Barth D, Rehbein S, Reid J F, Barrick R A
Merck Research Laboratories, Rohrdorf-Lauterbach, Germany.
Vet Parasitol. 1996 Oct 15;65(1-2):89-97. doi: 10.1016/0304-4017(96)00939-9.
The efficacy of an in-feed formulation (IVOMEC premix) containing 0.6% ivermectin was tested against Strongyloides ransomi in swine. The efficacy of ivermectin against patent infections of S. ransomi when given via the feed at 2 ppm for 7 days (Days 0-7) to provide 100 mcg ivermectin kg-1 body weight day-1 was evaluated in a study with 16 3-month-old male castrated piglets. Seven days prior to treatment each piglet was infected subcutaneously with 2500 infective larvae of S. ransomi. Fecal egg counts were carried out on Days -7, 0, 7 and 14, and worm counts on Day 14. Efficacy was 100% in all treated piglets. Two trials involving 40 pregnant gilts were carried out to evaluate the efficacy of ivermectin against the somatic larval stages of S. ransomi when given at a daily dose of 100 mcg kg-1 body weight for 7 days starting on Days 66, 78, 92 or 103 of pregnancy. The gilts were each experimentally infected with three subcutaneous injections of 250,000 infective larvae, with the last infection given between 12 and 30 days prior to commencement of treatment. Gilts were confirmed free of pre-existing intestinal stages of S. ransomi prior to ivermectin treatment. Fecal nematode egg counts were carried out in gilts/sows and piglets subsequently born. The Strongyloides larvae present in sow milk 1, 2 and 7 days post partum were counted. Fourteen days post natum, worm counts were performed in four randomly selected piglets for each litter. IVOMEC premix given to pregnant gilts prevented shedding of larvae in sow milk, egg output in feces and the establishment of S. ransomi in piglets.
对含0.6%伊维菌素的预混剂(IVOMEC预混剂)针对猪体内兰氏类圆线虫的疗效进行了测试。在一项研究中,对16头3月龄雄性去势仔猪评估了伊维菌素以2 ppm的剂量通过饲料给药7天(第0 - 7天),以提供100 mcg伊维菌素/千克体重/天,对兰氏类圆线虫显性感染的疗效。在治疗前7天,每头仔猪皮下接种2500条兰氏类圆线虫感染性幼虫。在第 - 7、0、7和14天进行粪便虫卵计数,并在第14天进行虫体计数。所有治疗仔猪的疗效均为100%。进行了两项涉及40头妊娠后备母猪的试验,以评估伊维菌素在妊娠第66、78、92或103天开始,以100 mcg/千克体重的日剂量给药7天,针对兰氏类圆线虫体幼虫期的疗效。每头后备母猪通过皮下注射三次250,000条感染性幼虫进行实验感染,最后一次感染在治疗开始前12至30天进行。在伊维菌素治疗前,确认后备母猪不存在兰氏类圆线虫的肠道前期感染。对后备母猪/母猪及其随后出生的仔猪进行粪便线虫虫卵计数。对产后1、2和7天母猪乳汁中的类圆线虫幼虫进行计数。产后14天,对每窝随机选择的4头仔猪进行虫体计数。给妊娠后备母猪投喂IVOMEC预混剂可防止母猪乳汁中幼虫排出、粪便中虫卵产出以及仔猪感染兰氏类圆线虫。