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

Betacoronavirus SARS-CoV-2, its genome, variety of genotypes and molecular-biological approaches to combat it

Year: 2020

Pages: 242-271

Number: Volume 13, issue 2

Type: scientific article

Summary:

This review focuses on betacoronavirus SARS-CoV-2, which caused a pandemic in the spring of 2020 in the form of a dangerous highly contagious coronavirus infection COVID-19. There was an explosive growth in the number of publications related to coronavirus worldwide in 2020, including questions of molecular biological detection of viral DNA and the creation of vaccines. The taxonomy of betacoronaviruses and the organization of their genome, represented by the (+) RNA chain, is briefly presented, including more detailed information about the surface glycoprotein in the form of S (Spike) protein. A hypothetical life cycle of betacoronavirus is described. It is shown that along with the high conservativeness of genomic sequences of various strains and isolates of SARS-CoV-2, there are mutations of individual nucleotides that lead to the replacement of amino acids in the protein sequence, among which the mis-sense mutation D614G presumably has a noticeable effect on the virus's contagiosity and the severity of the disease caused by it. It is suggested that D/G614 isolates should be detected, including using allele-specific reverse transcription PCR, since this may be clinically relevant information. The methods of detecting viral material using reverse transcription PCR and other methods of nucleic acid amplification are considered, and the diagnostic test systems for SARS-CoV-2 allowed for use in the Russian Federation are indicated. A summary of the types of vaccines being developed to control COVID-19 worldwide, including the Russian Federation, is provided. As of the end of May 2020 WHO has registered 131 candidate vaccines, of which 10 are undergoing clinical trials. A certain emphasis in describing the creation of vaccines is made on the use of plant technologies.

Keywords:

betacoronavirus, SARS-CoV, SARS-CoV-2, COVID-19, genome, RNA, sequencing, diagnostics, real-time PCR, LAMP, loop amplification, Spike protein, vaccine

References:

  1. Abbott T.R., Dhamdhere G., Liu Y., Lin X., Goudy L., Zeng L., Chemparathy A., Chmura S., Heaton N.S., Debs R., Pande T., Endy D., La Russa M.F., Lewis D.B., Qi L.S. Development of CRISPR as an Antiviral Strategy to Combat SARS-CoV-2 and Influenza. // Cell. 2020. V. 181(4). P. 865-876. e12. doi: 10.1016/j.cell.2020.04.020.
  2. Ahmed S.F., Quadeer A.A., McKay M.R. COVIDep platform for real-time reporting of vaccine target recommendations for SARS-CoV-2: Description and connections with COVID-19 immune responses and preclinical vaccine trials // bioRxiv. doi: 10.1101/2020.05.23.111385/.
  3. Baek Y.H., Um J., Antigua K.J.C., Park J.H., Kim Y., Oh S., Kim Y.I., Choi W.S., Kim S.G., Jeong J.H., Chin B.S., Nicolas H.D.G., Ahn J.Y., Shin K.S., Choi Y.K., Park J.S., Song M.S. Development of a reverse transcription-loop-mediated isothermal amplification as a rapid early-detection method for novel SARS-CoV-2 // Microbes Infect. 2020. 2020. doi: 10.1080/22221751.2020.1756698.
  4. Becerra-Flores M., Cardozo T. SARS-CoV-2 viral spike G614 mutation exhibits higher case fatality rate. // J. Clin. Pract. 2020. e13525. doi: 10.1111/ijcp.13525/
  5. Broughton J.P., Deng X., Yu G., Fasching C.L., Servellita V., Singh J., Miao X., Streithorst J.A., Granados A., Sotomayor-Gonzalez A., Zorn K., Gopez A., Hsu E., Gu W., Miller S., Pan C.-Y., Guevara H., Wadford D.A., Chen J.C., Chiu C.Y. CRISPR–Cas12-based detection of SARS-CoV-2 // Nature Biotechnol. 2020. V. 38(7). P. 870-874.doi: 10.1038/s41587-020-0513-4.
  6. Brufsky A. Distinct Viral Clades of SARS-CoV-2: Implications for Modeling of Viral Spread. // Med. Virol. 2020. doi: 10.1002/jmv.25902.
  7. Calina D., Docea A.O., Petrakis D., Egorov A.M., Ishmukhametov A.A., Gabibov A.G., Shtilman M.I., Kostoff R., Carvalho F., Vinceti M., Spandidos D.A., Tsatsakis A. Towards Effective COVID‑19 Vaccines: Updates, Perspectives and Challenges (Review) // J. Mol. Med. 2020. V. 46(1). P. 3-16. doi: 10.3892/ijmm.2020.4596.
  8. Callaway E. The race for coronavirus vaccines: a graphical guide // Nature. 2020. V. 580(7805). P. 576-577. doi: 10.1038/d41586-020-01221-y.
