Waves and variants of SARS-CoV-2: understanding the causes and effect of the COVID-19 catastrophe
Open accessAbstract
The coronavirus disease-19 has left a permanent mark on the history of the human race. Severe acute respiratory syndrome coronavirus-2 is a positive-sense single-stranded RNA virus, first reported in Wuhan, China, in December 2019 and from there took over the world. Being highly susceptible to mutations, the virus's numerous variants started to appear, and some were more lethal and infectious than the parent. The effectiveness of the vaccine is also affected severely against the new variant. In this study, the infectious mechanism of the coronavirus is explained with a focus on different variants and their respective mutations, which play a critical role in the increased transmissibility, infectivity, and immune escape of the virus. As India has already faced the second wave of the pandemic, the future outlook on the likeliness of a third wave with respect to the Indian variants such as kappa, delta, and Delta Plus is also discussed. This review article aims to reflect the catastrophe of the variants of SARS-CoV-2 and the possibility of developing even more severe variants in the near future.
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Claims the paper makes
21 of 36 cited sources checked · 7 supported · 0 flagged · accuracy not yet measured
- Background
Mutations in the RBD region are likely to disrupt antibody recognition.
“Mutations in the RBD region are likely to disrupt antibody recognition [53].”
Quote in the paperNot yet classified1 of 1 sources checked- cites [53] Wang R, Chen J, Gao K, et al. Vaccine-escape and fast-growing mutations in the United Kingdom, the United States, Singapore, Spain, India, and other COVID-19-devastated countries. Genomics. 2021;113:2158–70. source
- Finding
The D614G form is associated with a higher population of infection-capable open spike configurations and greater chance of ACE-2 binding.
“in the G614 form, due to the relaxation of tensile hydrogen bonds, a higher population of infection capable of open configurations results in higher chances of binding events with the host receptor ACE-2, thereby increasing the overall infectivity.”
Quote in the paperNot yet classified1 of 1 sources checked- cites [27] Mansbach RA, Chakraborty S, Nguyen K, et al. The SARS-CoV-2 spike variant D614G favors an open conformational state. Sci Adv. 2021;7(16):eabf3671. https://doi.org/10.1126/sciadv.abf3671. source
- Background
The spike protein enables viral entry into host cells through the ACE-2 receptor.
“The S gene encodes for the prominent homotrimeric, type I fusion and transmembrane glycoprotein which enables viral entry into the host target cell through the angiotensin-converting enzyme-2 (ACE-2) receptor [5, 6].”
Quote in the paperNot yet classified2 of 2 sources checked- cites [5] Tortorici MA, Veesler D. Structural insights into coronavirus entry. Adv Virus Res. 2019;105:93–116. source
The Introduction says spike promotes host attachment and membrane fusion during entry, and “Diversity of CoV receptors and entry mechanisms” identifies ACE2 as an entry receptor for SARS-CoV and HCoV-NL63. The same section describes other coronaviruses using different receptors, so the source does not support ACE2 as the entry receptor for coronaviruses generally. (LLM, conf=0.85)
Experimental — accuracy not yet measured - cites [6] Biswas S, Thakur V, Kaur P, et al. Blood clots in COVID-19 patients: Simplifying the curious mystery. Med Hypotheses. 2021;146:1371. source
- Finding
The paper says Lambda is more resistant to neutralization by convalescent sera and the Alpha variant than the parent D614G spike protein.
“The Lambda variant spike protein is found to be 3.3 times more resistant to neutralization by the convalescent sera than the parent D614G spike protein and 4.9 times to that of the Alpha variant ones.”
Quote in the paperNot yet classified1 of 1 sources checked- cites [55] Harvey WT, Carabelli AM, Jackson B, et al. SARS-CoV-2 variants, spike mutations and immune escape. Nat Rev Microbiol. 2021;19:409–24. source
The Variants of interest or concern section discusses modest reductions in neutralization of Alpha (B.1.1.7) by convalescent sera, but does not compare it with Lambda. Searches for Lambda and the claimed 3.3-fold and 4.9-fold comparisons found no passage addressing those results in our copy. (LLM, conf=0.76)
Experimental — accuracy not yet measured
- Finding
The Delta variant was first identified in Maharashtra, India, in October 2020 and is now found in more than 100 nations.
“The Delta (G/478 K.V1; B.1.617.2) variant, first identified in Maharashtra, India, in October 2020, is now found to be the dominant lineage detected in more than 100 nations and declared as VOC by the WHO on May 11, 2021 [74].”
Quote in the paperNot yet classified1 of 1 sources checked- cites [74] Bhutta ZA, Siddiqi S, Hafeez A, et al. Beyond the numbers: understanding the diversity of covid-19 epidemiology and response in South Asia. https://doi.org/10.1136/bmj.n1544. source
The 'How robust are the data?' section identifies Delta as B.1.617.2 and links its emergence and spread to India's spring 2021 surge. It does not say Delta was first identified in Maharashtra in October 2020 or found in more than 100 nations; it also does not substantiate the citing sentence's WHO designation date. (LLM, conf=0.83)
Experimental — accuracy not yet measured
- Finding
The Lambda variant originated in Peru in August 2020 and was declared a VOI by WHO on June 14, 2021.
“The Lambda (GR/452Q.V1) variant originated in Peru in August 2020 [49]. Previously known as C.37 or Andean variant, this could be a new emerging threat; therefore, WHO on June 14, 2021 declared this as a VOI [50].”
Quote in the paperNot yet classified1 of 2 sources checked- cites [49] Romero PE, Dávila-Barclay A, Salvatierra G, et al. The emergence of SARS-CoV-2 variant lambda (C.37) in South America. Microbiol Spectr. 2021. 9:e00789-21. https://doi.org/10.1128/Spectrum.00789-21. source
The Letter describes emergence in Peru as a hypothesis and says additional samples were being processed to confirm and date C.37’s origin. It reports the first Lima detection in December 2020, not an August 2020 origin. The WHO declaration is attached to a different citation in the citing sentence, so it is outside this verdict. (LLM, conf=0.87)
Experimental — accuracy not yet measured - cites [50] Weekly epidemiological update on COVID-19-29 June 2021, https://www.who.int/publications/m/item/weekly-epidemiological-update-on-covid-19---29-june-2021. Accessed 17 July 2021.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Background
The spike protein mediates entry into host cells by binding the ACE-2 receptor.
“The S gene encodes for the prominent homotrimeric, type I fusion and transmembrane glycoprotein which enables viral entry into the host target cell through the angiotensin-converting enzyme-2 (ACE-2) receptor [5, 6].”
Quote in the paperNot yet classified2 of 2 sources checked- cites [5] Tortorici MA, Veesler D. Structural insights into coronavirus entry. Adv Virus Res. 2019;105:93–116. source
The Introduction says the spike protein promotes host attachment and membrane fusion during entry. The section “Diversity of CoV receptors and entry mechanisms” identifies ACE2 as an entry receptor for SARS-CoV and HCoV-NL63, but also says other coronaviruses use different receptors. The unqualified claim that spike-mediated entry occurs through ACE2 is therefore broader than the source supports. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites [6] Biswas S, Thakur V, Kaur P, et al. Blood clots in COVID-19 patients: Simplifying the curious mystery. Med Hypotheses. 2021;146:1371. source
- Background
The paper says the pandemic is being driven by a competition between vaccination and newly emerging variants.
“Yet, this pandemic has become a race between effective vaccines and the new variants.”
Quote in the paperNot yet classified1 of 1 sources checked- cites [2] Mathieu E, Ritchie H, Ortiz-Ospina E, et al. A global database of COVID-19 vaccinations. Nat Hum Behav. 2021. https://doi.org/10.1038/S41562-021-01122-8 (Epub ahead of print 2021). source
The Discussion describes effective vaccines and asks whether their global rollout can proceed quickly enough to address the pandemic. It does not describe a race against newly emerging variants; variants appear in the title of a cited work in the References, not in the paper’s own account of the rollout. (LLM, conf=0.84)
Experimental — accuracy not yet measured
- Background
Membrane fusion is described as a key step required before viral entry into the host cell.
“The fusion of two membranes is the crucial step before the virus enters the host cell [11, 12].”
Quote in the paperNot yet classified1 of 2 sources checked- cites [11] Haque SM, Ashwaq O, Sarief A, et al. A comprehensive review about SARS-CoV-2. Future Virol. 2020;15:625. source
- cites [12] Moreira RA, Guzman HV, Boopathi S, et al. Characterization of structural and energetic differences between conformations of the SARS-CoV-2 spike protein. Materials (Basel). 2020;13:1–14.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Background
The receptor-binding domain directly contacts ACE-2 and contributes to host-cell attachment.
“RBD contains a core structure and a variable receptor-binding motif (RBM; 437–508 a.a.) which interacts and attaches with the host cell ACE-2 receptor (Fig. 2) [7].”
Quote in the paperNot yet classified1 of 1 sources checked- cites [7] Wan Y, Shang J, Graham R, et al. Receptor recognition by the novel coronavirus from Wuhan: an analysis based on decade-long structural studies of SARS Coronavirus. J Virol. 2020. https://doi.org/10.1128/JVI.00127-20 (Epub ahead of print 17 March 202). source
The Introduction (page unavailable) states that the SARS-CoV RBD has a core and an RBM that binds ACE2, and links RBD–ACE2 affinity to initial host-cell attachment. The Results model ACE2 recognition by the 2019-nCoV RBD. The cited sentence’s specific RBM range of amino acids 437–508 is not established in the passages from our copy. (LLM, conf=0.84)
Experimental — accuracy not yet measured
- Finding
The Lambda variant is described as having mutations that increase infectivity and immune escape.
“The L452Q and F490S mutations reported in the RBD region have been shown to increase the viral infectivity, rendering the virus more infectious and able to escape immune response from specific monoclonal antibodies [51, 52] or disrupt the ability of vaccine-generated antibodies to recognize the variant [53].”
Quote in the paperNot yet classified3 of 3 sources checked- cites [51] Deng X, Garcia-Knight MA, Khalid MM, et al. Transmission, infectivity, and neutralization of a spike L452R SARS-CoV-2 variant. Cell. 2021;184:3426-3437.e8. source
The Results section (page unavailable) reports a twofold reduction in neutralization by vaccine-recipient plasma against B.1.429, supporting a limited claim about reduced vaccine-antibody activity. The study concerns a California variant with L452R, not the Lambda variant or its L452Q and F490S mutations; it does not establish that vaccine-generated antibodies cannot recognize Lambda. (LLM, conf=0.87)
Experimental — accuracy not yet measured - cites [52] Greaney AJ, Starr TN, Gilchuk P, et al. Complete mapping of mutations to the SARS-CoV-2 spike receptor-binding domain that escape antibody recognition. Cell Host Microbe. 2021;29:44-57.e9. source
The Results section ('Mapping Escape from Each of 10 Human Monoclonal Antibodies'; page unavailable) reports that many mutations at site 490 confer escape from a specific monoclonal antibody. It does not identify F490S or L452Q as causing escape, or show that either mutation increases infectivity; the passages also do not describe the Lambda variant. (LLM, conf=0.81)
Experimental — accuracy not yet measured - cites [53] Wang R, Chen J, Gao K, et al. Vaccine-escape and fast-growing mutations in the United Kingdom, the United States, Singapore, Spain, India, and other COVID-19-devastated countries. Genomics. 2021;113:2158–70. source
In Results (‘Impacts of SARS-CoV-2 spike RBD mutations on COVID-19 vaccines’; page unavailable), Table 4 identifies F490S as a predicted vaccine-escape mutation, and the infectivity Results suggest it may lead to more infectious variants. The paper does not establish escape from vaccine-generated antibodies in vaccinated people, nor does it identify L452Q or the Lambda variant; the citing sentence presents the predicted effect more definitively than the source does. (LLM, conf=0.87)
Experimental — accuracy not yet measured
- Background
Widespread ACE-2 expression in multiple organs is described as a reason SARS-CoV-2 can infect tissues beyond the lungs.
“The widespread presence of ACE-2 receptors in different organs facilitates the extrapulmonary infection by SARS-CoV-2, causing associated complications such as acute respiratory distress syndrome (ARDS), cytokine storm, blood clots [6, 9], and possibly psychological and neurological problems [10].”
