National Research Council of Italy, Institute of Sciences of Food Production (CNR-ISPA), Bari, Italy.
Int J Food Microbiol. 2011 Feb 28;145(2-3):437-43. doi: 10.1016/j.ijfoodmicro.2011.01.015. Epub 2011 Jan 18.
An extensive use of Weissella (W.) confusa is currently being made for the production of a variety of fermented foods and beverages although some strains of this species have emerged as opportunistic pathogens for humans and animals. Nevertheless, no rapid methods are available for the reliable identification of W. confusa. We developed a novel PCR using AFLP (Amplified Fragment Length Polymorphism)-derived primers for the rapid and unequivocal identification of W. confusa. Fluorescent AFLP of 30 strains of W. confusa, Leuconostoc citreum, Lactobacillus (Lb.) brevis, Lb. rossiae, Lb. plantarum and Lb. buchneri allowed us to detect, purify and sequence several W. confusa specific AFLP fragments. The homology search in BLAST of a 303 bp nucleotide sequence revealed a ≤ 77% identity of the purified fragment with the lepA gene of several lactic acid bacteria. A PCR assay targeting 225 bp of this fragment was developed and tested against the DNA of 109 strains, including 34 foodborne and clinical W. confusa and 75 strains of 47 phylogenetically closely and distantly related species, resulting in 100% specificity with a detection limit of 16 pg. Being the first species-specific PCR to date developed for the rapid and unambiguous identification of W. confusa, this novel assay could be a reliable and efficient tool for detecting W. confusa not only in food and beverages, but also in clinical specimens, thus contributing to clarify its real significance in human and animal infections.
虽然有些 Weissella (W.) confusa 菌株已经成为人类和动物的机会性病原体,但目前仍广泛用于生产各种发酵食品和饮料。然而,目前还没有可靠的方法来快速鉴定 W. confusa。我们使用 AFLP(扩增片段长度多态性)衍生引物开发了一种新型 PCR,用于快速准确地鉴定 W. confusa。对 30 株 W. confusa、Leuconostoc citreum、Lactobacillus (Lb.) brevis、Lb. rossiae、Lb. plantarum 和 Lb. buchneri 的荧光 AFLP 分析允许我们检测、纯化和测序几个 W. confusa 特异性 AFLP 片段。BLAST 中的同源性搜索显示,纯化片段与几种乳酸菌的 lepA 基因的同一性≤77%。针对该片段的 225 bp 设计了 PCR 检测方法,并对包括 34 株食源性病原体和临床 W. confusa 以及 75 株亲缘关系密切和较远的 47 个物种的 109 株菌株的 DNA 进行了测试,特异性为 100%,检测限为 16 pg。作为迄今为止开发的用于快速明确鉴定 W. confusa 的首个种特异性 PCR,该新型检测方法不仅可以可靠且高效地用于检测食品和饮料中的 W. confusa,还可以用于临床标本,从而有助于阐明其在人类和动物感染中的实际意义。