Table 3. Transformation of isogenic and non-isogenic H.pylori strains by chromosomal DNA containing selectable markers of different sizes.
Recipient H.pylori strain | Transformation frequency (× 10–7) | ||
---|---|---|---|
Transfer of a point mutation (1 bp)a from RA4 | Transfer of aphA cassette (1.3 kb)b from RA3 | Transfer of hpyIIRM::aphA cassette (4.8 kb) from RA1 | |
6cc | 141 ± 32 | 100 ± 19 | 49 ± 40 |
J166d | 98 ± 7e | 4 ± 0.9 | <0.4 |
CH4d | 106 ± 38e | 3 ± 2 | <0.4 |
HPK1d | 222 ± 160e | 1 ± 0.7 | <0.5 |
7767d | 113 ± 67e | 3 ± 2 | <0.4 |
aStrepr point mutation.
baphA present in vacA.
cStrain 6c has the same clonal origin as strain 6a.
dStrain has different origin to strain 6a.
eStrain was transformed by the point mutation in rpsL (A128G) conferring Strepr at a significantly higher frequency (P < 0.05) than by the aphA cassette or by the hpyIIRM::aphA cassette.