Affiliation:
1. Department of Biochemistry, University of Nebraska, Lincoln, Nebraska 68588
2. Veterinary and Biomedical Science Department, University of Nebraska, Lincoln, Nebraska 68588
Abstract
ABSTRACT
Helicobacter hepaticus
is a gram-negative, spiral-shaped microaerophilic bacterium associated with chronic intestinal infection leading to hepatitis and colonic and hepatic carcinomas in susceptible strains of mice. In the closely related human pathogen
Helicobacter pylori
,
l
-proline is a preferred respiratory substrate and is found at significantly high levels in the gastric juice of infected patients. A previous study of the proline catabolic PutA flavoenzymes from
H. pylori
and
H. hepaticus
revealed that
Helicobacter
PutA generates reactive oxygen species during proline oxidation by transferring electrons from reduced flavin to molecular oxygen. We further explored the preference for proline as a respiratory substrate and the potential impact of proline metabolism on the redox environment in
Helicobacter
species during host infection by disrupting the
putA
gene in
H. hepaticus
. The resulting
putA
knockout mutant strain was characterized by oxidative stress analysis and mouse infection studies. The
putA
mutant strain of
H. hepaticus
exhibited increased proline levels and resistance to oxidative stress relative to that of the wild-type strain, consistent with proline's role as an antioxidant. The significant increase in stress resistance was attributed to higher proline content, as no upregulation of antioxidant genes was observed for the
putA
mutant strain. The wild-type and
putA
mutant
H. hepaticus
strains displayed similar levels of infection in mice, but in mice challenged with the
putA
mutant strain, significantly reduced inflammation was observed, suggesting a role for proline metabolism in
H. hepaticus
pathogenicity in vivo.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
38 articles.
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