Molecular diversity and evolutionary relationships of Tn1546-like elements in enterococci from humans and animals

被引:179
作者
Willems, RJL
Top, J
van den Braak, N
van Belkum, A
Mevius, DJ
Hendriks, G
van Santen-Verheuvel, M
van Embden, JDA
机构
[1] Natl Inst Publ Hlth & Environm, Res Lab Infect Dis, NL-3720 BA Bilthoven, Netherlands
[2] Erasmus Med Ctr Rotterdam, Dept Med Microbiol & Infect Dis, NL-3015 GD Rotterdam, Netherlands
[3] DLO, Inst Anim Sci & Hlth, Dept Bacteriol, NL-8200 AB Lelystad, Netherlands
关键词
D O I
10.1128/AAC.43.3.483
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We report on a detailed study on the molecular diversity and evolutionary relationships of Tn1546-like elements in vancomycin-resistant enterococci (VRE) from humans and animals. Restriction fragment length polymorphism (RFLP) analysis of the VanA transposon of 97 VRE revealed seven different Tn1546 types. Subsequent sequencing of the complete VanA transposons of 13 VRE isolates representing the seven RFLP types followed by sequencing of the identified polymorphic regions in 84 other VanA transposons resulted in the identification of 22 different Tn1546 derivatives. Differences between the Tn1546 types included point mutations in orf1, vanS, vanA, vanX, and vanY. Moreover, insertions of an ISI216V-IS3-like element in orf1, of IS1251 in the vanS-vanH intergenic region, and of IS1216V in the vanX-vanY intergenic region were found. The presence of insertion sequence elements was often associated with deletions in Tn1546. Identical Tn1546 types were found among isolates from humans and farm animals in The Netherlands, suggesting the sharing of a common vancomycin resistance gene pool. Application of the genetic analysis of Tn1546 to VRE isolates causing infections in hospitals in Oxford, United Kingdom, and Chicago, III., suggested the possibility of the horizontal transmission of the vancomycin resistance transposon. The genetic diversity in Tn1546 combined with epidemiological data suggest that the DNA polymorphism among Tn1546 variants can successfully be exploited for the tracing of the routes of transmission of vancomycin resistance genes.
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页码:483 / 491
页数:9
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