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脉冲场凝胶电泳用于比较与疫情相关的单核细胞增生李斯特菌菌株。

Pulsed-field gel electrophoresis applied for comparing Listeria monocytogenes strains involved in outbreaks.

作者信息

Buchrieser C, Brosch R, Catimel B, Rocourt J

机构信息

Laboratoire des Listeria, World Health Organization Collaborating Center for Foodborne Listeriosis, Institut Pasteur, Paris, France.

出版信息

Can J Microbiol. 1993 Apr;39(4):395-401. doi: 10.1139/m93-058.

Abstract

Recent food-borne outbreaks of human listeriosis as well as numerous sporadic cases have been mainly caused by Listeria monocytogenes serovar 4b strains. Thus, it was of interest to find out whether a certain clone or a certain few clones were responsible for these cases and especially for outbreaks. We used pulsed-field gel electrophoresis of large chromosomal DNA restriction fragments generated by ApaI, SmaI, or NotI to analyse 75 L. monocytogenes strains isolated during six major and eight smaller recent listeriosis outbreaks. These strains could be divided into 20 different genomic varieties. Thirteen of 14 strains isolated during major epidemics in Switzerland (1983-1987), the United States (California, 1985) and Denmark (1985-1987) demonstrated indistinguishable DNA restriction patterns. In contrast, strains responsible for the outbreaks in Canada (Nova Scotia, 1981), the United States (Massachusetts, 1983), France (Anjou, 1975-1976), New Zealand (1969), and Austria (1986) and some smaller outbreaks in France (1987, 1988, 1989) were each characterized by particular combinations of DNA restriction patterns. Seventy-seven percent of the tested strains could be classified into the previously described ApaI group A (Brosch et al. 1991), demonstrating a very close genomic relatedness. Because 49% of the epidemic strains selected for this study belonged to phagovar 2389/2425/3274/2671/47/108/340 or 2389/47/108/340, fifty-six additional strains of these phagovars, isolated from various origins, were also typed to determine whether differences in DNA restriction profiles between epidemic and randomly selected strains of the same phagovars could be pointed out. Variations in DNA patterns appeared more frequently within randomly selected strains than within epidemic strains.

摘要

近期食源性人类李斯特菌病的暴发以及众多散发病例主要由单核细胞增生李斯特菌血清型4b菌株引起。因此,弄清楚是否某个克隆或某几个克隆导致了这些病例尤其是暴发疫情,是很有意义的。我们使用脉冲场凝胶电泳分析由ApaI、SmaI或NotI产生的大染色体DNA限制性片段,对在最近六次主要和八次较小的李斯特菌病暴发期间分离出的75株单核细胞增生李斯特菌菌株进行分析。这些菌株可分为20种不同的基因组变种。在瑞士(1983 - 1987年)、美国(加利福尼亚州,1985年)和丹麦(1985 - 1987年)的主要疫情期间分离出的14株菌株中的13株,显示出难以区分的DNA限制性图谱。相比之下,在加拿大(新斯科舍省,1981年)、美国(马萨诸塞州,1983年)、法国(安茹,1975 - 1976年)、新西兰(1969年)和奥地利(1986年)的暴发疫情中以及法国一些较小的暴发疫情(1987年、1988年、1989年)中负责的菌株,各自具有特定的DNA限制性图谱组合特征。77%的测试菌株可归入先前描述的ApaI A组(Brosch等人,1991年),显示出非常密切的基因组相关性。由于本研究中选择的49%的疫情菌株属于噬菌型2389/2425/3274/2671/47/108/340或2389/47/108/340,还对从不同来源分离出的另外56株这些噬菌型菌株进行了分型,以确定同一噬菌型的疫情菌株和随机选择的菌株之间在DNA限制性图谱上是否存在差异。DNA图谱的变异在随机选择的菌株中比在疫情菌株中更频繁出现。

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