  9. Capell T., Twyman R.M., Armario-Najera V., Ma J.K-C., Schillberg S., Christou P. Potential Applications of Plant Biotechnology Against SARS-CoV-2 // Trends Plant Sci. V. 25(7). P. 635-643. doi: 10.1016/j.tplants.2020.04.009/
  10. Chan JF-W., Yuan S., Zhang A.J., Poon VK-M., Chan CC-S., Lee AC-Y., Fan Z., Li C., Liang R., Cao J., Tang K., Luo C., Cheng VC-C., Cai J-P., Chu H., Chan K-H., To KK-W., Sridhar S., Yuen K-Y. Surgical Mask Partition Reduces the Risk of Non-Contact Transmission in a Golden Syrian Hamster Model for Coronavirus Disease 2019 (COVID-19) // Infect. Dis. 2020. ciaa644. doi: 10.1093/cid/ciaa644.
  11. Chang T.J., Yang D.M., Wang M.L., Liang K.H., Tsai P.H., Chiou S.H., Lin T.H., Wang C.T. Genomic Analysis and Comparative Multiple Sequence of SARS-CoV2. // Chin. Med. Assoc. 2020. V. 83(6). P. 537-543. doi: 10.1097/JCMA.0000000000000335.
  12. Chemeris A.V. CRISPR / Cas systems (special thematic issue of the journal) // Biomics. 2017. V.9 (3). P. 148-154.
  13. Chemeris A.V., Bikbulatova S.M., Chemeris D.A., Baimiev Al.Kh., Knyazev A.V., Kuluyev B.R., Maksimov I.V. Should you be afraid of GMOs? A look of outside observers on hysteria around // Biomics. 2014. V.6. P.77-138.
  14. Chemeris A.V., Chemeris D.A., Baimiev Al.Kh., Knyazev A.V., Kuluev B.R., Maksimov I.V. The fight against GMOs as neo-Lysenkoism // Biomics. V.7. P. 1-39.
  15. Chen L., Liu W., Zhang Q., Xu K., Ye G., Wu W., Sun Z., Liu F., Wu K., Zhong B., Mei Y., Zhang W., Chen Y., Li Y., Shi M., Lan K., Liu Y. RNA based mNGS approach identifies a novel human coronavirus from two individual pneumonia cases in 2019 Wuhan outbreak // Emerg. Infections. 2020. V. 9(1). P. 313-319. doi: 10.1080/22221751.2020.1725399.
  16. Chubukova O.V., Khasanova S.S., Nikonorov Yu.M., Kulagin V.F., Chemeris A.V., Vakhitov V.A. Immunogenicity of the Puumala hantavirus N-protein for outbred mice after intramuscular injection of its gene // Problems Virol. V. 53 (4). P. 38-41.
  17. Corman V.M., Landt O., Kaiser M., Molenkamp R., Meijer A., Chu D.K.W., Bleicker T., Brünink S., Schneider J., Schmidt M.L., Mulders D.G.J.C., Haagmans B.L., van der Veer B., van den Brink S., Wijsman L., Goderski G., Romette J.L., Ellis J., Zambon M., Peiris M., Goossens H., Reusken C., Koopmans M.P.G., Drosten C. Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR // Euro Surveillance. 2020. V. 25 (3). 2000045. doi: 10.2807/1560-7917.ES.2020.25.3.2000045.
  18. Coutard B., Valle C., de Lamballerie X., Canard B., Seidah N.G., Decroly E. The spike glycoprotein of the new coronavirus 2019-nCoV contains a furin-like cleavage site absent in CoV of the same clade // Antiviral Res. V. 176. P. 104742. doi: 10.1016/j.antiviral.2020.104742.
  19. Curi L., Federico P.-B., Gimenez C.A. An ultrasensitive, rapid, and portable coronavirus SARS-CoV-2 sequence detection method based on CRISPR-Cas12 // bioRxiv. doi: 10.1101/2020.02.29.971127.
  20. Demurtas O.C., Massa S., Illiano E., De Martinis D., Chan P.K., Di Bonito P., Franconi R. Antigen Production in Plant to Tackle Infectious Diseases Flare Up: The Case of SARS // Plant Sci. 2016. V. 7. P. 54. doi: 10.3389/fpls.2016.00054.
  21. Deslandes A., Berti V., Tandjaoui-Lambotte Y., Alloui C., Carbonnelle E., Zahar J.R., Brichler S., Cohen Y. SARS-CoV-2 was already spreading in France in late December 2019 // J. Antimicrob. Agents. 2020. V. 55(6). P. 106006. doi: 10.1016/j.ijantimicag.2020.106006.
  22. Ding X., Yin K., Li Z., Liu C. All-in-One Dual CRISPR-Cas12a (AIOD-CRISPR) Assay: A Case for Rapid, Ultrasensitive and Visual Detection of Novel Coronavirus SARS-CoV-2 and HIV virus // bioRxiv. 2020. doi: 10.1101/2020.03.19.998724.
  23. Eaaswarkhanth M., Madhoun A.A., Al-Mulla F. Could the D614G substitution in the SARS-CoV-2 spike (S) protein be associated with higher COVID-19 mortality? // J. Infect. Dis. 2020. V. 96. P. 459–460. doi: 10.1016/j.ijid.2020.05.071.
