首页> 外文期刊>Molecular biotechnology >Molecular studies on the transmission of indian cassava mosaic virus (ICMV) and Sri Lankan Cassava Mosaic Virus (SLCMV) in cassava by bemisia tabaci and cloning of ICMV and SLCMV replicase gene from cassava
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Molecular studies on the transmission of indian cassava mosaic virus (ICMV) and Sri Lankan Cassava Mosaic Virus (SLCMV) in cassava by bemisia tabaci and cloning of ICMV and SLCMV replicase gene from cassava

机译:烟粉虱对印度木薯花叶病毒(ICMV)和斯里兰卡木薯花叶病毒(SLCMV)的传播分子生物学研究以及从木薯中克隆ICMV和SLCMV复制酶基因的分子研究

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摘要

Cassava mosaic disease, caused by cassava mosaic geminiviruses are transmitted by Bemisia tabaci. The B. tabaci adults from colonies reared on virus free cassava plant produced from apical meristem culture was studied to determine their ability to transmit Indian cassava mosaic virus (ICMV) and Sri Lankan cassava mosaic virus (SLCMV) from cassava to cassava. Virus free plants were confirmed by polymerase chain reaction (PCR) using geminivirus degenerate primers. The virus acquisition access period (AAP) of 48 h on virus infected cassava leaves and 48 h virus inoculation access periods on virus free healthy leaves were investigated. Both ICMV and SLCMV were absolutely transmitted by whiteflies reared on cassava. Virus specific primers were designed in the replicase region and used to detect virus in B. tabaci after different AAP. The PCR amplified replicase genes from virus transmitted cassava leaves were cloned the plasmid DNA was isolated from a recombinant colony of E. coli DH5α after their confirmation by colony PCR and sequenced them. The nucleotide sequences obtained from automated DNA sequencing were confirmed as ICMV and SLCMV replicase gene after homology searching by BLAST and found to be a new isolates. The nucleotide sequences of new isolates were submitted in GenBank (accession number JN652126 and JN595785).
机译:木薯花叶双生病毒引起的木薯花叶病由烟粉虱传播。研究了在由顶端分生组织培养产生的无病毒木薯植物上饲养的菌落中的烟粉虱成人,以确定其将木薯印度花叶病毒(ICMV)和斯里兰卡木薯花叶病毒(SLCMV)从木薯传播到木薯的能力。使用双生病毒简并引物通过聚合酶链反应(PCR)确认无病毒植物。研究了病毒感染的木薯叶上48 h的病毒获取访问期(AAP)和无病毒的健康叶上48 h病毒接种访问期。 ICMV和SLCMV均由木薯上饲养的粉虱绝对传播。在复制酶区域中设计了病毒特异性引物,并用于在不同AAP后检测烟粉虱中的病毒。从病毒传播的木薯叶中PCR扩增的复制酶基因被克隆,在通过菌落PCR确认后,从大肠杆菌DH5α的重组菌落中分离质粒DNA并对其进行测序。通过BLAST同源性搜索,从自动DNA测序获得的核苷酸序列被确认为ICMV和SLCMV复制酶基因,并且发现是新的分离物。新分离株的核苷酸序列在GenBank中提交(登录号JN652126和JN595785)。

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