Affiliation:
1. Department of Biochemistry, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China
Abstract
ABSTRACT
DNA sequencing upstream of the
Salmonella enterica
serovar Typhi
pilV
and
rci
genes previously identified in the ca. 118-kb major pathogenicity island (X.-L. Zhang, C. Morris, and J. Hackett, Gene 202:139–146, 1997) identified a further 10
pil
genes apparently forming a
pil
operon. The product of the
pilS
gene, prePilS protein (a putative type IVB structural prepilin) was purified, and an anti-prePilS antiserum was raised in mice. Mutants of serovar Typhi either lacking the whole
pil
operon or with an insertion mutation in the
pilS
gene were constructed, as was a strain in which the
pilN
to
pilV
genes were driven by the
tac
promoter. The
pil
+
strains synthesized type IVB pili, as judged by (i) visualization in the electron microscope of thin pili in culture supernatants of one such strain and (ii) the presence of PilS protein (smaller than the prePilS protein by removal of the leader peptide) on immunoblotting of material pelleted by high-speed centrifugation of either the culture supernatant or sonicates of
pil
+
strains. Control
pil
mutants did not express the PilS protein. A
pilS
mutant of serovar Typhi entered human intestinal INT407 cells in culture to levels only 5 to 25% of those of the wild-type strain, and serovar Typhi entry was strongly inhibited by soluble prePilS protein (50% inhibition of entry at 1.4 μM prePilS).
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
127 articles.
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