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A LysR-Type Transcriptional Regulator Controls Multiple Phenotypes in Acinetobacter baumannii

Acinetobacter baumannii is a multidrug-resistant, Gram-negative nosocomial pathogen that exhibits phenotypic heterogeneity resulting in virulent opaque (VIR-O) and avirulent translucent (AV-T) colony variants. Each variant has a distinct gene expression profile resulting in multiple phenotypic diffe...

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Autores principales: Tierney, Aimee R. P., Chin, Chui Yoke, Weiss, David S., Rather, Philip N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8601201/
https://www.ncbi.nlm.nih.gov/pubmed/34805000
http://dx.doi.org/10.3389/fcimb.2021.778331
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author Tierney, Aimee R. P.
Chin, Chui Yoke
Weiss, David S.
Rather, Philip N.
author_facet Tierney, Aimee R. P.
Chin, Chui Yoke
Weiss, David S.
Rather, Philip N.
author_sort Tierney, Aimee R. P.
collection PubMed
description Acinetobacter baumannii is a multidrug-resistant, Gram-negative nosocomial pathogen that exhibits phenotypic heterogeneity resulting in virulent opaque (VIR-O) and avirulent translucent (AV-T) colony variants. Each variant has a distinct gene expression profile resulting in multiple phenotypic differences. Cells interconvert between the VIR-O and AV-T variants at high frequency under laboratory conditions, suggesting that the genetic mechanism underlying the phenotypic switch could be manipulated to attenuate virulence. Therefore, our group has focused on identifying and characterizing genes that regulate this switch, which led to the investigation of ABUW_1132 (1132), a highly conserved gene predicted to encode a LysR-type transcriptional regulator. ABUW_1132 was shown to be a global regulator as the expression of 74 genes was altered ≥ 2-fold in an 1132 deletion mutant. The 1132 deletion also resulted in a 16-fold decrease in VIR-O to AV-T switching, loss of 3-OH-C(12)-HSL secretion, and reduced surface-associated motility. Further, the deletion of 1132 in the AV-T background caused elevated capsule production, which increased colony opacity and altered the typical avirulent phenotype of translucent cells. These findings distinguish 1132 as a global regulatory gene and advance our understanding of A. baumannii’s opacity-virulence switch.
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spelling pubmed-86012012021-11-19 A LysR-Type Transcriptional Regulator Controls Multiple Phenotypes in Acinetobacter baumannii Tierney, Aimee R. P. Chin, Chui Yoke Weiss, David S. Rather, Philip N. Front Cell Infect Microbiol Cellular and Infection Microbiology Acinetobacter baumannii is a multidrug-resistant, Gram-negative nosocomial pathogen that exhibits phenotypic heterogeneity resulting in virulent opaque (VIR-O) and avirulent translucent (AV-T) colony variants. Each variant has a distinct gene expression profile resulting in multiple phenotypic differences. Cells interconvert between the VIR-O and AV-T variants at high frequency under laboratory conditions, suggesting that the genetic mechanism underlying the phenotypic switch could be manipulated to attenuate virulence. Therefore, our group has focused on identifying and characterizing genes that regulate this switch, which led to the investigation of ABUW_1132 (1132), a highly conserved gene predicted to encode a LysR-type transcriptional regulator. ABUW_1132 was shown to be a global regulator as the expression of 74 genes was altered ≥ 2-fold in an 1132 deletion mutant. The 1132 deletion also resulted in a 16-fold decrease in VIR-O to AV-T switching, loss of 3-OH-C(12)-HSL secretion, and reduced surface-associated motility. Further, the deletion of 1132 in the AV-T background caused elevated capsule production, which increased colony opacity and altered the typical avirulent phenotype of translucent cells. These findings distinguish 1132 as a global regulatory gene and advance our understanding of A. baumannii’s opacity-virulence switch. Frontiers Media S.A. 2021-11-04 /pmc/articles/PMC8601201/ /pubmed/34805000 http://dx.doi.org/10.3389/fcimb.2021.778331 Text en Copyright © 2021 Tierney, Chin, Weiss and Rather https://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 Cellular and Infection Microbiology
Tierney, Aimee R. P.
Chin, Chui Yoke
Weiss, David S.
Rather, Philip N.
A LysR-Type Transcriptional Regulator Controls Multiple Phenotypes in Acinetobacter baumannii
title A LysR-Type Transcriptional Regulator Controls Multiple Phenotypes in Acinetobacter baumannii
title_full A LysR-Type Transcriptional Regulator Controls Multiple Phenotypes in Acinetobacter baumannii
title_fullStr A LysR-Type Transcriptional Regulator Controls Multiple Phenotypes in Acinetobacter baumannii
title_full_unstemmed A LysR-Type Transcriptional Regulator Controls Multiple Phenotypes in Acinetobacter baumannii
title_short A LysR-Type Transcriptional Regulator Controls Multiple Phenotypes in Acinetobacter baumannii
title_sort lysr-type transcriptional regulator controls multiple phenotypes in acinetobacter baumannii
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8601201/
https://www.ncbi.nlm.nih.gov/pubmed/34805000
http://dx.doi.org/10.3389/fcimb.2021.778331
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