{"title":"人类免疫缺陷病毒相关神经认知障碍中肠道微生物群衍生的神经调节氨基酸代谢失调:元基因组学和代谢组学的综合分析。","authors":"Xue Chen, Jiaqi Wei, Zhen Li, Yang Zhang, Xin Zhang, Ling Zhang, Xia Wang, Yulin Zhang, Tong Zhang","doi":"10.1002/ana.26963","DOIUrl":null,"url":null,"abstract":"<div>\n \n <section>\n \n <h3> Objective</h3>\n \n <p>Although accumulating evidence implicating altered gut microbiota in human immunodeficiency virus (HIV) infection and neurodegenerative disorders; however, the association between dysbiosis of the gut microbiota and metabolites in the pathogenesis of HIV-associated neurocognitive disorder (HAND) remains unclear.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Fecal and plasma samples were obtained from 3 cohorts (HAND, HIV–non-HAND, and healthy controls), metagenomic analysis and metabolomic profiling were performed to investigate alterations in the gut microbial composition and circulating metabolites in HAND.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>The gut microbiota of people living with HIV (PLWH) had an increased relative abundance of <i>Prevotella</i> and a decreased relative abundance of <i>Bacteroides</i>. In contrast, <i>Prevotella</i> and <i>Megamonas</i> were substantially decreased, and <i>Bacteroides</i> and <i>Phocaeicola</i> were increased in HAND patients. Moreover, untargeted metabolomics identified several neurotransmitters and certain amino acids associated with neuromodulation, and the differential metabolic pathways of amino acids associated with neurocognition were depleted in HAND patients. Notably, most neuromodulatory metabolites are associated with an altered abundance of specific gut bacteria.</p>\n </section>\n \n <section>\n \n <h3> Interpretation</h3>\n \n <p>Our findings provide new insights into the intricate interplay between the gut and microbiome-brain axis in the pathogenesis of HAND, highlighting the potential for developing novel therapeutic strategies that specifically target the gut microbiota. ANN NEUROL 2024;96:306–320</p>\n </section>\n </div>","PeriodicalId":127,"journal":{"name":"Annals of Neurology","volume":null,"pages":null},"PeriodicalIF":8.1000,"publicationDate":"2024-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dysregulation of Gut Microbiota-Derived Neuromodulatory Amino Acid Metabolism in Human Immunodeficiency Virus-Associated Neurocognitive Disorder: An Integrative Metagenomic and Metabolomic Analysis\",\"authors\":\"Xue Chen, Jiaqi Wei, Zhen Li, Yang Zhang, Xin Zhang, Ling Zhang, Xia Wang, Yulin Zhang, Tong Zhang\",\"doi\":\"10.1002/ana.26963\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <section>\\n \\n <h3> Objective</h3>\\n \\n <p>Although accumulating evidence implicating altered gut microbiota in human immunodeficiency virus (HIV) infection and neurodegenerative disorders; however, the association between dysbiosis of the gut microbiota and metabolites in the pathogenesis of HIV-associated neurocognitive disorder (HAND) remains unclear.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Fecal and plasma samples were obtained from 3 cohorts (HAND, HIV–non-HAND, and healthy controls), metagenomic analysis and metabolomic profiling were performed to investigate alterations in the gut microbial composition and circulating metabolites in HAND.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>The gut microbiota of people living with HIV (PLWH) had an increased relative abundance of <i>Prevotella</i> and a decreased relative abundance of <i>Bacteroides</i>. In contrast, <i>Prevotella</i> and <i>Megamonas</i> were substantially decreased, and <i>Bacteroides</i> and <i>Phocaeicola</i> were increased in HAND patients. Moreover, untargeted metabolomics identified several neurotransmitters and certain amino acids associated with neuromodulation, and the differential metabolic pathways of amino acids associated with neurocognition were depleted in HAND patients. Notably, most neuromodulatory metabolites are associated with an altered abundance of specific gut bacteria.