Stromberg Bert E, Gasbarre Louis C, Ballweber Lora R, Dargatz David A, Rodriguez Judith M, Kopral Christine A, Zarlenga Dante S
College of Veterinary Medicine, University of Minnesota, St. Paul, Minnesota (Stromberg); United States Department of Agriculture (USDA), Agricultural Research Service (ARS), Bovine Functional Genomics Lab, Beltsville, Maryland (Gasbarre); Colorado State University, Veterinary Diagnostic Laboratory, Fort Collins, Colorado (Ballweber); USDA, Animal and Plant Health Inspection Service (APHIS), Veterinary Service (VS) Centers for Epidemiology and Animal Health, Fort Collins, Colorado (Dargatz, Rodriguez, Kopral); USDA, ARS, Animal Parasitic Diseases Lab, Beltsville, Maryland, USA (Zarlenga).
Can J Vet Res. 2015 Oct;79(4):290-5.
During the United States Department of Agriculture (USDA) National Animal Health Monitoring System's (NAHMS) 2007-2008 beef study, 567 producers from 24 US States were offered the opportunity to collect fecal samples from weaned beef calves and have them evaluated for the presence of parasite eggs (Phase 1). Participating producers were provided with instructions and materials for sample collection. Up to 20 fresh fecal samples were collected from each of the 99 participating operations. Fresh fecal samples were submitted to one of 3 randomly assigned laboratories for evaluation. Upon arrival at the laboratories, all samples were processed for the enumeration of strongyle, Nematodirus, and Trichuris eggs using the modified Wisconsin technique. The presence or absence of coccidian oocysts and tapeworm eggs was also noted. In submissions where the strongyle eggs per gram exceeded 30, aliquots from 2 to 6 animals were pooled for DNA extraction. Extracted DNA was subjected to genus level polymerase chain reaction (PCR) identification for the presence of Ostertagia, Cooperia, Haemonchus, Oesophagostomum, and Trichostrongylus. In this study, 85.6% of the samples had strongyle type, Nematodirus, and Trichuris eggs. Among the samples evaluated, 91% had Cooperia, 79% Ostertagia, 53% Haemonchus, 38% Oesophagostomum, 18% Nematodirus, 7% Trichuris, and 3% Trichostrongylus. The prevalence of coccidia and tapeworm eggs was 59.9% and 13.7%, respectively.
在美国农业部(USDA)国家动物健康监测系统(NAHMS)2007 - 2008年的牛肉研究中,来自美国24个州的567名生产者有机会收集断奶牛肉犊的粪便样本,并对其进行寄生虫卵检测(第一阶段)。参与的生产者收到了样本收集的说明和材料。从99个参与养殖场中的每个养殖场最多收集20份新鲜粪便样本。新鲜粪便样本被提交到3个随机分配的实验室之一进行评估。样本抵达实验室后,使用改良的威斯康星技术对所有样本进行处理,以计数圆线虫、细颈线虫和鞭虫的虫卵。同时也记录球虫卵囊和绦虫卵的有无情况。在每克粪便中圆线虫卵超过30个的样本中,将2至6只动物的等分样本合并用于DNA提取。提取的DNA进行属水平的聚合酶链反应(PCR)鉴定,以检测奥斯特他线虫、古柏线虫、血矛线虫、食道口线虫和毛圆线虫的存在情况。在本研究中,样本中有85.6%含有圆线虫类、细颈线虫和鞭虫的虫卵。在评估的样本中,91%含有古柏线虫,79%含有奥斯特他线虫,53%含有血矛线虫,38%含有食道口线虫,18%含有细颈线虫,7%含有鞭虫,3%含有毛圆线虫。球虫和绦虫卵的检出率分别为59.9%和13.7%。