97 research outputs found

    Partial Activation of SA- and JA-Defensive Pathways in Strawberry upon Colletotrichum acutatum Interaction

    Get PDF
    [EN] Understanding the nature of pathogen host interaction may help improve strawberry (Fragaria x anahassa) cultivars. Plant resistance to pathogenic agents usually operates through a complex network of defense mechanisms mediated by a diverse array of signaling molecules. In strawberry, resistance to a variety of pathogens has been reported to be mostly polygenic and quantitatively inherited, making it difficult to associate molecular markers with disease resistance genes. Colletotrichum acutaturn spp. is a major strawberry pathogen, and completely resistant cultivars have not been reported. Moreover, strawberry defense network components and mechanisms remain largely unknown and poorly understood. Assessment of the strawberry response to C. acutatum included a global transcript analysis, and acidic hormones SA and JA measurements were analyzed after challenge with the pathogen. Induction of transcripts corresponding to the SA and JA signaling pathways and key genes controlling major steps within these defense pathways was detected. Accordingly, SA and JA accumulated in strawberry after infection. Contrastingly, induction of several important SA, JA, and oxidative stress-responsive defense genes, including FaPR1-1, FaLOX2, FaJAR1, FaPDF1, and FaGST1, was not detected, which suggests that specific branches in these defense pathways (those leading to FaPR1-2, FaPR2-1, FaPR2-2, FaAOS, FaPR5, and FaPR10) were activated. Our results reveal that specific aspects in SA and JA dependent signaling pathways are activated in strawberry upon interaction with C. acutatum. Certain described defense-associated transcripts related to these two known signaling pathways do not increase in abundance following infection. This finding suggests new insight into a specific putative molecular strategy for defense against this pathogen.Authors are grateful to Dr. JM Lopez-Aranda (IFAPA-Centro de Churriana) for providing micropropagated strawberry plants and to Nicolas Garcia-Caparros for technical assistance. Authors also want to thank Kevin M. Folta for his insightful comments on the paper. This work was supported by Junta de Andalucia, Spain [Proyectos de Excelencia P07-AGR-02482/P12-AGR-2174, and grants to Grupo-BIO278].Amil-Ruiz, F.; Garrido-Gala, J.; Gadea Vacas, J.; Blanco-Portales, R.; Munoz-Merida, A.; Trelles, O.; De Los Santos, B.... (2016). Partial Activation of SA- and JA-Defensive Pathways in Strawberry upon Colletotrichum acutatum Interaction. Frontiers in Plant Science. 7(1036). https://doi.org/10.3389/fpls.2016.01036S71036Acosta, I. F., & Farmer, E. E. (2010). Jasmonates. The Arabidopsis Book, 8, e0129. doi:10.1199/tab.0129Al-Shahrour, F., Diaz-Uriarte, R., & Dopazo, J. (2004). FatiGO: a web tool for finding significant associations of Gene Ontology terms with groups of genes. Bioinformatics, 20(4), 578-580. doi:10.1093/bioinformatics/btg455Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990). Basic local alignment search tool. Journal of Molecular Biology, 215(3), 403-410. doi:10.1016/s0022-2836(05)80360-2Amil-Ruiz, F., Blanco-Portales, R., Muñoz-Blanco, J., & Caballero, J. L. (2011). The Strawberry Plant Defense Mechanism: A Molecular Review. Plant and Cell Physiology, 52(11), 