独特的肠道细菌微生物群落作为HIV感染和进展的指标

S. Ako, C. Nkenfou, J. N. Assob, T. B. Pokam, M. Tongo, Enoh Jude Eteneneng, Mbanya Gladice Mbanya, E. Akum
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引用次数: 0

摘要

人类消化道的上皮细胞内层蕴藏着复杂的微生物群落。肠道免疫紊乱会促进肠道生态失调,进而诱发粘膜和外周慢性炎症。在最受影响的人群中,对HIV感染期间观察到的特定肠道微生物组变化的解释是有必要的。这是一项病例对照和比较研究设计,于2018年6月至2019年9月进行。在布埃亚地区医院共招募了40名成年志愿者(15名艾滋病毒阴性,25名艾滋病毒阳性)。血液分析CD4+ T细胞计数和HIV病毒载量。使用下一代Illumina®MiSeq™测序仪对所有参与者的粪便样本进行16S rRNA基因测序分析。生物标志物线性判别分析(LDA)结果表明,特异性肠道微生物群Lachnoclostridium sp32343-sp32393-sp32423群落可以作为HIV感染的指标。研究结果还表明,普通拟杆菌(seq 11和seq 42)、异种大单胞菌(seq 63)、普雷沃菌科未分类成员sp14289 (seq 51)、sp13942 (seq 4)和copi -普雷沃菌sp13942 (seq 5)可作为HIV病毒载量升高和CD4+ T细胞计数降低的肠道微生物组生物标志物。与此同时,肠道微生物组生物标志物鉴定出降低HIV病毒载量和增加CD4+ T细胞计数的有Succinivibrionaceae sp56244 (seq 47)、Eubacterium rectale (seq 8)、Megamonas funiformis (seq 1和seq 14)、Prevotella copri (seq 29、seq 34和seq 12)和未分类的Prevotellaceae sp13927 (seq 17)、sp13942 (seq 5)。Lachnoclostridium sp32343-sp32393-sp32423的特异性肠道微生物群落可以作为HIV存在的指标。一些肠道细菌微生物组可用于艾滋病毒疾病进展的管理。
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Unique Community of Gut Bacterial Microbiome as Indicator for HIV Infection and Progression
The human digestive tract harbors complex microbial communities within its epithelial cell lining. Disruption in enteric immunity will promote gut dysbiosis, which can successively induce chronic inflammation within the mucous membrane and periphery. Interpretation of the specific gut microbiome changes observed during HIV infection is warranted in populations most affected.This was a case-control and comparative study design carried out between June 2018 to September 2019. A total of 40 volunteer adult participants were recruited (15 HIV-negative and 25 HIV-positive) at the Buea Regional Hospital. Blood analysis was done for CD4+ T cell count and HIV viral load. Fecal samples from all participants were analyzed using the 16S rRNA gene sequencing on the next-generation Illumina® MiSeq™ sequencer. Biomarker Linear Discriminant Analysis (LDA) score from LEfSe analysis indicated that the specific gut microbiome, Lachnoclostridium sp32343-sp32393-sp32423 communities could serve as an indicator for HIV infection. Findings also showed that Bacteroides vulgatus (seq 11 & seq 42), Megamonas funiformis (seq 63), unclassified members of Prevotallaceae family sp14289 (seq 51), sp13942 (seq 4), and Prevotella copri-sp13942 (seq 5) could be used as gut microbiome biomarkers for increased HIV viral load and decreased CD4+ T cell count. Meanwhile gut microbiome biomarkers for decreased HIV viral load and increased CD4+ T cell count were identified as Succinivibrionaceae sp56244 (seq 47),  Eubacterium rectale (seq 8), Megamonas funiformis (seq 1 and seq 14), Prevotella copri (seq 29, seq 34, and seq 12) and unclassified Prevotellaceae sp13927 (seq 17), sp13942 (seq 5). Specific gut microbiome communities of Lachnoclostridium sp32343-sp32393-sp32423 could be used as an indicator of HIV presence. Some gut bacteria microbiome can be utilized in the management of HIV disease progression.
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