DC Field | Value | Language |
---|---|---|
dc.contributor.author | HoiyIn CHung | - |
dc.contributor.author | Ji Yeong Noh | - |
dc.contributor.author | Bon-Sang Koo | - |
dc.contributor.author | Jung Joo Hong | - |
dc.contributor.author | H K Kim | - |
dc.date.accessioned | 2022-04-28T15:31:25Z | - |
dc.date.available | 2022-04-28T15:31:25Z | - |
dc.date.issued | 2022 | - |
dc.identifier.issn | 20010370 | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/25813 | - |
dc.description.abstract | Since the outbreak of coronavirus disease (COVID-19) in 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has evolved into diverse variants. Here, an early isolate of SARS-CoV-2 was serially passaged in multiple cell lines of human origin in triplicate, and selected mutations were compared to those found in natural SARS-CoV-2 variants. In the spike protein, Q493R and Q498R substitutions from passaged viruses were consistent with those in the B.1.1.529 (Omicron) variant. Y144del and H655Y substitutions from passaged viruses were also reported in B.1.1.7 (Alpha), P.1 (Gamma), and B.1.1.529 (Omicron) variants. Several single nucleotide polymorphisms (SNPs) found in first-passaged viruses have also been identified as selected mutation sites in serially passaged viruses. Considering the consistent mutations found between serially passaged SARS-CoV-2 and natural variants, there may be host-specific selective mutation patterns of viral evolution in humans. Additional studies on the selective mutations in SARS-CoV-2 experiencing diverse host environments will help elucidate the direction of SARS-CoV-2 evolution. | - |
dc.publisher | Elsevier | - |
dc.title | SARS-CoV-2 mutations acquired during serial passage in human cell lines are consistent with several of those found in recent natural SARS-CoV-2 variants | - |
dc.title.alternative | SARS-CoV-2 mutations acquired during serial passage in human cell lines are consistent with several of those found in recent natural SARS-CoV-2 variants | - |
dc.type | Article | - |
dc.citation.title | Computational and Structural Biotechnology Journal | - |
dc.citation.number | 0 | - |
dc.citation.endPage | 1934 | - |
dc.citation.startPage | 1925 | - |
dc.citation.volume | 20 | - |
dc.contributor.affiliatedAuthor | HoiyIn CHung | - |
dc.contributor.affiliatedAuthor | Ji Yeong Noh | - |
dc.contributor.affiliatedAuthor | Bon-Sang Koo | - |
dc.contributor.affiliatedAuthor | Jung Joo Hong | - |
dc.contributor.alternativeName | 정회인 | - |
dc.contributor.alternativeName | 노지영 | - |
dc.contributor.alternativeName | 구본상 | - |
dc.contributor.alternativeName | 홍정주 | - |
dc.contributor.alternativeName | 김혜권 | - |
dc.identifier.bibliographicCitation | Computational and Structural Biotechnology Journal, vol. 20, pp. 1925-1934 | - |
dc.identifier.doi | 10.1016/j.csbj.2022.04.022 | - |
dc.subject.keyword | SARS-CoV-2 | - |
dc.subject.keyword | Variant | - |
dc.subject.keyword | Mutation | - |
dc.subject.keyword | SNP | - |
dc.subject.keyword | Evolution | - |
dc.subject.local | SARS-CoV-2 | - |
dc.subject.local | SARS-Cov-2 | - |
dc.subject.local | Variant | - |
dc.subject.local | variant | - |
dc.subject.local | mutation | - |
dc.subject.local | Mutation | - |
dc.subject.local | SNP | - |
dc.subject.local | SNPs | - |
dc.subject.local | Evolution | - |
dc.subject.local | evolution | - |
dc.description.journalClass | Y | - |
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