Ochman H, Whittam T S, Caugant D A, Selander R K
J Gen Microbiol. 1983 Sep;129(9):2715-26. doi: 10.1099/00221287-129-9-2715.
Electrophoretically demonstrable variation in 12 enzymes was studied in more than 1 600 isolates of Escherichia coli from human and animal sources and in 123 strains of the four species of Shigella. All 12 enzymes were polymorphic; and the number of allozymes (mobility variants), which were equated with alleles, averaged 9.3 per locus in E. coli. For Shigella species, the mean number of alleles was 2.9 per locus. Some 77% of the allozymes recorded in Shigella were shared with E. coli. A total of 302 unique genotypic combinations of alleles over the 12 loci (electrophoretic types, ETs) was distinguished, of which 279 represented E. coli and 23 were Shigella. Among electrophoretic types, mean allelic diversity per locus was 0.52 for E. coli and 0.29 for Shigella. It was estimated that there are, on the average, about 0.3 detectable codon differences per locus between pairs of strains of E. coli and Shigella, which is roughly equivalent to 1.2 amino acid differences per enzyme. Evidence that the enzyme loci studied are a random sample of the genome is provided by a significant positive correlation between estimates of genetic divergence between pairs of strains obtained by DNA reassociation tests and estimates of genetic distance between the same strains based on electrophoresis. A principal components analysis of allozyme profiles revealed that the 302 ETs fall into three overlapping clusters, reflecting strong non-random associations of alleles, largely at four loci. Each of the four ETs of E. coli that have been most frequently recovered from natural populations has an allozyme profile that is very similar to, or identical with, the hypothetical modal ET of one of the groups. ETs of Shigella fall into two of the groups. No biological significance can at present bbe attributed to the genetic structure revealed by Multilocus electrophoretic techniques. The electrophoretic data are fully compatible with other molecular and more conventional evidence of a close affinity between E. coli and Shigella, and they raise questions regarding the present assignments of certain strains to species. In support of evidence from DNA reassociation tests and serotyping, the present study suggests that S. sonnei is homogeneous in chromosomal genotype.
对来自人和动物源的1600多株大肠杆菌分离株以及123株四种志贺氏菌属菌株中的12种酶进行了电泳可显示的变异研究。所有12种酶均具有多态性;在大肠杆菌中,等同于等位基因的同工酶(迁移率变体)数量平均每个位点为9.3个。对于志贺氏菌属,每个位点的等位基因平均数为2.9个。志贺氏菌属中记录的约77%的同工酶与大肠杆菌共有。在12个位点上总共区分出302种独特的等位基因基因型组合(电泳类型,ETs),其中279种代表大肠杆菌,23种是志贺氏菌属。在电泳类型中,大肠杆菌每个位点的平均等位基因多样性为0.52,志贺氏菌属为0.29。据估计,大肠杆菌和志贺氏菌属菌株对之间每个位点平均约有0.3个可检测到的密码子差异,这大致相当于每种酶有1.2个氨基酸差异。通过DNA重结合试验获得的菌株对之间遗传差异估计值与基于电泳的相同菌株之间遗传距离估计值之间存在显著正相关,这为所研究的酶位点是基因组的随机样本提供了证据。对同工酶谱的主成分分析表明,302种ETs分为三个重叠的簇,反映了等位基因的强烈非随机关联,主要在四个位点。从自然群体中最常分离到的大肠杆菌的四种ETs中的每一种都有一种同工酶谱,与其中一组的假设模式ET非常相似或相同。志贺氏菌属的ETs分为其中两组。目前,多位点电泳技术揭示的遗传结构尚无生物学意义。电泳数据与大肠杆菌和志贺氏菌属之间密切亲缘关系的其他分子证据和更传统证据完全一致,并且它们对目前某些菌株的种属划分提出了疑问。为支持来自DNA重结合试验和血清分型的证据,本研究表明宋内志贺氏菌在染色体基因型上是同质的。