Affiliation:
1. Pathogen Molecular Biology and Biochemistry Unit, Department of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine,1 and
2. Digestive Diseases Research Centre, St. Bartholomew's and the Royal London School of Medicine and Dentistry, Whitechapel,2 London, United Kingdom
Abstract
ABSTRACT
Hemolysins have been found to possess a variety of functions in bacteria, including a role in virulence.
Helicobacter pylori
demonstrates hemolytic activity when cultured on unlysed blood agar plates which is increased under iron-limiting conditions. However, the role of an
H. pylori
hemolysin in virulence is unclear. Scrutiny of the
H. pylori
26695 genome sequence suggests the presence of at least two distinct hemolysins, HP1086 and HP1490, in this strain. Previous studies have shown that the in vitro hemolytic activity of
H. pylori
is reduced when it is coincubated with dextran 5000, suggesting the presence of a pore-forming cytolysin. HP1086 has homology to pore-forming cytolysins (TlyA) from other bacterial species, and the introduction of the cloned
H. pylori tlyA
gene into a nonhemolytic
Escherichia coli
strain conferred hemolytic activity. An
H. pylori tlyA
defined mutant showed reduced in vitro hemolytic activity, which appears to be due to pore formation, as the hemolytic activity of the wild-type strain is reduced to the same level as the
tlyA
mutant by the addition of dextran 5000. The mutant also showed reduced adhesion to human gastric adenocarcinoma cells and failed to colonize the gastric mucosa of mice. These data clearly suggest a role in virulence for
H. pylori
TlyA, contrary to the suggestion that hemolytic activity is an in vitro phenomenon for this pathogen.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
39 articles.
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