1873-1903. doi:10.1093/pcp/pcr136Amil-Ruiz, F., Garrido-Gala, J., Blanco-Portales, R., Folta, K. M., Muñoz-Blanco, J., & Caballero, J. L. (2013). Identification and Validation of Reference Genes for Transcript Normalization in Strawberry (Fragaria × ananassa) Defense Responses. PLoS ONE, 8(8), e70603. doi:10.1371/journal.pone.0070603Arroyo, F. T., Moreno, J., García-Herdugo, G., Santos, B. D. los, Barrau, C., Porras, M., … Romero, F. (2005). Ultrastructure of the early stages of Colletotrichum acutatum infection of strawberry tissues. Canadian Journal of Botany, 83(5), 491-500. doi:10.1139/b05-022Ashburner, M., Ball, C. A., Blake, J. A., Botstein, D., Butler, H., Cherry, J. M., … Sherlock, G. (2000). Gene Ontology: tool for the unification of biology. Nature Genetics, 25(1), 25-29. doi:10.1038/75556Aviv, D. H., Rustérucci, C., Iii, B. F. H., Dietrich, R. A., Parker, J. E., & Dangl, J. L. (2002). Runaway cell death, but not basal disease resistance, inlsd1is SA- andNIM1/NPR1-dependent. The Plant Journal, 29(3), 381-391. doi:10.1046/j.0960-7412.2001.01225.xBak, S., Beisson, F., Bishop, G., Hamberger, B., Höfer, R., Paquette, S., & Werck-Reichhart, D. (2011). Cytochromes P450. The Arabidopsis Book, 9, e0144. doi:10.1199/tab.0144Baniwal, S. K., Bharti, K., Chan, K. Y., Fauth, M., Ganguli, A., Kotak, S., … von Koskull-DÖring, P. (2004). Heat stress response in plants: a complex game with chaperones and more than twenty heat stress transcription factors. Journal of Biosciences, 29(4), 471-487. doi:10.1007/bf02712120Bhattacharjee, S. (2012). The Language of Reactive Oxygen Species Signaling in Plants. Journal of Botany, 2012, 1-22. doi:10.1155/2012/985298Birkenbihl, R. P., Diezel, C., & Somssich, I. E. (2012). Arabidopsis WRKY33 Is a Key Transcriptional Regulator of Hormonal and Metabolic Responses toward Botrytis cinerea Infection. Plant Physiology, 159(1), 266-285. doi:10.1104/pp.111.192641Caarls, L., Pieterse, C. M. J., & Van Wees, S. C. M. (2015). How salicylic acid takes transcriptional control over jasmonic acid signaling. Frontiers in Plant Science, 6. doi:10.3389/fpls.2015.00170Casado-Díaz, A., Encinas-Villarejo, S., Santos, B. de los, Schilirò, E., Yubero-Serrano, E.-M., Amil-Ruíz, F., … Caballero, J.-L. (2006). Analysis of strawberry genes differentially expressed in response to Colletotrichum infection. Physiologia Plantarum, 128(4), 633-650. doi:10.1111/j.1399-3054.2006.00798.xCharng, Y., Liu, H., Liu, N., Chi, W., Wang, C., Chang, S., & Wang, T. (2006). A Heat-Inducible Transcription Factor, HsfA2, Is Required for Extension of Acquired Thermotolerance in Arabidopsis. Plant Physiology, 143(1), 251-262. doi:10.1104/pp.106.091322Chung, S. H., Rosa, C., Scully, E. D., Peiffer, M., Tooker, J. F., Hoover, K., … Felton, G. W. (2013). Herbivore exploits orally secreted bacteria to suppress plant defenses. Proceedings of the National Academy of Sciences, 110(39), 15728-15733. doi:10.1073/pnas.1308867110Curry, K. J., Abril, M., Avant, J. B., & Smith, B. J. (2002). Strawberry Anthracnose: Histopathology of Colletotrichum acutatum and C. fragariae. Phytopathology®, 92(10), 1055-1063. doi:10.1094/phyto.2002.92.10.1055Debode, J., Van Hemelrijck, W., Baeyen, S., Creemers, P., Heungens, K., & Maes, M. (2009). Quantitative detection and monitoring ofColletotrichum acutatumin strawberry leaves using real-time PCR. Plant Pathology, 58(3), 504-514. doi:10.1111/j.1365-3059.2008.01987.xDempsey, D. A., & Klessig, D. F. (2012). SOS – too many signals for systemic acquired resistance? Trends in Plant