2011
DOI: 10.1128/aac.01529-10
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Dissemination of Multiple Drug Resistance Genes by Class 1 Integrons in Klebsiella pneumoniae Isolates from Four Countries: a Comparative Study

Abstract: A comparative genetic analysis of 42 clinical Klebsiella pneumoniae isolates, resistant to two or more antibiotics belonging to the broad-spectrum ␤-lactam group, sourced from Sydney, Australia, and three South American countries is presented. The study focuses on the genetic contexts of class 1 integrons, mobilizable genetic elements best known for their role in the rapid evolution of antibiotic resistance among Gram-negative pathogens. It was found that the class 1 integrons in this cohort were located in a … Show more

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Cited by 52 publications
(37 citation statements)
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“…The 100-bp deletion characteristic of Tn 4401 isoform a is indicated above the sequence. Primers used are shown below the sequence: KPCfw, KPCrv 15, 816U, 3098U, 4714 26.…”
Section: Resultsmentioning
confidence: 99%
“…The 100-bp deletion characteristic of Tn 4401 isoform a is indicated above the sequence. Primers used are shown below the sequence: KPCfw, KPCrv 15, 816U, 3098U, 4714 26.…”
Section: Resultsmentioning
confidence: 99%
“…In this study, the average level of intI1 genes detected was at least 2 orders of magnitude lower than that detected in hospital wastewaters in China, with tet and sul genes detected in a lower range as well (37). Class 1 integrons are responsible for the spread and carriage of antibiotic resistance gene cassettes in Gram-negative pathogens (38,39). The high concentrations of class 1 integrons detected in raw wastewater and the occurrence in ARB isolates were consistent with recent literature reports, e.g., 97% for E. coli isolates in Iran (40), 76% for E. coli and 43% for Salmonella isolates in Netherlands (41), 67% for E. coli isolates in Spain (42), and 63% for E. coli isolates in Thailand (43).…”
Section: Discussionmentioning
confidence: 99%
“…The presence of class 1 and 2 integrons was analyzed using primers designed to detect the corresponding integrase genes: HS463a and HS464 for intI1 [16], and HS501 and HS502 for intI2 [17]. In the subset of isolates that were positive for intI1, the Pc promoter region was amplified using primers Pre-Pc (5 0 GATGCGTGGAGACCGAAACCTT3 0 ) and Post-Pc (5 0 GCGACTGCCCTGCTGCGTAACAT 3 0 ).…”
Section: Variablesmentioning
confidence: 99%