Quote in the paperNot yet classified2 of 3 sources checked- cites [6] Biswas S, Thakur V, Kaur P, et al. Blood clots in COVID-19 patients: Simplifying the curious mystery. Med Hypotheses. 2021;146:1371. sourceExperimental — accuracy not yet measured
- cites [9] Thakur V, Ratho RK, Kumar P, et al. Multi-Organ Involvement in COVID-19: beyond pulmonary manifestations. J Clin Med. 2021;10:446. sourceExperimental — accuracy not yet measured
- cites [10] Thakur V, Jain A. COVID 2019-suicides: A global psychological pandemic. Brain Behav Immun. 2020;88:952. source
- Finding
The Alpha variant is described as increasing severity and death risk, with several mutations affecting binding and cleavage.
“This Alpha variant increased its severity (40–80%) through the air pathway and the associated case fatality is expected to be 55% higher with a higher death rate [60, 61].”
Quote in the paperNot yet classified1 of 2 sources checked- cites [60] Horby P, Bell I, Breuer J, et al. NERVTAG: Update note on B.1.1.7 severity, 11 February 2021 - GOV.UK. https://www.gov.uk/government/publications/nervtag-update-note-on-b117-severity-11-february-2021.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [61] Vasireddy D, Vasireddy D, Vanaparthy R, et al. Review of COVID-19 Variants and COVID-19 Vaccine Efficacy: What the Clinician Should Know? J Clin Med Res. 2021;13:317–25. source
The UK variant (B.1.1.7) section reports approximately 55% higher mortality and an increased death rate. But its 40–80% figure describes transmissibility, not severity; it links N501Y to tighter binding but does not say an Alpha mutation affects cleavage. Page numbers are unavailable in our copy. (LLM, conf=0.90)
Experimental — accuracy not yet measured
- Finding
The Delta variant is described as the dominant lineage in more than 100 countries and as driving the second wave in India.
“The Delta (G/478 K.V1; B.1.617.2) variant, first identified in Maharashtra, India, in October 2020, is now found to be the dominant lineage detected in more than 100 nations and declared as VOC by the WHO on May 11, 2021 [74]. Delta strain drives the second wave in India, where almost 4-lakh cases were reported per day.”
Quote in the paperNot yet classified1 of 1 sources checked- cites [74] Bhutta ZA, Siddiqi S, Hafeez A, et al. Beyond the numbers: understanding the diversity of covid-19 epidemiology and response in South Asia. https://doi.org/10.1136/bmj.n1544. source
In “How robust are the data?” (page not specified), the paper relates India’s spring 2021 surge to the emergence and spread of Delta, supporting the second-wave point. It does not say Delta was the dominant lineage in more than 100 countries; the claim also states the variant’s role in India more categorically than the paper does. (LLM, conf=0.87)
Experimental — accuracy not yet measured
- Background
The authors say that immune evasion can arise in chronically infected immunocompromised patients under treatment with immune plasma or monoclonal antibodies.
“The possible theories about the origin of novel variants are the evolution of circulating intermediate mutants in the chronically infected immunocompromised patients supporting high viral replication while on treatment with immune plasma or monoclonal antibodies [88, 89].”
Quote in the paperNot yet classified2 of 2 sources checked- cites [88] Choi B, Choudhary MC, Regan J, et al. Persistence and Evolution of SARS-CoV-2 in an Immunocompromised Host. N Engl J Med. 2020;383:2291–3. source
The main text reports persistent infection, high viral loads, and accelerated viral evolution in one immunocompromised patient, who later received a SARS-CoV-2 antibody cocktail. It does not report immune-plasma treatment or establish immune evasion, the origin of novel variants, or that antibody treatment drove the observed evolution. The indexed copy gives no page number. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites [89] Sa K, Da C, Rp D, et al. SARS-CoV-2 evolution during treatment of chronic infection. Nature. 2021;592:277–82. source
The Discussion (page not available) reports viral evolution during persistent infection in an immunocompromised patient treated with convalescent plasma, with evidence of reduced antibody susceptibility. The paper tested monoclonal antibodies in the laboratory but does not report monoclonal-antibody treatment of the patient; it also presents a single case, not an established explanation for the origin of novel variants. (LLM, conf=0.88)
Experimental — accuracy not yet measured
- Finding
Delta Plus variants AY.1 and AY.2 have become a new cause of global concern and may contribute to a third wave in India.
“Delta Plus variants known as AY.1 (B.1.617.2.1) and AY.2 (B.1.617.2.2) have now become a new cause of global concern.”
Quote in the paperNot yet classified - Finding
Delta strain drives the second wave in India.
“Delta strain drives the second wave in India, where almost 4-lakh cases were reported per day.”
Quote in the paperNot yet classified - Finding
Pfizer-BioNTech and Moderna vaccines showed decreased neutralization against Gamma variants.
“BNT162b/2 and mRNA-1273 mRNA-based vaccines showed decreased neutralization in Gamma variants.”
Quote in the paperNot yet classified - Finding
The Delta Plus variant has increased transmissibility, stronger binding to lung-cell receptors, and potential to reduce monoclonal antibody response.
“The Delta Plus variant has increased transmissibility, causes stronger binding to receptors of lung cells, and has the potential of reducing monoclonal antibody response.”
Quote in the paperNot yet classified - Finding
The Beta variant was identified in South Africa in October 2020 and showed a 50% increase in transmission.
“The Beta (B.1.351; GH/501Y.V2) variant was identified in Cape province of South Africa in October 2020 with 17 critical mutations, showing a 50% increase in transmission [67].”
Quote in the paperNot yet classified0 of 1 sources checked- cites [67] Estimates of severity and transmissibility of novel SARS-CoV-2 variant 501Y.V2 in South Africa | CMMID Repository, https://cmmid.github.io/topics/covid19/sa-novel-variant.html. Accessed 10 July 2021.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Finding
The Gamma variant was found responsible for reinfection in São Paulo State and for the second wave in Brazil.
“The Gamma variant was found to be responsible for the re-infection in São Paulo State and caused the second wave in Brazil [42].”
Quote in the paperNot yet classified0 of 1 sources checked- cites [42] Chakraborty C, Bhattacharya M, Sharma AR. Present variants of concern and variants of interest of severe acute respiratory syndrome coronavirus 2: Their significant mutations in S-glycoprotein, infectivity, re-infectivity, immune escape and vaccines activity. Rev Med Virol. 2021; p. e2270. source
- Finding
Vaccines have lower efficacy against Beta strains than against earlier variants.
“The majority of the vaccines have lower efficacy against Beta strains.”
Quote in the paperNot yet classified - Finding
The paper argues that SARS-CoV-2 variants and their spike mutations are critical drivers of increased transmissibility, infectivity, and immune escape.
“different variants and their respective mutations, which play a critical role in the increased transmissibility, infectivity, and immune escape of the virus.”
Quote in the paperNot yet classified - Finding
The paper states that current vaccines are ineffective against the new variants because no other mutations are involved in immune escape.
“The existing vaccines are ineffective against the new variants, and the reason is no other mutations are involved in immune escape.”
Quote in the paperNot yet classified0 of 1 sources checked- cites [42] Chakraborty C, Bhattacharya M, Sharma AR. Present variants of concern and variants of interest of severe acute respiratory syndrome coronavirus 2: Their significant mutations in S-glycoprotein, infectivity, re-infectivity, immune escape and vaccines activity. Rev Med Virol. 2021; p. e2270. source
- Finding
The Lambda variant is suspected to be more transmissible than the original virus and shows greater infectivity than Alpha and Gamma.
“This is suspected to be more transmissible than the original virus and is a matter of great concern, as this has been detected in the UK and other European countries. Studies have shown the greater infectivity of Lambda variants in comparison to Alpha and Gamma variants of the VOC category.”
Quote in the paperNot yet classified - Finding
The virus is highly susceptible to mutations, leading to many variants that can be more lethal and infectious than the parent strain.
“Being highly susceptible to mutations, the virus's numerous variants started to appear, and some were more lethal and infectious than the parent.”
Quote in the paperNot yet classified - Finding
The authors say the new variants may create a need to replace current vaccines quickly.
“There is no doubt that new variants evolved to have the characteristics of the immune escape, which may likely create the requirement to replace the current vaccines quickly.”
Quote in the paperNot yet classified - Finding
The Beta variant is reported to have increased transmission and mutations that help it evade neutralizing antibodies.
“The Beta (B.1.351; GH/501Y.V2) variant was identified in Cape province of South Africa in October 2020 with 17 critical mutations, showing a 50% increase in transmission [67].”
Quote in the paperNot yet classified0 of 1 sources checked- cites [67] Estimates of severity and transmissibility of novel SARS-CoV-2 variant 501Y.V2 in South Africa | CMMID Repository, https://cmmid.github.io/topics/covid19/sa-novel-variant.html. Accessed 10 July 2021.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Finding
The paper says Delta Plus has increased transmissibility and stronger binding to lung-cell receptors.
“The Delta Plus variant has increased transmissibility, causes stronger binding to receptors of lung cells, and has the potential of reducing monoclonal antibody response.”
Quote in the paperNot yet classified - Finding
The conclusion states that the new variants carry critical spike mutations that make them more transmissible, infectious, spreadable, and lethal.
“The new variants are loaded with various critical mutations in the spike protein, making them more transmissible, infective, spreadable, and lethal.”
Quote in the paperNot yet classified - Finding
The Gamma variant is said to have caused reinfection in São Paulo State and the second wave in Brazil.
“The Gamma variant was found to be responsible for the re-infection in São Paulo State and caused the second wave in Brazil [42].”
Quote in the paperNot yet classified0 of 1 sources checked- cites [42] Chakraborty C, Bhattacharya M, Sharma AR. Present variants of concern and variants of interest of severe acute respiratory syndrome coronavirus 2: Their significant mutations in S-glycoprotein, infectivity, re-infectivity, immune escape and vaccines activity. Rev Med Virol. 2021; p. e2270. source
- Background
Furin preactivation and proteolysis are required for fusion of the viral and host cell membranes.
“Preactivation and proteolysis by furin are required for the fusion of viral membranes and host cell membranes.”
Quote in the paperNot yet classified - Background
SARS-CoV-2 is the etiological agent responsible for the COVID-19 pandemic that originated in Wuhan, China, in early December 2019.
“Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the etiological agent responsible for this pandemic which originated in Wuhan, China, in early December 2019.”
Quote in the paperNot yet classified - Background
The Alpha variant was first identified in the UK in November 2020.
“The Alpha variant was first identified in the UK in November 2020 from a 58-year-old male [59].”
Quote in the paperNot yet classified0 of 1 sources checked- cites [59] Weekly epidemiological update - 2 February 2021, https://www.who.int/publications/m/item/weekly-epidemiological-update---2-february-2021. Accessed 17 July 2021.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Background
SARS-CoV-2 is susceptible to a high rate of mutations, which leads to the evolution of variants in a shorter period than anticipated.
“Being an RNA virus in nature, SARS-CoV-2 is susceptible to a high rate of mutations, leading to the evolution of various variants in a shorter period than anticipated.”
Quote in the paperNot yet classified - Background
Variants of interest are predicted to affect transmission, reduce therapeutic efficiency and antibody neutralization, and increase disease severity.
“SARS-CoV-2 variants have specific genetic markers that have been predicted to affect virus transmission, reduce therapeutics efficiency and neutralization capacity by antibodies or immune evasion, and increase disease severity [35].”
Quote in the paperNot yet classified0 of 1 sources checked- cites [35] SARS-CoV-2 Variant Classifications and Definitions, https://www.cdc.gov/coronavirus/2019-ncov/variants/variant-info.html. Accessed 10 July 2021.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Method
INSACOG was established in India to monitor genomic variations in SARS-CoV-2.
“Govt. of India established Indian SARS-CoV-2 Genomics Consortium (INSACOG) on 30th December 2020, currently working with the capacity of 28 Genome Sequencing Laboratories (GSLs) to monitor genomic variations in SARS-CoV-2 [103].”
Quote in the paperNot yet classified0 of 1 sources checked- cites [103] Indian SARS-CoV-2 Genomics Consortium (INSACOG) | Department of Biotechnology, https://dbtindia.gov.in/insacog. Accessed 10 July 2021.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Background
SARS-CoV-2 is presented as the causative agent of the COVID-19 pandemic, which began in Wuhan in late 2019 and spread worldwide.
“Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the etiological agent responsible for this pandemic which originated in Wuhan, China, in early December 2019.”
Quote in the paperNot yet classified - Method
The paper recommends standard public-health precautions such as masks, handwashing, ventilation, distancing, and vaccination.
“Generally, precautions at the personal level include the use of masks in crowded places, regular hand washing, and better ventilation in indoor spaces.”
Quote in the paperNot yet classified - Background
The paper reports that the existing vaccines are ineffective against new variants and links this to immune escape.
