中国农业科学 ›› 2012, Vol. 45 ›› Issue (14): 2801-2814.doi: 10.3864/j.issn.0578-1752.2012.14.003
周晓鸿, 田芳, 杜丽璞, 王轲, 林志珊, 叶兴国
收稿日期:
2012-02-15
出版日期:
2012-07-15
发布日期:
2012-05-07
通讯作者:
通信作者叶兴国,Tel:010-82109765;E-mail:yexg@mail.caas.net.cn
作者简介:
周晓鸿,E-mail:zhouxiaohong003@163.com
基金资助:
国家转基因研究专项(2011ZX08010-004)
ZHOU Xiao-Hong, TIAN Fang, DU Li-Pu, WANG Ke, LIN Zhi-Shan, YE Xing-Guo
Received:
2012-02-15
Online:
2012-07-15
Published:
2012-05-07
摘要: 植物与微生物在长期的侵染和抗侵染过程中逐渐形成了复杂的互作关系,二者相互利用、协同进化。一些病原微生物致病能力的变化或增强迫使植物提高抗病性,同时改进了植物的农艺性状、产量性状和品质性状。植物与微生物互作关系的分子生物学研究促进了植物基因工程育种途径的创立和生产潜力的提高,尤其微生物介导的基因转移已成为改良植物的重要工具。本文概括性综述了植物与一些主要有益微生物互作的应答反应、信号传导和分子基础,以及利用有益微生物对改良植物性状和生产水平的研究进展。描述了植物对主要有益微生物的应答途径,以及植物和农杆菌、根瘤菌、真菌及植物病毒互作的分子信号系统,并介绍了它们在基因工程、遗传育种和生产实践中的应用。对于人们正确认识有益微生物的两面性,改变传统观念,进一步利用有益微生物的正向作用提高植物抗病性、抗逆性、品质和生产潜力,培育优良作物品种等,具有一定参考价值。
周晓鸿, 田芳, 杜丽璞, 王轲, 林志珊, 叶兴国. 植物与有益微生物互作的分子基础及其应用的研究进展[J]. 中国农业科学, 2012, 45(14): 2801-2814.
ZHOU Xiao-Hong, TIAN Fang, DU Li-Pu, WANG Ke, LIN Zhi-Shan, YE Xing-Guo. Advances in Molecular Biology Research of Interaction between Plants and Beneficial Microorganisms and Their Applications in Plant Improvement[J]. Scientia Agricultura Sinica, 2012, 45(14): 2801-2814.
[1]Jones J D, Dangl J L. The plant immune system. Nature, 2006, 444(7117): 323-329.[2]Aderem A, Ulevitch R J. Toll-like receptors in the induction of the innate immune response. Nature, 2000, 406(6797): 782-787.[3]Madala N E, Molinaro A, Dubery I A. Distinct carbohydrate and lipid-based molecular patterns within lipopolysaccharides from Burkholderia cepacia contribute to defense-associated differential gene expression in Arabidopsis thaliana. Innate Immunity, 2012, 18(1): 140-154.[4]Lee J, Klessig D F, Nurnberger T. A harpin binding site in tobacco plasma membranes mediates activation of the pathogenesis-related gene HIN1 independent of extracellular calcium but dependent on mitogen-activated protein kinase activity. The Plant Cell, 2001, 13(5): 1079-1093.[5]Felix G, Duran J D, Volko S, Boller T. Plants have a sensitive perception system for the most conserved domain of bacterial flagellin. The Plant Journal, 1999, 18(3): 265-276.[6]Nurnberger T, Brunner F. Innate immunity in plants and animals: Emerging parallels between the recognition of general elicitors and pathogen-associated molecular patterns. Current Opinion in Plant Biology, 2002, 5(4): 318-324.[7]Zhang J, Shao F, Li Y, Cui H, Chen L, Li H, Zou Y, Long C, Lan L, Chai J, Chen S, Tang X, Zhou J M. A Pseudomonas syringae effector inactivates MAPKs to suppress PAMP-induced immunity in plants. Cell Host and Microbe, 2007, 1(3): 175-185.[8]Wittstock U, Gershenzon J. Constitutive plant toxins and their role in defense against herbivores and pathogens. Current Opinion in Plant Biology, 2002, 5(4): 300-307.[9]Blume B, Nurnberger T, Nass N, Scheel D. Receptor-mediated increase in cytoplasmic free calcium required for activation of pathogen defense in parsley. The Plant Cell, 2000, 12(8): 1425-1440.[10]Kim M C, Panstruga R, Elliott C, Muller J, Devoto A, Yoon H W, Park H C, Cho M J, Schulze-Lefert P. Calmodulin interacts with MLO protein to regulate defence against mildew in barley. Nature, 2002, 416(6879): 447-451.[11]Jabs T, Tschope M, Colling C, Hahlbrock K, Scheel D. Elicitor-stimulated ion fluxes and O2- from the oxidative burst are essential components in triggering defense gene activation and phytoalexin synthesis in parsley. Proceedings of the National Academy of Sciences of the United States of America, 1997, 94(9): 4800-4805.[12]Lamb C, Dixon R A. The oxidative burst in plant disease resistance. Annual Reviews Plant Physiology and Plant Molecular Biology, 1997, 48: 251-275.