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牛囊尾蚴的分子分化

Molecular differentiation of bovine sarcocysts.

作者信息

Akhlaghi Majedeh, Razavi Mostafa, Hosseini Arsalan

机构信息

Shiraz University, Shiraz, Islamic Republic of Iran.

出版信息

Parasitol Res. 2016 Jul;115(7):2721-8. doi: 10.1007/s00436-016-5020-7. Epub 2016 Mar 28.

Abstract

Cattle are common intermediate hosts of Sarcocystis, and the prevalence in adult bovine muscle is close to 100 % in most regions of the world. Three Sarcocystis spp. are known to infect cattle as intermediate hosts, namely, S. cruzi, S. hirsuta, and S. hominis. The aim of the present study was the molecular identification and differentiation of these three species, Neospora caninum and Besnoitia by PCR and RFLP methods. Tissue samples were obtained from diaphragmatic muscle of 101 cattle slaughtered in Shiraz, Fars Province, Iran, for both smear preparation and DNA extraction. The samples were digested by Pepsin, washed three times with PBS solution before taking smears, fixed in absolute methanol and stained with 10 % Giemsa. The slides were examined microscopically for Sarcocystis bradyzoites and DNA was extracted from 100 mg of Sarcocystis-infected meat samples. Since the primers also bind to 18S rRNA gene of some tissue cyst-forming coccidian protozoa, DNA was also extracted from 100 μl of tachyzoite-containing suspension of N. caninum and Besnoitia isolated from goat to compare RFLP pattern. Polymerase chain reaction (PCR) was performed on DNA of samples which were microscopically positive for Sarcocystis. Five restriction enzymes Dra1, EcoRV, RsaI, AvaI, and SspI were used for RFLP and DNA of one sample from protozoa was sequenced. Based on the RFLP results, 87 (98.9 %) DNA samples were cut with DraI, indicating infection by S. cruzi. One sample (1.1 %) of PCR products of infected samples was cut only with EcoRV which showed S. hominis infection. Forty-eight samples (53.3 %) of PCR products were cut with both DraI, EcoRV, or with DraI, EcoRV, and RsaI while none of them was cut with SspI, which shows the mixed infection of both S. cruzi and S. hominis and no infection with S. hirsuta. It seems by utilizing these restriction enzymes, RLFP could be a suitable method not only for identification of Sarcocystis species but also for differentiating them from N. caninum and Besnoitia.

摘要

牛是肉孢子虫常见的中间宿主,在世界大多数地区成年牛肌肉中的感染率接近100%。已知有三种肉孢子虫可感染牛作为中间宿主,即克鲁兹肉孢子虫、多毛肉孢子虫和人肉孢子虫。本研究的目的是通过PCR和RFLP方法对这三种肉孢子虫以及犬新孢子虫和贝诺孢子虫进行分子鉴定和区分。从伊朗法尔斯省设拉子屠宰的101头牛的膈肌获取组织样本,用于涂片制备和DNA提取。样本用胃蛋白酶消化,在涂片前用PBS溶液洗涤三次,用无水甲醇固定并用10%吉姆萨染色。在显微镜下检查涂片是否存在肉孢子虫缓殖子,并从100mg感染肉孢子虫的肉样中提取DNA。由于引物也与一些形成组织囊的球虫原生动物的18S rRNA基因结合,还从从山羊分离的犬新孢子虫和贝诺孢子虫含速殖子的100μl悬液中提取DNA,以比较RFLP模式。对显微镜下肉孢子虫呈阳性的样本DNA进行聚合酶链反应(PCR)。使用五种限制性内切酶Dra1、EcoRV、RsaI、AvaI和SspI进行RFLP分析,并对来自原生动物的一个样本的DNA进行测序。根据RFLP结果,87个(98.9%)DNA样本被DraI切割,表明感染了克鲁兹肉孢子虫。感染样本的PCR产物中有一个样本(1.1%)仅被EcoRV切割,显示感染了人肉孢子虫。48个(53.3%)PCR产物样本被DraI、EcoRV或DraI、EcoRV和RsaI同时切割,而没有一个被SspI切割,这表明同时感染了克鲁兹肉孢子虫和人肉孢子虫,未感染多毛肉孢子虫。似乎利用这些限制性内切酶,RLFP不仅可以作为鉴定肉孢子虫种类的合适方法,还可以将它们与犬新孢子虫和贝诺孢子虫区分开来。

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