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Primer-BLAST: a tool to design target-specific primers for polymerase chain reaction.Primer-BLAST:一种用于设计聚合酶链反应(PCR)目标特异性引物的工具。
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Effectiveness of qPCR permutations, internal controls and dilution as means for minimizing the impact of inhibition while measuring Enterococcus in environmental waters.qPCR 排列、内参和稀释在测量环境水中肠球菌时最小化抑制影响的有效性。
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Consecutive Serratia marcescens multiclone outbreaks in a neonatal intensive care unit.连续发生于新生儿重症监护病房的粘质沙雷氏菌多克隆爆发
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Expression and characterization of the chitinases from Serratia marcescens GEI strain for the control of Varroa destructor, a honey bee parasite.表达和表征粘质沙雷氏菌 GEI 菌株的几丁质酶,用于控制瓦螨,一种蜜蜂寄生虫。
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运用定量实时聚合酶链反应直接检测海洋及其他水生环境中的粘质沙雷氏菌。

Use of quantitative real-time PCR for direct detection of serratia marcescens in marine and other aquatic environments.

作者信息

Joyner Jessica, Wanless David, Sinigalliano Christopher D, Lipp Erin K

机构信息

Odum School of Ecology, University of Georgia, Athens, Georgia, USA.

出版信息

Appl Environ Microbiol. 2014 Mar;80(5):1679-83. doi: 10.1128/AEM.02755-13. Epub 2013 Dec 27.

DOI:10.1128/AEM.02755-13
PMID:24375136
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3957607/
Abstract

Serratia marcescens is the etiological agent of acroporid serratiosis, a distinct form of white pox disease in the threatened coral Acropora palmata. The pathogen is commonly found in untreated human waste in the Florida Keys, which may contaminate both nearshore and offshore waters. Currently there is no direct method for detection of this bacterium in the aquatic or reef environment, and culture-based techniques may underestimate its abundance in marine waters. A quantitative real-time PCR assay was developed to detect S. marcescens directly from environmental samples, including marine water, coral mucus, sponge tissue, and wastewater. The assay targeted the luxS gene and was able to distinguish S. marcescens from other Serratia species with a reliable quantitative limit of detection of 10 cell equivalents (CE) per reaction. The method could routinely discern the presence of S. marcescens for as few as 3 CE per reaction, but it could not be reliably quantified at this level. The assay detected environmental S. marcescens in complex sewage influent samples at up to 761 CE ml(-1) and in septic system-impacted residential canals in the Florida Keys at up to 4.1 CE ml(-1). This detection assay provided rapid quantitative abilities and good sensitivity and specificity, which should offer an important tool for monitoring this ubiquitous pathogen that can potentially impact both human health and coral health.

摘要

粘质沙雷氏菌是鹿角珊瑚白痘病(一种在受威胁的鹿角珊瑚中出现的独特形式的白痘病)的病原体。该病原体常见于佛罗里达礁岛群未经处理的人类粪便中,可能会污染近岸和离岸水域。目前,在水生或珊瑚礁环境中尚无直接检测这种细菌的方法,基于培养的技术可能会低估其在海水中的丰度。开发了一种定量实时聚合酶链反应(qPCR)检测方法,可直接从环境样本(包括海水、珊瑚黏液、海绵组织和废水)中检测粘质沙雷氏菌。该检测方法以luxS基因为靶点,能够将粘质沙雷氏菌与其他沙雷氏菌属物种区分开来,每个反应的可靠定量检测限为10个细胞当量(CE)。该方法通常能够识别每个反应低至3个CE的粘质沙雷氏菌的存在,但在此水平上无法进行可靠的定量。该检测方法在复杂的污水进水样本中检测到的环境粘质沙雷氏菌含量高达761 CE ml-1,在佛罗里达礁岛群受化粪池系统影响的住宅运河中检测到的含量高达4.1 CE ml-1。这种检测方法具有快速定量能力以及良好的灵敏度和特异性,应为监测这种可能对人类健康和珊瑚健康都有潜在影响的普遍存在的病原体提供重要工具。