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Metabolomic Analysis of Murine Tissues Infected with . | LitMetric

Metabolomic Analysis of Murine Tissues Infected with .

bioRxiv

Department of Veterinary Pathobiology, College of Veterinary Medicine, University of Missouri, Columbia, Missouri.

Published: November 2024

AI Article Synopsis

  • The study investigates how a gram-negative bacterial pathogen affects the metabolism of host tissues, specifically in infected mice over four weeks.
  • Notable metabolic changes were observed two weeks post-infection, with significant alterations in the reproductive tracts, spleens, and livers compared to uninfected tissues.
  • The research highlights that while certain metabolic pathways were impacted, treatments targeting GABA and glutaminolysis did not significantly change the bacteria's virulence, suggesting that the infection alters metabolism in ways that could influence inflammation and infection outcomes.

Article Abstract

is a gram negative, facultative, intracellular bacterial pathogen that constitutes a substantial threat to human and animal health. can replicate in a variety of tissues and can induce immune responses that alter host metabolite availability. Here, mice were infected with and murine spleens, livers, and female reproductive tracts were analyzed by GC-MS to determine tissue-specific metabolic changes at one-, two- and four- weeks post infection. The most remarkable changes were observed at two-weeks post-infection when relative to uninfected tissues, 42 of 329 detected metabolites in reproductive tracts were significantly altered by infection, while in spleens and livers, 68/205 and 139/330 metabolites were significantly changed, respectively. Several of the altered metabolites in host tissues were linked to the GABA shunt and glutaminolysis. Treatment of macrophages with GABA did not alter control of infection, and deletion of the putative GABA transporter BMEI0265 did not alter virulence. While glutaminolysis inhibition did not affect control of in macrophages, glutaminolysis was required for macrophage IL-1β production in response to . In sum, these results indicate that infection alters host tissue metabolism and that these changes could have effects on inflammation and the outcome of infection.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11601316PMC
http://dx.doi.org/10.1101/2024.11.16.623915DOI Listing

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