  24. El-Tholoth M., Bau H.H., Song J. A Single and Two-Stage, Closed-Tube, Molecular Test for the 2019 Novel Coronavirus (COVID-19) at Home, Clinic, and Points of Entry // ChemRxiv. 2020. doi: 10.26434/chemrxiv.11860137.v/
  25. Esposito S., Principi N., Leung CC, Migliori GB. Universal use of face masks for success against COVID-19: evidence and implications for prevention policies // Eur Respir J. V. 55(6). P. 2001260. doi: 10.1183/13993003.01260-2020
  26. Forster P., Forster L., Renfrew C., Forster M. Phylogenetic network analysis of SARS-CoV-2 genomes // Natl. Acad. Sci. USA. 2020. V. 117(17). P. 9241-9243. doi: 10.1073/pnas.2004999117.
  27. Gao Y., Yan L., Huang Y., Liu F., Zhao Y., Cao L., Wang T., Sun Q., Ming Z., Zhang L., Ge J., Zheng L., Zhang Y., Wang H., Zhu Y., Zhu C., Hu T., Hua T., Zhang B., Yang X., Li J., Yang H., Liu Z., Xu W., Guddat L.W., Wang Q., Lou Z., Rao Z. Structure of the RNA-dependent RNA polymerase from COVID-19 virus // Science. 2020. V. 368(6492). P. 779-782.. doi: 10.1126/science.abb7498.
  28. Garafutdinov R.R., Mavzyutov A.R., Alekseev Ya.I., Vorobiev A.A., Nikonorov Yu.M., Chubukova O.V., Matniyazov R.T., Baimiev An.Kh., Maksimov I.V., Kuluev B.R., Baimiev Al.Kh., Chemeris A.V. Human betacoronaviruses and their highly sensitive detection using PCR and other amplification methods // Biomics. 2020. V.12 (1). P. 121-179. doi: 31301/2221-6197.bmcs.2020-7. (In Russian)
  29. Giddings G., Allison G., Brooks D., Carter A. Transgenic plants as factories for biopharmaceuticals // Nat Biotechnol. V. 18(11). P. 1151-1155. doi: 10.1038/81132.
  30. Giritch A., Marillonnet S., Engler C., van Eldik G., Botterman J., Klimyuk V., Gleba Y. Rapid high-yield expression of full-size IgG antibodies in plants coinfected with noncompeting viral vectors // Natl. Acad. Sci. USA. 2006. V. 103(40). P. 14701-6. doi: 10.1073/pnas.0606631103.
  31. Gunasekaran B., Gothandam K.M. A Review on Edible Vaccines and Their Prospects // J. Med. Biol. Res. 2020. V. 53(2). e8749. doi: 10.1590/1414-431X20198749.
  32. Hiatt A., Cafferkey R., Bowdish K. Production of Antibodies in Transgenic Plants // 1989. V.342(6245). P.76-78. doi: 10.1038/342076a0.
  33. Hou T., Zeng W., Yang M., Chen W., Ren L., Ai J., Wu J., Liao Y., Gou X., Li Y., et al. 2020. Development and Evaluation of A CRISPR-based Diagnostic For 2019-novel Coronavirus // 2020.02.22.20025460.
  34. Ishige T., Murata S., Taniguchi T., Miyabe A., Kitamura K., Kawasaki K., Nishimura M., Igari H., Matsushita K. Highly sensitive detection of SARS-CoV-2 RNA by multiplex rRT-PCR for molecular diagnosis of COVID-19 by clinical laboratories. // Chim. Acta. 2020. V. 507. P. 139-142. doi: 10.1016/j.cca.2020.04.023.
  35. Khamsi R. If a coronavirus vaccine arrives, can the world make enough? // Nature. 2020. V. 580(7805). P. 578-580. doi: 10.1038/d41586-020-01063-8.
  36. Kim J.M., Chung Y.S., Jo H.J., Lee N.J., Kim M.S., Woo S.H., Park S., Kim J.W., Kim H.M., Han M.G. Identification of Coronavirus Isolated from a Patient in Korea with COVID-19 // Osong Public Health and Research Perspectives. 2020. V. 11 (1). P. 3-7. doi: 10.24171/j.phrp.2020.11.1.02.
  37. Kim S-J., Nguyen V-G., Park Y-H., Park B-K., Chung H-C. A Novel Synonymous Mutation of SARS-CoV-2: Is This Possible to Affect Their Antigenicity and Immunogenicity? // Vaccines (Basel). 2020. V. 8(2). E220. doi: 10.3390/vaccines8020220.
  38. Kirchdoerfer R.N., Ward A.B. Structure of the SARS-CoV nsp12 polymerase bound to nsp7 and nsp8 co-factors // Nature Commun. 2019. V. 10 (1). P. 2342. doi: 10.1038/s41467-019-10280-3.
