Omicron variant of SARS‐CoV‐2: Genomics, transmissibility, and responses to current COVID‐19 vaccines
Open accessAbstract
Currently, severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) has spread worldwide as an Omicron variant. This variant is a heavily mutated virus and designated as a variant of concern by the World Health Organization (WHO). WHO cautioned that the Omicron variant of SARS‐CoV‐2 held a very high risk of infection, reigniting anxieties about the economy's recovery from the 2‐year pandemic. The extensively mutated Omicron variant is likely to spread internationally, posing a high risk of infection surges with serious repercussions in some areas. According to preliminary data, the Omicron variant of SARS‐CoV‐2 has a higher risk of reinfection. On the other hand, whether the current COVID‐19 vaccines could effectively resist the new strain is still under investigation. However, there is very limited information on the current situation of the Omicron variant, such as genomics, transmissibility, efficacy of vaccines, treatment, and management. This review focused on the genomics, transmission, and effectiveness of vaccines against the Omicron variant, which will be helpful for further investigation of a new variant of SARS‐CoV‐2.
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Omicron showed very high transmissibility but lower severity than previously circulating strains.
“Omicron showed very high transmissibility but lower severity [17].”
From Vaccine effectiveness and duration of protection of COVID-19 mRNA vaccines against Delta and Omicron BA.1 symptomatic and severe COVID-19 outcomes in adults aged 50 years and over in France (2023) · cites this paper as [17]
Section 3 (page unavailable) describes rapid spread and high transmissibility. Section 5 (page unavailable) reports early evidence of fewer hospitalizations with Omicron than Delta, but says more data were needed to establish whether Omicron caused less severe disease. The claim presents that tentative severity finding as settled. (LLM, conf=0.88)
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- Authors
- Araf, Y., Akter, F., Tang, Y., Fatemi, R., Parvez, M. S. A., Zheng, C., & Hossain, M. G.
- Affiliations
- Fujian Medical University (CN)
- BRAC University (BD)
- State Key Laboratory of Veterinary Biotechnology (CN)
- East West University (BD)
- Shahjalal University of Science and Technology (BD)
- Bangladesh Agricultural University (BD)
- ORCID
- Venue
- Journal of Medical Virology
- Publisher
- Wiley
- Published
- 2022-01-23
- Volume
- 94
- Issue
- 5
- Pages
- 1825-1832
- ISSN
- 0146-6615 (ISSN-L)
- 1096-9071
- PMC
- PMC9015557
- OpenAlex
- W4205170082
- Cited by
- 862
- References
- 31
- Citations by year
- 2026: 23 · 2025: 88 · 2024: 162 · 2023: 280 · 2022: 305 · 2021: 4
- FWCI
- 32.26
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Medical Virology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- 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
- Omicron variant, SARS-CoV-2, COVID-19 pandemic, viral genomics, transmissibility, vaccine efficacy, variants of concern, reinfection, viral mutations, COVID-19 vaccines
- MeSH terms
- COVID-19, SARS-CoV-2, COVID-19 Vaccines, Humans, Genomics
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