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Multiple antibiotic susceptibility of polyphosphate kinase mutants (ppk1 and ppk2) from Pseudomonas aeruginosa PAO1 as revealed by global phenotypic analysis
Ortiz-Severín, Javiera; Varas, Macarena; Bravo-Toncio, Catalina; Guiliani, Nicolás; Chávez, Francisco P.
  • Ortiz-Severín, Javiera; University of Chile. Faculty of Science. Department of Biology. Systems Microbiology Laboratory. Santiago. CL
  • Varas, Macarena; University of Chile. Faculty of Science. Department of Biology. Systems Microbiology Laboratory. Santiago. CL
  • Bravo-Toncio, Catalina; University of Chile. Faculty of Science. Department of Biology. Systems Microbiology Laboratory. Santiago. CL
  • Guiliani, Nicolás; University of Chile. Faculty of Science. Department of Biology. Bacterial Communication Laboratory. Santiago. CL
  • Chávez, Francisco P; University of Chile. Faculty of Science. Department of Biology. Systems Microbiology Laboratory. Santiago. CL
Biol. Res ; 48: 1-6, 2015. ilus, tab
Artículo en Inglés | LILACS | ID: biblio-950786
ABSTRACT

BACKGROUND:

Pseudomonas aeruginosa is known to be a multidrug resistant opportunistic pathogen. Particularly, P. aeruginosa PAO1 polyphosphate kinase mutant (ppk1) is deficient in motility, quorum sensing, biofilm formation and virulence.

FINDINGS:

By using Phenotypic Microarrays (PM) we analyzed near 2000 phenotypes of P. aeruginosa PAO1 polyP kinase mutants (ppk1 and ppk2). We found that both ppk mutants shared most of the phenotypic changes and interestingly many of them related to susceptibility toward numerous and different type of antibiotics such as Ciprofloxacin, Chloramphenicol and Rifampicin.

CONCLUSIONS:

Combining the fact that ppk1 mutants have reduced virulence and are more susceptible to antibiotics, polyP synthesis and particularly PPK1, is a good target for the design of molecules with anti-virulence and anti-persistence properties.
Asunto(s)


Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Pseudomonas aeruginosa / Fosfotransferasas (Aceptor del Grupo Fosfato) / Farmacorresistencia Bacteriana Múltiple / Análisis por Micromatrices / Mutación Idioma: Inglés Revista: Biol. Res Asunto de la revista: Biologia Año: 2015 Tipo del documento: Artículo País de afiliación: Chile Institución/País de afiliación: University of Chile/CL

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Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Pseudomonas aeruginosa / Fosfotransferasas (Aceptor del Grupo Fosfato) / Farmacorresistencia Bacteriana Múltiple / Análisis por Micromatrices / Mutación Idioma: Inglés Revista: Biol. Res Asunto de la revista: Biologia Año: 2015 Tipo del documento: Artículo País de afiliación: Chile Institución/País de afiliación: University of Chile/CL