Cited by 210SARS-CoV-2 and COVID-19 ResearchCOVID-19 Clinical Research StudiesCOVID-19 epidemiological studies

Waves and variants of SARS-CoV-2: understanding the causes and effect of the COVID-19 catastrophe

Open access
Thakur, Vikram, Bhola, Shivam, Thakur, Pryanka, Patel, Sanjay Kumar Singh, Kulshrestha, Saurabh, Ratho, Radha Kanta, Kumar, Pradeep·2022·Infection

Abstract

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.

Integrity signals

Registry

Crossref · 10.1007/s15010-021-01734-2

Cites

89 of 89 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

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

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

    Minor

    The paper says existing vaccines are ineffective against new variants, yet elsewhere reports substantial effectiveness for two vaccines against Delta.

  • Delta mutation count disagrees with its list

    Minor

    The paper states that Delta has 13 spike-protein mutations, but the accompanying list contains 14 entries.

  • VOI count disagrees with the named list

    Minor

    The paper refers to five variants of interest, but its named VOI list contains six.

3 of 3

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

    Info

    The 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

1 of 1

Cites

1 retracted

Flagged first, then by citations

Research works printed but not linked: 3

  1. 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.
  2. 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
  3. 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

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
Venue
Infection
Published
2021-12-16
Volume
50
Issue
2
Pages
309-325
ISSN
  • 0300-8126 (ISSN-L)
  • 1439-0973
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
Open access
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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