Microbiome analysis of Brazilian women cervix reveals specific bacterial abundance correlation to RIG-like receptor gene expression

Front Immunol. 2023 Apr 25:14:1147950. doi: 10.3389/fimmu.2023.1147950. eCollection 2023.

Abstract

The relationship among microbiome, immunity and cervical cancer has been targeted by several studies, yet many questions remain unanswered. We characterized herein the virome and bacteriome from cervical samples and correlated these findings with innate immunity gene expression in a Brazilian convenience sample of HPV-infected (HPV+) and uninfected (HPV-) women. For this purpose, innate immune gene expression data were correlated to metagenomic information. Correlation analysis showed that interferon (IFN) is able to differentially modulate pattern recognition receptors (PRRs) expression based on HPV status. Virome analysis indicated that HPV infection correlates to the presence of Anellovirus (AV) and seven complete HPV genomes were assembled. Bacteriome results unveiled that vaginal community state types (CST) distribution was independent of HPV or AV status, although bacterial phyla distribution differed between groups. Furthermore, TLR3 and IFNαR2 levels were higher in the Lactobacillus no iners-dominated mucosa and we detected correlations among RIG-like receptors (RLR) associated genes and abundance of specific anaerobic bacteria. Collectively, our data show an intriguing connection between HPV and AV infections that could foster cervical cancer development. Besides that, TLR3 and IFNαR2 seem to create a protective milieu in healthy cervical mucosa (L. no iners-dominated), and RLRs, known to recognize viral RNA, were correlated to anaerobic bacteria suggesting that they might be related to dysbiosis.

Keywords: RIG-I-like receptor family; anellovirus; human papilloma virus (HPV); innate immunity recognition; microbiome and dysbiosis; squamous intraepithelial lesion of the cervix; toll-like receptors (TLR); virome analysis.

MeSH terms

  • Bacteria / genetics
  • Brazil
  • Cervix Uteri
  • Female
  • Gene Expression
  • Humans
  • Microbiota*
  • Papillomavirus Infections*
  • Toll-Like Receptor 3 / genetics
  • Uterine Cervical Neoplasms* / genetics
  • Uterine Cervical Neoplasms* / metabolism

Substances

  • Toll-Like Receptor 3

Grants and funding

This study was supported by grants from the Brazilian National Science Council (CNPq; # 309850/2020-7), from the Swiss Bridge Foundation (# L0V 3024060) and from intramural resources of the Brazilian National Cancer Institute to MAS.