Quan Ke Thai,
Department of Saigon University, 273 An Duong Vuong, Ward 3 District 5, Ho Chi
Minh city, Vietnam. Phuoc Huynh, department of aVNU HCMC University of Science,
227 Nguyen Van Cu, Ward 4 District 5, Ho Chi Minh city, Vietnam. Yen Le Thi,
department of DSI1191, Saigon University, 273 An Duong Vuong, Ward 3 District
5, Ho Chi Minh city, Vietnam. Huyen
Nguyen Thi Thuong, department of Department of Biology, HCMC University of
Education, 280 An Duong Vuong Ward 4 District 5, Ho Chi Minh city, Vietnam. Wrote
a research article about, Genetic Diversity of Omicron Spike Variants in
Vietnam. Entitled, Genetic diversity of SARS-CoV-2 Omicron variants’ spike gene
in Vietnam. This research paper published by the International Journal of Biosciences | IJB. an open access scholarly research journal on Biosciences.
under the affiliation of the International Network For Natural Sciences|
INNSpub. an open access multidisciplinary research journal publisher.
Abstract
The recently emerging Omicron is of prime concern because this variant has been the cause of current large outbreaks. Omicron becomes more dangerous when numerous content mutations in the Spike (S) gene lead to more than 30 substitutions of amino acids in spike protein. Omicron variant had been identified as Variants Of Concern (VOC) when it had transmission rate overtake previous VOCs. In this report, we focus on analyzing the genetic diversity of the S gene of Omicron variants in Vietnam. Our results indicate the high level of haplotype diversity when confirmed 362 haplotypes and the haplotype diversity index at 0.9160 ± 0.0037. The analysis of nucleotide diversity display nucleotide diversity at 0.0053 ± 0.0026 and recorded 318 polymorphic sites with the average number of mutations of 40 ± 9. Almost missense mutations appeared in the RBD region, and deletion and insertion occurred in the NTD region. Besides, we note conserved mutation in the S gene of Omicron in Vietnam, namely C21618T G21987A T22200G G22578A C22674T T22679C C22686T A22688G G22775A A22786C G22813T T22882G G22992A C22995A A23013C A23040G A23055G A23063T T23075C A23403G C23525T T23599G C23604A C23854A G23948T A24424T T24469A, and C25000T. Furthermore, the genetic networks of the S gene provided more correlation between infection and mutation in this gene. Ultimately, we propose the close relation between BA.2 and BA.4, BA.5 through the network, in which necessary focus T22917G (L452R), T23018G (F486V), and other novel mutations will appear in the S gene. The network provided the whole picture of Omicron variants in Vietnam, supporting the tracing of the source of a new outbreak in the future.
Introduction
The recently emerging
Omicron is of prime concern because this variant has been the cause of current
large outbreaks. Omicron becomes more dangerous when numerous content mutations
in the Spike (S) gene lead to more than 30 substitutions of amino acids in
spike protein. Omicron variant had been identified as Variants Of Concern (VOC)
when it had transmission rate overtake previous VOCs. In this report, we focus
on analyzing the genetic diversity of the S gene of Omicron variants in
Vietnam. Our results indicate the high level of haplotype diversity when
confirmed 362 haplotypes and the haplotype diversity index at 0.9160 ± 0.0037.
The analysis of nucleotide diversity display nucleotide diversity at 0.0053 ±
0.0026 and recorded 318 polymorphic sites with the average number of mutations
of 40 ± 9. Almost missense mutations appeared in the RBD region, and deletion
and insertion occurred in the NTD region. Besides, we note conserved mutation
in the S gene of Omicron in Vietnam, namely C21618T G21987A T22200G G22578A
C22674T T22679C C22686T A22688G G22775A A22786C G22813T T22882G G22992A C22995A
A23013C A23040G A23055G A23063T T23075C A23403G C23525T T23599G C23604A C23854A
G23948T A24424T T24469A, and C25000T. Furthermore, the genetic networks of the
S gene provided more correlation between infection and mutation in this gene.
Ultimately, we propose the close relation between BA.2 and BA.4, BA.5 through
the network, in which necessary focus T22917G (L452R), T23018G (F486V), and
other novel mutations will appear in the S gene. The network provided the whole
picture of Omicron variants in Vietnam, supporting the tracing of the source of
a new outbreak in the future.
appearance of the Delta
variant is almost eliminated, breaking the achievements preventing the pandemic
in some countries. Delta's rapid transmission is determined mainly by the spike
protein's L452R, T478K, and E484Q N501Y mutations (Kumar, Singh et al., 2021)
(Fan, Hu et al., 2021). In addition, some substitutions, such as E484K, D614G,
and P681H/R, have also been conserved in many different VOC variants
(Papanikolaou, Chrysovergis et al., 2022) (Lubinski, Frazier et al., 2021) .
