Urinary Tract Infections in a South American Population: Dynamic Spread of Class 1 Integrons and Multidrug Resistance by Homologous and Site-Specific Recombination

Author:

Márquez Carolina12,Labbate Maurizio3,Raymondo Claudia2,Fernández Jimena2,Gestal Alicia M.4,Holley Marita3,Borthagaray Graciela2,Stokes H. W.3

Affiliation:

1. Cátedra de Microbiología, Instituto de Química Biológica, Facultad de Ciencias—UDELAR, Montevideo, Uruguay

2. Cátedra de Microbiología, Facultad de Química—UDELAR, Montevideo, Uruguay

3. Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney, New South Wales 2109, Australia

4. School of Molecular and Microbial Sciences, University of Sydney, Sydney, New South Wales 2006, Australia

Abstract

ABSTRACT One hundred four bacterial strains mediating urinary tract infections in separate individuals from a Uruguayan community were isolated. Forty-six strains conferred a multidrug resistance phenotype. All 104 strains were examined for the presence of class 1, 2, and 3 integrons. Class 1 integrons were found in 21 isolates across four distinct bacterial genera. A large class 1 integron in a Klebsiella pneumoniae strain was fully sequenced and was 29,093 bp in length. This integron probably arose by homologous recombination since it was embedded in a hybrid Tn 21 -like transposon backbone which comprised a Tn 5036 -like tnp transposition module at the IRi integron end and a Tn 21 mer module at the IRt integron end. The parent integron/transposon that contributed the Tn 5036 module was not related to Tn 1696 since the integron insertion points in the transposon backbones were 16 bases apart. Examination of the other 20 class 1 integron-containing strains revealed further evidence of genetic exchange. This included a strain that possessed a Tn 5036 module at the IRt end but not at the IRi end and another that possessed a tnp module beyond IRi that was a hybrid of Tn 21 and Tn 5051 and that is presumed to have arisen by site-specific recombination. This study highlights the ability of different genetic elements to act cooperatively to spread and rearrange antibiotic resistance in a community.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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