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当幼虫继续发育时确定抗蠕虫药物的抗性的方法。

Methods to determine resistance to anthelmintics when continuing larval development occurs.

机构信息

AgriScience Queensland, 41 Boggo Road, Dutton Park, QLD 4102, Australia.

Formerly AgriScience Queensland, 41 Boggo Road, Dutton Park, QLD 4102, Australia.

出版信息

Vet Parasitol. 2014 Jan 31;199(3-4):191-200. doi: 10.1016/j.vetpar.2013.11.002. Epub 2013 Nov 15.

DOI:10.1016/j.vetpar.2013.11.002
PMID:24314600
Abstract

The in vivo faecal egg count reduction test (FECRT) is the most commonly used test to detect anthelmintic resistance (AR) in gastrointestinal nematodes (GIN) of ruminants in pasture based systems. However, there are several variations on the method, some more appropriate than others in specific circumstances. While in some cases labour and time can be saved by just collecting post-drench faecal worm egg counts (FEC) of treatment groups with controls, or pre- and post-drench FEC of a treatment group with no controls, there are circumstances when pre- and post-drench FEC of an untreated control group as well as from the treatment groups are necessary. Computer simulation techniques were used to determine the most appropriate of several methods for calculating AR when there is continuing larval development during the testing period, as often occurs when anthelmintic treatments against genera of GIN with high biotic potential or high re-infection rates, such as Haemonchus contortus of sheep and Cooperia punctata of cattle, are less than 100% efficacious. Three field FECRT experimental designs were investigated: (I) post-drench FEC of treatment and controls groups, (II) pre- and post-drench FEC of a treatment group only and (III) pre- and post-drench FEC of treatment and control groups. To investigate the performance of methods of indicating AR for each of these designs, simulated animal FEC were generated from negative binominal distributions with subsequent sampling from the binomial distributions to account for drench effect, with varying parameters for worm burden, larval development and drench resistance. Calculations of percent reductions and confidence limits were based on those of the Standing Committee for Agriculture (SCA) guidelines. For the two field methods with pre-drench FEC, confidence limits were also determined from cumulative inverse Beta distributions of FEC, for eggs per gram (epg) and the number of eggs counted at detection levels of 50 and 25. Two rules for determining AR: (1) %reduction (%R)<95% and lower confidence limit <90%; and (2) upper confidence limit <95%, were also assessed. For each combination of worm burden, larval development and drench resistance parameters, 1000 simulations were run to determine the number of times the theoretical percent reduction fell within the estimated confidence limits and the number of times resistance would have been declared. When continuing larval development occurs during the testing period of the FECRT, the simulations showed AR should be calculated from pre- and post-drench worm egg counts of an untreated control group as well as from the treatment group. If the widely used resistance rule 1 is used to assess resistance, rule 2 should also be applied, especially when %R is in the range 90 to 95% and resistance is suspected.

摘要

体内粪便卵计数减少试验(FECRT)是检测放牧系统反刍动物胃肠道线虫(GIN)抗药性(AR)最常用的方法。然而,该方法有几种变体,在某些特定情况下,有些变体比其他变体更合适。虽然在某些情况下,通过仅收集处理组和对照组的驱虫后粪便蠕虫卵计数(FEC),或者处理组的驱虫前和驱虫后 FEC,可以节省劳动力和时间,但在某些情况下,需要对未经处理的对照组以及处理组进行驱虫前和驱虫后 FEC。使用计算机模拟技术来确定在测试期间持续幼虫发育的情况下,计算 AR 的最合适方法,这种情况经常发生在驱虫剂对具有高生物潜能或高再感染率的 GIN 属(如绵羊的捻转血矛线虫和牛的细颈线虫)的治疗效果低于 100%时。研究了三种田间 FECRT 实验设计:(I)处理组和对照组的驱虫后 FEC,(II)仅处理组的驱虫前和驱虫后 FEC,以及(III)处理组和对照组的驱虫前和驱虫后 FEC。为了研究每种设计指示 AR 的方法的性能,从具有后续抽样的二项分布中生成模拟动物 FEC,以考虑驱虫效果,蠕虫负担、幼虫发育和驱虫剂耐药性的参数各不相同。减少百分比和置信区间的计算基于农业常务委员会(SCA)指南。对于具有驱虫前 FEC 的两种田间方法,置信区间也可以从 FEC、每克粪便虫卵数(epg)和在检测水平为 50 和 25 时计数的卵数的累积逆 Beta 分布中确定。确定 AR 的两条规则:(1)%减少(%R)<95%,置信下限<90%;(2)置信上限<95%。对于每个蠕虫负担、幼虫发育和驱虫剂耐药性参数的组合,进行了 1000 次模拟,以确定理论百分比减少落入估计置信区间的次数,以及宣布耐药性的次数。当 FECRT 的测试期间发生持续的幼虫发育时,模拟结果表明,应该从未经处理的对照组以及处理组的驱虫前和驱虫后蠕虫卵计数中计算 AR。如果使用广泛使用的耐药性规则 1 来评估耐药性,则应应用规则 2,尤其是当 %R 在 90%至 95%之间并且怀疑存在耐药性时。

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