阿苯达唑对Nsukka屠宰场交易山羊产的圆形虫卵的体外防治效果:阿苯达唑耐药性的初步调查

I. Idika, V. J. Ebuk, E. Okoro, T. Nzeakor, N. M. Uzonnah, C. Nwosu
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摘要

采用体外卵孵化试验(EHA)模型,评价了阿苯达唑对Nsukka市屠宰场供屠宰山羊毛线虫寄生虫的杀灭效果。连续4个月,每周访问屠宰场1次,共取样240只山羊。每天至少从15只山羊的每个直肠收集粪便样本。每天用2.5% W/V的阿苯达唑对收集的粪样中回收的圆形卵进行孵化试验。在每个采样日对收集的粪便样本进行粪便培养,以恢复和鉴定山羊体内的线虫寄生虫。在240只山羊中,通过圆形虫卵观察到的毛线虫病患病率为94.6%(227/240)。粪便培养和幼虫鉴定显示,69.8%的圆形虫为弯血蜱,25.5%为色状毛线虫,4.8%为食道口虫。在EHA中,阿苯达唑的平均LC50值为0.16 μg/ml,略高于世界兽医寄生虫学发展协会(WAAVP)规定的0.1μg/ml作为抗虫指标的鉴别剂量。因此,迫切需要筛查尼日利亚线虫寄生虫种群中是否存在阿苯达唑耐药基因。
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In vitro Efficacy of Albendazole against Strongyle eggs recovered from Trade Goats slaughtered at the Nsukka Abattoir: A Preliminary Survey of Resistance to Albendazole
The efficacy of Albendazole against trichostrongyle nematode parasites in goats presented for slaughter at the Nsukka municipal abattoir was evaluated using the In vitro Egg hatch assay (EHA) model. The abattoir was visited once every week for 4 consecutive months during which a total of 240 goats were sampled. Fecal samples were collected per rectum from a minimum of 15 goats on each day of the visit. Egg Hatch Assay was performed on strongyle eggs recovered from pooled faecal sample on each day of sampling with a 2.5% W/V Albendazole. Faecal culture was also set up from the pooled faecal sample on each sampling day to recover and identify the nematode parasites present in the goats. Among the 240 goats sampled, the prevalence of trichostrongylosis as observed by the presence of strongyle eggs was 94.6% (227/240). Faecal culture and larval identification revealed 69.8% of the strongyles as Haemonchus contortus, while 25.5 and 4.8% were Trichostrongylus colubriformis and Oesophagostomum species respectively. In the EHA, Albendazole had mean LC50 value of 0.16 μg/ml which is slightly in excess of the discriminating dose of 0.1μg/ml as prescribed by the World Association for the Advancement of Veterinary Parasitology (WAAVP) as an indication of anthelmintic resistance. There is therefore an urgent need to screen the nematode parasite population in the Nigeria for the presence Albendazole resistance genes.
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