Assessment of transmission ability of barley yellow dwarf virus-PAV isolates by different populations of Rhopalosiphum padi and Sitobion avenae

Citation
B. Bencharki et al., Assessment of transmission ability of barley yellow dwarf virus-PAV isolates by different populations of Rhopalosiphum padi and Sitobion avenae, EUR J PL P, 106(5), 2000, pp. 455-464
Citations number
47
Categorie Soggetti
Plant Sciences
Journal title
EUROPEAN JOURNAL OF PLANT PATHOLOGY
ISSN journal
09291873 → ACNP
Volume
106
Issue
5
Year of publication
2000
Pages
455 - 464
Database
ISI
SICI code
0929-1873(200006)106:5<455:AOTAOB>2.0.ZU;2-F
Abstract
Populations of two aphid species from different geographic regions of Moroc co were tested for their ability to transmit five barley yellow dwarf virus -PAV (BYDV-PAV) type isolates using Clintland 64 oat as the test plant. Tra nsmission efficiencies were determined for 10 sub-populations of Rhopalosip hum padi and 12 sub-populations of Sitobion avenae. After a short acquisiti on access period (AAP) of 4 h, all populations transmitted the virus but wi th different efficiencies. R. padi (Rp-S) and S. avenae (Sa-S) collected in the Settat region were the most efficient vectors, with transmission rates of 38% and 27%, respectively. R. padi (Rp-C) collected at Chaouen and S. a venae (Sa-B) at Berkane, were poor transmitters with respective vectoring a bilities of 20% and 16%. These four sub-populations were chosen to study th e acquisition of BYDV-PAV and the retention of virus within aphids in more detail. The transmission after two AAPs of 4 h and 48 h were compared. Star ved aphids given a 4 h AAP had significantly higher transmission efficienci es than non-starved aphids. However, after a 48 h AAP, no difference was ob served in the transmission between starved and non-starved aphids. Intraspe cific variability was also detected by means of serial transfers of individ ual aphids after the given AAP. Following the first day of serial transfers , no differences were observed in transmission efficiency and virus titers for sub-populations within each species acquiring the virus during 48 h, bu t there was significant variation when the virus was acquired in 4 h. The l evels of PAV antigen retained by aphids fed on healthy plants declined rapi dly during the first day after acquisition, but remained fairly constant du ring the next 5-7 days depending on the length of the AAP. Virus antigen co uld be detected by ELISA in Rp-S and Sa-S for up to 11 days of serial trans fer, but it was shown that aphids could retain and transmit BYDV-PAV for at least 3 weeks.