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羊水弓形虫检测:四种不同分子生物学方法的比较

Detection of Toxoplasma gondii from amniotic fluid, a comparison of four different molecular biological methods.

作者信息

Nagy Bálint, Bán Zoltán, Beke Artúr, Nagy Gyula Richard, Lázár Levente, Papp Csaba, Tóth-Pál Erno, Papp Zoltán

机构信息

1st Department of Obstetrics and Gynecology, Semmelweis University, Hungary.

出版信息

Clin Chim Acta. 2006 Jun;368(1-2):131-7. doi: 10.1016/j.cca.2005.12.023. Epub 2006 Feb 3.

DOI:10.1016/j.cca.2005.12.023
PMID:16458874
Abstract

BACKGROUND

The infection caused by the parasite Toxoplasma gondii (T. gondii) is often asymptomatic or has mild symptoms. The infection can cause serious problems in pregnant women who acquire the infection during gestation and their fetuses are congenitally infected.

METHODS

We tested 64 amniotic fluid samples for the presence of T. gondii by using fluorescent PCR and DNA fragment analysis. Later we compared four different molecular biological methods for the detection of the presence of T. gondii on same frozen DNA samples. These methods are the conventional PCR, fluorescent PCR with DNA fragment analysis, quantitative real-time PCR with SYBRGreen I and with fluorescence energy transfer hybridization probe detection. We determined the detection limit of these methods.

RESULTS

The conventional PCR and quantitative real-time PCR with SYBRGreen I detection have the detection limit of 1000 parasites, followed by fluorescent PCR with the detection limit of 10-100 parasites. The real-time PCR using fluorescence energy transfer hybridization probes can detect one parasite. This is the most sensitive and the fastest method. We detected 5 T. gondii positive samples with all methods from the studied 64 amniotic fluids.

CONCLUSIONS

All studied molecular biological methods are suitable for the detection of congenital toxoplasmosis. The quantitative real-time PCR based methods are more sensitive, simple and easy to perform these are opening the avenue to find out the effect of the number of parasites on fetal abnormalities.

摘要

背景

由刚地弓形虫(T. gondii)引起的感染通常无症状或症状轻微。在孕期感染该寄生虫的孕妇及其先天性感染的胎儿中,这种感染可导致严重问题。

方法

我们采用荧光PCR和DNA片段分析检测了64份羊水样本中是否存在刚地弓形虫。随后,我们在相同的冷冻DNA样本上比较了四种不同的分子生物学方法来检测刚地弓形虫的存在。这些方法分别是常规PCR、带DNA片段分析的荧光PCR、使用SYBRGreen I的定量实时PCR以及荧光能量转移杂交探针检测。我们确定了这些方法的检测限。

结果

常规PCR和使用SYBRGreen I检测的定量实时PCR的检测限为1000个寄生虫,其次是检测限为10 - 100个寄生虫的荧光PCR。使用荧光能量转移杂交探针的实时PCR能够检测到一个寄生虫。这是最灵敏且最快的方法。在研究的64份羊水中,我们用所有方法均检测到了5份刚地弓形虫阳性样本。

结论

所有研究的分子生物学方法都适用于先天性弓形虫病的检测。基于定量实时PCR的方法更灵敏、简单且易于操作,这为探究寄生虫数量对胎儿异常的影响开辟了道路。

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