  39. Korber B., Fischer W.M., Gnanakaran S., Yoon H., Theiler J., Abfalterer W., Foley B., Giorgi E.E., Bhattacharya T., Parker M.D., Partridge D.G., Evans C.M., Freeman T.M., de Silva T.I., Sheffield COVID-19 Genomics Group, LaBranche C.C., Montefiori D.C. Spike mutation pipeline reveals the emergence of a more transmissible form of SARS-CoV-2 // bioRxiv. 2020. doi: 10.1101/2020.04.29.069054.
  40. Koyama T., Weeraratne D., Snowdon J.N., Parida L. Emergence of Drift Variants That May Affect COVID-19 Vaccine Development and Antibody Treatment // 2020. V. 9(5). E324. doi: 10.3390/pathogens9050324.
  41. Kuluev B.R., Baimiev An.Kh., Chemeris D.A., Matniyazov R.T., Gerashenkov G.A., Nikonorov Yu.M., Baimiev Al.Kh., Chemeris A.V. The use of CRISPR loci not for genome editing // Biomics. V.9. P. 271-283.
  42. Kuluev B.R., Vershinina Z.R., Knyazev A.V., Chemeris D.A., Baimiev An.Kh., Chumakov M.I., Baimiev Al.Kh., Chemeris A.V. "Hairy" plant roots - an important tool for researchers and a powerful phytochemical biofactory for industrial workers // Biomics. 2015. V. 7. No. 2. P. 70-120.
  43. Kurup VM, Thomas J. Edible Vaccines: Promises and Challenges // Biotechnol. 2020. V. 62(2). P. 79-90. doi: 10.1007/s12033-019-00222-1.
  44. Lam T.T., Shum M.H., Zhu H.C., Tong Y.G., Ni X.B., Liao Y.S., Wei W., Cheung W.Y., Li W.J., Li L.F., Leung G.M., Holmes E.C., Hu Y.L., Guan Y. Identifying SARS-CoV-2 related coronaviruses in Malayan pangolins // Nature. 2020. V. 583(7815). P. 282-285doi: 10.1038/s41586-020-2169-0/
  45. Lamb L.E., Bartolone S.N., Ward E., Chancellor M.B. Rapid Detection of Novel Coronavirus (COVID-19) by Reverse Transcription-Loop-Mediated Isothermal Amplification // 2020. doi: 10.1101/2020.02.19.20025155.
  46. Lei C., Qian K., Li T., Zhang S., Fu W., Ding M., Hu S. Neutralization of SARS-CoV-2 spike pseudotyped virus by recombinant ACE2-Ig // Commun. 2020. V. 11(1). P. 2070. doi: 10.1038/s41467-020-16048-4.
  47. Leung N.H.L, Chu D.K.W., Shiu E.Y.C., Chan K.H., McDevitt J.J., Hau B.J.P., Yen H.L., Li Y., Ip D.K.M., Peiris J.S.M., Seto W.H., Leung G.M., Milton D.K., Cowling B.J. Respiratory virus shedding in exhaled breath and efficacy of face masks // Med. 2020. V. 26(5). P. 676-680. doi: 10.1038/s41591-020-0843-2.
  48. Li H.Y., Ramalingam S., Chye M.L. Accumulation of recombinant SARS-CoV spike protein in plant cytosol and chloroplasts indicate potential for development of plant-derived oral vaccines // Biol. Med. (Maywood). 2006. V. 231(8). P. 1346-1352. doi: 10.1177/153537020623100808.
  49. Li X., Zai J., Zhao Q., Nie Q., Li Y., Foley B.T., Chaillon A. Evolutionary history, potential intermediate animal host, and cross-species analyses of SARS-CoV-2 // Med. Virol. 2020. V. 92(6). P. 602-611. doi: 10.1002/jmv.25731.
  50. Liu X., Feng J., Zhang Q., Guo D., Zhang L., Suo T., Hu W., Guo M., Wang X., Huang Z., Xiong Y., Chen G., Chen Y., Lan K. Analytical comparisons of SARS-COV-2 detection by qRT-PCR and ddPCR with multiple primer/probe sets // Microbes Infect. 2020. V. 9(1). P. 1175-1179. doi: 10.1080/22221751.2020.1772679.
  51. Lu R., Wu X., Wan Z., Li Y., Jin X., Zhang C. A Novel Reverse Transcription Loop-Mediated Isothermal Amplification Method for Rapid Detection of SARS-CoV-2 // J. Mol. Sci. 2020. V. 21(8). pii: E2826. doi: 10.3390/ijms21082826.
  52. Mason H.S., Lam D.M., Arntzen C.J. Expression of Hepatitis B Surface Antigen in Transgenic Plants // Natl. Acad. Sci. USA. 1992. V. 89(24). P. 11745-11749. doi: 10.1073/pnas.89.24.11745.
  53. Massa S., Paolini F., Marino C., Franconi R., Venuti A. Bioproduction of a Therapeutic Vaccine Against Human Papillomavirus in Tomato Hairy Root Cultures // Plant Sci. 2019. V. 10. P. 452. doi: 10.3389/fpls.2019.00452.
