Role of Vfr in regulating exotoxin A production by Pseudomonas aeruginosa

Author:

Davinic Marko1,Carty Nancy L.1,Colmer-Hamood Jane A.2,San Francisco Michael1,Hamood Abdul N.2

Affiliation:

1. Department of Biological Sciences, Texas Tech University, MS3131, Lubbock, TX 79409, USA

2. Department of Microbiology and Immunology, School of Medicine, Texas Tech University Health Sciences Center, 3601 4th Street, Lubbock, TX 79430, USA

Abstract

Pseudomonas aeruginosaexotoxin A (ETA) production depends on the virulence-factor regulator Vfr. Recent evidence indicates that theP. aeruginosairon-starvation sigma factor PvdS also enhances ETA production through the ETA-regulatory generegA. Mutants defective invfr,regAandpvdS, plasmids that overexpress these genes individually andlacZtranscriptional/translational fusion plasmids were utilized to examine the relationship betweenvfr,regAandpvdSin regulatingP. aeruginosaETA production. ETA concentration andregAexpression were reduced significantly in PAOΔvfr, butpvdSexpression was not affected. Overexpression of Vfr produced a limited increase in ETA production in PAOΔpvdS, but not PAOΔregA. Additionally, overexpression of either RegA or PvdS did not enhance ETA production in PAOΔvfr. RT-PCR analysis showed that iron did not affect the accumulation ofvfrmRNA in PAO1. These results suggest that: (i) Vfr enhancestoxAexpression in PAO1 both directly and indirectly throughregA, but not throughpvdS; (ii)vfrexpression is not regulated by iron; and (iii) both Vfr and PvdS cooperate in the presence of RegA to achieve a maximum level oftoxAexpression.

Publisher

Microbiology Society

Subject

Microbiology

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