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Vaginal lactobacilli produce anti-inflammatory β-carboline compounds.

Authors :
Glick VJ
Webber CA
Simmons LE
Martin MC
Ahmad M
Kim CH
Adams AND
Bang S
Chao MC
Howard NC
Fortune SM
Verma M
Jost M
Beura LK
James MJ
Lee SY
Mitchell CM
Clardy J
Kim KH
Gopinath S
Source :
Cell host & microbe [Cell Host Microbe] 2024 Nov 13; Vol. 32 (11), pp. 1897-1909.e7. Date of Electronic Publication: 2024 Oct 17.
Publication Year :
2024

Abstract

The optimal vaginal microbiome is a Lactobacillus-dominant community. Apart from Lactobacillus iners, the presence of Lactobacillus species is associated with reduced vaginal inflammation and reduced levels of pro-inflammatory cytokines. Loss of Lactobacillus-dominance is associated with inflammatory conditions, such as bacterial vaginosis (BV). We have identified that Lactobacillus crispatus, a key vaginal bacterial species, produces a family of β-carboline compounds with anti-inflammatory activity. These compounds suppress nuclear factor κB (NF-κB) and interferon (IFN) signaling downstream of multiple pattern recognition receptors in primary human cells and significantly dampen type I IFN receptor (IFNAR) activation in monocytes. Topical application of an anti-inflammatory β-carboline compound, perlolyrine, was sufficient to significantly reduce vaginal inflammation in a mouse model of genital herpes infection. These compounds are enriched in cervicovaginal lavage (CVL) of healthy people compared with people with BV. This study identifies a family of compounds by which vaginal lactobacilli mediate host immune homeostasis and highlights a potential therapeutic avenue for vaginal inflammation.<br />Competing Interests: Declaration of interests C.W., M.C.M., S.B., J.C., K.H.K., and S.G. are co-inventors on a patent related to this work.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1934-6069
Volume :
32
Issue :
11
Database :
MEDLINE
Journal :
Cell host & microbe
Publication Type :
Academic Journal
Accession number :
39423813
Full Text :
https://doi.org/10.1016/j.chom.2024.09.014