Science, 17(9), 538-545. doi:10.1016/j.tplants.2012.05.011Dodds, P. N., & Rathjen, J. P. (2010). Plant immunity: towards an integrated view of plant–pathogen interactions. Nature Reviews Genetics, 11(8), 539-548. doi:10.1038/nrg2812Doehlemann, G., Wahl, R., Horst, R. J., Voll, L. M., Usadel, B., Poree, F., … Kämper, J. (2008). Reprogramming a maize plant: transcriptional and metabolic changes induced by the fungal biotroph Ustilago maydis. The Plant Journal, 56(2), 181-195. doi:10.1111/j.1365-313x.2008.03590.xDong, X. (2004). NPR1, all things considered. Current Opinion in Plant Biology, 7(5), 547-552. doi:10.1016/j.pbi.2004.07.005Durgbanshi, A., Arbona, V., Pozo, O., Miersch, O., Sancho, J. V., & Gómez-Cadenas, A. (2005). Simultaneous Determination of Multiple Phytohormones in Plant Extracts by Liquid Chromatography−Electrospray Tandem Mass Spectrometry. Journal of Agricultural and Food Chemistry, 53(22), 8437-8442. doi:10.1021/jf050884bEl Oirdi, M., El Rahman, T. A., Rigano, L., El Hadrami, A., Rodriguez, M. C., Daayf, F., … Bouarab, K. (2011). Botrytis cinerea Manipulates the Antagonistic Effects between Immune Pathways to Promote Disease Development in Tomato. The Plant Cell, 23(6), 2405-2421. doi:10.1105/tpc.111.083394Encinas-Villarejo, S., Maldonado, A. M., Amil-Ruiz, F., de los Santos, B., Romero, F., Pliego-Alfaro, F., … Caballero, J. L. (2009). Evidence for a positive regulatory role of strawberry (Fragaria×ananassa) Fa WRKY1 and Arabidopsis At WRKY75 proteins in resistance. Journal of Experimental Botany, 60(11), 3043-3065. doi:10.1093/jxb/erp152Freeman, S., Horowitz, S., & Sharon, A. (2001). Pathogenic and Nonpathogenic Lifestyles in Colletotrichum acutatum from Strawberry and Other Plants. Phytopathology®, 91(10), 986-992. doi:10.1094/phyto.2001.91.10.986Freeman, S., Katan, T., & Shabi, E. (1998). Characterization of Colletotrichum Species Responsible for Anthracnose Diseases of Various Fruits. Plant Disease, 82(6), 596-605. doi:10.1094/pdis.1998.82.6.596Gfeller, A., Dubugnon, L., Liechti, R., & Farmer, E. E. (2010). Jasmonate Biochemical Pathway. Science Signaling, 3(109), cm3-cm3. doi:10.1126/scisignal.3109cm3Grellet-Bournonville, C. F., Martinez-Zamora, M. G., Castagnaro, A. P., & Díaz-Ricci, J. C. (2012). Temporal accumulation of salicylic acid activates the defense response against Colletotrichum in strawberry. Plant Physiology and Biochemistry, 54, 10-16. doi:10.1016/j.plaphy.2012.01.019Guidarelli, M., Carbone, F., Mourgues, F., Perrotta, G., Rosati, C., Bertolini, P., & Baraldi, E. (2011). Colletotrichum acutatum interactions with unripe and ripe strawberry fruits and differential responses at histological and transcriptional levels. Plant Pathology, 60(4), 685-697. doi:10.1111/j.1365-3059.2010.02423.xHeidrich, K., Wirthmueller, L., Tasset, C., Pouzet, C., Deslandes, L., & Parker, J. E. (2011). Arabidopsis EDS1 Connects Pathogen Effector Recognition to Cell Compartment-Specific Immune Responses. Science, 334(6061), 1401-1404. doi:10.1126/science.1211641Horowitz, S., Freeman, S., & Sharon, A. (2002). Use of Green Fluorescent Protein-Transgenic Strains to Study Pathogenic and Nonpathogenic Lifestyles in Colletotrichum acutatum. Phytopathology®, 92(7), 743-749. doi:10.1094/phyto.2002.92.7.743Ikeda, M., Mitsuda, N., & Ohme-Takagi, M. (2011). Arabidopsis HsfB1 and HsfB2b Act as Repressors of the Expression of Heat-Inducible Hsfs But Positively Regulate the Acquired Thermotolerance. Plant Physiology, 157(3), 1243-1254. doi:10.1104/pp.111.179036Ikeda, M., & Ohme-Takagi, M. (2009). A Novel Group of Transcriptional Repressors in Arabidopsis. Plant and Cell Physiology, 50(5), 970-975. doi:10.1093/pcp/pcp048Khan, A. A., & Shih, D. S. (2004). Molecular cloning, characterization, and expression analysis of two class II chitinase genes from the strawberry plant. Plant Science, 166(3), 753-762. doi:10.1016/j.plantsci.2003.11.015Krinke, O., Ruelland, E., Valentová, O., Vergnolle, C., Renou, J.