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Accès à distance ? S'identifier sur le proxy UCLouvain

Not in your usual Top 10: protists that infect plants and algae

  1. Adl Sina M., Simpson Alastair G. B., Lane Christopher E., Lukeš Julius, Bass David, Bowser Samuel S., Brown Matthew W., Burki Fabien, Dunthorn Micah, Hampl Vladimir, Heiss Aaron, Hoppenrath Mona, Lara Enrique, le Gall Line, Lynn Denis H., McManus Hilary, Mitchell Edward A. D., Mozley-Stanridge Sharon E., Parfrey Laura W., Pawlowski Jan, Rueckert Sonja, Shadwick Laura, Schoch Conrad L., Smirnov Alexey, Spiegel Frederick W., The Revised Classification of Eukaryotes, 10.1111/j.1550-7408.2012.00644.x
  2. Agarwal Arati, Kaul Vijay, Faggian Robert, Rookes James E., Ludwig-Müller Jutta, Cahill David M., Analysis of global host gene expression during the primary phase of the Arabidopsis thaliana?Plasmodiophora brassicae interaction, 10.1071/fp11026
  3. Aist James R., Williams P. H., The cytology and kinetics of cabbage root hair penetration by Plasmodiophora brassicae, 10.1139/b71-284
  4. Amano Hideomi, Suginaga Reiko, Arashima Koichi, Noda Hiroyuki, Immunological detection of the fungal parasite, Pythium sp.; the causative organism of red rot disease in Porphyra yezoensis, 10.1007/bf00003550
  5. Amon James P., Thraustochytrids and Labyrinthulids of Terrestrial, Aquatic and Hypersaline Environments of the Great Salt Lake, USA, 10.2307/3759339
  6. ARASAKI S., Studies on the Wasting Disease of the Cultured Lavers (Porphyra tenera), 10.2331/suisan.13.74
  7. Balendres Mark A., Nichols David S., Tegg Robert S., Wilson Calum R., Metabolomes of Potato Root Exudates: Compounds That Stimulate Resting Spore Germination of the Soil-Borne PathogenSpongospora subterranea, 10.1021/acs.jafc.6b03904
  8. Beakes Gordon W., Glockling Sally L., Sekimoto Satoshi, The evolutionary phylogeny of the oomycete “fungi”, 10.1007/s00709-011-0269-2
  9. Bi Kai, He Zhangchao, Gao Zhixiao, Zhao Ying, Fu Yanping, Cheng Jiasen, Xie Jiatao, Jiang Daohong, Chen Tao, Integrated omics study of lipid droplets from Plasmodiophora brassicae, 10.1038/srep36965
  10. Bigelow D.M., Olsen M.W., Gilbertson R.L., Labyrinthula terrestris sp. nov., a new pathogen of turf grass, 10.1080/15572536.2006.11832852
  11. Bittara Francisco G., Thompson Asunta L., Gudmestad Neil C., Secor Gary A., Field Evaluation of Potato Genotypes for Resistance to Powdery Scab on Tubers and Root Gall Formation Caused by Spongospora subterranea, 10.1007/s12230-016-9526-4
  12. Bockelmann Anna-Christina, Tams Verena, Ploog Jana, Schubert Philipp R., Reusch Thorsten B. H., Quantitative PCR Reveals Strong Spatial and Temporal Variation of the Wasting Disease Pathogen, Labyrinthula zosterae in Northern European Eelgrass (Zostera marina) Beds, 10.1371/journal.pone.0062169
  13. Brakel Janina, Werner Franziska Julie, Tams Verena, Reusch Thorsten B. H., Bockelmann Anna-Christina, Current European Labyrinthula zosterae Are Not Virulent and Modulate Seagrass (Zostera marina) Defense Gene Expression, 10.1371/journal.pone.0092448
  14. Bulman, The Mycota VII, Part A, Systematics and Evolution, 99 (2014)
  15. Bulman Simon, Candy Judith M., Fiers Mark, Lister Ros, Conner Anthony J., Eady Colin C., Genomics of Biotrophic, Plant-infecting Plasmodiophorids Using In Vitro Dual Cultures, 10.1016/j.protis.2010.09.004
  16. Bulman, Plant Pathol., 47, 759 (1998)
  17. Burki Fabien, Keeling Patrick J., Rhizaria, 10.1016/j.cub.2013.12.025
  18. Burki Fabien, Kudryavtsev Alexander, Matz Mikhail V, Aglyamova Galina V, Bulman Simon, Fiers Mark, Keeling Patrick J, Pawlowski Jan, Evolution of Rhizaria: new insights from phylogenomic analysis of uncultivated protists, 10.1186/1471-2148-10-377
  19. Butler Claire E., Jaskowska Eleanor, Kelly Steven, Genome Sequence of Phytomonas françai , a Cassava ( Manihot esculenta ) Latex Parasite , 10.1128/genomea.01266-16
  20. Camargo Erney Plessmann, Phytomonas and Other Trypanosomatid Parasites of Plants and Fruit, Advances in Parasitology (1999) ISBN:9780120317424 p.29-112, 10.1016/s0065-308x(08)60148-7
  21. Carré Patrick, Pouzet André, Rapeseed market, worldwide and in Europe, 10.1051/ocl/2013054
  22. Chen, Front. Plant Sci., 6, 1183 (2015)
  23. Chitrampalam Periasamy, Goldberg Natalie, Olsen Mary W., Labyrinthula species associated with turfgrasses in Arizona and New Mexico, 10.1007/s10658-015-0701-0
  24. Christianen Marjolijn J. A., van Belzen Jim, Herman Peter M. J., van Katwijk Marieke M., Lamers Leon P. M., van Leent Peter J. M., Bouma Tjeerd J., Low-Canopy Seagrass Beds Still Provide Important Coastal Protection Services, 10.1371/journal.pone.0062413
