Lactobacillus gasseri and Gardnerella vaginalis produce extracellular vesicles that contribute to the function of the vaginal microbiome and modulate host-Trichomonas vaginalis interactions.

Trichomonas vaginalis extracellular vesicles host-pathogen interaction vaginal microbiome

Journal

Molecular microbiology
ISSN: 1365-2958
Titre abrégé: Mol Microbiol
Pays: England
ID NLM: 8712028

Informations de publication

Date de publication:
24 Jul 2023
Historique:
revised: 22 06 2023
received: 10 01 2023
accepted: 06 07 2023
medline: 24 7 2023
pubmed: 24 7 2023
entrez: 24 7 2023
Statut: aheadofprint

Résumé

Trichomonas vaginalis is an extracellular protozoan parasite of the human urogenital tract, responsible for a prevalent sexually transmitted infection. Trichomoniasis is accompanied by a dysbiotic microbiome that is characterised by the depletion of host-protective commensals such as Lactobacillus gasseri, and the flourishing of a bacterial consortium that is comparable to the one seen for bacterial vaginosis, including the founder species Gardnerella vaginalis. These two vaginal bacteria are known to have opposite effects on T. vaginalis pathogenicity. Studies on extracellular vesicles (EVs) have been focused on the direction of a microbial producer (commensal or pathogen) to a host recipient, and largely in the context of the gut microbiome. Here, taking advantage of the simplicity of the human cervicovaginal microbiome, we determined the molecular cargo of EVs produced by L. gasseri and G. vaginalis and examined how these vesicles modulate the interaction of T. vaginalis and host cells. We show that these EVs carry a specific cargo of proteins, which functions can be attributed to the opposite roles that these bacteria play in the vaginal biome. Furthermore, these bacterial EVs are delivered to host and protozoan cells, modulating host-pathogen interactions in a way that mimics the opposite effects that these bacteria have on T. vaginalis pathogenicity. This is the first study to describe side-by-side the protein composition of EVs produced by two bacteria belonging to the opposite spectrum of a microbiome and to demonstrate that these vesicles modulate the pathogenicity of a protozoan parasite. Such as in trichomoniasis, infections and dysbiosis co-occur frequently resulting in significant co-morbidities. Therefore, studies like this provide the knowledge for the development of antimicrobial therapies that aim to clear the infection while restoring a healthy microbiome.

Identifiants

pubmed: 37485746
doi: 10.1111/mmi.15130
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Faculty Research Development Fund, University of Auckland
Organisme : HRC Explorer Grant
Organisme : Hugo Charitable Trust Fellowship
Organisme : Maurice and Phyllis Paykel Trust

Informations de copyright

© 2023 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd.

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Auteurs

Anastasiia Artuyants (A)

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

Jiwon Hong (J)

School of Biological Sciences, University of Auckland, Auckland, New Zealand.
Surgical and Translational Research Centre, University of Auckland, Auckland, New Zealand.

Priscila Dauros-Singorenko (P)

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

Anthony Phillips (A)

School of Biological Sciences, University of Auckland, Auckland, New Zealand.
Surgical and Translational Research Centre, University of Auckland, Auckland, New Zealand.

Augusto Simoes-Barbosa (A)

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

Classifications MeSH