Czyzewska Izabela, Furowicz Antoni J
Katedra Immunologii i Mikrobiologii Wydziału Biotechnologii i Hodowli Zwierzat Akademii Rolniczej w Szczecinic.
Przegl Epidemiol. 2003;57(2):263-70.
The purpose of the work has been to identify Yersinia pseudotuberculosis strains and to demonstrate their potential pathogenicity using PCR reaction. Investigations included 167 samples of the water and 32 samples of the soil from westpomeranian region. Based on the analysis of PCR reactions the research confirmed the presence of DNA Y. pseudotuberculosis strain in 6 of the water samples and in 1 of the soil sample. The strains have been identified by nucleotide sequence of the ypm gene, which is specific only for mentioned species. Genotypic analysis demonstrated also the presence of genes, which confirmed their virulence. The PCR reaction should be used in the microbiological diagnostic of Y. pseudotuberculosis strains, isolated from animals and from environment, because it is very specific, fast and sensitive method.
这项工作的目的是鉴定假结核耶尔森菌菌株,并通过聚合酶链反应(PCR)来证明其潜在致病性。调查包括来自西波美拉尼亚地区的167份水样和32份土壤样本。基于PCR反应分析,研究证实6份水样和1份土壤样本中存在假结核耶尔森菌菌株的DNA。这些菌株已通过ypm基因的核苷酸序列进行鉴定,该基因仅对上述物种具有特异性。基因型分析还表明存在证实其毒力的基因。PCR反应应用于从动物和环境中分离出的假结核耶尔森菌菌株的微生物诊断,因为它是一种非常特异、快速且灵敏的方法。