Affiliation:
1. Department of Biological Science, Institute of Molecular Biology and Nutrition, College of Natural Science and Mathematics, California State University Fullerton, Fullerton, California 92834-6850
2. Department of Microbiology, Miami University, Oxford, Ohio 45056
3. Division of Molecular Genetics, Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom
Abstract
ABSTRACT
The multiresistance plasmid pJHCMW1, harbored by a clinical
Klebsiella pneumoniae
strain isolated from a neonate with meningitis, was sequenced. A circular sequence of 11,354 bp was generated, of which 7,993 bp make up Tn
1331
, a transposon including the antibiotic resistance genes
aac
(
6
′)
-Ib
,
aadA1
,
bla
OXA-9
, and
bla
TEM-1
. The gene
aac
(
6
′)
-Ib
is included in a gene cassette, and both
aadA1
and
bla
OXA-9
are included in a single-gene cassette that may have arisen as a consequence of a recombination event involving two integrons. The pJHCMW1 plasmid replicates through a ColE1-like RNA-regulated mechanism, includes a functional
oriT
, and two loci with similarity to XerCD site-specific recombination target sites involved in plasmid stabilization by the resolution of multimers. One of these two loci,
mwr
, is active and has been the subject of previous studies, and the other,
dxs
, is not functional but binds the recombinase XerD with low affinity. Two additional open reading frames were identified, one with low similarity to two hypothetical membrane proteins from
Mycobacterium tuberculosis
and
Mycobacterium leprae
and the other with low similarity to
psiB
, a gene encoding a function that facilitates the establishment of the transferring plasmid in the recipient bacterial cell during the process of conjugation.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
73 articles.
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