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基于荧光的实时环介导等温扩增(LAMP)检测猪等孢球虫卵囊的方法探索。

Exploration of fluorescence-based real-time loop-mediated isothermal amplification (LAMP) assay for detection of Isospora suis oocysts.

作者信息

Huang Cuiqin, Wen Fuli, Yue Liangping, Chen Renfeng, Zhou Wei, Hu Lingying, Chen Meizhen, Wang Shoukun

机构信息

College of Life Sciences, Longyan University, 1 Dongxiao Rd. N, Xinlluo District, Longyan, Fujian Province 364012, China; Fujian Provincial Key Labatory for the Prevention and Control of Animal Infectious Diseases and Biotechnology, Longyan 364000, Fujian, China.

College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou 350002, Fujian, China; Animal Pharmaceutical Engineering Laboratory of Fujian Province, Fuzhou 350002, Fujian, China.

出版信息

Exp Parasitol. 2016 Jun;165:1-6. doi: 10.1016/j.exppara.2016.03.001. Epub 2016 Mar 8.

Abstract

Isospora suis is an intestinal protozoan parasite in pigs. The 2-3 weeks old piglets are most often infected by I. suis because their immune system is not fully developed. The infection exhibits clinical features such as diarrhea and dehydration and seriously affects the economic interests of farmers. The traditional method of identifying I. suis relies on the detection of fecal oocysts, which depends heavily on the accumulation of experience. Thus, missed detection, and false alarms often occur during detection. With the development of molecular-based detection methods, development of a simple, convenient and more sensitive method for the detection of I. suis is an urgent need. In this study, based on the 18S rRNA gene sequence, a fluorescence -based real-time loop-mediated isothermal amplification (LAMP) assay was established for the detection of I. suis. The results showed that the assay is highly specific and sensitive, with a detection limit of 2.74 × 10(2) copies/μL recombinant plasmid of I. suis, corresponding to 1 fg/μL plasmid when converted to DNA concentration. The sensitivity is about 100 times higher than conventional PCR. Additionally, DNA extracted from a certain number of oocysts was used for detection, and it showed that the LAMP assay had a detection limit of 5 oocysts, lower than that of 13 oocysts of conventional PCR. The established LAMP assay overcomes the shortage of the traditional microscopy-based method, and provides a valuable way for molecular detection of I. suis.

摘要

猪等孢球虫是猪肠道内的一种原生动物寄生虫。2 - 3周龄的仔猪最常感染猪等孢球虫,因为它们的免疫系统尚未完全发育。感染表现出腹泻和脱水等临床特征,严重影响养殖户的经济利益。传统的猪等孢球虫鉴定方法依赖于粪便中卵囊的检测,这在很大程度上依赖于经验积累。因此,检测过程中经常出现漏检和误报的情况。随着基于分子的检测方法的发展,开发一种简单、便捷且更灵敏的猪等孢球虫检测方法迫在眉睫。在本研究中,基于18S rRNA基因序列,建立了一种基于荧光的实时环介导等温扩增(LAMP)检测方法用于检测猪等孢球虫。结果表明,该检测方法具有高度特异性和灵敏性,猪等孢球虫重组质粒的检测限为2.74×10(2)拷贝/μL,换算为DNA浓度时相当于1 fg/μL质粒。其灵敏度比传统PCR高约100倍。此外,用从一定数量卵囊中提取的DNA进行检测,结果表明LAMP检测方法的检测限为5个卵囊,低于传统PCR的13个卵囊。所建立的LAMP检测方法克服了传统显微镜检测方法的不足,为猪等孢球虫的分子检测提供了一种有价值的方法。

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