Cited 25 time in
Human Coronavirus OC43 as a Low-Risk Model to Study COVID-19
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Mi Il | - |
| dc.contributor.author | Lee, Choongho | - |
| dc.date.accessioned | 2024-08-08T08:30:59Z | - |
| dc.date.available | 2024-08-08T08:30:59Z | - |
| dc.date.issued | 2023-02 | - |
| dc.identifier.issn | 1999-4915 | - |
| dc.identifier.issn | 1999-4915 | - |
| dc.identifier.uri | https://scholarworks.dongguk.edu/handle/sw.dongguk/20474 | - |
| dc.description.abstract | The coronavirus disease 2019 (COVID-19) pandemic has had irreversible and devastating impacts on every aspect of human life. To better prepare for the next similar pandemic, a clear understanding of coronavirus biology is a prerequisite. Nevertheless, the high-risk nature of the causative agent of COVID-19, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), requires the use of a cumbersome biosafety level-3 (BSL-3) confinement facility. To facilitate the development of preventive and therapeutic measures against SARS-CoV-2, one of the endemic strains of low-risk coronaviruses has gained attention as a useful research alternative: human coronavirus OC43 (HCoV-OC43). In this review, its history, classification, and clinical manifestations are first summarized. The characteristics of its viral genomes, genes, and evolution process are then further explained. In addition, the host factors necessary to support the life cycle of HCoV-OC43 and the innate, as well as adaptive, immunological responses to HCoV-OC43 infection are discussed. Finally, the development of in vitro and in vivo systems to study HCoV-OC43 and its application to the discovery of potential antivirals for COVID-19 by using HCoV-OC43 models are also presented. This review should serve as a concise guide for those who wish to use HCoV-OC43 to study coronaviruses in a low-risk research setting. | - |
| dc.format.extent | 17 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | MDPI | - |
| dc.title | Human Coronavirus OC43 as a Low-Risk Model to Study COVID-19 | - |
| dc.type | Article | - |
| dc.publisher.location | 스위스 | - |
| dc.identifier.doi | 10.3390/v15020578 | - |
| dc.identifier.scopusid | 2-s2.0-85148976670 | - |
| dc.identifier.wosid | 000940542700001 | - |
| dc.identifier.bibliographicCitation | Viruses, v.15, no.2, pp 1 - 17 | - |
| dc.citation.title | Viruses | - |
| dc.citation.volume | 15 | - |
| dc.citation.number | 2 | - |
| dc.citation.startPage | 1 | - |
| dc.citation.endPage | 17 | - |
| dc.type.docType | Review | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Virology | - |
| dc.relation.journalWebOfScienceCategory | Virology | - |
| dc.subject.keywordPlus | HEMAGGLUTINATING ENCEPHALOMYELITIS VIRUS | - |
| dc.subject.keywordPlus | HUMAN RESPIRATORY CORONAVIRUS | - |
| dc.subject.keywordPlus | BOVINE CORONAVIRUS | - |
| dc.subject.keywordPlus | ESTERASE PROTEIN | - |
| dc.subject.keywordPlus | NEURAL CELLS | - |
| dc.subject.keywordPlus | PERSISTENT INFECTION | - |
| dc.subject.keywordPlus | ANTIVIRAL ACTIVITY | - |
| dc.subject.keywordPlus | MOLECULAR-BIOLOGY | - |
| dc.subject.keywordPlus | BAT CORONAVIRUS | - |
| dc.subject.keywordPlus | NEURONAL CELLS | - |
| dc.subject.keywordAuthor | COVID-19 | - |
| dc.subject.keywordAuthor | human coronavirus | - |
| dc.subject.keywordAuthor | biosafety level | - |
| dc.subject.keywordAuthor | OC43 | - |
| dc.subject.keywordAuthor | low-risk model | - |
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