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2
Genotyping of Giardia duodenalis in children in upper Egypt using assemblage- specific PCR technique.采用虫种特异性聚合酶链反应技术对埃及上埃及地区儿童肠道贾第虫进行基因分型。
PLoS One. 2020 Oct 1;15(10):e0240119. doi: 10.1371/journal.pone.0240119. eCollection 2020.
3
Multilocus genotyping of Giardia duodenalis isolated from patients in Egypt.
Molecular Genotyping of in Humans in the Yazd County, Central of Iran.
伊朗中部亚兹德县人类的分子基因分型
Iran J Parasitol. 2024 Jan-Mar;19(1):98-104. doi: 10.18502/ijpa.v19i1.15216.
4
From microbes to molecules.从微生物到分子。
Trop Parasitol. 2022 Jan-Jun;12(1):1-2. doi: 10.4103/tp.tp_34_22. Epub 2022 Jun 26.
从埃及患者中分离出的十二指肠贾第虫的多位点基因分型。
Acta Trop. 2019 Aug;196:66-71. doi: 10.1016/j.actatropica.2019.05.012. Epub 2019 May 14.
4
Formalin-ethyl acetate concentration, FLOTAC Pellet and anal swab techniques for the diagnosis of intestinal parasites.用于诊断肠道寄生虫的福尔马林-乙酸乙酯浓缩法、FLOTAC沉淀法和肛门拭子技术。
Parasitol Res. 2018 Nov;117(11):3567-3573. doi: 10.1007/s00436-018-6054-9. Epub 2018 Aug 18.
5
Molecular characterization of Cryptosporidium spp. and Giardia duodenalis in children in Egypt.埃及儿童中隐孢子虫属和十二指肠贾第鞭毛虫的分子特征。
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聚合酶链反应-限制性片段长度多态性与组装特异性引物在儿童[具体内容缺失]特征分析中的比较

Comparison of polymerase chain reaction-restriction fragment length polymorphism and assemblage-specific primers for characterization of in children.

作者信息

Elhadad Heba, Abdo Sarah, Salem Aziza I, Mohamed Mostafa A, El-Taweel Hend A, El-Abd Eman A

机构信息

Department of Parasitology, Medical Research Institute, Alexandria University, Alexandria, Egypt.

Department of Parasitology, Faculty of Medicine, Medical Research Institute, Alexandria University, Alexandria, Egypt.

出版信息

Trop Parasitol. 2022 Jan-Jun;12(1):41-47. doi: 10.4103/tp.tp_28_21. Epub 2022 Jun 26.

DOI:10.4103/tp.tp_28_21
PMID:35923264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9341145/
Abstract

BACKGROUND

is a diarrheagenic eukaryotic parasite that consists of at least eight morphologically identical but genetically distinct genotypes. Human giardiasis is caused mainly by A and B assemblages.

AIM AND OBJECTIVES

The study aimed to compare the performance of polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and assemblage-specific primers in genotyping of .

MATERIALS AND METHODS

Stool samples of 315 children were microscopically screened for . Positive samples were genotyped using assemblage-specific primers and semi-nested PCR-RFLP techniques.

RESULTS

The prevalence of was 18.1%. The detected genotypes using and approaches were assemblage A (15.8% vs. 12.7%) and assemblage B (36.8% vs. 74.5%) as single infections and mixed assemblages A and B (47.4% vs. 12.7%). The two approaches showed a moderate agreement (kappa index = 0.413, < 0.001). PCR-RFLP of gene revealed that sub-assemblages BIII and BIV were equally detected (30.9% each). The remaining samples were equally divided between sub-assemblage AII, mixed BIII and BIV, and mixed AII and BIII (12.7% each). A significant association was detected between the retrieved sub-assemblages and the presence of symptoms.

CONCLUSIONS

Although both approaches confirmed the predominance of assemblage B, the use of assemblage-specific primers is more effective in elucidating the true picture of mixed assemblage infection.

摘要

背景

贾第虫是一种致腹泻的真核寄生虫,至少由八种形态相同但基因不同的基因型组成。人类贾第虫病主要由A和B基因型引起。

目的

本研究旨在比较聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和基因型特异性引物在贾第虫基因分型中的性能。

材料与方法

对315名儿童的粪便样本进行显微镜检查以筛查贾第虫。对阳性样本使用基因型特异性引物和半巢式PCR-RFLP技术进行基因分型。

结果

贾第虫的患病率为18.1%。使用两种方法检测到的基因型,单一感染时为A基因型(分别为15.8%和12.7%)和B基因型(分别为36.8%和74.5%),A和B基因型混合感染时为(分别为47.4%和12.7%)。两种方法显示出中等一致性(kappa指数=0.413,P<0.001)。贾第虫基因的PCR-RFLP显示,BIII和BIV亚基因型的检测率相同(均为30.9%)。其余样本在AII亚基因型、BIII和BIV混合亚基因型以及AII和BIII混合亚基因型之间平均分配(各占12.7%)。在检测到的亚基因型与症状之间发现了显著关联。

结论

虽然两种方法都证实了B基因型的优势,但使用基因型特异性引物在阐明混合基因型感染的真实情况方面更有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7680/9341145/06309a27fbef/TP-12-41-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7680/9341145/06309a27fbef/TP-12-41-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7680/9341145/b2d0085abefa/TP-12-41-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7680/9341145/06309a27fbef/TP-12-41-g002.jpg