Involvement of an ATP-dependent protease, PA0779/AsrA, in inducing heat shock in response to tobramycin in Pseudomonas aeruginosa

Antimicrobial Agents and Chemotherapy

Volumn 55, Issue 5, 2011, Pages 1874-1882

  Kindrachuk, Kristen N ^a   Fernández, Lucía ^a   Bains, Manjeet ^a   Hancock, Robert E W ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ENDOPEPTIDASE LA; TOBRAMYCIN;

ANTIBIOTIC SENSITIVITY; ARTICLE; BACTERIAL GENE; BACTERIAL STRAIN; BACTERIUM MUTANT; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; DRUG EXPOSURE; GENE ASRA; GENE EXPRESSION REGULATION; HEAT SHOCK; MICROARRAY ANALYSIS; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PSEUDOMONAS AERUGINOSA; TRANSPOSON; WILD TYPE;

ANTI-BACTERIAL AGENTS; ATP-DEPENDENT PROTEASES; BACTERIAL PROTEINS; HEAT-SHOCK RESPONSE; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PSEUDOMONAS AERUGINOSA; TOBRAMYCIN;

EID: 79955525591     PISSN: 00664804     EISSN: 10986596     Source Type: Journal    
DOI: 10.1128/AAC.00935-10     Document Type: Article

References (47)

