7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Diagnostic kit for rice blight resistance

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Blight-resistant rice lines are the most effective solution for bacterial blight, caused by Xanthomonas oryzae pv. oryzae ( Xoo). Key resistance mechanisms involve SWEET genes as susceptibility factors. Bacterial transcription activator-like (TAL) effectors bind to effector-binding elements (EBEs) in SWEET gene promoters and induce SWEET genes. EBE variants that cannot be recognized by TAL effectors abrogate induction, causing resistance. Here we describe a diagnostic kit to enable analysis of bacterial blight in the field and identification of suitable resistant lines. Specifically, we include a SWEET promoter database, RT–PCR primers for detecting SWEET induction, engineered reporter rice lines to visualize SWEET protein accumulation and knock-out rice lines to identify virulence mechanisms in bacterial isolates. We also developed CRISPR–Cas9 genome-edited Kitaake rice to evaluate the efficacy of EBE mutations in resistance, software to predict the optimal resistance gene set for a specific geographic region, and two resistant ‘mega’ rice lines that will empower farmers to plant lines that are most likely to resist rice blight.

          Abstract

          Strategic deployment of blight-resistant rice lines is enabled by a molecular diagnostic kit.

          Related collections

          Most cited references35

          • Record: found
          • Abstract: found
          • Article: not found

          Sugar transporters for intercellular exchange and nutrition of pathogens.

          Sugar efflux transporters are essential for the maintenance of animal blood glucose levels, plant nectar production, and plant seed and pollen development. Despite broad biological importance, the identity of sugar efflux transporters has remained elusive. Using optical glucose sensors, we identified a new class of sugar transporters, named SWEETs, and show that at least six out of seventeen Arabidopsis, two out of over twenty rice and two out of seven homologues in Caenorhabditis elegans, and the single copy human protein, mediate glucose transport. Arabidopsis SWEET8 is essential for pollen viability, and the rice homologues SWEET11 and SWEET14 are specifically exploited by bacterial pathogens for virulence by means of direct binding of a bacterial effector to the SWEET promoter. Bacterial symbionts and fungal and bacterial pathogens induce the expression of different SWEET genes, indicating that the sugar efflux function of SWEET transporters is probably targeted by pathogens and symbionts for nutritional gain. The metazoan homologues may be involved in sugar efflux from intestinal, liver, epididymis and mammary cells.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            High-efficiency TALEN-based gene editing produces disease-resistant rice.

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Os8N3 is a host disease-susceptibility gene for bacterial blight of rice.

              Many bacterial diseases of plants depend on the interaction of type III effector genes of the pathogen and disease-susceptibility genes of the host. The host susceptibility genes are largely unknown. Here, we show that expression of the rice gene Os8N3, a member of the MtN3 gene family from plants and animals, is elevated upon infection by Xanthomonas oryzae pv. oryzae strain PXO99(A) and depends on the type III effector gene pthXo1. Os8N3 resides near xa13, and PXO99(A) failed to induce Os8N3 in rice lines with xa13. Silencing of Os8N3 by inhibitory RNA produced plants that were resistant to infection by strain PXO99(A) yet remained susceptible to other strains of the pathogen. The effector gene avrXa7 from strain PXO86 enabled PXO99(A) compatibility on either xa13- or Os8N3-silenced plants. The findings indicate that Os8N3 is a host susceptibility gene for bacterial blight targeted by the type III effector PthXo1. The results support the hypothesis that X. oryzae pv. oryzae commandeers the regulation of otherwise developmentally regulated host genes to induce a state of disease susceptibility. Furthermore, the results support a model in which the pathogen induces disease susceptibility in a gene-for-gene manner.
                Bookmark

                Author and article information

                Contributors
                yangbi@missouri.edu
                frommew@hhu.de
                Journal
                Nat Biotechnol
                Nat. Biotechnol
                Nature Biotechnology
                Nature Publishing Group US (New York )
                1087-0156
                1546-1696
                28 October 2019
                28 October 2019
                2019
                : 37
                : 11
                : 1372-1379
                Affiliations
                [1 ]ISNI 0000 0001 2176 9917, GRID grid.411327.2, Institute for Molecular Physiology and Cluster of Excellence on Plant Sciences (CEPLAS), , Heinrich Heine University of Düsseldorf, ; Düsseldorf, Germany
                [2 ]ISNI 0000 0001 0660 6765, GRID grid.419498.9, Max Planck Institute for Plant Breeding Research, ; Cologne, Germany
                [3 ]ISNI 0000 0001 2162 3504, GRID grid.134936.a, Division of Plant Sciences, Bond Life Sciences Center, , University of Missouri, ; Columbia, MO USA
                [4 ]ISNI 0000 0001 0729 330X, GRID grid.419387.0, International Rice Research Institute, ; Metro Manila, Philippines
                [5 ]ISNI 0000 0004 1936 8091, GRID grid.15276.37, Department of Plant Pathology, , University of Florida, ; Gainesville, FL USA
                [6 ]ISNI 0000 0004 1936 7312, GRID grid.34421.30, Department of Genetics, Development and Cell Biology, , Iowa State University, ; Ames, IA USA
                [7 ]ISNI 0000 0001 2097 0141, GRID grid.121334.6, IRD, CIRAD, , Université Montpellier, IPME, ; Montpellier, France
                [8 ]ISNI 0000 0004 0466 6352, GRID grid.34424.35, Donald Danforth Plant Science Center, ; St. Louis, MO USA
                [9 ]ISNI 0000 0001 0943 978X, GRID grid.27476.30, Institute of Transformative Bio-Molecules (WPI-ITbM), , Nagoya University, ; Aichi, Japan
                [10 ]GRID grid.449728.4, Present Address: College of Agriculture and Food Science, , University of the Philippines, ; Los Baños, Philippines
                Author information
                http://orcid.org/0000-0002-1654-4921
                http://orcid.org/0000-0002-9905-2454
                http://orcid.org/0000-0001-9517-5249
                http://orcid.org/0000-0002-2293-3384
                http://orcid.org/0000-0001-6465-0115
                Article
                268
                10.1038/s41587-019-0268-y
                6831515
                31659338
                4363f009-6044-448b-8536-95dc42406124
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 27 February 2019
                : 28 August 2019
                Funding
                Funded by: BMGF
                Funded by: Alexander von Humboldt Foundation and BMGF
                Categories
                Resource
                Custom metadata
                © The Author(s), under exclusive licence to Springer Nature Limited 2019

                Biotechnology
                pathogenesis,plant biotechnology,plant breeding,infection,biotechnology
                Biotechnology
                pathogenesis, plant biotechnology, plant breeding, infection, biotechnology

                Comments

                Comment on this article