eISSN: 2221-6197 DOI: 10.31301/2221-6197

The enigmas of the new coronavirus SARS-CoV-2

Year: 2021

Pages: 75-99

Number: Volume 13, issue 1

Type: scientific article

Summary:

The emergence of the new SARS-CoV-2 coronavirus has given rise to many enigmas, to which there are no answers yet. However, the degree of threat to humanity, due to the fact that by the beginning of February 2021, more than 100 million people were ill in the world, of which 2 million died, led to the fact that the efforts of many researchers were aimed at combating this disease, including massive sequencing of the complete genomes of SARS-CoV-2, as this is necessary for diagnostics and prediction of the epidemiological situation, including in the long term. Currently, a fairly high level of conservativeness of the SARS-CoV-2 genome is shown, but there is also a significant variability of intra-host viral RNA, confirming the concept of the existence of quasispecies for RNA-containing viruses. As of February 2021, the complete genomes of almost half a million coronavirus isolates have been sequenced worldwide, and a number of nomenclatures have been proposed to streamline their analysis, including the convenient dynamic nomenclature Pango lineage. Variations of SARS-CoV-2 genomes in the form of consensus SNPs (Single Nucleotide Polymorphism) and intra-host iSNVs (intra-host Single Nucleotide Variant) were demonstrated. Taking into account iSNV and minor mutations, about 85% of the 29.9 thousand nucleotides viral genome were changed at least once, but only a very few of them turned into major mutations due to certain features that ensure the predominant distribution of such strains. The example of the S-protein gene, taking into account iSNV, minor and major mutations, shows its significant variability, which is detected when sequencing hundreds of thousands of SARS-CoV-2 genomes. On the basis of the analysis of 400 complete SARS-CoV-2 genomes isolated on the territory of the Russian Federation during 2020, the dynamics of the circulation of individual strains with acquired major mutations, the representation of which is slightly different from the changes in the SARS-CoV-2 genome in the rest world, is estimated. The possibility of long-term persistence of the new coronavirus in the human body is note, while the reservoirs for the latent existence of SARS-CoV-2, in contrast, for example, to the herpes simple virus, remain unknown. There is no consensus on the possibility of reactivation of SARS-CoV-2 or reinfection. The latter is theoretically possible in cases where SARS-CoV-2 strains belonging to other genetic lineages and clades are found in the body of the "re-infected". This, however, does not exclude the possibility of mutating the virus within a single host. Despite significant progress in monitoring the spread of SARS-CoV-2, many questions remain, but as knowledge of the biology of the new coronavirus accumulates, they will also be answered.

Keywords:

coronavirus, SARS-CoV-2, quasispecies, genome, RNA, sequencing, S-protein, consensus mutations, intrahost mutations, SNP, iSNV, persistence, reinfection, COVID-19

References:

1. Alvarez-Moreno CA, Rodríguez-Morales AJ. Testing Dilemmas: Post negative, positive SARS-CoV-2 RT-PCR - is it a reinfection? Travel Med Infect Dis. 2020. V.35. P.101743. doi: 10.1016/j.tmaid.2020.101743

2. Armero A., Berthet N., Avarre J.C. Intra-Host Diversity of SARS-Cov-2 Should Not Be Neglected: Case of the State of Victoria, Australia. Viruses. 2021. V. 13(1). P. 133. doi: 10.3390/v13010133

3.Baric R.S. Emergence of a Highly Fit SARS-CoV-2 Variant. N Engl J Med. 2020. V. 383(27). P. 2684-2686. doi: 10.1056/NEJMcibr2032888

4.Bendall M.L., Gibson K.M., Steiner M.C., Rentia U., Pérez-Losada M., Crandall K.A. HAPHPIPE: Haplotype Reconstruction and Phylodynamics for Deep Sequencing of Intra-Host Viral Populations. Mol. Biol. Evol. 2020. msaa315. doi: 10.1093/molbev/msaa315

