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

dc.contributor.authorRead, David Alan
dc.contributor.authorFeatherstone, Jonathan
dc.contributor.authorRees, David Jasper Gilbert
dc.contributor.authorThompson, Genevieve Dawn
dc.contributor.authorRoberts, Ronel
dc.contributor.authorFlett, Bradley Charles
dc.contributor.authorMashingaidze, Kingston
dc.contributor.authorBerger, David Kenneth
dc.contributor.authorWelgemoed, Tanya
dc.contributor.authorPietersen, Gerhard
dc.contributor.authorSchulze, Susanna Elizabeth
dc.contributor.authorKiula, Barnabas Anthony
dc.contributor.authorKullaya, Alois
dc.contributor.authorMbega, Ernest
dc.date.accessioned2019-09-03T11:07:09Z
dc.date.issued2019-02
dc.description.abstractMaize 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.departmentForestry and Agricultural Biotechnology Institute (FABI)en_ZA
dc.description.departmentMicrobiology and Plant Pathologyen_ZA
dc.description.departmentPlant Production and Soil Scienceen_ZA
dc.description.embargo2020-02-01
dc.description.librarianam2019en_ZA
dc.description.urihttps://link.springer.com/journal/42161en_ZA
dc.identifier.citationRead, 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.issn1125-4653 (print)
dc.identifier.issn2239-7264 (online)
dc.identifier.other10.1007/s42161-018-0152-5
dc.identifier.urihttp://hdl.handle.net/2263/71265
dc.language.isoenen_ZA
dc.publisherSpringeren_ZA
dc.rights© Società Italiana di Patologia Vegetale (S.I.Pa.V.) 2018en_ZA
dc.subjectEmerging virusen_ZA
dc.subjectStunting symptomsen_ZA
dc.subjectRNA sequencingen_ZA
dc.subjectMaize yellow mosaic virus (MaYMV)en_ZA
dc.subjectMaize (Zea mays)en_ZA
dc.subjectTanzaniaen_ZA
dc.titleFirst report of maize yellow mosaic virus (MaYMV) on maize (Zea mays) in Tanzaniaen_ZA
dc.typeArticleen_ZA

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