TY - JOUR
T1 - Proteomic analysis of colony morphology variants of Burkholderia pseudomallei defines a role for the arginine deiminase system in bacterial survival
AU - Chantratita, Narisara
AU - Tandhavanant, Sarunporn
AU - Wikraiphat, Chanthiwa
AU - Trunck, Lily A.
AU - Rholl, Drew A.
AU - Thanwisai, Aunchalee
AU - Saiprom, Natnaree
AU - Limmathurotsakul, Direk
AU - Korbsrisate, Sunee
AU - Day, Nicholas P.J.
AU - Schweizer, Herbert P.
AU - Peacock, Sharon J.
N1 - Funding Information:
We thank staff at the Mahidol-Oxford Tropical Medicine Research Unit and the Department of Microbiology and Immunology for their assistance and support. We also thank the BioService Unit (BSU), National Science and Technology Development Agency, Pathumthani, Thailand for their assistance in 2D-gel electrophoresis and MALDI-TOF MS. N.C is supported by a Wellcome Trust Career Development award in Public Health and Tropical Medicine, UK (grant 087769/Z/08/Z ). This research was financially supported by Thailand Research Fund (TRF) (grant MRG5280010 ) and the Wellcome Trust. SP is supported by the Wellcome Trust and the NIHR Cambridge Biomedical Research Centre . HPS is supported by grant AI065357 from the National Institute of Allergy and Infectious Diseases, National Institutes of Health .
PY - 2012/1/4
Y1 - 2012/1/4
N2 - Colony morphology variation of Burkholderia pseudomallei is a notable feature of a proportion of primary clinical cultures from patients with melioidosis. Here, we examined the hypothesis that colony morphology switching results in phenotypic changes associated with enhanced survival under adverse conditions. We generated isogenic colony morphology types II and III from B. pseudomallei strain 153 type I, and compared their protein expression profiles using 2D gel electrophoresis. Numerous proteins were differentially expressed, the most prominent of which were flagellin, arginine deiminase (AD) and carbamate kinase (CK), which were over-expressed in isogenic types II and III compared with parental type I. AD and CK (encoded by arcA and arcC) are components of the arginine deiminase system (ADS) which facilitates acid tolerance. Reverse transcriptase PCR of arcA and arcC mRNA expression confirmed the proteomic results. Transcripts of parental type I strain 153 arcA and arcC were increased in the presence of arginine, in a low oxygen concentration and in acid. Comparison of wild type with arcA and arcC defective mutants demonstrated that the B. pseudomallei ADS was associated with survival in acid, but did not appear to play a role in intracellular survival or replication within the mouse macrophage cell line J774A.1. These data provide novel insights into proteomic alterations that occur during the complex process of morphotype switching, and lend support to the idea that this is associated with a fitness advantage in vivo.
AB - Colony morphology variation of Burkholderia pseudomallei is a notable feature of a proportion of primary clinical cultures from patients with melioidosis. Here, we examined the hypothesis that colony morphology switching results in phenotypic changes associated with enhanced survival under adverse conditions. We generated isogenic colony morphology types II and III from B. pseudomallei strain 153 type I, and compared their protein expression profiles using 2D gel electrophoresis. Numerous proteins were differentially expressed, the most prominent of which were flagellin, arginine deiminase (AD) and carbamate kinase (CK), which were over-expressed in isogenic types II and III compared with parental type I. AD and CK (encoded by arcA and arcC) are components of the arginine deiminase system (ADS) which facilitates acid tolerance. Reverse transcriptase PCR of arcA and arcC mRNA expression confirmed the proteomic results. Transcripts of parental type I strain 153 arcA and arcC were increased in the presence of arginine, in a low oxygen concentration and in acid. Comparison of wild type with arcA and arcC defective mutants demonstrated that the B. pseudomallei ADS was associated with survival in acid, but did not appear to play a role in intracellular survival or replication within the mouse macrophage cell line J774A.1. These data provide novel insights into proteomic alterations that occur during the complex process of morphotype switching, and lend support to the idea that this is associated with a fitness advantage in vivo.
KW - Arginine deiminase system
KW - Burkholderia pseudomallei
KW - Colony variation
KW - Melioidosis
KW - Proteomic analysis
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U2 - 10.1016/j.jprot.2011.10.015
DO - 10.1016/j.jprot.2011.10.015
M3 - Article
C2 - 22062159
AN - SCOPUS:84355166444
SN - 1874-3919
VL - 75
SP - 1031
EP - 1042
JO - Journal of Proteomics
JF - Journal of Proteomics
IS - 3
ER -