Alvi Mughees Aizaz, Alshammari Ayed, Ali Rana Muhammad Athar, Ul Haq Shahbaz, Bashir Rizwan, Li Li, Saqib Muhammad, Sajid Muhammad Sohail, Ghafoor Muzafar, Imran Muhammad, Ijaz Muhammad Umar, Fu Bao-Quan, Saeed Mohd, Ahmad Irfan, Liu You-Yu, Yan Hong-Bin, Jia Wan-Zhong
State Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, National Para-Reference Laboratory for Animal Echinococcosis, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.
Department of Clinical Medicine and Surgery, University of Agriculture, Faisalabad, Pakistan.
Front Vet Sci. 2023 Jun 16;10:1191271. doi: 10.3389/fvets.2023.1191271. eCollection 2023.
Cystic echinococcosis (CE) is a neglected zoonotic disease caused by (). The parasite affects a wide range of livestock and wild animals. In this study, the population diversity of the species was investigated based on mitochondrial cytochrome b (b) and NADH dehydrogenase subunit 5 (5) genes. In addition to this, β-tubulin gene isoforms of were amplified to determine the resistance against benzimidazoles. For this purpose, 40 cyst samples from cattle ( = 20) and buffaloes ( = 20) were collected from the main abattoir of Sialkot. DNA extraction was performed using Qiagen Blood and Tissue Kits. Amplification was performed through PCR. Each amplicon was confirmed by GelRed™ stained agarose gel (2%). Samples were sequenced in a DNA analyzer and viewed for any misread nucleotide by using MEGA (v.11). Corrections in nucleotide sequence and multiple sequence alignment were made through the same software. NCBI-BLAST was used for sample specific sequences to identify them as belonging to a particular species. Diversity indices were estimated using DnaSP (v.6) while phylogenetic analysis was inferred using the Bayesian method using MrBayes (v.1.1). β-tubulin gene isoforms sequence analysis was performed to find out the candidate gene causing benzimidazole resistance. All 40 isolates were found positive for BLAST-based searches of sequences of each isolate for each gene (5 and b) confirmed their maximum similarity with the G1 genotype. Overall, high haplotype diversity (Hd = 1.00; Hd = 0.833) and low nucleotide diversity ( = 0.00560; = 0.00763) was identified based on diversity indices. For both the genes, non-significant values of Tajima's D (5 = -0.81734; b = -0.80861) and Fu's Fs (5 = -1.012; b = 0.731) indicate recent population expansion. Bayesian phylogeny-based results of and sequences confirmed their genotypic status as distinct from other species. This study shed light on the status of benzimidazole resistance in for the very first time from Pakistan. The findings of this study will significantly add in the information available on genetic diversity of based on and genes sequences.
囊型包虫病(CE)是一种由()引起的被忽视的人畜共患病。该寄生虫会感染多种家畜和野生动物。在本研究中,基于线粒体细胞色素b(cyt b)和烟酰胺腺嘌呤二核苷酸脱氢酶亚基5(ND5)基因,对该物种的种群多样性进行了调查。除此之外,扩增了该虫的β-微管蛋白基因亚型,以确定其对苯并咪唑类药物的抗性。为此,从锡亚尔科特的主要屠宰场收集了40份来自牛(n = 20)和水牛(n = 20)的囊肿样本。使用Qiagen血液和组织试剂盒进行DNA提取。通过聚合酶链反应(PCR)进行扩增。每个扩增产物用GelRed™染色的2%琼脂糖凝胶进行确认。样本在DNA分析仪中进行测序,并使用MEGA(v.11)查看是否存在任何误读的核苷酸。通过同一软件对核苷酸序列进行校正和多序列比对。使用NCBI-BLAST对样本特异性序列进行鉴定,以确定它们属于特定物种。使用DnaSP(v.6)估计多样性指数,同时使用MrBayes(v.1.1)通过贝叶斯方法进行系统发育分析。进行β-微管蛋白基因亚型序列分析以找出导致苯并咪唑抗性的候选基因。所有40个分离株基于每个基因(ND5和cyt b)的序列进行基于BLAST的搜索均呈阳性,证实它们与G1基因型的最大相似性。总体而言,基于多样性指数确定单倍型多样性较高(Hd ND5 = 1.00;Hd cyt b = 0.833),核苷酸多样性较低(πND5 = 0.00560;πcyt b = 0.00763)。对于这两个基因,Tajima's D(ND5 = -0.81734;cyt b = -0.80861)和Fu's Fs(ND5 = -1.012;cyt b = 0.731)的非显著值表明种群近期有所扩张。基于贝叶斯系统发育的ND5和cyt b序列结果证实了它们的基因型状态与其他该虫物种不同。本研究首次揭示了巴基斯坦该虫对苯并咪唑类药物的抗性状况。本研究结果将显著增加基于ND5和cyt b基因序列的该虫遗传多样性方面的现有信息。