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优化样本量和DNA提取方法以提高对致病疫霉不同繁殖体的PCR检测

Optimization of Sample Size and DNA Extraction Methods to Improve PCR Detection of Different Propagules of Phytophthora infestans.

作者信息

Wangsomboondee T, Ristaino J B

机构信息

Department of Plant Pathology, North Carolina State University, Raleigh 27695.

出版信息

Plant Dis. 2002 Mar;86(3):247-253. doi: 10.1094/PDIS.2002.86.3.247.

Abstract

The plant pathogen Phytophthora infestans causes a destructive blight of potato tubers and foliage. A rapid polymerase chain reaction (PCR) assay has been developed for detection of P. infestans in potato tubers. In this study, the effect of method of DNA extraction on different propagule types and the minimal number of propagules of P. infestans detectable by PCR were assessed using the PINF and internal transcribed spacer (ITS)5 primers. Sensitivity of the primers for PCR was high, and DNA was detectable at concentrations as low as 10 pg/ml. Zoospores and oospores responded differently to different extraction methods, whereas all extraction methods worked equally well for sporangia. Freeze-thaw DNA lysis, in which propagules were frozen at -80°C and thawed at 65°C three times for 15 min each, or direct PCR, in which propagules were placed directly in the reaction mix, were effective methods for PCR detection of sporangia or zoospores but were not effective methods for PCR detection of DNA in oospores of P. infestans. DNA from a single sporangium or oospore could be amplified by PCR after hexadecyltrimethyl-ammonium bromide (CTAB) or NaOH lysis extraction methods, whereas DNA from a single zoospore could be amplified by CTAB or direct PCR methods. "IsoCode" Stixs, used in forensic applications, were used to collect the pathogen from leaf and tuber lesions and provided another simple method to extract template DNA. PCR detection of the pathogen in infected tubers using PINF and ITS5 primers was compared to tissue isolation or visual observation. The probability of detection of P. infestans in infected tubers at 7 days post inoculation using the PCR assay, tissue isolation, or visual observation was 0.90, 0.80, and 0.75, respectively. The PINF and ITS5 primers provide a powerful tool for rapid and sensitive detection of zoospores, sporangia, and oospores of P. infestans when used with appropriate extraction methods, and could easily be deployed to reduce spread of the pathogen in potato tubers.

摘要

植物病原菌致病疫霉会引发马铃薯块茎和叶片的毁灭性疫病。已开发出一种快速聚合酶链反应(PCR)检测方法,用于检测马铃薯块茎中的致病疫霉。在本研究中,使用PINF和内转录间隔区(ITS)5引物评估了DNA提取方法对不同繁殖体类型的影响以及PCR可检测到的致病疫霉最少繁殖体数量。引物对PCR的灵敏度很高,DNA浓度低至10 pg/ml时即可检测到。游动孢子和卵孢子对不同提取方法的反应不同,而所有提取方法对孢子囊的效果相同。冻融DNA裂解(将繁殖体在-80°C冷冻,然后在65°C解冻3次,每次15分钟)或直接PCR(将繁殖体直接放入反应混合物中)是检测孢子囊或游动孢子的有效PCR方法,但不是检测致病疫霉卵孢子中DNA的有效方法。十六烷基三甲基溴化铵(CTAB)或氢氧化钠裂解提取方法后,单个孢子囊或卵孢子的DNA可通过PCR扩增,而单个游动孢子的DNA可通过CTAB或直接PCR方法扩增。用于法医应用的“IsoCode”Stixs用于从叶片和块茎病斑中收集病原体,并提供了另一种提取模板DNA的简单方法。将使用PINF和ITS5引物对感染块茎中的病原体进行PCR检测与组织分离或目视观察进行了比较。接种后7天,使用PCR检测、组织分离或目视观察在感染块茎中检测到致病疫霉的概率分别为0.90、0.80和0.75。当与适当的提取方法一起使用时,PINF和ITS5引物为快速、灵敏地检测致病疫霉的游动孢子、孢子囊和卵孢子提供了强大工具,并且可以很容易地用于减少病原体在马铃薯块茎中的传播。

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