1. Askeland, R. A., and S. M. Morrison. 1983. Cyanide production by Pseudomonas fluorescens and Pseudomonas aeruginosa. Appl. Environ. Microbiol. 45:1802-1807.
2. Bissonnette, S. A., I. Rivera-Rivera, R. T. Sauer, and T. A. Baker. 2010. The IbpA and IbpB small heat-shock proteins are substrates of the AAA+ Lon protease. Mol. Microbiol. 75:1539-1549.
3. Borriello, G., L. Richards, G. D. Ehrlich, and P. S. Stewart. 2006. Arginine or nitrate enhances antibiotic susceptibility of Pseudomonas aeruginosa in biofilms. Antimicrob. Agents Chemother. 50:382-384.
4. Bryan, L. E., and S. Kwan. 1981. Aminoglycoside-resistant mutants of Pseudomonas aeruginosa deficient in cytochrome d, nitrite reductase, and aerobic transport. Antimicrob. Agents Chemother. 19:958-964.
5. Bryan, L. E., and S. Kwan. 1983. Roles of ribosomal binding, membrane potential, and electron transport in bacterial uptake of streptomycin and gentamicin. Antimicrob. Agents Chemother. 23:835-845.
6. Carterson, A. J., et al. 2004. The transcriptional regulator AlgR controls cyanide production in Pseudomonas aeruginosa. J. Bacteriol. 186:6837-6844. (Pubitemid 39332123)
7. Castric, P. A. 1983. Hydrogen cyanide production by Pseudomonas aeruginosa at reduced oxygen levels. Can. J. Microbiol. 29:1344-1349.
8. Castric, P. A. 1975. Hydrogen cyanide, a secondary metabolite of Pseudomonas aeruginosa. Can. J. Microbiol. 21:613-618.
9. Choi, K. H., A. Kumar, and H. P. Schweizer. 2006. A 10-min method for preparation of highly electrocompetent Pseudomonas aeruginosa cells: application for DNA fragment transfer between chromosomes and plasmid transformation. J. Microbiol. Methods 64:391-397.
10. Clinical and Laboratory Standards Institute. 2006. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically. Approved standard, 7th ed. (M7-A7). CLSI, Wayne, PA.
11. Davis, B. D., L. L. Chen, and P. C. Tai. 1986. Misread protein creates membrane channels: an essential step in the bactericidal action of aminoglycosides. Proc. Natl. Acad. Sci. U. S. A. 83:6164-6168.
12. El'Garch, F., K. Jeannot, D. Hocquet, C. Llanes-Barakat, and P. Plesiat. 2007. Cumulative effects of several nonenzymatic mechanisms on the resistance of Pseudomonas aeruginosa to aminoglycosides. Antimicrob. Agents Chemother. 51:1016-1021.
13. Field, T. R., A. White, J. S. Elborn, and M. M. Tunney. 2005. Effect of oxygen limitation on the in vitro antimicrobial susceptibility of clinical isolates of Pseudomonas aeruginosa grown planktonically and as biofilms. Eur. J. Clin. Microbiol. Infect. Dis. 24:677-687.
14. Foweraker, J. E., C. R. Laughton, D. F. Brown, and D. Bilton. 2005. Phenotypic variability of Pseudomonas aeruginosa in sputa from patients with acute infective exacerbation of cystic fibrosis and its impact on the validity of antimicrobial susceptibility testing. J. Antimicrob. Chemother. 55:921-927.
15. Hocquet, D., et al. 2003. MexXY-OprM efflux pump is necessary for a adaptive resistance of Pseudomonas aeruginosa to aminoglycosides. Antimicrob. Agents Chemother. 47:1371-1375.
16. Irvin, R. T., J. W. Govan, J. A. Fyfe, and J. W. Costerton. 1981. Heterogeneity of antibiotic resistance in mucoid isolates of Pseudomonas aeruginosa obtained from cystic fibrosis patients: role of outer membrane proteins. Antimicrob. Agents Chemother. 19:1056-1063.
17. Jacobs, M. A., et al. 2003. Comprehensive transposon mutant library of Pseudomonas aeruginosa. Proc. Natl. Acad. Sci. U. S. A. 100:14339-14344.
18. King, P., D. M. Citron, D. C. Griffith, O. Lomovskaya, and M. N. Dudley. 2010. Effect of oxygen limitation on the in vitro activity of levofloxacin and other antibiotics administered by the aerosol route against Pseudomonas aeruginosa from cystic fibrosis patients. Diagn. Microbiol. Infect. Dis. 66:181-186.
19. Kohanski, M. A., D. J. Dwyer, B. Hayete, C. A. Lawrence, and J. J. Collins. 2007. A common mechanism of cellular death induced by bactericidal antibiotics. Cell 130:797-810.
20. Kohanski, M. A., D. J. Dwyer, J. Wierzbowski, G. Cottarel, and J. J. Collins. 2008. Mistranslation of membrane proteins and two-component system activation trigger antibiotic-mediated cell death. Cell 135:679-690.
21. Koskenkorva, T., et al. 2008. Transcriptional activity of Pseudomonas aeruginosa fhp promoter is dependent on two regulators in addition to FhpR. Arch. Microbiol. 189:385-396.
22. Koskenkorva-Frank, T. S., and P. T. Kallio. 2009. Induction of Pseudomonas aeruginosa fhp and fhpR by reactive oxygen species. Can. J. Microbiol. 55:657-663.
23. Levin, B. R., and D. E. Rozen. 2006. Non-inherited antibiotic resistance. Nat. Rev. Microbiol. 4:556-562.