[13]Fellbrich G, Blume B, Brunner F, Hirt H, Kroj T, Ligterink W, Romanski A, Nurnberger T. Phytophthora parasitica elicitor-induced reactions in cells of Petroselinum crispum. Plant Cell and Physiologist, 2000, 41(6): 692-701.[14]Ryals J A, Neuenschwander U H, Willits M G, Molina A, Steiner H Y, Hunt M D. Systemic acquired resistance. The Plant Cell, 1996, 8(10): 1809-1819.[15]Kunkel B N, Brooks D M. Cross talk between signaling pathways in pathogen defense. Current Opinion in Plant Biology, 2002, 5(4): 325-331.[16]von Saint Paul V,Zhang W, Kanawati B, Geist B, Faus-Kessler T, Schmitt-Kopplin P, Schaffner A R. The Arabidopsis glucosyltransferase UGT76B1 conjugates isoleucic acid and modulates plant defense and senescence. The Plant Cell, 2011, 23(11): 4124-4145.[17]Kumar D, Klessig D F. High-affinity salicylic acid-binding protein 2 is required for plant innate immunity and has salicylic acid-stimulated lipase activity. Proceedings of the National Academy of Sciences of the United States of America, 2003, 100(26): 16101-16106.[18]Falk A, Feys B J, Frost L N, Jones J D, Daniels M J, Parker J E. EDS1, an essential component of R gene-mediated disease resistance in Arabidopsis has homology to eukaryotic lipases. Proceedings of the National Academy of Sciences of the United States of America, 1999, 96(6): 3292-3297.[19]Jirage D, Tootle T L, Reuber T L, Frost L N, Feys B J, Parker J E, Ausubel F M, Glazebrook J. Arabidopsis thaliana PAD4 encodes a lipase-like gene that is important for salicylic acid signaling. Proceedings of the National Academy of Sciences of the United States of America, 1999, 96(23): 13583-13588.[20]Feys B J, Parker J E. Interplay of signaling pathways in plant disease resistance. Trends in Genetics, 2000, 16(10): 449-455.[21]Slaymaker D H, Navarre D A, Clark D, del Pozo O, Martin G B, Klessig D F. The tobacco salicylic acid-binding protein 3 (SABP3) is the chloroplast carbonic anhydrase, which exhibits antioxidant activity and plays a role in the hypersensitive defense response. Proceedings of the National Academy of Sciences of the United States of America, 2002, 99(18): 11640-11645.[22]Mukhtar M S, Nishimura M T, Dangl J. NPR1 in plant defense: It's not over'til it's turned over. Cell, 2009, 137(5): 804-806.[23]Després C, Chubak C, Rochon A, Clark R, Bethune T, Desveaux D, Fobert P R. The Arabidopsis NPR1 disease resistance protein is a novel cofactor that confers redox regulation of DNA binding activity to the basic domain/leucine zipper transcription factor TGA1. The Plant Cell , 2003, 15(9): 2181-2191.[24]Young J M, Kuykendall L D, Martinez-Romero E, Kerr A, Sawada H. Classification and nomenclature of Agrobacterium and Rhizobium. International Journal of Systematic and Evolutionary Microbiology, 2003, 53(5): 1689-1695.[25]史晓霞, 师尚礼, 杨 晶, 王正凤. 豆科植物根瘤茵分类研究进展. 草坪与草原, 2006(1): 12-16.Shi X X, Shi S L, Yang J, Wang Z F. Research advancement in taxonomy of Rhizobium leguminosarum. Grassland and Turf, 2006(1): 12-16. (in Chinese)[26]Stachel S E, Nester E W. The genetic and transcriptional organization of the vir region of the A6 Ti plasmid of Agrobacterium tumefaciens. The EMBO Journal, 1986, 5(7): 1445-1454.[27]Altabe S, de Iannino N I, De Mendoza D, Ugalde R. Expression of the Agrobacterium tumefaciens chvB virulence region in Azospirillum spp. Journal of bacteriology, 1990, 172(5): 2563-2567.[28]Brencic A, Winans S C. Detection of and response to signals involved in host-microbe interactions by plant-associated bacteria. Microbiology and Molecular Biology Reviews, 2005, 69(1): 155-194.[29]Jin S, Roitsch T, Ankenbauer R G, Gordon M P, Nester E W. The VirA protein of Agrobacterium tumefaciens is autophosphorylated and is essential for vir gene regulation. Journal of Bacteriology, 1990, 172(2): 525-530.