“The existing vaccines are ineffective against the new variants, and the reason is no other mutations are involved in immune escape.”
Quote in the paperNot yet classified - Background
The authors report that SARS-CoV-2 can mutate rapidly because it is an RNA virus, which leads to many variants appearing in a short time.
“Being an RNA virus in nature, SARS-CoV-2 is susceptible to a high rate of mutations, leading to the evolution of various variants in a shorter period than anticipated.”
Quote in the paperNot yet classified - Background
The Delta Plus sublineages are described as having mutations that increase attachment, immune evasion, and transmissibility.
“In addition to three mutations, E484Q, L452R, and P614R, these new sub-lineages have additional K417N mutations in the spike proteins that enhance virus attachment to the infected cells and have immune evasion properties as in the Beta variant (B.1.351 lineage).”
Quote in the paperNot yet classified - Background
The paper states that variants of interest are expected to affect transmission, antibody neutralization, therapeutic efficacy, and disease severity.
“SARS-CoV-2 variants have specific genetic markers that have been predicted to affect virus transmission, reduce therapeutics efficiency and neutralization capacity by antibodies or immune evasion, and increase disease severity [35].”
Quote in the paperNot yet classified0 of 1 sources checked- cites [35] SARS-CoV-2 Variant Classifications and Definitions, https://www.cdc.gov/coronavirus/2019-ncov/variants/variant-info.html. Accessed 10 July 2021.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Method
India established INSACOG to monitor genomic variation in SARS-CoV-2 using genome-sequencing laboratories.
“To counteract the unprecedented public health challenge, Govt. of India established Indian SARS-CoV-2 Genomics Consortium (INSACOG) on 30th December 2020, currently working with the capacity of 28 Genome Sequencing Laboratories (GSLs) to monitor genomic variations in SARS-CoV-2 [103].”
Quote in the paperNot yet classified0 of 1 sources checked- cites [103] Indian SARS-CoV-2 Genomics Consortium (INSACOG) | Department of Biotechnology, https://dbtindia.gov.in/insacog. Accessed 10 July 2021.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Background
Alpha, Beta, Gamma, and Delta are described as the four variants of concern responsible for later waves of the pandemic.
“There are four variants of concern, i.e. Alpha, Beta, Gamma, and Delta variants distributed throughout the globe and responsible for a second and third wave of the pandemic.”
Quote in the paperNot yet classified0 of 1 sources checked- cites [58] About Variants of the Virus that Causes COVID-19 | CDC, https://www.cdc.gov/coronavirus/2019-ncov/variants/variant.html. Accessed 10 July 2021.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Background
The paper argues that furin cleavage and preactivation are required for viral and host membrane fusion.
“Preactivation and proteolysis by furin are required for the fusion of viral membranes and host cell membranes.”
Quote in the paperNot yet classified
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Blanket vaccine-ineffectiveness claim conflicts with reported Delta efficacy
MinorThe paper says existing vaccines are ineffective against new variants, yet elsewhere reports substantial effectiveness for two vaccines against Delta.
“The existing vaccines are ineffective against the new variants”
“The Pfizer-BioNTech and Oxford-AstraZeneca were 88% and 60% effective against the SARS-CoV-2 Delta variant, 2 weeks after the second dose.”
Delta mutation count disagrees with its list
MinorThe paper states that Delta has 13 spike-protein mutations, but the accompanying list contains 14 entries.
“13 mutations are present in spike protein”
“T19R, G142D, 156del, 157del, R158G, L452R, T478K, D614G, P681R, D950R, P871R, T95I, A222V*, and K417N*”
VOI count disagrees with the named list
MinorThe paper refers to five variants of interest, but its named VOI list contains six.
“D614G is the only substitution mutation that is present in all the five VOI and four VOC”
“Epsilon, Eta, Iota, Kappa, Zeta, and Lambda are the variants of interest circulating throughout the world.”
Cited works that were retracted
Works this paper cites that were later retracted, from the retraction notices publishers deposit. Major when the notice came out before this paper was published.
Cites a retracted work: 10.1016/j.bbi.2020.04.062
InfoThe cited work was retracted on 2023-12-09 (notice 10.1016/j.bbi.2023.10.024), not before this paper was published (2021-12-16).
Cited work 10.1016/j.bbi.2020.04.062 · retracted 2023-12-09 · notice 10.1016/j.bbi.2023.10.024 · this paper published 2021-12-16
“The widespread presence of ACE-2 receptors in different organs facilitates the extrapulmonary infection by SARS-CoV-2, causing associated complications such as acute respiratory distress syndrome (ARDS), cytokine storm, blood clots [6, 9], and possibly psychological and neurological problems [10].”
Cites
1 retracted
REMOVED: COVID 2019-suicides: A global psychological pandemic
Thakur, V., & Jain, A. (2020) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2020.04.062 · Cited by 380 · cited 1× · see citing works
“The widespread presence of ACE-2 receptors in different organs facilitates the extrapulmonary infection by SARS-CoV-2, causing associated complications such as acute respiratory distress syndrome (ARDS), cytokine storm, blood clots [6, 9], and possibly psychological and neurological problems [10].”
BackgroundSelf-citationRetractedA pneumonia outbreak associated with a new coronavirus of probable bat origin
Zhou, P., Yang, X.-L., Wang, X.-G., Hu, B., Zhang, L., Zhang, W., Si, H.-R., Zhu, Y., Li, B., Huang, C.-L., et al. (2020) · Nature · doi:10.1038/s41586-020-2012-7 · Cited by 21,969 · cited 1× · see citing works
“96% of genome identity with horseshoe bat virus RaTG13 Rhinolophus affinis [3].”
BackgroundHoffmann, M., Kleine-Weber, H., Schroeder, S., Krüger, N., Herrler, T., Erichsen, S., Schiergens, T. S., Herrler, G., Wu, N.-H., Nitsche, A., et al. (2020) · Cell · doi:10.1016/j.cell.2020.02.052 · Cited by 20,286 · cited 2× · see citing works
“The ACE-2 receptors are normally expressed in type II pneumocytes in the alveoli, nasal mucosa, epithelial cells of lungs, kidney, and heart, enterocytes of the small intestine, and endothelial cells of blood vessels, making them vulnerable to SARS-CoV-2 [8].”
BackgroundCryo-EM structure of the 2019-nCoV spike in the prefusion conformation
Wrapp, D., Wang, N., Corbett, K. S., Goldsmith, J. A., Hsieh, C.-L., Abiona, O., Graham, B. S., & McLellan, J. S. (2020) · Science · doi:10.1126/science.abb2507 · Cited by 8,897 · cited 1× · see citing works
“The S2 subunit is composed of a fusion peptide (FP), heptapeptide domains 1 and 2 (HPD1, HPD2), transmembrane domain (TM), and cytoplasm domain (CD) and is involved in membrane fusion [14].”
BackgroundU1 snRNP regulates cancer cell migration and invasion in vitro
Oh, J.-M., Venters, C. C., Di, C., Pinto, A. M., Wan, L., Younis, I., Cai, Z., Arai, C., So, B. R., Duan, J., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-13993-7 · Cited by 7,157 · see citing works
WHO Coronavirus Disease (COVID-19) Dashboard
(2020) · Bangladesh Physiotherapy Journal · doi:10.46945/bpj.10.1.03.01 · Cited by 5,545 · see citing works
The proximal origin of SARS-CoV-2
Andersen, K. G., Rambaut, A., Lipkin, W. I., Holmes, E. C., & Garry, R. F. (2020) · Nature Medicine · doi:10.1038/s41591-020-0820-9 · Cited by 5,081 · see citing works
Wan, Y., Shang, J., Graham, R., Baric, R. S., & Li, F. (2020) · Journal of Virology · doi:10.1128/jvi.00127-20 · Cited by 4,341 · see citing works
Korber, B., Fischer, W. M., Gnanakaran, S., Yoon, H., Theiler, J., Abfalterer, W., Hengartner, N., Giorgi, E. E., Bhattacharya, T., Foley, B., et al. (2020) · Cell · doi:10.1016/j.cell.2020.06.043 · Cited by 4,281 · cited 1× · see citing works
“D–G substitution in the C-terminal region of the S1 domain of spike protein [23] (Fig.”
BackgroundSARS-CoV-2 variants, spike mutations and immune escape
Harvey, W. T., Carabelli, A. M., Jackson, B., Gupta, R. K., Thomson, E. C., Harrison, E. M., Ludden, C., Reeve, R., Rambaut, A., COVID-19 Genomics UK (COG-UK) Consortium, et al. (2021) · Nature Reviews Microbiology · doi:10.1038/s41579-021-00573-0 · Cited by 3,528 · cited 1× · see citing works
“D614G is again associated with the increase in transmissibility, infectivity, and viral load, making the Lambda variant even more lethal [55].”
BackgroundChan, J. F., Kok, K., Zhu, Z., Chu, H., To, K. K., Yuan, S., & Yuen, K. (2020) · Emerging Microbes & Infections · doi:10.1080/22221751.2020.1719902 · Cited by 3,063 · cited 1× · see citing works
“The SARS-CoV-2 genome of 30,000 nucleotides includes 5’UTR, followed by ORF1a and ORF1ab, four structural genes (spike S, envelope E, membrane M, nucleocapsid N), accessory proteins, and 3 ́ UTR with poly-A tail [4].”
BackgroundEstimated transmissibility and impact of SARS-CoV-2 lineage B.1.1.7 in England
Davies, N. G., Abbott, S., Barnard, R. C., Jarvis, C. I., Kucharski, A. J., Munday, J. D., Pearson, C. A. B., Russell, T. W., Tully, D. C., Washburne, A. D., et al. (2021) · Science · doi:10.1126/science.abg3055 · Cited by 2,633 · see citing works
Estimated transmissibility and impact of SARS-CoV-2 lineage B.1.1.7 in England
Davies, N. G., Abbott, S., Barnard, R. C., Jarvis, C. I., Kucharski, A. J., Munday, J. D., Pearson, C. A. B., Russell, T. W., Tully, D. C., Washburne, A. D., et al. (2020) · doi:10.1101/2020.12.24.20248822 · Cited by 2,557 · see citing works
Tegally, H., Wilkinson, E., Giovanetti, M., Iranzadeh, A., Fonseca, V., Giandhari, J., Doolabh, D., Pillay, S., San, E. J., Msomi, N., et al. (2020) · doi:10.1101/2020.12.21.20248640 · Cited by 2,535 · see citing works
A global database of COVID-19 vaccinations
Mathieu, E., Ritchie, H., Ortiz-Ospina, E., Roser, M., Hasell, J., Appel, C., Giattino, C., & Rodés-Guirao, L. (2021) · Nature Human Behaviour · doi:10.1038/s41562-021-01122-8 · Cited by 1,974 · cited 1× · see citing works
“54 billion people have already been vaccinated with at least one dose of the SARSCoV-2 vaccine irrespective of the brand name [2].”
BackgroundStarr, T. N., Greaney, A. J., Hilton, S. K., Ellis, D., Crawford, K. H. D., Dingens, A. S., Navarro, M. J., Bowen, J. E., Tortorici, M. A., Walls, A. C., et al. (2020) · Cell · doi:10.1016/j.cell.2020.08.012 · Cited by 1,956 · see citing works
Isolation and characterization of a bat SARS-like coronavirus that uses the ACE2 receptor
Ge, X.-Y., Li, J.-L., Yang, X.-L., Chmura, A. A., Zhu, G., Epstein, J. H., Mazet, J. K., Hu, B., Zhang, W., Peng, C., et al. (2013) · Nature · doi:10.1038/nature12711 · Cited by 1,778 · see citing works
Spike mutation D614G alters SARS-CoV-2 fitness
Plante, J. A., Liu, Y., Liu, J., Xia, H., Johnson, B. A., Lokugamage, K. G., Zhang, X., Muruato, A. E., Zou, J., Fontes-Garfias, C. R., et al. (2021) · Nature · doi:10.1038/s41586-020-2895-3 · Cited by 1,558 · cited 1× · see citing works
“[26] studied replication kinetics of the D614G variant in human lung epithelial cell line Calu-3 and found 2.”