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Interpretation</h3>\\n \\n <p>Our findings provide new insights into the intricate interplay between the gut and microbiome-brain axis in the pathogenesis of HAND, highlighting the potential for developing novel therapeutic strategies that specifically target the gut microbiota. ANN NEUROL 2024;96:306–320</p>\\n </section>\\n </div>\",\"PeriodicalId\":127,\"journal\":{\"name\":\"Annals of Neurology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":8.1000,\"publicationDate\":\"2024-05-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of Neurology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/ana.26963\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Neurology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ana.26963","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
目的:尽管有越来越多的证据表明肠道微生物群的改变与人类免疫缺陷病毒(HIV)感染和神经退行性疾病有关,但肠道微生物群失调与代谢物在HIV相关神经认知障碍(HAND)发病机制中的关联仍不清楚:方法:从3个队列(HAND、HIV-非HAND和健康对照组)中获取粪便和血浆样本,进行元基因组分析和代谢组分析,研究HAND患者肠道微生物组成和循环代谢物的改变:结果:HIV 感染者(PLWH)的肠道微生物群中,普雷沃特氏菌(Prevotella)的相对丰度增加,乳杆菌(Bacteroides)的相对丰度降低。相比之下,HAND 患者的普雷沃特氏菌和 Megamonas 大量减少,而 Bacteroides 和 Phocaeicola 增加。此外,非靶向代谢组学发现了几种神经递质和某些与神经调节相关的氨基酸,而与神经认知相关的氨基酸的不同代谢途径在 HAND 患者中被耗尽。值得注意的是,大多数神经调节代谢物与特定肠道细菌丰度的改变有关:我们的研究结果为了解肠道和微生物脑轴在 HAND 发病机制中错综复杂的相互作用提供了新的视角,凸显了开发专门针对肠道微生物群的新型治疗策略的潜力。ann neurol 2024.
Dysregulation of Gut Microbiota-Derived Neuromodulatory Amino Acid Metabolism in Human Immunodeficiency Virus-Associated Neurocognitive Disorder: An Integrative Metagenomic and Metabolomic Analysis
Objective
Although accumulating evidence implicating altered gut microbiota in human immunodeficiency virus (HIV) infection and neurodegenerative disorders; however, the association between dysbiosis of the gut microbiota and metabolites in the pathogenesis of HIV-associated neurocognitive disorder (HAND) remains unclear.
Methods
Fecal and plasma samples were obtained from 3 cohorts (HAND, HIV–non-HAND, and healthy controls), metagenomic analysis and metabolomic profiling were performed to investigate alterations in the gut microbial composition and circulating metabolites in HAND.
Results
The gut microbiota of people living with HIV (PLWH) had an increased relative abundance of Prevotella and a decreased relative abundance of Bacteroides. In contrast, Prevotella and Megamonas were substantially decreased, and Bacteroides and Phocaeicola were increased in HAND patients. Moreover, untargeted metabolomics identified several neurotransmitters and certain amino acids associated with neuromodulation, and the differential metabolic pathways of amino acids associated with neurocognition were depleted in HAND patients. Notably, most neuromodulatory metabolites are associated with an altered abundance of specific gut bacteria.
Interpretation
Our findings provide new insights into the intricate interplay between the gut and microbiome-brain axis in the pathogenesis of HAND, highlighting the potential for developing novel therapeutic strategies that specifically target the gut microbiota. ANN NEUROL 2024;96:306–320
期刊介绍:
Annals of Neurology publishes original articles with potential for high impact in understanding the pathogenesis, clinical and laboratory features, diagnosis, treatment, outcomes and science underlying diseases of the human nervous system. Articles should ideally be of broad interest to the academic neurological community rather than solely to subspecialists in a particular field. Studies involving experimental model system, including those in cell and organ cultures and animals, of direct translational relevance to the understanding of neurological disease are also encouraged.