September-2020
South Africa was the first country to detect the novel variant of SARS-CoV-2 from specimens collected on 11 November and 14 November 2021. The first Omicron variant was reported to WHO by the South African Department of Health on 24 November 2021 [ 6 ]. On 25 November 2021, the United Kingdom Health Security Agency designated the B.1.1.529 Omicron variant as a Variant Under Monitoring (VUI-21-NOV-01) and, just one day later, it was designated as a VOC by the WHO; the variant was later named Omicron [ 4 , 7 ]. The rapid spread of this variant in South Africa and surrounding countries alarmed the WHO. This could be due to the large number of mutations on the spike protein in the Omicron variant as compared to other VOCs. However, Omicron has been reported to be less severe than the previous variants [ 8 , 9 ]. Three days after the announcement of Omicron on 29 November 2021, by the WHO, this novel variant was detected in Australia, Belgium, Canada, the Czech Republic, Denmark, France, Germany, Italy, Netherlands, and the United Kingdom [ 10 ]. As of 25 December 2021, Omicron had been reported in 108 countries, with nearly 150,000 confirmed cases and 26 deaths, creating an alarming situation worldwide [ 11 ]. The emergence of the Omicron variant in South Africa has also revealed a vaccination gap between the richest and the poorest. Whilst an average of 60% of the population of Europeans has been vaccinated, it is appalling to see that only 5–10% of the African population has been vaccinated [ 12 ]. This could be one of the major factors contributing to the emergence of VOCs. Japan also reported the first two cases of the novel Omicron variant at the end of November 2021 among international travelers returning to the country with the undetected Omicron variant [ 13 ]. India reported the first two cases of the Omicron variant on 3rd December 2021 among international travelers [ 14 ]. In Germany, two suspected cases of the new Omicron variant were first reported on 27 November 2021 and, as the New Year began, this novel Omicron became one of the most dominant variants in Germany, despite protective measures at the initial stage in January 2022 [ 15 , 16 ]. This new variant has been spreading worldwide and has been reported in 180 countries as of 4 February 2022. As of 11 February 2022, the UK reported a maximum number of Omicron cases (422,993) followed by the USA (359,236), Denmark (69,789), Germany (48,866), Canada (30,687), and France (27,487), while an increasing number of cases can be seen on a daily basis in many other countries [ 16 ]. Jansen et al. [ 17 ] reported that the Omicron variant has a shorter incubation period than the previous variants, with similar clinical symptoms. Preliminary data conducted by the National Institute of Infectious Diseases shows a high viral load three to six days after the onset of symptoms [ 18 ].
As the Omicron variant continues to evolve and mutate, new sequences (sub-lineages) of the Omicron variant were reported by the WHO in December 2021, namely: BA.1, BA.2, and BA.3 [ 19 ]. Over the past two months, the BA.1 variant has escalated globally. However, in the last weeks of January 2022, the BA.2 sub-lineage had increased internationally and had already become dominant in Denmark. As of 11 February 2022, BA.2 had been detected in at least 70 countries and 44 U.S. states, according to the data uploaded in GISAID, and a total number of 55,404 sequences in the BA.2 lineage have been detected since the lineage was identified [ 20 , 21 ]. A preprint uploaded in medRxix [ 22 ], concluded that Omicron BA.2 is more dominant and transmissible than the parent Omicron variant (BA.1). It possesses immune-escaped advantages among vaccinated individuals; however, it does not increase its transmissibility to vaccinated individuals with breakthrough infections. India is another country where BA.2 is rapidly replacing the Delta and Omicron BA.1 variants, as per the report [ 23 ]. Data uploaded on GISAID suggest that the BA.2 variant is increasing rapidly in proportion to the original BA.1 variant, thus dominating the parental variant based on the sequence frequency [ 24 ].
The Omicron variant has the highest number of mutations observed so far, as compared to the other VOCs such as Alpha, Beta, Gamma, and Delta. This variant contains more than 30 mutations in the spike protein, which binds to the ACE2 receptor in the human cell for invasion, and out of which, 15 modifications are observed in a Receptor Binding Domain (RBD), an area strongly associated with humoral immune evasion [ 25 ], thus, increasing its transmissibility and thereby causing the possibility of evading vaccine-induced antibodies [ 26 ]. Researchers from China constructed and studied the binding affinity between the complex structure of the human ACE2 protein and the RBD of the Omicron variant spike protein (S-protein) using atomistic molecular dynamics simulations. They observed that mutations in the RBD of the SARS-CoV-2 Omicron variant resulted in a higher binding affinity to the human ACE2 protein [ 27 ].
There are two distinct mechanisms for the entry of SARS-CoV-2 into a human cell: cell-surface entry and endosomal entry, where TMPRSS2-mediated S protein activation takes place at the plasma membrane and cathepsin-mediated activation takes place in the endolysosome at the cytoplasmic region, respectively [ 28 ]. A researcher from Glasgow University in the UK demonstrated the replication process of different SARS-CoV-2 variants and their mechanisms in entering the human cell. An HIV-pseudotype was evaluated for entry assay. The study reveals that Omicron, like pangolin CoV, uses the endocytosis pathway to enter human cells and is independent of the TMPRSS2 present on the cell surface. This study was further supported by using drug inhibitors targeting either the TMPRSS2 (Camostat) or the cathepsins (E64d). As compared to another variant spike, the Omicron spike shows a reduced syncytium formation, thereby causing fewer lung infections [ 29 ].
In November 2021, Omicron (B.1.1.529) emerged as a VOC. Wahid et al. [ 26 ] had earlier reported the triplet mutation (K417N + E484K + N501Y) in the Beta (B.1.351) and Gamma (P.1) variants, which were highly transmissible, leading to greater COVID-19 hospitalizations, ICU admissions, and even deaths. Such mutations have increased the immune escape potential leading to a decrease in the neutralization of antibodies (such as those found in the Pfizer and Moderna vaccines). The Omicron variant contains overall 50 mutations, with 30 mutations [ 25 ] on the spike protein, which include: A67V, del69/70, T95I, G142D, del143/145, N211I, del212/212, G339D, S371L, S373P, S375F, S477N, T478K, E484A, Q493R, G496S, Q498R, N501Y, Y505H, T547K, D614G, H655Y, N679K, P681H, N764K, D796Y, N856K, Q954H, N969K, and L981F, of which 15 modifications are located at the RBD region [ 30 ]. Cecylia et al. [ 27 ] conducted atomistic molecular dynamics simulations to study the binding interactions between the human ACE2 protein and the RBD of the Omicron spike protein (S-protein). The analysis shows that the Omicron RBD binds more strongly to the human ACE2 protein than does the original Wuhan strain. However, the SARS-CoV-2 Omicron RBD shows weaker binding affinity than the Delta variant [ 31 ]. Most COVID-19 strains contain at least one change from the original Wuhan sequence, D614G, altering the virus’s ability to escape the immune response. The N501Y mutation is present in all VOCs, except the Delta variant [ 32 ]. Interestingly, Omicron’s spike protein mutations, such as D614G, N501Y, and K417N, are found in some other VOCs, thus making the virus more infectious—a prospect that is very concerning.