  25. Cock J. Mark, Sterck Lieven, Rouzé Pierre, Scornet Delphine, Allen Andrew E., Amoutzias Grigoris, Anthouard Veronique, Artiguenave François, Aury Jean-Marc, Badger Jonathan H., Beszteri Bank, Billiau Kenny, Bonnet Eric, Bothwell John H., Bowler Chris, Boyen Catherine, Brownlee Colin, Carrano Carl J., Charrier Bénédicte, Cho Ga Youn, Coelho Susana M., Collén Jonas, Corre Erwan, Da Silva Corinne, Delage Ludovic, Delaroque Nicolas, Dittami Simon M., Doulbeau Sylvie, Elias Marek, Farnham Garry, Gachon Claire M. M., Gschloessl Bernhard, Heesch Svenja, Jabbari Kamel, Jubin Claire, Kawai Hiroshi, Kimura Kei, Kloareg Bernard, Küpper Frithjof C., Lang Daniel, Le Bail Aude, Leblanc Catherine, Lerouge Patrice, Lohr Martin, Lopez Pascal J., Martens Cindy, Maumus Florian, Michel Gurvan, Miranda-Saavedra Diego, Morales Julia, Moreau Hervé, Motomura Taizo, Nagasato Chikako, Napoli Carolyn A., Nelson David R., Nyvall-Collén Pi, Peters Akira F., Pommier Cyril, Potin Philippe, Poulain Julie, Quesneville Hadi, Read Betsy, Rensing Stefan A., Ritter Andrés, Rousvoal Sylvie, Samanta Manoj, Samson Gaelle, Schroeder Declan C., Ségurens Béatrice, Strittmatter Martina, Tonon Thierry, Tregear James W., Valentin Klaus, von Dassow Peter, Yamagishi Takahiro, Van de Peer Yves, Wincker Patrick, The Ectocarpus genome and the independent evolution of multicellularity in brown algae, 10.1038/nature09016
  26. Coelho Susana M., Godfroy Olivier, Arun Alok, Le Corguillé Gildas, Peters Akira F., Cock J. Mark, Genetic regulation of life cycle transitions in the brown alga Ectocarpus, 10.4161/psb.6.11.17737
  27. Collado-Mercado E, Radway JC, Collier JL, Novel uncultivated labyrinthulomycetes revealed by 18S rDNA sequences from seawater and sediment samples, 10.3354/ame01361
  28. Cox, Phytopathology, 98, 1567 (2014)
  29. DEAN RALPH, VAN KAN JAN A. L., PRETORIUS ZACHARIAS A., HAMMOND-KOSACK KIM E., DI PIETRO ANTONIO, SPANU PIETRO D., RUDD JASON J., DICKMAN MARTY, KAHMANN REGINE, ELLIS JEFF, FOSTER GARY D., The Top 10 fungal pathogens in molecular plant pathology : Top 10 fungal pathogens, 10.1111/j.1364-3703.2011.00783.x
  30. Desoignies , N. 2012 Polymyxa betae - Beta vulgaris
  31. DESOIGNIES NICOLAS, LEGREVE ANNE, In Vitro Dual Culture of Polymyxa betae in Agrobacterium rhizogenes Transformed Sugar Beet Hairy Roots in Liquid Media : IN VITRO CULTURE OF POLYMYXA BETAE, 10.1111/j.1550-7408.2011.00563.x
  32. Desoignies N., Carbonell J., Moreau J.-S., Conesa A., Dopazo J., Legrève A., Molecular interactions between sugar beet andPolymyxa betaeduring its life cycle : Molecular interactions between sugar beet andPolymyxa betae, 10.1111/aab.12095
  33. Devos Sylvie, Laukens Kris, Deckers Peter, Van Der Straeten Dominique, Beeckman Tom, Inzé Dirk, Van Onckelen Harry, Witters Erwin, Prinsen Els, A Hormone and Proteome Approach to Picturing the Initial Metabolic Events DuringPlasmodiophora brassicaeInfection onArabidopsis, 10.1094/mpmi-19-1431
  34. Di Lucca Alfredo Giovanni Trelles, Trinidad Chipana Edwin Fernando, Talledo Albújar Michael John, Dávila Peralta Waldo, Montoya Piedra Ysabel Catalina, Arévalo Zelada Jorge Luis, Slow wilt: another form of Marchitez in oil palm associated with trypanosomatids in Peru, 10.1590/s1982-56762013000600008
  35. Diederichsen Elke, Frauen Martin, Linders Enrico G. A., Hatakeyama Katsunori, Hirai Masashi, Status and Perspectives of Clubroot Resistance Breeding in Crucifer Crops, 10.1007/s00344-009-9100-0
  36. Dieryck Benjamin, Weyns Jeannine, Doucet Diane, Bragard Claude, Legrève Anne, Acquisition and Transmission ofPeanut clump virusbyPolymyxa graminison Cereal Species, 10.1094/phyto-12-10-0335
  37. Dixon Geoffrey R., The Occurrence and Economic Impact of Plasmodiophora brassicae and Clubroot Disease, 10.1007/s00344-009-9090-y
  38. Douhan Greg W., Olsen Mary W., Herrell Amanda, Winder Charles, Wong Frank, Entwistle Kate, Genetic diversity of Labyrinthula terrestris, a newly emergent plant pathogen, and the discovery of new Labyrinthulid organisms, 10.1016/j.mycres.2009.08.002
  39. Faggian Robert, Strelkov Stephen E., Detection and Measurement of Plasmodiophora brassicae, 10.1007/s00344-009-9092-9
  40. Fahling M., Graf H., Siemens J., Pathotype Separation of Plasmodiophora brassicae by the Host Plant, 10.1046/j.1439-0434.2003.00744.x
  41. Falloon Richard E., Genet Russell A., Wallace Andrew R., Butler Ruth C., Susceptibility of potato (Solanum tuberosum) cultivars to powdery scab (caused by Spongospora subterranea f. sp. subterranea), and relationships between tuber and root infection, 10.1071/ap03040
  42. Falloon R. E., Merz U., Butler R. C., Curtin D., Lister R. A., Thomas S. M., Root infection of potato bySpongospora subterranea: knowledge review and evidence for decreased plant productivity, 10.1111/ppa.12419