5.Biswas S.K., Mudi S.R. Spike protein D614G and RdRp P323L: the SARS-CoV-2 mutations associated with severity of COVID-19. Genomics Inform. 2020. V. 18(4). e44. doi: 10.5808/GI.2020.18.4.e44

6.Cantin E.M., Lange W., Openshaw H. Application of polymerase chain reaction assays to studies of herpes simplex virus latency. Intervirology. 1991. V. 32(2). P. 93-100. doi: 10.1159/000150189

7.Cella E, Benedetti F, Fabris S, Borsetti A, Pezzuto A, Ciotti M, Pascarella S, Ceccarelli G, Zella D, Ciccozzi M, Giovanetti M. SARS-CoV-2 Lineages and Sub-Lineages Circulating Worldwide: A Dynamic Overview. Chemotherapy. 2021. V.18. P.1-5. doi: 10.1159/000515340

8.Chen T., Hudnall S.D. Anatomical mapping of human herpesvirus reservoirs of infection. Mod. Pathol. 2006. 19(5). P. 726-37. doi: 10.1038/modpathol.3800584

9.Chen Z, Boon SS, Wang MH, Chan RWY, Chan PKS. Genomic and evolutionary comparison between SARSCoV-2 and other human coronaviruses. J Virol Methods. 2021. V.289. P.114032. doi: 10.1016/j.jviromet.2020.114032

10. Cheng X, Virk N, Chen W, Ji S, Ji S, Sun Y, Wu X. CpG usage in RNA viruses: data and hypotheses. PLoS One. 2013. V.8(9). e74109. doi: 10.1371/journal.pone.0074109

11. Colson P., Finaud M., Levy N., Lagier J.C., Raoult D. Evidence of SARS-CoV-2 re-infection with a different genotype. J. Infect. 2021. V. 82(4). P. 84-123. doi: 10.1016/j.jinf.2020.11.011

12. Dao T.L., Hoang V.T., Gautret P. Recurrence of SARS-CoV-2 viral RNA in recovered COVID-19 patients: a narrative review. Eur. J. Clin. Microbiol. Infect. Dis. 2021. V. 40(1). P. 13-25. doi: 10.1007/s10096-020-04088-z

13. Davies N.G., Jarvis C.I.; CMMID COVID-19 Working Group, Edmunds WJ, Jewell NP, Diaz-Ordaz K., Keogh R.H. Increased mortality in community-tested cases of SARS-CoV-2 lineage B.1.1.7. Nature. 2021. doi: 10.1038/s41586-021-03426-1

14. Digard P, Lee HM, Sharp C, Grey F, Gaunt E. Intragenome variability in the dinucleotide composition of SARS-CoV-2. Virus Evol. 2020. V.6(2). P.veaa057. doi: 10.1093/ve/veaa057

15. Du P., Song C., Li R., Song Y., Li J., Ding N., Zhang J., Song R., Han J., Gao G., Yue J., Duan A., Huang Y., An J., Wang J., Zhang F., Chen C., Zeng H. Specific redistribution of SARS-CoV-2 variants in the respiratory system and intestinal tract. Clin. Infect. Dis. 2020. ciaa1617. doi: 10.1093/cid/ciaa1617

16. Erol A. Are the emerging SARS-COV-2 mutations friend or foe? Immunol. Lett. 2021. V. 230. P. 63-64. doi: 10.1016/j.imlet.2020.12.014

17. Eskier D., Suner A., Oktay Y., Karakülah G. Mutations of SARS-CoV-2 nsp14 exhibit strong association with increased genome-wide mutation load. Peer J. 2020. V.8. e10181. doi: 10.7717/peerj.10181

18. Fiorentini S, Messali S, Zani A, Caccuri F, Giovanetti M, Ciccozzi M, Caruso A. First detection of SARS-CoV-2
spike protein N501 mutation in Italy in August, 2020. Lancet Infect Dis. 2021. S1473-3099(21)00007-4. doi:
10.1016/S1473-3099(21)00007-4

19. Forster P., Forster L., Renfrew C., Forster M. Phylogenetic network analysis of SARS-CoV-2 genomes. Proc. Natl. Acad. Sci. USA. 2020. V.117(17). P. 9241-9243. doi: 10.1073/pnas.2004999117

