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The Complex Genetic Context of bla (PER-1) Flanked by Miniature Inverted-Repeat Transposable Elements in Acinetobacter johnsonii

On a large plasmid of Acinetobacter johnsonii strain XBB1 from hospital sewage, bla (PER-1) and ISCR1 were found in a complex Tn402-like integron carrying an arr3-aacA4 cassette array. The integron was truncated by the same 439-bp miniature inverted-repeat transposable element (MITE) at both ends. b...

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Detalles Bibliográficos
Autor principal: Zong, Zhiyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3934969/
https://www.ncbi.nlm.nih.gov/pubmed/24587208
http://dx.doi.org/10.1371/journal.pone.0090046
Descripción
Sumario:On a large plasmid of Acinetobacter johnsonii strain XBB1 from hospital sewage, bla (PER-1) and ISCR1 were found in a complex Tn402-like integron carrying an arr3-aacA4 cassette array. The integron was truncated by the same 439-bp miniature inverted-repeat transposable element (MITE) at both ends. bla (PER-1) and its complex surroundings might have been mobilized by the MITEst into an orf of unknown function, evidenced by the presence of the characteristic 5-bp direct target repeats. The same 439-bp MITEs have also been found flanking class 1 integrons carrying metallo-β-lactamases genes bla (IMP-1), bla (IMP-5) and bla (VIM-2) before but without ISCR1. Although the cassette arrays are different, integrons have always been truncated by the 439-bp MITEs at the exact same locations. The results suggested that MITEs might be able to mobilize class 1 integrons via transposition or homologous recombination and therefore represent a possible common mechanism for mobilizing antimicrobial resistance determinants.