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Transposable gentamicin resistance in IncW plasmids from Hammersmith Hospital
Journal of General Microbiology
|November 1, 1980
Abstract:
A transposon, Tn733, encoding the gentamicin acetyltransferase AAC(3) was found on two gentamicin R plasmids of IncW at Hammersmith Hospital. Transposon TN733 has a molecular mass of 5.8 megadaltons and gives a characteristic 2.4 megadalton fragment on digestion with EcoRI. The appearance of gentamicin resistance on a transposon will increase the chances of spread of this gene.
Insights
A novel transposon, Tn733, carrying the gentamicin resistance gene AAC(3) was identified on IncW plasmids. This discovery highlights a potential mechanism for the increased spread of antibiotic resistance.
Area of Science:
- Molecular biology
- Microbiology
- Genetics
Background:
- Gentamicin resistance is a growing public health concern.
- Plasmids, particularly those of the IncW group, are known vectors for antibiotic resistance genes.
- Transposons facilitate the movement and dissemination of genetic elements, including those conferring antibiotic resistance.
Purpose of the Study:
- To characterize a newly identified transposon, Tn733, associated with gentamicin resistance.
- To investigate the genetic basis of gentamicin resistance in plasmids from Hammersmith Hospital.
- To assess the implications of transposon-mediated resistance for the spread of antibiotic resistance.
Main Methods:
- Plasmid isolation and characterization.
- Molecular analysis of transposon Tn733, including restriction enzyme digestion (EcoRI).
- Identification of the gentamicin acetyltransferase gene AAC(3).
Main Results:
- Transposon Tn733, encoding AAC(3), was identified on two IncW gentamicin resistance plasmids.
- Tn733 has a molecular mass of 5.8 megadaltons.
- Digestion of Tn733 with EcoRI produced a characteristic 2.4 megadalton fragment.
Conclusions:
- The presence of gentamicin resistance on a mobile genetic element like Tn733 increases the likelihood of its dissemination.
- This finding underscores the importance of monitoring transposon-mediated antibiotic resistance.
- Further research is needed to understand the prevalence and impact of Tn733 in clinical settings.