  54. Mercatelli D., Giorgi, F.M. Geographic and Genomic Distribution of SARS-CoV-2 Mutations // Preprints 2020, 2020040529 doi: 10.20944/preprints202004.0529.v1.
  55. Metsky H.C., Freije C.A., Kosoko-Thoroddsen T-SF., Sabeti P.C., Myhrvold C. 2020. CRISPR-based surveillance for COVID-19 using genomically-comprehensive machine learning design // 2020. doi: 10.1101/2020.02.26.967026.
  56. Miller A., Reandelar M.J., Fasciglione K., Roumenova V., Li Y., Otazu G.H. Correlation between universal BCG vaccination policy and reduced morbidity and mortality for COVID-19: an epidemiological study // 2020. doi: 10.1101/2020.03.24.20042937.
  57. Minskaia E., Hertzig T. Gorbalenya A.E., Campanacci V., Cambillau C., Canard B., Ziebuhr J. Discovery of an RNA virus 3'->5' exoribonuclease that is critically involved in coronavirus RNA synthesis // Natl. Acad. Sci. USA. 2006. V. 103 (13). P. 5108-5113. doi: 10.1073/pnas.0508200103.
  58. Moein S.T., Hashemian S.M.R., Mansourafshar B., Khorram-Tousi A., Tabarsi P., Doty R.L.. Smell Dysfunction: A Biomarker for COVID-19 // Forum Allergy Rhinol. 2020. 10.1002/alr.22587. doi: 10.1002/alr.22587.
  59. Moorlag S.J.C.F.M., Arts R.J.W., van Crevel R., Netea M.G. Non-specific effects of BCG vaccine on viral infections // Microbiol. Infect. 2019. V. 25(12). P.1473-1478. doi: 10.1016/j.cmi.2019.04.02.
  60. Moriya C., Horiba S., Kurihara K., Kamada T., Takahara Y., Inoue M., Iida A., Hara H., Shu T., Hasegawa M., Matano T. Intranasal Sendai Viral Vector Vaccination Is More Immunogenic Than Intramuscular Under Pre-Existing Anti-Vector Antibodies // 2011. V. 29(47). P. 8557-8663. doi: 10.1016/j.vaccine.2011.09.028.
  61. Nguyen T., Duong Bang D., Wolff A. 2019 Novel Coronavirus Disease (COVID-19): Paving the Road for Rapid Detection and Point-of-Care Diagnostics // Micromachines (Basel). V. 11(3). pii: E306. doi: 10.3390/mi11030306.
  62. Nikitin N., Petrova E., Trifonova E., Karpova O. Influenza virus aerosols in the air and their infectiousness // Virol. 2014. 859090. doi: 10.1155/2014/859090.
  63. Ogando N.S., Ferron F., Decroly E., Canard B., Posthuma C.C., Snijder E.J. The Curious Case of the Nidovirus Exoribonuclease: Its Role in RNA Synthesis and Replication Fidelity // Microbiol. 2019. V.10. 1813. doi: 10.3389/fmicb.2019.01813.
  64. O'Neill L.A.J., Netea M.G. BCG-induced Trained Immunity: Can It Offer Protection Against COVID-19? // Rev. Immunol. 2020. V. 20(6). P.335-337. doi: 10.1038/s41577-020-0337-y.
  65. Onishchenko G.G., Govorun V.M., Sergienko V.I., Akopian T.A., Momynaliev K.T., Vereshchagin V.A., Lazarev V.N., Vasilev N.T., Markov V.I., Merkulov V.A., Maksimov V.A., Melnikov V.A., Lopukhin Y.M. Structural organization of the genome of SARS-associated coronavirus (Strain SoD) isolated on the territory of the Russian Federation // Exp. Biol. Med. 2004. V. 137 (2). P. 197-199. doi: 10.1023/b:bebm.0000028139.02582.97.
  66. Pachetti M., Marini B., Benedetti F., Giudici F., Mauro E., Storici P., Masciovecchio C., Angeletti S., Ciccozzi M., Gallo R.C., Zella D., Ippodrino R. Emerging SARS-CoV-2 mutation hot spots include a novel RNA-dependent-RNA polymerase variant. // Transl. Med. 2020. V. 18(1). P. 179. doi: 10.1186/s12967-020-02344-6.
  67. Padron-Regalado E. Vaccines for SARS-CoV-2: Lessons From Other Coronavirus Strains // Dis. Ther. 2020. V. 9(2). P. 1-20. doi: 10.1007/s40121-020-00300-x.
  68. Park G.S., Ku K., Baek S.H., Kim S.J., Kim S.I., Kim B.T., Maeng J.S. Development of Reverse Transcription Loop-Mediated Isothermal Amplification Assays Targeting Severe Acute Respiratory Syndrome Coronavirus 2 // Mol. Diagn. 2020. pii: S1525-1578(20)30090-8. doi: 10.1016/j.jmoldx.2020.03.006.