-P., Taconnat, L., … Zachowski, A. (2007). Phosphatidylinositol 4-Kinase Activation Is an Early Response to Salicylic Acid in Arabidopsis Suspension Cells. Plant Physiology, 144(3), 1347-1359. doi:10.1104/pp.107.100842Kubigsteltig, I., Laudert, D., & Weiler, E. W. (1999). Structure and regulation of the Arabidopsis thaliana allene oxide synthase gene. Planta, 208(4), 463-471. doi:10.1007/s004250050583Leandro, L. F. S., Gleason, M. L., Nutter, F. W., Wegulo, S. N., & Dixon, P. M. (2001). Germination and Sporulation of Colletotrichum acutatum on Symptomless Strawberry Leaves. Phytopathology®, 91(7), 659-664. doi:10.1094/phyto.2001.91.7.659Leon-Reyes, A., Van der Does, D., De Lange, E. S., Delker, C., Wasternack, C., Van Wees, S. C. M., … Pieterse, C. M. J. (2010). Salicylate-mediated suppression of jasmonate-responsive gene expression in Arabidopsis is targeted downstream of the jasmonate biosynthesis pathway. Planta, 232(6), 1423-1432. doi:10.1007/s00425-010-1265-zLi, J., Brader, G., Kariola, T., & Tapio Palva, E. (2006). WRKY70 modulates the selection of signaling pathways in plant defense. The Plant Journal, 46(3), 477-491. doi:10.1111/j.1365-313x.2006.02712.xLi, J., Brader, G., & Palva, E. T. (2004). The WRKY70 Transcription Factor: A Node of Convergence for Jasmonate-Mediated and Salicylate-Mediated Signals in Plant Defense. The Plant Cell, 16(2), 319-331. doi:10.1105/tpc.016980Liu, P.-P., von Dahl, C. C., Park, S.-W., & Klessig, D. F. (2011). Interconnection between Methyl Salicylate and Lipid-Based Long-Distance Signaling during the Development of Systemic Acquired Resistance in Arabidopsis and Tobacco. Plant Physiology, 155(4), 1762-1768. doi:10.1104/pp.110.171694Lodha, T. D., & Basak, J. (2011). Plant–Pathogen Interactions: What Microarray Tells About It? Molecular Biotechnology, 50(1), 87-97. doi:10.1007/s12033-011-9418-2López-Ráez, J. A., Verhage, A., Fernández, I., García, J. M., Azcón-Aguilar, C., Flors, V., & Pozo, M. J. (2010). Hormonal and transcriptional profiles highlight common and differential host responses to arbuscular mycorrhizal fungi and the regulation of the oxylipin pathway. Journal of Experimental Botany, 61(10), 2589-2601. doi:10.1093/jxb/erq089Maas, J. L. (Ed.). (1998). Compendium of Strawberry Diseases, Second Edition. doi:10.1094/9780890546178Makowski, R. M. D., & Mortensen, K. (1998). Latent infections and penetration of the bioherbicide agent Colletotrichum gloeosporioides f. sp. malvae in non-target field crops under controlled environmental conditions. Mycological Research, 102(12), 1545-1552. doi:10.1017/s0953756298006960Maleck, K., Levine, A., Eulgem, T., Morgan, A., Schmid, J., Lawton, K. A., … Dietrich, R. A. (2000). The transcriptome of Arabidopsis thaliana during systemic acquired resistance. Nature Genetics, 26(4), 403-410. doi:10.1038/82521Marcel, S., Sawers, R., Oakeley, E., Angliker, H., & Paszkowski, U. (2010). Tissue-Adapted Invasion Strategies of the Rice Blast