A pilot study of microbial signatures of liver disease in those with HIV mono-infection in Rio de Janeiro, Brazil. (1st January 2022)
- Record Type:
- Journal Article
- Title:
- A pilot study of microbial signatures of liver disease in those with HIV mono-infection in Rio de Janeiro, Brazil. (1st January 2022)
- Main Title:
- A pilot study of microbial signatures of liver disease in those with HIV mono-infection in Rio de Janeiro, Brazil
- Authors:
- Yanavich, Carolyn
Perazzo, Hugo
Li, Fan
Tobin, Nicole
Lee, David
Zabih, Sara
Morata, Michelle
Almeida, Cristiane
Veloso, Valdilea G.
Grinsztejn, Beatriz
Aldrovandi, Grace M. - Abstract:
- Abstract : 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 andAbstract : 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. … (more)
- Is Part Of:
- AIDS. Volume 36:Number 1(2022)
- Journal:
- AIDS
- Issue:
- Volume 36:Number 1(2022)
- Issue Display:
- Volume 36, Issue 1 (2022)
- Year:
- 2022
- Volume:
- 36
- Issue:
- 1
- Issue Sort Value:
- 2022-0036-0001-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-01-01
- Subjects:
- 16S sequencing -- fatty liver -- HIV infection -- liver disease -- microbiome -- shotgun sequencing
AIDS (Disease) -- Periodicals
Acquired Immunodeficiency Syndrome
AIDS (Disease)
Periodicals
Periodicals
616.9792005 - Journal URLs:
- http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&PAGE=toc&D=ovft&AN=00002030-000000000-00000 ↗
http://journals.lww.com/aidsonline/pages/default.aspx?desktopMode=true ↗
http://journals.lww.com/pages/default.aspx ↗ - DOI:
- 10.1097/QAD.0000000000003084 ↗
- Languages:
- English
- ISSNs:
- 0269-9370
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 0773.083000
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