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Capsule Protects Acinetobacter baumannii From Inter-Bacterial Competition Mediated by CdiA Toxin

Currently, Acinetobacter baumannii is considered as one of the most important infectious agents causing hospital acquired infections worldwide. It has been observed that many clinically important pathogens express contact-dependent growth inhibition (CDI) phenomenon, which modulates cell–cell and ce...

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Autores principales: Krasauskas, Renatas, Skerniškytė, Jūratė, Martinkus, Julius, Armalytė, Julija, Sužiedėlienė, Edita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396552/
https://www.ncbi.nlm.nih.gov/pubmed/32849318
http://dx.doi.org/10.3389/fmicb.2020.01493
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author Krasauskas, Renatas
Skerniškytė, Jūratė
Martinkus, Julius
Armalytė, Julija
Sužiedėlienė, Edita
author_facet Krasauskas, Renatas
Skerniškytė, Jūratė
Martinkus, Julius
Armalytė, Julija
Sužiedėlienė, Edita
author_sort Krasauskas, Renatas
collection PubMed
description Currently, Acinetobacter baumannii is considered as one of the most important infectious agents causing hospital acquired infections worldwide. It has been observed that many clinically important pathogens express contact-dependent growth inhibition (CDI) phenomenon, which modulates cell–cell and cell–environment interactions, potentially allowing bacteria to adapt to ever-changing conditions. Mainly, these systems are used for the inhibition of the growth of genetically different individuals within the same species. In this work, by performing cell competition assays with three genotypically different (as determined by pulse-field gel electrophoresis) clinical A. baumannii isolates II-c, II-a, and II-a1, we show that A. baumannii capsule is the main feature protecting from CDI-mediated inhibition. We also observed that for one clinical isolate, the two-component BfmRS system, contributed to the resistance against CDI-mediated inhibition. Moreover, we were able to demonstrate, that the effector protein CdiA is released into the growth media and exhibits its inhibitory activity without the requirement of a cell–cell contact. Lastly, by evaluating the remaining number of the cells pre-mixed with the CdiA and performing live/dead assay, we demonstrate that purified CdiA protein causes a rapid cell growth arrest. Our results indicate, that capsule efficiently protects A. baumannii from a CDI-mediated inhibition by a clinical A. baumannii V15 strain, which is able to secrete CdiA effector into the growth media and cause target cell growth arrest without a cell–cell contact.
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spelling pubmed-73965522020-08-25 Capsule Protects Acinetobacter baumannii From Inter-Bacterial Competition Mediated by CdiA Toxin Krasauskas, Renatas Skerniškytė, Jūratė Martinkus, Julius Armalytė, Julija Sužiedėlienė, Edita Front Microbiol Microbiology Currently, Acinetobacter baumannii is considered as one of the most important infectious agents causing hospital acquired infections worldwide. It has been observed that many clinically important pathogens express contact-dependent growth inhibition (CDI) phenomenon, which modulates cell–cell and cell–environment interactions, potentially allowing bacteria to adapt to ever-changing conditions. Mainly, these systems are used for the inhibition of the growth of genetically different individuals within the same species. In this work, by performing cell competition assays with three genotypically different (as determined by pulse-field gel electrophoresis) clinical A. baumannii isolates II-c, II-a, and II-a1, we show that A. baumannii capsule is the main feature protecting from CDI-mediated inhibition. We also observed that for one clinical isolate, the two-component BfmRS system, contributed to the resistance against CDI-mediated inhibition. Moreover, we were able to demonstrate, that the effector protein CdiA is released into the growth media and exhibits its inhibitory activity without the requirement of a cell–cell contact. Lastly, by evaluating the remaining number of the cells pre-mixed with the CdiA and performing live/dead assay, we demonstrate that purified CdiA protein causes a rapid cell growth arrest. Our results indicate, that capsule efficiently protects A. baumannii from a CDI-mediated inhibition by a clinical A. baumannii V15 strain, which is able to secrete CdiA effector into the growth media and cause target cell growth arrest without a cell–cell contact. Frontiers Media S.A. 2020-07-17 /pmc/articles/PMC7396552/ /pubmed/32849318 http://dx.doi.org/10.3389/fmicb.2020.01493 Text en Copyright © 2020 Krasauskas, Skerniškytė, Martinkus, Armalytė and Sužiedėlienė. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Krasauskas, Renatas
Skerniškytė, Jūratė
Martinkus, Julius
Armalytė, Julija
Sužiedėlienė, Edita
Capsule Protects Acinetobacter baumannii From Inter-Bacterial Competition Mediated by CdiA Toxin
title Capsule Protects Acinetobacter baumannii From Inter-Bacterial Competition Mediated by CdiA Toxin
title_full Capsule Protects Acinetobacter baumannii From Inter-Bacterial Competition Mediated by CdiA Toxin
title_fullStr Capsule Protects Acinetobacter baumannii From Inter-Bacterial Competition Mediated by CdiA Toxin
title_full_unstemmed Capsule Protects Acinetobacter baumannii From Inter-Bacterial Competition Mediated by CdiA Toxin
title_short Capsule Protects Acinetobacter baumannii From Inter-Bacterial Competition Mediated by CdiA Toxin
title_sort capsule protects acinetobacter baumannii from inter-bacterial competition mediated by cdia toxin
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396552/
https://www.ncbi.nlm.nih.gov/pubmed/32849318
http://dx.doi.org/10.3389/fmicb.2020.01493
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