Gibson Keylie M, Steiner Margaret C, Kassaye Seble, Maldarelli Frank, Grossman Zehava, Pérez-Losada Marcos, Crandall Keith A
Computational Biology Institute, Milken Institute School of Public Health, George Washington University, Washington, DC, United States.
Department of Medicine, Georgetown University, Washington, DC, United States.
Front Microbiol. 2019 Mar 8;10:369. doi: 10.3389/fmicb.2019.00369. eCollection 2019.
Washington, DC consistently has one of the highest annual rates of new HIV-1 diagnoses in the United States over the last 10 years. To guide intervention and prevention strategies to combat DC HIV infection, it is helpful to understand HIV transmission dynamics in a historical context. Toward this aim, we conducted a retrospective study (years 1987-2015) of 3,349 HIV sequences (1,026 bp) from 1,996 individuals living in the DC area belonging to three different cohorts. We coupled HIV sequence data with clinical information (sex, risk factor, race/ethnicity, viral load, subtype, anti-retroviral regimen) to identify circulating drug resistant mutations (DRM) and transmission clusters and assess their persistence over time. Of the transmission clusters identified in the DC area, 78.0 and 31.7% involved MSM and heterosexuals, respectively. The longest spread of time for a single cluster was 5 years (2007-2012) using a distance-based network inference approach and 27 years (1987-2014) using a maximum likelihood phylogenetic approach. We found eight subtypes and nine recombinants. Genetic diversity increased steadily over time with a slight peak in 2009 and remained constant thereafter until 2015. Nucleotide diversity also increased over time while relative genetic diversity (BEAST) remained relatively steady over the last 28 years with slight increases since 2000 in subtypes B and C. Sequences from individuals on drug therapy contained the highest total number of DRMs (1,104-1,600) and unique DRMs (63-97) and the highest proportion (>20%) of resistant individuals. Heterosexuals (43.94%), MSM (40.13%), and unknown (44.26%) risk factors showed similar prevalence of DRMs, while injection drug users had a lower prevalence (33.33%). Finally, there was a 60% spike in the number of codons with DRMs between 2007 and 2010. Past patterns of HIV transmission and DRM accumulation over time described here will help to predict future efficacy of ART drugs based on DRMs persisting over time and identify risk groups of interest for prevention and intervention efforts within the DC population. Our results show how longitudinal data can help to understand the temporal dynamics of HIV-1 at the local level.
在过去10年里,华盛顿特区一直是美国新感染HIV-1年发病率最高的地区之一。为指导抗击华盛顿特区HIV感染的干预和预防策略,在历史背景下了解HIV传播动态很有帮助。为此,我们对来自华盛顿特区地区1996名个体的3349条HIV序列(1026个碱基对)进行了一项回顾性研究(1987 - 2015年),这些个体分属三个不同队列。我们将HIV序列数据与临床信息(性别、风险因素、种族/族裔、病毒载量、亚型、抗逆转录病毒疗法方案)相结合,以识别循环耐药突变(DRM)和传播簇,并评估它们随时间的持续性。在华盛顿特区地区识别出的传播簇中,分别有78.0%和31.7%涉及男男性行为者(MSM)和异性恋者。使用基于距离的网络推断方法,单个簇最长传播时间为5年(2007 - 2012年);使用最大似然系统发育方法,最长传播时间为27年(1987 - 2014年)。我们发现了8种亚型和9种重组型。遗传多样性随时间稳步增加,在2009年略有峰值,此后一直保持稳定直至2015年。核苷酸多样性也随时间增加,而相对遗传多样性(贝叶斯进化分析采样树方法)在过去28年里保持相对稳定,自2000年以来B型和C型亚型略有增加。接受药物治疗个体的序列中DRM总数(1104 - 1600个)和独特DRM(63 - 97个)最多,耐药个体比例最高(>20%)。异性恋者(43.94%)、男男性行为者(40.13%)和风险因素未知者(44.26%)的DRM流行率相似,而注射吸毒者的流行率较低(33.33%)。最后,2007年至2010年期间,带有DRM的密码子数量激增60%。这里描述的HIV过去传播模式和DRM随时间的积累情况,将有助于根据随时间持续存在的DRM预测抗逆转录病毒治疗药物的未来疗效,并识别华盛顿特区人群中预防和干预工作的重点风险群体。我们的结果显示了纵向数据如何有助于在地方层面理解HIV-1的时间动态。