Twigg Homer L, Knox Kenneth S, Zhou Jin, Crothers Kristina A, Nelson David E, Toh Evelyn, Day Richard B, Lin Huaiying, Gao Xiang, Dong Qunfeng, Mi Deming, Katz Barry P, Sodergren Erica, Weinstock George M
1 Department of Medicine.
2 Department of Medicine, University of Arizona, Tucson, Arizona.
Am J Respir Crit Care Med. 2016 Jul 15;194(2):226-35. doi: 10.1164/rccm.201509-1875OC.
Previous work found the lung microbiome in healthy subjects infected with HIV was similar to that in uninfected subjects. We hypothesized the lung microbiome from subjects infected with HIV with more advanced disease would differ from that of an uninfected control population.
To measure the lung microbiome in an HIV-infected population with advanced disease.
16s RNA gene sequencing was performed on acellular bronchoalveolar lavage (BAL) fluid from 30 subjects infected with HIV with advanced disease (baseline mean CD4 count, 262 cells/mm(3)) before and up to 3 years after starting highly active antiretroviral therapy (HAART) and compared with 22 uninfected control subjects.
The lung microbiome in subjects infected with HIV with advanced disease demonstrated decreased alpha diversity (richness and diversity) and greater beta diversity compared with uninfected BAL. Differences improved with HAART, but still persisted up to 3 years after starting therapy. Population dispersion in the group infected with HIV was significantly greater than in the uninfected cohort and declined after treatment. There were differences in the relative abundance of some bacteria between the two groups at baseline and after 1 year of therapy. After 1 year on HAART, HIV BAL contained an increased abundance of Prevotella and Veillonella, bacteria previously associated with lung inflammation.
The lung microbiome in subjects infected with HIV with advanced disease is altered compared with an uninfected population both in diversity and bacterial composition. Differences remain up to 3 years after starting HAART. We speculate an altered lung microbiome in HIV infection may contribute to chronic inflammation and lung complications seen in the HAART era.
先前的研究发现,感染HIV的健康受试者的肺部微生物群与未感染受试者的相似。我们推测,疾病进展更严重的HIV感染者的肺部微生物群将与未感染的对照人群不同。
测量患有晚期疾病的HIV感染人群的肺部微生物群。
对30名患有晚期疾病的HIV感染者(基线平均CD4细胞计数为262个/mm³)在开始高效抗逆转录病毒治疗(HAART)之前及之后长达3年的无细胞支气管肺泡灌洗(BAL)液进行16s RNA基因测序,并与22名未感染的对照受试者进行比较。
与未感染的BAL相比,患有晚期疾病的HIV感染者的肺部微生物群显示出α多样性(丰富度和多样性)降低以及β多样性增加。HAART治疗后差异有所改善,但在开始治疗后3年仍持续存在。HIV感染组的总体离散度明显大于未感染队列,且治疗后有所下降。两组在基线和治疗1年后某些细菌的相对丰度存在差异。在接受HAART治疗1年后,HIV感染者的BAL中普雷沃菌属和韦荣球菌属的丰度增加,这些细菌以前与肺部炎症有关。
与未感染人群相比,患有晚期疾病的HIV感染者的肺部微生物群在多样性和细菌组成方面均发生了改变。开始HAART治疗后3年差异仍然存在。我们推测,HIV感染中肺部微生物群的改变可能导致HAART时代出现的慢性炎症和肺部并发症。