  43. Fourqurean James W., Duarte Carlos M., Kennedy Hilary, Marbà Núria, Holmer Marianne, Mateo Miguel Angel, Apostolaki Eugenia T., Kendrick Gary A., Krause-Jensen Dorte, McGlathery Karen J., Serrano Oscar, Seagrass ecosystems as a globally significant carbon stock, 10.1038/ngeo1477
  44. Gachon C. M. M., Strittmatter M., Muller D. G., Kleinteich J., Kupper F. C., Detection of Differential Host Susceptibility to the Marine Oomycete Pathogen Eurychasma dicksonii by Real-Time PCR: Not All Algae Are Equal, 10.1128/aem.01885-08
  45. Gachon Claire M.M., Sime-Ngando Télesphore, Strittmatter Martina, Chambouvet Aurélie, Kim Gwang Hoon, Algal diseases: spotlight on a black box, 10.1016/j.tplants.2010.08.005
  46. Gau Rebecca D., Merz Ueli, Falloon Richard E., Brunner Patrick C., Global Genetics and Invasion History of the Potato Powdery Scab Pathogen, Spongospora subterranea f.sp. subterranea, 10.1371/journal.pone.0067944
  47. van de Graaf P., Wale S. J., Lees A. K., Factors affecting the incidence and severity of Spongospora subterranea infection and galling in potato roots, 10.1111/j.1365-3059.2007.01686.x
  48. Graf H., Fähling M, Siemens J., Chromosome Polymorphism of the Obligate Biotrophic Parasite Plasmodiophora brassicae : Chromosome polymorphism, 10.1046/j.1439-0434.2003.00805.x
  49. Gravot Antoine, Richard Gautier, Lime Tanguy, Lemarié Séverine, Jubault Mélanie, Lariagon Christine, Lemoine Jocelyne, Vicente Jorge, Robert-Seilaniantz Alexandre, Holdsworth Michael J., Manzanares-Dauleux Maria J., Hypoxia response in Arabidopsis roots infected by Plasmodiophora brassicae supports the development of clubroot, 10.1186/s12870-016-0941-y
  50. Grenville-Briggs Laura, Gachon Claire M. M., Strittmatter Martina, Sterck Lieven, Küpper Frithjof C., van West Pieter, A Molecular Insight into Algal-Oomycete Warfare: cDNA Analysis of Ectocarpus siliculosus Infected with the Basal Oomycete Eurychasma dicksonii, 10.1371/journal.pone.0024500
  51. Groner, Dis. Aquat. Organ., 118, 159 (2016)
  52. Grsic-Rausch Slobodanka, Kobelt Peter, Siemens Johannes M., Bischoff Markus, Ludwig-Müller Jutta, Expression and Localization of Nitrilase during Symptom Development of the Clubroot Disease in Arabidopsis, 10.1104/pp.122.2.369
  53. Gutiérrez Pablo, Bulman Simon, Alzate Juan, Ortíz Mary Carmen, Marín Mauricio, Mitochondrial genome sequence of the potato powdery scab pathogenSpongospora subterranea, 10.3109/19401736.2013.873898
  54. Gutiérrez Sánchez Pablo Andrés, Alzate Juan Fernando, Montoya Mauricio Marín, Analysis of Carbohydrate Metabolism Genes of Spongospora subterranea Using 454 Pyrosequencing : Análisis de Genes del Metabolismo de Carbohidratos de Spongospora subterranea Utilizando Pirosecuenciación 454, 10.15446/rfnam.v67n2.44166
  55. Hannaert V., Saavedra E., Duffieux F., Szikora J.-P., Rigden D. J., Michels P. A. M., Opperdoes F. R., Plant-like traits associated with metabolism of Trypanosoma parasites, 10.1073/pnas.0335769100
  56. Hatakeyama Katsunori, Suwabe Keita, Tomita Rubens Norio, Kato Takeyuki, Nunome Tsukasa, Fukuoka Hiroyuki, Matsumoto Satoru, Identification and Characterization of Crr1a, a Gene for Resistance to Clubroot Disease (Plasmodiophora brassicae Woronin) in Brassica rapa L., 10.1371/journal.pone.0054745
  57. Hwang Eun Kyoung, Park Chan Sun, Kakinuma Makoto, Physicochemical responses ofPythium porphyrae(Oomycota), the causative organism of red rot disease inPorphyrato acidification, 10.1111/j.1365-2109.2009.02284.x
  58. JACKSON ANDREW P., Genome evolution in trypanosomatid parasites, 10.1017/s0031182014000894
  59. Jackson, Oceanogr. Mar. Biol., 39, 269 (2001)
  60. Jahn Linda, Mucha Stefanie, Bergmann Sabine, Horn Cornelia, Staswick Paul, Steffens Bianka, Siemens Johannes, Ludwig-Müller Jutta, The Clubroot Pathogen (Plasmodiophora brassicae) Influences Auxin Signaling to Regulate Auxin Homeostasis in Arabidopsis, 10.3390/plants2040726
  61. Jashni Mansoor Karimi, Mehrabi Rahim, Collemare Jérôme, Mesarich Carl H., de Wit Pierre J. G. M., The battle in the apoplast: further insights into the roles of proteases and their inhibitors in plant–pathogen interactions, 10.3389/fpls.2015.00584
  62. Jaskowska Eleanor, Butler Claire, Preston Gail, Kelly Steven, Phytomonas: Trypanosomatids Adapted to Plant Environments, 10.1371/journal.ppat.1004484
  63. Johnson Dennis A., Cummings Thomas F., Effect of Powdery Scab Root Galls on Yield of Potato, 10.1094/pdis-11-14-1170-re
  64. Jones John T., Haegeman Annelies, Danchin Etienne G. J., Gaur Hari S., Helder Johannes, Jones Michael G. K., Kikuchi Taisei, Manzanilla-López Rosa, Palomares-Rius Juan E., Wesemael Wim M. L., Perry Roland N., Top 10 plant-parasitic nematodes in molecular plant pathology : Top 10 plant-parasitic nematodes, 10.1111/mpp.12057
