Sorghum ergot, initially restricted to Asia and Africa, was recently found
in the Americas and Australia. Three species causing the disease have been
reported: Claviceps sorghi in India, C. sorghicola in Japan, and C. african
a in all ergot-positive countries. The objective of our study was to study
the intraspecific variation in C. africana isolates in the Americas, Africa
, India. and Australia. We confirmed C. africana, C. sorghi, and C. sorghic
ola as different species using differences in nucleotide sequences of inter
nal transcribed spacer 1 and 5.8S rDNA regions. Sequences of this region ob
tained from the representative American, Indian, and Australian isolates of
C. africana were identical. In addition, random amplified polymorphic DNA
(RAPD) banding patterns of sorghum ergot pathogen isolates from the United
States, Mexico, Puerto Rico, Bolivia, Australia, and India were evaluated w
ith nearly 100 primers. A total of 65 primers gave identical patterns for a
ll isolates, which confirmed that all were C. africana. The identity of RAP
D pattern and rDNA sequence of Indian isolates with those of C. africana co
nfirmed that the species is now present in India. Only 20 primers gave smal
l pattern differences and 7 of them were used for routine testing. All of t
he American isolates were identical and three isolates of the same type wer
e also found in South Africa, suggesting Africa as the origin of the invasi
on clone in the Americas. Australian and Indian isolates were distinguishab
le by a single band difference; therefore, migration from the Asian region
to Australia is suspected. Another distinct group was found in Africa. Clus
ter analysis of the informative bands revealed that the American and Africa
n group are on the same moderately (69%) supported clade. Isolates from Aus
tralia and India belonged to another clade.