  69. Peng H., Yang L.T., Wang L.Y., Li J., Huang J., Lu Z.Q., Koup R.A., Bailer R.T., Wu C.Y. Long-lived memory T lymphocyte responses against SARS coronavirus nucleocapsid protein in SARS-recovered patients // Virology. 2006. V. 351(2). P. 466-475. doi: 10.1016/j.virol.2006.03.036.
  70. Penney C.A., Thomas D.R., Deen S.S., Walmsley A.M. Plant-made vaccines in support of the Millennium Development Goals // Plant Cell Rep. 2011. V. 30(5). P. 789-798. doi: 10.1007/s00299-010-0995-5.
  71. Pinto D., Park Y-J., Beltramello M., Walls A.C., Tortorici M.A., Bianchi S., Jaconi S., Culap K., Zatta F., De Marco A., Peter A., Guarino B., Spreafico R., Cameroni E., Case J.B., Chen R.E., Havenar-Daughton C., Snell G., Telenti A., Virgin H.W., Lanzavecchia A., Diamond M.S., Fink K., Veesler D., Corti D. Cross-neutralization of SARS-CoV-2 by a Human Monoclonal SARS-CoV Antibody // 2020. V. 583(7815). P. 290-295.. doi: 10.1038/s41586-020-2349-y. Online ahead of print.
  72. Pogrebnyak N., Golovkin M., Andrianov V., Spitsin S., Smirnov Y., Egolf R., Koprowski H. Severe acute respiratory syndrome (SARS) S protein production in plants: development of recombinant vaccine // Natl. Acad. Sci. USA. 2005. V. 102 (25). P. 9062-7. doi: 10.1073/pnas.0503760102.
  73. Poon L.L., Chan K.H., Wong O.K., Yam W.C., Yuen K.Y., Guan Y., Lo Y.M., Peiris J.S. Early diagnosis of SARS coronavirus infection by real time RT-PCR // Clin. Virol. 2003. V. 28 (3). P. 233-238. doi: 10.1016/j.jcv.2003.08.004.
  74. Rosales-Mendoza S. Will plant-made biopharmaceuticals play a role in the fight against COVID-19? // Opin. Biol. Ther. 2020. V. 20(6). P. 545-548. doi: 10.1080/14712598.2020.1752177.
  75. Rosales-Mendoza S., Márquez-Escobar V.A., González-Ortega O., Nieto-Gómez R., Arévalo-Villalobos J.I. What Does Plant-Based Vaccine Technology Offer to the Fight against COVID-19? // Vaccines (Basel). V. 8(2). E183. doi: 10.3390/vaccines8020183.
  76. Saha P., Majumder R, Chakraborty S, Srivastava AK, Mandal M, Sarkar S. Mutations in Spike Protein of SARS-CoV-2 Modulate Receptor Binding, Membrane Fusion and Immunogenicity: An Insight into Viral Tropism and Pathogenesis of COVID-19 // 2020. doi : 10.26434/chemrxiv.12320567.v1.
  77. Seong M.W., Kim S.Y., Corman V.M., Kim T.S., Cho S.I., Kim M.J., Lee S.J., Lee J.S., Seo S.H., Ahn J.S., Yu B.S., Park N., Oh M.D., Park W.B., Lee J.Y., Kim G., Joh J.S., Jeong I., Kim E.C., Drosten C., Park S.S. Microevolution of Outbreak-Associated Middle East Respiratory Syndrome Coronavirus, South Korea, 2015 // Infect. Dis. 2016. V. 22(2). P. 327-330. doi:. 103201/eid2202.151700.
  78. Shakoor S., Rao AQ, Shahid N, Yaqoob A, Samiullah TR, Shakoor S, Latif A, Tabassum B, Khan MAU, Shahid AA, Husnain T. Role of Oral Vaccines as an Edible Tool to Prevent Infectious Diseases // Acta Virol. V. 63(3). P. 245-252. doi: 10.4149/av_2019_301.
  79. Shanmugaraj B., Siriwattananon K., Wangkanont K., Phoolcharoen W. Perspectives on Monoclonal Antibody Therapy as Potential Therapeutic Intervention for Coronavirus disease-19 (COVID-19) // Asian Pac. J. Allergy Immunol. V. 38(1). P. 10-18. doi: 10.12932/AP-200220-0773.
  80. Sharma A. It is too soon to attribute ADE to COVID-19 // Microbes Infect. V. 22(4-5). P. 158. doi: 10.1016/j.micinf.2020.03.005.
  81. Skarjinskaia M., Ruby K., Araujo A., Taylor K., Gopalasamy-Raju V., Musiychuk K., Chichester JA, Palmer GA, de la Rosa P., Mett V., Ugulava N, Streatfield SJ., Yusibov V. Hairy Roots as a Vaccine Production and Delivery System // Biochem. Eng. Biotechnol. 2013. V. 134. P. 115-134. doi: 10.1007/10_2013_184.
