4.4 Article

A pilot study of microbial signatures of liver disease in those with HIV mono-infection in Rio de Janeiro, Brazil

期刊

AIDS
卷 36, 期 1, 页码 49-58

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAD.0000000000003084

关键词

16S sequencing; fatty liver; HIV infection; liver disease; microbiome; shotgun sequencing

资金

  1. LAPCLIN-AIDS (Laboratorio de Pesquisa Clinica em IST/AIDS) from INI/FIOCRUZ (Instituto Nacional de Infectologica Evandro Chagas Fundacao Oswaldo Cruz)
  2. University of California Los Angeles (UCLA)
  3. UCLA Center for AIDS Research (CFAR) [NIH/NIAIDAI028697]
  4. International Society for Infectious Diseases (ISID Research Grant 2016)
  5. Fundacao Carlos Chagas Filho de Amparo a Pesquisa do Estado do Rio de Janeiro [E-26/110.268/2014]
  6. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [405.211/2016-3]
  7. Programa Ciencias Sem Fronteiras -Bolsa Jovens Talentos/CNPq [407.410/2013-9, 301.520/2014-3]

向作者/读者索取更多资源

The relationship between the microbiome and liver disease in HIV-infection was examined by analyzing the rectal microbiome. The study found distinct microbial profiles in HIV mono-infected individuals with steatosis or fibrosis, some of which are similar to those associated with non-alcoholic fatty liver disease in HIV-negative populations. Further studies are needed to understand the role of the gut microbiota in the pathogenesis of liver disease in HIV-infected persons.
Objective: The rectal microbiome was examined to assess the relationship between the microbiome and liver disease in HIV-infection. Design: Eighty-two HIV-1 mono-infected individuals from the PROSPEC-HIV-study (NCT02542020) were grouped into three liver health categories based on results of controlled attenuation parameter (CAP) and liver stiffness measurement (LSM) of transient elastography: normal (n = 30), steatosis (n = 30), or fibrosis (n = 22). Methods: Liver steatosis and fibrosis were defined by CAP at least 248 dB/m and LSM at least 8.0 kPa, respectively. 16S rRNA gene and whole genome shotgun metagenomic sequencing were performed on rectal swabs. Bacterial differences were assessed using zero-inflated negative binomial regression and random forests modeling; taxonomic drivers of functional shifts were identified using FishTaco. Results: Liver health status explained four percentage of the overall variation (r(2) = 0.04, P = 0.003) in bacterial composition. Participants with steatosis had depletions of Akkermansia muciniphila and Bacteroides dorei and enrichment of Prevotella copri, Finegoldia magna, and Ruminococcus bromii. Participants with fibrosis had depletions of Bacteroides stercoris and Parabacteroides distasonis and enrichment of Sneathia sanguinegens. In steatosis, functional analysis revealed increases in primary and secondary bile acid synthesis encoded by increased Eubacterium rectale, F. magna, and Faecalibacterium prausnitzii and decreased A. muciniphila, Bacteroides fragilis and B. dorei. Decreased folate biosynthesis was driven by similar changes in microbial composition. Conclusion: HIV mono-infection with steatosis or fibrosis had distinct microbial profiles. Some taxa are similar to those associated with non-alcoholic fatty liver disease in HIV-negative populations. Further studies are needed to define the role of the gut microbiota in the pathogenesis of liver disease in HIV-infected persons.

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