20. Freed N.E., Vlková M., Faisal M.B., Silander O.K. Rapid and inexpensive whole-genome sequencing of SARS-CoV-2 using 1200 bp tiled amplicons and Oxford Nanopore Rapid Barcoding. Biol. Methods Protoc. 2020. V. 5(1):bpaa014. doi: 10.1093/biomethods/bpaa014

21. Garafutdinov R.R., Mavzyutov A.R., Alekseev Ya.I., Vorobev A.A., Nikonorov Yu.M., Chubukova O.V., Matniyazov R.T., Baymiev An.Kh., Maksimov I.V., Kuluev B.R., Baymiev Al.Kh., Chemeris A.V. Human betacoronaviruses and their highly sensitive detection by PCR and other amplification methods. Biomics. 2020. V.12(1). P. 121-179. DOI: 10.31301/2221-
6197.bmcs.2020-7 (In Russian)

22. Garafutdinov R.R., Mavzyutov A.R., Nikonorov Yu.M., Chubukova O.V., Matniyazov R.T., Baymiev An.Kh., Maksimov I.V., Miftakhov I.Yu., Khalikova E.Yu., Kuluev B.R., Baymiev Al.Kh., Chemeris A.V. Betacoronavirus SARS-CoV-2, its
genome, variety of genotypes and molecular-biological approaches to combat it. Biomics. 2020. V.12(2). P. 242-
271. DOI: 10.31301/2221-6197.bmcs.2020-15 (In Russian)

23. Gibson K.M., Steiner M.C., Rentia U., Bendall M.L., Pérez-Losada M., Crandall K.A. Validation of Variant Assembly Using HAPHPIPE with Next-Generation Sequence Data from Viruses. Viruses. 2020. V. 12(7). P. 758. doi: 10.3390/v12070758

24. Gohl D.M., Garbe J., Grady P., Daniel J., Watson R.H.B., Auch B., Nelson A., Yohe S., Beckman K.B. A rapid, cost-effective tailed amplicon method for sequencing SARS-CoV-2. BMC Genomics. 2020. V. 21(1). P. 863. doi: 10.1186/s12864-020-07283-6

25. Grubaugh N.D., Gangavarapu K., Quick J., Matteson N.L., De Jesus J.G., Main B.J., Tan A.L., Paul L.M., Brackney D.E., Grewal S., Gurfield N., Van Rompay K.K.A., Isern S., Michael S.F., Coffey L.L., Loman N.J., Andersen K.G. An amplicon-based sequencing framework for accurately measuring intrahost virus diversity using PrimalSeq and iVar. Genome Biol. 2019. V. 20(1). P. 8. doi: 10.1186/s13059-018-1618-7

26. Itokawa K., Sekizuka T., Hashino M., Tanaka R., Kuroda M. Disentangling primer interactions improves SARS-CoV-2 genome sequencing by multiplex tiling PCR. PLoS One. 2020. V. 15(9). e0239403. doi: 10.1371/journal.pone.0239403

27. Itokawa K., Sekizuka T., Hashino M., Tanaka R., Kuroda M. Disentangling primer interactions improves SARS-Cov-2 genome sequencingby the ARTIC Networks multiplex PCR. bioRxiv. 2020.03.10.985150. doi.org/10/1101/2020.03.10.985150

28. Jackson C.B., Zhang L., Farzan M., Choe H. Functional importance of the D614G mutation in the SARS-CoV-2 spike protein. Biochem. Biophys. Res. Commun. 2021. V. 538. P. 108-115. doi: 10.1016/j.bbrc.2020.11.026

29. Jaworski E., Langsjoen R.M., Judy B., Newman P., Plante J.A., Plante K.S., Miller A.L., Zhou Y., Swetnam D., Dong J., Ren P., Pyles R.B., Ksiazek T., Menachery V.D., Weaver S.C., Routh A. Tiled-ClickSeq for targeted sequencing of complete coronavirus genomes with simultaneous capture of RNA recombination and minority variants. bioRxiv. 2021. 2021.03.10.434828. doi: 10.1101/2021.03.10.434828

