NlpC/P60 peptidoglycan hydrolases of Trichomonas vaginalis have complementary activities that empower the protozoan to control host-protective lactobacilli.


Journal

PLoS pathogens
ISSN: 1553-7374
Titre abrégé: PLoS Pathog
Pays: United States
ID NLM: 101238921

Informations de publication

Date de publication:
08 2023
Historique:
received: 13 12 2022
accepted: 18 07 2023
revised: 28 08 2023
medline: 29 8 2023
pubmed: 16 8 2023
entrez: 16 8 2023
Statut: epublish

Résumé

Trichomonas vaginalis is a human protozoan parasite that causes trichomoniasis, a prevalent sexually transmitted infection. Trichomoniasis is accompanied by a shift to a dysbiotic vaginal microbiome that is depleted of lactobacilli. Studies on co-cultures have shown that vaginal bacteria in eubiosis (e.g. Lactobacillus gasseri) have antagonistic effects on T. vaginalis pathogenesis, suggesting that the parasite might benefit from shaping the microbiome to dysbiosis (e.g. Gardnerella vaginalis among other anaerobes). We have recently shown that T. vaginalis has acquired NlpC/P60 genes from bacteria, expanding them to a repertoire of nine TvNlpC genes in two distinct clans, and that TvNlpCs of clan A are active against bacterial peptidoglycan. Here, we expand this characterization to TvNlpCs of clan B. In this study, we show that the clan organisation of NlpC/P60 genes is a feature of other species of Trichomonas, and that Histomonas meleagridis has sequences related to one clan. We characterized the 3D structure of TvNlpC_B3 alone and with the inhibitor E64 bound, probing the active site of these enzymes for the first time. Lastly, we demonstrated that TvNlpC_B3 and TvNlpC_B5 have complementary activities with the previously described TvNlpCs of clan A and that exogenous expression of these enzymes empower this mucosal parasite to take over populations of vaginal lactobacilli in mixed cultures. TvNlpC_B3 helps control populations of L. gasseri, but not of G. vaginalis, which action is partially inhibited by E64. This study is one of the first to show how enzymes produced by a mucosal protozoan parasite may contribute to a shift on the status of a microbiome, helping explain the link between trichomoniasis and vaginal dysbiosis. Further understanding of this process might have significant implications for treatments in the future.

Identifiants

pubmed: 37585473
doi: 10.1371/journal.ppat.1011563
pii: PPATHOGENS-D-22-02149
pmc: PMC10461829
doi:

Substances chimiques

Peptidoglycan 0
N-Acetylmuramoyl-L-alanine Amidase EC 3.5.1.28

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1011563

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/W013630/1
Pays : United Kingdom

Informations de copyright

Copyright: © 2023 Barnett et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have no competing interest.

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Auteurs

Michael J Barnett (MJ)

School of Biological Sciences, University of Auckland, Auckland, New Zealand.

Jully Pinheiro (J)

School of Biological Sciences, University of Auckland, Auckland, New Zealand.

Jeremy R Keown (JR)

School of Biological Sciences, University of Auckland, Auckland, New Zealand.

Jacob Biboy (J)

Centre for Bacterial Cell Biology, Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.

Joe Gray (J)

Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.

Ioana-Wilhelmina Lucinescu (IW)

Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.

Waldemar Vollmer (W)

Centre for Bacterial Cell Biology, Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.

Robert P Hirt (RP)

Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.

Augusto Simoes-Barbosa (A)

School of Biological Sciences, University of Auckland, Auckland, New Zealand.

David C Goldstone (DC)

School of Biological Sciences, University of Auckland, Auckland, New Zealand.
Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.

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