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Molecular Features of the V1-V4 Coding Region of Sexually Transmitted Human Immunodeficiency Virus Type 1

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dc.contributor.author최준용-
dc.date.accessioned2017-11-02T08:14:23Z-
dc.date.available2017-11-02T08:14:23Z-
dc.date.issued2017-
dc.identifier.issn0022-1899-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/154237-
dc.description.abstractBACKGROUND: Investigations into which human immunodeficiency virus type 1 (HIV-1) sequence features may be selected for transmission during sexual exposure have been hampered by the small number of characterized transmission pairs in individual studies. METHODS: To boost statistical power to detect differences in glycosylation, length, and electrical charge in the HIV-1 V1-V4 coding region, we reanalyzed all available 2485 env sequences derived from 114 subjects representing 58 transmission pairs from previous studies using mixed-effects linear regression and an approach to approximate the unobserved transmitted virus. RESULTS : The recipient partner had a shorter V1-V4 region and fewer potential N-linked glycosylation sites (PNGS) than sequences from the source partner. We also detected a trend toward more PNGS and lower isoelectric points in transmitted sequences with source partner and the evolutionary tendency to shorten V1-V4 sequences, reduce the number of PNGS, and lower isoelectric points in the recipient following transmission. CONCLUSIONS: By using all available well-characterized env sequences from transmission pairs via sexual exposure, we were able to identify several important virologic factors that may be important in the development of biomedical preventive interventions-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherOxford University Press-
dc.relation.isPartOfJOURNAL OF INFECTIOUS DISEASES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnalysis of Variance-
dc.subject.MESHEvolution, Molecular-
dc.subject.MESHGlycosylation-
dc.subject.MESHHIV Envelope Protein gp120/chemistry-
dc.subject.MESHHIV Envelope Protein gp120/genetics*-
dc.subject.MESHHIV Envelope Protein gp120/metabolism-
dc.subject.MESHHIV Infections/transmission*-
dc.subject.MESHHIV Infections/virology*-
dc.subject.MESHHIV-1/genetics*-
dc.subject.MESHHIV-1/metabolism-
dc.subject.MESHHIV-1/pathogenicity-
dc.subject.MESHHumans-
dc.subject.MESHPeptide Fragments/genetics*-
dc.titleMolecular Features of the V1-V4 Coding Region of Sexually Transmitted Human Immunodeficiency Virus Type 1-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Internal Medicine-
dc.contributor.googleauthorJun Yong Choi-
dc.contributor.googleauthorSergei L. Kosakovsky Pond-
dc.contributor.googleauthorChristy M. Anderson-
dc.contributor.googleauthorDouglas D. Richman-
dc.contributor.googleauthorDavey M. Smith-
dc.identifier.doi10.1093/infdis/jix184-
dc.contributor.localIdA04191-
dc.relation.journalcodeJ01454-
dc.identifier.eissn1537-6613-
dc.identifier.pmid28419276-
dc.identifier.urlhttps://academic.oup.com/jid/article-lookup/doi/10.1093/infdis/jix184-
dc.subject.keywordHIV-
dc.subject.keywordenv-
dc.subject.keywordtransmitted virus-
dc.subject.keywordviral evolution-
dc.contributor.alternativeNameChoi, Jun Yong-
dc.contributor.affiliatedAuthorChoi, Jun Yong-
dc.citation.titleJournal of Infectious Diseases-
dc.citation.volume215-
dc.citation.number10-
dc.citation.startPage1506-
dc.citation.endPage1513-
dc.identifier.bibliographicCitationJOURNAL OF INFECTIOUS DISEASES, Vol.215(10) : 1506-1513, 2017-
dc.date.modified2017-11-01-
dc.identifier.rimsid42206-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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