Cloning and characterization of a Bacteroides conjugal tetracycline-erythromycin resistance element by using a shuttle cosmid vector
Open Access
- 1 March 1989
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 171 (3) , 1294-1302
- https://doi.org/10.1128/jb.171.3.1294-1302.1989
Abstract
The Bacteroides conjugal tetracycline resistance (Tcr) elements appear not to be plasmids. In many cases, resistance to erythromycin (Emr) is cotransferred with Tcr. Using a newly constructed shuttle cosmid, pNJR1, we cloned 44 to 50 kilobase pairs of a conjugal Tcr Emr element on overlapping cosmid clones. Cosmid libraries were made in Escherichia coli with DNA from the original clinical Bacteroides thetaiotaomicron DOT strain containing Tcr Emr-DOT or from a Bacteroides uniformis Tcr Emr-DOT transconjugant strain. The cosmid clones were mobilized from E. coli into B. uniformis in groups of 10 to 20 per filter mating, with selection for Tcr or Emr transconjugants. The Tcr and Emr genes were cloned both separately and together on 30-kilobase-pair fragments. Several of the Tcr clones also contained transfer genes that permitted self-transfer of the cosmid from B. uniformis donors to E. coli or B. uniformis recipients. Neither the Tcr nor the Emr gene conferred resistance on E. coli, and the transfer-proficient clones did not self-transfer out of E. coli. Southern blot analysis was used to compare DNA from independently isolated Bacteroides strains carrying conjugal Tcr or Tcr Emr elements and their respective B. uniformis transconjugants. Results of these analyses indicate that there are large regions of homology, including regions outside the Tcr and Emr genes, but that the elements are not identical. Some Tcr clones contained a region which hybridized to chromosomal DNA from the wild-type B. uniformis recipient strain that did not carry the Tcr Emr-DOT element. This region of homology appeared not to be a junction fragment. It was not required in a Bacteroides recipient for successful transfer of the Tcr Emr element. Although we are not sure we have cloned a junction fragment between the Tcr Emr-DOT element and the B. uniformis chromosome, the preliminary function and restriction map appears to be linear.This publication has 37 references indexed in Scilit:
- Extrachromosomal systems and gene transmission in anaerobic bacteriaPlasmid, 1987
- Vectors with restriction site banks V. pJRD215, a wide-host-range cosmid vector with multiple cloning sitesGene, 1987
- Recent Advances inBacteroidesGeneticsCRC Critical Reviews in Microbiology, 1987
- Expression in Escherichia coli of cryptic tetracycline resistance genes from Bacteroides R plasmidsPlasmid, 1984
- A Broad Host Range Mobilization System for In Vivo Genetic Engineering: Transposon Mutagenesis in Gram Negative BacteriaBio/Technology, 1983
- Novel antibiotic resistance transfer in BacteroidesAntimicrobial Agents and Chemotherapy, 1982
- DNase-resistant transfer of chromosomal cat and tet insertions by filter mating in pneumococcusPlasmid, 1980
- Taxonomy of the Bacteroides: I. Deoxyribonucleic Acid Homologies Among Bacteroides fragilis and Other Saccharolytic Bacteroides SpeciesInternational Journal of Systematic and Evolutionary Microbiology, 1978
- A complementation analysis of the restriction and modification of DNA in Escherichia coliJournal of Molecular Biology, 1969
- Preparation of transforming deoxyribonucleic acid by phenol treatmentBiochimica et Biophysica Acta (BBA) - Specialized Section on Nucleic Acids and Related Subjects, 1963