期刊
MOLECULAR AND BIOCHEMICAL PARASITOLOGY
卷 180, 期 1, 页码 62-67出版社
ELSEVIER
DOI: 10.1016/j.molbiopara.2011.07.007
关键词
Sheep; Strongylid nematodes; PCR; Diagnosis; DNA extraction; McMaster faecal worm egg count
资金
- Australian Research Council (ARC)
Patent strongylid nematode infections were identified using McMaster worm egg counts (WEC) and PCR assays (ITS-2 nuclear ribosomal DNA) to screen genomic DNA extracted directly from lamb faecal samples. Lambs from four different farms in southern Western Australia were sampled rectally on two separate occasions, with McMaster WECs and PCRs conducted oh a total of 858 samples. Negative controls (n=96) (WEC <50 eggs per gram [epg]) and positive controls (n=96) (faecal samples spiked with a 100 mu L suspension of third-stage larvae (L-3) containing approximately equal proportions of Teladorsagia circumcincta, Trichostrongylus colubriformis, Haemonchus contortus, Oesophagostomum spp. and Chabertia ovina) were generated. All control samples amplified in accordance with positive controls. High levels of agreement (Kappa values >= 0.93) were identified between the two diagnostic tests. PCRs detected an additional 2.0% of samples as strongylid-positive but there was no significant difference in the number of strongylid-positive samples identified using PCR or McMaster WEC. (C) 2011 Elsevier B.V. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据