Similarly, the H655Y, N679K, and P681H mutations in the Omicron spike protein, also found in the Alpha and Delta variants, could increase the transmission of the virus [ 6 , 33 , 34 ]. It has the deletion at spike protein (Δ69–70), position 69–70, similar to the Alpha and Eta variants, that leads to the S-gene dropout or S-gene target failure. This phenomenon may provide a useful proxy to measure the prevalence of the Omicron variant. The rapid transmission of the Omicron variant across the globe could be due to the presence of these larger numbers of mutations in the spike protein, unlike the Delta variant, and thus evading immune response [ 33 ]. However, this phenomenon does not apply to the BA.2 sub-lineage of the Omicron variant, as it does not contain the deletion at S: 69–70 and is S-gene target positive (SGTP) on PCR diagnostic assays [ 35 ]. The comparison and mutual sharing of the spike protein mutations of the Omicron sub-lineages, BA.1, BA.2, and BA.3, are represented by a Venn diagram, as shown in Figure 1 .
Comparison of spike protein mutations of Omicron sub-lineage: BA.1, BA.2, and BA.3. (GISAID: https://www.epicov.org/epi3/frontend#58aca ) (Accessed on 10 February 2022). This Venn diagram represents the common mutation present among the sub-linages of Omicron variant; G142D, T478K, D614G, H655Y N679K, P681H, N764K, D796Y, Q954H, N969K. B.A.1 (30); A67V, del69/70, T95I, G142D, del143/145, N211I, del212/212, G339D, S371L, S373P, S375F, S477N, T478K, E484A, Q493R, G496S, Q498R, N501Y, Y505H, T547K, D614G, H655Y, N679K, P681H, N764K, D796Y, N856K, Q954H, N969K, L981F. B.A.2 (29); T19I, L24S, del25/27, G142D, V213G, G339D, S371F, S373P, S375F, T376A, D405N, R408S, K417N, N440K, S477N, T478K, E484A, Q493R, Q498R, N501Y, Y505H, D614G, H655Y, N679K, P681H, N764K, D796Y, Q954H, N969K. B.A.3 (16); A67V, del69/70, T95I, G142D, del143/145, N211I, del212/212, T478K, D614G, H655Y, N679K, P681H, N764K, D796Y, Q954H, N969K.
The combination of N501Y + Q498R may increase the binding affinity to ACE2, while other substitutions may lead to a decrease in the binding affinity to the ACE2 in the Omicron spike protein. Kinases’, such as PI3K/AKT, signaling are essential in SARS-CoV-2 entry. Based on molecular docking, Bexultan et al. [ 36 ] analyzed the interaction between the potential kinases and the N501Y mutation and observed that the N501Y mutation did not enhance binding to epidermal growth factor receptors (EGFR) due to the mutations. The N501Y mutation-containing lineages might become more infectious since several kinases are elevated in cancer patients. Therefore, additional care for cancer management should be taken into consideration. Mannar et al. [ 37 ] analyzed a cryo-electron microscopy structure between the spike proteins of the Omicron variant in complex with human ACE2. The structure depicts two additional new salt bridges and hydrogen bonds formed by the mutated residues R493, S496, and R498 in the RBD with the ACE2. This enhances other mutations, such as K417N, which is known to reduce the ACE2 binding affinity to the spike protein. These strong interactions at the ACE2 interface may contribute to the rapid spread of the Omicron variant [ 38 ]. Zhuoming et al. [ 39 ] reported that E484K could escape neutralization by convalescent sera, while S477N was resistant to neutralization by multiple mAbs, thus needing further investigation. The increase in binding affinity to the ACE2 receptor by N501Y could aid in an increase in transmission. The combination of N501Y and Q498R may also increase the binding affinity even more; however, other substitutions in the Omicron spike protein are expected to decrease binding to the ACE2. A cluster of mutations (such as H655Y, N679K, P681H) present at the S1–S2 furin cleavage site in the Omicron variant may increase spike cleavage and could aid in transmission. The N679K present at the furin cleavage site adds to the polybasic nature and is associated with an increase in transmission. The P681H mutation (also found in Alpha) enhances spike cleavage, and could also aid in transmission. At this position, an alternate mutation (P681R) is found in Delta [ 40 ]. In India, Surendra et al. [ 41 ] found a major mutation at the P681 position with an R (P681R) similar to the Delta variant (B.167.2) of about 9.71% instead of the H (P681H) mutation. This variant is of considerable public concern, as it is increasing at a high rate in many countries, including the U.S., due to its increased transmissibility and immune evasion. In the nucleocapsid (N) protein region, the Omicron variant also possesses two additional mutations such as R203K and G204R (found in ancestral mutation) that enhance sub-genomic RNA expression and viral RNA binding with key host proteins, thus increasing the viral load [ 42 , 43 ]. Phylogenetic analysis, based on the prevalence of high numbers of mutations, revealed that the Omicron variant is closely related to the Gamma (P.1) variant [ 44 ], and may possess similar characteristics at the molecular level [ 45 ].
The emergence of mutations in SARS-CoV-2 has resulted in five SARS-CoV-2 variants, namely: the Alpha, Beta, Gamma, Delta, and Omicron variants. The World Health Organization has designated such variants as VOC [ 46 ]. This has resulted in investigating the performance of the potential impact on diagnosis. A rapid diagnostic antigen test is cheap and offers quick results at the point of care when the viral load is high and, hence, provides utility in clinical and public health settings. The rapid test is approved in many countries, including Australia, for self-testing [ 47 ]. However, it is less sensitive than the RT-PCR-based method [ 48 ].