24. Lewenza, S., et al. 2005. Construction of a mini-Tn5-luxCDABE mutant library in Pseudomonas aeruginosa PAO1: a tool for identifying differentially regulated genes. Genome Res. 15:583-589. (Pubitemid 41057821)
25. Lin, J. T., M. B. Connelly, C. Amolo, S. Otani, and D. S. Yaver. 2005. Global transcriptional response of Bacillus subtilis to treatment with subinhibitory concentrations of antibiotics that inhibit protein synthesis. Antimicrob. Agents Chemother. 49:1915-1926.
26. MacLeod, D. L., et al. 2000. Aminoglycoside-resistance mechanisms for cystic fibrosis Pseudomonas aeruginosa isolates are unchanged by long-term, intermittent, inhaled tobramycin treatment. J. Infect. Dis. 181:1180-1184.
27. Matsunaga, K., H. Yamaki, T. Nishimura, and N. Tanaka. 1986. Inhibition of DNA replication initiation by aminoglycoside antibiotics. Antimicrob. Agents Chemother. 30:468-474.
28. McPhee, J. B., et al. 2006. Contribution of the PhoP-PhoQ and PmrA-PmrB two-component regulatory systems to Mg2+-induced gene regulation in Pseudomonas aeruginosa. J. Bacteriol. 188:3995-4006. (Pubitemid 43825404)
29. Morita, Y., C. Gilmour, D. Metcalf, and K. Poole. 2009. Translational control of the antibiotic inducibility of the PA5471 gene required for mexXY multidrug efflux gene expression in Pseudomonas aeruginosa. J. Bacteriol. 191:4966-4975.
30. Morita, Y., M. L. Sobel, and K. Poole. 2006. Antibiotic inducibility of the MexXY multidrug efflux system of Pseudomonas aeruginosa: involvement of the antibiotic-inducible PA5471 gene product. J. Bacteriol. 188:1847-1855. (Pubitemid 43346863)
31. Ngo, J. K., and K. J. Davies. 2009. Mitochondrial Lon protease is a human stress protein. Free Radic. Biol. Med. 46:1042-1048.
32. Overhage, J., M. Bains, M. D. Brazas, and R. E. W. Hancock. 2008. Swarming of Pseudomonas aeruginosa is a complex adaptation leading to increased production of virulence factors and antibiotic resistance. J. Bacteriol. 190:2671-2679.
33. Pai, V. B., and M. C. Nahata. 2001. Efficacy and safety of aerosolized tobramycin in cystic fibrosis. Pediatr. Pulmonol. 32:314-327.
34. Pessi, G., and D. Haas. 2001. Dual control of hydrogen cyanide biosynthesis by the global activator GacA in Pseudomonas aeruginosa PAO1. FEMS Microbiol. Lett. 200:73-78.
35. Phillips, T. A., R. A. VanBogelen, and F. C. Neidhardt. 1984. lon gene product of Escherichia coli is a heat-shock protein. J. Bacteriol. 159:283-287.
36. Qiu, D., F. H. Damron, T. Mima, H. P. Schweizer, and H. D. Yu. 2008. PBAD-based shuttle vectors for functional analysis of toxic and highly regulated genes in Pseudomonas and Burkholderia spp. and other bacteria. Appl. Environ. Microbiol. 74:7422-7426.
37. Reimmann, C., et al. 1997. The global activator GacA of Pseudomonas aeruginosa PAO positively controls the production of the autoinducer N-butyryl-homoserine lactone and the formation of the virulence factors pyocyanin, cyanide, and lipase. Mol. Microbiol. 24:309-319.
38. Rotanova, T. V., et al. 2006. Slicing a protease: structural features of the ATP-dependent Lon proteases gleaned from investigations of isolated domains. Protein Sci. 15:1815-1828. (Pubitemid 44141499)
39. Schurek, K. N., et al. 2008. Novel genetic determinants of low-level aminoglycoside resistance in Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 52:4213-4219.
40. Schurr, M. J., and V. Deretic. 1997. Microbial pathogenesis in cystic fibrosis: co-ordinate regulation of heat-shock response and conversion to mucoidy in Pseudomonas aeruginosa. Mol. Microbiol. 24:411-420.
41. Sobel, M. L., G. A. McKay, and K. Poole. 2003. Contribution of the MexXY multidrug transporter to aminoglycoside resistance in Pseudomonas aeruginosa clinical isolates. Antimicrob. Agents Chemother. 47:3202-3207.
42. Tanaka, N., K. Matsunaga, H. Yamaki, and T. Nishimura. 1984. Inhibition of initiation of DNA synthesis by aminoglycoside antibiotics. Biochem. Biophys. Res. Commun. 122:460-465.
43. Williams, H. D., J. E. Zlosnik, and B. Ryall. 2007. Oxygen, cyanide and energy generation in the cystic fibrosis pathogen Pseudomonas aeruginosa. Adv. Microb. Physiol. 52:1-71.
44. Worlitzsch, D., et al. 2002. Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients. J. Clin. Invest. 109:317-325.
45. Yamamoto, M., et al. 2009. Role of MexZ and PA5471 in transcriptional regulation of mexXY in Pseudomonas aeruginosa. Microbiology 155:3312-3321.
46. Yeung, A. T., et al. 2009. Swarming of Pseudomonas aeruginosa is controlled by a broad spectrum of transcriptional regulators, including MetR. J. Bacteriol. 191:5592-5602.
47. Zhao, K., M. Liu, and R. R. Burgess. 2005. The global transcriptional response of Escherichia coli to induced sigma 32 protein involves sigma 32 regulon activation followed by inactivation and degradation of sigma 32 in vivo. J. Biol. Chem. 280:17758-17768.