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RNA-seq reveals the critical role of OtpR in regulating Brucella melitensis metabolism and virulence under acidic stress

The response regulator OtpR is critical for the growth, morphology and virulence of Brucella melitensis. Compared to its wild type strain 16 M, B. melitensis 16 MΔotpR mutant has decreased tolerance to acid stress. To analyze the genes regulated by OtpR under acid stress, we performed RNA-seq whole...

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Autores principales: Liu, Wenxiao, Dong, Hao, Li, Jing, Ou, Qixing, Lv, Yujin, Wang, Xiaolei, Xiang, Zuoshuang, He, Yongqun, Wu, Qingmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542472/
https://www.ncbi.nlm.nih.gov/pubmed/26242322
http://dx.doi.org/10.1038/srep10864
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author Liu, Wenxiao
Dong, Hao
Li, Jing
Ou, Qixing
Lv, Yujin
Wang, Xiaolei
Xiang, Zuoshuang
He, Yongqun
Wu, Qingmin
author_facet Liu, Wenxiao
Dong, Hao
Li, Jing
Ou, Qixing
Lv, Yujin
Wang, Xiaolei
Xiang, Zuoshuang
He, Yongqun
Wu, Qingmin
author_sort Liu, Wenxiao
collection PubMed
description The response regulator OtpR is critical for the growth, morphology and virulence of Brucella melitensis. Compared to its wild type strain 16 M, B. melitensis 16 MΔotpR mutant has decreased tolerance to acid stress. To analyze the genes regulated by OtpR under acid stress, we performed RNA-seq whole transcriptome analysis of 16 MΔotpR and 16 M. In total, 501 differentially expressed genes were identified, including 390 down-regulated and 111 up-regulated genes. Among these genes, 209 were associated with bacterial metabolism, including 54 genes involving carbohydrate metabolism, 13 genes associated with nitrogen metabolism, and seven genes associated with iron metabolism. The 16 MΔotpR also decreased capacity to utilize different carbon sources and to tolerate iron limitation in culture experiments. Notably, OtpR regulated many Brucella virulence factors essential for B. melitensis intracellular survival. For instance, the virB operon encoding type IV secretion system was significantly down-regulated, and 36 known transcriptional regulators (e.g., vjbR and blxR) were differentially expressed in 16 MΔotpR. Selected RNA-seq results were experimentally confirmed by RT-PCR and RT-qPCR. Overall, these results deciphered differential phenomena associated with virulence, environmental stresses and cell morphology in 16 MΔotpR and 16 M, which provided important information for understanding the detailed OtpR-regulated interaction networks and Brucella pathogenesis.
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spelling pubmed-45424722015-09-01 RNA-seq reveals the critical role of OtpR in regulating Brucella melitensis metabolism and virulence under acidic stress Liu, Wenxiao Dong, Hao Li, Jing Ou, Qixing Lv, Yujin Wang, Xiaolei Xiang, Zuoshuang He, Yongqun Wu, Qingmin Sci Rep Article The response regulator OtpR is critical for the growth, morphology and virulence of Brucella melitensis. Compared to its wild type strain 16 M, B. melitensis 16 MΔotpR mutant has decreased tolerance to acid stress. To analyze the genes regulated by OtpR under acid stress, we performed RNA-seq whole transcriptome analysis of 16 MΔotpR and 16 M. In total, 501 differentially expressed genes were identified, including 390 down-regulated and 111 up-regulated genes. Among these genes, 209 were associated with bacterial metabolism, including 54 genes involving carbohydrate metabolism, 13 genes associated with nitrogen metabolism, and seven genes associated with iron metabolism. The 16 MΔotpR also decreased capacity to utilize different carbon sources and to tolerate iron limitation in culture experiments. Notably, OtpR regulated many Brucella virulence factors essential for B. melitensis intracellular survival. For instance, the virB operon encoding type IV secretion system was significantly down-regulated, and 36 known transcriptional regulators (e.g., vjbR and blxR) were differentially expressed in 16 MΔotpR. Selected RNA-seq results were experimentally confirmed by RT-PCR and RT-qPCR. Overall, these results deciphered differential phenomena associated with virulence, environmental stresses and cell morphology in 16 MΔotpR and 16 M, which provided important information for understanding the detailed OtpR-regulated interaction networks and Brucella pathogenesis. Nature Publishing Group 2015-08-05 /pmc/articles/PMC4542472/ /pubmed/26242322 http://dx.doi.org/10.1038/srep10864 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Liu, Wenxiao
Dong, Hao
Li, Jing
Ou, Qixing
Lv, Yujin
Wang, Xiaolei
Xiang, Zuoshuang
He, Yongqun
Wu, Qingmin
RNA-seq reveals the critical role of OtpR in regulating Brucella melitensis metabolism and virulence under acidic stress
title RNA-seq reveals the critical role of OtpR in regulating Brucella melitensis metabolism and virulence under acidic stress
title_full RNA-seq reveals the critical role of OtpR in regulating Brucella melitensis metabolism and virulence under acidic stress
title_fullStr RNA-seq reveals the critical role of OtpR in regulating Brucella melitensis metabolism and virulence under acidic stress
title_full_unstemmed RNA-seq reveals the critical role of OtpR in regulating Brucella melitensis metabolism and virulence under acidic stress
title_short RNA-seq reveals the critical role of OtpR in regulating Brucella melitensis metabolism and virulence under acidic stress
title_sort rna-seq reveals the critical role of otpr in regulating brucella melitensis metabolism and virulence under acidic stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542472/
https://www.ncbi.nlm.nih.gov/pubmed/26242322
http://dx.doi.org/10.1038/srep10864
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