  65. Jubault M., Hamon C., Gravot A., Lariagon C., Delourme R., Bouchereau A., Manzanares-Dauleux M. J., Differential Regulation of Root Arginine Catabolism and Polyamine Metabolism in Clubroot-Susceptible and Partially Resistant Arabidopsis Genotypes, 10.1104/pp.108.117432
  66. Jubault Mélanie, Lariagon Christine, Taconnat Ludivine, Renou Jean-Pierre, Gravot Antoine, Delourme Régine, Manzanares-Dauleux Maria J., Partial resistance to clubroot in Arabidopsis is based on changes in the host primary metabolism and targeted cell division and expansion capacity, 10.1007/s10142-013-0312-9
  67. Kamoun Sophien, Furzer Oliver, Jones Jonathan D. G., Judelson Howard S., Ali Gul Shad, Dalio Ronaldo J. D., Roy Sanjoy Guha, Schena Leonardo, Zambounis Antonios, Panabières Franck, Cahill David, Ruocco Michelina, Figueiredo Andreia, Chen Xiao-Ren, Hulvey Jon, Stam Remco, Lamour Kurt, Gijzen Mark, Tyler Brett M., Grünwald Niklaus J., Mukhtar M. Shahid, Tomé Daniel F. A., Tör Mahmut, Van Den Ackerveken Guido, McDowell John, Daayf Fouad, Fry William E., Lindqvist-Kreuze Hannele, Meijer Harold J. G., Petre Benjamin, Ristaino Jean, Yoshida Kentaro, Birch Paul R. J., Govers Francine, The Top 10 oomycete pathogens in molecular plant pathology : Top 10 oomycete plant pathogens, 10.1111/mpp.12190
  68. Kanyuka Konstantin, Ward Elaine, Adams Michael J., Polymyxa graminis and the cereal viruses it transmits: a research challenge, 10.1046/j.1364-3703.2003.00177.x
  69. Kawamura Y., Yokoo K., Tojo M., Hishiike M., Distribution ofPythium porphyrae, the Causal Agent of Red Rot Disease ofPorphyraespp., in the Ariake Sea, Japan, 10.1094/pd-89-1041
  70. Kerrigan J. L., Olsen M. W., Martin S. B., Rapid Blight, 10.1094/phi-i-2012-0621-01
  71. Kim Gwang Hoon, Moon Kyoung-Hyoun, Kim Je-Yoon, Shim Junbo, Klochkova Tatyana A., A revaluation of algal diseases in Korean Pyropia (Porphyra) sea farms and their economic impact, 10.4490/algae.2014.29.4.249
  72. Kitajima E. W., Flagellate Protozoon Associated with Poor Development of the Root System of Cassava in the Espirito Santo State, Brazil, 10.1094/phyto-76-638
  73. Klewer, Luerssen, Graf, Siemens, Restriction Fragment Length Polymorphism Markers to Characterize Plasmodiophora brassicae Single-spore Isolates with Different Virulence Patterns, 10.1046/j.1439-0434.2001.00595.x
  74. Klochkova Tatyana A., Shim Jun Bo, Hwang Mi Sook, Kim Gwang Hoon, Host–parasite interactions and host species susceptibility of the marine oomycete parasite, Olpidiopsis sp., from Korea that infects red algae, 10.1007/s10811-011-9661-8
  75. Klochkova Tatyana A., Shin Yoon Ju, Moon Kyoung-Hyoun, Motomura Taizo, Kim Gwang Hoon, New species of unicellular obligate parasite, Olpidiopsis pyropiae sp. nov., that plagues Pyropia sea farms in Korea, 10.1007/s10811-015-0595-4
  76. Klochkova Tatyana A., Jung Sokyong, Kim Gwang Hoon, Host range and salinity tolerance of Pythium porphyrae may indicate its terrestrial origin, 10.1007/s10811-016-0947-8
  77. Kombrink Anja, Thomma Bart P. H. J., LysM Effectors: Secreted Proteins Supporting Fungal Life, 10.1371/journal.ppat.1003769
  78. Koreny L., Sobotka R., Kovarova J., Gnipova A., Flegontov P., Horvath A., Obornik M., Ayala F. J., Lukes J., Aerobic kinetoplastid flagellate Phytomonas does not require heme for viability, 10.1073/pnas.1201089109
  79. La Barre Stéphane, Potin Philippe, Leblanc Catherine, Delage Ludovic, The Halogenated Metabolism of Brown Algae (Phaeophyta), Its Biological Importance and Its Environmental Significance, 10.3390/md8040988
  80. Lafont, C.r. séances Soc. biol. ses. fil., 66, 1011 (1909)
  81. Lamb Joleah B., van de Water Jeroen A. J. M., Bourne David G., Altier Craig, Hein Margaux Y., Fiorenza Evan A., Abu Nur, Jompa Jamaluddin, Harvell C. Drew, Seagrass ecosystems reduce exposure to bacterial pathogens of humans, fishes, and invertebrates, 10.1126/science.aal1956
  82. Legrève Anne, Vanpee Brigitte, Delfosse Philippe, Maraite Henri, 10.1023/a:1008784823899
  83. Legrève Anne, Delfosse Philippe, Maraite Henri, Phylogenetic analysis of Polymyxa species based on nuclear 5.8S and internal transcribed spacers ribosomal DNA sequences, 10.1017/s0953756201005391
  84. Lemarié, Plant Cell Physiol., 56, 2158 (2015)
  85. Lindholm Tore, Lindqvist Christer, Sjöqvist Conny, Occurrence and Activity of Slime Nets,Labyrinthulasp. Among Aquatic Plants in Cold and Oligohaline Baltic Sea Waters, 10.5735/085.053.0225
  86. Loureiro Rafael, Gachon Claire M. M., Rebours Céline, Seaweed cultivation: potential and challenges of crop domestication at an unprecedented pace, 10.1111/nph.13278