Fungus Magnaporthe oryzae. The Plant Cell, 22(9), 3177-3187. doi:10.1105/tpc.110.078048Ndamukong, I., Abdallat, A. A., Thurow, C., Fode, B., Zander, M., Weigel, R., & Gatz, C. (2007). SA-inducible Arabidopsis glutaredoxin interacts with TGA factors and suppresses JA-responsive PDF1.2 transcription. The Plant Journal, 50(1), 128-139. doi:10.1111/j.1365-313x.2007.03039.xPajerowska-Mukhtar, K. M., Wang, W., Tada, Y., Oka, N., Tucker, C. L., Fonseca, J. P., & Dong, X. (2012). The HSF-like Transcription Factor TBF1 Is a Major Molecular Switch for Plant Growth-to-Defense Transition. Current Biology, 22(2), 103-112. doi:10.1016/j.cub.2011.12.015Pe�a-Cort�s, H., Barrios, P., Dorta, F., Polanco, V., S�nchez, C., S�nchez, E., & Ram�rez, I. (2004). Involvement of Jasmonic Acid and Derivatives in Plant Response to Pathogen and Insects and in Fruit Ripening. Journal of Plant Growth Regulation, 23(3), 246-260. doi:10.1007/s00344-004-0035-1Pernas, M., Ryan, E., & Dolan, L. (2010). SCHIZORIZA Controls Tissue System Complexity in Plants. Current Biology, 20(9), 818-823. doi:10.1016/j.cub.2010.02.062Pieterse, C. M. J., Leon-Reyes, A., Van der Ent, S., & Van Wees, S. C. M. (2009). Networking by small-molecule hormones in plant immunity. Nature Chemical Biology, 5(5), 308-316. doi:10.1038/nchembio.164Rahman, T. A. E., Oirdi, M. E., Gonzalez-Lamothe, R., & Bouarab, K. (2012). Necrotrophic Pathogens Use the Salicylic Acid Signaling Pathway to Promote Disease Development in Tomato. Molecular Plant-Microbe Interactions®, 25(12), 1584-1593. doi:10.1094/mpmi-07-12-0187-rRen, C.-M., Zhu, Q., Gao, B.-D., Ke, S.-Y., Yu, W.-C., Xie, D.-X., & Peng, W. (2008). Transcription Factor WRKY70 Displays Important but No Indispensable Roles in Jasmonate and Salicylic Acid Signaling. Journal of Integrative Plant Biology, 50(5), 630-637. doi:10.1111/j.1744-7909.2008.00653.xRietz, S., Stamm, A., Malonek, S., Wagner, S., Becker, D., Medina-Escobar, N., … Parker, J. E. (2011). Different roles of Enhanced Disease Susceptibility1 (EDS1) bound to and dissociated from Phytoalexin Deficient4 (PAD4) in Arabidopsis immunity. New Phytologist, 191(1), 107-119. doi:10.1111/j.1469-8137.2011.03675.xRobert-Seilaniantz, A., Grant, M., & Jones, J. D. G. (2011). Hormone Crosstalk in Plant Disease and Defense: More Than Just JASMONATE-SALICYLATE Antagonism. Annual Review of Phytopathology, 49(1), 317-343. doi:10.1146/annurev-phyto-073009-114447Cristina, M., Petersen, M., & Mundy, J. (2010). Mitogen-Activated Protein Kinase Signaling in Plants. Annual Review of Plant Biology, 61(1), 621-649. doi:10.1146/annurev-arplant-042809-112252Rouhier, N. (2006). Genome-wide analysis of plant glutaredoxin systems. Journal of Experimental Botany, 57(8), 1685-1696. doi:10.1093/jxb/erl001Ruepp, A. (2004). The FunCat, a functional annotation scheme for systematic classification of proteins from whole genomes. Nucleic Acids Research, 32(18), 5539-5545. doi:10.1093/nar/gkh894Rusterucci, C. (2001). The Disease Resistance Signaling Components EDS1 and PAD4 Are Essential Regulators of the Cell Death Pathway Controlled by LSD1 in Arabidopsis. THE PLANT CELL ONLINE, 13(10), 2211-2224. doi:10.1105/tpc.13.10.2211Sarowar, S., Zhao, Y., Soria-Guerra, R. E., Ali, S., Zheng, D., Wang, D., & Korban, S. S. (2011). Expression profiles of differentially regulated genes during the early stages of apple flower infection with Erwinia amylovora. Journal of Experimental Botany, 62(14), 