Sunde Marianne
Section of Bacteriology, National Veterinary Institute, 0033 Oslo, Norway.
J Antimicrob Chemother. 2005 Dec;56(6):1019-24. doi: 10.1093/jac/dki377. Epub 2005 Oct 20.
The aim of the study was to investigate the prevalence of integrons and to characterize inserted gene cassettes in Escherichia coli isolated from meat and meat products of Norwegian origin.
The strains investigated (n = 241 resistant out of 944 investigated) were collected within the frame of the Norwegian monitoring programme for antimicrobial resistance in bacteria from feed, food and animals (NORM-VET) during the years 2000-2003. PCR and DNA sequencing were used for detection of the integrase genes and gene cassettes within the integrons.
Integrons were detected in 43 (18%) of the 241 resistant isolates. Class 1 integrons were detected in 29 (12%) strains and class 2 integrons were detected in 14 (6%) strains. Ten different gene cassettes were detected: dfrA1, dfr2a, dfrA12, aadA1, aadA2, catB2, oxa-30, sat, sat1 and orfF. The dfrA1 + aadA1 combination was the most prevalent cassette combination, detected in 12 of 29 class 1 integrons. Twelve (of 14) class 2 integrons contained a cassette area consistent with that on Tn7, the remaining two contained the cassettes sat + sat1 + aadA1. Nearly one-third of the class 1 integrons (9 of 29) lacked the sul1 gene. Ten gene cassettes (one dfr2a, two catB2 and seven aadA1) were expressed at levels below breakpoint values normally used to classify strains as resistant.
Integrons of class 1 or 2 were present in approximately 18% of the resistant E. coli strains investigated. Certain cassette combinations in class 1 integrons seem to be more widespread than others, like the dfrA1 + aadA1. Low-level expression of antimicrobial resistance, caused by the expression of certain gene cassettes in some integrons represents an obstacle in classifying strains as susceptible or resistant.
本研究旨在调查整合子的流行情况,并对从挪威产肉类及肉制品中分离出的大肠杆菌中插入的基因盒进行特征分析。
所研究的菌株(944株中241株耐药)是在2000年至2003年挪威饲料、食品和动物细菌抗菌药物耐药性监测计划(NORM-VET)框架内收集的。采用聚合酶链反应(PCR)和DNA测序检测整合酶基因及整合子内的基因盒。
在241株耐药菌株中,43株(18%)检测到整合子。29株(12%)菌株检测到1类整合子,14株(6%)菌株检测到2类整合子。检测到10种不同的基因盒:dfrA1、dfr2a、dfrA12、aadA1、aadA2、catB2、oxa-30、sat、sat1和orfF。dfrA1 + aadA1组合是最常见的基因盒组合,在29个1类整合子中的12个中检测到。14个2类整合子中有12个含有与Tn7上一致的基因盒区域,其余2个含有sat + sat1 + aadA1基因盒。近三分之一的1类整合子(29个中的9个)缺乏sul1基因。10个基因盒(1个dfr2a、2个catB2和7个aadA1)的表达水平低于通常用于将菌株分类为耐药的断点值。
在所研究的耐药大肠杆菌菌株中,约18%存在1类或2类整合子。1类整合子中的某些基因盒组合似乎比其他组合更广泛,如dfrA1 + aadA1。某些整合子中特定基因盒的表达导致抗菌药物耐药性的低水平表达,这在将菌株分类为敏感或耐药方面构成了障碍。