Abstract
Sonicated chlamydospores of P. parasitica var. nicotianae were mixed into autoclaved Astatula sand to achieve defined inoculum densities. Individual 4 wk old susceptible tobacco plants were exposed to infested soil. After 50 days at 25.degree. C in a growth room, the percentages of infection were 23, 27, 50, 81, 92, 98 and 1O0 for plants originally exposed to 50, 75, 100, 250, 500, 1000 and 5000 chlamydospores/kg of soil, respectively. Motile zoospores were added to individual plants growing in flooded sand. After 28 days at 25.degree. C in a growth room, the percentages of infection were 10, 22, 35, 55, 82, 93 and 100 for plants originally exposed to 5, 15, 25, 50, 100, 200 and 300 zoospores/plant, respectively. Sonicated oospores that were frozen and either left untreated or treated with cellulase or gluculase (glucuronidase and sulfatase) enzymes were mixed into autoclaved soil at densities of 500-100,00O spores/kg of soil. The oospores were plated on various media to determine germination percentages. None of the enzyme-treated or untreated oospores germinated after 96-128 h at 25.degree. C and 12 h light on various media and none of the tobacco plants were infected after exposure to infested soil for 50 days at 25.degree. C in a growth room.