30. Kannan S.R., Spratt A.N., Quinn T.P., Heng X., Lorson C.L., Sönnerborg A., Byrareddy S.N., Singh K. Infectivity of SARS-CoV-2: there Is Something More than D614G? J. Neuroimmune Pharmacol. 2020. V. 15(4). P. 574-577. doi: 10.1007/s11481-020-09954-3

31. Kim D., Lee J.Y., Yang J.S., Kim J.W., Kim V.N., Chang H. The Architecture of SARS-CoV-2 Transcriptome. Cell. 2020. V, 181(4). P. 914-921.e10. doi: 10.1016/j.cell.2020.04.011

32. Komissarov AB, Safina KR, Garushyants SK, Fadeev AV, Sergeeva MV, Ivanova AA, Danilenko DM, Lioznov D, Shneider OV, Shvyrev N, Spirin V, Glyzin D, Shchur V, Bazykin GA. Genomic epidemiology of the early stages of the SARS-CoV-2 outbreak in Russia. Nat Commun. 2021. V.12(1). P.649. doi: 10.1038/s41467-020-20880-z

33. Kozlovskaya L, Piniaeva A, Ignatyev G, Selivanov A, Shishova A, Kovpak A, Gordeychuk I, Ivin Y, Berestovskaya A, Prokhortchouk E, Protsenko D, Rychev M, Ishmukhametov A. Isolation and phylogenetic analysis of SARS-CoV-2 variants collected in Russia during the COVID-19 outbreak. Int J Infect Dis. 2020. V.99. P.40-46. doi: 10.1016/j.ijid.2020.07.024

34. Lauring A.S., Andino R. Quasispecies theory and the behavior of RNA viruses. PLoS Pathog. 2010. V. 6(7). e1001005. doi: 10.1371/journal.ppat.1001005

35. Leung K., Shum M.H., Leung G.M., Lam T.T., Wu J.T. Early transmissibility assessment of the N501Y mutant strains of SARS-CoV-2 in the United Kingdom, October to November 2020. Euro Surveill. 2021. V. 26(1). 2002106. doi: 10.2807/1560-7917.ES.2020.26.1.2002106.

36. Li Q., Zheng X.S., Shen X.R., Si H.R., Wang X., Wang Q., Li B., Zhang W., Zhu Y., Jiang R.D., Zhao K., Wang H., Shi Z.L., Zhang H.L., Du R.H., Zhou P. Prolonged shedding of severe acute respiratory syndrome coronavirus 2 in patients with COVID-19. Emerg. Microbes Infect. 2020. V. 9(1). P. 2571-2577. doi: 10.1080/22221751.2020.1852058

37. Maggi F., Novazzi F., Genoni A., Baj A., Spezia P.G., Focosi D., Zago C., Colombo A., Cassani G., Pasciuta R., Tamborini A., Rossi A., Prestia M., Capuano R., Azzi L., Donadini A., Catanoso G., Grossi P.A., Maffioli L., Bonelli G. Imported SARS-CoV-2 Variant P.1 in Traveler Returning from Brazil to Italy. Emerg. Infect. Dis. 2021. V. 27(4). P. 1249-1251. doi: 10.3201/eid2704.210183

38. Mahase E. Covid-19: What new variants are emerging and how are they being investigated? BMJ. 2021. V. 18. 372:n158. doi: 10.1136/bmj.n158

39. Maurano M.T., Ramaswami S., Zappile P., Dimartino D., Boytard L., Ribeiro-Dos-Santos A.M., Vulpescu N.A. Westby G., Shen G., Feng X., Hogan M.S., RagonnetCronin M., Geidelberg L., Marier C., Meyn P., Zhang Y., Cadley J., Ordoñez R., Luther R., Huang E., Guzman E., Arguelles-Grande C., Argyropoulos K.V., Black M., Serrano A., Call M.E., Kim M.J., Belovarac B., Gindin T., Lytle A., Pinnell J., Vougiouklakis T., Chen J., Lin L.H., Rapkiewicz A., Raabe V., Samanovic M.I., Jour G., Osman I., Aguero-Rosenfeld M., Mulligan M.J., Volz E.M., Cotzia P., Snuderl M., Heguy A. Sequencing identifies multiple early introductions of SARS-CoV-2 to the New York City region. Genome Res. 2020. V. 30(12). P. 1781-1788. doi: 10.1101/gr.266676.120

