Organic Hydroperoxide Resistance Gene ohr (VPA1681) Confers Protection against Organic Peroxides in the Presence of Alkyl Hydroperoxide Reductase Genes in Vibrio parahaemolyticus
Vibrio parahaemolyticus is the most prevalent foodborne pathogen in Taiwan and some other coastal Asian countries, and its antioxidative activity contributes to the tolerance of this bacterium to different environmental stresses. This study reports on the function of the organic hydroperoxide resist...
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Published in | Applied and environmental microbiology Vol. 87; no. 21; p. e0086121 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Microbiology
14.10.2021
|
Subjects | |
Online Access | Get full text |
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Summary: | Vibrio parahaemolyticus
is the most prevalent foodborne pathogen in Taiwan and some other coastal Asian countries, and its antioxidative activity contributes to the tolerance of this bacterium to different environmental stresses. This study reports on the function of the organic hydroperoxide resistance gene (
ohr
; VPA1681) and its gene regulator
ohrR
(VPA1682) in this pathogen.
The marine foodborne enteropathogen
Vibrio parahaemolyticus
contains the chief organic peroxide reductases AphC1-AhpC2 and a putative organic hydroperoxide resistance enzyme (Ohr; VPA1681) against different peroxides. This study investigated the function of the Ohr under the presence of AhpC1-AhpC2 in this pathogen by gene mutation. Experimental results demonstrated that the
ohr
gene product was a weak scavenger of H
2
O
2
only in the mutant strains that lacked the peroxide sensor/regulator
oxyR
and
ahpC1
-
ahpC2
genes. The Ohr of
V. parahaemolyticus
was highly effective at scavenging organic peroxide, as demonstrated by assaying the defective changes in the Δ
ohr
mutant strain and determining the detoxifying activity of the purified recombinant
V. parahaemolyticus
Ohr
vp
protein in the reduced form. The Ohr and AhpC1-AhpC2 exhibited similar functions against organic peroxides; however, only the
ΔahpC1ΔahpC2
mutant strain showed a significant increase in susceptibility to several disinfectants, organic acids, and antibiotics compared with the wild-type strain. The transcription of the
ohr
gene depended on exogenous cumene hydroperoxide (cumene) stress and was markedly enhanced in the
ΔohrR
(VPA1682) mutant strains. This study revealed the organic hydroperoxide reductase activity of the Ohr in
V. parahaemolyticus
, and its role probably depends on sophisticated regulation by OhrR.
IMPORTANCE
Vibrio parahaemolyticus
is the most prevalent foodborne pathogen in Taiwan and some other coastal Asian countries, and its antioxidative activity contributes to the tolerance of this bacterium to different environmental stresses. This study reports on the function of the organic hydroperoxide resistance gene (
ohr
; VPA1681) and its gene regulator,
ohrR
(VPA1682), in this pathogen. The strain with the
ohr
gene had effective protection against organic peroxide, and the recombinant Ohr
vp
was active in its reduced form. The function of Ohr was significant mostly in strains in which the function of AhpC1-AhpC2 was limited. The
ohrR
repressor of the
ohr
gene was effective at low concentrations of organic peroxide. Other common
Vibrio
species that contain homologous
ohr
,
ohrR
,
ahpC1
, and
ahpC2
genes, which are phylogenetically close to those of
V. parahaemolyticus
, may share similar functions to those revealed in this study. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Citation Chen N-X, Chu Y-J, Ni B, Hsu P, Wong H. 2021. Organic hydroperoxide resistance gene ohr (VPA1681) confers protection against organic peroxides in the presence of alkyl hydroperoxide reductase genes in Vibrio parahaemolyticus. Appl Environ Microbiol 87:e00861-21. https://doi.org/10.1128/AEM.00861-21. Present address: Bin Ni, School of Medicine, Jiangsu University, Zhenjiang, Jiangsu, China. |
ISSN: | 0099-2240 1098-5336 1098-5336 |
DOI: | 10.1128/AEM.00861-21 |