Recently, a new variant is thought to be more infectious than the Delta variant
and maintains from 30 to 45 mutations in the spike protein (Wei, Shan et al.,
2021) (Kumar, Thambiraja et al., 2022). According to PANGO Lineages, this
variant belongs to lineage B.1.1.529, named Omicron by WHO and classified as a
VOC variant. Since December 2021, Omicron has almost replaced Delta as the
primary source of infection infections in the United States (Fall, Eldesouki et
al., 2022). After that, the Omicron variant became almost universally dominant
and gradually replaced the previously dangerous Delta variant (Chaguza, Coppi
et al., 2022).
Vietnam is one of the
infrequent countries that has succeeded in controlling the epidemic situation
in the early stages of the pandemic outbreak in the world. Vietnam has
successfully gone 99 days with no community transmission, and most cases (60%)
in Vietnam are due to entry from China, Europe, and the United States (Thai,
Rabaa et al., 2021). Examination of genomics indicated that the nucleotide
similarity of the sequences in Vietnam in the two outbreaks was very high
(minimum 99.96%, mean 99.97%), combined with familiar mutation exhibiting that
virus is not competent to silently infect the community from April 2020
(Phuong, Tung et al., 2021). In Vietnam, each epidemic wave corresponds to the
emergence of a new variant with a more robust infectious fitness. During the
third wave of epidemics (beginning on January 28, 2021), the outbreak in
northern Vietnam occurred rapidly with the main contribution of Alpha variants
(Chau, Hong et al., 2021). Then, the fourth wave (beginning on April 27, 2021)
had been the worst ever experienced by the country. In May 2021, all patients
in Vietnam were derived by the Delta variant (Nguyen, Wong et al., 2021). In
November, this wave had caused 99.9% of total deaths in the country (Hoang,
Pham et al., 2022). The Vietnamese government has had to implement
unprecedented strict epidemic prevention measures, including encouraging people
to isolate themselves at home, mobilizing the participation of the army and
military medics, and setting up field hospitals. However, the epidemic
situation had been still difficult to control because the Delta variant has
high transmissibility.
After November 2021,
when the vaccination rate in Vietnam reached a relatively high threshold,
government took to restore social life under "new normal" conditions.
The gradual easing of
epidemic prevention measures has facilitated the spread of the virus in the
community. The first case confirmed that the Omicron variant was recorded in
Vietnam on December 19, 2021. Until March 2022, the Omicron became the primary
circulating variant and the cause of infections in the Hanoi capital. On March
12, 2022, Vietnam recorded the highest number of infections ever at 454,179
cases/day. This number is much larger than the previous wave of epidemics
caused by the Delta variants. Proposes that Omicron will become the dominant
variant in Vietnam shortly. Despite the sudden increase in cases, the mortality
rate tends to be the opposite.
The number of deaths
caused by the Omicron on March 13, 2022, is 95 cases, and the average of the
last seven days is 82. These concerns were lower than Delta's 803 cases on
September 1, 2021, and the average of the last seven days in 360 cases
(according to Vietnam's Ministry of Health). The current research literature
indicates that the Omicron variants are more infectious than previously
recorded variants (Ren, Wang et al., 2022) (He, Hong et al., 2021). On the
other hand, Omicron can cause symptoms less severe (Callaway and Ledford, 2021)
(Kupferschmidt and Vogel, 2021) (Ren, Wang et al., 2022). Even so, the high
transmission rate of Omicron will pose a significant challenge for diagnostics
and vaccine strategies. Therefore, tracking the genetic shifts of these
variants is significant. For these reasons, the genetic diversity of the S gene
of Omicron variants isolated in Vietnam was investigated. By constructing a
network, the genetic relationship of Omicron variants would be revealed,
supporting the tracing of a infection source of a new outbreak in the future.
Reference
Abbas Q, Kusakin
A. 2022. Follow-up investigation and detailed mutational characterization
of the SARS-CoV-2 Omicron variant lineages (BA.1, BA.2, BA.3 and BA.1.1). bioRxiv:
2022.2002.2025.481941. http://dx.doi.org/10.1101/2022.02.25.481941.
Alouane T, Laamarti
M. 2020. Genomic Diversity and Hotspot Mutations in 30,983 SARS-CoV-2
Genomes: Moving Toward a Universal Vaccine for the “Confined Virus”?
Pathogens 9(10). http://dx.doi.org/10.3390/pathogens9100829.
Berrio A, Gartner
V. 2020. Positive selection within the genomes of SARS-CoV-2 and other
Coronaviruses independent of impact on protein function. Peer J 8, e10234. http://dx.doi.org/10.7717/peerj.10234.
Callaway E, Ledford H. 2021.
