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. 1998 Mar;180(5):1159-65.
doi: 10.1128/JB.180.5.1159-1165.1998.

Chromosomal regions specific to pathogenic isolates of Escherichia coli have a phylogenetically clustered distribution

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Chromosomal regions specific to pathogenic isolates of Escherichia coli have a phylogenetically clustered distribution

E F Boyd et al. J Bacteriol. 1998 Mar.

Abstract

We studied the ancestry of virulence-associated genes in Escherichia coli by examining chromosomal regions specific to pathogenic isolates. The four virulence determinants examined were the alpha-hemolysin (hly) loci hlyI and hlyII, the type II capsule gene cluster kps, and the P (pap) and S (sfa) fimbria gene clusters. All four loci were shown previously to be associated with pathogenicity islands of uropathogenic E. coli isolates. The hly, kps, sfa, and pap regions each have an unexpected clustered distribution among the E. coli collection of reference (ECOR) strains, but all these regions were absent from a collection of diarrheagenic E. coli isolates. Strains in the ECOR subgroup B2 typically had a combination of at least three of the four loci, and all strains in subgroup D had a copy of the kps and pap clusters. In contrast, only four strains in subgroup A had either hly, kps, sfa, or pap, and no subgroup A strains had all four together. Strains of subgroup B1 were devoid of all four virulence regions, with the exception of one isolate that had a copy of the sfa gene cluster. This phylogenetic distribution of strain-specific sequences corresponds to the ECOR groups with the largest genome size, namely, B2 and D. We propose that the pathogenicity islands are ancestral to subgroups B2 and D and were acquired after speciation, with subsequent horizontal transfer into some group A, B1, and E lineages. These results suggest that the hly, kps, sfa, and pap pathogenicity determinants may play a role in the evolution of enteric bacteria quite apart from, and perhaps with precedence over, their ability to cause disease.

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Figures

FIG. 1
FIG. 1
Gene organization of kps, sfa, pap, and hly gene clusters. (A and B) Organization of pap and sfa gene clusters. Boxes indicate genes, and uppercase letters indicate gene designation(s). (C) The kps genes in region 1 (five genes [kpsSCUDE]) and region 3 (two genes [kpsMT]) are conserved among E. coli isolates that synthesize serologically distinct capsules. The number of genes in the central region 2 (kpsDBACES) reflects the size and complexity of the polysaccharide repeating unit. (D) The alpha-hemolysin determinant from E. coli J96 is represented; it consists of four genes. Black bars below gene clusters indicate the position of DNA fragments used as probes.
FIG. 2
FIG. 2
Distribution of the kps, sfa, pap, and hly complexes among the ECOR collection of natural isolates. The tree is based on electrophoretic variation among 38 enzymes (15). Only for the pap operon did the three probes used give differing results.
FIG. 3
FIG. 3
Distribution of polymorphic nucleotide and amino acid sites along the kspD, papH, and hlyA genes among ECOR isolates. Vertical numbers indicate the nucleotide position along the gene. Dots indicate nucleotide identity.
FIG. 4
FIG. 4
Evolutionary relationships among three chromosomal loci. Pairwise genetic distances were estimated from the numbers of substitutions (18, 24). Letters indicate subgroups of the ECOR strains, and numbers indicate genetic distance.

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