Deerain et al. [ 49 ] evaluated ten commercially available rapid antigen test kits, based on nucleocapsid protein antigens, to check their diagnostic performance (sensitivity) between the Delta and Omicron variants. Overall, they observed no sensitivity difference among the variants. The detection limit of all the kits for the Delta variant was 6.50 log10 copies per mL (Ct 25.4), and 6.39 log10 copies per mL (Ct 25.8) for the Omicron variant. Similarly, Puhach et al. [ 50 ] evaluated seven Ag-RDTs for their sensitivity to the Omicron variant and compared them to other VOCs such as Alpha, Beta, Gamma, and Delta. A trend toward lower sensitivity for Omicron detection compared to the other VOCs was observed. As per the data retrieved on 28 December 2021 (the Food and Drug Administration), it suggests that the antigen test provides a rapid result, and does detect the Omicron variant, but is not a very reliable or sensitive diagnostic testing option [ 51 ].
The Paul Ehrlich Institute (PEI) has also investigated and evaluated the sensitivity of 198 rapid antigen tests (Qualitative Lateral Flow Tests) using uniform sample material marketed in Germany until the end of January 2022. The current state-of-the-art was defined as corresponding to a minimum sensitivity of 75% for the pools with Cq ≤ 25. However, the results do not allow any conclusions regarding the specificity of the tests [ 52 ]. Some studies have also demonstrated that up to 50% of the positive cases detected by rapid tests are false positives as compared to PCR diagnostics tests. A recent small preprint study that has not been peer-reviewed found that the antigen test fails to detect the virus on day zero of 30 individuals who turn out to be COVID positive in the PCR test. The PCR tests also indicated a higher viral load [ 53 ]. However, a study performed in January 2022, in California, on 731 individuals’ shows that the Abbott BinaxNOW rapid tests could detect the Omicron variant, as they did with other variants, especially when people have higher viral load and were symptomatic [ 54 ]. The Abbott BinaxNOW Rapid Antigen Test can be a useful adjunct to RT-PCR testing for the detection of SARS-CoV-2 infections [ 55 ].
The RT-PCR test is considered to be the ‘gold standard’ for detecting coronavirus. In the RT-PCR, two or more spike genes are targeted; therefore, there are chances to detect one of the genes in case of any mutations, thus highlighting its advantage for the Omicron variant. Ever since the detection of SARS-CoV-2 in 2019, it has undergone a broad process of replication and mutation in the spike proteins and RBD, generating a vast number of VOIs and VOCs. Due to this mutation, a phenomenon called ‘S-gene dropout’ or ‘S-gene target failure’ has been reported [ 7 ]. This vast mutation has jeopardized the reliability of currently used diagnostic kits for detecting SARS-CoV-2 and, hence, requires a regular re-evaluation of commercially available kits based on the emerging VOIs and VOCs [ 56 ]. ‘S-gene target failure’ has been suggested as a marker in identifying the Omicron variant. However, with the emergence of the new BA.2 sub-lineage of Omicron (which does not contain 69/70del in the spike protein), it cannot be considered as a marker for the presence of Omicron and requires confirmation of Omicron by sequencing [ 4 ]. This phenomenon has been supported by Metzger et al. [ 57 ], who obtained a piece of information and collected 39 assays of the most commonly used PCR tests in Switzerland and Liechtenstein, targeting genomic loci such as the ORF1ab region, the RdRp gene, the S gene, the E gene, the N gene, and the M gene. Only two assays showed S-gene dropout for Omicron out of eight assays targeting the S gene. Hence, gene sequencing data analysis is required to confirm the presence of the Omicron variant.
Whole-genome sequencing of Omicron with next-generation sequencing (NGS) might serve as a gold standard to detect SARS-CoV-2 variants despite being time-consuming and costly. It also requires large data processing. Fu et al. [ 58 ] compared and evaluated the Allplex SARS-CoV-2 Master Assay and Variants I Assay (a direct PCR-based variant analysis) to detect HV69/70 deletion, Y144 deletion, E484K, N501Y, and P681H spike mutations with NGS for 115 samples and observed sensitivity of 98.7% with the Master Assay and 100% with the Variants I Assay. These assays can be utilized as useful tools to rapidly monitor selected and updated VOCs in resource-limited settings. Currently, the CDC is working to understand the new Omicron variant and the effectiveness of commercially available diagnostic tools and authorized medical countermeasures, such as vaccines and therapeutics, against this variant, and is providing technical support to monitor the epidemiologic and clinical features of novel variants [ 59 ].
The emergence of COVID-19 has led to the development of various repurposed and therapeutic drugs, including antivirals and antibody drugs. The U.S. Food and Drug Administration (FDA) have authorized the use of these drugs for emergency purposes in COVID-19 patients with serious illnesses, as per the panel’s recommendation. Meanwhile many anti-viral drugs and mAbs are under investigation.
The in vitro studies performed by IGM Biosciences, Inc. indicate the novel antibody IGM-6268 exhibits potential neutralizing activity against the Omicron variant and all other VOCs and VOIs [ 60 ]. Some of the recent advances in therapies that have been approved and authorized for emergency use in COVID-19 patients and are suitable for the Omicron variant are being discussed in this section ( Table 2 ).
List of drugs which has been approved and authorized by FDA for emergency use in COVID-19 patients. (Source: FDA homepage, Medlineplus, Medicalletter).