40. Mavzyutov A.R., Garafutdinov R.R., Khalikova E.Yu., Yuldashev R.A., Khusainova R.I., Chubukova O.V., Gimalov F.R., Matniyazov R.T., Alekseev Ya.I., Vorobev A.A., Vershinina Z.R., Miftakhov I.Yu., Nikonorov Yu.M., Maksimov I.V., Kuluev B.R., Baymiev An.Kh., Baymiev Al.Kh., Chemeris A.V. Problematic aspects of diagnostics of SARS-CoV-2 coronavirus
infection using reverse-transcriptional PCR. Biomics. 2020. V.12(4). P. 564-590. DOI: 10.31301/2221-6197.bmcs.2020-50 (In Russian)

41. Mostafa H.H., Fissel J.A., Fanelli B., Bergman Y., Gniazdowski V., Dadlani M., Carroll K.C., Colwell R.R., Simner P.J. Metagenomic Next-Generation Sequencing of Nasopharyngeal Specimens Collected from Confirmed and Suspect COVID-19 Patients. mBio. 2020. V. 11(6). e01969-20. doi: 10.1128/mBio.01969-20

42. Motayo B.O., Oluwasemowo O.O., Olusola B.A., Akinduti P.A., Arege O.T., Obafemi Y.D., Faneye A.O., Isibor P.O., Aworunse O.S., Oranusi S.U. Evolution and genetic diversity of SARS-CoV-2 in Africa using whole genome sequences. Int J Infect Dis. 2021. V. 103. P. 282 - 287. doi: 10.1016/j.ijid.2020.11.190

43. Moyo-Gwete T., Madzivhandila M., Makhado Z., Ayres F., Mhlanga D., Oosthuysen B., Lambson B.E., Kgagudi P., Tegally H., Iranzadeh A., Doolabh D., Tyers L., Chinhoyi L.R., Mennen M., Skelm S., Wibmer C.K., Bhiman J.N., Ueckermann V., Rossouw T., Boswell M., de Oliveira T., Williamson C., Burgers W.A., Ntusi N., Morris L., Moore P.L. SARS-CoV-2 501Y.V2 (B.1.351) elicits cross-reactive neutralizing antibodies. bioRxiv. 2021 Mar 6:2021.03.06.434193. doi: 10.1101/2021.03.06.434193

44. Paden C.R., Tao Y., Queen K., Zhang J., Li Y., Uehara A., Tong S. Rapid, Sensitive, Full-Genome Sequencing of Severe Acute Respiratory Syndrome Coronavirus 2. Emerg. Infect. Dis. 2020. V. 26(10). P. 2401-2405. doi: 10.3201/eid2610.201800

45. Pillay S., Giandhari J., Tegally H., Wilkinson E., Chimukangara B., Lessells R., Moosa Y., Mattison S., Gazy I., Fish M., Singh L., Khanyile K.S., San J.E., Fonseca V., Giovanetti M., Alcantara L.C.Jr., de Oliveira T. Whole Genome Sequencing of SARS-CoV-2: Adapting Illumina Protocols for Quick and Accurate Outbreak Investigation during a Pandemic. Genes (Basel). 2020. V. 11(8). P. 949. doi: 10.3390/genes11080949

46. Platto S., Wang Y., Zhou J., Carafoli E. History of the COVID-19 pandemic: Origin, explosion, worldwide spreading. Biochem. Biophys. Res. Commun. 2021. V. 538. P. 14-23. doi: 10.1016/j.bbrc.2020.10.087