4851-4861. doi:10.1093/jxb/err147Sasaki, Y. (2001). Monitoring of Methyl Jasmonate-responsive Genes in Arabidopsis by cDNA Macroarray: Self-activation of Jasmonic Acid Biosynthesis and Crosstalk with Other Phytohormone Signaling Pathways. DNA Research, 8(4), 153-161. doi:10.1093/dnares/8.4.153Schenk, P. M., Kazan, K., Manners, J. M., Anderson, J. P., Simpson, R. S., Wilson, I. W., … Maclean, D. J. (2003). Systemic Gene Expression in Arabidopsis during an Incompatible Interaction with Alternaria brassicicola. Plant Physiology, 132(2), 999-1010. doi:10.1104/pp.103.021683Simpson, D. W. (1991). Resistance toBotrytis cinereain pistillate genotypes of the cultivated strawberryFragaria ananassa. Journal of Horticultural Science, 66(6), 719-723. doi:10.1080/00221589.1991.11516203Shulaev, V., Sargent, D. J., Crowhurst, R. N., Mockler, T. C., Folkerts, O., Delcher, A. L., … Mane, S. P. (2010). The genome of woodland strawberry (Fragaria vesca). Nature Genetics, 43(2), 109-116. doi:10.1038/ng.740Song, W. C., Funk, C. D., & Brash, A. R. (1993). Molecular cloning of an allene oxide synthase: a cytochrome P450 specialized for the metabolism of fatty acid hydroperoxides. Proceedings of the National Academy of Sciences, 90(18), 8519-8523. doi:10.1073/pnas.90.18.8519Spoel, S. H., & Dong, X. (2012). How do plants achieve immunity? Defence without specialized immune cells. Nature Reviews Immunology, 12(2), 89-100. doi:10.1038/nri3141Spoel, S. H., Johnson, J. S., & Dong, X. (2007). Regulation of tradeoffs between plant defenses against pathogens with different lifestyles. Proceedings of the National Academy of Sciences, 104(47), 18842-18847. doi:10.1073/pnas.0708139104Staswick, P. E., & Tiryaki, I. (2004). The Oxylipin Signal Jasmonic Acid Is Activated by an Enzyme That Conjugates It to Isoleucine in Arabidopsis. The Plant Cell, 16(8), 2117-2127. doi:10.1105/tpc.104.023549Ten Hove, C. A., Willemsen, V., de Vries, W. J., van Dijken, A., Scheres, B., & Heidstra, R. (2010). SCHIZORIZA Encodes a Nuclear Factor Regulating Asymmetry of Stem Cell Divisions in the Arabidopsis Root. Current Biology, 20(5), 452-457. doi:10.1016/j.cub.2010.01.018Turner, J. G., Ellis, C., & Devoto, A. (2002). The Jasmonate Signal Pathway. The Plant Cell, 14(suppl 1), S153-S164. doi:10.1105/tpc.000679Tusher, V. G., Tibshirani, R., & Chu, G. (2001). Significance analysis of microarrays applied to the ionizing radiation response. Proceedings of the National Academy of Sciences, 98(9), 5116-5121. doi:10.1073/pnas.091062498Uknes, S., Mauch-Mani, B., Moyer, M., Potter, S., Williams, S., Dincher, S., … Ryals, J. (1992). Acquired resistance in Arabidopsis. The Plant Cell, 4(6), 645-656. doi:10.1105/tpc.4.6.645Vargas, W. A., Martín, J. M. S., Rech, G. E., Rivera, L. P., Benito, E. P., Díaz-Mínguez, J. M., … Sukno, S. A. (2012). Plant Defense Mechanisms Are Activated during Biotrophic and Necrotrophic Development of Colletotricum graminicola in Maize. Plant Physiology, 158(3), 1342-1358. doi:10.1104/pp.111.190397Venugopal, S. C., Jeong, R.-D., Mandal, M. K., Zhu, S., Chandra-Shekara, A. C., Xia, Y., … Kachroo, P. (2009). Enhanced Disease Susceptibility 1 and Salicylic Acid Act Redundantly to Regulate Resistance Gene-Mediated Signaling. PLoS Genetics, 5(7), e1000545. doi:10.1371/journal.pgen.1000545Vlot, A. C., Liu, P.-P., Cameron, R. K., Park, S.