A method was developed to isolate teliospores of Tilletia indica from infes
ted grain. The technique was evaluated to determine its sensitivity for det
ection and quantification of teliospores, the time required to conduct an i
ndividual test, and its utility for the detection and identification of the
pathogen for phytosanitary regulation and seed certification. A seed wash
of a 50-g grain sample was washed through 53-mu m and 20-mu m pore size nyl
on screens to remove unwanted debris and to concentrate and isolate teliosp
ores. The material retained in the 20-mu m screen was suspended for direct
microscopic examination or plated on water agar for teliospore germination
and identification by polymerase chain reaction (PCR) utilizing two pairs o
f T. indica-specific primers. The reliability of detection for both light m
icroscopy and PCR are 100% at an infestation of five teliospores per 50-g s
ample. The proportion of teliospores recovered from grain samples artificia
lly infested with T. indica was 0, 82, 88, 81, and 82%, respectively, at in
festation levels of 0, 1, 2, 5, and 10 teliospores per 50-g wheat sample. E
xtraction efficiency was comparable to the centrifuge seed-wash method curr
ently used by most seed health laboratories. Sample analysis using size-sel
ective sieving was more than 83% faster than the standard centrifuge seed w
ash.