  87. Lovelock David A., Donald Caroline E., Conlan Xavier A., Cahill David M., Salicylic acid suppression of clubroot in broccoli (Brassicae oleracea var. italica) caused by the obligate biotroph Plasmodiophora brassicae, 10.1007/s13313-012-0167-x
  88. Ludwig-Müller Jutta, Belowground Defence Strategies Against Clubroot (Plasmodiophora brassicae), Belowground Defence Strategies in Plants (2016) ISBN:9783319423173 p.195-219, 10.1007/978-3-319-42319-7_9
  89. Ludwig-Müller Jutta, Prinsen Els, Rolfe Stephen A., Scholes Julie D., Metabolism and Plant Hormone Action During Clubroot Disease, 10.1007/s00344-009-9089-4
  90. Ludwig-Müller Jutta, Jülke Sabine, Geiß Kathleen, Richter Franziska, Mithöfer Axel, Šola Ivana, Rusak Gordana, Keenan Sandi, Bulman Simon, A novel methyltransferase from the intracellular pathogenPlasmodiophora brassicaemethylates salicylic acid : Salicylic acid methyltransferase fromP. brassicae, 10.1111/mpp.12185
  91. Ludwig-Müller Jutta, Auer Susann, Jülke Sabine, Marschollek Sabine, Manipulation of Auxin and Cytokinin Balance During the Plasmodiophora brassicae–Arabidopsis thaliana Interaction, Methods in Molecular Biology (2017) ISBN:9781493968299 p.41-60, 10.1007/978-1-4939-6831-2_3
  92. Lukeš Julius, Skalický Tomáš, Týč Jiří, Votýpka Jan, Yurchenko Vyacheslav, Evolution of parasitism in kinetoplastid flagellates, 10.1016/j.molbiopara.2014.05.007
  93. Malinowski Robert, Smith Jody A., Fleming Andrew J., Scholes Julie D., Rolfe Stephen A., Gall formation in clubroot-infected Arabidopsis results from an increase in existing meristematic activities of the host but is not essential for the completion of the pathogen life cycle : Gall formation in clubroot infection, 10.1111/j.1365-313x.2012.04983.x
  94. Malinowski Robert, Novák Ondřej, Borhan M. Hossein, Spíchal Lukáš, Strnad Miroslav, Rolfe Stephen A., The role of cytokinins in clubroot disease, 10.1007/s10658-015-0845-y
  95. MANSFIELD JOHN, GENIN STEPHANE, MAGORI SHIMPEI, CITOVSKY VITALY, SRIARIYANUM MALINEE, RONALD PAMELA, DOW MAX, VERDIER VALÉRIE, BEER STEVEN V., MACHADO MARCOS A., TOTH IAN, SALMOND GEORGE, FOSTER GARY D., Top 10 plant pathogenic bacteria in molecular plant pathology : Top 10 plant pathogenic bacteria, 10.1111/j.1364-3703.2012.00804.x
  96. Martin Daniel L., Chiari Ylenia, Boone Emily, Sherman Timothy D., Ross Cliff, Wyllie-Echeverria Sandy, Gaydos Joseph K., Boettcher Anne A., Functional, Phylogenetic and Host-Geographic Signatures of Labyrinthula spp. Provide for Putative Species Delimitation and a Global-Scale View of Seagrass Wasting Disease, 10.1007/s12237-016-0087-z
  97. Maslov Dmitri A., Votýpka Jan, Yurchenko Vyacheslav, Lukeš Julius, Diversity and phylogeny of insect trypanosomatids: all that is hidden shall be revealed, 10.1016/j.pt.2012.11.001
  98. MCGHEE R. BARCLAY, MCGHEE ANN H., Biology and Structure ofPhytomonas stahelisp. n., a Trypanosomatid Located in Sieve Tubes of Coconut and Oil Palms, 10.1111/j.1550-7408.1979.tb04633.x
  99. MCGRANN GRAHAM R. D., GRIMMER MICHAEL K., MUTASA-GÖTTGENS EFFIE S., STEVENS MARK, Progress towards the understanding and control of sugar beet rhizomania disease, 10.1111/j.1364-3703.2008.00514.x
  100. McKone KL, Tanner CE, Role of salinity in the susceptibility of eelgrass Zostera marina to the wasting disease pathogen Labyrinthula zosterae, 10.3354/meps07860
  101. Medina Jorge Mansur, Rodrigues Juliany Cola Fernandes, Moreira Otacilio C, Atella Geórgia, Souza Wanderley de, Barrabin Hector, Mechanisms of growth inhibition of Phytomonas serpens by the alkaloids tomatine and tomatidine, 10.1590/0074-02760140097
  102. Merz U., Falloon R. E., Review: Powdery Scab of Potato—Increased Knowledge of Pathogen Biology and Disease Epidemiology for Effective Disease Management, 10.1007/s11540-008-9105-2
  103. Michel Gurvan, Tonon Thierry, Scornet Delphine, Cock J. Mark, Kloareg Bernard, The cell wall polysaccharide metabolism of the brown alga Ectocarpus siliculosus. Insights into the evolution of extracellular matrix polysaccharides in Eukaryotes, 10.1111/j.1469-8137.2010.03374.x
  104. Moxham Susan E., Buczacki S.T., Chemical composition of the resting spore wall of Plasmodiophora brassicae, 10.1016/s0007-1536(83)80013-8
  105. Muehlstein LK, Perspectives on the wasting disease of eelgrass Zostera marina, 10.3354/dao007211
  106. Muehlstein Lisa K., The host – pathogen interaction in the wasting disease of eelgrass, Zostera marina, 10.1139/b92-258
  107. Muehlstein L. K., Porter D., Short F. T., Labyrinthula sp., a marine slime mold producing the symptoms of wasting disease in eelgrass, Zostera marina, 10.1007/bf00392553