-W., Yang, Y., Kumar, D., … Klessig, D. F. (2008). Identification of likely orthologs of tobacco salicylic acid-binding protein 2 and their role in systemic acquired resistance inArabidopsis thaliana. The Plant Journal, 56(3), 445-456. doi:10.1111/j.1365-313x.2008.03618.xWang, D., Amornsiripanitch, N., & Dong, X. (2006). A Genomic Approach to Identify Regulatory Nodes in the Transcriptional Network of Systemic Acquired Resistance in Plants. PLoS Pathogens, 2(11), e123. doi:10.1371/journal.ppat.0020123Wang, D. (2005). Induction of Protein Secretory Pathway Is Required for Systemic Acquired Resistance. Science, 308(5724), 1036-1040. doi:10.1126/science.1108791Wang, G.-F., Seabolt, S., Hamdoun, S., Ng, G., Park, J., & Lu, H. (2011). Multiple Roles of WIN3 in Regulating Disease Resistance, Cell Death, and Flowering Time in Arabidopsis. Plant Physiology, 156(3), 1508-1519. doi:10.1104/pp.111.176776Wiermer, M., Feys, B. J., & Parker, J. E. (2005). Plant immunity: the EDS1 regulatory node. Current Opinion in Plant Biology, 8(4), 383-389. doi:10.1016/j.pbi.2005.05.010Windram, O., Madhou, P., McHattie, S., Hill, C., Hickman, R., Cooke, E., … Denby, K. J. (2012). Arabidopsis Defense against Botrytis cinerea: Chronology and Regulation Deciphered by High-Resolution Temporal Transcriptomic Analysis. Th

    Incidence and drug treatment of emotional distress after cancer diagnosis : a matched primary care case-control study

    Get PDF
    Notes This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License.Peer reviewedPublisher PD

    Long-term adherence to IFN beta-1a treatment when using rebismart1device in patients with relapsing-remitting multiple sclerosis

    Get PDF
    The effectiveness of disease-modifying drugs in the treatment of multiple sclerosis is associated with adherence. RebiSmart® electronic device provides useful information about adherence to the treatment with subcutaneous (sc) interferon (IFN) ß-1a (Rebif®). The aim of the study was to determine long-term adherence to this treatment in patients with relapsing- remitting multiple sclerosis (RRMS). This retrospective multicentre observational study analysed 258 patients with RRMS who were receiving sc IFN ß-1a (Rebif®) treatment by using RebiSmart® until replacement (36 months maximum lifetime) or treatment discontinuation. Adherence was calculated with data (injection dosage, time, and date) automatically recorded by RebiSmart®. Patients in the study had a mean age of 41 years with a female proportion of 68%. Mean EDSS score at start of treatment was 1.8 (95% CI, 1.6-1.9). Overall adherence was 92.6%(95% CI, 90.6-94.5%). A total of 30.2% of patients achieved an adherence rate of 100%, 80.6% at least 90%, and only 13.2% of patients showed a suboptimal adherence (<80%). A total of 59.9% of subjects were relapse-free after treatment initiation. Among 106 subjects (41.1%) who experienced, on average, 1.4 relapses, the majority were mild (40.6%) or moderate (47.2%). Having experienced relapses from the beginning of the treatment was the only variable significantly related to achieving an adherence of at least 80% (OR = 3.06, 1.28-7.31). Results of this study indicate that sc IFN ß-1a administration facilitated by RebiSmart® could lead to high rates of adherence to a prescribed dose regimen over 36 months

    The STF2p Hydrophilin from Saccharomyces cerevisiae Is Required for Dehydration Stress Tolerance

    Get PDF
