J. Antimicrob. Chemother.

OBJECTIVES AND METHODS: armA is a novel plasmid-borne 16S rRNA methyltransferase that confers high-level resistance to 4,6-disubstituted deoxystreptamines. Recently, we have isolated from a high-level broad-spectrum aminoglycoside-resistant Escherichia coli animal isolate a plasmid, pMUR050, that bore the armA gene. In order to elucidate the genetic basis for the spread of armA, we have determined the complete nucleotide sequence of pMUR050. RESULTS: armA was borne by a complex transposon composite flanked by two direct repeats of IS26. The transposon composite included a class one integron with sul1 for resistance to sulphonamides and ant3''9 conferring resistance to spectinomycin-streptomycin, and a macrolide efflux pump and mefE/mel conferring high-level resistance to erythromycin. We identified in GenBank that another plasmid, pCTX-M3, from a Polish Citrobacter freundii human isolate, bore the same genetic structure, including armA. CONCLUSIONS: armA is present in human and animal isolates within a novel transposon composite. Further spread of armA between bacteria of diverse origin is to be expected.

Source:http://purl.uniprot.org/citations/16027145

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http://purl.uniprot.org/cit...rdfs:commentOBJECTIVES AND METHODS: armA is a novel plasmid-borne 16S rRNA methyltransferase that confers high-level resistance to 4,6-disubstituted deoxystreptamines. Recently, we have isolated from a high-level broad-spectrum aminoglycoside-resistant Escherichia coli animal isolate a plasmid, pMUR050, that bore the armA gene. In order to elucidate the genetic basis for the spread of armA, we have determined the complete nucleotide sequence of pMUR050. RESULTS: armA was borne by a complex transposon composite flanked by two direct repeats of IS26. The transposon composite included a class one integron with sul1 for resistance to sulphonamides and ant3''9 conferring resistance to spectinomycin-streptomycin, and a macrolide efflux pump and mefE/mel conferring high-level resistance to erythromycin. We identified in GenBank that another plasmid, pCTX-M3, from a Polish Citrobacter freundii human isolate, bore the same genetic structure, including armA. CONCLUSIONS: armA is present in human and animal isolates within a novel transposon composite. Further spread of armA between bacteria of diverse origin is to be expected.lld:uniprot
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http://purl.uniprot.org/cit...uniprot:nameJ. Antimicrob. Chemother.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorMoreno M.A.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorGonzalez-Zorn B.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorDominguez L.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorTeshager T.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorCatalan A.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorEscudero J.A.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorPorrero C.lld:uniprot
http://purl.uniprot.org/cit...uniprot:date2005lld:uniprot
http://purl.uniprot.org/cit...uniprot:pages583-585lld:uniprot
http://purl.uniprot.org/cit...uniprot:titleGenetic basis for dissemination of armA.lld:uniprot
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