Rapid identification of virulence genes in enterotoxigenic Escherichia coli isolates associated with diarrhoea in Queensland piggeries

被引:26
作者
Do, T
Stephens, C
Townsend, K
Wu, X
Chapman, T
Chin, J
McCormick, B
Bara, M
Trott, DJ [1 ]
机构
[1] Univ Queensland, Sch Vet Sci, Brisbane, Qld 4072, Australia
[2] Toowoomba Vet Lab, Anim & Plant Hlth Serv, Dept Primary Ind, Toowoomba, Qld 4350, Australia
[3] Elizabeth Macarthur Agr Inst, Camden, NSW 2570, Australia
[4] Natl Escherichia Coli Reference & Serotyping Lab, Dept Primary Ind, Epsom, Vic 3552, Australia
关键词
D O I
10.1111/j.1751-0813.2005.tb12745.x
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Objective To identify virulence genes in enterotoxigenic E coli (ETEC) isolates associated with diarrhoea in neonatal, 1 to 3 week-old and weaned pigs in south east Queensland. Design Multiplex PCR and serotyping were applied to E coli isolates obtained over a 5-year period (1998-2002) from cases diagnosed at Toowoomba Veterinary Laboratory. Procedure A total of 126 isolates from 25 different Queensland piggeries were tested for haemolytic activity on 5% sheep blood agar and by multiplex PCR for the presence of five commonly recognised fimbrial (F4, F5, F6, F41 and F18) and three enterotoxin genes (STa, STb, LT). A subset of 62 representative isolates were serotyped by slide agglutination. For comparative purposes, multiplex PCR was also performed on the DNA of 31 ETEC isolates from 9 serotypes originating from piggeries in southern New South Wales. Results A total of 113 (89.7%) of the isolates from Queensland possessed ETEC virulence genes, including 14 of 15 isolates from neonatal pigs (93.3%), 18 of 23 isolates from 1 to 3 week old pigs (78.3%) and 81 of 88 isolates from weaned pigs (92.1%). F4:STa:STb:LT (serotype 0149) was the most prevalent pathotype in neonatal and 1-3 week old pigs and F4:STa:STb:LT (serotype 0149) and F18:STa:STb:LT (serotype 0141) were most prevalent in weaned pigs. In comparison; isolates obtained from neonatal pigs from New South Wales belonged to a more diverse range of pathotypes and serotypes. Conclusion Multiplex PCR was a rapid and specific method for detecting the presence of ETEC virulence genes in porcine E coli isolates. For isolates obtained from cases of suspected colibacillosis in Queensland, growth of a heavy pure culture of haemolytic E coli was a sensitive prognostic indicator of the presence of ETEC virulence genes in the isolate. ETEC pathotypes and serotypes remained stable in Queensland piggeries over the five-year study period and appear to have changed little over the last three decades.
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页码:293 / 299
页数:7
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