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. 1976 Sep;10(3):411–416. doi: 10.1128/aac.10.3.411

Mutants of Pseudomonas aeruginosa That Show Specific Hypersensitivity to Aminoglycosides

B J Mills 1, B W Holloway 1
PMCID: PMC429762  PMID: 825027

Abstract

A class of mutants in Pseudomonas aeruginosa have been found that are tolerant to aeruginocin 41 and also hypersensitive to aminoglycosides. They do not show any changes in susceptibility to a wide range of other toxic agents, including antibiotics and surfactants. This tol locus, tolA, has been mapped at 10 min from the FP2 origin and linked to carA (carbamyl phosphate synthetase) by transduction and conjugation. By selecting for revertants of the hypersensitivity phenotype, revertants to tol+ were found, indicating that it is the tolA locus that is responsible for this specific hypersensitivity. The results indicate that a specific mechanism exists for the intrinsic resistance of P. aeruginosa to aminoglycosides.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Boon T. Inactivation of ribosomes in vitro by colicin E 3 . Proc Natl Acad Sci U S A. 1971 Oct;68(10):2421–2425. doi: 10.1073/pnas.68.10.2421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bowman C. M., Dahlberg J. E., Ikemura T., Konisky J., Nomura M. Specific inactivation of 16S ribosomal RNA induced by colicin E3 in vivo. Proc Natl Acad Sci U S A. 1971 May;68(5):964–968. doi: 10.1073/pnas.68.5.964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bryan L. E., Van Den Elzen H. M., Tseng J. T. Transferable drug resistance in Pseudomonas aeruginosa. Antimicrob Agents Chemother. 1972 Jan;1(1):22–29. doi: 10.1128/aac.1.1.22. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chandler P. M., Krishnapillai V. Phenotypic properties of R factors of Pseudomonas aeruginosa: R factors readily transferable between Pseudomonas and the Enterobacteriaceae. Genet Res. 1974 Jun;23(3):239–250. doi: 10.1017/s0016672300014890. [DOI] [PubMed] [Google Scholar]
  5. Changeux J. P., Thiéry J. On the mode of action of colicins: a model of regulation at the membrane level. J Theor Biol. 1967 Nov;17(2):315–318. doi: 10.1016/0022-5193(67)90175-0. [DOI] [PubMed] [Google Scholar]
  6. Davies J. K., Reeves P. Genetics of resistance to colicins in Escherichia coli K-12: cross-resistance among colicins of group A. J Bacteriol. 1975 Jul;123(1):102–117. doi: 10.1128/jb.123.1.102-117.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Dunn N. W., Holloway B. W. Pleiotrophy of p-fluorophenylalanine-resistant and antibiotic hypersensitive mutants of Pseudomonas aeruginosa. Genet Res. 1971 Oct;18(2):185–197. doi: 10.1017/s0016672300012593. [DOI] [PubMed] [Google Scholar]
  8. Hill C., Holland I. B. Genetic basis of colicin E susceptibility in Escherichia coli. I. Isolation and properties of refractory mutants and the preliminary mapping of their mutations. J Bacteriol. 1967 Sep;94(3):677–686. doi: 10.1128/jb.94.3.677-686.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Holloway B. W., Rossiter H., Burgess D., Dodge J. Aeruginocin tolerant mutants of Pseudomonas aeruginosa. Genet Res. 1973 Dec;22(3):239–253. doi: 10.1017/s0016672300013069. [DOI] [PubMed] [Google Scholar]
  10. Jacoby G. A. Properties of R plasmids determining gentamicin resistance by acetylation in Pseudomonas aeruginosa. Antimicrob Agents Chemother. 1974 Sep;6(3):239–252. doi: 10.1128/aac.6.3.239. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kawakami Y., Mikoshiba F., Nagasaki S., Matsumoto H., Tazaki T. Prevalence of Pseudomonas aeruginosa strains possessing R factor in a hospital. J Antibiot (Tokyo) 1972 Oct;25(10):607–609. doi: 10.7164/antibiotics.25.607. [DOI] [PubMed] [Google Scholar]
  12. Lundbäck A. K., Nordström K. Mutations in Escherichia coli K-12 decreasing the rate of streptomycin uptake: synergism with R-factor-mediated capacity to inactivate streptomycin. Antimicrob Agents Chemother. 1974 May;5(5):500–507. doi: 10.1128/aac.5.5.500. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Mitsuhashi S., Kobayashi F., Yamaguchi M. Enzymatic inactivation of gentamicin C components by cell-free extract from Pseudomonas aeruginosa. J Antibiot (Tokyo) 1971 Jun;24(6):400–401. doi: 10.7164/antibiotics.24.400. [DOI] [PubMed] [Google Scholar]
  14. Nomura M., Witten C. Interaction of colicins with bacterial cells. 3. Colicin-tolerant mutations in Escherichia coli. J Bacteriol. 1967 Oct;94(4):1093–1111. doi: 10.1128/jb.94.4.1093-1111.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Ozaki M., Mizushima S., Nomura M. Identification and functional characterization of the protein controlled by the streptomycin-resistant locus in E. coli. Nature. 1969 Apr 26;222(5191):333–339. doi: 10.1038/222333a0. [DOI] [PubMed] [Google Scholar]
  16. Roberts L. M., Reeve E. C. Two mutations giving low-level streptomycin resistance in Escherichia coli K 12. Genet Res. 1970 Dec;16(3):359–365. doi: 10.1017/s0016672300002640. [DOI] [PubMed] [Google Scholar]
  17. Stadler J., Adelberg E. A. Temperature dependence of sex-factor maintenance in Escherichia coli K-12. J Bacteriol. 1972 Jan;109(1):447–449. doi: 10.1128/jb.109.1.447-449.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Stanisich V., Holloway B. W. Conjugation in Pseudomonas aeruginosa. Genetics. 1969 Feb;61(2):327–339. doi: 10.1093/genetics/61.2.327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Tseng J. T., Bryan L. E. The effect of complement and other cell wall reagents on tetracycline and streptomycin resistance in Pseudomonas aeruginosa. Can J Microbiol. 1974 Aug;20(8):1101–1107. doi: 10.1139/m74-172. [DOI] [PubMed] [Google Scholar]
  20. Watson J. M., Holloway B. W. Suppressor mutations in Pseudomonas aeruginosa. J Bacteriol. 1976 Mar;125(3):780–786. doi: 10.1128/jb.125.3.780-786.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Yamada T., Davies J. A genetic and biochemical study of streptomycin- and spectinomycin-resistance in Salmonella typhimurium. Mol Gen Genet. 1971;110(3):197–210. doi: 10.1007/BF00337833. [DOI] [PubMed] [Google Scholar]

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