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Appl. Environ. Microbiol., Jan 1996, 87-93, Vol 62, No. 1
MA Ferreira, PW Tooley, E Hatziloukas, C Castro and NW Schaad
Mitochondrial DNA (mtDNA) from five isolates of Tilletia indica was
isolated and digested with several restriction enzymes. A 2.3-kb EcoRI
fragment was chosen, cloned, and shown to hybridize with total DNA
restricted with EcoRI from T. indica and not from a morphologically similar
smut fungus, Tilletia barclayana. The clone was partially sequenced, and
primers were designed and tested under high-stringency conditions in PCR
assays. The primer pair Ti1/Ti4 amplified a 2.3-kb fragment from total DNA
of 17 T. indica isolates from India, Pakistan, and Mexico. DNA from 25
isolates of other smut fungi (T. barclayana, Tilletia foetida, Tilletia
caries, Tilletia fusca, and Tilletia controversa) did not produce any
bands, as detected by ethidium bromide- stained agarose gels and Southern
hybridizations. The sensitivity of the assay was determined and increased
by using a single nested primer in a second round of amplification, so that
1 pg of total mycelial DNA could be detected. The results indicated that
the primers which originated from a cloned mtDNA sequence can be used to
differentiate T. indica from other Tilletia species and have the potential
to identify teliospores contaminating wheat seeds.
Copyright © 1996, American Society for Microbiology
Isolation of a species-specific mitochondrial DNA sequence for identification of Tilletia indica, the Karnal bunt of wheat fungus
Departmento de Biologia Celular, Universidade de Brasilia, D.F., Brazil.
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