The GO system prevents ROS-induced mutagenesis and killing in Pseudomonas aeruginosa

被引:34
作者
Sanders, Laurie H. [1 ]
Sudhakaran, Julee [1 ]
Sutton, Mark D. [1 ]
机构
[1] SUNY Buffalo, Sch Med & Biomed Sci, Dept Biochem, Buffalo, NY 14214 USA
关键词
base excision repair; DNA damage; mutations; reactive oxygen species; pathogenesis; GENERATES G.C->T.A TRANSVERSIONS; CYSTIC-FIBROSIS PATIENTS; ESCHERICHIA-COLI; DNA-POLYMERASES; HIGH-FREQUENCY; MUTATOR LOCUS; LUNG-DISEASE; RPOB GENE; RESISTANCE; MUTATIONS;
D O I
10.1111/j.1574-6968.2009.01550.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Inactivation of the Pseudomonas aeruginosa mutM, mutY, or mutT gene conferred a 2.4-, 17.2-, or 38.1-fold increase in spontaneous mutation frequency, respectively. Importantly, the mutY and mutT strains each displayed a robust H2O2-induced mutation frequency. In addition, the mutM, mutY, and mutT mutations severely sensitized P. aeruginosa to killing by H2O2, suggesting that these gene products act to repair one or more cytotoxic lesions in P. aeruginosa. Nucleotide sequence analysis of a fragment of the rpoB gene from rifampicin resistant mutM-, mutY-, and, mutT-deficient strains was consistent with this conclusion. These findings are discussed in terms of possible roles for mutM, mutY, and mutT in contributing to survival and mutagenesis of P. aeruginosa colonizing the airways of cystic fibrosis patients.
引用
收藏
页码:89 / 96
页数:8
相关论文
共 28 条
[1]  
[Anonymous], 2005, DNA REPAIR MUTAGENES
[2]   Recognition of formamidopyrimidine by Escherichia coli and mammalian thymine glycol glycosylases -: Distinctive paired base effects and biological and mechanistic implications [J].
Asagoshi, K ;
Yamada, T ;
Okada, Y ;
Terato, H ;
Ohyama, Y ;
Seki, S ;
Ide, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (32) :24781-24786
[3]   MUTM, A 2ND MUTATOR LOCUS IN ESCHERICHIA-COLI THAT GENERATES G.C-]T.A TRANSVERSIONS [J].
CABRERA, M ;
NGHIEM, Y ;
MILLER, JH .
JOURNAL OF BACTERIOLOGY, 1988, 170 (11) :5405-5407
[4]   Occurrence of hypermutable Pseudomonas aeruginosa in cystic fibrosis patients is associated with the oxidative stress caused by chronic lung inflammation [J].
Ciofu, O ;
Riis, B ;
Pressler, T ;
Poulsen, HE ;
Hoiby, N .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (06) :2276-2282
[5]   Use of the rpoB gene to determine the specificity of base substitution mutations on the Escherichia coli chromosome [J].
Garibyan, L ;
Huang, T ;
Kim, M ;
Wolff, E ;
Nguyen, A ;
Nguyen, T ;
Diep, A ;
Hu, KB ;
Iverson, A ;
Yang, HJ ;
Miller, JH .
DNA REPAIR, 2003, 2 (05) :593-608
[6]   Opportunistic infections in lung disease:: Pseudomonas infections in cystic fibrosis [J].
Gomez, Marisa I. ;
Prince, Alice .
CURRENT OPINION IN PHARMACOLOGY, 2007, 7 (03) :244-251
[7]   Lack of association between hypermutation and antibiotic resistance development in Pseudomonas aeruginosa isolates from intensive care unit patients [J].
Gutiérrez, O ;
Juan, C ;
Pérez, JL ;
Oliver, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (09) :3573-3575
[8]   Hypermutable bacteria isolated from humans - a critical analysis [J].
Hall, Lucinda M. C. ;
Henderson-Begg, Stephaine K. .
MICROBIOLOGY-SGM, 2006, 152 :2505-2514
[9]  
Hazra TK, 2000, J BIOL CHEM, V275, P27762
[10]   Comprehensive transposon mutant library of Pseudomonas aeruginosa [J].
Jacobs, MA ;
Alwood, A ;
Thaipisuttikul, I ;
Spencer, D ;
Haugen, E ;
Ernst, S ;
Will, O ;
Kaul, R ;
Raymond, C ;
Levy, R ;
Liu, CR ;
Guenthner, D ;
Bovee, D ;
Olson, MV ;
Manoil, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (24) :14339-14344