Drugs | Dosage | Method of Administration | Duration | Side Effect | Mode of Action | Efficacy of Monoclonal Antibodies/ Drugs against SARS-CoV-2 Variants | Reference |
---|---|---|---|---|---|---|---|
Sarilumab | Single dose of sarilumab 400 mg | Intravenous infusion | Sarilumab infusion should be used within 4 h of preparation | Neutropenia, thrombocytopenia and GI perforation | Suppress cytokine storm | Effective against COVID-19 | [ , , ] |
Tocilizumab (Actemra) | 12 mg/kg in patients weighing <30 kg and 8 mg/kg in those weighing ≥30 kg (max dose 800 mg) | Intravenous infusion | Administered as a single IV infusion over 60 min | Neutropenia, thrombocytopenia, serum hepatic transaminase elevations, gastrointestinal perforations, and anaphylaxis | Inhibits binding of the proinflammatory cytokine IL-6 to its receptors | Effective against COVID-19 | [ , ] |
Dexamethasone (DEX) | DEX 6 mg | Orally or Intravenous infusion | Once daily for up to 10 days or until hospital discharge, whichever comes first | Avascular necrosis, Adrenal insufficiency, Increased BP, Peripheral edema, and Myopathy | Suppress inflammation | Effective against COVID-19 | [ ] |
Baricitinib (Olumiant) | 4 mg | Orally | Once daily while hospitalized for up to 14 days | Lymphoma and other malignancies, Thrombosis, GI perforation and serious cardiac-related events (e.g., MI, stroke) | Inhibits viral endocytosis | Effective against COVID-19 | [ ] |
Remdesivir (Veklury) | 200 mg IV on day 1, followed by 100 mg once daily | Intravenous infusion | Treatment duration is 5–10 days | Nausea, Hypersensitivity reactions | Inhibits viral RNA-dependent RNA polymerase | Active against Omicron and all other variants: Alpha, Beta, Gamma and Delta | [ , ] |
Molnupiravir | 800 mg every 12 h | Orally | Treatment should be started within 5 days of symptom onset | Diarrhea, nausea, and dizziness | Targets viral RNA polymerase, inducing mutagenesis and inhibiting SARS-CoV-2 replication | Active against the entire variants: Alpha, Beta, Gamma, Delta and Omicron | [ , ] |
Paxlovid (Ritonavir-Boosted Nirmatrelvir) | 300/100 mg (2 nirmatrelvir tablets and 1 ritonavir tablet taken together) twice daily | Orally | Treatment should be started within 5 days of symptom onset | Dysgeusia, diarrhea, hypertension, and myalgia | Inhibits the SARS-CoV-2 main protease (Mpro), preventing viral replication. | Active against entire SARS-CoV-2 variant including, omicron | [ ] |
Bamlanivimab Plus etesevimab | 700 mg (one vial) of Bamlanivimab and 1400 mg (two vials) of etesevimab | single Intravenous infusion | One-time dose right after COVID-positive test and within 10 days after the onset of infection symptoms | Bleeding, bruising, pain, soreness, or swelling at injection sit | Binds to spike protein RBD of SARS-CoV-2 | Active against two SARS-CoV-2 variant: Alpha and Delta | [ , , ] |
Casirivimab plus imdevimab (REGEN-COV) | 600 mg of casirivimab and 600 mg of imdevimabis diluted together in 50, 100, 150, or 250 mL of normal saline at a maximum rate of 310 mL/hr (180 mL/hr if diluted in 50 mL) | Intravenous infusion or Subcutaneous injection | After a positive SARS-CoV-2 test result and within 10 days of COVID-19 symptom onset | Pain, bleeding, bruising of the skin, soreness, swelling, or infection at injection site | Bind at different sites on the RBD of the spike protein of SARS-CoV-2. | Active against all SARS-CoV-2 variant: Alpha, Beta, Gamma, Delta, Omicron | [ , , ] |
Sotrovimab | 500 mg of sotrovimab diluted in 50 or 100 mL of normal saline | Intravenous infusion | After a positive viral test for SARS-CoV-2 and within 10 days of symptom onset | Rash (2%) and diarrhea (1%). Hypersensitivity reactions, including anaphylaxis | Binds at the epitope sites on the spike protein and prevent membrane fusion after the virus binds to the human ACE2 receptor | Active against the entire variants: Alpha, Beta, Gamma, Delta and Omicron | [ , , ] |
Tixagevimab plus cilgavimab | 150 mg of each antibody is administered. | Intramuscular injection | one time as two shots (one after another) | Headache (6%) and fatigue (4%). | Binds to non-overlapping region of the SARS-CoV-2 spike protein. | Active against the entire variants: Alpha, Beta, Gamma, Delta and Omicron | [ , , ] |
Bebtelovimab | 175 mg/2 mL vials | Intravenous infusion | Treatment should be started within 7 days of symptom onset | Rash, pruritus, and infusion-related reactions | Binds to the spike protein and prevents its attachment to the human receptor | Active against the Omicron variant of SARS-CoV-2 (Neutralize BA.1 and BA.2omicron variant) | [ ] |
Amid Omicron, WHO continues to approve new COVID-19 treatments for hospitalized patients, according to their disease severity. The arthritis drugs tocilizumab and sarilumab [ 61 , 62 ], which have been found to have efficacy in the treatment of COVID-19 patients with moderate to severe COVID-19 pneumonia, have recently been approved by WHO [ 63 ]. Similarly, dexamethasone, which is effective at reining in lung-damaging inflammation [ 64 ], and Baricitinib a Janus kinase (JAK) inhibitor, are also approved by WHO for treatment in COVID-19 patients as per the panel’s recommendation [ 65 ]. Recently, studies have shown that dextromethorphan treatment was characterized by regulation of adaptive immunity and other specific local innate; however, it was not associated with the regulation of pro-inflammatory pathways in COVID-19 acute respiratory distress syndrome (CARDS) [ 66 ].
Recently, the U.S. FDA issued an emergency use authorization (EUA) for Pfizer’s Paxlovid (nirmatrelvir tablets and ritonavir tablets) for the treatment of COVID-19 patients with mild–moderate symptoms and those at high risk of progressing into severe illness. This should be prescribed immediately, within five days after diagnosis of COVID-19 [ 67 ]. During the biochemical assay, the nirmatrelvir drug was shown to inhibit the 3CL protease associated with the Omicron (B.1.1.529) variant [ 68 ]. In vitro studies also suggest that Paxlovid has the potential to maintain plasma concentrations, thus preventing Omicron and other variants from replicating.
Molnupiravir, an oral antiviral drug, is a small molecule of the synthetic nucleoside derivative N-hydroxycytidine (NHC). It targets viral RNA polymerase and inhibits SARS-CoV-2 replication. It was granted EUA by the FDA’s Antimicrobial Drugs Advisory Committee on 23 December 2021, for the treatment of COVID-19 [ 69 ].
The antiviral drug Veklury (remdesivir) was approved by the FDA in 2020 for the treatment of COVID-19 in adult and pediatric patients, and those of old age [ 70 ]. These three drugs: molnupiravir, remdesivir, and paxlovid have shown neutralizing activity against other VOCs, including the novel Omicron variant [ 71 ]. Many antiviral drugs such as Ivermectin, Interferon Alfa, Interferon Beta, Interferon Lambda, and Nitazoxanide are still under evaluation for the treatment of COVID-19. All these drugs have paved the way as new hopes to fight against the COVID-19 pandemic.
The emergence of COVID-19 has led to the development of various treatments. Monoclonal antibodies (mAbs) are a novel class of antiviral intervention [ 72 ]; they target the RBD of the SARS-CoV-2 spike protein, which is highly mutated in the Omicron variant [ 73 ]. They are one of the most effective therapeutic strategies to neutralize viral replication. This has been shown proven in a previous experiment conducted by researchers from the Baylor University Medical Centre, Dallas, Texas in the US, where dual mAb therapy was shown to reduce viral transmission [ 74 ].