BackgroundGenomics and epidemiology of the P.1 SARS-CoV-2 lineage in Manaus, Brazil
Faria, N. R., Mellan, T. A., Whittaker, C., Claro, I. M., Candido, D. D. S., Mishra, S., Crispim, M. A. E., Sales, F. C. S., Hawryluk, I., McCrone, J. T., et al. (2021) · Science · doi:10.1126/science.abh2644 · Cited by 1,461 · see citing works
The Impact of Mutations in SARS-CoV-2 Spike on Viral Infectivity and Antigenicity
Li, Q., Wu, J., Nie, J., Zhang, L., Hao, H., Liu, S., Zhao, C., Zhang, Q., Liu, H., Nie, L., et al. (2020) · Cell · doi:10.1016/j.cell.2020.07.012 · Cited by 1,420 · cited 1× · see citing works
“Being a glycosylated protein, the mutations and the site-specific glycans on infection and immune response play a vital role in anticipating the future of the COVID-19 disease [20].”
BackgroundSARS-CoV-2 spike-protein D614G mutation increases virion spike density and infectivity
Zhang, L., Jackson, C. B., Mou, H., Ojha, A., Peng, H., Quinlan, B. D., Rangarajan, E. S., Pan, A., Vanderheiden, A., Suthar, M. S., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-19808-4 · Cited by 1,387 · cited 1× · see citing works
“[24] reported a more efficient entry of pseudovirus SG614 with less S1 domain shedding in ACE-2 expressing cells.”
BackgroundMultiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity
Garcia-Beltran, W. F., Lam, E. C., St. Denis, K., Nitido, A. D., Garcia, Z. H., Hauser, B. M., Feldman, J., Pavlovic, M. N., Gregory, D. J., Poznansky, M. C., et al. (2021) · Cell · doi:10.1016/j.cell.2021.03.013 · Cited by 1,353 · see citing works
mRNA vaccine-elicited antibodies to SARS-CoV-2 and circulating variants
Wang, Z., Schmidt, F., Weisblum, Y., Muecksch, F., Barnes, C. O., Finkin, S., Schaefer-Babajew, D., Cipolla, M., Gaebler, C., Lieberman, J. A., et al. (2021) · Nature · doi:10.1038/s41586-021-03324-6 · Cited by 1,343 · cited 13× · see citing works
“This variant has substitutions in the spike glycoprotein at A67V, E484K, D614G, Q677H, and F888L with three deletions at 69Hdel, 70Vdel, and 144del [42].”
BackgroundInfluentialEfficacy of the ChAdOx1 nCoV-19 Covid-19 Vaccine against the B.1.351 Variant
Madhi, S. A., Baillie, V., Cutland, C. L., Voysey, M., Koen, A. L., Fairlie, L., Padayachee, S. D., Dheda, K., Barnabas, S. L., Bhorat, Q. E., et al. (2021) · New England Journal of Medicine · doi:10.1056/nejmoa2102214 · Cited by 1,257 · see citing works
Persistence and Evolution of SARS-CoV-2 in an Immunocompromised Host
Choi, B., Choudhary, M. C., Regan, J., Sparks, J. A., Padera, R. F., Qiu, X., Solomon, I. H., Kuo, H.-H., Boucau, J., Bowman, K., et al. (2020) · New England Journal of Medicine · doi:10.1056/nejmc2031364 · Cited by 1,246 · cited 1× · see citing works
“The possible theories about the origin of novel variants are the evolution of circulating intermediate mutants in the chronically infected immunocompromised patients supporting high viral replication while on treatment with immune plasma or monoclonal antibodies [88, 89].”
BackgroundGreaney, A. J., Loes, A. N., Crawford, K. H. D., Starr, T. N., Malone, K. D., Chu, H. Y., & Bloom, J. D. (2021) · Cell Host & Microbe · doi:10.1016/j.chom.2021.02.003 · Cited by 1,178 · see citing works
Greaney, A. J., Loes, A. N., Crawford, K. H. D., Starr, T. N., Malone, K. D., Chu, H. Y., & Bloom, J. D. (2021) · doi:10.1101/2020.12.31.425021 · Cited by 1,178 · cited 1× · see citing works
“This variant has substitutions in the spike protein at T95I, G142D, E154K, D614G, P681R, Q1071H, and L452R, E484Q in its RBD region, which may provide this variant reduced resistance to neutralization by post-vaccination sera [47].”
BackgroundThe Molecular Biology of Coronaviruses
Lai, M. M. C., & Cavanagh, D. R. (1997) · Advances in virus research · doi:10.1016/s0065-3527(08)60286-9 · Cited by 1,153 · see citing works
Naqvi, A. A. T., Fatima, K., Mohammad, T., Fatima, U., Singh, I. K., Singh, A. K., Atif, S. M., Hariprasad, G., Hasan, G. M., & Hassan, M. I. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2020.165878 · Cited by 1,118 · cited 1× · see citing works
“Non-covalently bound S1 and S2 subunits in the pre-fusion state facilitate binding to the host receptor [15].”
BackgroundSARS-CoV-2 evolution during treatment of chronic infection
Kemp, S. A., Collier, D. A., Datir, R. P., Ferreira, I. A. T. M., Gayed, S., Jahun, A., Hosmillo, M., Rees-Spear, C., Mlcochova, P., Lumb, I. U., et al. (2021) · Nature · doi:10.1038/s41586-021-03291-y · Cited by 1,097 · see citing works
Transmission of SARS-CoV-2 on mink farms between humans and mink and back to humans
Munnink, B. B. O., Sikkema, R. S., Nieuwenhuijse, D. F., Molenaar, R. J., Münger, E., Molenkamp, R., van der Spek, A. N., Tolsma, P., Rietveld, A., Brouwer, M., et al. (2020) · Science · doi:10.1126/science.abe5901 · Cited by 1,087 · see citing works
Greaney, A. J., Starr, T. N., Gilchuk, P., Zost, S. J., Binshtein, E., Loes, A. N., Hilton, S. K., Huddleston, J., Eguia, R., Crawford, K. H. D., et al. (2021) · Cell Host & Microbe · doi:10.1016/j.chom.2020.11.007 · Cited by 1,016 · see citing works
Yang, Y., Islam, M. S., Wang, J., Li, Y., & Chen, X. (2020) · International Journal of Biological Sciences · doi:10.7150/ijbs.45538 · Cited by 965 · cited 1× · see citing works
“China treated 85% of the COVID-19 patients using traditional medicines such as root extract of Isatis indigotica and extract of Houttuynia cordata [99, 100].”
BackgroundEffectiveness of the BNT162b2 Covid-19 Vaccine against the B.1.1.7 and B.1.351 Variants
Abu-Raddad, L. J., Chemaitelly, H., & Butt, A. A. (2021) · New England Journal of Medicine · doi:10.1056/nejmc2104974 · Cited by 899 · cited 1× · see citing works
“Pfizer vaccine showed only 75% efficacy [84], whereas AstraZeneca AZD1222 vaccine failed in preventing even mild and moderate COVID-19 infection in South African trials [85, 86].”
ResultSARS-CoV-2: Structure, Biology, and Structure-Based Therapeutics Development
Wang, M.-Y., Zhao, R., Gao, L.-J., Gao, X.-F., Wang, D.-P., & Cao, J.-M. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.587269 · Cited by 874 · cited 1× · see citing works
“During transition from the close to open (upstate) configuration, RBM is up and receptor-accessible conformation enables the binding to the ACE-2 receptor, which is associated with the strong receptor [21].”
BackgroundStructural insights into coronavirus entry
(2019) · Advances in Virus Research · doi:10.1016/bs.aivir.2019.08.002 · Cited by 769 · cited 1× · see citing works
“The S gene encodes for the prominent homotrimeric, type I fusion and transmembrane glycoprotein which enables viral entry into the host target cell through the angiotensin-converting enzyme-2 (ACE-2) receptor [5, 6].”
BackgroundResurgence of COVID-19 in Manaus, Brazil, despite high seroprevalence
Sabino, E. C., Buss, L. F., Carvalho, M. P. S., Prete, C. A., Crispim, M. A. E., Fraiji, N. A., Pereira, R. H. M., Parag, K. V., da Silva Peixoto, P., Kraemer, M. U. G., et al. (2021) · The Lancet · doi:10.1016/s0140-6736(21)00183-5 · Cited by 758 · see citing works
SARS-CoV-2 B.1.1.7 sensitivity to mRNA vaccine-elicited, convalescent and monoclonal antibodies
Collier, D. A., De Marco, A., Ferreira, I. A. T. M., Meng, B., Datir, R., Walls, A. C., Kemp S, S. A., Bassi, J., Pinto, D., Fregni, C. S., et al. (2021) · doi:10.1101/2021.01.19.21249840 · Cited by 729 · see citing works
Sensitivity of SARS-CoV-2 B.1.1.7 to mRNA vaccine-elicited antibodies
Collier, D. A., De Marco, A., Ferreira, I. A. T. M., Meng, B., Datir, R. P., Walls, A. C., Kemp, S. A., Bassi, J., Pinto, D., Silacci-Fregni, C., et al. (2021) · Nature · doi:10.1038/s41586-021-03412-7 · Cited by 728 · see citing works
Liu, Z., VanBlargan, L. A., Bloyet, L.-M., Rothlauf, P. W., Chen, R. E., Stumpf, S., Zhao, H., Errico, J. M., Theel, E. S., Liebeskind, M. J., et al. (2021) · Cell Host & Microbe · doi:10.1016/j.chom.2021.01.014 · Cited by 725 · see citing works
Transmission, infectivity, and neutralization of a spike L452R SARS-CoV-2 variant
Deng, X., Garcia-Knight, M. A., Khalid, M. M., Servellita, V., Wang, C., Morris, M. K., Sotomayor-González, A., Glasner, D. R., Reyes, K. R., Gliwa, A. S., et al. (2021) · Cell · doi:10.1016/j.cell.2021.04.025 · Cited by 651 · see citing works
Deng, X., Garcia-Knight, M. A., Khalid, M. M., Servellita, V., Wang, C., Morris, M. K., Sotomayor-González, A., Glasner, D. R., Reyes, K. R., Gliwa, A. S., et al. (2021) · doi:10.1101/2021.03.07.21252647 · Cited by 651 · see citing works
Increased resistance of SARS-CoV-2 variant P.1 to antibody neutralization
Wang, P., Casner, R. G., Nair, M. S., Wang, M., Yu, J., Cerutti, G., Liu, L., Kwong, P. D., Huang, Y., Shapiro, L., et al. (2021) · Cell Host & Microbe · doi:10.1016/j.chom.2021.04.007 · Cited by 636 · see citing works
Wrobel, A. G., Benton, D. J., Xu, P., Roustan, C., Martin, S. R., Rosenthal, P. B., Skehel, J. J., & Gamblin, S. J. (2020) · Nature Structural & Molecular Biology · doi:10.1038/s41594-020-0468-7 · Cited by 544 · cited 1× · see citing works
“Some studies have indicated the importance of the furin cleavage site for causing conformational changes required for the binding of RBD to the ACE-2 receptor [18].”
BackgroundRecurrent deletions in the SARS-CoV-2 spike glycoprotein drive antibody escape
McCarthy, K. R., Rennick, L. J., Nambulli, S., Robinson-McCarthy, L. R., Bain, W. G., Haidar, G., & Duprex, W. P. (2021) · Science · doi:10.1126/science.abf6950 · Cited by 535 · see citing works
SARS-CoV-2 immune evasion by the B.1.427/B.1.429 variant of concern
McCallum, M., Bassi, J., De Marco, A., Chen, A., Walls, A. C., Di Iulio, J., Tortorici, M. A., Navarro, M.-J., Silacci-Fregni, C., Saliba, C., et al. (2021) · Science · doi:10.1126/science.abi7994 · Cited by 412 · see citing works
SARS-CoV-2 spike E484K mutation reduces antibody neutralisation
Jangra, S., Ye, C., Rathnasinghe, R., Stadlbauer, D., Alshammary, H., Amoako, A. A., Awawda, M. H., Beach, K. F., Bermúdez-González, M. C., Chernet, R. L., et al. (2021) · The Lancet Microbe · doi:10.1016/s2666-5247(21)00068-9 · Cited by 385 · cited 1× · see citing works
“This variant showed reduced neutralization by bamlanivimab and etesevimab monoclonal antibodies and convalescent sera [43, 44].”
BackgroundTemporal signal and the phylodynamic threshold of SARS-CoV-2
Duchêne, S., Featherstone, L. A., Haritopoulou-Sinanidou, M., Rambaut, A., Lemey, P., & Baele, G. (2020) · Virus Evolution · doi:10.1093/ve/veaa061 · Cited by 385 · see citing works
Emergence of a Novel SARS-CoV-2 Variant in Southern California
Zhang, W., Davis, B. D., Chen, S. S., Sincuir Martinez, J. M., Plummer, J. T., & Vail, E. (2021) · JAMA · doi:10.1001/jama.2021.1612 · Cited by 371 · cited 1× · see citing works
“V1) variant first identified in California, the USA in 2021, showed a 20% increase in transmission possibly attributed to the L452R and D614G substitutions in the spike protein [36].”