  108. Muller D. G., Kupper F. C., Kupper H., Infection experiments reveal broad host ranges of Eurychasma dicksonii (Oomycota) and Chytridium polysiphoniae (Chytridiomycota), two eukaryotic parasites in marine brown algae (Phaeophyceae), 10.1111/j.1440-1835.1999.tb00301.x
  109. Nakamura Yoji, Sasaki Naobumi, Kobayashi Masahiro, Ojima Nobuhiko, Yasuike Motoshige, Shigenobu Yuya, Satomi Masataka, Fukuma Yoshiya, Shiwaku Koji, Tsujimoto Atsumi, Kobayashi Takanori, Nakayama Ichiro, Ito Fuminari, Nakajima Kazuhiro, Sano Motohiko, Wada Tokio, Kuhara Satoru, Inouye Kiyoshi, Gojobori Takashi, Ikeo Kazuho, The First Symbiont-Free Genome Sequence of Marine Red Alga, Susabi-nori (Pyropia yezoensis), 10.1371/journal.pone.0057122
  110. Neuhauser Sigrid, Bulman Simon, Kirchmair Martin, Plasmodiophorids: The Challenge to Understand Soil-Borne, Obligate Biotrophs with a Multiphasic Life Cycle, Molecular Identification of Fungi (2010) ISBN:9783642050411 p.51-78, 10.1007/978-3-642-05042-8_3
  111. Neuhauser Sigrid, Kirchmair Martin, Gleason Frank H., The ecological potentials of Phytomyxea (“plasmodiophorids”) in aquatic food webs, 10.1007/s10750-010-0508-0
  112. Neuhauser Sigrid, Kirchmair Martin, Bulman Simon, Bass David, Cross-kingdom host shifts of phytomyxid parasites, 10.1186/1471-2148-14-33
  113. O'Brien, Australas. Plant Pathol., 46, 1 (2017)
  114. Olsen Jeanine L., Rouzé Pierre, Verhelst Bram, Lin Yao-Cheng, Bayer Till, Collen Jonas, Dattolo Emanuela, De Paoli Emanuele, Dittami Simon, Maumus Florian, Michel Gurvan, Kersting Anna, Lauritano Chiara, Lohaus Rolf, Töpel Mats, Tonon Thierry, Vanneste Kevin, Amirebrahimi Mojgan, Brakel Janina, Boström Christoffer, Chovatia Mansi, Grimwood Jane, Jenkins Jerry W., Jueterbock Alexander, Mraz Amy, Stam Wytze T., Tice Hope, Bornberg-Bauer Erich, Green Pamela J., Pearson Gareth A., Procaccini Gabriele, Duarte Carlos M., Schmutz Jeremy, Reusch Thorsten B. H., Van de Peer Yves, The genome of the seagrass Zostera marina reveals angiosperm adaptation to the sea, 10.1038/nature16548
  115. OLSEN MARY W., Labyrinthula terrestris: a new pathogen of cool-season turfgrasses, 10.1111/j.1364-3703.2007.00425.x
  116. Olsen YS, Duarte CM, Combined effect of warming and infection by Labyrinthula sp. on the Mediterranean seagrass Cymodocea nodosa, 10.3354/meps11343
  117. Pan Jingwen, del Campo Javier, Keeling Patrick J., Reference Tree and Environmental Sequence Diversity of Labyrinthulomycetes, 10.1111/jeu.12342
  118. Park Chan Sun, Hwang Eun Kyoung, Biochemical characterization of Pyropia yezoensis-AP1 strain accompanies the resistance reaction to the red rot disease pathogen, Pythium porphyrae, 10.1007/s10811-015-0527-3
  119. Park Chan Sun, Kakinuma Makoto, Amano Hideomi, 10.1023/a:1011982105124
  120. Park Chan Sun, Kakinuma Makoto, Amano Hideomi, Forecasting infections of the red rot disease on Porphyra yezoensis Ueda (Rhodophyta) cultivation farms, 10.1007/s10811-006-9031-0
  121. PARTHASARATHY M. V., VAN SLOBBE W. G., SOUDANT C., Trypanosomatid Flagellate in the Phloem of Diseased Coconut Palms, 10.1126/science.192.4246.1346
  122. PÄSOLD SUSANNE, SIEGEL INA, SEIDEL CLAUDIA, LUDWIG-MÜLLER JUTTA, Flavonoid accumulation in Arabidopsis thaliana root galls caused by the obligate biotrophic pathogen Plasmodiophora brassicae : Flavonoids in Arabidopsis clubroots, 10.1111/j.1364-3703.2010.00628.x
  123. Petersen, Overs. K. Danske Vidensk. Selsk. Forh., 5, 439 (1905)
  124. Porcel Betina M., Denoeud France, Opperdoes Fred, Noel Benjamin, Madoui Mohammed-Amine, Hammarton Tansy C., Field Mark C., Da Silva Corinne, Couloux Arnaud, Poulain Julie, Katinka Michael, Jabbari Kamel, Aury Jean-Marc, Campbell David A., Cintron Roxana, Dickens Nicholas J., Docampo Roberto, Sturm Nancy R., Koumandou V. Lila, Fabre Sandrine, Flegontov Pavel, Lukeš Julius, Michaeli Shulamit, Mottram Jeremy C., Szöőr Balázs, Zilberstein Dan, Bringaud Frédéric, Wincker Patrick, Dollet Michel, The Streamlined Genome of Phytomonas spp. Relative to Human Pathogenic Kinetoplastids Reveals a Parasite Tailored for Plants, 10.1371/journal.pgen.1004007
  125. PRESTON TERENCE M., KING CONRAD A., Actin-Based Motility in the Net Slime MouldLabyrinthula: Evidence for the Role of Myosin in Gliding Movement, 10.1111/j.1550-7408.2005.00064.x
  126. Qu Xinshun, Christ Barbara J., Genetic variation and phylogeny ofSpongospora subterranea f.sp.subterranea based on ribosomal DNA sequence analysis, 10.1007/bf02870199
  127. Ritter Andrés, Goulitquer Sophie, Salaün Jean-Pierre, Tonon Thierry, Correa Juan A., Potin Philippe, Copper stress induces biosynthesis of octadecanoid and eicosanoid oxygenated derivatives in the brown algal kelpLaminaria digitata, 10.1111/j.1469-8137.2008.02626.x
