Hafner G J, Harding R M, Dale J L
Centre for Molecular Biotechnology, Queensland University of Technology, Brisbane, Australia.
J Gen Virol. 1995 Sep;76 ( Pt 9):2279-85. doi: 10.1099/0022-1317-76-9-2279.
The systemic movement and replication of banana bunchy top virus (BBTV) DNA component one were investigated. Strand-specific RNA probes and PCR were used to indicate the presence of the virus in various parts of infected banana plants during infection on the basis of dsDNA replicative intermediates of BBTV. The strand-specific probes were not only able to detect the presence of the virus but also gave an indication of where the virus replicated. The results using both the virion sense and complementary to virion sense specific probes were essentially the same indicating that BBTV initially replicated for a short period at the site of inoculation, and subsequently moved down the pseudostem to the basal meristematic region and ultimately into the roots and newly formed leaves. The virus was detected in the leaves formed prior to inoculation after 21 days using PCR but was not detected by the RNA probes. This indicated that the virus had the ability to move into these leaves but may not have replicated or accumulated to significant levels. The appearance of multimeric forms of BBTV suggested that the virus may have replicated via a rolling circle mechanism. Additionally, BBTV DNA component one did not appear to replicate in its aphid vector, Pentalonia nigronervosa.
对香蕉束顶病毒(BBTV)DNA组分一的系统移动和复制进行了研究。基于BBTV的双链DNA复制中间体,使用链特异性RNA探针和PCR来指示在感染期间病毒在受感染香蕉植株各个部位的存在情况。链特异性探针不仅能够检测到病毒的存在,还能指示病毒复制的位置。使用病毒粒子正义链和与病毒粒子正义链互补的特异性探针得到的结果基本相同,表明BBTV最初在接种部位短暂复制,随后沿假茎向下移动到基部分生组织区域,并最终进入根部和新形成的叶片。接种21天后,使用PCR在接种前形成的叶片中检测到了病毒,但RNA探针未检测到。这表明病毒有能力移动到这些叶片中,但可能没有复制或积累到显著水平。BBTV多聚体形式的出现表明该病毒可能通过滚环机制进行复制。此外,BBTV DNA组分一似乎不在其蚜虫传播介体黑脉金斑蚜中复制。