TABLE 1.
Sequence diversity of selected loci among analyzed P. aeruginosa strainsa
| Species | Gene locus | Mean nucleotide substitutions (%) among pairs of strains | dS | dN | GenBank accession no. of reference strain or reference |
|---|---|---|---|---|---|
| P. aeruginosa | oriC | 0.40 | M30125 | ||
| citS | 0.25 | 1.18 ± 0.31 | 0.00 | M29728 | |
| ampC | 0.38 | 1.11 ± 0.33 | 0.15 ± 0.07 | X54719 | |
| oprI | 0.15 | 1.28 ± 0.71 | 0.00 | X58714 | |
| fliC | 11.5 | ||||
| fliC a-type | 0.59 | 3.41 ± 0.61 | 0.74 ± 0.17 | M57501 | |
| fliC b-type | 0.05 | 0.26 ± 0.19 | 0.00 | U54775 | |
| pilA | 71.3 | ||||
| pilA group I | 13.3 | M21652 | |||
| pilA group II | 29.7 | M11323 | |||
| E. coli | gapA | 0.2 | 0.78 ± 0.28 | 0.09 ± 0.04 | 33 |
| putP | 2.4 | 9.04 ± 1.46 | 0.15 ± 0.11 | 31 | |
| mdh | 1.1 | 3.70 ± 0.65 | 0.15 ± 0.09 | 4 | |
| gnd | 7.2b | 32 | |||
| icd | 1.8 | 57 | |||
| aceK | 2.9 | 34 | |||
| Salmonella enterica | gapA | 3.8 | 15.55 ± 1.49 | 0.61 ± 0.15 | 33 |
| putP | 4.6 | 16.70 ± 1.88 | 0.60 ± 0.23 | 31 | |
| mdh | 4.5 | 20.13 ± 1.72 | 0.48 ± 0.16 | 4 | |
| gnd | 3.8 | 21.80 ± 1.40 | 0.44 ± 0.10 | 32 | |
| icd | 5.6 | 29.35 ± 2.00 | 0.25 ± 0.09 | 57 | |
| aceK | 5.7 | 28.39 ± 1.76 | 1.05 ± 0.14 | 34 |
Strain DSM 1128 is excluded because of its unusually high sequence variability in all analyzed loci. dS and dN indicate the average number of synonymous or nonsynonymous nucleotide substitutions using Jukes-Cantor corrections. To avoid hypervariable regions, the a-type and b-type flagellin genes were considered separately and the hypervariable pilin genes were excluded. For comparison, the following sequence variations are shown: glyceraldehyde-3-phosphate dehydrogenase gene (gapA), proline permease gene (putP), malate dehydrogenase gene (mdh), 6-phosphogluconate dehydrogenase gene (gnd), isocitrate dehydrogenase gene (icd), and isocitrate dehydrogenase kinase-phosphatase gene (aceK) in about 30 E. coli and Salmonella strains representing the major phylogenetic lineages.
Reflects high frequency of recombination within and among taxonomic groups because of close linkage with genes that are subject to diversifying selection (32).