Kovtunovych Gennadiy, Lytvynenko Tetyana, Negrutska Valentyna, Lar Olena, Brisse Sylvain, Kozyrovska Natalia
Department of Regulatory Cell Mechanisms, Institute of Molecular Biology and Genetics of the National Academy of Sciences, Zabolotnoho Str 150, Kyiv 03143, Ukraine.
Res Microbiol. 2003 Oct;154(8):587-92. doi: 10.1016/S0923-2508(03)00148-7.
Bacteria of the genus Klebsiella are important opportunistic pathogens responsible for nosocomial infections that are increasingly resistant to antimicrobial agents. Distinctive identification of the species K. oxytoca, K. pneumoniae, K. planticola, K. ornithinolytica and K. terrigena is difficult based on phenotypic tests and misidentifications are frequent in routine clinical microbiology. We developed a specific method to discriminate K. oxytoca from the other species of the genus Klebsiella, based on the PCR amplification of the polygalacturonase (pehX) gene. A PCR amplicon of 344 bp was obtained in all 35 K. oxytoca strains tested, but in none of the 29 K. pneumoniae, 12 K. planticola/K. ornithinolytica and 7 K. terrigena strains tested. The test was also negative for polygalacturonate-degrading species of the genus Erwinia. Analysis of 24 strains designated as K. pneumoniae from international collections (NCTC, PZH) revealed previous misidentification of six K. oxytoca strains. Key biochemical tests fully confirmed the pehX PCR results. The new K. oxytoca identification assay should be useful for both clinical and ecological monitoring of K. oxytoca strains, as well as for controlling the previous identification of collection strains.
克雷伯氏菌属细菌是重要的机会致病菌,可引发医院感染,且对抗菌药物的耐药性日益增强。基于表型试验,很难对产酸克雷伯菌、肺炎克雷伯菌、植生克雷伯菌、解鸟氨酸克雷伯菌和土生克雷伯菌进行明确鉴别,在常规临床微生物学中经常出现错误鉴定。我们开发了一种基于多聚半乳糖醛酸酶(pehX)基因PCR扩增的方法,用于区分产酸克雷伯菌与克雷伯氏菌属的其他菌种。在所检测的35株产酸克雷伯菌中,均获得了一条344 bp的PCR扩增产物,但在29株肺炎克雷伯菌、12株植生克雷伯菌/解鸟氨酸克雷伯菌和7株土生克雷伯菌中均未获得。对欧文氏菌属中能降解多聚半乳糖醛酸的菌种进行检测,结果也为阴性。对来自国际菌种保藏中心(NCTC、PZH)的24株标记为肺炎克雷伯菌的菌株进行分析,发现其中6株产酸克雷伯菌之前被错误鉴定。关键生化试验完全证实了pehX PCR结果。这种新的产酸克雷伯菌鉴定方法对于产酸克雷伯菌菌株的临床和生态监测,以及控制之前对保藏菌株的鉴定都应是有用的。