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Development and analysis of furazolidone-resistant Escherichia coli mutants

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Authors
Martínez Puchol, Sandra
Gómes, Cláudia
Pons, Maria J.
Ruíz Roldan, Lidia
Torrents De La Peña, Alba
Ochoa, Theresa J.
Ruíz, Joaquim
Issue Date
2015-06-15
Keywords
Enterobacteriaceae
Nitrofuran
Resistance mechanisms

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Citation
Mart ınez-Puchol S, Gomes C, Pons MJ, Ruiz-Rold an L, Torrents de la Pe~na A, Ochoa TJ, Ruiz J. Development and analysis of furazolidone-resistant Escherichia coli mutants. APMIS 2015.
Publisher
John Wiley & Sons, Inc.
Journal
Acta pathologica, microbiologica et Immunológica Scandinavica (APMIS.)
URI
http://hdl.handle.net/10757/556955
DOI
10.1111/apm.12401
PubMed ID
26011027
Additional Links
http://www.ncbi.nlm.nih.gov/pubmed/26011027
Abstract
Furazolidone-resistant mutants were obtained from four clinical isolates of diarrhoeagenic Escherichia coli. The stability of the resistance and the frequency of mutation were established. The minimal inhibitory concentration of furazolidone, nitrofurantoin, nalidixic acid, ampicillin, chloramphenicol and tetracycline was established both in the presence and absence of the efflux pump inhibitor Phe-Arg-β-Naphtylamyde. The presence of mutations in the nitroreductase genes nfsA and nfsB was analysed by PCR; sequencing and their enzymatic activity was assessed by a spectrophotometric assay. Alterations in outer membrane proteins were studied by SDS-PAGE. The frequency of mutation ranged from <9.6 × 10-10 to 9.59 × 10-7 . Neither an effect on efflux pumps inhibited by Phe-Arg-β-Naphtylamyde nor cross-resistance with the antibiotics studied was observed. Nineteen mutants (52.94%) presented mutations in the nitroreductase-encoding genes: 17 in the nfsA gene (15 mutants with an internal stop codon, 2 with amino acid changes), 2 in the nfsB (all amino acid changes). Alterations in the outer membrane proteins OmpA and OmpW were also observed. Although more studies are necessary to find other resistance mechanisms, present data showed the low potential of selecting furazolidone-resistant mutants, together with the lack of cross-resistance with unrelated antimicrobial agents.
Type
info:eu-repo/semantics/article
Rights
info:eu-repo/semantics/openAccess
Language
eng
Description
Revisión por pares
[email protected]
ISSN
1600-0463
ae974a485f413a2113503eed53cd6c53
10.1111/apm.12401
Scopus Count
Collections
Medicina

entitlement

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