Shayan Parviz, Eslami Ali, Borji Hassan
Department of Parasitology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.
Parasitol Res. 2007 Apr;100(5):1063-8. doi: 10.1007/s00436-006-0357-y. Epub 2006 Nov 30.
Benzimidazole compounds, especially albendazole, are the most commonly used anthelmintics for deworming of small ruminants in Iran. It is believed that the therapeutic effects of the benzimidazoles (BZs) come through their binding capacity to the beta-tubulin isotype 1. Substitution of phenylalanine to tyrosine at position 200 of this polypeptide confers resistance to BZs. Several investigators developed different biological- and molecular-based techniques to demonstrate the occurrence of resistance in helminthes against BZs. To address the determination of resistance at position 200 of beta-tubulin isotype 1, we developed an innovative restriction site created polymerase chain reaction-restriction fragment length polymorphism, in which nucleotide A at the position of 637 upstream flanked by the first two coding sequences of the phenylalanine (TT) triplet was substituted through the nucleotide G. The introduced modification in forward primer (UTvet MF-primer) leads to the creation of restriction site (AACGTT) for PSP1. Therefore, in the case of normal allele only, PSP1 can cut the corresponding PCR product. In the first step, the genomic DNA was isolated from each single Teladorsagia circumcincta collected either from the abomasa of untreated (n = 35) or of 5 mg/kg BW 2.5% albendazole suspension-treated (n = 40) sheep. It was amplified with the primer pair, creating PCR product of 403 bp in length. In the second step, the PCR product was extracted from agarose gel and amplified with the modified forward primer (UTvet MF-primer) and the same reverse primer as in step 1, creating a PCR product of 222 bp. The PCR product was then cut with PSP1 to obtain in the case of normal allele two DNA products (183 and 39 bp). Eight of the 35 worms collected from the untreated sheep were BZ(SS) homozygotes, and the rest (27) were BZ(RS) heterozygotes. In our preliminary experiment, we could not find a BZ(RR) homozygote form within the examined samples. Five out of 40 worms collected from the albendazole-treated sheep were BZ(RR) homozygotes, whereas the rest (35) were BZ(RS) heterozygotes. No BZ(SS) homozygote form was detected within this group.
苯并咪唑类化合物,尤其是阿苯达唑,是伊朗用于小反刍动物驱虫最常用的驱虫药。据信,苯并咪唑类药物(BZs)的治疗作用是通过它们与β-微管蛋白同种型1的结合能力来实现的。该多肽第200位的苯丙氨酸被酪氨酸取代会导致对BZs产生抗性。一些研究人员开发了不同的基于生物学和分子的技术来证明蠕虫对BZs产生抗性的情况。为了确定β-微管蛋白同种型1第200位的抗性,我们开发了一种创新的限制性位点创建聚合酶链反应-限制性片段长度多态性方法,其中苯丙氨酸(TT)三联体的前两个编码序列侧翼的第637位的核苷酸A被核苷酸G取代。正向引物(UTvet MF-引物)中引入的修饰导致产生了PSP1的限制性位点(AACGTT)。因此,仅在正常等位基因的情况下,PSP1才能切割相应的PCR产物。第一步,从未经处理(n = 35)或经5 mg/kg体重2.5%阿苯达唑悬浮液处理(n = 40)的绵羊皱胃中收集的每一条环纹奥斯特线虫中分离基因组DNA。用引物对进行扩增,产生长度为403 bp的PCR产物。第二步,从琼脂糖凝胶中提取PCR产物,并用修饰后的正向引物(UTvet MF-引物)和与第一步相同的反向引物进行扩增,产生长度为222 bp的PCR产物。然后用PSP1切割PCR产物,在正常等位基因的情况下获得两个DNA产物(183和39 bp)。从未经处理的绵羊收集的35条蠕虫中有8条是BZ(SS)纯合子,其余(27条)是BZ(RS)杂合子。在我们的初步实验中,在所检测的样本中未发现BZ(RR)纯合子形式。从经阿苯达唑处理的绵羊收集的40条蠕虫中有5条是BZ(RR)纯合子,而其余(35条)是BZ(RS)杂合子。在该组中未检测到BZ(SS)纯合子形式。