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从新鲜牛肉和甜瓜中进行沙门氏菌属的PCR检测及微生物分离。

PCR detection and microbiological isolation of Salmonella spp. from fresh beef and cantaloupes.

作者信息

Gallegos-Robles M A, Morales-Loredo A, Alvarez-Ojeda G, Osuna-García J A, Martínez I O, Morales-Ramos L H, Fratamico P

机构信息

Univ. Juárez del Estado de Durango, Venecia, Gomez Palacio, Durango, México.

出版信息

J Food Sci. 2009 Jan-Feb;74(1):M37-40. doi: 10.1111/j.1750-3841.2008.01006.x.

Abstract

Species belonging to the genus Salmonella are an important cause of enteric fevers, gastroenteritis, and septicemia, and the pathogens are commonly transmitted through contaminated food. In this study, polymerase chain reaction (PCR) amplification of a 287-bp region of the invA gene was compared to a microbiological technique to determine the presence of Salmonella in retail beef and in cantaloupe rinse samples. Both methods showed the same level of sensitivity, detecting 1 CFU/25 g of meat after enrichment for 24 h at 42 degrees C. The presence of Salmonella was determined in 50 commercial top sirloin beef samples that were not artificially inoculated. Three samples were positive by the microbiological method, and these samples and an additional sample were positive by the PCR. Both methods were also used to test surface rinses of cantaloupes collected from 4 farms in Nayarit, Mexico. Salmonella was detected by the microbiological method in 9 of 20 samples (45%), whereas the pathogen was detected by the PCR in 11 samples (55%). This study demonstrates the utility of the PCR targeting the invA gene to determine the presence of Salmonella spp. in beef and cantaloupe samples.

摘要

沙门氏菌属的细菌是引起伤寒、肠胃炎和败血症的重要病因,这些病原体通常通过受污染的食物传播。在本研究中,将invA基因287bp区域的聚合酶链反应(PCR)扩增与一种微生物技术进行比较,以确定零售牛肉和哈密瓜冲洗液样本中沙门氏菌的存在情况。两种方法显示出相同的灵敏度水平,在42℃富集24小时后,均能检测出每25克肉中含有1个菌落形成单位(CFU)。对50份未人工接种的市售上等牛里脊牛肉样本进行了沙门氏菌检测。微生物学方法检测出3份样本呈阳性,这些样本以及另外1份样本经PCR检测也呈阳性。两种方法还用于检测从墨西哥纳亚里特州4个农场采集的哈密瓜表面冲洗液。微生物学方法在20份样本中的9份(45%)检测到沙门氏菌,而PCR在11份样本(55%)中检测到该病原体。本研究证明了靶向invA基因的PCR技术在确定牛肉和哈密瓜样本中沙门氏菌属存在情况方面的实用性。

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