Detection of maize rough dwarf virus by enzyme‐linked immunosorbent assay in plant hosts and in the planthopper vector

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Abstract
SUMMARY: SVPs were efficiently detected by ELISA in individual male and female insects. Females carried more virus per insect and per unit fresh weight, but no significant difference was detected between males and females in vector efficiency. Of insects positive in ELISA, 15–20% were unable to transmit the virus to host plants. Storage of viruliferous hoppers at‐20°C decreased the level of viral antigen detected by half in about 240 days.Subviral particles (SVPs) of maize rough dwarf virus were detected in the planthopper vector Laodelphax striatellus and in maize and barley plants using double antibody sandwich ELISA. In purified preparations diluted in buffer, as little as 36 ng/ml of SVPs was detectable whereas after dilution in extracts of healthy frozen planthoppers the sensitivity was reduced to 50 ng/ml. Freezing the hoppers prior to extraction lowered to one third the background reading due to normal components. Neither the dissociated proteins of the SVP nor the viral double‐stranded RNA contributed to the ELISA readings.