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通过多位点酶电泳对幽门螺杆菌进行群体遗传分析:广泛的等位基因多样性和重组群体结构。

Population genetic analysis of Helicobacter pylori by multilocus enzyme electrophoresis: extensive allelic diversity and recombinational population structure.

作者信息

Go M F, Kapur V, Graham D Y, Musser J M

机构信息

Section of Gastroenterology, Department of Medicine, Veterans Affairs Medical Center, Houson, TX, USA.

出版信息

J Bacteriol. 1996 Jul;178(13):3934-8. doi: 10.1128/jb.178.13.3934-3938.1996.

Abstract

Genetic diversity and relationships in 74 Helicobacter pylori isolates recovered from patients assigned to distinct clinical categories were estimated by examination of allelic variation in six genes encoding metabolic housekeeping enzymes by multilocus enzyme electrophoresis. Seventy-three distinct allele profiles, representing multilocus chromosomal genotypes, were identified. All six loci were highly polymorphic, with an average of 11.2 alleles per locus. The mean genetic diversity in the sample was 0.735, a value that exceeds the level of diversity recorded in virtually all bacterial species studied by multilocus enzyme electrophoresis. A high frequency of occurrence of null alleles (lack of enzyme activity) was identified and warrants further investigation at the molecular level. Lack of linkage disequilibrium (nonrandom association (of alleles over loci) indicates that horizontal transfer and recombination of metabolic enzyme genes have contributed to the generation of chromosomal diversity in H. pylori. In this sample of isolates, there was no statistically significant association of multilocus enzyme electrophoretic types or cluster of related chromosomal types and disease category.

摘要

通过多位点酶电泳检测编码代谢管家酶的六个基因中的等位基因变异,对从不同临床分类患者中分离出的74株幽门螺杆菌的遗传多样性和关系进行了评估。确定了代表多位点染色体基因型的73种不同的等位基因谱。所有六个位点都具有高度多态性,每个位点平均有11.2个等位基因。样本中的平均遗传多样性为0.735,这一数值超过了几乎所有通过多位点酶电泳研究的细菌物种所记录的多样性水平。已鉴定出无效等位基因(缺乏酶活性)的高发生率,值得在分子水平上进一步研究。缺乏连锁不平衡(等位基因在不同位点的非随机关联)表明代谢酶基因的水平转移和重组促成了幽门螺杆菌染色体多样性的产生。在这个分离株样本中,多位点酶电泳类型或相关染色体类型簇与疾病类别之间没有统计学上显著的关联。

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