47. Rambaut A, Holmes EC, O'Toole Á, Hill V, McCrone JT, Ruis C, du Plessis L, Pybus OG. A dynamic nomenclature proposal for SARS-CoV-2 lineages to assist genomic epidemiology. Nat Microbiol. 2020. V.5(11). P.1403-1407. doi: 10.1038/s41564-020-0770-5

48. Rambaut A, Holmes EC, O'Toole Á, Hill V, McCrone JT, Ruis C, du Plessis L, Pybus OG. Addendum: A dynamic nomenclature proposal for SARS-CoV-2 lineages to assist genomic epidemiology. Nat Microbiol. 2021. V.6(3).P.415. doi: 10.1038/s41564-021-00872-5

49. Rato S., Golumbeanu M., Telenti A., Ciuffi A. Exploring viral infection using single-cell sequencing. Virus Res. 2017. V. 239. P. 55-68. doi: 10.1016/j.virusres.2016.10.016

50. Riggioni C, Comberiati P, Giovannini M, Agache I, Akdis M, Alves-Correia M, Antó JM, Arcolaci A, Azkur AK, Azkur D, Beken B, Boccabella C, Bousquet J, Breiteneder H, Carvalho D, De Las Vecillas L, Diamant Z, Eguiluz-Gracia I, Eiwegger T, Eyerich S, Fokkens W, Gao YD, Hannachi F, Johnston SL, Jutel M, Karavelia A, Klimek L, Moya B, Nadeau KC, O'Hehir R, O'Mahony L, Pfaar O, Sanak M, Schwarze J, Sokolowska M, Torres MJ, van de Veen W, van Zelm MC, Wang Y, Zhang L, Jiménez-Saiz R, Akdis CA. A compendium answering 150 questions on COVID-19 and SARS-CoV-2. Allergy. 2020. V.75(10). P.2503-2541. doi: 10.1111/all.14449

51. Salehi-Vaziri M., Jalali T., Farahmand B., Fotouhi F., Banifazl M., Pouriayevali M.H., Sadat Larijani M., Afzali N., Ramezani A. Clinical characteristics of SARS-CoV-2 by re-infection vs. reactivation: a case series from Iran. Eur. J. Clin. Microbiol. Infect. Dis. 2021. V. 18. P. 1–7. doi: 10.1007/s10096-021-04221-6

52. Sapoval N., Mahmoud M., Jochum M.D., Liu Y., Elworth R.A.L., Wang Q., Albin D., Ogilvie H.A., Lee M.D., Villapol S., Hernandez K.M., Maljkovic Berry I., Foox J., Beheshti A., Ternus K., Aagaard K.M., Posada D., Mason C.E., Sedlazeck F.J., Treangen T.J. SARSCoV-2 genomic diversity and the implications for qRTPCR diagnostics and transmission. Genome Res. 2021. V. 31(4):635-644. doi: 10.1101/gr.268961.120

53. Selhorst P., Van Ierssel S., Michiels J., Mariën J., Bartholomeeusen K., Dirinck E., Vandamme S., Jansens H., Ariën K.K. Symptomatic SARS-CoV-2 reinfection of a health care worker in a Belgian nosocomial outbreak despite primary neutralizing antibody response. Clin. Infect. Dis. 2020. ciaa1850. doi: 10.1093/cid/ciaa1850

54. Sender R, Bar-On YM, Flamholz A, Gleizer S, Bernsthein B, Phillips R, Milo R. The total number and mass of SARS-CoV-2 virions in an infected person. medRxiv. 2020. Nov 17; 2020.11.16.20232009. doi: 10.1101/2020.11.16.20232009

55. Singh J., Samal J., Kumar V., Sharma J., Agrawal U., Ehtesham N.Z., Sundar D., Rahman S.A., Hira S., Hasnain S.E. Structure-Function Analyses of New SARSCoV-2 Variants B.1.1.7, B.1.351 and B.1.1.28.1: Clinical, Diagnostic, Therapeutic and Public Health Implications. Viruses. 2021. V. 13(3). 439. doi: 10.3390/v13030439

