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PMID: 2615657 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Genetic transfer systems in Bacteroides: cloning and mapping of the transferable tetracycline-resistance locus.

Molecular microbiology ·Vol. 3 ·No. 11 ·1989-11-00 ·Pages 1617-23

Guiney DG, Hasegawa P, Bouic K, Matthews B

Abstract

Conjugation systems that transfer antibiotic resistance in the absence of detectable plasmids are common in Bacteroides, but the mechanism of transfer is poorly understood. We found that linked transfer of tetracycline (TcR) and clindamycin (ClR) resistance by Bacteroides fragilis strain 1126 is induced by growth in either Tc or Cl. We cloned the transferable TcR locus as a 13 kb fragment on the shuttle vector pPH6 in Escherichia coli and showed that this region expresses TcR in Bacteroides but not E. coli. The TcR gene was mapped to a 3 kb region and the ClR gene was shown not to be present in the 13 kb insert. Homologous TcR genes are found in B. fragilis V479 and 1792. Using pulsed-field electrophoresis, the transferable TcR gene was shown to be physically associated with high molecular-weight DNA, suggesting that it is located on the chromosome. A new TcR shuttle vector, pPH7 delta 1.1, was constructed to facilitate use of this selective marker in Bacteroides genetics.

MeSH Terms
Bacteroides/drug effects,genetics Chromosome Mapping Cloning, Molecular Conjugation, Genetic DNA, Bacterial/genetics Drug Resistance, Microbial/genetics Genetic Vectors Molecular Weight Tetracycline/pharmacology Transfection
Chemicals
DNA, Bacterial Tetracycline
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Guiney D G
Department of Medicine, University of California, San Diego 92103.
Hasegawa P
Bouic K
Matthews B
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
1989-11-00
Pages
1617-23
Language
English
Region
England
NLM ID
8712028
Subset
IM
Grants
NIAID NIH HHS · AI16463 · United States
NIDCR NIH HHS · DE07344 · United States
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