Currently, four anti-SARS-CoV-2 mAb products: bamlanivimab plus etesevimab, casirivimab plus imdevimab (REGEN-COV), sotrovimab, and tixagevimab plus cilgavimab (Evusheld) have been authorized by the FDA for emergency used to treat COVID-19-positive, non-hospitalized patients who are likely to develop more serious disease at the later stage [ 75 ]. The bebtelovimab monoclonal antibody was approved recently [ 76 ]. Such mAbs as casirivimab plus imdevimab, and bamlanivimab plus etesevimab, which have shown effectiveness in the previous VOCs, have reduced neutralization in the Omicron variant [ 77 ].
Recently, Emi et al. [ 78 ] assessed the neutralizing activities of mAbs using a live-virus focus reduction neutralization assay (FRNT) against the Omicron variant and other VOCs. Etesevimab, bamlanivimab and imdevimab did not neutralize Omicron. Casirivimab showed reduced neutralization against the Omicron variant. COV2-2196 (tixagevimab), COV2-2130 (cilgavimab), and S309 (marketed as sotrovimab) retained neutralizing activity against the Omicron variant. Thus, there are two authorized monoclonal antibody treatments against Omicron—Sotrovimab and Evusheld. Early reports also suggest that bamlanivimab and C144-LS antibodies have reduced efficacy against the Omicron variant. Based on early modeling, studies have shown casirivimab plus imdevimab (REGN-COV2), as well as the Rockefeller University antibody C135, to be effective against the Omicron variant [ 79 ]. Some of the monoclonal antibodies authorized by the FDA for emergency use are listed below.
These mAbs bind at the overlapping sites in the spike protein RBD of SARS-CoV-2; blocking its attachment to the human ACE2 receptor. The FDA has banned the use of these mAbs in some areas of the United State due to the progression of variant resistance [ 80 ]. However, the FDA has approved a EUA to allow the use of this mAbs injection in certain non-hospitalized adults and children and infants (≥2 years of age) who have mild to moderate COVID-19 symptoms with a risk of progressing to serious illness [ 81 ].
These are recombinant human mAbs that prevent the entry of the virus into human cell by targeting the spike protein of SARS-CoV-2. The FDA has authorized the use of these mAbs to treat mild to moderate SARS-CoV-2-positive adults and pediatric patients. It is also administered to patients above 65 years of age with chronic medical conditions. However, it is not authorized for hospitalized COVID-19 patients with oxygen therapy [ 82 ]. Recently, the FDA rescinded its authorization of these drugs, due to the prevalence of the Omicron variant [ 83 ].
This mAb targets an epitope region in the spike protein RBD that is conserved between SARS-CoV and SARS-CoV-2. This monoclonal antibody has been shown to neutralize the Omicron variant. However, it is not authorized for use in COVID-19 patients who are hospitalized with mechanical ventilation [ 84 ].
The tixagevimab and cilgavimab monoclonal antibodies bind to non-overlapping sites of the SARS-CoV-2 spike protein, preventing the interaction between the virus and the ACE2 receptor. The FDA has approved a EUA to allow certain adults and children 12 years of age and older to receive this mAbs injection. The combination has shown to somewhat decrease neutralizing activity in in vitro against the Omicron variant [ 85 ].
This mAbs has not been approved and has only been authorized for emergency use by the FDA for treatment of mild to moderate COVID-19 patients (≥12 years old) with a high risk of progressing to severe illness. It neutralizes the SARS-CoV-2 spike glycoprotein RBD, thereby inhibiting the entry of the virus into a human cell. Bebtelovimab is active and has shown some neutralizing activity against other VOCs, including the Omicron variant [ 76 ].
Thus, the abilities of all these monoclonal antibodies and anti-viral therapies to fight and neutralize the Alpha, Beta, Gamma, and Delta VOCs—including the novel Omicron variant—have paved the way for hope in the future to make a potential therapeutic and diagnostic intervention.
The emergence of the novel Omicron variant has created chaos worldwide. Just after the announcement of Omicron as a VOC by WHO, this novel variant had already spread globally. This rapid spread of the Omicron variant has concerned global health bodies. This is due to a high level of mutation; overall, Omicron has 50 mutations, with 30 mutations on its spike protein. This review gives an overview, highlighting concerns about the emergence of the Omicron variant, its vast array of mutations, the impact of diagnosis methods to detect the novel Omicron variant, and the novel advancement in therapeutic drugs.
The Omicron variant possesses a phenomenon called S-gene dropout, due to the deletion of the amino acid at spike protein position 69–70. This acts as a marker to measure the prevalence of the Omicron variant during diagnosis. However, this phenomenon does not apply to the BA.2 sub-lineage of the Omicron variant. A vast number of mutation and phylogenetic analyses revealed that the Omicron variant may possess similar characteristics to the Gamma (P.1) variant at the molecular level, predicting that drugs suitable for gamma may equally work for the novel Omicron variant.
Recent in vitro studies indicate that Novel Antibody IGM-6268 exhibits potential neutralizing activity against the Omicron variant, as well as other VOCs and VOIs. Interestingly, three drugs namely: molnupiravir, remdesivir, and paxlovid have been approved and authorized by the FDA for emergency use, as they show neutralizing activity against other VOCs, including the novel Omicron variant. This article has a limitation, as it lacks clinical data on the efficacy of mAbs and anti-viral drugs for the treatment of patients with the Omicron variant. Here, we have only described mAbs and anti-viral drugs authorized by the FDA for emergency use in hospitalized and non-hospitalized COVID-19 patients.
It is almost inescapable that there will be the emergence of a new variant, as long as there is a loophole in one part of the world that is unprotected.
It has been more than two years since the emergence of this COVID-19 pandemic. Despite several measures and protocols to control the virus, it has dominated the world. High levels of effort and mass vaccination campaigns to restrain the spread of this virus have become useless with the emergence of novel variants. COVID-19 has escalated around the globe within a short period and the outcome is devastating, with global health concerns and economic fallout. The emergence of a new VOC every year with the accumulation of a large number of mutations is of concern. The vast array of mutations in SARS-CoV-2 has recently given rise to the most mutated Omicron variant of SARS-CoV-2. The emergence of mutations could be due to the transmissibility of the virus from person to person, leading to its escape from population immunity and frequent transmission. It is the nature of the virus to mutate. This novel Omicron variant has shown itself to be resistant to vaccination and requires booster doses. The hypothesis of its epizootic transfer needs validation and should be thoroughly investigated. At present, there is no specific data and evidence to get rid of SARS-CoV-2. Moreover, the etiology of SARS-CoV-2 is poorly understood. As of now, some anti-viral and monoclonal antibody drugs are being authorized by the FDA for emergency use, as per the panel’s recommendation. This COVID-19 is not going away soon, and may remain forever. The only way to tackle this situation is to follow appropriate protocol and measurements as per the WHO recommendations, such as quarantine, keeping good personal hygiene, social distancing, wearing a mask, and vaccination. In addition, strengthening the level of research for the development of potential vaccines and anti-viral drugs, and a proper strategy to tackle the situation in case of new variants should be evaluated at the global level. It is also very important to monitor and expand genomic surveillance to keep track of the emergence of new variants, thus avoiding the spread of new diseases worldwide.
