Department of Microbiology, CDB, Hospital Clinic, University of Barcelona, Barcelona, Spain.
Molecuar Core Facilty, Hospital Clínic de Barcelona, Barcelona, Spain.
BMC Microbiol. 2024 Jun 8;24(1):201. doi: 10.1186/s12866-024-03335-z.
People living with HIV (PLWH) are at increased risk of acquisition of multidrug resistant organisms due to higher rates of predisposing factors. The gut microbiome is the main reservoir of the collection of antimicrobial resistance determinants known as the gut resistome. In PLWH, changes in gut microbiome have been linked to immune activation and HIV-1 associated complications. Specifically, gut dysbiosis defined by low microbial gene richness has been linked to low Nadir CD4 + T-cell counts. Additionally, sexual preference has been shown to strongly influence gut microbiome composition in PLWH resulting in different Prevotella or Bacteroides enriched enterotypes, in MSM (men-who-have-sex-with-men) or no-MSM, respectively. To date, little is known about gut resistome composition in PLWH due to the scarcity of studies using shotgun metagenomics. The present study aimed to detect associations between different microbiome features linked to HIV-1 infection and gut resistome composition.
Using shotgun metagenomics we characterized the gut resistome composition of 129 HIV-1 infected subjects showing different HIV clinical profiles and 27 HIV-1 negative controls from a cross-sectional observational study conducted in Barcelona, Spain. Most no-MSM showed a Bacteroides-enriched enterotype and low microbial gene richness microbiomes. We did not identify differences in resistome diversity and composition according to HIV-1 infection or immune status. However, gut resistome was more diverse in MSM group, Prevotella-enriched enterotype and gut micorbiomes with high microbial gene richness compared to no-MSM group, Bacteroides-enriched enterotype and gut microbiomes with low microbial gene richness. Additionally, gut resistome beta-diversity was different according to the defined groups and we identified a set of differentially abundant antimicrobial resistance determinants based on the established categories.
Our findings reveal a significant correlation between gut resistome composition and various host variables commonly associated with gut microbiome, including microbiome enterotype, microbial gene richness, and sexual preference. These host variables have been previously linked to immune activation and lower Nadir CD4 + T-Cell counts, which are prognostic factors of HIV-related comorbidities. This study provides new insights into the relationship between antibiotic resistance and clinical characteristics of PLWH.
由于较高的易患因素,艾滋病毒感染者(PLWH)获得耐药菌的风险增加。肠道微生物组是由多种抗菌药物抗性决定因素组成的主要储存库,称为肠道抗药性组。在 PLWH 中,肠道微生物组的变化与免疫激活和 HIV-1 相关并发症有关。具体来说,肠道微生物群落的改变与低微生物基因丰富度相关,与低 Nadir CD4+T 细胞计数相关。此外,性取向已被证明强烈影响 PLWH 的肠道微生物组组成,导致 MSM(男男性行为者)或非 MSM 中分别存在不同的普雷沃氏菌或拟杆菌富集肠型。迄今为止,由于使用宏基因组学进行研究的稀缺性,很少有关于 PLWH 肠道抗药性组组成的研究。本研究旨在检测与 HIV-1 感染相关的不同微生物组特征与肠道抗药性组组成之间的关联。
使用宏基因组学,我们对来自西班牙巴塞罗那进行的一项横断面观察性研究的 129 名 HIV-1 感染患者和 27 名 HIV-1 阴性对照者的肠道抗药性组组成进行了特征描述,这些患者具有不同的 HIV 临床特征。大多数非 MSM 表现出拟杆菌富集肠型和低微生物基因丰富度的微生物组。我们没有发现根据 HIV-1 感染或免疫状态,抗药性组的多样性和组成有差异。然而,与非 MSM 组相比,MSM 组的肠道抗药性组更加多样化,表现为普雷沃氏菌富集肠型和高微生物基因丰富度的肠道微生物组。此外,根据定义的组,肠道抗药性组的β多样性不同,我们根据已建立的类别确定了一组差异丰富的抗菌药物抗性决定因素。
我们的研究结果表明,肠道抗药性组的组成与各种与肠道微生物组相关的宿主变量之间存在显著相关性,包括微生物组肠型、微生物基因丰富度和性取向。这些宿主变量先前与免疫激活和较低的 Nadir CD4+T 细胞计数有关,这是 HIV 相关合并症的预后因素。本研究为 PLWH 抗生素耐药性与临床特征之间的关系提供了新的见解。