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[通过脉冲场凝胶电泳对血液科分离的嗜麦芽窄食单胞菌进行分子分型]

[Molecular typing by pulsed field gel electrophoresis of Stenotrophomonas maltophilia isolated in a department of hematology].

作者信息

Fabe C, Rodriguez P, Cony-Makhoul P, Parneix P, Bebear C, Maugein J

机构信息

Laboratoire de Bactériologie, Hôpital Haut Lévêque, Pessac, France.

出版信息

Pathol Biol (Paris). 1996 May;44(5):435-41.

PMID:8758490
Abstract

Stenotrophomonas maltophilia is an important nosocomial pathogen. The increased isolates of S. maltophilia among hematology unit patients led to an epidemiological survey. Over 26 months, 24 strains isolated from 23 patients and an environmental isolate from blood pressure armband have been identified. The isolated were first analysed by the use of phenotypical markers: biotype, antibiotic susceptibility, but the minor differences observed justified a genotypic analysis. Pulsed field gel electrophoresis of genomic DNA was carried with XbaI and DraI restriction endonucleases by contour-clamped homogeneous electric field method (CHEF). The data obtained showed a great genomic diversity within the species S. maltophilia. Nevertheless, the same restriction profile was found for 3 patients and 3 other profiles were obtained for 3 couples of patients hospitalized at the same time. All the other strains isolated from subjects hospitalized during the same period exhibited pulsotypes independent from each other. Compared to biotypes and antibiotic susceptibility, these results indicate field only with non modified primers, and the absence of 460 mutations was confirmed by sequencing. Two isolates P1 and P2, from a transplanted patient were amplified with both primers MCMM and MCMW: sequencing analysis shown the presence of a mixture of strains, one of them harbouring A- > G 1378 mutation. One resistant strain was amplified neither with MCMM nor with MCMW: a C- > T silent mutation at nt 1368 was present. As sequencing analysis confirmed PCR results, discriminative PCR enables isolates to be rapidly assessed for the presence or absence of 460 mutations. Moreover, it can distinguish Met to Val from Met to Ile mutations, and allows the analysis of mixtures of sensitive and resistant strains.

摘要

嗜麦芽窄食单胞菌是一种重要的医院病原体。血液科患者中嗜麦芽窄食单胞菌分离株的增加促使开展了一项流行病学调查。在26个月的时间里,已从23名患者中鉴定出24株菌株以及从血压臂带中分离出的1株环境菌株。首先利用表型标记物对分离株进行分析:生物型、抗生素敏感性,但观察到的细微差异证明有必要进行基因分型分析。采用轮廓夹钳均匀电场法(CHEF),用XbaI和DraI限制性内切酶对基因组DNA进行脉冲场凝胶电泳。获得的数据显示嗜麦芽窄食单胞菌物种内存在很大的基因组多样性。然而,发现3名患者具有相同的限制性图谱,同时住院的另外3对患者获得了另外3种图谱。同期住院患者分离出的所有其他菌株呈现出相互独立的脉冲型。与生物型和抗生素敏感性相比,这些结果表明仅使用未修饰引物时,通过测序确认不存在460个突变。来自一名移植患者的两株分离株P1和P2用引物MCMM和MCMW进行扩增:测序分析显示存在菌株混合物,其中之一含有A->G 1378突变。一株耐药菌株既不能用MCMM也不能用MCMW扩增:在核苷酸1368处存在C->T沉默突变。由于测序分析证实了PCR结果,鉴别性PCR能够快速评估分离株是否存在460个突变。此外,它可以区分甲硫氨酸到缬氨酸的突变和甲硫氨酸到异亮氨酸的突变,并允许分析敏感和耐药菌株的混合物。

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