School of Veterinary and Life Sciences, Murdoch University, Murdoch, Western Australia 6150, Australia.
South Australian Research and Development Institute, 33 Flemington Street, Glenside, SA 5065, Australia.
Exp Parasitol. 2014 Feb;137:46-52. doi: 10.1016/j.exppara.2013.12.004. Epub 2013 Dec 16.
A novel quantitative PCR (qPCR) for Giardia at the glutamate dehydrogenase (gdh) locus was developed and validated. The qPCR was used to screen a total of 3412 lamb faecal samples collected from approximately 1189 lambs at three sampling periods (weaning, post-weaning and pre-slaughter) from eight farms across South Australia (SA), New South Wales (NSW), Victoria (Vic) and Western Australia (WA). The overall prevalence was 20.2% (95% CI 18.9-21.6) and of the 690 positives, 473 were successfully typed. In general, the prevalence of Giardia varied widely across the different farms with the highest prevalence in one WA farm (42.1%) at pre-slaughter sampling and the lowest prevalence in one Victorian farm (7.2%) at weaning. The range of cyst shedding at weaning, post-weaning and pre-slaughter overall across all states was 63-1.3×10(9) cysts g(-1) (median=1.7×10(4)), 63-1.1×10(9) cysts g(-1) (median=9.6×10(3)), 63-4.7×10(9) cysts g(-1) (median=8.1×10(4)) respectively. Assemblage specific primers at the triose phosphate isomerase (tpi) locus identified assemblage A in 22.4% (106/473) of positive samples typed, assemblage E in 75.9% (359/473) and mixed A and E assemblages in 1.7% (8/473) of samples. A subset of representative samples from the 8 farms (n=32) were typed at both the gdh and beta-giardin loci and confirmed these results and identified sub-assemblage AII in 16 representative assemblage A isolates across the 8 farms. This demonstrates a prevalence of Giardia previously not recognised in Australian sheep, highlighting a need for further research to quantify the production impacts of this protozoan parasite.
开发并验证了一种针对贾第虫谷氨酸脱氢酶(gdh)基因座的新型实时定量 PCR(qPCR)方法。使用该 qPCR 共检测了来自南澳大利亚州(SA)、新南威尔士州(NSW)、维多利亚州(Vic)和西澳大利亚州(WA)8 个农场的 1189 只羔羊的 3412 份粪便样本。总体流行率为 20.2%(95%CI 18.9-21.6),690 份阳性样本中有 473 份成功分型。总体而言,不同农场之间贾第虫的流行率差异很大,WA 一个农场的流行率最高(宰前采样时为 42.1%),而维州一个农场的流行率最低(断奶时为 7.2%)。在所有州,断奶、断奶后和宰前的包囊脱落范围为 63-1.3×10(9)个包囊 g(-1)(中位数=1.7×10(4))、63-1.1×10(9)个包囊 g(-1)(中位数=9.6×10(3))、63-4.7×10(9)个包囊 g(-1)(中位数=8.1×10(4))。三磷酸甘油醛异构酶(tpi)基因座的种特异性引物在 473 份阳性样本中鉴定出 22.4%(106/473)为 A 组、75.9%(359/473)为 E 组和 1.7%(8/473)为 AE 混合组。从 8 个农场中选择了代表性样本子集(n=32),在 gdh 和β-微管蛋白基因座进行了分型,并确认了这些结果,并在 8 个农场的 16 个代表性 A 组分离株中鉴定出亚组 AII。这表明在澳大利亚绵羊中存在以前未被识别的贾第虫,这突显了进一步研究量化这种原生动物寄生虫对生产影响的必要性。