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

Identification and characterization of novel endolysins targeting Gardnerella vaginalis biofilms to treat bacterial vaginosis
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 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.
Arroyo-Moreno, Sara
b32353f8-270c-409b-9469-e50fa733d287
Cummings, Matthew
1de2cc15-8cfc-49b1-ba94-a79a07bdb5e7
Corcoran, David B.
85739873-0b9e-428a-aba6-0aced70d1784
Coffey, Aidan
446b0f10-7f4d-4841-9312-de7a24c14426
McCarthy, Ronan R.
0b2cf2e0-b0ff-4c92-aa04-92d91182d1f2
Arroyo-Moreno, Sara
b32353f8-270c-409b-9469-e50fa733d287
Cummings, Matthew
1de2cc15-8cfc-49b1-ba94-a79a07bdb5e7
Corcoran, David B.
85739873-0b9e-428a-aba6-0aced70d1784
Coffey, Aidan
446b0f10-7f4d-4841-9312-de7a24c14426
McCarthy, Ronan R.
0b2cf2e0-b0ff-4c92-aa04-92d91182d1f2

Arroyo-Moreno, Sara, Cummings, Matthew, Corcoran, David B., Coffey, Aidan and McCarthy, Ronan R. (2022) Identification and characterization of novel endolysins targeting Gardnerella vaginalis biofilms to treat bacterial vaginosis. NPJ Biofilms and Microbiomes, 8 (29). (doi:10.1038/s41522-022-00285-0).

Record type: Article

Abstract

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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Published date: 19 April 2022

Identifiers

Local EPrints ID: 506160
URI: http://eprints.soton.ac.uk/id/eprint/506160
PURE UUID: 687ebc9d-47d8-4ed0-b97b-244d024c8c9e
ORCID for Ronan R. McCarthy: ORCID iD orcid.org/0000-0002-7480-6352

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Date deposited: 29 Oct 2025 17:40
Last modified: 01 Nov 2025 03:12

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Contributors

Author: Sara Arroyo-Moreno
Author: Matthew Cummings
Author: David B. Corcoran
Author: Aidan Coffey
Author: Ronan R. McCarthy ORCID iD

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