An acidic, endochitinase gene (pcht28) isolated from Lycopersicon chilense
was introduced into tomato (L. esculentum) through Agrobacterium-mediated t
ransformation, using the CAMV 35S promoter. Transgenic plants demonstrated
a high level of constitutive expression of pcht28 and chitinase enzyme acti
vity. Kanamycin-resistant R1 plants (resulting from self-pollination of tra
nsgenic plants) as well as R2 plants were evaluated for their tolerance to
Verticillium dahliae (race 1 and 2 for R1 plants and race 2 for R2 plants)
in the greenhouse. They demonstrated a significantly (P<0.05) higher level
of tolerance to the fungi compared to the nontransgenic plants, as measured
by foliar disease symptoms, vascular discoloration, and vascular discolora
tion index. The transgenic plants produced in this study represent a source
of genetic resistance to Verticillium dahliae.