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Two Type VI Secretion Systems of Enterobacter cloacae Are Required for Bacterial Competition, Cell Adherence, and Intestinal Colonization

Enterobacter cloacae has emerged as an opportunistic pathogen in healthcare-associated infections. Analysis of the genomic sequences of several E. cloacae strains revealed the presence of genes that code for expression of at least one type VI secretion system (T6SS). Here, we report that E. cloacae...

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Autores principales: Soria-Bustos, Jorge, Ares, Miguel A., Gómez-Aldapa, Carlos A., González-y-Merchand, Jorge A., Girón, Jorge A., De la Cruz, Miguel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541819/
https://www.ncbi.nlm.nih.gov/pubmed/33072020
http://dx.doi.org/10.3389/fmicb.2020.560488
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author Soria-Bustos, Jorge
Ares, Miguel A.
Gómez-Aldapa, Carlos A.
González-y-Merchand, Jorge A.
Girón, Jorge A.
De la Cruz, Miguel A.
author_facet Soria-Bustos, Jorge
Ares, Miguel A.
Gómez-Aldapa, Carlos A.
González-y-Merchand, Jorge A.
Girón, Jorge A.
De la Cruz, Miguel A.
author_sort Soria-Bustos, Jorge
collection PubMed
description Enterobacter cloacae has emerged as an opportunistic pathogen in healthcare-associated infections. Analysis of the genomic sequences of several E. cloacae strains revealed the presence of genes that code for expression of at least one type VI secretion system (T6SS). Here, we report that E. cloacae strain ATCC 13047 codes for two functional T6SS named T6SS-1 and T6SS-2. T6SS-1 and T6SS-2 were preferentially expressed in tryptic soy broth and tissue culture medium (DMEM), respectively. Mutants in T6SS-1-associated genes clpV1 and hcp1 significantly affected their ability of inter- and intra-bacterial killing indicating that T6SS-1 is required for bacterial competition. In addition, the Hcp effector protein was detected in supernatants of E. cloacae cultures and a functional T6SS-1 was required for the secretion of this protein. A clpV2 mutant was impaired in both biofilm formation and adherence to epithelial cells, supporting the notion that these phenotypes are T6SS-2 dependent. In vivo data strongly suggest that both T6SSs are required for intestinal colonization because single and double mutants in clpV1 and clpV2 genes were defective in gut colonization in mice. We conclude that the two T6SSs are involved in the pathogenesis scheme of E. cloacae with specialized functions in the interaction with other bacteria and with host cells.
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spelling pubmed-75418192020-10-17 Two Type VI Secretion Systems of Enterobacter cloacae Are Required for Bacterial Competition, Cell Adherence, and Intestinal Colonization Soria-Bustos, Jorge Ares, Miguel A. Gómez-Aldapa, Carlos A. González-y-Merchand, Jorge A. Girón, Jorge A. De la Cruz, Miguel A. Front Microbiol Microbiology Enterobacter cloacae has emerged as an opportunistic pathogen in healthcare-associated infections. Analysis of the genomic sequences of several E. cloacae strains revealed the presence of genes that code for expression of at least one type VI secretion system (T6SS). Here, we report that E. cloacae strain ATCC 13047 codes for two functional T6SS named T6SS-1 and T6SS-2. T6SS-1 and T6SS-2 were preferentially expressed in tryptic soy broth and tissue culture medium (DMEM), respectively. Mutants in T6SS-1-associated genes clpV1 and hcp1 significantly affected their ability of inter- and intra-bacterial killing indicating that T6SS-1 is required for bacterial competition. In addition, the Hcp effector protein was detected in supernatants of E. cloacae cultures and a functional T6SS-1 was required for the secretion of this protein. A clpV2 mutant was impaired in both biofilm formation and adherence to epithelial cells, supporting the notion that these phenotypes are T6SS-2 dependent. In vivo data strongly suggest that both T6SSs are required for intestinal colonization because single and double mutants in clpV1 and clpV2 genes were defective in gut colonization in mice. We conclude that the two T6SSs are involved in the pathogenesis scheme of E. cloacae with specialized functions in the interaction with other bacteria and with host cells. Frontiers Media S.A. 2020-09-24 /pmc/articles/PMC7541819/ /pubmed/33072020 http://dx.doi.org/10.3389/fmicb.2020.560488 Text en Copyright © 2020 Soria-Bustos, Ares, Gómez-Aldapa, González-y-Merchand, Girón and De la Cruz. 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
Soria-Bustos, Jorge
Ares, Miguel A.
Gómez-Aldapa, Carlos A.
González-y-Merchand, Jorge A.
Girón, Jorge A.
De la Cruz, Miguel A.
Two Type VI Secretion Systems of Enterobacter cloacae Are Required for Bacterial Competition, Cell Adherence, and Intestinal Colonization
title Two Type VI Secretion Systems of Enterobacter cloacae Are Required for Bacterial Competition, Cell Adherence, and Intestinal Colonization
title_full Two Type VI Secretion Systems of Enterobacter cloacae Are Required for Bacterial Competition, Cell Adherence, and Intestinal Colonization
title_fullStr Two Type VI Secretion Systems of Enterobacter cloacae Are Required for Bacterial Competition, Cell Adherence, and Intestinal Colonization
title_full_unstemmed Two Type VI Secretion Systems of Enterobacter cloacae Are Required for Bacterial Competition, Cell Adherence, and Intestinal Colonization
title_short Two Type VI Secretion Systems of Enterobacter cloacae Are Required for Bacterial Competition, Cell Adherence, and Intestinal Colonization
title_sort two type vi secretion systems of enterobacter cloacae are required for bacterial competition, cell adherence, and intestinal colonization
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541819/
https://www.ncbi.nlm.nih.gov/pubmed/33072020
http://dx.doi.org/10.3389/fmicb.2020.560488
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