First report of maize yellow mosaic virus (MaYMV) on maize (Zea mays) in Tanzania

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dc.contributor.author Read, David Alan
dc.contributor.author Featherstone, Jonathan
dc.contributor.author Rees, David Jasper Gilbert
dc.contributor.author Thompson, Genevieve Dawn
dc.contributor.author Roberts, Ronel
dc.contributor.author Flett, Bradley Charles
dc.contributor.author Mashingaidze, Kingston
dc.contributor.author Berger, David Kenneth
dc.contributor.author Welgemoed, Tanya
dc.contributor.author Pietersen, Gerhard
dc.contributor.author Schulze, Susanna Elizabeth
dc.contributor.author Kiula, Barnabas Anthony
dc.contributor.author Kullaya, Alois
dc.contributor.author Mbega, Ernest
dc.date.accessioned 2019-09-03T11:07:09Z
dc.date.issued 2019-02
dc.description.abstract Maize yellow mosaic virus (MaYMV) has been reported from China, Ecuador, Brazil and Burkino Faso on maize since 2016 and appears to be an emerging virus with a wide global distribution. Thirty-five maize samples with varying degrees of mosaic and stunting symptoms, were collected in May/June 2015 from the regions of Mara, Arusha, Manyara, Kilimanjaro, Morogoro and Pwani in Tanzania. Total RNA was extracted from leaf material, which was used to prepare RNAtag libraries according to Shishkin et al. (2015). Sequencing was carried out on an Illumina HiSeq2500 instrument. The reads from each dataset were taxonomically classified using the Kaiju software package (Menzel et al. 2016), with thirty datasets having reads showing homology to MaYMV, as well as either/both Maize chlorotic mottle virus and potyviruses. Trimmed datasets were assembled using CLC Genomics Workbench 9 de Novo assembly tool on default settings, with the exception of the following: “minimum contig length” (2000 bp), “length fraction” (0.9), “similarity fraction” (0.9). This yielded seven full/near full genomes with GenBank accession numbers MG664788 – MG664794, sharing 97.9–99.9% sequence homology. These sequences shared a 96.3–96.5% (KU291105) and 97–97.3% (KU291103) nucleotide identity with those from China. Seven positive samples were tested with RT-PCR, using the PCR primers MaYMV-F and MaYMV-R (Chen et al. 2016). Six samples produced the expected RT-PCR amplicon of 750 bp, with one potentially below the detection limit for RT-PCR. An RNA-seq negative sample did not produce the MaYMV amplicon but was positive for a maize control RT-PCR (actin), as expected. The identities of the amplicons were confirmed in four samples using Sanger sequencing. Next generation sequencing and PCR confirmed MaYMV positive samples in all sampled regions except Pwani. The broad geographical distribution of MaYMV in samples from this study suggests that the virus is well established in Tanzania. en_ZA
dc.description.department Forestry and Agricultural Biotechnology Institute (FABI) en_ZA
dc.description.department Microbiology and Plant Pathology en_ZA
dc.description.department Plant Production and Soil Science en_ZA
dc.description.embargo 2020-02-01
dc.description.librarian am2019 en_ZA
dc.description.uri https://link.springer.com/journal/42161 en_ZA
dc.identifier.citation Read, D.A., Featherstone, J., Rees, D.J.G. et al. First report of maize yellow mosaic virus (MaYMV) on maize (Zea mays) in Tanzania. Journal of Plant Pathology (2019) 101: 203. https://doi.org/10.1007/s42161-018-0152-5. en_ZA
dc.identifier.issn 1125-4653 (print)
dc.identifier.issn 2239-7264 (online)
dc.identifier.other 10.1007/s42161-018-0152-5
dc.identifier.uri http://hdl.handle.net/2263/71265
dc.language.iso en en_ZA
dc.publisher Springer en_ZA
dc.rights © Società Italiana di Patologia Vegetale (S.I.Pa.V.) 2018 en_ZA
dc.subject Emerging virus en_ZA
dc.subject Stunting symptoms en_ZA
dc.subject RNA sequencing en_ZA
dc.subject Maize yellow mosaic virus (MaYMV) en_ZA
dc.subject Maize (Zea mays) en_ZA
dc.subject Tanzania en_ZA
dc.title First report of maize yellow mosaic virus (MaYMV) on maize (Zea mays) in Tanzania en_ZA
dc.type Article en_ZA


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