Rodrigues Janaelia Ferreira Vasconcelos, Monteiro Jomar Patricio, Almeida Thayany Magalhães, Molento Marcelo Beltrão
Federal University of Paraná, UFPR, Av. Cel. Francisco H. dos Santos, 100, Curitiba, PR CEP: 81530-000, Brazil; Laboratory of Veterinary Clinical Parasitology, Federal University of Paraná, UFPR, R: dos Funcionários, 1540, Curitiba, PR CEP: 81530-000, Brazil.
Embrapa Caprinos e Ovinos, Estrada Sobral-Groaíras, Km 04. C.P.: 145, Sobral, CE CEP: 62010-970, Brazil.
Vet Parasitol. 2025 Feb;334:110394. doi: 10.1016/j.vetpar.2025.110394. Epub 2025 Jan 14.
Haemonchus contortus is a gastrointestinal parasite that affects ruminants (cattle, sheep, etc.), having a significant welfare impact worldwide. The rise of anthelmintic resistance poses a growing challenge to adequate control, compromising the success of treatments. This study presents a systematic review of the molecular mechanisms involved in the resistance of H. contortus to anthelmintic drugs. Following an extensive literature search (9075 total articles/excluding duplications), 61 articles were examined. From these, benzimidazoles (BZD) and macrocyclic lactone (ML) were the most reported drug classes (17 and 29, respectively). The mutations in the β-tubulin gene were the primary mechanism of BZD resistance. Important comparisons from early reports of resistance mechanisms to ML (published before 2020) mainly based on parasite-population gene expression (e.g., ligand-gated chloride channels, LGCC, and P-glycoproteins, PGP) with more recent genomic and transcriptomic data (e.g., transcription factor, cky-1 gene) are highlighted. Additionally, resistance mechanisms to levamisole (LEV) and monepantel are discussed, showing evidence of polymorphisms in genes related to the nicotinic acetylcholine receptors (nAChR). Considering the available data, it is possible to divide the reports into two technological periods, evidencing that the availability of a chromosome-level genome for H. contortus in association with experiments based on controlled genetic crosses and transcriptome-wide data allowed for the visualization of genes and polymorphisms that were previously indistinguishable from unrelated genetic variation (i.e., genetic noise). Therefore, the study of anthelmintic resistance mechanisms is facing new possibilities, reflecting the large data banks and the speed at which this information is being processed. We suggest that new publications on drug resistance should adopt the approaches and refer to this new era of scientific discoveries. Consistent data interpretation, including artificial intelligence (AI) support, will help us to suggest novel biological mechanisms involved in drug resistance and predict its evolution, allowing a more comprehensible approach toward sustainable parasite control strategies.
捻转血矛线虫是一种影响反刍动物(牛、羊等)的胃肠道寄生虫,在全球范围内对动物福利有重大影响。驱虫药耐药性的上升对充分控制寄生虫构成了越来越大的挑战,危及治疗的成功率。本研究对捻转血矛线虫对驱虫药耐药性所涉及的分子机制进行了系统综述。在广泛的文献检索(共9075篇文章/不包括重复文章)之后,审查了61篇文章。其中,苯并咪唑类(BZD)和大环内酯类(ML)是报道最多的药物类别(分别为17篇和29篇)。β-微管蛋白基因突变是BZD耐药性的主要机制。从早期关于ML耐药机制的报告(2020年之前发表)进行的重要比较主要基于寄生虫群体基因表达(例如配体门控氯离子通道、LGCC和P-糖蛋白、PGP),并突出了更新的基因组和转录组数据(例如转录因子、cky-1基因)。此外,还讨论了左旋咪唑(LEV)和莫能菌素的耐药机制,显示了与烟碱型乙酰胆碱受体(nAChR)相关基因存在多态性的证据。考虑到现有数据,可以将报告分为两个技术阶段,这表明捻转血矛线虫染色体水平基因组的可用性,以及基于可控遗传杂交和全转录组数据的实验,使得以前与无关遗传变异(即遗传噪声)无法区分的基因和多态性得以显现。因此,驱虫药耐药机制的研究正面临新的可能性,反映了庞大的数据库以及处理这些信息的速度。我们建议关于耐药性的新出版物应采用这些方法并参考这个科学发现的新时代。包括人工智能(AI)支持在内的一致数据解释,将有助于我们提出涉及耐药性的新生物学机制并预测其演变,从而对可持续的寄生虫控制策略采取更易于理解的方法。