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Characterization of an R-plasmid associated with ampicillin resistance in Shigella dysenteriae type 1 isolated from
Abstract:
Ampicillin-resistant strains of Shigella dysenteriae type 1 isolated in epidemics in Mexico, Central America, and Bangla Desh were examined for the presence of plasmid deoxyribonucleic acid (DNA) by gel electrophoresis. All strains contained a heterogeneous population of plasmids. Transfer experiments to Escherichia coli K-12 indicated that the ampicillin resistance determinant (Ap(r)) was located on a 5.5-megadalton (Mdal) plasmid identical in all Shiga strains examined, as judged by DNA hybridization and by its molecular properties. This 5.5-Mdal plasmid contained the ampicillin transposon (TnA) sequences. There was not a high degree of homology between the Shiga Ap(r) plasmid DNA and DNA obtained from Ap(r)Salmonella typhi strains isolated from typhoid epidemics in Mexico, previous to the dysentery outbreaks. Although low, the degree of reassociation observed indicated that probably part of the TnA sequence was present in S. typhi DNA. The DNA hybridization experiments showed, in addition, that there was a high degree of homology among Ap(r) plasmids isolated from different enterobacteria, and this identity was confirmed by restriction endonuclease activity. These results together with their similarities in molecular and replicative properties indicate that the Ap(r) plasmids, as was suggested for the Sm(r) Su(r) plasmids, possibly evolved once and then epidemiologically spread in the Enterobacteriaceae.
Insights
Ampicillin resistance in Shigella dysenteriae type 1 is linked to a specific 5.5-megadalton plasmid. This plasmid, containing ampicillin transposon sequences, appears to have spread among Enterobacteriaceae, potentially originating from a single evolutionary event.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- Ampicillin resistance is a significant challenge in treating bacterial infections.
- Shigella dysenteriae type 1 outbreaks have been associated with ampicillin resistance.
Purpose of the Study:
- To investigate the genetic basis of ampicillin resistance in Shigella dysenteriae type 1.
- To determine the origin and spread of ampicillin-resistant plasmids in Enterobacteriaceae.
Main Methods:
- Gel electrophoresis to identify plasmid DNA.
- Conjugation experiments to transfer ampicillin resistance.
- DNA hybridization and restriction endonuclease analysis to compare plasmids.
Main Results:
- All ampicillin-resistant Shigella dysenteriae type 1 strains harbored a 5.5-megadalton plasmid carrying the ampicillin resistance determinant (Ap(r)).
- This plasmid contained ampicillin transposon (TnA) sequences and showed high homology with plasmids from other enterobacteria.
- Limited homology was found between the Shigella Ap(r) plasmid and DNA from ampicillin-resistant Salmonella typhi.
Conclusions:
- The ampicillin resistance in Shigella dysenteriae type 1 is plasmid-mediated and associated with a specific 5.5-Mdal TnA-containing plasmid.
- This Ap(r) plasmid likely evolved once and spread epidemiologically within the Enterobacteriaceae family.