BackgroundModerate mutation rate in the SARS coronavirus genome and its implications
Zhao, Z., Li, H., Wu, X., Zhong, Y., Zhang, K., Zhang, Y.-P., Boerwinkle, E., & Fu, Y.-X. (2004) · BMC Evolutionary Biology · doi:10.1186/1471-2148-4-21 · Cited by 286 · cited 1× · see citing works
“028, indicating strong purifying selection [32].”
On the origin and evolution of SARS-CoV-2
Singh, D., & Yi, S. V. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00604-z · Cited by 281 · cited 1× · see citing works
“The mutations in the spike protein such as deletions, substitutions, and recombinations mainly in RBD can virtually create a highly lethal variant to a highly transmissible one, possibly due to the alteration in ACE-2 binding affinity [34].”
BackgroundEmergence of a new SARS-CoV-2 variant in the UK
Tang, J. W.-T., Tambyah, P. A., & Hui, D. S. C. (2020) · Journal of Infection · doi:10.1016/j.jinf.2020.12.024 · Cited by 278 · see citing works
Structures of MERS-CoV spike glycoprotein in complex with sialoside attachment receptors
Park, Y.-J., Walls, A. C., Wang, Z., Sauer, M. M., Li, W., Tortorici, M. A., Bosch, B.-J., DiMaio, F., & Veesler, D. (2019) · Nature Structural & Molecular Biology · doi:10.1038/s41594-019-0334-7 · Cited by 260 · cited 1× · see citing works
“The new variants are found and predicted to exploit a cellular attachment promoting factor to increase the variant’s efficiency in terms of both infection and transmission to infect ACE2 cells in the upper respiratory tract [13].”
BackgroundA Review of COVID-19 (Coronavirus Disease-2019) Diagnosis, Treatments and Prevention
Hafeez, A., Ahmad, S., Siddqui, S. A., et al. (2020) · Eurasian Journal of Medicine and Oncology · doi:10.14744/ejmo.2020.90853 · Cited by 252 · cited 1× · see citing works
“Various approved vaccines with high efficacy are available, so vaccination is a must as a preventive measure (Table 2) [96].”
BackgroundSARS-CoV-2 B.1.1.7 and B.1.351 spike variants bind human ACE2 with increased affinity
Ramanathan, M., Ferguson, I., Miao, W., & Khavari, P. A. (2021) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(21)00262-0 · Cited by 218 · see citing works
Covid-19: The E484K mutation and the risks it poses
Wise, J. (2021) · BMJ · doi:10.1136/bmj.n359 · Cited by 211 · see citing works
Will SARS-CoV-2 variants of concern affect the promise of vaccines?
Gupta, R. K. (2021) · Nature reviews. Immunology · doi:10.1038/s41577-021-00556-5 · Cited by 206 · see citing works
The SARS-CoV-2 Spike variant D614G favors an open conformational state
Mansbach, R. A., Chakraborty, S., Nguyen, K., Montefiori, D. C., Korber, B., & Gnanakaran, S. (2021) · Science Advances · doi:10.1126/sciadv.abf3671 · Cited by 206 · see citing works
Trypsin Treatment Unlocks Barrier for Zoonotic Bat Coronavirus Infection
Menachery, V. D., Dinnon, K. H., Yount, B. L., McAnarney, E. T., Gralinski, L. E., Hale, A., Graham, R. L., Scobey, T., Anthony, S. J., Wang, L., et al. (2020) · Journal of Virology · doi:10.1128/jvi.01774-19 · Cited by 205 · cited 1× · see citing works
“The spike protein is cleaved by host type II transmembrane serine proteases (TMPRSS2) and furin at the S1/S2 polybasic cleavage site (PRRA) having arginine residues that empower the high cleavability (S2) [16, 17].”
BackgroundAllen, H., Vusirikala, A., Flannagan, J., Twohig, K. A., Zaidi, A., Chudasama, D. Y., Lamagni, T. L., Groves, N., Turner, C., Rawlinson, C., et al. (2021) · The Lancet Regional Health - Europe · doi:10.1016/j.lanepe.2021.100252 · Cited by 202 · see citing works
Review of COVID-19 Variants and COVID-19 Vaccine Efficacy: What the Clinician Should Know?
Vasireddy, D., Vanaparthy, R., Mohan, G., Malayala, S. V., & Atluri, P. (2021) · Journal of Clinical Medicine Research · doi:10.14740/jocmr4518 · Cited by 197 · cited 1× · see citing works
“This Alpha variant increased its severity (40–80%) through the air pathway and the associated case fatality is expected to be 55% higher with a higher death rate [60, 61].”
BackgroundWang, R., Chen, J., Gao, K., & Wei, G.-W. (2021) · Genomics · doi:10.1016/j.ygeno.2021.05.006 · Cited by 191 · cited 2× · see citing works
“Mutations in the RBD region are likely to disrupt antibody recognition [53].”
BackgroundDifferences between First wave and Second wave of COVID-19 in India
Jain, V. K., Iyengar, K. P., & Vaishya, R. (2021) · Diabetes & Metabolic Syndrome: Clinical Research & Reviews · doi:10.1016/j.dsx.2021.05.009 · Cited by 180 · cited 2× · see citing works
“Even with a much higher positive rate, the death rate was reported to be less than that of the first wave possibly due to vast scientific understanding of the disease and its presentation with many available drugs and approved vaccines, higher availability of medical infrastructure and facilities [28].”
Multi-Organ Involvement in COVID-19: Beyond Pulmonary Manifestations
Thakur, V., Ratho, R. K., Kumar, P., Bhatia, S. K., Bora, I., Mohi, G. K., Saxena, S. K., Devi, M., Yadav, D., & Mehariya, S. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10030446 · Cited by 147 · cited 1× · see citing works
“The widespread presence of ACE-2 receptors in different organs facilitates the extrapulmonary infection by SARS-CoV-2, causing associated complications such as acute respiratory distress syndrome (ARDS), cytokine storm, blood clots [6, 9], and possibly psychological and neurological problems [10].”
BackgroundSelf-citationGiacomo, S. D., Mercatelli, D., Rakhimov, A., & Giorgi, F. (2021) · Journal of Medical Virology · doi:10.1002/jmv.27062 · Cited by 140 · cited 1× · see citing works
“The T478K mutation is found to be more adapted and influences the virus affinity to the human cells, leading toward increased viral infectivity [78].”
BackgroundA Comprehensive Review About SARS-CoV-2
Haque, S. M., Ashwaq, O., Sarief, A., & Azad John Mohamed, A. K. (2020) · Future Virology · doi:10.2217/fvl-2020-0124 · Cited by 121 · cited 1× · see citing works
“The fusion of two membranes is the crucial step before the virus enters the host cell [11, 12].”
BackgroundChakraborty, C., Bhattacharya, M., & Sharma, A. R. (2022) · Reviews in Medical Virology · doi:10.1002/rmv.2270 · Cited by 111 · cited 15× · see citing works
“This variant has substitutions in the spike glycoprotein at A67V, E484K, D614G, Q677H, and F888L with three deletions at 69Hdel, 70Vdel, and 144del [42].”
BackgroundInfluentialA clade of SARS-CoV-2 viruses associated with lower viral loads in patient upper airways
Lorenzo-Redondo, R., Nam, H. H., Roberts, S. C., Simons, L. M., Jennings, L. J., Qi, C., Achenbach, C. J., Hauser, A. R., Ison, M. G., Hultquist, J. F., et al. (2020) · EBioMedicine · doi:10.1016/j.ebiom.2020.103112 · Cited by 111 · see citing works
A Unique Clade of SARS-CoV-2 Viruses is Associated with Lower Viral Loads in Patient Upper Airways
Lorenzo-Redondo, R., Nam, H. H., Roberts, S. C., Simons, L. M., Jennings, L. J., Qi, C., Achenbach, C. J., Hauser, A. R., Ison, M. G., Hultquist, J. F., et al. (2020) · doi:10.1101/2020.05.19.20107144 · Cited by 111 · cited 1× · see citing works
“Studies correlated D614G mutation with higher viral load in nasopharyngeal aspirate, supporting the advantage in transmission, fitness advantage, and enhanced infectivity in COVID19 patients [25].”
BackgroundSARS-CoV-2 infection and viral load are associated with the upper respiratory tract microbiome
Rosas-Salazar, C., Kimura, K. S., Shilts, M. H., Strickland, B. A., Freeman, M. H., Wessinger, B. C., Gupta, V., Brown, H. M., Rajagopala, S. V., Turner, J. H., et al. (2021) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2021.02.001 · Cited by 92 · see citing works
The Emergence of Sars-CoV-2 Variant Lambda (C.37) in South America
Romero, P. E., Dávila-Barclay, A., Salvatierra, G., González, L., Cuicapuza, D., Solís, L., Marcos-Carbajal, P., Huancachoque, J., Maturrano, L., & Tsukayama, P. (2021) · Microbiology Spectrum · doi:10.1128/spectrum.00789-21 · Cited by 85 · see citing works
Blood clots in COVID-19 patients: Simplifying the curious mystery
Biswas, S., Thakur, V., Kaur, P., Khan, A., Kulshrestha, S., & Kumar, P. (2021) · Medical Hypotheses · doi:10.1016/j.mehy.2020.110371 · Cited by 74 · cited 2× · see citing works
“The widespread presence of ACE-2 receptors in different organs facilitates the extrapulmonary infection by SARS-CoV-2, causing associated complications such as acute respiratory distress syndrome (ARDS), cytokine storm, blood clots [6, 9], and possibly psychological and neurological problems [10].”
BackgroundSelf-citationZhou, H., Dcosta, B. M., Samanovic, M. I., Mulligan, M. J., Landau, N. R., & Tada, T. (2021) · mBio · doi:10.1128/mbio.01386-21 · Cited by 68 · see citing works
Coronavirus entry: how we arrived at SARS-CoV-2
Whittaker, G. R., Daniel, S., & Millet, J. K. (2021) · Current Opinion in Virology · doi:10.1016/j.coviro.2021.02.006 · Cited by 67 · cited 2× · see citing works
“1 3 surface, and cysteine-type cathepsin protease is responsible for the intracellular compartment cleavage, which indicates the possibility of the multiple activation triggers set up by the SARS-CoV-2 to infect the cell with critical efficiency [19].”
BackgroundMoreira, R. A., Guzman, H. V., Boopathi, S., Baker, J. L., & Poma, A. B. (2020) · Materials · doi:10.3390/ma13235362 · Cited by 55 · cited 1× · see citing works
“The fusion of two membranes is the crucial step before the virus enters the host cell [11, 12].”
BackgroundTada, T., Zhou, H., Dcosta, B. M., Samanovic, M. I., Mulligan, M. J., & Landau, N. R. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.02.450959 · Cited by 51 · cited 2× · see citing works
“The monoclonal antibody (REGN10987) in the Regeneron REGN-COV2 therapy is reported to be ineffective, i.e. the Lambda variant is found to be 3.6 times more resistant to neutralization by REGN10987 [57].”
BackgroundInfluentialNeutralization Potential of Covishield Vaccinated Individuals Sera Against B.1.617.1
Yadav, P. D., Sapkal, G. N., Abraham, P., Deshpande, G., Nyayanit, D. A., Patil, D. Y., Gupta, N., Sahay, R. R., Shete, A. M., Kumar, S., et al. (2022) · Clinical Infectious Diseases · doi:10.1093/cid/ciab483 · Cited by 51 · see citing works
Deploying Biomolecules as Anti-COVID-19 Agents
Patel, S. K. S., Lee, J.-K., & Kalia, V. C. (2020) · Indian Journal of Microbiology · doi:10.1007/s12088-020-00893-4 · Cited by 49 · see citing works
Self-citationMutant coronavirus in the United Kingdom sets off alarms, but its importance remains unclear
(2020) · AAAS Articles DO Group · doi:10.1126/science.abg2626 · Cited by 46 · cited 1× · see citing works
“high accumulation of immune complexes escapes mutants, and develop immune evasion facilitating the emergence of highly infective variants [90].”
BackgroundCong, Y., Feng, Y., Ni, H., Zhi, F., Miao, Y., Fang, B., Zhang, L., & Zhang, J. Z. H. (2021) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.1c00241 · Cited by 40 · cited 1× · see citing works
“These interactions reinforce the binding between the spike protein of the SARS-CoV-2 and the ACE-2 of the host cell [22].”
