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利用幼虫发育试验预测左旋咪唑对捻转血矛线虫和蛇形毛圆线虫的体内疗效。

The use of the larval development assay for predicting the in vivo efficacy of levamisole against Haemonchus contortus and Trichostrongylus colubriformis.

作者信息

Ruffell Angela, Raza Ali, Elliott Timothy P, Kotze Andrew C

机构信息

CSIRO Agriculture and Food, Brisbane, Queensland, Australia.

Invetus, Trevenna Road, Armidale, New South Wales, Australia.

出版信息

Vet Parasitol. 2018 Aug 30;260:6-11. doi: 10.1016/j.vetpar.2018.07.013. Epub 2018 Jul 30.

Abstract

The larval development assay has been used for many years to measure the sensitivity of the free-living life stages of trichostrongylid nematodes to anthelmintics. The assay has applications in both drug discovery and the diagnosis of drug resistance. We revisited the usefulness of the larval development assay for diagnosis of resistance to levamisole using field-derived isolates of Haemonchus contortus and Trichostrongylus colubriformis showing varying levels of resistance to this drug in vivo. Each of the resistant isolates showed a plateau in their larval development assay dose-response at the highest drug concentrations tested, representing a highly-resistant fraction, amounting to between 6.9 and 55.1% of the populations. The remaining population fractions for the resistant isolates showed IC values from 1.4- to 17.8-fold higher than their corresponding susceptible isolate of the same species. We used a data set from the DrenchRite test user manual to derive equations describing the relationship between the IC values for these low / moderate resistance components of each population and in vivo drug efficacy, and then used these equations to estimate the expected in vivo efficacy of levamisole against this population component of each isolate. A combination of this expected efficacy, with the known zero efficacy of the drug in vivo against the highly-resistant population fractions in each isolate, allowed us to calculate a predicted drug efficacy for the whole population for each isolate. The predicted levamisole efficacies for the three resistant H. contortus isolates were 88.8, 84.1 and 43.7%. These compared favourably with the actual efficacy of the drug against these isolates as determined in faecal egg count reduction tests or total worm count studies: 79, 66.3 and 40.6%, respectively. Similarly, for T. colubriformis, predicted efficacies of 82.0 and 1.8% compared favourably with the actual efficacies of 65-92 % and 0%, respectively. This study illustrates the usefulness of the larval development assay as a diagnostic tool for predicting in vivo efficacy of levamisole against H. contortus and T. colubriformis.

摘要

幼虫发育试验多年来一直用于测定毛圆科线虫自由生活阶段对驱虫药的敏感性。该试验在药物研发和耐药性诊断中均有应用。我们利用从野外分离得到的捻转血矛线虫和蛇形毛圆线虫分离株,重新评估了幼虫发育试验在诊断左旋咪唑耐药性方面的实用性,这些分离株在体内对该药物表现出不同程度的耐药性。在最高测试药物浓度下,每个耐药分离株的幼虫发育试验剂量反应均出现平台期,代表了一个高耐药部分,占群体的6.9%至55.1%。耐药分离株的其余群体部分显示出的半数抑制浓度(IC)值比同一物种相应的敏感分离株高1.4至17.8倍。我们使用来自DrenchRite测试用户手册的数据集推导方程,描述每个群体中这些低/中度耐药成分的IC值与体内药物疗效之间的关系,然后使用这些方程估计左旋咪唑对每个分离株该群体成分的预期体内疗效。将这种预期疗效与药物在体内对每个分离株中高耐药群体部分已知的零疗效相结合,使我们能够计算每个分离株整个群体的预测药物疗效。对三个耐药捻转血矛线虫分离株的预测左旋咪唑疗效分别为88.8%、84.1%和43.7%。与在粪便虫卵计数减少试验或总虫数研究中确定的该药物对这些分离株的实际疗效相比,结果较为理想:分别为79%、66.3%和40.6%。同样,对于蛇形毛圆线虫,预测疗效分别为82.0%和1.8%,与实际疗效分别为65 - 92%和0%相比,结果较为理想。本研究说明了幼虫发育试验作为一种诊断工具在预测左旋咪唑对捻转血矛线虫和蛇形毛圆线虫体内疗效方面的实用性。

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