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伊朗地表水中隐孢子虫和贾第虫灵敏检测方法的开发

Development of sensitive detection of cryptosporidium and giardia from surface water in iran.

作者信息

Mahmoudi Mr, Ashrafi K, Abedinzadeh H, Tahvildar-Bideruni F, Haghighi A, Bandehpour M, Taghipour Lailabadi N, Kazemi B

机构信息

Department of Parasitology and Mycology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Parasitol. 2011 Aug;6(3):43-51.

Abstract

BACKGROUND

The protozoan parasites Cryptosporidium spp. and Giardia are known to occur widely in both raw and drinking waters. They are two of the causative agents of waterborne outbreaks of gastroenteritis throughout the world. In the present study, a PCR assay and FA were developed for detection of Cryptosporidium oocysts and Giardia cyst in environmental samples.

METHODS

We have detected Cryptosporidium spp. oocysts and Giardia cysts in seeded and unseeded environmental water samples by PCR method. Water samples were spiked with oocysts (50, 100,300,500) and filtrated with a 1.2-µm pore size cellulose nitrate and follow by DNA extraction and purification by QIAamp DNA mini kit. Nested-PCR assay amplified an 850 bp fragment of 18s rRNA gene specific for Cryptosporidium and 435 bp fragment of glutamate dehydrogenase (GDH) target gene for Giardia. Also many river water from north of Iran, be checked by these methods.

RESULTS

Cryptosporidium and Giardia DNAs were detected in seeded water sample and Giardia was detected in all 5 water samples from river in north of Iran by nested- PCR and FA. Also in one river water sample, Cryptosporidium was detected.

CONCLUSION

This protocol is effective for detection of these waterborne parasites in treated and untreated water samples. This study can also serve as a platform for further investigations and research water source in Iran.

摘要

背景

原生动物寄生虫隐孢子虫属和贾第虫已知在原水和饮用水中广泛存在。它们是全球水源性肠胃炎暴发的两种致病因子。在本研究中,开发了一种聚合酶链反应(PCR)检测方法和荧光抗体(FA)检测方法,用于检测环境样品中的隐孢子虫卵囊和贾第虫包囊。

方法

我们通过PCR方法检测了接种和未接种的环境水样中的隐孢子虫属卵囊和贾第虫包囊。水样接种卵囊(50、100、300、500个)后,用孔径为1.2μm的硝酸纤维素膜过滤,然后用QIAamp DNA微型试剂盒进行DNA提取和纯化。巢式PCR检测扩增出隐孢子虫特异性的18s rRNA基因的850 bp片段和贾第虫的谷氨酸脱氢酶(GDH)靶基因的435 bp片段。还用这些方法检测了伊朗北部的许多河水。

结果

通过巢式PCR和FA在接种水样中检测到隐孢子虫和贾第虫的DNA,在伊朗北部河流的所有5个水样中检测到贾第虫。在一个河水样中还检测到了隐孢子虫。

结论

该方案对于检测处理和未处理水样中的这些水源性寄生虫有效。本研究也可为伊朗进一步调查和研究水源提供一个平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5ee/3279887/82277aaaf5d1/IJP-6-043-g001.jpg

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