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从家禽中选择性富集弯曲杆菌属用于与DNA杂交结合的方法。

Methods for Selective Enrichment of Campylobacter spp. from Poultry for Use in Conjunction with DNA Hybridization.

作者信息

Stern Norman J, Mozola Mark A

机构信息

Poultry Microbiological Safety Research Unit, Richard B. Russell Research Center, Agricultural Research Service, U.S. Department of Agriculture, P.O Box 5677, Athens, Georgia 30613.

GENE-TRAK Systems Corporation, 31 New York Avenue, Framington, Massachusetts 01701.

出版信息

J Food Prot. 1992 Oct;55(10):767-770. doi: 10.4315/0362-028X-55.10.767.

Abstract

A DNA hybridization test was investigated for application to the detection of Campylobacter spp. in poultry samples. The test chemistry involves solution phase hybridization and detection by means of an enzymatically generated colorimetric endpoint. DNA probes used in the test system are targeted to unique sequences of ribosomal RNA and are specific for Campylobacter jejuni , Campylobacter coli , Campylobacter lari , and Campylobacter fetus subsp. fetus . Initial experiments with pure cultures of C. jejuni established the sensitivity limit of the DNA hybridization assay at approximately 10 CFU per sample. Experiments were designed to define optimal conditions for recovery and selective enrichment of Campylobacter spp. from chicken carcasses for use in conjunction with the DNA hybridization assay. Following overnight enrichment, cultures were swabbed onto Campy-Cefex agar plates and allowed to incubate for 24 h. This overnight growth was then suspended and assayed with the DNA probe. The remainder of the overnight enrichment was centrifuged and the resulting pellet was analyzed. Thirty-eight chicken carcasses were assayed for Campylobacter spp. by DNA probe and culture methodology employing culture enrichment and selective plating. Culture procedures isolated Campylobacter spp. from 23 carcasses, while the DNA probe assay detected the organism from 21 carcasses. The DNA probe registered five "false" positives and seven "false" negatives relative to the cultural bacteriologic approach.

摘要

研究了一种DNA杂交试验,用于检测家禽样本中的弯曲杆菌属。该试验化学方法涉及溶液相杂交,并通过酶促产生的比色终点进行检测。试验系统中使用的DNA探针靶向核糖体RNA的独特序列,对空肠弯曲杆菌、结肠弯曲杆菌、拉氏弯曲杆菌和胎儿弯曲杆菌胎儿亚种具有特异性。用空肠弯曲杆菌纯培养物进行的初步实验确定了DNA杂交试验的灵敏度极限约为每个样本10 CFU。设计实验以确定从鸡尸体中回收和选择性富集弯曲杆菌属的最佳条件,以便与DNA杂交试验结合使用。过夜富集后,将培养物用拭子接种到弯曲杆菌-头孢菌素琼脂平板上,培养24小时。然后将过夜生长物悬浮并用DNA探针进行检测。将过夜富集物的其余部分离心,并对所得沉淀进行分析。采用培养富集和选择性平板接种的DNA探针和培养方法对38个鸡尸体进行了弯曲杆菌属检测。培养程序从23个尸体中分离出弯曲杆菌属,而DNA探针检测从21个尸体中检测到该菌。相对于培养细菌学方法,DNA探针记录了5个“假”阳性和7个“假”阴性。

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