BackgroundCovid-19: Single vaccine dose is 33% effective against variant from India, data show
Iacobucci, G. (2021) · BMJ · doi:10.1136/bmj.n1346 · Cited by 33 · cited 1× · see citing works
“Pfizer-BioNTech and Moderna vaccines showed decreased neutralization [80].”
BackgroundMoreira, R. A., Guzman, H. V., Boopathi, S., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.01.363499 · Cited by 29 · see citing works
Ferraz, M. V. F., Moreira, E. G., Coêlho, D. F., Wallau, G. L., & Lins, R. D. (2021) · Chemical Communications · doi:10.1039/d1cc01747k · Cited by 24 · cited 1× · see citing works
“The cross-reactivity between the variants and the elicited neutralizing antibodies is the critical factor where high cross-reactivity results in higher chances of neutralizing a virus; otherwise, the variant can easily escape the immune system [92].”
BackgroundBeyond the numbers: understanding the diversity of covid-19 epidemiology and response in South Asia
Bhutta, Z. A., Siddiqi, S., Hafeez, A., Islam, M., Nundy, S., Qadri, F., & Sultan, F. (2021) · BMJ · doi:10.1136/bmj.n1544 · Cited by 22 · see citing works
Molecular epidemiology of SARS CoV-2: a review of current data on genetic variability of the virus
Parczewski, M., & Ciechanowicz, A. (2020) · Polish Archives of Internal Medicine · doi:10.20452/pamw.15550 · Cited by 17 · cited 1× · see citing works
“Although 3 ́–5 ́ exonuclease proofreading activity slows the mutation rate, accumulating amino acid mutations alters the cell tropism, transmissibility, and pathogenicity of SARS-CoV-2 [33].”
BackgroundPanzera, Y., Goñi, N., Calleros, L., Ramos, N., Frabasile, S., Marandino, A. E., Tomás, G., Techera, C., Grecco, S., Fuques, E., et al. (2021) · Microbiology Resource Announcements · doi:10.1128/mra.00410-21 · Cited by 11 · see citing works
Covid-19: Delaying end of lockdown will allow more people to be vaccinated, UK government announces
Mahase, E. (2021) · BMJ · doi:10.1136/bmj.n1552 · Cited by 4 · see citing works
Emergence and Expansion of the SARS-CoV-2 Variant B.1.526 Identified in New York
Annavajhala, M. K., Mohri, H., Wang, P., Nair, M., Zucker, J. E., Sheng, Z., Gomez-Simmonds, A., Kelley, A. L., Tagliavia, M., Huang, Y., et al. (2021) · doi:10.1101/2021.02.23.21252259
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- Delta variant triggers dangerous new phase in the pandemic | Science | AAAS, https://www.sciencemag.org/news/2021/06/delta-variant-triggers-dangerous-new-phase-pandemic. Accessed 17 July 2021.
- Madhi SA, Baillie V, Cutland CL, et al. Efficacy of the ChAdOx1 nCoV-19 Covid-19 vaccine against the B.1.351 variant. N Engl J Med. 2021;384:1885–98. https://doi.org/10.1056/NEJMoa2102214. · DOI · Paper page
- Status of COVID-19 Vaccines within WHO EUL/PQ evaluation process Manufacturer / WHO EUL holder Name of Vaccine NRA of Record Platform EOI accepted Pre-submission meeting held Dossier accepted for review* Status of assessment** Decision date***.
Cited by
Sorted by citations
Khandia, R., Singhal, S., Alqahtani, T., Kamal, M. A., El-Shall, N. A., Nainu, F., Desingu, P. A., & Dhama, K. (2022) · Environmental Research · doi:10.1016/j.envres.2022.112816 · Cited by 300 · see citing works
SARS‐CoV‐2 variants and vulnerability at the global level
Chavda, V. P., Patel, A., & Vaghasiya, D. D. (2022) · Journal of Medical Virology · doi:10.1002/jmv.27717 · Cited by 132 · see citing works
“Even monoclonal antibodies are ineffective in this case and are expected to lose some efficiency in the Delta form.(40,89)”
BackgroundNutritional and Functional New Perspectives and Potential Health Benefits of Quinoa and Chia Seeds
Agarwal, A., Rizwana, Tripathi, A. D., Kumar, T., Sharma, K. P., & Patel, S. K. S. (2023) · Antioxidants · doi:10.3390/antiox12071413 · Cited by 135 · see citing works
Self-citationOmicron (B.1.1.529) variant of SARS‐CoV‐2: Concerns, challenges, and recent updates
Mohapatra, R. K., Tiwari, R., Sarangi, A. K., Islam, M. R., Chakraborty, C., & Dhama, K. (2022) · Journal of Medical Virology · doi:10.1002/jmv.27633 · Cited by 84 · see citing works
SARS-CoV-2 seroprevalence in children worldwide: a systematic review and meta-analysis
Naeimi, R., Sepidarkish, M., Mollalo, A., Parsa, H., Mahjour, S., Safarpour, F., Almukhtar, M., Mechaal, A., Chemaitelly, H. S., Sartip, B., et al. (2022) · EClinicalMedicine · doi:10.1016/j.eclinm.2022.101786 · Cited by 69 · see citing works
Mohapatra, R. K., Tiwari, R., Sarangi, A. K., et al. (2022) · Journal of Medical Virology · doi:10.1002/jmv.27585 · Cited by 79 · see citing works
Mutational cascade of SARS-CoV-2 leading to evolution and emergence of omicron variant
Bansal, K., & Kumar, S. (2022) · Virus Research · doi:10.1016/j.virusres.2022.198765 · Cited by 75 · see citing works
Endotheliopathy in Acute COVID-19 and Long COVID
Vassiliou, A. G., Vrettou, C. S., Keskinidou, C., Dimopoulou, I., Kotanidou, Α., & Orfanos, S. E. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24098237 · Cited by 55 · see citing works
Global impact of delta plus variant and vaccination
Chavda, V., & Apostolopoulos, V. (2022) · Expert Review of Vaccines · doi:10.1080/14760584.2022.2044800 · Cited by 46 · see citing works
“the modified version of the delta variant which has brought a devastating second COVID-19 wave in India and it has been declared as a ‘variant of concern (VOC)’ by the World Health Organization [5,6].”
BackgroundInfluentialUnderstanding Mutations in Human SARS-CoV-2 Spike Glycoprotein: A Systematic Review & Meta-Analysis
Kumar, R., Srivastava, Y., Muthuramalingam, P., Singh, S. K., Verma, G., Tiwari, S., Tandel, N., Beura, S. K., Panigrahi, A. R., Maji, S., et al. (2023) · Viruses · doi:10.3390/v15040856 · Cited by 55 · see citing works
“1 lineage and are similar to the Delta variants [84].”
BackgroundSelf-citationKumar, P., Park, H., Yuk, Y., Kim, H.-Y., Jang, J., Pagolu, R., Park, S., Yeo, C., & Choi, K. (2023) · Critical Reviews in Biotechnology · doi:10.1080/07388551.2023.2176740 · Cited by 43 · see citing works
“Coronaviruses remain a future threat to humans and the environment [5].”
BackgroundSelf-citationAhiakpa, J. K., Cosmas, N. T., Anyiam, F. E., Enalume, K. O., Lawan, I., Gabriel, I. B., Oforka, C. L., Dahir, H. G., Salisu, T. F., Nwobodo, M. A., et al. (2022) · PLoS ONE · doi:10.1371/journal.pone.0268230 · Cited by 41 · see citing works
Piepenbrink, M. S., Park, J., Deshpande, A. A., Loos, A., Ye, C., Basu, M., Sarkar, S., Khalil, A. M., Chauvin, D., Woo, J. C., et al. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1010691 · Cited by 40 · see citing works
SARS-CoV-2 variants: Impact on biological and clinical outcome
Mahilkar, S., Agrawal, S. R., Chaudhary, S., Parikh, S., Sonkar, S. C., Verma, D. K., Chitalia, V., Mehta, D., Koner, B. C., Vijay, N., et al. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.995960 · Cited by 35 · see citing works
Jalal, K., Khan, K., Basharat, Z., Abbas, M., Uddin, R., Ali, F., Khan, S. A., & Hassan, S. S. U. (2022) · Environmental science and pollution research international · doi:10.1007/s11356-022-19979-1 · Cited by 32 · see citing works
Kar, J., Ramrao, D. P., Zomuansangi, R., Lalbiaktluangi, C., Singh, S. M., Joshi, N. C., Kumar, A., Kaushalendra, K., Mehta, S., Yadav, M. K., et al. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1034471 · Cited by 36 · see citing works
“These new variants have critical mutations which increase their transmissibility, infectivity, contagiousness as well as their lethality, which further necessitates the need for novel antivirals (Thakur et al., 2021).”
BackgroundEstimation of the basic reproduction number of Alpha and Delta variants of COVID-19 pandemic in Iran
Sheikhi, F., Yousefian, N., Tehranipoor, P., & Kowsari, Z. (2022) · PLoS ONE · doi:10.1371/journal.pone.0265489 · Cited by 28 · see citing works
“It is reported that one dose of COVID-19 vaccine does not provide adequate resistance against Delta variant [8].”
BackgroundHospitalization burden and epidemiology of the COVID-19 pandemic in Spain (2020–2021)
Carretero, R. G., Gómez, O. V., Gil-Prieto, R., & de Miguel, Á. G. (2023) · BMC Infectious Diseases · doi:10.1186/s12879-023-08454-y · Cited by 29 · see citing works
Khan, K., Khan, S., Jalal, K., Ul-haq, Z., & Uddin, R. (2022) · Virology · doi:10.1016/j.virol.2022.05.001 · Cited by 25 · see citing works
“These mutations have a higher impact on the pace of transmission and the immunological escape mechanism (Tao et al., 2021; Thakur et al., 2021).”
Hajek, A., & König, H. (2022) · PLoS ONE · doi:10.1371/journal.pone.0265544 · Cited by 30 · see citing works
“While individuals can protect themselves via the vaccination against Covid-19 (for an overview regarding the efficacy of different approved vaccines, please see [13]), they can also protect others by reducing the likelihood of transmission (community protection [10]).”
BackgroundAli, A. M., Tofiq, A. M., Rostam, H. M., Ali, K. M., & Tawfeeq, H. M. (2022) · Journal of Medical Virology · doi:10.1002/jmv.28098 · Cited by 26 · see citing works
Baindara, P., Dinata, R., Mandal, S. M., & Schrum, A. G. (2022) · Infectious Disease Reports · doi:10.3390/idr14020029 · Cited by 26 · see citing works
“Largely, much of the analysis of major sequence alterations between different variants has emphasized SARS-CoV-2 spike glycoprotein [11], where the receptor binding domain (RBD) and amino (N)-terminal domain (NTD) are particularly relevant to infectivity [7].”
BackgroundBsoul, E. A., & Loomer, P. M. (2022) · PLoS ONE · doi:10.1371/journal.pone.0264323 · Cited by 25 · see citing works
Bhola, S., Trisal, J., Thakur, V., Kaur, P., Kulshrestha, S., Bhatia, S. K., & Kumar, P. (2022) · Neurological Sciences · doi:10.1007/s10072-022-05875-6 · Cited by 39 · see citing works
Self-citationTherapeutic Approaches in Pancreatic Cancer: Recent Updates
Kumar, L., Kumar, S., Sandeep, K., & Patel, S. K. S. (2023) · Biomedicines · doi:10.3390/biomedicines11061611 · Cited by 25 · see citing works
“Furthermore, global perspectives have been significantly altered in the current pandemic toward therapeutic strategies for sustainable approaches to maintain good health and the economy [30,31].”
