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本文引用的文献

1
Quantitative real-time PCR analysis of total and propidium monoazide-resistant fecal indicator bacteria in wastewater.废水中总粪便指示菌和叠氮溴化丙锭抗性粪便指示菌的定量实时聚合酶链反应分析
Water Res. 2009 Nov;43(19):4790-801. doi: 10.1016/j.watres.2009.05.031. Epub 2009 May 29.
2
Unusual Cryptosporidium genotypes in human cases of diarrhea.腹泻患者中出现的不寻常隐孢子虫基因型。
Emerg Infect Dis. 2008 Nov;14(11):1800-2. doi: 10.3201/eid1411.080239.
3
Cryptosporidium source tracking in the Potomac River watershed.波托马克河流域隐孢子虫的溯源追踪
Appl Environ Microbiol. 2008 Nov;74(21):6495-504. doi: 10.1128/AEM.01345-08. Epub 2008 Sep 5.
4
Cryptosporidium ryanae n. sp. (Apicomplexa: Cryptosporidiidae) in cattle (Bos taurus).牛(Bos taurus)中的瑞安隐孢子虫(Cryptosporidium ryanae)新种(顶复门:隐孢子虫科)
Vet Parasitol. 2008 Oct 1;156(3-4):191-8. doi: 10.1016/j.vetpar.2008.05.024. Epub 2008 May 23.
5
Cryptosporidium fayeri n. sp. (Apicomplexa: Cryptosporidiidae) from the Red Kangaroo (Macropus rufus).来自红袋鼠(大赤袋鼠)的费氏隐孢子虫新种(顶复门:隐孢子虫科)
J Eukaryot Microbiol. 2008 Jan-Feb;55(1):22-6. doi: 10.1111/j.1550-7408.2007.00299.x.
6
Quantifying fungal viability in air and water samples using quantitative PCR after treatment with propidium monoazide (PMA).使用单叠氮丙锭(PMA)处理后,通过定量PCR对空气和水样中的真菌活力进行定量分析。
J Microbiol Methods. 2008 Feb;72(2):180-4. doi: 10.1016/j.mimet.2007.11.017. Epub 2007 Nov 28.
7
Enumeration of viable Listeria monocytogenes cells by real-time PCR with propidium monoazide and ethidium monoazide in the presence of dead cells.在存在死细胞的情况下,使用单叠氮化丙锭和单叠氮化乙锭通过实时聚合酶链反应对单核细胞增生李斯特氏菌活细胞进行计数。
Appl Environ Microbiol. 2007 Dec;73(24):8028-31. doi: 10.1128/AEM.01198-07. Epub 2007 Oct 12.
8
Photoactivated ethidium monoazide directly cleaves bacterial DNA and is applied to PCR for discrimination of live and dead bacteria.光活化单叠氮溴化乙锭可直接切割细菌DNA,并应用于聚合酶链反应以区分活细菌和死细菌。
Microbiol Immunol. 2007;51(8):763-75. doi: 10.1111/j.1348-0421.2007.tb03966.x.
9
Use of propidium monoazide for live/dead distinction in microbial ecology.单叠氮碘化丙啶在微生物生态学中用于区分活死细胞的应用。
Appl Environ Microbiol. 2007 Aug;73(16):5111-7. doi: 10.1128/AEM.02987-06. Epub 2007 Jun 22.
10
Molecular monitoring of disinfection efficacy using propidium monoazide in combination with quantitative PCR.使用单叠氮碘化丙啶结合定量PCR对消毒效果进行分子监测。
J Microbiol Methods. 2007 Aug;70(2):252-60. doi: 10.1016/j.mimet.2007.04.014. Epub 2007 May 1.

隐孢子虫丙啶单叠氮化物-PCR,一种基于分子生物学的技术,用于鉴定活隐孢子虫卵囊的基因型。

Cryptosporidium propidium monoazide-PCR, a molecular biology-based technique for genotyping of viable Cryptosporidium oocysts.

机构信息

National Exposure Research Laboratory, U.S. Environmental Protection Agency, Mailstop: 320, 26 W. Martin Luther King Dr., Cincinnati, OH 45268, USA.

出版信息

Appl Environ Microbiol. 2009 Nov;75(21):6856-63. doi: 10.1128/AEM.00540-09. Epub 2009 Sep 11.

DOI:10.1128/AEM.00540-09
PMID:19749067
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2772443/
Abstract

Cryptosporidium is an important waterborne protozoan parasite that can cause severe diarrhea and death in the immunocompromised. The current methods used to monitor for Cryptosporidium oocysts in water are the microscopy-based USEPA methods 1622 and 1623. These methods assess total levels of oocysts in source waters, but do not determine oocyst viability or genotype. Recently, propidium monoazide (PMA) has been used in conjunction with molecular diagnostic tools to identify species and assess the viability of bacteria. The goal of this study was the development of a Cryptosporidium PMA-PCR (CryptoPMA-PCR) assay that includes PMA treatment prior to PCR analysis in order to prevent the amplification of DNA from dead oocysts. The results demonstrated that PMA penetrates only dead oocysts and blocks amplification of their DNA. The CryptoPMA-PCR assay can also specifically detect live oocysts within a mixed population of live and dead oocysts. More importantly, live oocysts, not dead oocysts, were detected in raw waste or surface water samples spiked with Cryptosporidium oocysts. This proof-of-concept study is the first to demonstrate the use of PMA for pre-PCR treatment of Cryptosporidium oocysts. The CryptoPMA-PCR assay is an attractive approach to specifically detect and genotype viable Cryptosporidium oocysts in the water, which is critical for human health risk assessment.

摘要

隐孢子虫是一种重要的水传播原生动物寄生虫,可导致免疫功能低下者严重腹泻和死亡。目前用于监测水中隐孢子虫卵囊的方法是基于显微镜的美国环保署方法 1622 和 1623。这些方法评估源水中卵囊的总水平,但不能确定卵囊的活力或基因型。最近,吖啶橙(PMA)已与分子诊断工具结合使用,以鉴定物种并评估细菌的活力。本研究的目的是开发一种隐孢子虫 PMA-PCR(CryptoPMA-PCR)检测方法,该方法在 PCR 分析前进行 PMA 处理,以防止从死亡卵囊中扩增 DNA。结果表明,PMA 仅穿透死亡卵囊并阻止其 DNA 的扩增。CryptoPMA-PCR 检测方法还可以特异性检测活卵囊在活卵囊和死卵囊混合群体中。更重要的是,在添加隐孢子虫卵囊的原始废物或地表水样品中检测到的是活卵囊,而不是死卵囊。这项概念验证研究首次证明了 PMA 可用于隐孢子虫卵囊的 PCR 前处理。CryptoPMA-PCR 检测方法是一种有吸引力的方法,可特异性检测和基因分型水中有活力的隐孢子虫卵囊,这对于人类健康风险评估至关重要。