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Transcriptome profiling in imipenem-selected Acinetobacter baumannii

BACKGROUND: Carbapenem-resistance in Acinetobacter baumannii has gradually become a global challenge. To identify the genes involved in carbapenem resistance in A. baumannii, the transcriptomic responses of the completely sequenced strain ATCC 17978 selected with 0.5 mg/L (IPM-2 m) and 2 mg/L (IPM-8...

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Autores principales: Chang, Kai-Chih, Kuo, Han-Yueh, Tang, Chuan Yi, Chang, Cheng-Wei, Lu, Chia-Wei, Liu, Chih-Chin, Lin, Huei-Ru, Chen, Kuan-Hsueh, Liou, Ming-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192346/
https://www.ncbi.nlm.nih.gov/pubmed/25260865
http://dx.doi.org/10.1186/1471-2164-15-815
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author Chang, Kai-Chih
Kuo, Han-Yueh
Tang, Chuan Yi
Chang, Cheng-Wei
Lu, Chia-Wei
Liu, Chih-Chin
Lin, Huei-Ru
Chen, Kuan-Hsueh
Liou, Ming-Li
author_facet Chang, Kai-Chih
Kuo, Han-Yueh
Tang, Chuan Yi
Chang, Cheng-Wei
Lu, Chia-Wei
Liu, Chih-Chin
Lin, Huei-Ru
Chen, Kuan-Hsueh
Liou, Ming-Li
author_sort Chang, Kai-Chih
collection PubMed
description BACKGROUND: Carbapenem-resistance in Acinetobacter baumannii has gradually become a global challenge. To identify the genes involved in carbapenem resistance in A. baumannii, the transcriptomic responses of the completely sequenced strain ATCC 17978 selected with 0.5 mg/L (IPM-2 m) and 2 mg/L (IPM-8 m) imipenem were investigated using RNA-sequencing to identify differences in the gene expression patterns. RESULTS: A total of 88 and 68 genes were differentially expressed in response to IPM-2 m and IPM-8 m selection, respectively. Among the expressed genes, 50 genes were highly expressed in IPM-2 m, 30 genes were highly expressed in IPM-8 m, and 38 genes were expressed common in both strains. Six groups of genes were simultaneously expressed in IPM-2 m and IPM-8 m mutants. The three gene groups involved in DNA recombination were up-regulated, including recombinase, transposase and DNA repair, and beta-lactamase OXA-95 and homologous recombination. The remaining gene groups involved in biofilm formation were down-regulated, including quorum sensing, secretion systems, and the csu operon. The antibiotic resistance determinants, including RND efflux transporters and multidrug resistance pumps, were over-expressed in response to IPM-2 m selection, followed by a decrease in response to IPM-8 m selection. Among the genes over-expressed in both strains, bla(OXA-95,) previously clustered with the bla(OXA-51-like) family, showed 14-fold (IPM-2 m) to 330-fold (IPM-8 m) over-expression. The expression of bla(OXA-95) in IPM-2 m and IPM-8 m cells was positively correlated with the rate of imipenem hydrolysis, as demonstrated through Liquid Chromatography-Mass Spectrometry/Mass Spectrometry, suggesting that bla(OXA-95) plays a critical role in conferring carbapenem resistance. In addition, A. baumannii shows an inverse relationship between carbapenem resistance and biofilm production. CONCLUSION: Gene recombination and bla(OXA-95) play critical roles in carbapenem resistance in A. baumannii. Taken together, the results of the present study provide a foundation for future studies of the network systems associated with carbapenem resistance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-815) contains supplementary material, which is available to authorized users.
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spelling pubmed-41923462014-10-11 Transcriptome profiling in imipenem-selected Acinetobacter baumannii Chang, Kai-Chih Kuo, Han-Yueh Tang, Chuan Yi Chang, Cheng-Wei Lu, Chia-Wei Liu, Chih-Chin Lin, Huei-Ru Chen, Kuan-Hsueh Liou, Ming-Li BMC Genomics Research Article BACKGROUND: Carbapenem-resistance in Acinetobacter baumannii has gradually become a global challenge. To identify the genes involved in carbapenem resistance in A. baumannii, the transcriptomic responses of the completely sequenced strain ATCC 17978 selected with 0.5 mg/L (IPM-2 m) and 2 mg/L (IPM-8 m) imipenem were investigated using RNA-sequencing to identify differences in the gene expression patterns. RESULTS: A total of 88 and 68 genes were differentially expressed in response to IPM-2 m and IPM-8 m selection, respectively. Among the expressed genes, 50 genes were highly expressed in IPM-2 m, 30 genes were highly expressed in IPM-8 m, and 38 genes were expressed common in both strains. Six groups of genes were simultaneously expressed in IPM-2 m and IPM-8 m mutants. The three gene groups involved in DNA recombination were up-regulated, including recombinase, transposase and DNA repair, and beta-lactamase OXA-95 and homologous recombination. The remaining gene groups involved in biofilm formation were down-regulated, including quorum sensing, secretion systems, and the csu operon. The antibiotic resistance determinants, including RND efflux transporters and multidrug resistance pumps, were over-expressed in response to IPM-2 m selection, followed by a decrease in response to IPM-8 m selection. Among the genes over-expressed in both strains, bla(OXA-95,) previously clustered with the bla(OXA-51-like) family, showed 14-fold (IPM-2 m) to 330-fold (IPM-8 m) over-expression. The expression of bla(OXA-95) in IPM-2 m and IPM-8 m cells was positively correlated with the rate of imipenem hydrolysis, as demonstrated through Liquid Chromatography-Mass Spectrometry/Mass Spectrometry, suggesting that bla(OXA-95) plays a critical role in conferring carbapenem resistance. In addition, A. baumannii shows an inverse relationship between carbapenem resistance and biofilm production. CONCLUSION: Gene recombination and bla(OXA-95) play critical roles in carbapenem resistance in A. baumannii. Taken together, the results of the present study provide a foundation for future studies of the network systems associated with carbapenem resistance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-815) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-26 /pmc/articles/PMC4192346/ /pubmed/25260865 http://dx.doi.org/10.1186/1471-2164-15-815 Text en © Chang et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Chang, Kai-Chih
Kuo, Han-Yueh
Tang, Chuan Yi
Chang, Cheng-Wei
Lu, Chia-Wei
Liu, Chih-Chin
Lin, Huei-Ru
Chen, Kuan-Hsueh
Liou, Ming-Li
Transcriptome profiling in imipenem-selected Acinetobacter baumannii
title Transcriptome profiling in imipenem-selected Acinetobacter baumannii
title_full Transcriptome profiling in imipenem-selected Acinetobacter baumannii
title_fullStr Transcriptome profiling in imipenem-selected Acinetobacter baumannii
title_full_unstemmed Transcriptome profiling in imipenem-selected Acinetobacter baumannii
title_short Transcriptome profiling in imipenem-selected Acinetobacter baumannii
title_sort transcriptome profiling in imipenem-selected acinetobacter baumannii
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192346/
https://www.ncbi.nlm.nih.gov/pubmed/25260865
http://dx.doi.org/10.1186/1471-2164-15-815
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