56. Subramanian S. The Long-Term Evolutionary History of Gradual Reduction of CpG Dinucleotides in the SARSCoV-2 Lineage. Biology (Basel). 2021. V.10(1). P.52. doi: 10.3390/biology10010052

57. Taiaroa G., DanielRawlinson, Featherstone L, Miranda Pitt M., Caly L., Druce J., Purcell D., Harty L., Tran T., Roberts J., Scott N., Catton M., Williamson D., Coin L., Duchene S. Direct RNA sequencing and early evolution of SARS-CoV-2. bioRxiv. 2020. 03.05.976167. doi.org/10.1101/2020.03.05.976167

58. Tang J.W., Toovey O.T.R., Harvey K.N., Hui D.D.S. Introduction of the South African SARS-CoV-2 variant 501Y.V2 into the UK. J Infect. 2021. V. 82(4). P. e8–e10. doi: 10.1016/j.jinf.2021.01.007

59. Tillett R.L., Sevinsky J.R., Hartley P.D., Kerwin H., Crawford N., Gorzalski A., Laverdure C., Verma S.C., Rossetto C.C., Jackson D., Farrell M.J., Van Hooser S., Pandori M. Genomic evidence for reinfection with SARSCoV-2: a case study. Lancet Infect. Dis. 2021. V. 21(1). P. 52-58. doi: 10.1016/S1473-3099(20)30764-7

60. To K.K., Hung I.F., Ip J.D., Chu A.W., Chan W.M., Tam A.R., Fong C.H., Yuan S., Tsoi H.W., Ng A.C., Lee L.L., Wan P., Tso E., To W.K., Tsang D., Chan K.H., Huang J.D., Kok K.H., Cheng V.C., Yuen K.Y. COVID19 re-infection by a phylogenetically distinct SARScoronavirus-2 strain confirmed by whole genome sequencing. Clin. Infect. Dis. 2020. ciaa1275. doi: 10.1093/cid/ciaa1275

61. Turner J.S., Day A., Alsoussi W.B., Liu Z., O'Halloran J.A., Presti R.M., Patterson B.K., Whelan S.P.J., Ellebedy A.H., Mudd P.A. SARS-CoV-2 Viral RNA Shedding for More Than 87 Days in an Individual With an Impaired CD8+ T Cell Response. Front. Immunol. 2021. V. 11. 618402. doi: 10.3389/fimmu.2020.618402

62. Tyson J.R., James P., Stoddart D., Sparks N., Wickenhagen A., Hall G., Choi J.H., Lapointe H., Kamelian K., Smith A.D., Prystajecky N., Goodfellow I., Wilson S.J., Harrigan R., Snutch T.P., Loman N.J., Quick J. Improvements to the ARTIC multiplex PCR method for SARS-CoV-2 genome sequencing using nanopore. bioRxiv. 2020. 2020.09.04.283077. doi: 10.1101/2020.09.04.283077

63. Vacca D., Fiannaca A., Tramuto F., Cancila V., La Paglia L., Mazzucco W., Gulino A., La Rosa M., Maida C.M., Morello G., Belmonte B., Casuccio A., Maugeri R., Iacopino G., Vitale F., Tripodo C., Urso A. Direct RNA nanopore sequencing of SARS-CoV-2 extracted from critical material from swabs. medRxiv. 2020.12.21.20191346. doi.org/10.1101/2020.12.21.20191346

64. Valesano A.L., Rumfelt K.E., Dimcheff D.E., Blair C.N., Fitzsimmons W.J., Petrie J.G., Martin E.T., Lauring A.S. Temporal dynamics of SARS-CoV-2 mutation accumulation within and across infected hosts. bioRxiv. 2021. 2021.01.19.427330. doi: 10.1101/2021.01.19.427330

65. Wang D., Wang Y., Sun W., Zhang L., Ji J., Zhang Z., Cheng X., Li Y., Xiao F., Zhu A., Zhong B., Ruan S., Li J., Ren P., Ou Z., Xiao M., Li M., Deng Z., Zhong H., Li F., Wang W.J., Zhang Y., Chen W., Zhu S., Xu X., Jin X., Zhao J., Zhong N., Zhang W., Zhao J., Li J., Xu Y. Population Bottlenecks and Intra-host Evolution During Human-to-Human Transmission of SARS-CoV-2. Front. Med. (Lausanne). 2021. V. 8. P. 585358. doi: 10.3389/fmed.2021.585358.

