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通过对小亚基核糖体DNA序列进行PCR扩增检测火鸡盲肠粪便中的火鸡组织滴虫。

Detection of Histomonas meleagridis in turkeys cecal droppings by PCR amplification of the small subunit ribosomal DNA sequence.

作者信息

Huber Karine, Chauve C, Zenner L

机构信息

UMR 958 Protozoaires Entéricoles des Volailles, INRA-ENVL, 1, Avenue Bourgelat, 69280 Marcy L'Etoile, France.

出版信息

Vet Parasitol. 2005 Aug 10;131(3-4):311-6. doi: 10.1016/j.vetpar.2005.05.012.

Abstract

Histomonas meleagridis is a protozoan parasite that may cause histomoniasis, a disease of gallinaceous fowl characterized by necrotic typhlitis, hepatitis and high mortality. Diagnosis of this disease is based on direct identification or on cultivation of the parasite. With the aim of developing more sensitive, rapid and useful tools for parasite detection, PCR that amplified a DNA target of 209 pb of the 18S rRNA gene was designed to detect the genome of H. meleagridis and to differentiate it from the genome of Tetratrichomonas gallinarum, another common protozoan parasite of fowl. The sensitivity of the test was evaluated using serial diluted samples of cultured H. meleagridis and showed positive amplification for concentrations comprised between 10 and 10(-1)parasites/ml of culture. The sensitivity for cecal droppings samples was assessed using spiked material and was comprised between 3 x 10(3) and 3 x 10(5)parasites/ml of stool. The reliability of the PCR for the detection of Histomonas infection was also evaluated by experimental infection of turkeys. Results of the PCR appeared to be in agreement with the development of the clinical signs and of the cecal lesions. The PCR developed in this study may be a useful tool in the detection and identification of H. meleagridis for rapid, routine screening as a supplement to direct identification or cultivation of the parasite.

摘要

火鸡组织滴虫是一种原生动物寄生虫,可引起组织滴虫病,这是一种鸡形目禽类疾病,其特征为坏死性盲肠炎、肝炎和高死亡率。该疾病的诊断基于寄生虫的直接鉴定或培养。为了开发更灵敏、快速且实用的寄生虫检测工具,设计了一种PCR方法,该方法可扩增18S rRNA基因209 pb的DNA靶点,用于检测火鸡组织滴虫的基因组,并将其与鸡四毛滴虫(另一种常见的禽类原生动物寄生虫)的基因组区分开来。使用培养的火鸡组织滴虫系列稀释样本评估了该检测方法的灵敏度,结果显示,对于浓度在10至10(-1)个寄生虫/毫升培养物之间的样本,PCR呈阳性扩增。使用加标材料评估了盲肠粪便样本的灵敏度,灵敏度范围为3×10(3)至3×10(5)个寄生虫/毫升粪便。还通过对火鸡进行实验性感染,评估了PCR检测组织滴虫感染的可靠性。PCR结果似乎与临床症状和盲肠病变的发展情况一致。本研究中开发的PCR可能是一种有用的工具,可用于火鸡组织滴虫的检测和鉴定,作为直接鉴定或培养寄生虫的补充方法,用于快速、常规筛查。

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