Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
J Virol. 2020 Jun 1;94(12). doi: 10.1128/JVI.00151-20.
Concurrent sexually transmitted infections (STI) can increase the probability of HIV-1 transmission primarily by increasing the viral load present in semen. In this study, we explored the relationship of HIV-1 in blood and seminal plasma in the presence and absence of urethritis and after treatment of the concurrent STI. Primer ID deep sequencing of the V1/V3 region of the HIV-1 gene was done for paired blood and semen samples from antiretroviral therapy (ART)-naive men living in Malawi with ( = 19) and without ( = 5) STI-associated urethritis; for a subset of samples, full-length genes were generated for sequence analysis and to test entry phenotype. Cytokine concentrations in the blood and semen were also measured, and a reduction in the levels of proinflammatory cytokines was observed following STI treatment. We observed no difference in the prevalence of diverse compartmentalized semen-derived lineages in men with or without STI-associated urethritis, and these viral populations were largely stable during STI treatment. Clonal amplification of one or a few viral sequences accounted for nearly 50% of the viral population, indicating a recent bottleneck followed by limited viral replication. We conclude that the male genital tract is a site where virus can be brought in from the blood, where localized sustained replication can occur, and where specific genotypes can be amplified, perhaps initially by cellular proliferation but further by limited viral replication. HIV-1 infection is a sexually transmitted infection that coexists with other STI. Here, we examined the impact of a concurrent STI resulting in urethritis on the HIV-1 population within the male genital tract. We found that viral populations remain largely stable even with treatment of the STI. These results show that viral populations within the male genital tract are defined by factors beyond transient inflammation associated with a concurrent STI.
同时感染性传播感染(STI)会增加 HIV-1 传播的可能性,主要是通过增加精液中存在的病毒载量。在这项研究中,我们探讨了在存在和不存在尿道炎的情况下以及在同时治疗性传播感染后,血液和精液中 HIV-1 的关系。使用引物 ID 对来自马拉维的抗逆转录病毒治疗(ART)初治男性的配对血液和精液样本进行 HIV-1 基因 V1/V3 区的深度测序,这些男性患有( = 19)和不患有( = 5)与 STI 相关的尿道炎;对于一部分样本,生成全长基因进行序列分析并测试进入表型。还测量了血液和精液中的细胞因子浓度,并观察到 STI 治疗后促炎细胞因子水平降低。我们观察到在患有或不患有与 STI 相关的尿道炎的男性中,不同分隔精液衍生谱系的流行率没有差异,并且这些病毒群体在 STI 治疗期间基本保持稳定。一个或几个病毒序列的克隆扩增占病毒群体的近 50%,表明随后发生了有限的病毒复制,出现了近期瓶颈。我们的结论是,男性生殖道是病毒可以从血液中进入的部位,在那里可以发生局部持续复制,并且可以扩增特定的基因型,可能最初是通过细胞增殖,但随后是有限的病毒复制。HIV-1 感染是一种与其他 STI 共存的性传播感染。在这里,我们研究了并发 STI 导致尿道炎对男性生殖道内 HIV-1 群体的影响。我们发现,即使治疗性传播感染,病毒群体仍基本保持稳定。这些结果表明,男性生殖道内的病毒群体是由与并发 STI 相关的短暂炎症以外的因素决定的。