As. Sekhon et al., AN EXOANTIGEN TEST FOR THE RAPID IDENTIFICATION OF MEDICALLY SIGNIFICANT FUSARIUM SPECIES, Journal of medical and veterinary mycology, 33(5), 1995, pp. 287-289
The accurate identification of Fusarium species can take 2-3 weeks. Pr
eliminary exoantigen studies indicate that a mature culture suspected
of being a Fusarium species may be immunologically identified 48 h aft
er receipt. Exoantigen extracts of 10-day-old slant cultures of Fusari
um chlamydosporum, Fusarium moniliforme (= Fusarium verticilloides), F
usarium oxysporum, Fusarium proliferation and Fusarium solani and part
ially purified reference homologous and heterologous shake culture ext
racts (6-week-old) were reacted against rabbit ant-F. chlamydosporum,
F.moniliforme, F. oxysporum, F. proliferatum and F. solani sera, in a
micro-immunodiffusion procedure. The results indicated that all the st
rains belonging to a given species produced 1-3 bands of identity only
when tested against its homologous antiserum and reference antigen. N
o cross-reactions were observed with the heterologous antisera. Furthe
rmore, extracts from isolate of Fusarium dimerum, Fusarium equiseti, F
usarium roseum complex, Acremonium species, Cylindrocarpon, Fonsecaea
pedrosoi and Trichoderma species did not react with any of the prepare
d Fusarium species' antisera. Our data suggest that the exoantigen pro
cedure is a rapid and reliable tool for the accurate immuno-identifica
tion of the medically Fusarium species studied.