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Identification and characterization of novel endolysins targeting Gardnerella vaginalis biofilms to treat bacterial vaginosis

Bacterial vaginosis (BV) is a recurrent dysbiosis that is frequently associated with preterm birth, increased risk for acquisition of human immunodeficiency virus (HIV) and other sexually transmitted infections (STIs). The overgrowth of a key pathobiont, Gardnerella vaginalis, as a recalcitrant biof...

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Autores principales: Arroyo-Moreno, Sara, Cummings, Matthew, Corcoran, David B., Coffey, Aidan, McCarthy, Ronan R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018826/
https://www.ncbi.nlm.nih.gov/pubmed/35440653
http://dx.doi.org/10.1038/s41522-022-00285-0
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author Arroyo-Moreno, Sara
Cummings, Matthew
Corcoran, David B.
Coffey, Aidan
McCarthy, Ronan R.
author_facet Arroyo-Moreno, Sara
Cummings, Matthew
Corcoran, David B.
Coffey, Aidan
McCarthy, Ronan R.
author_sort Arroyo-Moreno, Sara
collection PubMed
description Bacterial vaginosis (BV) is a recurrent dysbiosis that is frequently associated with preterm birth, increased risk for acquisition of human immunodeficiency virus (HIV) and other sexually transmitted infections (STIs). The overgrowth of a key pathobiont, Gardnerella vaginalis, as a recalcitrant biofilm is central to the development of this dysbiosis. Overgrowth of vaginal biofilms, seeded by initial G. vaginalis colonization, leads to recurrent symptomatic BV which is poorly resolved by classically used antibiotics. In this light, the use of bacteriophages and/or their proteins, represents a promising alternative. Here we identify 84 diverse anti-Gardnerella endolysins across 7 protein families. A subset of 36 endolysin candidates were refactored and overexpressed in an E. coli BL21 (DE3) system and 5 biochemically and structurally diverse endolysins were fully characterized. Each candidate endolysin showed good lytic activity against planktonic G. vaginalis ATCC14018, as well as G. vaginalis clinical isolates. These endolysin candidates were assayed in biofilm prevention and disruption assays, with biofilm disruption at low microgram concentrations (5 μg/ml) observed. In addition to clonal G. vaginalis biofilms, endolysin candidates could also successfully disrupt polyspecies biofilms. Importantly, none of our candidates showed lytic activity against commensal lactobacilli present in the vaginal microbiota such as L. crispatus, L. jensenii, L. gasseri, and L. iners or against Atopobium vaginae (currently classified as Fannyhessa vaginae). The potency and selectivity of these novel endolysins constitute a promising alternative treatment to combat BV, avoiding problems associated with antibiotic resistance, while retaining beneficial commensal bacteria in the vaginal flora. The diverse library of candidates reported here represents a strong repository of endolysins for further preclinical development.
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spelling pubmed-90188262022-04-28 Identification and characterization of novel endolysins targeting Gardnerella vaginalis biofilms to treat bacterial vaginosis Arroyo-Moreno, Sara Cummings, Matthew Corcoran, David B. Coffey, Aidan McCarthy, Ronan R. NPJ Biofilms Microbiomes Article Bacterial vaginosis (BV) is a recurrent dysbiosis that is frequently associated with preterm birth, increased risk for acquisition of human immunodeficiency virus (HIV) and other sexually transmitted infections (STIs). The overgrowth of a key pathobiont, Gardnerella vaginalis, as a recalcitrant biofilm is central to the development of this dysbiosis. Overgrowth of vaginal biofilms, seeded by initial G. vaginalis colonization, leads to recurrent symptomatic BV which is poorly resolved by classically used antibiotics. In this light, the use of bacteriophages and/or their proteins, represents a promising alternative. Here we identify 84 diverse anti-Gardnerella endolysins across 7 protein families. A subset of 36 endolysin candidates were refactored and overexpressed in an E. coli BL21 (DE3) system and 5 biochemically and structurally diverse endolysins were fully characterized. Each candidate endolysin showed good lytic activity against planktonic G. vaginalis ATCC14018, as well as G. vaginalis clinical isolates. These endolysin candidates were assayed in biofilm prevention and disruption assays, with biofilm disruption at low microgram concentrations (5 μg/ml) observed. In addition to clonal G. vaginalis biofilms, endolysin candidates could also successfully disrupt polyspecies biofilms. Importantly, none of our candidates showed lytic activity against commensal lactobacilli present in the vaginal microbiota such as L. crispatus, L. jensenii, L. gasseri, and L. iners or against Atopobium vaginae (currently classified as Fannyhessa vaginae). The potency and selectivity of these novel endolysins constitute a promising alternative treatment to combat BV, avoiding problems associated with antibiotic resistance, while retaining beneficial commensal bacteria in the vaginal flora. The diverse library of candidates reported here represents a strong repository of endolysins for further preclinical development. Nature Publishing Group UK 2022-04-19 /pmc/articles/PMC9018826/ /pubmed/35440653 http://dx.doi.org/10.1038/s41522-022-00285-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Arroyo-Moreno, Sara
Cummings, Matthew
Corcoran, David B.
Coffey, Aidan
McCarthy, Ronan R.
Identification and characterization of novel endolysins targeting Gardnerella vaginalis biofilms to treat bacterial vaginosis
title Identification and characterization of novel endolysins targeting Gardnerella vaginalis biofilms to treat bacterial vaginosis
title_full Identification and characterization of novel endolysins targeting Gardnerella vaginalis biofilms to treat bacterial vaginosis
title_fullStr Identification and characterization of novel endolysins targeting Gardnerella vaginalis biofilms to treat bacterial vaginosis
title_full_unstemmed Identification and characterization of novel endolysins targeting Gardnerella vaginalis biofilms to treat bacterial vaginosis
title_short Identification and characterization of novel endolysins targeting Gardnerella vaginalis biofilms to treat bacterial vaginosis
title_sort identification and characterization of novel endolysins targeting gardnerella vaginalis biofilms to treat bacterial vaginosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018826/
https://www.ncbi.nlm.nih.gov/pubmed/35440653
http://dx.doi.org/10.1038/s41522-022-00285-0
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