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Quantification of Cryptosporidium parvum in anaerobic digesters treating manure by (reverse-transcription) quantitative real-time PCR, infectivity and excystation tests

机译:通过(逆转录)定量实时荧光定量PCR,感染性和兴奋试验检测定量处理粪便的厌氧消化池中的小隐孢子虫

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The survival of Cryptosporidium parvum oocysts in anaerobic digesters treating manure was investigated for mesophilic, thermophilic, and a combined treatment (mesophilic-thermophilic-mesophilic) under different retention times of oocysts in the reactors. C. parvum DNA was extracted with an optimised protocol, and its amount determined by quantitative real-time PCR (qPCR). Results indicated noteworthy differences in DNA content after the different treatments. DNA was not degraded during the process. However, excystation and infectivity tests showed a reduction of viable oocyst numbers of >= 2 and >= 5 log units after the thermophilic treatment in two different experiments. Thus qPCR-targeting DNA can overestimate the number of oocysts that survive and remain viable after anaerobic digestion. However, targeting DNA is suitable to indicate the presence or absence of oocysts. Reverse transcription qPCR (RT-qPCR) targeting C. parvum hsp70 mRNA successfully indicated the presence of viable fraction of oocysts.
机译:研究了在处理粪便的厌氧消化池中小隐隐孢子虫卵囊的中温,嗜热和联合处理(中温-嗜温-中温)的存活率。用优化的方案提取小球藻DNA,并通过定量实时PCR(qPCR)确定其数量。结果表明,不同处理后DNA含量明显不同。在此过程中,DNA没有降解。然而,在两个不同的实验中,高温处理后的兴奋性和感染性测试显示存活卵囊数量减少了> = 2和> = 5 log单位。因此,靶向qPCR的DNA可能高估了在无氧消化后存活并保持活力的卵囊的数量。但是,靶向DNA适合指示卵囊的存在或不存在。靶向小球藻hsp70 mRNA的逆转录qPCR(RT-qPCR)成功表明卵囊中存在有活力的部分。

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