Urinary tract infections in a South American population: Dynamic spread of class 1 integrons and multidrug resistance by homologous and site-specific recombination
- Publication Type:
- Journal Article
- Citation:
- Journal of Clinical Microbiology, 2008, 46 (10), pp. 3417 - 3425
- Issue Date:
- 2008-10-01
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Full metadata record
| Field | Value | Language |
|---|---|---|
| dc.contributor.author | Márquez, C | en_US |
| dc.contributor.author |
Labbate, M |
en_US |
| dc.contributor.author | Raymondo, C | en_US |
| dc.contributor.author | Fernández, J | en_US |
| dc.contributor.author | Gestal, AM | en_US |
| dc.contributor.author | Holley, M | en_US |
| dc.contributor.author | Borthagaray, G | en_US |
| dc.contributor.author | Stokes, HW | en_US |
| dc.date.issued | 2008-10-01 | en_US |
| dc.identifier.citation | Journal of Clinical Microbiology, 2008, 46 (10), pp. 3417 - 3425 | en_US |
| dc.identifier.issn | 0095-1137 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10453/8846 | |
| dc.description.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 Tn21-like transposon backbone which comprised a Tn5036-like tnp transposition module at the IRi integron end and a Tn21 mer module at the IRt integron end. The parent integron/transposon that contributed the Tn5036 module was not related to Tn1696 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 Tn5036 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 Tn21 and Tn5051 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. Copyright © 2008, American Society for Microbiology. All Rights Reserved. | en_US |
| dc.relation.ispartof | Journal of Clinical Microbiology | en_US |
| dc.relation.isbasedon | 10.1128/JCM.00835-08 | en_US |
| dc.subject.classification | Microbiology | en_US |
| dc.subject.mesh | Humans | en_US |
| dc.subject.mesh | Enterobacteriaceae | en_US |
| dc.subject.mesh | Enterobacteriaceae Infections | en_US |
| dc.subject.mesh | Urinary Tract Infections | en_US |
| dc.subject.mesh | DNA, Bacterial | en_US |
| dc.subject.mesh | DNA Transposable Elements | en_US |
| dc.subject.mesh | Sequence Alignment | en_US |
| dc.subject.mesh | Sequence Analysis, DNA | en_US |
| dc.subject.mesh | Drug Resistance, Multiple, Bacterial | en_US |
| dc.subject.mesh | Recombination, Genetic | en_US |
| dc.subject.mesh | Base Sequence | en_US |
| dc.subject.mesh | Integrons | en_US |
| dc.subject.mesh | Gene Order | en_US |
| dc.subject.mesh | Molecular Sequence Data | en_US |
| dc.subject.mesh | Adolescent | en_US |
| dc.subject.mesh | Adult | en_US |
| dc.subject.mesh | Aged | en_US |
| dc.subject.mesh | Aged, 80 and over | en_US |
| dc.subject.mesh | Middle Aged | en_US |
| dc.subject.mesh | Child | en_US |
| dc.subject.mesh | Child, Preschool | en_US |
| dc.subject.mesh | Infant | en_US |
| dc.subject.mesh | Infant, Newborn | en_US |
| dc.subject.mesh | Uruguay | en_US |
| dc.subject.mesh | Female | en_US |
| dc.subject.mesh | Male | en_US |
| dc.title | Urinary tract infections in a South American population: Dynamic spread of class 1 integrons and multidrug resistance by homologous and site-specific recombination | en_US |
| dc.type | Journal Article | |
| utslib.citation.volume | 10 | en_US |
| utslib.citation.volume | 46 | en_US |
| utslib.for | 0605 Microbiology | en_US |
| utslib.for | 06 Biological Sciences | en_US |
| utslib.for | 07 Agricultural and Veterinary Sciences | en_US |
| utslib.for | 11 Medical and Health Sciences | en_US |
| pubs.embargo.period | Not known | en_US |
| pubs.organisational-group | /University of Technology Sydney | |
| pubs.organisational-group | /University of Technology Sydney/Faculty of Science | |
| pubs.organisational-group | /University of Technology Sydney/Faculty of Science/School of Life Sciences | |
| utslib.copyright.status | closed_access | |
| pubs.issue | 10 | en_US |
| pubs.publication-status | Published | en_US |
| pubs.volume | 46 | en_US |
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 Tn21-like transposon backbone which comprised a Tn5036-like tnp transposition module at the IRi integron end and a Tn21 mer module at the IRt integron end. The parent integron/transposon that contributed the Tn5036 module was not related to Tn1696 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 Tn5036 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 Tn21 and Tn5051 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. Copyright © 2008, American Society for Microbiology. All Rights Reserved.
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