  82. Srivatsan S., Han P.D., van Raay K., Wolf C.R., McCulloch D.J., Kim A.E., Brandstetter E., Martin B., Gehring J., Chen W., Seattle Flu Study Investigators, Kosuri S., Konnick E.Q., Lockwood C.M., Rieder M.J., Nickerson D.A., Chu H.Y., Shendure J., Starita L.M. Preliminary support for a “dry swab, extraction free” protocol for SARS-CoV-2 testing via RT-qPCR // 2020. V. 9(1). P. 1259-1268. doi: 10.1101/2020.04.22.056283.
  83. Suo T., Liu X., Guo M., Feng J., Hu W., Yang Y., Zhang Q., Wang X., Sajid M., Guo D., et al. ddPCR: a more sensitive and accurate tool for SARS-CoV-2 detection in low viral load specimens // Micr. Infect. 2020. V. 9(1). P. 1259-1268. doi: 10.1080/22221751.2020.1772678.
  84. te Velthuis A.J., Arnold J.J., Cameron C.E., van den Worm S.H., Snijder E.J. The RNA polymerase activity of SARS-coronavirus nsp12 is primer dependent // Nucleic Acids 2010. V. 38 (1). P. 203-214. doi: 10.1093/nar/gkp904
  85. Tetro J.A. Is COVID-19 receiving ADE from other coronaviruses? // Microbes Infect. V. 22(2). P. 72-73. doi: 10.1016/j.micinf.2020.02.006.
  86. van Dorp L., Acman M., Richard D., Shaw L.P., Ford C.E., Ormond L., Owen C.J., Pang J., Tana C.C.S., Boshier F.A.T., Ortiz A.T., Balloux F. Emergence of genomic diversity and recurrent mutations in SARS-CoV-2 // Genet. Evol. 2020. V.83. P. 104351.doi: 10.1016/j.meegid.2020.104351.
  87. Vershinina Z.R., Kuluev B.R., Maksimov I.V., Mikhailova E.V., Gumerova G.R., Maleev G.V., Knyazev A.V., Baimiev An.Kh., Baimiev Al.Kh., Chemeris A.V. GMOs can not be banned! // Biomics. T.12 (1). P. 80-120. doi: 10.31301/2221-6197.bmcs.2020-6/
  88. Visseaux B., Le Hingrat Q., Collin G., Bouzid D., Lebourgeois S., Le Pluart D., Deconinck L., Lescure F.X., Lucet J.C., Bouadma L., Timsit J.F., Descamps D., Yazdanpanah Y., Casalino E., Houhou-Fidouh N.; Emergency Department influenza study group. Evaluation of the QIAstat-Dx Respiratory SARS-CoV-2 Panel, the first rapid multiplex PCR commercial assay for SARS-CoV-2 detection // Clin. Microbiol. 2020. V. 58(8). e00630-20. doi: 10.1128/JCM.00630-20.
  89. Waggoner J.J., Stittleburg V., Pond R., Saklawi Y., Sahoo M.K., Babiker A., et al. Triplex real-time RT-PCR for severe acute respiratory syndrome coronavirus 2 // Infect. Dis. 2020. V. 26(7). P. 1633-1635. doi: 10.3201/eid2607.201285.
  90. Walls A.C., Park Y.J., Tortorici M.A., Wall A., McGuire A.T., Veesler D. Structure, Function, and Antigenicity of the SARS-CoV-2 Spike Glycoprotein // 2020. V. 181(2). P. 281-292.e6. doi: 10.1016/j.cell.2020.02.058.
  91. Wan Y., Shang J., Sun S., Tai W., Chen J., Geng Q., He L., Chen Y., Wu J., Shi Z., Zhou Y., Du L., Li F. Molecular Mechanism for Antibody-Dependent Enhancement of Coronavirus Entry // Virol. 2020. V. 94(5). e02015-19. doi: 10.1128/JVI.02015-19.
  92. Wang C, .Li W., Drabek D., Okba N.M.A., van Haperen R., Osterhaus A.D.M.E., van Kuppeveld F.J.M., Haagmans B.L., Grosveld F., Bosch B.J. A human monoclonal antibody blocking SARS-CoV-2 infection // Commun. 2020. V. 11(1). P. 2251. doi: 10.1038/s41467-020-16256-y.
  93. Wang C., Liu Z., Chen Z., Huang X., Xu M., He T., Zhang Z. The establishment of reference sequence for SARS-CoV-2 and variation analysis // Med. Virol. 2020. V. 92(6). P. 667-675. doi: 10.1002/jmv.25762.
  94. Wölfel R., Corman V.M., Guggemos W., Seilmaier M., Zange S., Müller M.A., Niemeyer D., Jones T.C., Vollmar P., Rothe C., Hoelscher M., Bleicker T., Brünink S., Schneider J., Ehmann R., Zwirglmaier K., Drosten C., Wendtner C. Virological assessment of hospitalized patients with COVID-2019 // Nature. 2020. V. 591(7809). P. 465-469. doi: 10.1038/s41586-020-2196-x.
