Long PCRs of transposons in the structural analysis of genes encoding acquired glycopeptide resistance in enterococci

被引:17
作者
Haaheim, H
Dahl, KH
Simonsen, GS
Olsvik, O
Sundsfjord, A [1 ]
机构
[1] Univ Tromso, Sch Med, Dept Med Microbiol, N-9037 Tromso, Norway
[2] Univ Tromso Hosp, N-9012 Tromso, Norway
关键词
D O I
10.2144/98243st02
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Glycopeptide-resistant enterococci (GRE) associated with multiple antibiotic resistance present a major challenge to clinical practice and infection control due to limited or nonexistent antimicrobial treatment options. The genes encoding VanA- and VanB-type glycopeptide resistance have been shown to reside on transposons Tn1546 and Tn1547, respectively These transferable genetic elements may carry the resistance determinants between and within different ecological niches Molecular epidemiological studies of nosocomial outbreaks of VanA- and VanB-type GRE indicate horizontal transfer of glycopeptide resistance genes as an important mechanism for the spread of GRE. To target infection control and better understand the epidemiology of GRE, outbreak investigations and molecular epidemiological studies should therefore apply at least two different approaches, i.e., molecular-typing methods to analyze bacterial genomic heterogeneity and structural analysis of mobile resistance determinants. Here we describe the development and use of long PCRs in the structural analysis of vanA and vanB gene clusters in GRE.
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页码:432 / +
页数:4
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