P. Mehta et al., TRANSMISSION OF TOMATO YELLOW LEAF CURL GEMINIVIRUS BY BEMISIA-TABACI(HOMOPTERA, ALEYRODIDAE), Journal of economic entomology, 87(5), 1994, pp. 1291-1297
The sweetpotato whitefly, Bemisie tebaci (Gennadius), is an economical
ly important pest worldwide. A new biotype of sweetpotato whitefly, bi
otype B, causes extensive damage by direct feeding and by the transmis
sion of plant viruses, such as geminiviruses. Because of the importanc
e of whitefly-transmitted geminiviruses, studies were conducted to qua
ntify the characteristics of tomato yellow leaf curl geminivirus (TYLC
V) transmission by the vector B. tabaci. Transmission of an isolate of
TYLCV from Egypt was achieved with one adult B. tabaci per plant, but
the efficiency of transmission increased fourfold when the number of
adults were increased to five per plant. B. tabaci transmitted TYLCV a
fter a minimum acquisition-access period of 15 min, and rate of transm
ission increased as the acquisition-access period was lengthened and r
eached a maximum after 24 h. A minimum inoculation-access period of 15
min was observed with the rate of transmission increasing as the inoc
ulation-access period was lengthened, reaching a maximum after a 12-h
inoculation-access period. When B. tabaci were transferred serially af
ter acquisition, adults were unable to transmit TYLCV until 24 h after
the initiation of the acquisition-access period regardless of the len
gth of acquisition provided. The 24-h transmission threshold from init
ial vector access to a TYLCV-infected plant until transmission of the
virus includes both the acquisition-access period and the latent perio
d during which the virus circulates within the vector. Retention of TY
LCV from the nymphal to adult stages of B. tabaci was supportive of a
circulative mode of transmission. TYLCV titer in B. tabaci after an ac
quisition-access period of 12 h continuously increased on a non-TYLCV
host starting at 12 h, reaching a peak at 108 h and remaining stable f
rom 132 to 180 h after the acquisition-access period. These data indic
ate multiplication of the virus in the vector as the most likely expla
nation for the continuous increase of TYLCV titer.