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开发一种用于贾第虫的定量 PCR(qPCR)方法,并分析澳大利亚四个州绵羊中贾第虫的流行情况、囊包脱落情况和基因型。

Development of a quantitative PCR (qPCR) for Giardia and analysis of the prevalence, cyst shedding and genotypes of Giardia present in sheep across four states in Australia.

机构信息

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.

出版信息

Exp Parasitol. 2014 Feb;137:46-52. doi: 10.1016/j.exppara.2013.12.004. Epub 2013 Dec 16.

Abstract

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.

摘要

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。

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