  95. Wu F., Zhao S., Yu B., Chen Y.M., Wang W., Song Z.G., Hu Y., Tao Z.W., Tian J.H., Pei Y.Y., Yuan M.L., Zhang Y.L., Dai F.H., Liu Y., Wang Q.M., Zheng J.J., Xu L., Holmes E.C., Zhang Y.Z. A new coronavirus associated with human respiratory disease in China // Nature. 2020. V. 579 (7798). P. 265-269. doi: 10.1038/s41586-020-2008-3.
  96. Ye Z.W., Yuan S., Yuen K.S., Fung S.Y., Chan C.P., Jin D.Y. Zoonotic origins of human coronaviruses // J. Biol. Sci. 2020. V. 16 (10). P. 1686-1697. doi: 10.7150/ijbs.45472.
  97. Yin C. Genotyping coronavirus SARS-CoV-2: methods and implications // 2020. pii: S0888-7543(20)30318-9. doi: 10.1016/j.ygeno.2020.04.016.
  98. Yip M.S., Leung H.L., Li P.H., Cheung C.Y., Dutry I., Li D., Daëron M., Bruzzone R., Peiris J.S., Jaume M. Antibody-dependent enhancement of SARS coronavirus infection and its role in the pathogenesis of SARS // Hong Kong Med. J. V. 22(3) Suppl 4). P. 25-31.
  99. Yu F., Yan L., Wang N., Yang S., Wang L., Tang Y., Gao G., Wang S., Ma C., Xie R., Wang F., Tan C., Zhu L., Guo Y., Zhang F. Quantitative Detection and Viral Load Analysis of SARS-CoV-2 in Infected Patients // Infect. Dis. 2020. pii: ciaa345. doi: 10.1093/cid/ciaa345.
  100. Zaychuk T., Nechipurenko Y., Adjubey A., Onikienko S., Chereshnev V., Zainutdinov S., Kochneva G., Netesov S., Matveeva O. Review of technologies for creating vaccines against beta-coronaviruses and Sendai virus as possible vaccine vector // Biol. preprint.
  101. Zhao Z., Li H., Wu X., Zhong Y., Zhang K., Zhang Y.P., Boerwinkle E., Fu Y.X. Moderate mutation rate in the SARS coronavirus genome and its implications // BMC Evol. Biol. 2004. V. 4. 21. doi: 10.1186/1471-2148-4-21/
  102. Zheng N., Xia R., Yang C., Yin B., Li Y., Duan C., Liang L., Guo H., Xie Q. Boosted Expression of the SARS-CoV Nucleocapsid Protein in Tobacco and Its Immunogenicity in Mice // 2009. V. 27(36). P.5001-5007. doi: 10.1016/j.vaccine.2009.05.073.
  103. Zhong X, Qi G, Yang J, Xing G, Liu J, Yang X. [High-efficiency Expression of a Receptor-Binding Domain of SARS-CoV Spike Protein in Tobacco Chloroplasts] // Sheng Wu Gong Cheng Xue Bao. V. 30(6). P. 920-930. [Article in Chinese].
  104. Zhou P., Yang X.L., Wang X.G., Hu B., Zhang L., Zhang W., Si H.R., Zhu Y., Li B., Huang C.L., Chen H.D., Chen J., Luo Y., Guo H., Jiang R.D., Liu M.Q., Chen Y., Shen X.R., Wang X., Zheng X.S., Zhao K, Chen Q.J., Deng F., Liu L.L., Yan B., Zhan F.X., Wang Y.Y., Xiao G.F., Shi Z.L. A pneumonia outbreak associated with a new coronavirus of probable bat origin // 2020. V. 579(7798). P. 270-273. doi: 10.1038/s41586-020-2012-7.
  105. Zhu N., Zhang D., Wang W., Li X., Yang B., Song J., Zhao X., Huang B., Shi W., Lu R., Niu P., Zhan F., Ma X., Wang D., Xu W., Wu G., Gao G.F., Tan W. A Novel Coronavirus from Patients with Pneumonia in China, 2019 // New Engl. J. Med. 2020. V. 382 (8). P. 727-733. doi: 10.1056/NEJMoa2001017.
  106. Zhu N., Zhang D., Wang W., Li X., Yang B., Song J., Zhao X., Huang B., Shi W., Lu R., Niu P., Zhan F., Ma X., Wang D., Xu W., Wu G., Gao G.F., Tan W. A Novel Coronavirus from Patients with Pneumonia in China, 2019 // New Eng. J. Med. 2020. V. 382 (8). P. 727-733. doi: 10.1056/NEJMoa2001017.
  107. Zou L., Ruan F., Huang M., Liang L., Huang H., Hong Z., Yu J., Kang M., Song Y., Xia J., Guo Q., Song T., He J., Yen H.L., Peiris M., Wu J. SARS-CoV-2 Viral Load in Upper Respiratory Specimens of Infected Patients // New Engl. J. Med. V. 382(12). P. 1177-1179. doi: 10.1056/NEJMc2001737.
Download pdf
up
eISSN: 2221-6197 DOI: 10.31301/2221-6197