66. Wang Y., Wang D., Zhang L., Sun W., Zhang Z., Chen W., Zhu A., Huang Y., Xiao F., Yao J., Gan M., Li F., Luo L., Huang X., Zhang Y., Wong S.S., Cheng X, Ji J., Ou Z., Xiao M., Li M., Li J., Ren P., Deng Z., Zhong H., Xu X., Song T., Mok C.K.P., Peiris M., Zhong N., Zhao J., Li Y., Li J., Zhao J. Intra-host variation and evolutionary dynamics of SARS-CoV-2 populations in COVID-19 patients. Genome Med. 2021. V. 13(1). P. 30. doi: 10.1186/s13073-021-00847-5

67. Wibmer C.K., Ayres F., Hermanus T., Madzivhandila M., Kgagudi P., Oosthuysen B., Lambson B.E., de Oliveira T., Vermeulen M., van der Berg K., Rossouw T., Boswell M., Ueckermann V., Meiring S., von Gottberg A., Cohen C., Morris L., Bhiman J.N., Moore P.L. SARSCoV-2 501Y.V2 escapes neutralization by South African COVID-19 donor plasma. bioRxiv. 2021 Jan 19:2021.01.18.427166. doi: 10.1101/2021.01.18.427166

68. Xia X. Extreme Genomic CpG Deficiency in SARSCoV-2 and Evasion of Host Antiviral Defense. Mol Biol Evol. 2020. V.37(9).P.2699-2705. doi: 10.1093/molbev/msaa094

69. Xiao M., Liu X., Ji J., Li M., Li J., Yang L., Sun W., Ren P., Yang G., Zhao J., Liang T., Ren H., Chen T., Zhong H., Song W., Wang Y., Deng Z., Zhao Y., Ou Z., Wang D., Cai J., Cheng X., Feng T., Wu H., Gong Y. Yang H., Wang J., Xu X., Zhu S., Chen F., Zhang Y., Chen W., Li Y., Li J. Multiple approaches for massively parallel sequencing of SARS-CoV-2 genomes directly from clinical samples. Genome Med. 2020. V. 12(1). P. 57. doi: 10.1186/s13073-020-00751-4

70. Xu Y., Kang L., Shen Z., Li X., Wu W., Ma W., Fang C., Yang F., Jiang X., Gong S., Zhang L., Li M. Hybrid capture-based sequencing enables unbiased recovery of SARCoV-2 genomes from fecal samples and characterization of the dynamics of intra-host variants. bioRxiv. 2020. 07.30.230102. doi.org/10.1101/2020.07.30.230102

71. Zhou D., Dejnirattisai W., Supasa P., Liu C., Mentzer A.J., Ginn H.M., Zhao Y., Duyvesteyn H.M.E., Tuekprakhon A., Nutalai R., Wang B., Paesen G.C., Lopez-Camacho C., Slon-Campos J., Hallis B., Coombes N., Bewley K., Charlton S., Walter T.S., Skelly D., Lumley S.F., Dold C., Levin R., Dong T., Pollard A.J., Knight J.C., Crook D., Lambe T., Clutterbuck E., Bibi S., Flaxman A., Bittaye M., Belij-Rammerstorfer S., Gilbert S., James W., Carroll M.W., Klenerman P., Barnes E.,
Dunachie S.J., Fry E.E., Mongkolsapaya J., Ren J., Stuart D.I., Screaton G.R. Evidence of escape of SARS-CoV-2
variant B.1.351 from natural and vaccine-induced sera. Cell. 2021. S0092-8674(21)00226-9. doi: 10.1016/j.cell.2021.02.037

Download pdf
up
eISSN: 2221-6197 DOI: 10.31301/2221-6197