    The yeast Saccharomyces cerevisiae is able to overcome cell dehydration; cell metabolic activity is arrested during this period but restarts after rehydration. The yeast genes encoding hydrophilin proteins were characterised to determine their roles in the dehydration-resistant phenotype, and STF2p was found to be a hydrophilin that is essential for survival after the desiccation-rehydration process. Deletion of STF2 promotes the production of reactive oxygen species and apoptotic cell death during stress conditions, whereas the overexpression of STF2, whose gene product localises to the cytoplasm, results in a reduction in ROS production upon oxidative stress as the result of the antioxidant capacity of the STF2p protein

    A phylogenetic classification of the world’s tropical forests

    Get PDF
    Knowledge about the biogeographic affinities of the world’s tropical forests helps to better understand regional differences in forest structure, diversity, composition and dynamics. Such understanding will enable anticipation of region specific responses to global environmental change. Modern phylogenies, in combination with broad coverage of species inventory data, now allow for global biogeographic analyses that take species evolutionary distance into account. Here we present the first classification of the world’s tropical forests based on their phylogenetic similarity. We identify five principal floristic regions and their floristic relationships: (1) Indo-Pacific, (2) Subtropical, (3) African, (4) American, and (5) Dry forests. Our results do not support the traditional Neo- versus Palaeo-tropical forest division, but instead separate the combined American and African forests from their Indo-Pacific counterparts. We also find indications for the existence of a global dry forest region, with representatives in America, Africa, Madagascar and India. Additionally, a northern hemisphere Subtropical forest region was identified with representatives in Asia and America, providing support for a link between Asian and American northern hemisphere forests

    Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

    Get PDF

    Trichomonas vaginalis: Clinical relevance, pathogenicity and diagnosis

    Get PDF
    Trichomonas vaginalis is the etiological agent of trichomoniasis, the most prevalent non-viral sexually transmitted disease worldwide. Trichomoniasis is a widespread, global health concern and occurring at an increasing rate. Infections of the female genital tract can cause a range of symptoms, including vaginitis and cervicitis, while infections in males are generally asymptomatic. The relatively mild symptoms, and lack of evidence for any serious sequelae, have historically led to this disease being under diagnosed, and under researched. However, growing evidence that T. vaginalis infection is associated with other disease states with high morbidity in both men and women has increased the efforts to diagnose and treat patients harboring this parasite. The pathology of trichomoniasis results from damage to the host epithelia, caused by a variety of processes during infection and recent work has highlighted the complex interactions between the parasite and host, commensal microbiome and accompanying symbionts. The commercial release of a number of nucleic acid amplification tests (NAATs) has added to the available diagnostic options. Immunoassay based Point of Care testing is currently available, and a recent initial evaluation of a NAAT Point of Care system has given promising results, which would enable testing and treatment in a single visit
    corecore