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使用比较PCR-RFLP方法评估捻转血矛线虫对苯并咪唑的抗性

Evaluation of Benzimidazole Resistance in Haemonchus contortus Using Comparative PCR-RFLP Methods.

作者信息

Nabavi R, Shayan P, Shokrani Hr, Eslami A, Bokaie S

机构信息

Department of Parasitology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.

出版信息

Iran J Parasitol. 2011 Jun;6(2):45-53.

Abstract

BACKGROUND

In order to deworm the ruminants especially of sheep in Iran, consumption of benzimidazoles has more than 2 decades history and today farmers are using imidazothiazoles, macrocyclic lactones and mostly benzimidazole compounds (BZs) to treat infected farm animals. It has been demonstrated that the most common molecular mechanism leading to BZsresistance in Haemonchus contortus is a single mutation at amino acid 200 (phenylalanine to tyrosine) of the isotype 1 of beta tubulin gene. According to the report of such mutations in Iranian Teladorsagia circumcincta isolates with Restriction Site Created PCR-RFLP, we decided to evaluate the frequency of such mutations in H. contortus in three different geographical areas of Iran.

METHODS

A total of 102 collected adult male H. contortus were evaluated with PCR-RFLP (using PSP1406I as restriction enzyme). By means of a second step to compare function of different methods and to increase sensitivity of detection mechanism, a third of samples were examined by another PCR-RFLP method (using TaaI as restriction enzyme) and finally beta tubulin gene of two samples was sequenced.

RESULTS

All of samples were detected as BZss homozygote. Finally, beta tubulin gene sequencing of two samples showed no point mutation at codon 200.

CONCLUSION

It seems that BZresistance of H. contortus in Iran is not a serious problem as anticipated before.

摘要

背景

为给伊朗的反刍动物尤其是绵羊驱虫,苯并咪唑的使用已有20多年历史,如今农民们使用咪唑噻唑、大环内酯类药物,且大多使用苯并咪唑类化合物(BZs)来治疗受感染的农场动物。已证明,导致捻转血矛线虫对BZs产生抗性的最常见分子机制是β微管蛋白基因1型的第200位氨基酸(苯丙氨酸突变为酪氨酸)发生单一突变。根据伊朗环形泰勒虫分离株中此类突变的限制性内切酶切位点创建PCR-RFLP报告,我们决定评估伊朗三个不同地理区域捻转血矛线虫中此类突变的频率。

方法

使用PCR-RFLP(以PSP1406I作为限制性内切酶)对总共102条采集的成年雄性捻转血矛线虫进行评估。通过第二步比较不同方法的功能并提高检测机制的灵敏度,三分之一的样本通过另一种PCR-RFLP方法(以TaaI作为限制性内切酶)进行检测,最后对两个样本的β微管蛋白基因进行测序。

结果

所有样本均被检测为BZs纯合子。最后,两个样本的β微管蛋白基因测序显示第200密码子无点突变。

结论

看来伊朗捻转血矛线虫对BZs的抗性并非如之前预期的那样是一个严重问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49a5/3279878/6b1e7ca95a4e/IJP-6-045-g001.jpg

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