This research was funded by two industry–academia collaboration projects, VtR Inc-CGU, R.O.C., project grant (SCRPD1L0221), DOXABIO-CGU, R.O.C., project grant (SCRPD1K0131), and also the CGU project grant (UZRPD1L0011).
Conceptualization, B.M.K., R.P.P. and C.-M.C.; methodology, B.M.K. and S.K.; validation, R.P.P.; formal analysis, B.M.K. and M.S.; investigation, B.M.K., M.S., S.K. and R.P.P.; resources, B.M.K. and S.K.; data curation, B.M.K.; writing—original draft preparation, B.M.K.; writing—review and editing, B.M.K., M.S., S.K., R.P.P. and C.-M.C.; visualization, B.M.K.; supervision, R.P.P. and C.-M.C.; project administration, R.P.P.; funding acquisition, C.-M.C. All authors have read and agreed to the published version of the manuscript.
Informed consent statement, data availability statement, conflicts of interest.
The authors declare no conflict of interest.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
In November 2021, the World Health Organization (WHO) first identified the Omicron mutation of the COVID-19 virus as a variant of concern. It quickly became the most common strain worldwide.
Since then, several sub-variants of Omicron have surfaced, including BA.2, BA.3, BA.4, and BA.5. By the summer of 2022, the BA.5 variant was the most dominant strain in the US. The BA.5 and BA.4 variants appear to be the most contagious types of COVID-19 so far, according to the CDC. In January of 2023, a new Omicron variant called XBB.1.16 was reported and labeled as “one to watch” by the WHO.
Omicron variants seem to cause less serious illness than earlier types of this coronavirus. The COVID-19 vaccines still work well to protect people against hospitalization and death. Th e new bivalent vaccine targets both the original strain as well as Omicron.
Your chances of getting any variant of COVID-19 are greatest if you haven't gotten the COVID-19 vaccine. It's still possible to get the virus if you've been vaccinated (breakthrough infection), but your symptoms should be milder and your chances of having to go to the hospital are much less.
Several other things raise your risk of getting very sick from COVID-19, including
Early studies found that cold-like symptoms were common in those with Omicron. They reported that the top five symptoms related to the variant were:
But other common COVID-19 symptoms, such as cough, fever, and loss of smell or taste, are still important signs to watch out for in case of any COVID-19 variant.
WHO experts have said there isn’t any data that suggests Omicron causes symptoms that are different from the ones produced by other COVID-19 variants.
Omicron symptoms day by day
A 2020 study from the University of Southern California found that COVID-19 symptoms tend to come in this order:
If your symptoms follow this pattern, you may want to take a COVID-19 test , seek care, and begin to self-isolate.
How long do you stay contagious with Omicron?
This variant has a shorter incubation time than those that came before it — about 3 days. If you have it, you can spread the virus to others from 1-2 days before your symptoms start until 2-3 days after they've cleared up. Even if you never show symptoms, you can still be contagious. Ten days after your symptoms begin or you test positive for COVID-19, you should no longer be contagious, as long as you're feeling better and your fever has stopped.
Studies show that the incubation period for Omicron is 3.42 days. This is shorter than the ones for the Alpha, Beta, and Delta variants.
Omicron typically causes less severe disease than other variants. However, some people may still get very sick, need to be hospitalized, and could die from an Omicron infection.
Having a less severe case of COVID-19 is especially true for instances of reinfection or breakthrough cases in people who are fully vaccinated. One early study shows that a previous infection only gives a 19% protection rate. It puts the chances of getting reinfected at almost 5½ times higher with this variant than with the Delta variant .
Remember that even a relatively mild case of COVID-19 can cause long COVID: symptoms that last weeks or months after the first illness has passed.
Omicron spreads more easily than earlier variants of COVID-19, including Delta. Researchers think this is mostly because this strain is better able to get around people's immune defenses, even if they've been vaccinated.
Omicron BA.2 or “ stealth ” subvariant. Scientists named this variant Omicron BA.2 to distinguish it from the original Omicron variant, BA.1. At first, scientists thought BA.2 wasn’t as contagious as BA.1 and would fade away soon. That didn’t happen. Starting in January 2022, BA.2 appeared to be at least as easy to transmit as BA.1.
A January 2022 study in Denmark showed no difference in the number of hospitalizations caused by BA.2 and BA.1. It also showed that as BA.2 cases went up, BA.1 cases went down. But other countries (Great Britain, Norway, and Sweden) reported a slower increase in the number of BA.2 cases.
Early studies show that current vaccines and boosters seem to work at least against this variant, protecting against a first infection as well as against serious illness.
BA.4 subvariant. Experts first detected the BA.4 subvariant in South Africa in early 2022, followed shortly by the BA.5 subvariant. Since then, the number of countries and cases linked to these variants has spiked.
Both BA.4 and BA.5 have mutations that make them different from previous Omicron subvariants. These mutations affect the "spike" proteins that help the virus latch onto and infect your cells. This makes infection easier. It also helps BA.4 and BA.5 evade virus-fighting antibodies from previous infections with COVID-19.
BA.5 subvariant. BA.5 seems to spread more easily than BA.4. In late July 2022, BA.5 was responsible for about 78% of COVID cases in the U.S., compared to 13% for BA.4. Along with the spike protein mutation, BA.5 has additional mutations that distinguish it from BA.4.
Experts believe that symptoms of BA.4 and BA.5 are similar to those of past variants. They include:
XBB subvariant. This subvariant is a combination of two BA.2 strains. It has mutations that help it evade immunity better than other variants. It also attaches more tightly to cells, making it easier to spread. It arose in mid-2022 and quickly became the cause of a majority of COVID-19 cases in the U.S. But it didn't cause a big jump in the number of cases. Because it has so many mutations, you could easily be reinfected with this one if you already had COVID-19 caused by another strain of the virus.
EG.5 or “ Eris ” subvariant. This descendant of the XBB subvariant first appeared in February of 2023. And by August of that year, it had become the most common and fastest-spreading subvariant in the U.S. While it spreads rapidly, experts have found that it's not more severe than strains that came before it.