  128. Rodgers KL, Shears NT, Modelling kelp forest primary production using in situ photosynthesis, biomass and light measurements, 10.3354/meps11801
  129. Rolfe Stephen A., Strelkov Stephen E., Links Matthew G., Clarke Wayne E., Robinson Stephen J., Djavaheri Mohammad, Malinowski Robert, Haddadi Parham, Kagale Sateesh, Parkin Isobel A. P., Taheri Ali, Borhan M. Hossein, The compact genome of the plant pathogen Plasmodiophora brassicae is adapted to intracellular interactions with host Brassica spp, 10.1186/s12864-016-2597-2
  130. SCHOLTHOF KAREN-BETH G., ADKINS SCOTT, CZOSNEK HENRYK, PALUKAITIS PETER, JACQUOT EMMANUEL, HOHN THOMAS, HOHN BARBARA, SAUNDERS KEITH, CANDRESSE THIERRY, AHLQUIST PAUL, HEMENWAY CYNTHIA, FOSTER GARY D., Top 10 plant viruses in molecular plant pathology : Top 10 plant viruses, 10.1111/j.1364-3703.2011.00752.x
  131. Schuller Astrid, Kehr Julia, Ludwig-Müller Jutta, Laser Microdissection Coupled to Transcriptional Profiling of Arabidopsis Roots Inoculated by Plasmodiophora brassicae Indicates a Role for Brassinosteroids in Clubroot Formation, 10.1093/pcp/pct174
  132. Schwelm Arne, Fogelqvist Johan, Knaust Andrea, Jülke Sabine, Lilja Tua, Bonilla-Rosso German, Karlsson Magnus, Shevchenko Andrej, Dhandapani Vignesh, Choi Su Ryun, Kim Hong Gi, Park Ju Young, Lim Yong Pyo, Ludwig-Müller Jutta, Dixelius Christina, The Plasmodiophora brassicae genome reveals insights in its life cycle and ancestry of chitin synthases, 10.1038/srep11153
  133. Schwelm Arne, Berney Cédric, Dixelius Christina, Bass David, Neuhauser Sigrid, The Large Subunit rDNA Sequence of Plasmodiophora brassicae Does not Contain Intra-species Polymorphism, 10.1016/j.protis.2016.08.008
  134. Sekimoto Satoshi, Beakes Gordon W., Gachon Claire M.M., Müller Dieter G., Küpper Frithjof C., Honda Daiske, The Development, Ultrastructural Cytology, and Molecular Phylogeny of the Basal Oomycete Eurychasma dicksonii, Infecting the Filamentous Phaeophyte Algae Ectocarpus siliculosus and Pylaiella littoralis, 10.1016/j.protis.2007.11.004
  135. Seward Emily A., Votýpka Jan, Kment Petr, Lukeš Julius, Kelly Steven, Description of Phytomonas oxycareni n. sp. from the Salivary Glands of Oxycarenus lavaterae, 10.1016/j.protis.2016.11.002
  136. Shah Farhat A., Falloon Richard E., Butler Ruth C., Lister Ros A., Low amounts of Spongospora subterranea sporosorus inoculum cause severe powdery scab, root galling and reduced water use in potato (Solanum tuberosum), 10.1007/s13313-011-0110-6
  137. Siemens Johannes, Keller Ingo, Sarx Johannes, Kunz Sabine, Schuller Astrid, Nagel Wolfgang, Schmülling Thomas, Parniske Martin, Ludwig-Müller Jutta, Transcriptome Analysis ofArabidopsisClubroots Indicate a Key Role for Cytokinins in Disease Development, 10.1094/mpmi-19-0480
  138. Siemens Johannes, Bulman Simon, Rehn Frank, Sundelin Thomas, Molecular Biology of Plasmodiophora brassicae, 10.1007/s00344-009-9091-x
  139. Smith Madeleine J., Adams Michael J., Ward Elaine, Evidence that Polymyxa species may infect Arabidopsis thaliana : Evidence for infection of Arabidopsis by Polymyxa, 10.1111/j.1574-6968.2011.02236.x
  140. Smith Madeleine J., Adams Michael J., Ward Elaine, Ribosomal DNA analyses reveal greater sequence variation inPolymyxaspecies than previously thought and indicate the possibility of new ribotype-host-virus associations : Ribotype-host-virus associations inPolymyxaspp., 10.1111/1758-2229.12026
  141. Song Tao, Chu Mingguang, Lahlali Rachid, Yu Fengqun, Peng Gary, Shotgun Label-free Proteomic Analysis of Clubroot (Plasmodiophora brassicae) Resistance Conferred by the Gene Rcr1 in Brassica rapa, 10.3389/fpls.2016.01013
  142. Natural Products From Marine Algae, ISBN:9781493926831, 10.1007/978-1-4939-2684-8
  143. Stowell , L.J. Martin , S.B. Olsen , M.W. Bigelow , D. Kohout , M. Peterson , P.D. Camberato , J. Gelernter , W.D. 2005 APSnet Features http://www.apsnet.org/publications/apsnetfeatures/Pages/RapidBlight.aspx
  144. Strelkov Stephen E., Hwang Sheau-Fang, Manolii Victor P., Cao Tiesen, Feindel David, Emergence of new virulence phenotypes of Plasmodiophora brassicae on canola (Brassica napus) in Alberta, Canada, 10.1007/s10658-016-0888-8
  145. Strittmatter Martina, Grenville-Briggs Laura J., Breithut Lisa, Van West Pieter, Gachon Claire M. M., Küpper Frithjof C., Infection of the brown algaEctocarpus siliculosusby the oomyceteEurychasma dicksoniiinduces oxidative stress and halogen metabolism : Physiological response ofEctocarpusto infection, 10.1111/pce.12533
  146. Sullivan Brooke K., Sherman Timothy D., Damare Varada S., Lilje Osu, Gleason Frank H., Potential roles of Labyrinthula spp. in global seagrass population declines, 10.1016/j.funeco.2013.06.004
