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一种用于在资源匮乏地区检测无症状蓝氏贾第鞭毛虫感染并进行基因分型的改良PCR-RFLP检测方法。

An Improved PCR-RFLP Assay for Detection and Genotyping of Asymptomatic Giardia lamblia Infection in a Resource-Poor Setting.

作者信息

Hawash Yoursry, Ghonaim M M, Al-Shehri S S

机构信息

Department of Medical Laboratory Science, College of Applied Medical Sciences, Taif University, Taif 21944, Saudi Arabia ; Department of Medical Parasitology, National Liver Institute, Menoufia University, Shebin El-Koom, Menoufia 23513, Egypt.

Department of Medical Laboratory Science, College of Applied Medical Sciences, Taif University, Taif 21944, Saudi Arabia ; Medical Microbiology and Immunology Department, Faculty of Medicine, Menoufia University, Shebin El-Koom, Menoufia 23513, Egypt.

出版信息

Korean J Parasitol. 2016 Feb;54(1):1-8. doi: 10.3347/kjp.2016.54.1.1. Epub 2016 Feb 26.

Abstract

Laboratory workers, in resource-poor countries, still consider PCR detection of Giardia lamblia more costly and more time-consuming than the classical parasitological techniques. Based on 2 published primers, an in-house one-round touchdown PCR-RFLP assay was developed. The assay was validated with an internal amplification control included in reactions. Performance of the assay was assessed with DNA samples of various purities, 91 control fecal samples with various parasite load, and 472 samples of unknown results. Two cysts per reaction were enough for PCR detection by the assay with exhibited specificity (Sp) and sensitivity (Se) of 100% and 93%, respectively. Taking a published small subunit rRNA reference PCR test results (6%; 29/472) as a nominated gold standard, G. lamblia was identified in 5.9% (28/472), 5.2%, (25/472), and 3.6% (17/472) by PCR assay, RIDA(®) Quick Giardia antigen detection test (R-Biopharm, Darmstadt, Germany), and iodine-stained smear microscopy, respectively. The percent agreements (kappa values) of 99.7% (0.745), 98.9% (0.900), and 97.7% (0.981) were exhibited between the assay results and that of the reference PCR, immunoassay, and microscopy, respectively. Restriction digestion of the 28 Giardia-positive samples revealed genotype A pattern in 12 and genotype B profile in 16 samples. The PCR assay with the described format and exhibited performance has a great potential to be adopted in basic clinical laboratories as a detection tool for G. lamblia especially in asymptomatic infections. This potential is increased more in particular situations where identification of the parasite genotype represents a major requirement as in epidemiological studies and infection outbreaks.

摘要

在资源匮乏的国家,实验室工作人员仍然认为,与传统寄生虫学技术相比,聚合酶链反应(PCR)检测蓝氏贾第鞭毛虫的成本更高、耗时更长。基于2条已发表的引物,开发了一种内部单轮降落PCR-限制性片段长度多态性分析方法。该分析方法通过在反应中加入内部扩增对照进行验证。使用不同纯度的DNA样本、91份不同寄生虫载量的对照粪便样本以及472份结果未知的样本对该分析方法的性能进行评估。每次反应2个包囊足以通过该分析方法进行PCR检测,其特异性(Sp)和灵敏度(Se)分别为100%和93%。以一项已发表的小亚基核糖体RNA(rRNA)参考PCR检测结果(6%;29/472)作为指定的金标准,通过PCR分析、RIDA(®)Quick Giardia抗原检测试验(德国达姆施塔特的R-Biopharm公司)和碘染色涂片显微镜检查,分别在5.9%(28/472)、5.2%(25/472)和3.6%(17/472)的样本中检测到蓝氏贾第鞭毛虫。该分析方法的结果与参考PCR、免疫分析和显微镜检查结果之间的一致性百分比(kappa值)分别为99.7%(0.745)、98.9%(0.900)和97.7%(0.981)。对28份贾第鞭毛虫阳性样本进行限制性酶切分析,结果显示12份样本为基因型A模式,16份样本为基因型B模式。所述形式且性能良好的PCR分析方法有很大潜力在基础临床实验室中作为蓝氏贾第鞭毛虫的检测工具被采用,尤其是在无症状感染的情况下。在寄生虫基因型鉴定是主要要求的特殊情况下,如在流行病学研究和感染暴发中,这种潜力会更大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6026/4792328/36c2dcde1102/kjp-54-1-1f1.jpg

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