Hazrati Tappeh Khosro, Manafi Gholamreza, Asgharzadeh Mohammad, Manafi Farideh
Center for Research of Cellular and Molecular of Urmia, Urmia University of Medical Sciences, Urmia, Iran.
Dept. of Medical Parasitology, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Iran J Parasitol. 2014 Oct-Dec;9(4):541-7.
Giardia lamblia is one of the most prevalent intestinal flagellate protozoa that infects a wide range of vertebrate hosts causing severe intestinal disorder in children.This study was performed to determine subspecies of G.lamblia by the PCR-RFLP method, targeting the glutamate dehydrogenase(gdh)locus, in hospitalized children at Urmia Mutahhari Hospital, West Azerbaijan Province,Iran and determining the infection transformational storages in this area.
Overall, 720 stool specimens were collected from the hospitalized children, 34 samples were positive and Giardia cysts were detected under the microscope. Cysts were partially purified by the sucrose density gradient method and then washed with sterile distilled water to remove effectively the PCR inhibitors. Genomic DNA of G. lamblia isolates was extracted by freeze-thaw cycles followed by phenol/ chloroform/isoamyl alcohol method. The single step PCR-RFLP assay was used to differentiate the assemblages between A and B, which were found in humans. In this method, 432 bp expected size was amplified, and then for detection of subspecies, specific restriction RsaI and BspLI enzymes were used.
Totally 34 samples were positive in terms of Giardia cyst out of 720 examined samples microscopically, so the parasite spread rate is reported 4.72%. Analysis PCR-RFLP on these samples revealed that 28 samples (93.3%) have the genotype BIII and 2 samples (6.7%) belong to the subgroup BIV.
PCR-RFLP is a proper analytical method for determining the genotype among parasite types, using the glutamate dehydrogenizes zone's genes. Based on the results, an animal origin of infection cycle is suggested.
蓝氏贾第鞭毛虫是最常见的肠道鞭毛虫原生动物之一,可感染多种脊椎动物宿主,导致儿童严重肠道疾病。本研究旨在通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,以谷氨酸脱氢酶(gdh)基因座为靶点,确定伊朗西阿塞拜疆省乌尔米亚穆塔哈里医院住院儿童中蓝氏贾第鞭毛虫的亚种,并确定该地区的感染传播情况。
总共从住院儿童中收集了720份粪便标本,其中34份样本呈阳性,显微镜下检测到贾第虫囊肿。通过蔗糖密度梯度法对囊肿进行部分纯化,然后用无菌蒸馏水洗涤,以有效去除PCR抑制剂。采用冻融循环结合苯酚/氯仿/异戊醇法提取蓝氏贾第鞭毛虫分离株的基因组DNA。采用单步PCR-RFLP分析法区分在人类中发现的A和B两种组合。在该方法中,扩增出预期大小为432 bp的片段,然后使用特异性限制性内切酶RsaI和BspLI检测亚种。
在720份经显微镜检查的样本中,共有34份样本的贾第虫囊肿呈阳性,因此报告的寄生虫传播率为4.72%。对这些样本进行的PCR-RFLP分析显示,28份样本(93.3%)具有BIII基因型,2份样本(6.7%)属于BIV亚组。
PCR-RFLP是一种利用谷氨酸脱氢酶区域基因确定寄生虫类型基因型的合适分析方法。根据结果,提示感染周期的动物源性。