How bad is Omicron? What scientists know so far. Nature 600(7888), 197-199. http://dx.doi.org/10.1038/d41586-021-03614-z.
Campbell F, Archer
B. 2021. Increased transmissibility and global spread of SARS-CoV-2
variants of concern as at June 2021. Euro surveillance : bulletin Europeen sur
les maladies transmissibles = European communicable disease bulletin 26(24), 2100509. http://dx.doi.org/10.2807/15607917.ES.2021.26.24.2100509.
Candido KL, Eich
CR. 2022. Spike protein of SARS-CoV-2 variants: a brief review and
practical implications. Braz J Microbiol. http://dx.doi.org/10.1007/s42770-022-00743-z.
Chaguza C, Coppi
A. 2022. Rapid emergence of SARS-CoV-2 Omicron variant is associated with
an infection advantage over Delta in vaccinated persons. Med (New York,
N.Y.): http://dx.doi.org/10.1016/j.medj.2022.1003.1010.
Chau NVV, Hong
NTT. 2021. Rapid whole-genome sequencing to inform COVID-19 outbreak
response in Vietnam. The Journal of infection 82(6), 276-316. http://dx.doi.org/10.1016/j.jinf.2021.03.017.
Chaw SM, Tai JH. 2020.
The origin and underlying driving forces of the SARS-CoV-2 outbreak. J Biomed
Sci 27(1), 73. http://dx.doi.org/10.1186/s12929-020-00665-8.
Colson P, Delerce
J. 2022. First cases of infection with the 21L/BA.2 Omicron variant in
Marseille, France. J Med Virol 94(7), 3421-3430. http://dx.doi.org/10.1002/jmv.27695.
Di Giacomo S,
Mercatelli D. 2021. Preliminary report on severe acute respiratory
syndrome coronavirus 2 (SARS-CoV-2) Spike mutation T478K. J Med Virol 93(9), 5638-5643. http://dx.doi.org/10.1002/jmv.27062.
Durmaz B, Abdulmajed
O. 2020. Mutations Observed in the SARS-CoV-2 Spike Glycoprotein and Their
Effects in the Interaction of Virus with ACE-2 Receptor. Medeniyet Medical
Journal 35(3), 253-260. http://dx.doi.org/10.5222/MMJ.2020.98048.
Excoffier L, Lischer HE. 2010.
Arlequin suite ver 3.5: a new series of programs to perform population genetics
analyses under Linux and Windows. Mol Ecol Resour 10(3), 564-567. http://dx.doi.org/10.1111/j.1755-0998.2010.02847.x.
Fall A, Eldesouki
RE. 2022. A Quick Displacement of the SARS-CoV-2 variant Delta with
Omicron: Unprecedented Spike in COVID-19 Cases Associated with Fewer Admissions
and Comparable Upper Respiratory Viral Loads. medRxiv : the preprint server for
health sciences: 2022.2001.2026.22269927. http://dx.doi.org/10.1101/2022.01.26.22269927.
Fan LQ, Hu XY. 2021.
Biological Significance of the Genomic Variation and Structural Dynamics of
SARS-CoV-2 B.1.617. Frontiers in microbiology 12, 750725-750725. http://dx.doi.org/10.3389/fmicb.2021.750725.
Goher SS, Ali F. 2021.
The Delta Variant Mutations in the Receptor Binding Domain of SARS-CoV-2 Show
Enhanced Electrostatic Interactions with the ACE2. Med Drug Discov:
100114. http://dx.doi.org/10.1016/j.medidd.2021.100114.
He X, Hong W. 2021.
SARS-CoV-2 Omicron variant: Characteristics and prevention. MedComm 2(4), 838-845. http://dx.doi.org/10.1002/mco2.110.
Hoang VT, Pham
TD. 2022. Seroprevalence of SARS-CoV-2 among high-density communities and
hyper-endemicity of COVID-19 in Vietnam. Trop Med Int Health. http://dx.doi.org/10.1111/tmi.13744.
Kim Y, Gaudreault
NN. 2022. Effects of Spike Mutations in SARS-CoV-2 Variants of Concern on
Human or Animal ACE2-Mediated Virus Entry and Neutralization 10(3), e0178921. http://dx.doi.org/10.1128/spectrum.01789-21.
Kumar S, Thambiraja TS. 2022.
Omicron and Delta variant of SARS-CoV-2: A comparative computational study of
spike protein. Journal of Medical Virology 94(4), 1641-1649. http://dx.doi.org/10.1002/jmv.27526.
Kumar V, Singh J. 2021.
Possible Link between Higher Transmissibility of Alpha, Kappa and Delta
Variants of SARS-CoV-2 and Increased Structural Stability of Its Spike Protein
and hACE2 Affinity. International journal of molecular sciences 22(17), 9131. http://dx.doi.org/10.3390/ijms22179131.
