Multidisciplinary Analysis of a Nontoxigenic Clostridium difficile Strain with Stable Resistance to Metronidazole

被引:33
作者
Moura, Ines [1 ]
Monot, Marc [2 ]
Tani, Chiara [3 ]
Spigaglia, Patrizia [1 ]
Barbanti, Fabrizio [1 ]
Norais, Nathalie [3 ]
Dupuy, Bruno [2 ]
Bouza, Emilio [4 ]
Mastrantonio, Paola [1 ]
机构
[1] Ist Super Sanita, Dept Infect Parasit & Immune Mediated Dis, I-00161 Rome, Italy
[2] Inst Pasteur, Lab Pathogenese Bacteries Anaerobies, Paris, France
[3] Novartis Vaccines & Diagnost, Struct Mass Spectrometry & Prote Unit, Siena, Italy
[4] Hosp Gen Univ Gregorio Maranon, Madrid, Spain
关键词
ESCHERICHIA-COLI; SUSCEPTIBILITY;
D O I
10.1128/AAC.02350-14
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Stable resistance to metronidazole in a nontoxigenic Clostridium difficile strain was investigated at both the genomic and proteomic levels. Alterations in the metabolic pathway involving the pyruvate-ferredoxin oxidoreductase were found, suggesting that reduction of metronidazole, required for its activity, may be less efficient in this strain. Proteomic studies also showed a cellular response to oxidative stress.
引用
收藏
页码:4957 / 4960
页数:4
相关论文
共 21 条
[1]   CcpA-mediated repression of Clostridium difficile toxin gene expression [J].
Antunes, Ana ;
Martin-Verstraete, Isabelle ;
Dupuy, Bruno .
MOLECULAR MICROBIOLOGY, 2011, 79 (04) :882-899
[2]   Horizontal gene transfer converts non-toxigenic Clostridium difficile strains into toxin producers [J].
Brouwer, Michael S. M. ;
Roberts, Adam P. ;
Hussain, Haitham ;
Williams, Rachel J. ;
Allan, Elaine ;
Mullany, Peter .
NATURE COMMUNICATIONS, 2013, 4
[3]   Proteomic Analysis of a NAP1 Clostridium difficile Clinical Isolate Resistant to Metronidazole [J].
Chong, Patrick M. ;
Lynch, Tarah ;
McCorrister, Stuart ;
Kibsey, Pamela ;
Miller, Mark ;
Gravel, Denise ;
Westmacott, Garrett R. ;
Mulvey, Michael R. .
PLOS ONE, 2014, 9 (01)
[4]  
Clinical and Laboratory Standards Institute, 2007, M11A7 CLIN LAB STAND, pM11
[5]   progressiveMauve: Multiple Genome Alignment with Gene Gain, Loss and Rearrangement [J].
Darling, Aaron E. ;
Mau, Bob ;
Perna, Nicole T. .
PLOS ONE, 2010, 5 (06)
[6]  
European Committee on Antimicrobial Susceptibility Testing, 2013, CLIN BREAKP TABL VER
[7]   The Changing Epidemiology of Clostridium difficile Infections [J].
Freeman, J. ;
Bauer, M. P. ;
Baines, S. D. ;
Corver, J. ;
Fawley, W. N. ;
Goorhuis, B. ;
Kuijper, E. J. ;
Wilcox, M. H. .
CLINICAL MICROBIOLOGY REVIEWS, 2010, 23 (03) :529-+
[8]   Prospects for aminoacyl-tRNA synthetase inhibitors as new antimicrobial agents [J].
Hurdle, JG ;
O'Neill, AJ ;
Chopra, I .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (12) :4821-4833
[9]   Proteomic analysis of the insoluble subproteome of Clostridium difficile strain 630 [J].
Jain, Shailesh ;
Graham, Robert L. J. ;
McMullan, Geoff ;
Ternan, Nigel G. .
FEMS MICROBIOLOGY LETTERS, 2010, 312 (02) :151-159
[10]   Molecular basis of metronidazole resistance in pathogenic bacteria and protozoa [J].
Land, KM ;
Johnson, PJ .
DRUG RESISTANCE UPDATES, 1999, 2 (05) :289-294