Abstract
SUMMARYPreparations were made from chervil plants doubly infected with carrot mottle virus (CMotV) and its helper virus, carrot red leaf (CRLV), on which it depends for transmission by the aphid Cavariella aegopodii, by the procedure developed previously for CRLV. The preparations contained 25 nm isometric particles which were indistinguishable from those of CRLV but possessed aphid‐transmissible infectivity of both viruses and manually transmissible infectivity of CMotV. Only one sedimenting and buoyant density component was detected. The manually transmissible CMotV infectivity was resistant to freezing and to organic solvents, treatments that destroyed the CMotV infectivity in extracts from singly infected plants. The aphid‐transmissible CMotV infectivity in preparations from CRLV/ CMotV‐infected plants, and that in extracts from CRLV/CMotV‐carrying C. aegopodii, was abolished by treatment with CRLV antiserum but not with normal serum. These results show that transmission of CMotV by C. aegopodii is dependent on the packaging of its RNA in coats composed partially or entirely of CRLV particle protein.The aphid Myzus persicae does not transmit CRLV or CMotV from plants mixedly or singly infected with these viruses but it is a vector of beet western yellows virus (BWYV) and potato leafroll virus (PLRV) and it transmitted CMotV from plants that also contained either of these viruses. This suggests that the coat proteins of BWYV and PLRV can substitute for that of CRLV in packaging CMotV nucleic acid and thereby confer on it their own vector specificities.
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