Affiliation:
1. Université de Paris-Sud, Faculté de Pharmacie, Département de Microbiologie, Unité EA 35-34, 92296 ChÂtenay-Malabry Cedex, France
Abstract
ABSTRACT
Recent investigations of the
Clostridium difficile
genome have revealed the presence of a cluster of 17 genes, 11 of which encode proteins with similar two-domain structures, likely to be surface-anchored proteins. Two of these genes have been proven to encode proteins involved in cell adherence:
slpA
encodes the precursor of the two proteins of the S-layer, P36 and P47, whereas
cwp66
encodes the Cwp66 adhesin. To gain further insight into the function of this cluster, we further focused on
slpA
,
cwp66
, and
cwp84,
the latter of which encodes a putative surface-associated protein with homology to numerous cysteine proteases. It displayed nonspecific proteolytic activity when expressed as a recombinant protein in
Escherichia coli
. Polymorphism of
cwp66
and
cwp84
genes was analyzed in 28 strains, and transcriptional organization of the three genes was explored by Northern blots. The
slpA
gene is strongly transcribed during the entire growth phase as a bicistronic transcript;
cwp66
is transcribed only in the early exponential growth phase as a polycistronic transcript encompassing the two contiguous genes upstream. The putative proteins encoded by the cotranscribed genes have no significant homology with known proteins but may have a role in adherence. No correlation could be established between sequence patterns of Cwp66 and Cwp84 and virulence of the strains. The
cwp84
gene is strongly transcribed as a monocistronic message. This feature, together with the highly conserved sequence pattern of
cwp84
, suggests a significant role in the physiopathology of
C. difficile
for the Cwp84 protease, potentially in the maturation of surface-associated adhesins encoded by the gene cluster.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
38 articles.
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