10 research outputs found

    Transcriptional response of virus-infected cassava and identification of putative sources of resistance for cassava brown streak disease

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    Cassava (Manihot esculenta) is a major food staple in sub-Saharan Africa, which is severely affected by cassava brown streak disease (CBSD). The aim of this study was to identify resistance for CBSD as well as to understand the mechanism of putative resistance for providing effective control for the disease. Three cassava varieties; Kaleso, Kiroba and Albert were inoculated with cassava brown streak viruses by grafting and also using the natural insect vector the whitefly, Bemisia tabaci. Kaleso expressed mild or no disease symptoms and supported low concentrations of viruses, which is a characteristic of resistant plants. In comparison, Kiroba expressed severe leaf but milder root symptoms, while Albert was susceptible with severe symptoms both on leaves and roots. Real-time PCR was used to estimate virus concentrations in cassava varieties. Virus quantities were higher in Kiroba and Albert compared to Kaleso. The Illumina RNA-sequencing was used to further understand the genetic basis of resistance. More than 700 genes were uniquely overexpressed in Kaleso in response to virus infection compared to Albert. Surprisingly, none of them were similar to known resistant gene orthologs. Some of the overexpressed genes, however, belonged to the hormone signalling pathways and secondary metabolites, both of which are linked to plant resistance. These genes should be further characterised before confirming their role in resistance to CBSD

    Number of reads generated from the RNA-Seq analysis and the corresponding gene expression range obtained for resistant Kaleso and susceptible Albert cassava varieties.

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    <p>Number of reads generated from the RNA-Seq analysis and the corresponding gene expression range obtained for resistant Kaleso and susceptible Albert cassava varieties.</p

    Relative changes of virus titre in cassava plants for a) CBSV and b) UCBSV.

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    <p>Virus quantities were normalised to the concentration of virus detected in Albert at the first week time point.</p

    Fold enrichment of NAC-protein genes in infected cassavas as measured by RNA-Seq and RT-qPCR.

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    <p>Fold enrichment of NAC-protein genes in infected cassavas as measured by RNA-Seq and RT-qPCR.</p

    Number of cassava plants infected with CBSV or UCBSV in roots and leaves over a period of 12 weeks after virus inoculation by grafting as confirmed by RT-PCR.

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    <p>Number of cassava plants infected with CBSV or UCBSV in roots and leaves over a period of 12 weeks after virus inoculation by grafting as confirmed by RT-PCR.</p
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