Interactions between host and gut microbiota in gestational diabetes mellitus and their impacts on offspring

BMC Microbiol. 2024 May 10;24(1):161. doi: 10.1186/s12866-024-03255-y.

Abstract

Gestational diabetes mellitus (GDM) is characterized by insulin resistance and low-grade inflammation, and most studies have demonstrated gut dysbiosis in GDM pregnancies. Overall, they were manifested as a reduction in microbiome diversity and richness, depleted short chain fatty acid (SCFA)-producing genera and a dominant of Gram-negative pathogens releasing lipopolysaccharide (LPS). The SCFAs functioned as energy substance or signaling molecules to interact with host locally and beyond the gut. LPS contributed to pathophysiology of diseases through activating Toll-like receptor 4 (TLR4) and involved in inflammatory responses. The gut microbiome dysbiosis was not only closely related with GDM, it was also vital to fetal health through vertical transmission. In this review, we summarized gut microbiota signature in GDM pregnancies of each trimester, and presented a brief introduction of microbiome derived SCFAs. We then discussed mechanisms of microbiome-host interactions in the physiopathology of GDM and associated metabolic disorders. Finally, we compared offspring microbiota composition from GDM with that from normal pregnancies, and described the possible mechanism.

Keywords: Gestational diabetes mellitus (GDM); Gut microbiota; Host-microbiome interactions; Metabolism; Offspring.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteria / classification
  • Bacteria / genetics
  • Bacteria / isolation & purification
  • Bacteria / metabolism
  • Diabetes, Gestational* / metabolism
  • Diabetes, Gestational* / microbiology
  • Dysbiosis* / microbiology
  • Fatty Acids, Volatile* / metabolism
  • Female
  • Gastrointestinal Microbiome*
  • Host Microbial Interactions
  • Humans
  • Lipopolysaccharides / metabolism
  • Pregnancy

Substances

  • Fatty Acids, Volatile
  • Lipopolysaccharides