Literature DB >> 23687271

Gene expression and physiological role of Pseudomonas aeruginosa methionine sulfoxide reductases during oxidative stress.

Adisak Romsang1, Sopapan Atichartpongkul, Wachareeporn Trinachartvanit, Paiboon Vattanaviboon, Skorn Mongkolsuk.   

Abstract

Pseudomonas aeruginosa PAO1 has two differentially expressed methionine sulfoxide reductase genes: msrA (PA5018) and msrB (PA2827). The msrA gene is expressed constitutively at a high level throughout all growth phases, whereas msrB expression is highly induced by oxidative stress, such as sodium hypochlorite (NaOCl) treatment. Inactivation of either msrA or msrB or both genes (msrA msrB mutant) rendered the mutants less resistant than the parental PAO1 strain to oxidants such as NaOCl and H2O2. Unexpectedly, msr mutants have disparate resistance patterns when exposed to paraquat, a superoxide generator. The msrA mutant had a higher paraquat resistance level than the msrB mutant, which had a lower paraquat resistance level than the PAO1 strain. The expression levels of msrA showed an inverse correlation with the paraquat resistance level, and this atypical paraquat resistance pattern was not observed with msrB. Virulence testing using a Drosophila melanogaster model revealed that the msrA, msrB, and, to a greater extent, msrA msrB double mutants had an attenuated virulence phenotype. The data indicate that msrA and msrB are essential genes for oxidative stress protection and bacterial virulence. The pattern of expression and mutant phenotypes of P. aeruginosa msrA and msrB differ from previously characterized msr genes from other bacteria. Thus, as highly conserved genes, the msrA and msrB have diverse expression patterns and physiological roles that depend on the environmental niche where the bacteria thrive.

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Year:  2013        PMID: 23687271      PMCID: PMC3719549          DOI: 10.1128/JB.00167-13

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  59 in total

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4.  Identification and characterization of a putative active site for peptide methionine sulfoxide reductase (MsrA) and its substrate stereospecificity.

Authors:  J Moskovitz; J M Poston; B S Berlett; N J Nosworthy; R Szczepanowski; E R Stadtman
Journal:  J Biol Chem       Date:  2000-05-12       Impact factor: 5.157

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Authors:  C K Stover; X Q Pham; A L Erwin; S D Mizoguchi; P Warrener; M J Hickey; F S Brinkman; W O Hufnagle; D J Kowalik; M Lagrou; R L Garber; L Goltry; E Tolentino; S Westbrock-Wadman; Y Yuan; L L Brody; S N Coulter; K R Folger; A Kas; K Larbig; R Lim; K Smith; D Spencer; G K Wong; Z Wu; I T Paulsen; J Reizer; M H Saier; R E Hancock; S Lory; M V Olson
Journal:  Nature       Date:  2000-08-31       Impact factor: 49.962

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Authors:  S Dhandayuthapani; M W Blaylock; C M Bebear; W G Rasmussen; J B Baseman
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Authors:  V K Singh; J Moskovitz; B J Wilkinson; R K Jayaswal
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Journal:  Nat Rev Microbiol       Date:  2017-04-19       Impact factor: 60.633

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4.  Effects of Chlorine Stress on Pseudomonas aeruginosa Biofilm and Analysis of Related Gene Expressions.

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Journal:  Curr Microbiol       Date:  2016-05-05       Impact factor: 2.188

5.  Roles of RcsA, an AhpD Family Protein, in Reactive Chlorine Stress Resistance and Virulence in Pseudomonas aeruginosa.

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7.  Significance of four methionine sulfoxide reductases in Staphylococcus aureus.

Authors:  Vineet K Singh; Manisha Vaish; Trintje R Johansson; Kyle R Baum; Robert P Ring; Saumya Singh; Sanjay K Shukla; Jackob Moskovitz
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8.  Pseudomonas aeruginosa IscR-Regulated Ferredoxin NADP(+) Reductase Gene (fprB) Functions in Iron-Sulfur Cluster Biogenesis and Multiple Stress Response.

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9.  The iron-sulphur cluster biosynthesis regulator IscR contributes to iron homeostasis and resistance to oxidants in Pseudomonas aeruginosa.

Authors:  Adisak Romsang; Jintana Duang-Nkern; Panithi Leesukon; Kritsakorn Saninjuk; Paiboon Vattanaviboon; Skorn Mongkolsuk
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10.  The Oxidative Stress Agent Hypochlorite Stimulates c-di-GMP Synthesis and Biofilm Formation in Pseudomonas aeruginosa.

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Journal:  Front Microbiol       Date:  2017-11-22       Impact factor: 5.640

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