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解读HIV-1C感染的多样性:密切相关的多个病毒谱系的传播

Deciphering Multiplicity of HIV-1C Infection: Transmission of Closely Related Multiple Viral Lineages.

作者信息

Novitsky Vlad, Moyo Sikhulile, Wang Rui, Gaseitsiwe Simani, Essex M

机构信息

Harvard T. H. Chan School of Public Health, Boston, Massachusetts, United States of America.

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

出版信息

PLoS One. 2016 Nov 28;11(11):e0166746. doi: 10.1371/journal.pone.0166746. eCollection 2016.

Abstract

BACKGROUND

A single viral variant is transmitted in the majority of HIV infections. However, about 20% of heterosexually transmitted HIV infections are caused by multiple viral variants. Detection of transmitted HIV variants is not trivial, as it involves analysis of multiple viral sequences representing intra-host HIV-1 quasispecies.

METHODOLOGY

We distinguish two types of multiple virus transmission in HIV infection: (1) HIV transmission from the same source, and (2) transmission from different sources. Viral sequences representing intra-host quasispecies in a longitudinally sampled cohort of 42 individuals with primary HIV-1C infection in Botswana were generated by single-genome amplification and sequencing and spanned the V1C5 region of HIV-1C env gp120. The Maximum Likelihood phylogeny and distribution of pairwise raw distances were assessed at each sampling time point (n = 217; 42 patients; median 5 (IQR: 4-6) time points per patient, range 2-12 time points per patient).

RESULTS

Transmission of multiple viral variants from the same source (likely from the partner with established HIV infection) was found in 9 out of 42 individuals (21%; 95 CI 10-37%). HIV super-infection was identified in 2 patients (5%; 95% CI 1-17%) with an estimated rate of 3.9 per 100 person-years. Transmission of multiple viruses combined with HIV super-infection at a later time point was observed in one individual.

CONCLUSIONS

Multiple HIV lineages transmitted from the same source produce a monophyletic clade in the inferred phylogenetic tree. Such a clade has transiently distinct sub-clusters in the early stage of HIV infection, and follows a predictable evolutionary pathway. Over time, the gap between initially distinct viral lineages fills in and initially distinct sub-clusters converge. Identification of cases with transmission of multiple viral lineages from the same source needs to be taken into account in cross-sectional estimation of HIV recency in epidemiological and population studies.

摘要

背景

大多数HIV感染是由单一病毒变体传播的。然而,约20%的异性传播HIV感染是由多种病毒变体引起的。检测传播的HIV变体并非易事,因为这涉及对代表宿主内HIV-1准种的多个病毒序列进行分析。

方法

我们区分了HIV感染中两种类型的多病毒传播:(1)来自同一来源的HIV传播,以及(2)来自不同来源的传播。通过单基因组扩增和测序,在博茨瓦纳42例原发性HIV-1C感染患者的纵向采样队列中生成了代表宿主内准种的病毒序列,这些序列跨越了HIV-1C env gp120的V1C5区域。在每个采样时间点(n = 217;42例患者;每位患者中位数为5(四分位间距:4 - 6)个时间点,每位患者范围为2 - 12个时间点)评估最大似然系统发育和成对原始距离的分布。

结果

42例个体中有9例(21%;95%置信区间10 - 37%)发现了来自同一来源(可能来自已感染HIV的性伴侣)的多种病毒变体传播。在2例患者(5%;95%置信区间1 - 17%)中鉴定出HIV重复感染,估计发生率为每100人年3.9例。在1例个体中观察到多种病毒传播与后期HIV重复感染相结合的情况。

结论

从同一来源传播的多个HIV谱系在推断的系统发育树中产生一个单系分支。这样的分支在HIV感染早期有短暂不同的亚群,并遵循可预测的进化途径。随着时间的推移,最初不同的病毒谱系之间的差距会缩小,最初不同的亚群会汇聚。在流行病学和人群研究中对HIV近期感染的横断面估计中,需要考虑识别来自同一来源传播多种病毒谱系的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47c3/5125632/8100843418a4/pone.0166746.g001.jpg

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