Affiliation:
1. School of Molecular Biosciences, Washington State University, Pullman, Washington
2. USDA Western Regional Research Center, Albany, California
Abstract
ABSTRACT
Campylobacter jejuni
, a spiral-shaped gram-negative bacterium, is a leading bacterial cause of human food-borne illness. Acute disease is associated with
C. jejuni
invasion of the intestinal epithelium. Further, maximal host cell invasion requires the secretion of proteins termed
Campylobacter
invasion antigens (Cia). As bile acids are known to alter the pathogenic behavior of other gastrointestinal pathogens, we hypothesized that the virulence potential of
Campylobacter
may be triggered by the bile acid deoxycholate (DOC). In support of this hypothesis, culturing
C. jejuni
with a physiologically relevant concentration of DOC significantly altered the kinetics of cell invasion, as shown by gentamicin protection assays. In contrast to
C. jejuni
harvested from Mueller-Hinton (MH) agar plates,
C. jejuni
harvested from MH agar plates supplemented with DOC secreted the Cia proteins, as judged by metabolic labeling experiments. DOC was also found to induce the expression of the
ciaB
gene, as determined by β-galactosidase reporter, real-time reverse transcription-PCR, and microarray analyses. Microarray analysis further revealed that DOC induced the expression of virulence genes (
ciaB, cmeABC, dccR
, and
tlyA
). In summary, we demonstrated that it is possible to enhance the pathogenic behavior of
C. jejuni
by modifying the culture conditions. These results provide a foundation for identifying genes expressed by
C. jejuni
in response to in vivo-like culture conditions.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
101 articles.
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