BackgroundSelf-citationGlobal COVID-19 vaccination challenges: Inequity of access and vaccine hesitancy
Dagovetz, M., Momchilov, K., Blank, L., Khorsandi, J., Rizzo, A., Khabbache, H., Sitibondo, A., Gómez-Salgado, J. C., Chirico, F., & Batra, K. (2025) · Journal of Medicine Surgery and Public Health · doi:10.1016/j.glmedi.2025.100197 · Cited by 27 · see citing works
Pandemic responsiveness: Evidence from social distancing and lockdown policy during COVID-19
Besley, T. J., & Dray, S. (2022) · PLoS ONE · doi:10.1371/journal.pone.0267611 · Cited by 23 · see citing works
Laine, L. M., Skön, M., Väisänen, E., Julkunen, I., & Österlund, P. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1016108 · Cited by 21 · see citing works
Mushebenge, A. G.-A., Ugbaja, S. C., Mbatha, N. A., Khan, R. B., & Kumalo, H. M. (2023) · COVID · doi:10.3390/covid3090100 · Cited by 22 · see citing works
Śliż, D., Wiecha, S., Gąsior, J. S., Kasiak, P. S., Ulaszewska, K., Postula, M. A., Małek, Ł. A., & Mamcarz, A. (2022) · Nutrients · doi:10.3390/nu14245381 · Cited by 15 · see citing works
Aksenova, A. Y., Likhachev, I. V., Grishin, S. Y., & Galzitskaya, O. V. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113502 · Cited by 16 · see citing works
“include Alpha, Beta, Gamma, Delta, and Omicron and are characterized by different transmissivity and/or pathogenicity, have caused consequent SARS-CoV-2 waves in the human population across the world [3].”
BackgroundForecasting dominance of SARS-CoV-2 lineages by anomaly detection using deep AutoEncoders
Rancati, S., Nicora, G., Prosperi, M., Bellazzi, R., Salemi, M., & Marini, S. (2024) · Briefings in Bioinformatics · doi:10.1093/bib/bbae535 · Cited by 16 · see citing works
“Unfortunately, as hundreds, if not thousands, of SARS-CoV-2 (sub)lineages continue to emerge, it is unfeasible to conduct experimental risk assessments or predict which ones will gain dominance in any area of the world, a practical limit as to how often vaccine composition changes need to be…”
BackgroundMachado, R. R. G., Walker, J. L., Scharton, D., Rafael, G. H., Mitchell, B. M., Reyna, R. A., de Souza, W. M., Liu, J., Walker, D. H., Plante, J. A., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-40033-2 · Cited by 19 · see citing works
Virulence Profiles of Wild-Type, P.1 and Delta SARS-CoV-2 Variants in K18-hACE2 Transgenic Mice
Santos, Y. D. S., Gamón, T. H., de Azevedo, M. D., Telezynski, B. L., de Souza, E. E., de Oliveira, D. B. D., Dombrowski, J., Rosa-Fernandes, L., Palmisano, G., Carvalho, L. J. D. M., et al. (2023) · Viruses · doi:10.3390/v15040999 · Cited by 16 · see citing works
Chrysostomou, A. C., Vrancken, B., Haralambous, C., Alexandrou, M., Aristokleous, A., Christodoulou, C., Gregoriou, I., Ioannides, M., Kalakouta, O., Karagiannis, C., et al. (2022) · Viruses · doi:10.3390/v15010108 · Cited by 5 · see citing works
“The L452R and T478K S protein RBD mutations are reported to improve transmission and confer immune evasion [73,99,100].”
BackgroundSharma, P., Kumari, R., Yadav, M. K., et al. (2022) · Indian Journal of Microbiology · doi:10.1007/s12088-022-01018-9 · Cited by 16 · see citing works
Temesgan, W. Z., Aklil, M. B., Yacob, H. S., Mekonnen, E. T., Tegegne, E. T., Tesfa, E. B., Melese, E., & Seyoum, T. (2022) · PLoS ONE · doi:10.1371/journal.pone.0264237 · Cited by 16 · see citing works
Kalyoncu, S., Yılmaz, S., Kuyucu, A. Z., Sayili, D., Mert, O., Soytürk, H., Gullu, S., Akinturk, H., Çıtak, E., Arslan, M., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-32021-9 · Cited by 15 · see citing works
Pagen, D. M. E., Brinkhues, S., Dukers–Muijrers, N. H. T. M., den Heijer, C. D. J., Bouwmeester-Vincken, N., Hanssen, D. A. T., van Loo, I. H. M., Savelkoul, P. H. M., & Hoebe, C. J. P. A. (2022) · PLoS ONE · doi:10.1371/journal.pone.0268057 · Cited by 14 · see citing works
Piepenbrink, M. S., Park, J., Desphande, A., Loos, A., Ye, C., Basu, M., Sarkar, S., Chauvin, D., Woo, J. C., Lovalenti, P., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.05.483133 · Cited by 13 · see citing works
“Although first generation SARS-CoV-2 vaccines have been highly effective at preventing severe disease, including from VoC, the humoral immunity induced by vaccination and natural infection is overwhelmingly dependent on a neutralizing antibody response targeted to the Receptor Binding Domain (RBD) of the Spike (S) gly…”
BackgroundInfluentialAl-Hindawi, A., AlDallal, U., Waly, Y. M., Hussain, M., Shelig, M., ElMitwalli, O. S., Deen, G. R., & Henari, F. Z. (2022) · Nanomaterials · doi:10.3390/nano12203550 · Cited by 11 · see citing works
“Hence, adequate containment of the virus’s new variants depends heavily upon advancements of accurate, rapid, yet affordable means of diagnosis, especially in developing countries [16].”
BackgroundPlant-Derived Natural Compounds as an Emerging Antiviral in Combating COVID-19
Singh, M., Lo, S.-H., Dubey, R., et al. (2023) · Indian Journal of Microbiology · doi:10.1007/s12088-023-01121-5 · Cited by 12 · see citing works
Jones, R., & Ponomarenko, A. (2023) · Infectious Disease Reports · doi:10.3390/idr15050058 · Cited by 15 · see citing works
SARS-CoV-2 variants of concern: a review
Sarkar, M. S., & Madabhavi, I. (2022) · Monaldi Archives for Chest Disease · doi:10.4081/monaldi.2022.2337 · Cited by 12 · see citing works
Wang, H., Churqui, M. P., Tunovic, T., Enache, L., Johansson, A., Kärmander, A., Nilsson, S., Lagging, M., Andersson, M. E., Dotevall, L., et al. (2022) · iScience · doi:10.1016/j.isci.2022.105000 · Cited by 14 · see citing works
“The Delta variant did not cause another wave of COVID-19 in Sweden, although it has been shown to be more transmissible and cause more severe diseases than the Alpha variant (Thakur et al., 2022).”
Impacts of COVID-19 on family violence in Thailand: prevalence and influencing factors
Napa, W., Neelapaichit, N., Kongsakon, R., Chotivitayataragorn, S., & Udomsubpayakul, U. (2023) · BMC Women s Health · doi:10.1186/s12905-023-02440-x · Cited by 12 · see citing works
“Because of mutations of the coronavirus, COVID-19 outbreaks have occurred in multiple waves [2].”
BackgroundKlivleyeva, N. G., Lukmanova, G. V., Глебова, Т. И., Шаменова, М. Г., Ongarbayeva, N. S., Saktaganov, N. T., Baimukhametova, A. M., Baiseiit, S. B., Ismagulova, D., Kassymova, G., et al. (2023) · Indian Journal of Microbiology · doi:10.1007/s12088-023-01064-x · Cited by 11 · see citing works
Alghamdi, F. A., Owen, R., Ashton, R. E. M., Obotiba, A. D., Meertens, R. M., Hyde, E., Faghy, M. A., KNAPP, K. M., Rogers, P., & Strain, W. D. (2022) · Radiography · doi:10.1016/j.radi.2022.08.009 · Cited by 12 · see citing works
Chan, F. H. M., Ataíde, R., Richards, J. S., & Narh, C. A. (2022) · Viruses · doi:10.3390/v14071434 · Cited by 10 · see citing works
“VOCs including the Alpha, Beta, Gamma, and Delta variants, associated with the GRY, GH, GR, and G/GK clades, respectively, were responsible for large waves of SARS-CoV-2 transmission and COVID-19 cases in most parts of the world in 2021 [56,57].”
BackgroundIdentification of Kukoamine A, Zeaxanthin, and Clexane as New Furin Inhibitors
Zaragoza-Huesca, D., Martínez-Cortés, C., Banegas‐Luna, A. J., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052796 · Cited by 11 · see citing works
“5 million deaths globally [24], and the demonstrated capacity of SARS-CoV-2 to generate new variants keeps health organizations on alert since different mutations from these variants can affect vaccine efficacy [25].”
BackgroundBivalent mRNA vaccine effectiveness against SARS-CoV-2 variants of concern
Kumari, M., Su, S.-C., Liang, K.-H., Lin, H.-T., Lu, Y.-F., Chen, K.-C., Wy, C., & Wu, H. (2023) · Journal of Biomedical Science · doi:10.1186/s12929-023-00936-0 · Cited by 9 · see citing works
Irenge, L. M., Bulakali, H. M., Akonkwa, A. I., Ambroise, J., & Gala, J. (2023) · Epidemiology and Infection · doi:10.1017/s0950268823000158 · Cited by 8 · see citing works
“Because of the emergence of SARS-CoV-2 variants linked to successive waves of the COVID-19 disease, SARS-CoV-2 has evolved at a rapid rate since its initial characterization [2].”
BackgroundBronchiectasis and COVID-19 infection: a two-way street
Oscullo, G., Gómez-Olivas, J. D., Beauperthuy, T., Bekki, A., García‐Ortega, A., Matera, M. G., Cazzola, M., & Martínez‐García, M. Á. (2022) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002447 · Cited by 10 · see citing works
“The new variants have led to multiple waves of COVID-19 around the world, each of them with different characteristics as regards the variant’s virulence and power of transmission, the country’s vaccination rate, the clinical severity, and the characteristics of affected individuals (with the first waves bringing highe…”
BackgroundTolksdorf, B., Heinze, J., Niemeyer, D., Röhrs, V., Berg, J., Drosten, C., & Kurreck, J. (2024) · Antiviral Research · doi:10.1016/j.antiviral.2024.105879 · Cited by 9 · see citing works
Persistent Endothelial Lung Damage and Impaired Diffusion Capacity in Long COVID
Asimakos, A., Vassiliou, A. G., Keskinidou, C., et al. (2023) · Journal of Personalized Medicine · doi:10.3390/jpm13091351 · Cited by 9 · see citing works
“The wide range of the clinical spectrum of COVID-19 has revealed the need for the development of novel precise and early prediction models that could provide more conclusive information than those that are given by the basic epidemiological and laboratory data [4–7].”
The Impact of COVID-19 on Health and Well-Being: Foreign Medical Students in Eastern Europe
Konstantinov, V., Gritsenko, V., Reznik, A., & Isralowitz, R. (2022) · The social science · doi:10.3390/socsci11090393 · Cited by 8 · see citing works
Thairu, Y., Babalola, O., Ajayi, A. A., et al. (2022) · Journal of Pharmaceutical Research International · doi:10.9734/jpri/2022/v34i44a36328 · Cited by 9 · see citing works
The immunological impact of revaccination in a hybrid-immune world
Bausch-Jurken, M. T., & Alter, G. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1588259 · Cited by 8 · see citing works
Boix‐Besora, A., Gòdia, F., & Cervera, L. (2023) · Vaccines · doi:10.3390/vaccines11111641 · Cited by 8 · see citing works
“Despite not presenting alarmingly high mutation ratios, during the COVID-19 pandemic, SARS-CoV-2 experienced different sequence variations, which resulted in changes on its transmissibility, severity, and immune escape [20,41].”
BackgroundSilva, J. P., de Lima, A. D., Alvim, L., Malta, F., Mendonça, C. P., de Carvalho, A. H. B., Rios, J. S. H., Fonseca, P., Queiroz, D. C., Santos, L. C. G. D. A. E., et al. (2023) · Viruses · doi:10.3390/v15041017 · Cited by 9 · see citing works
“While VOIs, VUMs, and FMVs have unclear impacts on human health [9], the VOCs are associated with immune escape and have the potential for higher transmissibility and virulence [10,11].”
BackgroundStanhope, B. J., Peterson, B., Knight, B., Decadiz, R. N., Pan, R., Davis, P., Fraser, A., Nuth, M., vanWestrienen, J., Wendlandt, E. B., et al. (2022) · Frontiers in Public Health · doi:10.3389/fpubh.2022.1042647 · Cited by 7 · see citing works
“Hence, unique variant panels can be very useful to detect variants with no ambiguity when there are multiple variants in the community; the same is true for mixed infections (55).”
BackgroundMohanty, M., Mishra, B., Singh, A. K., et al. (2022) · Cureus · doi:10.7759/cureus.32354 · Cited by 8 · see citing works
Xu, Z., Zou, Y., Gao, X., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1041331 · Cited by 8 · see citing works
“Although COVID-19 vaccination has proven useful in reducing the risk of SARSCoV-2 infection, severe clinical outcomes, and mortality of COVID-19, the efficacy of which is limited due to the high mutation frequency of SARS-CoV-2 (Aydogdu et al., 2022; Thakur et al., 2022).”
