Affiliation:
1. Department of Microbiology and Molecular Genetics1 and
2. Shipley Institute of Medicine,2 Harvard Medical School, Boston, Massachusetts 02115
Abstract
ABSTRACT
The
Vibrio cholerae
genome contains a 5.4-kb
pil
gene cluster that resembles the
Aeromonas hydrophila tap
gene cluster and other type IV-A pilus assembly operons. The region consists of five complete open reading frames designated
pilABCD
and
yacE
, based on the nomenclature of related genes from
Pseudomonas aeruginosa
and
Escherichia coli
K-12. This cluster is present in both classical and El Tor biotypes, and the
pilA
and
pilD
genes are 100% conserved. The
pilA
gene encodes a putative type IV pilus subunit. However, deletion of
pilA
had no effect on either colonization of infant mice or adherence to HEp-2 cells, demonstrating that
pilA
does not encode the primary subunit of a pilus essential for these processes. The
pilD
gene product is similar to other type IV prepilin peptidases, proteins that process type IV signal sequences. Mutational analysis of the
pilD
gene showed that
pilD
is essential for secretion of cholera toxin and hemagglutinin-protease, mannose-sensitive hemagglutination (MSHA), production of toxin-coregulated pili, and colonization of infant mice. Defects in these functions are likely due to the lack of processing of N termini of four Eps secretion proteins, four proteins of the MSHA cluster, and TcpB, all of which contain type IV-A leader sequences. Some
pilD
mutants also showed reduced adherence to HEp-2 cells, but this defect could not be complemented in
trans
, indicating that the defect may not be directly due to a loss of
pilD
. Taken together, these data demonstrate the effectiveness of the
V. cholerae
genome project for rapid identification and characterization of potential virulence factors.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
141 articles.
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