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Identification of a Novel Ciprofloxacin Tolerance Gene, aciT, Which Contributes to Filamentation in Acinetobacter baumannii

Fluoroquinolones are one of the most prescribed broad-spectrum antibiotics. However, their effectiveness is being compromised by high rates of resistance in clinically important organisms, including Acinetobacter baumannii. We sought to investigate the transcriptomic and proteomic responses of the c...

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Autores principales: Naidu, Varsha, Shah, Bhumika, Kamath, Karthik S., Chien, Arthur, Nagy, Stephanie, Pokhrel, Alaska, Molloy, Mark, Hassan, Karl A., Paulsen, Ian T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8316044/
https://www.ncbi.nlm.nih.gov/pubmed/33820764
http://dx.doi.org/10.1128/AAC.01400-20
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author Naidu, Varsha
Shah, Bhumika
Kamath, Karthik S.
Chien, Arthur
Nagy, Stephanie
Pokhrel, Alaska
Molloy, Mark
Hassan, Karl A.
Paulsen, Ian T.
author_facet Naidu, Varsha
Shah, Bhumika
Kamath, Karthik S.
Chien, Arthur
Nagy, Stephanie
Pokhrel, Alaska
Molloy, Mark
Hassan, Karl A.
Paulsen, Ian T.
author_sort Naidu, Varsha
collection PubMed
description Fluoroquinolones are one of the most prescribed broad-spectrum antibiotics. However, their effectiveness is being compromised by high rates of resistance in clinically important organisms, including Acinetobacter baumannii. We sought to investigate the transcriptomic and proteomic responses of the clinical A. baumannii strain AB5075-UW upon exposure to subinhibitory concentrations of ciprofloxacin. Our transcriptomics and proteomics analyses found that the most highly expressed genes and proteins were components of the intact prophage phiOXA. The next most highly expressed gene (and its protein product) under ciprofloxacin stress was a hypothetical gene, ABUW_0098, named here the Acinetobacter ciprofloxacin tolerance (aciT) gene. Disruption of this gene resulted in higher susceptibility to ciprofloxacin, and complementation of the mutant with a cloned aciT gene restored ciprofloxacin tolerance to parental strain levels. Microscopy studies revealed that aciT is essential for filamentation during ciprofloxacin stress in A. baumannii. Sequence analysis of aciT indicates the encoded protein is likely to be localized to the cell membrane. Orthologs of aciT are found widely in the genomes of species from the Moraxellaceae family and are well conserved in Acinetobacter species, suggesting an important role. With these findings taken together, this study has identified a new gene conferring tolerance to ciprofloxacin, likely by enabling filamentation in response to the antibiotic.
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spelling pubmed-83160442021-11-18 Identification of a Novel Ciprofloxacin Tolerance Gene, aciT, Which Contributes to Filamentation in Acinetobacter baumannii Naidu, Varsha Shah, Bhumika Kamath, Karthik S. Chien, Arthur Nagy, Stephanie Pokhrel, Alaska Molloy, Mark Hassan, Karl A. Paulsen, Ian T. Antimicrob Agents Chemother Mechanisms of Resistance Fluoroquinolones are one of the most prescribed broad-spectrum antibiotics. However, their effectiveness is being compromised by high rates of resistance in clinically important organisms, including Acinetobacter baumannii. We sought to investigate the transcriptomic and proteomic responses of the clinical A. baumannii strain AB5075-UW upon exposure to subinhibitory concentrations of ciprofloxacin. Our transcriptomics and proteomics analyses found that the most highly expressed genes and proteins were components of the intact prophage phiOXA. The next most highly expressed gene (and its protein product) under ciprofloxacin stress was a hypothetical gene, ABUW_0098, named here the Acinetobacter ciprofloxacin tolerance (aciT) gene. Disruption of this gene resulted in higher susceptibility to ciprofloxacin, and complementation of the mutant with a cloned aciT gene restored ciprofloxacin tolerance to parental strain levels. Microscopy studies revealed that aciT is essential for filamentation during ciprofloxacin stress in A. baumannii. Sequence analysis of aciT indicates the encoded protein is likely to be localized to the cell membrane. Orthologs of aciT are found widely in the genomes of species from the Moraxellaceae family and are well conserved in Acinetobacter species, suggesting an important role. With these findings taken together, this study has identified a new gene conferring tolerance to ciprofloxacin, likely by enabling filamentation in response to the antibiotic. American Society for Microbiology 2021-05-18 /pmc/articles/PMC8316044/ /pubmed/33820764 http://dx.doi.org/10.1128/AAC.01400-20 Text en © Crown copyright 2021. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Mechanisms of Resistance
Naidu, Varsha
Shah, Bhumika
Kamath, Karthik S.
Chien, Arthur
Nagy, Stephanie
Pokhrel, Alaska
Molloy, Mark
Hassan, Karl A.
Paulsen, Ian T.
Identification of a Novel Ciprofloxacin Tolerance Gene, aciT, Which Contributes to Filamentation in Acinetobacter baumannii
title Identification of a Novel Ciprofloxacin Tolerance Gene, aciT, Which Contributes to Filamentation in Acinetobacter baumannii
title_full Identification of a Novel Ciprofloxacin Tolerance Gene, aciT, Which Contributes to Filamentation in Acinetobacter baumannii
title_fullStr Identification of a Novel Ciprofloxacin Tolerance Gene, aciT, Which Contributes to Filamentation in Acinetobacter baumannii
title_full_unstemmed Identification of a Novel Ciprofloxacin Tolerance Gene, aciT, Which Contributes to Filamentation in Acinetobacter baumannii
title_short Identification of a Novel Ciprofloxacin Tolerance Gene, aciT, Which Contributes to Filamentation in Acinetobacter baumannii
title_sort identification of a novel ciprofloxacin tolerance gene, acit, which contributes to filamentation in acinetobacter baumannii
topic Mechanisms of Resistance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8316044/
https://www.ncbi.nlm.nih.gov/pubmed/33820764
http://dx.doi.org/10.1128/AAC.01400-20
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