During November 2004, veinal chlorosis on mature cassava leaves, typical of cassava brown streak disease (CBSD), was observed at Mukono in central Uganda. Five out of 11 cultivars at the site showed CBSD symptoms (incidence range 4 to 64%). In a survey of farmers' fields, CBSD was observed in Wakiso and Mukono districts. Incidence of cassava mosaic disease was also recorded and averaged 60% for landraces (range 16.7 to 100%) and 20% for resistant varieties (range 0 to 65%). Leaf samples of plants with CBSD symptoms produced an amplicon of 222 bp using reverse transcription-polymerase chain reaction with primers that amplify a fragment of the coat protein (CP) gene of Cassava brown streak virus. Sequence comparisons based on the amplified CP gene fragment indicated that the isolates have 77 to 82.9% nucleotide and 43.9 to 56.8% amino acid identity with those from Mozambique and Tanzania. There was 95.9 to 99.5% nucleotide and 85.1 to 90.5% amino acid identity among the Ugandan isolates. These results confirm the re-emergence of CBSD in Uganda after it was first observed in the 1930s in cassava introduced from Tanzania and controlled by eradication. Prior to this report, CBSD was known to be restricted to the coastal lowlands of East Africa.

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Two whitefly species, Bemisia afer (Priesner & Hosny) and B. tabaci (Gennadius) were used in transmission experiments with Cassava brown streak virus (CBSV) (Ipomovirus; Potyviridae). Adults of whiteflies were given access to CBSV by containing them in clip cages on CBSV-infected cassava plants. Whiteflies were then transferred, together or separately, to CBSD-susceptible cassava plants of var. ÔAlbertÕ in a controlled environment. In glasshouse experiments, whiteflies were caged with CBSV-infected and virusfree cassava plants. Transmission of CBSV was sporadic and occurred in three of seven experiments when inoculated by B. afer and B. tabaci or B. tabaci alone, but not by B. afer alone. However, rate of transmission was low (maximum 22%) even when using high whitefly numbers of up to 120 per target plant. Successful transmission was confirmed by the detection of CBSV by reverse transcription-polymerase chain reaction. Spread of cassava brown streak disease (CBSD) in the field in Tanzania coincided with increases in whitefly numbers; further supporting the evidence that B. tabaci is a vector of CBSV. The results of this study establish for the first time that B. tabaci is the vector of CBSV, similar to other ipomoviruses.www.blackwell-synergy.com