To find out if you have the virus , you’ll need to take a COVID-19 test. You can access at-home tests or see a doctor to get one. If you test positive, more testing would be needed to tell if your case was caused by this variant. But this process takes a long time and is expensive. Experts don’t usually do it for each positive COVID-19 case. The tests are also done anonymously to protect people’s privacy, so you won’t get that information.
Researchers continue to look at how well current COVID-19 treatments help with Omicron cases. Because of the genetic changes in this variant, some treatments will continue to be effective, while others may be less useful. Your doctor may suggest antiviral medicines or monoclonal antibody treatments as an outpatient depending on your risk factors for serious disease from COVID-19.
Corticosteroids and IL6 receptor blockers still help people with severe COVID-19 infections.
How long does Omicron last?
This variant has an incubation period of just over 3 days. If you have Omicron or any variant of COVID-19, you will likely have symptoms for a couple of weeks. You're contagious from 1-2 days before your symptoms start until 2-3 days after they're gone. You can be contagious even if you don't have symptoms. You shouldn't be contagious anymore about 10 days after you first have symptoms or a positive COVID-19 test, as long as you're not having symptoms or a fever .
The BA.4 and BA.5 variants are close enough to the original Omicron virus, and existing COVID-19 vaccines help prevent serious illness. So, it's important to get your COVID-19 vaccine and boosters.
The new bivalent booster vaccine targets both the original strain as well as Omicron.
Omicron booster
In October of 2022, the FDA authorized updated booster COVID-19 vaccines. These are bivalent vaccines, which means that they target both the original strain of the virus and the Omicron BA subvariants. You get this booster as a single dose.
If you’re an adult, you can get your booster as soon as 2 months after your most recent COVID-19 vaccine. But to get the maximum benefit, it’s best to wait at least 6 months when the antibody levels from your vaccine have gone down. If you’ve had COVID-19 recently, wait for 3 months from the date you first had symptoms or your positive test result if you didn’t have symptoms.
You can get the booster at the same time as any other vaccines you may need, including the flu vaccine.
Visit the CDC website to see current booster recommendations for people aged 65 and older, children between the ages of 6 months and 5 years, and those with weakened immune systems .
When you get your booster, you may have side effects that include:
These side effects are likely to be mild and should go away within a few days.
There are many things you can do to protect yourself against Omicron and other COVID-19 variants:
Get vaccinated. Vaccines are still the best public health step to protect people against serious illness from COVID-19. Get boosters if you're eligible.
Wear a high-quality mask. Your mask will protect you and those around you from all variants. The CDC suggests that you wear a mask in public indoor areas, regardless of whether you’ve had the COVID-19 vaccine, if the COVID-19 community level is high, or if you prefer to be masked. Also, wear a mask if you or a family member are at high risk for severe COVID-19 disease even if the community level is at medium.
Social distance. It’s important to continue to social distance to stop the spread of any variant of COVID-19 when there is a threat in the area.
Get a test. Self-tests or tests given by medical professionals can tell you if you have COVID-19 or not. These tools can help you take steps to protect others from Omicron and other variants.
Other safety measures. Open your windows to improve ventilation, keep your hands clean, stay away from crowded or poorly ventilated areas, and cough or sneeze into your elbow or a tissue.
Omicron is a variant of SARS-CoV-2, the virus that causes COVID-19.
What is Omicron?
Omicron is a variant of SARS-CoV-2 , the virus that causes COVID-19. A short time after it was identified, it became the dominant variant around the world.
Is Omicron a mutation?
All viruses mutate (or change) over time. Some of these changes don't alter the virus much. But others affect how they operate: They may help them adapt to the immune defenses of their host organisms so they can continue to spread. Or they can make the illness they cause more severe or harder to treat. The virus that causes COVID-19 has mutated several times since it first appeared. This means that there are several different variations or lineages that people can catch and spread to others.
Why is Omicron serious?
The incubation period for this variation of the virus is very short. You're contagious as soon as the day after you've been infected and before you have any symptoms. This makes it easy for someone to spread the illness to many other people very quickly before they realize they're sick and start to isolate themselves.
When did Omicron start?
The Omicron variation was first identified in late November 2021. The first case in the U.S. was confirmed one week later.
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SEAR/PR/ 1777
New Delhi, 18 December 2021 –
With seven countries in South-East Asia Region confirming cases of the new COVID-19 variant Omicron, the World Health Organization today emphasized on urgent scale up of public health and social measures to curtail its further spread.
“Countries can – and must – prevent the spread of Omicron with the proven health and social measures. Our focus must continue to be to protect the least protected and those at high risk,” said Dr Poonam Khetrapal Singh, Regional Director, WHO South-East Asia Region.
The overall threat posed by Omicron largely depends on three key questions – its transmissibility; how well the vaccines and prior SARS-CoV-2 infection protect against it, and how virulent the variant is as compared to other variants.
From what we know so far, Omicron appears to spread faster than the Delta variant which has been attributed to the surge in cases across the world in the last several months, the Regional Director said.
Emerging data from South Africa suggests increased risk of re-infection with Omicron, she said, adding that there is still limited data on the clinical severity associated with Omicron. Further information is needed to fully understand the clinical picture of those infected with Omicron. We expect more information in the coming weeks.
Omicron should not be dismissed as mild, the Regional Director said, adding that even if it does cause less severe disease, the sheer number of cases could once again overwhelm health systems. Hence, health care capacity including ICU beds, oxygen availability, adequate health care staff and surge capacity need to be reviewed and strengthened at all levels.
“We must continue to do it all. Protect yourself and protect each other. Get vaccinated, wear a mask, keep a distance, open windows, clean your hands and cough and sneeze safely. Continue to take all precautions even after taking vaccine doses,” the Regional Director said.
On the impact of the new variant on vaccines, Dr Khetrapal Singh said preliminary data suggests that that vaccines may likely have reduced effectiveness against infections by the Omicron variant. However, studies are underway to better understand the extent to which Omicron may evade vaccine and/or infection derived immunity and the extent to which current vaccines continue to protect against severe disease and death associated with Omicron. Globally, the pandemic is driven by the Delta variant, against which the vaccines continue to provide a robust level of protection from severe disease, hospitalization, and death. Hence, our efforts to scale-up vaccination coverage must continue.
“Vaccines are an important tool in our fight against the pandemic, but, as we know, vaccines alone will not get any country out of this pandemic. We must scale up vaccination and at the same time implement public health and social measures, which have proven critical to limiting transmission of COVID-19 and reducing deaths,” the Regional Director said.