  147. Sullivan Brooke K., Robinson Katie L., Trevathan-Tackett Stacey M., Lilje Erna S., Gleason Frank H., Lilje Osu, The First Isolation and Characterisation of the Protist Labyrinthula sp. in Southeastern Australia, 10.1111/jeu.12387
  148. Tamada Tetsuo, Kondo Hideki, Biological and genetic diversity of plasmodiophorid-transmitted viruses and their vectors, 10.1007/s10327-013-0457-3
  149. Trevathan-Tackett Stacey M., Lane Amy L., Bishop Nichole, Ross Cliff, Metabolites derived from the tropical seagrass Thalassia testudinum are bioactive against pathogenic Labyrinthula sp, 10.1016/j.aquabot.2014.12.005
  150. Tsirigoti Amerssa, Beakes Gordon W., Hervé Cécile, Gachon Claire M. M., Katsaros Christos, Attachment, penetration and early host defense mechanisms during the infection of filamentous brown algae by Eurychasma dicksonii, 10.1007/s00709-014-0721-1
  151. Tsui Clement K.M., Marshall Wyth, Yokoyama Rinka, Honda Daiske, Lippmeier J. Casey, Craven Kelly D., Peterson Paul D., Berbee Mary L., Labyrinthulomycetes phylogeny and its implications for the evolutionary loss of chloroplasts and gain of ectoplasmic gliding, 10.1016/j.ympev.2008.09.027
  152. Uppalapati Srinivasa Rao, Fujita Yuji, Carbohydrate regulation of attachment, encystment, and appressorium formation by Pythium porphyrae (Oomycota) zoospores on Porphyra yezoensis (Rhodophyta), 10.1046/j.1529-8817.2000.99099.x
  153. Uppalapati S. R., Fujita Y., The Relative Resistances of Porphyra Species (Bangiales, Rhodophyta) to Infection by Pythium porphyrae (Peronosporales, Oomycota), 10.1515/bot.2001.001
  154. Vaïanopoulos C., Bragard C., Moreau V., Maraite H., Legrève A., Identification and Quantification ofPolymyxa graminisf. sp.temperataandP. graminisf. sp.tepidaon Barley and Wheat, 10.1094/pdis-91-7-0857
  155. Vergeer L.H.T., Aarts T.L., de Groot J.D., The ‘wasting disease’ and the effect of abiotic factors (light intensity, temperature, salinity) and infection with Labyrinthula zosterae on the phenolic content of Zostera marina shoots, 10.1016/0304-3770(95)00480-n
  156. Vishniac H. S., The Nutritional Requirements of Isolates of Labyrinthula spp., 10.1099/00221287-12-3-455
  157. WALSH J. A., CLAY C. M., MILLER A., A new virus disease of watercress in England, 10.1111/j.1365-2338.1989.tb00420.x
  158. Ward Elaine, Kanyuka Kostya, Motteram Juliet, Kornyukhin Dmitry, Adams Michael J., The use of conventional and quantitative real-time PCR assays for Polymyxa graminis to examine host plant resistance, inoculum levels and intraspecific variation, 10.1111/j.1469-8137.2004.01291.x
  159. Ward L. I., Fenn M. G. E., Henry C. M., A rapid method for direct detection of Polymyxa DNA in soil, 10.1111/j.1365-3059.2004.01017.x
  160. Woronin, Arb. St. Petersburger naturf. Ges., 8, 169 (1877)
  161. Wu Shuangxiu, Sun Jing, Chi Shan, Wang Liang, Wang Xumin, Liu Cui, Li Xingang, Yin Jinlong, Liu Tao, Yu Jun, Transcriptome sequencing of essential marine brown and red algal species in China and its significance in algal biology and phylogeny, 10.1007/s13131-014-0435-4
  162. Young Edward Lorraine, Studies on Labyrinthula. The Etiologic Agent of the Wasting Disease of Eel-Grass, 10.2307/2437469
  163. Zamani-Noor N., Variation in pathotypes and virulence ofPlasmodiophora brassicaepopulations in Germany, 10.1111/ppa.12573
  164. Zambounis A., Elias M., Sterck L., Maumus F., Gachon C. M. M., Highly Dynamic Exon Shuffling in Candidate Pathogen Receptors ... What if Brown Algae Were Capable of Adaptive Immunity?, 10.1093/molbev/msr296
  165. Zhang Dapeng, Burroughs A. Maxwell, Vidal Newton D., Iyer Lakshminarayan M., Aravind L., Transposons to toxins: the provenance, architecture and diversification of a widespread class of eukaryotic effectors, 10.1093/nar/gkw221
  166. Zhang Xiaoli, Liu Yumei, Fang Zhiyuan, Li Zhansheng, Yang Limei, Zhuang Mu, Zhang Yangyong, Lv Honghao, Comparative Transcriptome Analysis between Broccoli (Brassica oleracea var. italica) and Wild Cabbage (Brassica macrocarpa Guss.) in Response to Plasmodiophora brassicae during Different Infection Stages, 10.3389/fpls.2016.01929
  167. Ziegler A., Fomitcheva V., Zakri A. M., Kastirr U., Occurrence ofPolymyxa graminisRibotypes in Germany and Their Association with Different Host Plants and Viruses, 10.1556/0806.43.2015.051
  168. Stahel, Phytopathol. Z., 4, 539 (1931)
  169. Lopez, Oleagineux, 30, 243 (1975)
  170. Kastelein , P. 1987
  171. FAO 2014 http://www.fao.org/figis/
Bibliographic reference Schwelm, Arne ; Badstöber, Julia ; Bulman, Simon ; Desoignies, Nicolas ; Etemadi, Mohammad ; et. al. Not in your usual Top 10: protists that infect plants and algae. In: Molecular Plant Pathology, Vol. 19, no. 4, p. 1029-1044 (2017)
Permanent URL http://hdl.handle.net/2078.1/188113