First Report of Dasheen mosaic virus Infecting Taro (Colocasia esculenta) from Ethiopia
- D. B. Kidanemariam , Holetta National Agricultural Biotechnology Research Center, Ethiopian Institute of Agricultural Research, Addis Ababa, Ethiopia
- M. W. Macharia
- J. Harvey
- T. Holton , Biosciences east and central Africa-International Livestock Research Institute, Nairobi, Kenya
- A. Sukal
- A. P. James †
- R. M. Harding , Centre for Tropical Crops and Biocommodities, Queensland University of Technology, Brisbane, Australia
- A. D. Abraham , Department of Biotechnology, Addis Ababa Science and Technology University, Addis Ababa, Ethiopia.
Dasheen mosaic virus (DsMV) is a member of the family Potyviridae, genus Potyvirus, and infects taro (Colocasia esculenta L.) and other aroids wherever they grow. DsMV infection results in characteristic feathery mottle and mosaic symptoms on leaves and can cause up to 60% production losses on taro and other edible aroids (Lebot 2009; Reyes et al. 2006). In June 2012, taro plants showing mosaic, feathery mottle, and yellowing symptoms were observed in a germplasm collection at the Areka Agricultural Research Center, Wolayita Zone, southern Ethiopia, and leaf samples were collected. Taro plants maintained in the collection were originally obtained from farmer’s fields in south and southwest Ethiopia. The samples were initially tested for potyviruses by antigen-coated plate (ACP) ELISA using the potyvirus group PathoScreen kit (Agdia, U.S.A.) and all eight samples tested positive. Subsequently, the samples were screened for the presence of DsMV using DsMV-specific double antibody sandwich (DAS) ELISA (Agdia, U.S.A.), with all eight samples again testing positive. Total RNA was then extracted from the samples using the ZR RNA MiniPrep kit (ZYMO, U.S.A.), cDNA was synthesized using the RevertAid First Strand cDNA Synthesis Kit (Thermo Fisher Scientific, U.K.), and PCR carried out using degenerate primers NIb2F/3R targeting the NIb-coding region (Zheng et al. 2010). Amplicons of the expected size (∼350 bp) were generated from all eight samples and were cloned and sequenced. Sequencing was carried out at the SegoliP Unit at BecA-ILRI Hub (Nairobi, Kenya) and sequences were analyzed using CLC Main Workbench v6.9.2 (QIAGEN, U.S.A). The eight sequences (deposited in GenBank as accession nos. MG709254–MG709261) shared 86 to 100% nucleotide identity. BLAST analysis showed a maximum of 88 and 96% identity at the nucleotide and amino acid levels, respectively, to DsMV isolate SdP from China (JX083210) infecting the aroid Pinellia pedatisecta. The minimum nucleotide identity of 86% between sequences probably suggests several introductions of DsMV into southern Ethiopia, although further characterization of DsMV isolates of known provenance will be required to determine the possible origins of the different DsMV isolates detected. To the best of our knowledge, this is the first report of DsMV infecting taro in Ethiopia. Taro is widely grown and is an important staple food crop in south Ethiopia. The presence of DsMV presents a serious threat to taro production and further work is needed to determine the geographic distribution, incidence, and yield losses associated with DsMV infection in taro-growing areas in Ethiopia.
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Funding: Biosciences East and Central Africa (BecA-ILRI hub) through the African Biosciences Challenge Fund program.