BackgroundThe Differentiation and Maintenance of SARS-CoV-2-Specific Follicular Helper T Cells
Wang, Y.-F., Tian, Q., & Ye, L. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.953022 · Cited by 6 · see citing works
“The emerging incompetent immune protection from vaccination or immunological memory of convalescent individuals is more associated with the rapid evolution of SARS-CoV-2 variants (Thakur et al., 2022; Woldemeskel et al., 2022).”
BackgroundGoux, H., Green, J., Wilson, A., Sozhamannan, S., Richard, S., Colombo, R., Lindholm, D., Jones, M. U., Agan, B., Larson, D., et al. (2024) · mBio · doi:10.1128/mbio.02737-24 · Cited by 7 · see citing works
Thakur, I., Chatterjee, A., Ghosh, A. K., et al. (2024) · Journal of Family Medicine and Primary Care · doi:10.4103/jfmpc.jfmpc_1884_23 · Cited by 7 · see citing works
“In contrast, there was no statistically significant difference in Wave‑2 and Wave‑3 [Table 3].”
BackgroundInfluentialCarretero, R. G., Gómez, O. V., Ordoñez-Garcia, M., Garrido-Peño, N., Gil-Prieto, R., & de Miguel, Á. G. (2023) · Viruses · doi:10.3390/v15071616 · Cited by 7 · see citing works
“Antiviral drugs, including remdesivir, target the replication of the SARS-CoV-2 virus.”
BackgroundInfluentialLenguiya, L. H., Fritz, M., de Fonclare, D. D. R., et al. (2023) · Viruses · doi:10.3390/v15040933 · Cited by 6 · see citing works
SARS-CoV-2 S Mutations: A Lesson from the Viral World to Understand How Human Furin Works
Cassari, L., Pavan, A., Zoia, G., Chinellato, M., Zeni, E., Grinzato, A., Rothenberger, S., Cendron, L., Dettin, M., & Pasquato, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054791 · Cited by 7 · see citing works
Ali, A. M., Tofiq, A. M., Rostam, H. M., et al. (2022) · Journal of Medical Virology · doi:10.1002/jmv.28313 · Cited by 7 · see citing works
Rajkumar, R. P. (2022) · Frontiers in Communication · doi:10.3389/fcomm.2022.867511 · Cited by 7 · see citing works
“This time period was selected as it represented a time when most countries had recovered from the initial “wave” of the COVID-19 pandemic, but several countries experienced second or third “waves (Thakur et al., 2021; El-Shabasy et al., 2022).”
BackgroundEstrela, P. F. N., dos Santos, C. A., Resende, P. C., et al. (2022) · The Analyst · doi:10.1039/d2an01625g · Cited by 7 · see citing works
Mediavilla, J. R., Lozy, T., Lee, A., Kim, J. S., Kan, V. W., Titova, E., Amin, A., Zody, M. C., Corvelo, A., Oschwald, D. M., et al. (2023) · Viruses · doi:10.3390/v15081699 · Cited by 7 · see citing works
Genomic evolution of the SARS-CoV-2 Variants of Concern: COVID-19 pandemic waves in India
Bhardwaj, P., Mishra, S. K., Behera, S. P., Zaman, K., Kant, R., & Singh, R. (2023) · EXCLI journal · doi:10.17179/excli2023-6098 · Cited by 7 · see citing works
“During the first wave of pandemic population the age group of 35.1±15.9 were majorly affected (Dhar et al., 2021; Thakur et al., 2022).”
InfluentialHorne, B. D., & Bunker, T. (2022) · Nutrients · doi:10.3390/nu15010020 · Cited by 6 · see citing works
“The evolving pandemic, although ignored in some areas, is allowing the rise of more infectious and virulent SARS-CoV-2 variants that are increasingly able to evade the human immune system and that are decreasingly responsive to therapies including vaccines and antivirals [41].”
BackgroundBhayana, S., Kalra, M., & Sachdeva, A. (2022) · Pediatric Hematology Oncology Journal · doi:10.1016/j.phoj.2022.05.003 · Cited by 6 · see citing works
“The culprit of the second wave was a delta strain (B.1.617.2) that was z 2.5 times more transmissible than the strain of the fi rst wave [9,10].”
InfluentialAhiakpa, J. K., Cosmas, N. T., Anyiam, F. E., Enalume, K. O., Lawan, I., Gabriel, I. B., Oforka, C. L., Dahir, H. G., Fausat, S. T., Nwobodo, M. A., et al. (2022) · medRxiv · doi:10.1101/2022.02.06.22270405 · Cited by 6 · see citing works
Bhundoo, A. K., Pillay, J. D., & Wilke, J. (2025) · Journal of Medical Internet Research · doi:10.2196/64856 · Cited by 8 · see citing works
“One study concluded that some older participants lacked technological skills that may be necessary for optimal online PA participation, whereas others lacked the financial capacity to fully engage with online PA resources [25].”
Valle, F. G., Demelo-Rodríguez, P., Alonso-Beato, R., et al. (2024) · Journal of Thrombosis and Thrombolysis · doi:10.1007/s11239-024-03026-6 · Cited by 5 · see citing works
Regional geographies and public health lessons of the COVID-19 pandemic in the Arctic
Tiwari, S., Petrov, A. N., Golosov, N., Devlin, M. K., Mark, W., DeGroote, J. P., Degai, T. S., & Ksenofontov, S. (2024) · Frontiers in Public Health · doi:10.3389/fpubh.2023.1324105 · Cited by 6 · see citing works
Hou, R., Traverson, L., Chabrol, F., Gautier, L., Oliveira, S. R. D. A., David, P., Lucet, J., Zinszer, K., & Ridde, V. (2023) · Health Systems & Reform · doi:10.1080/23288604.2023.2223812 · Cited by 5 · see citing works
Swami, A., Mohanty, A., Jamwal, A., et al. (2023) · Journal of Medical Microbiology · doi:10.1099/jmm.0.001685 · Cited by 5 · see citing works
Verkhivker, G. M., Alshahrani, M., & Gupta, G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076642 · Cited by 4 · see citing works
“An insightful review reflected on the evolutionary origins underlying the increased transmissibility, infectivity, and immune escape of the Omicron mutations, reinforcing the notion that the emergence of highly infective new variants may be driven by adaptive evolution through the development of increasingly diverse a…”
BackgroundZamani, S., Alizadeh, M. R., Shahrestanaki, E., et al. (2022) · PLoS ONE · doi:10.1371/journal.pone.0277413 · Cited by 5 · see citing works
Southern Europe Managing the First Phase of the Covid-19 Pandemic: The Crucial Effect of Timing
Verney, S., Real-Dato, J., & Teruel, J. R. (2022) · South European Society & Politics · doi:10.1080/13608746.2022.2306710 · Cited by 5 · see citing works
Daily, A. M., DiNatale, R. G., Koenig, H. G., et al. (2022) · Urology · doi:10.1016/j.urology.2022.05.037 · Cited by 5 · see citing works
Yang, N., & Yang, S. (2022) · Materials Today Communications · doi:10.1016/j.mtcomm.2022.103824 · Cited by 5 · see citing works
Palmowski, L., Hagedorn, A., Witowski, A., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-94483-3 · Cited by 4 · see citing works
Effect of COVID-19 vaccination coverage on transmission and mortality during Omicron dominance
Ogbodo, S. C., Damba, J. J., Olaoye, O. C., et al. (2025) · Academia Medicine · doi:10.20935/acadmed7536 · Cited by 4 · see citing works
Chakraborty, C., Bhattacharya, M., & Lee, S. (2025) · Osong Public Health and Research Perspectives · doi:10.24171/j.phrp.2024.0186 · Cited by 4 · see citing works
“In 2020, the initial Wuhan strain and the Alpha variant accounted for the majority of COVID-19-related deaths [30].”
Singapore's COVID‐19 Genomic Surveillance Programme: Strategies and Insights From a Pandemic Year
Tan, H. Y., Khamis, N. H., Goh, A., Mah, T. K. L., Yeo, B., Ngan, J. Y., Ding, Y., Lin, C., Chae, S., Lee, P. L., et al. (2024) · Influenza and Other Respiratory Viruses · doi:10.1111/irv.70060 · Cited by 4 · see citing works
Post COVID-19 era: Re-emergence of known and future (X) viral pathogens
Thakur, P., Thakur, V., Sapra, M., Srivastava, S., & Patel, S. K. S. (2024) · Vacunas · doi:10.1016/j.vacun.2024.02.001 · Cited by 6 · see citing works
Self-citationA mouse xenograft long‐term replication yields a SARS‐CoV‐2 Delta mutant with increased lethality
Kim, D., Kim, M., Kim, J.-S., Baek, K., Park, H., Park, S., Kang, B. M., Kim, S., Kim, M., Mostafa, M. N., et al. (2024) · Journal of Medical Virology · doi:10.1002/jmv.29459 · Cited by 4 · see citing works
Mediavilla, J. R., Lozy, T., Lee, A., et al. (2023) · Preprints.org · doi:10.20944/preprints202307.1532.v1 · Cited by 4 · see citing works
Shafiq, N., Jannat, A., Munir, H., Rashid, M., & Parveen, S. (2023) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2023.2234993 · Cited by 5 · see citing works
“The introduction of novel variants of the SARS-CoV-2, namely (VoCs), are creating successive phases of COVID-19 epidemics over the world, potentially inflicting substantial morbidity and death due to a huge rise in cases (Thakur et al., 2022).”
Bernauer, E., Alebrand, F., & Heurich, M. (2023) · Viruses · doi:10.3390/v15061324 · Cited by 4 · see citing works
Houston, A. D., Tovey, C., Rogers-Smith, K., et al. (2023) · BMJ Military Health · doi:10.1136/military-2022-002248 · Cited by 4 · see citing works
Jarraya, A., Kammoun, M., Kanoun, M., et al. (2022) · Italian Journal of Gynaecology and Obstetrics · doi:10.36129/jog.2022.85 · Cited by 4 · see citing works
“Furthermore, since its emergence, SARS-CoV2 hasn't stopped mutating [2].”
BackgroundUpdates on Palliative Medicine in the COVID-19 Era
Varrassi, G., & Rekatsina, M. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11020315 · Cited by 4 · see citing works
“Today, two years after the start of the pandemic, the situation has not changed much, as new variants of the virus arrive, usually with initial unknown severity of disease and consequences to patients and healthcare systems [31,32], but with a lot of demands by the media for ready answers and instant solutions.”
BackgroundScoping Review of Triage Modifications to Emergency Medical Care in Hospitals Post-COVID-19
Nash, C. (2025) · Emergency Care and Medicine · doi:10.3390/ecm2010006 · Cited by 5 · see citing works
“…case of severe acute respiratory syndrome coro-navirus 2 [1]—the SARS-CoV-2 virus that resulted in the COVID-19 pandemic [2] over a series of waves and variants [3]—an assessment showed that intensive care clinicians were often uncertain regarding the meaning of triage in disaster situations [4].”
- Authors
- Thakur, V., Bhola, S., Thakur, P., Patel, S. K. S., Kulshrestha, S., Ratho, R. K., & Kumar, P.
- Affiliations
- Government Medical College (IN)
- Shoolini University (IN)
- Post Graduate Institute of Medical Education and Research (IN)
- Konkuk University (KR)
- Corresponding author
- Ratho, Radha Kanta
- Kumar, Pradeep
- ORCID
- Venue
- Infection
- Published
- 2021-12-16
- Volume
- 50
- Issue
- 2
- Pages
- 309-325
- ISSN
- 0300-8126 (ISSN-L)
- 1439-0973
- PMC
- PMC8675301
- OpenAlex
- W4200591468
- Cited by
- 210
- References
- 86
- Citations by year
- 2026: 6 · 2025: 18 · 2024: 41 · 2023: 55 · 2022: 70
- FWCI
- 11.67
- Type
- journal article
- Language
- en
- Update notices
- correction (2022-01-14)
- Open access
- bronze
- doi.org
- Locations
- Infection (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (submittedVersion)
- Topics
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
- Health Sciences › Medicine › Infectious Diseases › COVID-19 Clinical Research Studies
- Physical Sciences › Mathematics › Modeling and Simulation › COVID-19 epidemiological studies
- Keywords
- SARS-CoV-2, COVID-19 pandemic, viral variants, Omicron variant, Delta variant, Kappa variant, viral mutations, immune evasion
- MeSH terms
- COVID-19, SARS-CoV-2, COVID-19 Vaccines, Humans, Mutation, Pandemics
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