Affiliation:
1. Department of Molecular Genetics and Biochemistry and Graduate Program in Molecular Virology and Microbiology, University of Pittsburgh School of Medicine, East 1240 Biomedical Science Tower, Pittsburgh, Pennsylvania 15261
Abstract
ABSTRACT
Plasmid pXO1 encodes the tripartite anthrax toxin, which is the major virulence factor of
Bacillus anthracis
. In spite of the important role of pXO1 in anthrax pathogenesis, very little is known about its replication and maintenance in
B. anthracis
. We cloned a 5-kb region of the pXO1 plasmid into an
Escherichia coli
vector and showed that this plasmid can replicate when introduced into
B. anthracis
. Mutational analysis showed that open reading frame 45 (
repX
) of pXO1 was required for the replication of the miniplasmid in
B. anthracis
. Interestingly,
repX
showed limited homology to bacterial FtsZ proteins that are involved in cell division. A mutation in the predicted GTP binding domain of RepX abolished its replication activity. Genes almost identical to
repX
are contained on several megaplasmids in members of the
Bacillus cereus
group, including a
B. cereus
strain that causes an anthrax-like disease. Our results identify a novel group of FtsZ-related initiator proteins that are required for the replication of virulence plasmids in
B. anthracis
and possibly in related organisms. Such replication proteins may provide novel drug targets for the elimination of plasmids encoding the anthrax toxin and other virulence factors.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
85 articles.
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