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JAC Advance Access published online on August 15, 2008

Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkn331
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© The Author 2008. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org

Original research

Prevalence and diversity of integrons and associated resistance genes in faecal Escherichia coli isolates of healthy humans in Spain

Laura Vinué1, Yolanda Sáenz1,2, Sergio Somalo1, Esther Escudero3, Miguel Ángel Moreno3, Fernanda Ruiz-Larrea1 and Carmen Torres1,2,*

1 Área de Bioquímica y Biología Molecular, Universidad de La Rioja, Logroño, Spain 2 CIBIR, Unidad de Microbiología Molecular, Logroño, Spain 3 Departamento de Sanidad Animal, Facultad de Veterinaria, Universidad Complutense de Madrid, Madrid, Spain

Received 18 April 2008; returned 22 May 2008; revised 21 July 2008; accepted 23 July 2008


* Correspondence address. Área de Bioquímica y Biología Molecular, Departamento de Agricultura y Alimentación, Universidad de La Rioja, Madre de Dios 51, 26006 Logroño, Spain. Tel: +34-941-299750; Fax: +34-941-299721; E-mail: carmen.torres{at}unirioja.es

Objectives: To analyse the prevalence and diversity of integrons in faecal Escherichia coli isolates from healthy humans in Spain.

Methods: One hundred E. coli isolates were obtained in Levine agar plates from faecal samples of 100 healthy humans during March to October 2007. Susceptibility to 16 antimicrobial agents was determined by the disc diffusion method. The presence and characterization of class 1, 2 and 3 integrons, as well as the presence of other antimicrobial resistance genes, were performed by PCR and DNA sequencing.

Results: Integrases associated with class 1 and/or class 2 integrons were identified in 29 E. coli isolates (intI1 gene in 26 isolates, intI2 in 1 isolate and intI1 + intI2 in 2 isolates), the remaining 71 isolates being free of these integrons. Seven different gene cassette arrangements were demonstrated in 27 of the 28 intI1-positive isolates and were as follows (number of isolates): dfrA1 + aadA1 (12), aadA (8), dfrA17 + aadA5 (3), dfrA7 (1), dfrA5 (1), dfrA1 (1) and dfrA12 + orfF + aadA2 (1). Four isolates presented defective class 1 integrons lacking the 3'-conserved region. The three isolates containing class 2 integrons harboured the dfrA1 + sat + aadA1 gene cassette array in their variable region. Integron-positive isolates showed higher percentages of resistance to streptomycin, ampicillin, tetracycline, trimethoprim, sulfamethoxazole, chloramphenicol and nalidixic acid than integron-negative isolates. Sixty-five percent of the integron-positive isolates belonged to phylogenetic groups A or D.

Conclusions: A high prevalence of integrons was detected in faecal E. coli of healthy humans. Individuals in the community could be a reservoir of integron-containing E. coli isolates.

Key Words: E. coli , antimicrobial resistance , gene cassettes


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