Public health and social measures include surveillance and response such as testing, genetic sequencing, contact tracing, isolation, and quarantine. They include personal protective measures such as masks; physical distancing; avoiding crowded, closed and confined settings; ensuring hand hygiene and respiratory etiquette. Physical distancing measures include regulating the number and flow of people attending gatherings, maintaining distance in public or workplaces.
WHO has been advocating for the measures to be tailored to local settings and conditions, and implemented in a timely manner to be effective.
Media Contacts
Shamila Sharma
Public Information and Advocacy Officer WHO South-East Asia Regional Office
IMAGES
COMMENTS
1. INTRODUCTION. The SARS‐CoV‐2 virus has infected over 260 000 000 people globally with over 5 000 000 people dying from the coronavirus disease‐2019 (COVID‐19) over the past 2 years since it was first discovered. 1 A herculean effort has been put forth to combat COVID‐19 through scientific research, public health and patient care. 2 Unlike many diseases, where preventative measures ...
On Nov 25, 2021, about 23 months since the first reported case of COVID-19 and after a global estimated 260 million cases and 5·2 million deaths,1 a new SARS-CoV-2 variant of concern (VoC), omicron,2 was reported. Omicron emerged in a COVID-19-weary world in which anger and frustration with the pandemic are rife amid widespread negative impacts on social, mental, and economic wellbeing ...
Omicron (B.1.1.529), a highly mutated SARS-CoV-2 variant, has emerged in the south of African continent in the November 2021. ... The aggressive surge of Omicron is making it the major corona virus strain, displacing the worldwide prevalent Delta form. As of now, PCR tests have been used to detect this variant. However, Omicron is expected to ...
The sub-lineages of the SARS-CoV-2 Omicron variant. a The Omicron variant has evolved into three sub-lineages: BA.1, BA.2, and BA.3.b Venn diagram showing the mutations located on the S protein ...
On Nov 25, 2021, about 23 months since the first reported case of COVID-19 and after a global estimated 260 million cases and 5·2 million deaths, 1 a new SARS-CoV-2 variant of concern (VoC), omicron, 2 was reported. Omicron emerged in a COVID-19-weary world in which anger and frustration with the pandemic are rife amid widespread negative impacts on social, mental, and economic wellbeing.
In April, New York officials announced that two new subvariants, which evolved from BA.2, were spreading rapidly in the state. One of them, known as BA.2.12.1, quickly outcompeted BA.2., becoming ...
Gauteng's R value was well below 1 in September — when Delta was the predominant variant and cases were falling — suggesting that Omicron has the potential to spread much faster and infect ...
A Scientist's Guide to Understanding Omicron. SARS-CoV-2 virus particles which cause COVID-19. Azaibi Tamin Hannah A. Bullock/CDC, via Associated Press. Dr. Bloom's lab at Fred Hutchinson ...
Three research papers were published recently to compare the virological properties of the Omicron variant with the earlier variants of concern (VOC). 1,2,3 The SARS-CoV-2 B.1.1.529 variant ...
Update on Omicron. On 26 November 2021, WHO designated the variant B.1.1.529 a variant of concern, named Omicron, on the advice of WHO's Technical Advisory Group on Virus Evolution (TAG-VE). This decision was based on the evidence presented to the TAG-VE that Omicron has several mutations that may have an impact on how it behaves, for example ...
Published on December 6, 2021. Throughout the COVID-19 pandemic, several coronavirus variants have emerged as the virus, SARS-CoV-2, continues to mutate and evolve. Many of these variants' mutations have little or no impact on how the virus affects humans. But others, such as the genetic changes in the delta variant, can make the coronavirus ...
Earlier versions of SARS-CoV-2 relied on a cellular receptor, ACE2, to bind to the cells, and on a cellular enzyme called TMPRSS2 to cleave its spike protein, granting the virus entry. Omicron has ...
Scientists around the world are racing to understand the Omicron variant, and there are some clearer signs than a week ago. Today's newsletter will try to answer four big questions about Omicron ...
The first intrinsic driver enhancing the spread of the Omicron variants is the change in the pathway of virus entry into the cell (Figure 4a). Despite the greater efficiency of membrane fusion channels for cell entry compared to endosomal channels [ 19 ], several studies have reported that the Omicron variants still tend to enter cells via ...
The worry since scientists first saw the list of mutations on Omicron is it would make vaccines less effective. It just looks so different to the original virus that was used to design the vaccines.
Omicron (pronounced ah·me·kraan) is the thirteenth variant of SARS-CoV-2, the coronavirus that causes COVID-19, named by the World Health Organization, using a Greek letter naming scheme. It is the fourth variant designated by the WHO as a "variant of concern" after Delta, which is currently responsible for most cases and deaths around ...
The Technical Advisory Group on SARS-CoV-2 Virus Evolution (TAG-VE) is an independent group of experts that periodically monitors and evaluates the evolution of SARS-CoV-2 and assesses if specific mutations and combinations of mutations alter the behaviour of the virus. The TAG-VE was convened on 26 November 2021 to assess the SARS-CoV-2 variant: B.1.1.529.
The Omicron variant is spreading widely and infecting large numbers of people, including the vaccinated and those previously infected with the virus. While spikes in cases have been the norm for ...
Scientists are seeking to understand if vaccines will work against Omicron. Scientists in South Africa and around the world are working at pace to discover more about a newly identified strain of the COVID-19 virus. On November 26th the World Health Organization (WHO) designated variant B.1.1.529 as a 'variant of concern' and named it Omicron.
Goats and Soda. Omicron is spreading at lightning speed. Scientists are trying to figure out why. A colorized electron micrograph image of a cell (red) infected with with SARS-CoV-2 virus ...
The scientific community has already sketched out a preliminary picture of omicron, the latest variant of the coronavirus, and which was first detected three weeks ago in the south of Africa.The variant, with a never-before-seen number of mutations, is spreading across the planet at an unprecedented speed compared to its predecessors. The European authorities have warned that the growth of ...
Similarly, the H655Y, N679K, and P681H mutations in the Omicron spike protein, also found in the Alpha and Delta variants, could increase the transmission of the virus [6,33,34]. It has the deletion at spike protein (Δ69-70), position 69-70, similar to the Alpha and Eta variants, that leads to the S-gene dropout or S-gene target failure.
Omicron is a variant of SARS-CoV-2, the virus that causes COVID-19. It first appeared in November 2021 and quickly became the dominant variant around the world.
SEAR/PR/1777New Delhi, 18 December 2021 - With seven countries in South-East Asia Region confirming cases of the new COVID-19 variant Omicron, the World Health Organization today emphasized on urgent scale up of public health and social measures to curtail its further spread. "Countries can - and must - prevent the spread of Omicron with the proven health and social measures.