Kupferschmidt K, Vogel G. 2021.
How bad is Omicron? Some clues are emerging. Science 374(6573), 1304-1305. http://dx.doi.org/10.1126/science.acx9782.
Lan J, Ge J. 2020.
Structure of the SARS-CoV-2 spike receptor-binding domain bound to the ACE2
receptor. Nature 581(7807), 215-220. http://dx.doi.org/10.1038/s41586-020-2180-5.
Leigh JW, Bryant D. 2015.
popart: full-feature software for haplotype network construction. Methods in
Ecology and Evolution 6(9), 1110-1116. https://doi.org/10.1111/2041-210X.12410.
Lubinski B, Frazier
LE. 2021. Spike protein cleavage-activation mediated by the SARS-CoV-2
P681R mutation: a case-study from its first appearance in variant of interest
(VOI) A.23.1 identified in Uganda. bioRxiv : the preprint server for biology:
2021.2006.2030.450632. http://dx.doi.org/10.1101/2021.06.30.450632.
Mohapatra RK, Kandi
V. 2022. The recently emerged BA.4 and BA.5 lineages of Omicron and their
global health concerns amid the ongoing wave of COVID-19 pandemic –
Correspondence. Int J Surg 103, 106698. http://dx.doi.org/10.1016/j.ijsu.2022.106698.
Motozono C, Toyoda
M. 2021. SARS-CoV-2 spike L452R variant evades cellular immunity and
increases infectivity. Cell Host Microbe 29(7), 1124-1136
e1111. http://dx.doi.org/10.1016/j.chom.2021.06.006.
Nguyen TP, Wong
ZS. 2021. Rapid impact assessments of COVID-19 control measures against
the Delta variant and short-term projections of new confirmed cases in Vietnam.
J Glob Health 11, 03118. http://dx.doi.org/10.7189/jogh.11.03118.
Ni D, Lau K. 2021.
Structural analysis of the Spike of the Omicron SARS-COV-2 variant by cryo-EM
and implications for immune evasion. bioRxiv: 2021.2012.2027.474250. http://dx.doi.org/10.1101/2021.12.27.474250.
O’Toole A,. Pybus
OG. 2022. Pango lineage designation and assignment using SARS-CoV-2 spike
gene nucleotide sequences. BMC Genomics 23(1), 121. http://dx.doi.org/10.1186/s12864-022-08358-2.
Ou J, Lan W. 2022.
Tracking SARS-CoV-2 Omicron diverse spike gene mutations identifies multiple
inter-variant recombination events. Signal Transduct Target Ther 7(1), 138. http://dx.doi.org/10.1038/s41392-022-00992-2.
Ovsyannikova IG,
Haralambieva IH. 2020. The role of host genetics in the immune response to
SARS-CoV-2 and COVID-19 susceptibility and severity. Immunol Rev 296(1), 205-219. http://dx.doi.org/10.1111/imr.12897.
Papanikolaou V,
Chrysovergis A. 2022. From delta to Omicron: S1-RBD/S2 mutation/deletion
equilibrium in SARS-CoV-2 defined variants. Gene 814, 146134-146134. http://dx.doi.org/10.1016/j.gene.2021.146134.
Phuong HVM, Tung
TS. 2021. Novel Mutation of SARS-CoV-2, Vietnam, July 2020. Emerging
infectious diseases 27(5), 1519-1521. http://dx.doi.org/10.3201/eid2705.210013.
Ren SY, Wang WB. 2022.
Omicron variant (B.1.1.529) of SARS-CoV-2: Mutation, infectivity, transmission,
and vaccine resistance. World journal of clinical cases 10(1), 1-11. http://dx.doi.org/10.12998/wjcc.v10.i1.1.
Singh D, Yi SV. 2021.
On the origin and evolution of SARS-CoV-2. Exp Mol Med 53(4), 537-547. http://dx.doi.org/10.1038/s12276-021-00604-z.
Tegally H, Moir
M. 2022. Continued Emergence and Evolution of Omicron in South Africa: New
BA.4 and BA.5 lineages. medRxiv: 2022.2005.2001.22274406. http://dx.doi.org/10.1101/2022.05.01.22274406.
Thai PQ, Rabaa
MA. 2021. The First 100 Days of Severe Acute Respiratory Syndrome
Coronavirus 2 (SARS-CoV-2) Control in Vietnam. Clin Infect Dis 72(9), e334-e342. http://dx.doi.org/10.1093/cid/ciaa1130.
Wei C, Shan KJ. 2021. Evidence for a mouse origin of the SARS-CoV-2 Omicron variant. J Genet Genomics 48(12), 1111-1121. http://dx.doi.org/10.1016/j.jgg.2021.12.003









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