Affiliation:
1. Program in Molecular Biology, Loyola University Medical Center, Maywood, Illinois 60153
2. Department of Medicine, Hines VA Hospital, Hines, Illinois 60141
3. Departments of Medicine and Microbiology and Immunology
Abstract
ABSTRACT
Horizontal DNA transfer contributes significantly to the dissemination of antibiotic resistance genes in
Bacteroides fragilis
. To further our understanding of DNA transfer in
B. fragilis
, we isolated and characterized a new transfer factor, cLV25. cLV25 was isolated from
B. fragilis
LV25 by its capture on the nonmobilizable
Escherichia coli-Bacteroides
shuttle vector pGAT400ΔBglII. Similar to other
Bacteroides
sp. transfer factors, cLV25 was mobilized in
E. coli
by the conjugative plasmid R751. Using Tn
1000
mutagenesis and deletion analysis of cLV25, two mobilization genes,
bmgA
and
bmgB
, were identified, whose predicted proteins have similarity to DNA relaxases and mobilization proteins, respectively. In particular, BmgA and BmgB were homologous to MocA and MocB, respectively, the two mobilization proteins of the
B. fragilis
mobilizable transposon Tn
4399
. A
cis
-acting origin of transfer (
oriT
) was localized to a 353-bp region that included nearly all of the intergenic region between
bmgB
and
orf22
and overlapped with the 3′ end of
orf22
. This
oriT
contained a putative
nic
site sequence but showed no significant similarity to the
oriT
regions of other transfer factors, including Tn
4399
. Despite the lack of sequence similarity between the
oriT
s of cLV25 and Tn
4399
, a mutation in the cLV25 putative DNA relaxase,
bmgA
, was partially complemented by Tn
4399
. In addition to the functional cross-reaction with Tn
4399
, a second distinguishing feature of cLV25 is that predicted proteins have similarity to proteins encoded not only by Tn
4399
but by several
Bacteroides
sp. transfer factors, including NBU1, NBU2, CTnDOT, Tn
4555
, and Tn
5520
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
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