Martinsson K, Nilsson O
Nord Vet Med. 1985 Mar-Apr;37(2):80-9.
The full potential of anthelmintics now available for single dose treatment is not achieved because the devising system for worm control in piglets/weaners is not efficiently applicable in practice. Therefore an in-feed medication programme for growing young pigs, allowing only one feed lot to be handled by the farmer, was tested in two studies. Study A Feed containing 0.0225% thiophanate was continuously fed almost ad lib. to piglets from birth right up to about 25 kg body weight when ready for fattening. This control measure effectively prevented A. suum and Oesophagostomum from becoming established during the whole pre-fattening period, thus allowing "worm-free" weaners to be produced. -33% of animals receiving unmedicated feed harboured mature Oesophagostomum already at an age of 63 days when first examined. Three out of 97 unmedicated pigs were then A. suum egg-count positive. At the same time all medicated pigs, except one with a low Oesophagostomum egg output, were egg-count negative. All medicated were still egg-count negative at 23-29 days after the withdrawal of the feed. About 30% of unmedicated pigs were then shedding eggs of A. suum and Oesophagostomum respectively. At 45-49 days after the withdrawal of the medicated feed 8% of previously medicated pigs and 43% of unmedicated pigs were A. suum egg-count positive. The corresponding figures for Oesophagostomum egg-count positive pigs were 6% and 40% respectively. The acquisition of worm infections by previously medicated pigs most probably was made in the fattening unit after the withdrawal of the thiophanate medicated feed. Study B In this study it was further substantiated that in-feed medication of pigs with thiophanate prevents A. suum from becoming established. All treated pigs were A. suum egg-count negative at Day 43 and 46 after the withdrawal of the medicated feed whereas about 62% of untreated control pigs were shedding A. suum eggs at the same time. This finding justify the proposal that the in-feed medication performed prevented larval migration. Furthermore it was shown that the in-feed medication must proceed right up to the transfer of piglets to the fattening unit in order to achieve its full potential. Farrowing pens may be heavily contaminated with infective Oesophagostomum larvae at the end of the pre-fattening period resulting in sudden and heavy nodular worm infections after the withdrawal of the medicated feed.
现有的单剂量驱虫药的全部潜力尚未实现,因为仔猪/断奶仔猪的蠕虫控制设计系统在实际应用中效率不高。因此,在两项研究中对一种适用于生长育肥猪的饲料给药方案进行了测试,该方案允许养殖户只管理一个饲养栏。研究A:含0.0225% 甲基托布津的饲料几乎不限量地持续喂给从出生到体重约25千克准备育肥的仔猪。这种控制措施有效地防止了猪蛔虫和结节虫在整个育肥前期定殖,从而能够培育出 “无蠕虫” 的断奶仔猪。-33% 食用未加药饲料的动物在63日龄首次检查时就已感染成熟的结节虫。97头未加药的猪中有3头猪蛔虫虫卵计数呈阳性。与此同时,所有加药的猪,除了一头结节虫虫卵排出量低的猪外,虫卵计数均为阴性。在停止喂食后23 - 29天,所有加药猪的虫卵计数仍为阴性。此时,约30% 未加药的猪分别排出猪蛔虫和结节虫的虫卵。在停止喂食含药饲料45 - 49天后,8% 先前加药的猪和43% 未加药的猪猪蛔虫虫卵计数呈阳性。结节虫虫卵计数呈阳性的猪的相应数字分别为6% 和40%。先前加药的猪感染蠕虫很可能是在停用甲基托布津加药饲料后在育肥单元中发生的。研究B:在这项研究中,进一步证实了用甲基托布津对猪进行饲料给药可防止猪蛔虫定殖。在停用含药饲料后的第43天和第46天,所有处理过的猪猪蛔虫虫卵计数均为阴性,而约62% 未处理的对照猪在同一时间排出猪蛔虫虫卵。这一发现证明了所进行的饲料给药可防止幼虫移行这一观点。此外,研究表明,饲料给药必须持续到仔猪转入育肥单元,才能充分发挥其潜力。在育肥前期结束时,产仔栏可能被感染性结节虫幼虫严重污染,导致停用含药饲料后突然发生严重的结节虫感染。