Abstract
Millions have died due to the COVID-19 pandemic. The irrepressible propensity of the pandemic, which was highlighted by the outbreak of the Delta variant, should not be underestimated. The Omicron SARS-CoV-2 variant is thought to have originated from Africa. Sequences of the omicron variant show that it carries the highest number of point mutations detected in a betacoronavirus. High hospitalization numbers due to the Omicron variant has retriggered precautionary restrictions and border closures even in countries which have attained herd immunity by mass vaccinations. Surveillance systems for accurate screening of the Omicron variant are needed to guide implementation of hygiene principles and restrictions. Development of vaccines against the variants is important as the pandemic evolves. Whether Omicron is the last variant depends on the success of the local and global public-health strategies against SARS-CoV-2.
Key Words: Delta variant, Omicron variant, Mutations, Vaccine, SARS-CoV-2, South Africa, Variant of concern
When the pneumonia of unknown etiology was reported in Wuhan, China, a pandemic of this scale was inconceivable. The virus was called severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) as the cause of the coronavirus disease 2019 (COVID-19). This highly transmissible virus infected more than 262 million cases and caused more than 5.2 million fatalities as of 30 November 2021 (https://www.worldometers.info/coronavirus/). SARS-CoV-2 is a single-stranded-RNA virus with a genome that is prone to mutations in relatively short periods of time (1). Millions of sequences have shown that only few mutations effectively cause a more severe disease with high transmissibility and infectivity. The viral genetic variations have affected the pandemic course in 2021. The new variants have caused new peaks of infections globally (2., 3., 4.). Following mass vaccinations in five continents, many countries have eased or lifted the pandemic-related restrictions; however, experts expected new waves of the positive cases (5., 6., 7). Availability of mass-sequencing facilities enabled many countries to actively track emergence of the new SARS-CoV-2 variants (8), leading to discoveries of many variants, including variants of interest (VOIs) or variants of concerns (VOCs) (9).
In late November 2021, news of emergence of a new variant, called B.1.1.529 or Omicron, triggered an urgent WHO meeting on 26 November 2021 to critically assess the various aspects of the variant reported by South Africa (10). The initial patient clusters infected were, however, identified by sequencing in Botswana, confirming that the dominating variant was not Delta. According to the latest news, at least 50 countries have confirmed Omicron cases; however, this number is growing (According to the https://www.gisaid.org/hcov19-variants/: December 2021).
The rapid spread of Omicron in South Africa is concerning because of its many mutations. The Omicron genome carries at least 50 new mutations with 30 located in the sequence of the viral Spike protein, which has been the target of developed vaccines (11). Two years into the pandemic, new viral variants have emerged with point mutations mainly in the Spike protein. According to updated GISAID sequence analyses (https://www.gisaid.org/hcov19-variants/), of 183 submitted sequences, 124 (67%) were reported in South Africa until 30 November 2021. Comparison of the sequences of all the variants of concern and variants of interest shows that Omicron shares many mutations with four other VOCs, including Alpha, Beta, Gamma, and Delta (Figure 1 . https://covariants.org/shared-mutations). For example, P681H is shared among Omicron and two VOCs (Alpha and Delta). D614G, the most common mutation, is present also in the Omicron genome. These Omicron mutations has raised concern among the scientists and decision-makers, calling for adaptation of strategies in the fight against SARS-CoV-2. Initial assessments suggest that the Omicron variant could more avidly bind to the human host cells than the former dominant variants, including Alpha and Delta (12,13). The Omicron mutations have implications for its functional biology, potentially adversely affecting the vaccine effectiveness worldwide. If the effectiveness of the approved vaccines are affected, the Omicron variant may not be the last VOC we encounter during this pandemic.
Whether hospitalizations due to the Omicron variant will increase globally is unpredictable now. However, considering restoring some public-health countermeasures is prudent to avoid further casualties, even in countries with optimal rates of full vaccination. Detection and spread of the Omicron VOC in many more countries is expected; however, avoiding case surges with Delta and Omicron variants is ideal to assist the healthcare facilities in many countries. Nevertheless, some experts predict that the disease due to the Omicron VOC is less severe than with other variants. Emergence of the Delta variant was not reported opportunely, but Omicron was quickly reported by the relevant authorities. Subsequently, border closures and counter-responses were implemented to curb the spread of the variant (14).
While mass production of the vaccines in 2021 is an important health measure against the pandemic, persistent emergence of the new SARS-CoV-2 variants will likely require additional countermeasures, including longer quarantine periods, physical distancing especially indoors, travel bans, mask wearing, and targeted vaccination campaigns. Reducing the chance of emergence of new viral variants may be difficult; however, preventing uncontrolled spread of the virus may facilitate this ideal aim. Sequencing facilities to accurately screen and track the spread of the variants is necessary for guiding the public-health countermeasures. Developing vaccines with broader efficacies is critical, considering the emergence of the variants such as Omicron.
Conflict of Interest
None.
Funding
None.
Footnotes
Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.arcmed.2022.01.001.
Appendix. Supplementary materials
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