Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, 501 D.W. Brooks Drive, Athens, GA, 30602, USA.
Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, 501 D.W. Brooks Drive, Athens, GA, 30602, USA.
Int J Parasitol Drugs Drug Resist. 2021 Apr;15:134-143. doi: 10.1016/j.ijpddr.2021.02.004. Epub 2021 Feb 18.
A population of Haemonchus contortus that was highly resistant to benzimidazoles and avermectin/milbemycins with a subpopulation that was resistant to levamisole, was replaced with a susceptible laboratory isolate of H. contortus in a flock of sheep. The anthelmintic susceptibility and population genetics of the newly established population were evaluated for 3.5 years using in vivo, in vitro, and molecular methods. Successful replacement of the resistant population with a susceptible population was confirmed using phenotypic and genotypic measurements; larval development assay indicated full anthelmintic susceptibility; albendazole treatment yielded 98.7% fecal egg count reduction; pyrosequence genotyping of single nucleotide polymorphisms in positions 167 and 200 of the isotype-1 beta tubulin gene were present at 0.0 and 1.7%, respectively; microsatellite genotyping indicated the background haplotype was similar to the susceptible isolate; and haplotypes of the isotype-1 beta tubulin gene were similar to the susceptible isolate. To sustain the susceptibility of the new population, targeted selective treatment was implemented using albendazole. Surprisingly, within 1.5 years post-replacement, the population reverted to a resistant phenotype. Resistance to albendazole, ivermectin, and moxidectin was confirmed via fecal egg count reduction test, larval development assay, and pyrosequencing-based genotyping. Targeted selective treatment was then carried out using levamisole. However, within one year, resistance was detected to levamisole. Population genetics demonstrated a gradual change in the genetic structure of the population until the final population was similar to the initial resistant population. Genetic analyses showed a lack of diversity in the susceptible isolate, suggesting the susceptible isolate had reduced environmental fitness compared to the resistant population, providing a possible explanation for the rapid reversion to resistance. This work demonstrates the power of combining molecular, in vitro, and in vivo assays to study phenotypic and genotypic changes in a field population of nematodes, enabling improved insights into the epidemiology of anthelmintic resistance.
一个对苯并咪唑类药物和阿维菌素/米尔贝肟高度耐药的捻转血矛线虫种群,其中一个亚群对左旋咪唑耐药,在一群绵羊中被一个易感性的实验室分离株捻转血矛线虫取代。使用体内、体外和分子方法,在 3.5 年内评估了新建立种群的驱虫敏感性和群体遗传学。通过表型和基因型测量证实了耐药种群被易感性种群成功取代;幼虫发育试验表明完全驱虫敏感性;阿苯达唑治疗产生 98.7%的粪便卵计数减少;在 167 位和 200 位的 1 型β微管蛋白基因的单核苷酸多态性的焦测序基因分型分别为 0.0%和 1.7%;微卫星基因分型表明背景单倍型与易感性分离株相似;并且 1 型β微管蛋白基因的单倍型与易感性分离株相似。为了维持新种群的敏感性,使用阿苯达唑实施了靶向选择性治疗。令人惊讶的是,在替换后 1.5 年内,种群恢复到耐药表型。通过粪便卵计数减少试验、幼虫发育试验和基于焦测序的基因分型证实了对阿苯达唑、伊维菌素和莫昔克丁的耐药性。然后使用左旋咪唑进行靶向选择性治疗。然而,在一年内,检测到左旋咪唑耐药。群体遗传学表明,种群的遗传结构逐渐发生变化,直到最终种群与初始耐药种群相似。遗传分析显示,易感性分离株缺乏多样性,这表明易感性分离株的环境适应性比耐药种群差,这可能是耐药性迅速恢复的原因之一。这项工作展示了结合分子、体外和体内试验研究线虫田间种群表型和基因型变化的能力,为驱虫耐药性的流行病学提供了更好的见解。