[30]Wise A A, Fang F, Lin Y H, He F, Lynn D G, Binns A N. The receiver domain of hybrid histidine kinase VirA: An enhancing factor for vir gene expression in Agrobacterium tumefaciens. Journal of Bacteriology, 2010, 192(6): 1534-1542.[31]Mantis N J, Winans S C. The chromosomal response regulatory gene chvI of Agrobacterium tumefaciens complements an Escherichia coli phoB mutation and is required for virulence. Journal of Bacteriology, 1993, 175(20): 6626-6636.[32]Cangelosi G A, Martinetti G, Leigh J A, Lee C C, Thienes C, Nester E W. Role for Agrobacterium tumefaciens ChvA protein in export of beta-1,2-glucan. Journal of Bacteriology, 1989, 171(3): 1609-1615.[33]Matthysse A G, Yarnall H, Boles S B, McMahan S. A region of the Agrobacterium tumefaciens chromosome containing genes required for virulence and attachment to host cells. Biochimica et Biophysica Acta, 2000, 1490(1/2): 208-212.[34]Wood D W, Setubal J C, Kaul R, Monks D E, Kitajima J P, Okura V K, Zhou Y, Chen L, Wood G E, Almeida N F, Jr., Woo L, Chen Y, Paulsen I T, Eisen J A, Karp P D, Bovee D, Sr., Chapman P, Clendenning J, Deatherage G, Gillet W, Grant C, Kutyavin T, Levy R, Li M J, McClelland E, Palmieri A, Raymond C, Rouse G, Saenphimmachak C, Wu Z, Romero P, Gordon D, Zhang S, Yoo H, Tao Y, Biddle P, Jung M, Krespan W, Perry M, Gordon-Kamm B, Liao L, Kim S, Hendrick C, Zhao Z Y, Dolan M, Chumley F, Tingey S V, Tomb J F, Gordon M P, Olson M V, Nester E W. The genome of the natural genetic engineer Agrobacterium tumefaciens C58. Science, 2001, 294(5550): 2317-2323.[35]Goodner B, Hinkle G, Gattung S, Miller N, Blanchard M, Qurollo B, Goldman B S, Cao Y, Askenazi M, Halling C, Mullin L, Houmiel K, Gordon J, Vaudin M, Iartchouk O, Epp A, Liu F, Wollam C, Allinger M, Doughty D, Scott C, Lappas C, Markelz B, Flanagan C, Crowell C, Gurson J, Lomo C, Sear C, Strub G, Cielo C, Slater S. Genome sequence of the plant pathogen and biotechnology agent Agrobacterium tumefaciens C58. Science, 2001, 294(5550): 2323-2328.[36]Nair G R, Liu Z, Binns A N. Reexamining the role of the accessory plasmid pAtC58 in the virulence of Agrobacterium tumefaciens strain C58. Plant Physiology, 2003, 133(3): 989-999.[37]Schroder G, Lanka E. The mating pair formation system of conjugative plasmids-A versatile secretion machinery for transfer of proteins and DNA. Plasmid, 2005, 54(1): 1-25.[38]Gelvin S B. Agrobacterium-mediated plant transformation: The biology behind the "gene-jockeying" tool. Microbiology and Molecular Biology Reviews, 2003, 67(1): 16-37[39]Djamei A, Pitzschke A, Nakagami H, Rajh I, Hirt H. Trojan horse strategy in Agrobacterium transformation: Abusing MAPK defense signaling. Science, 2007, 318(5849): 453-456.[40]Tzfira T, Vaidya M, Citovsky V. Involvement of targeted proteolysis in plant genetic transformation by Agrobacterium. Nature, 2004, 431(7004): 87-92.[41]Chen I, Christie P J, Dubnau D. The ins and outs of DNA transfer in bacteria. Science, 2005, 310(5753): 1456-1460.[42]Guo M, Hou Q, Hew C L, Pan S Q. Agrobacterium VirD2-binding protein is involved in tumorigenesis and redundantly encoded in conjugative transfer gene clusters. Molecular Plant-Microbe Interactions, 2007, 20(10): 1201-1212.[43]Guo M, Jin S, Sun D, Hew C L, Pan S Q. Recruitment of conjugative DNA transfer substrate to Agrobacterium type IV secretion apparatus. Proceedings of the National Academy of Sciences of the United States of America, 2007, 104(50): 20019-20024.[44]Ditt R F, Nester E W, Comai L. Plant gene expression response to Agrobacterium tumefaciens. Proceedings of the National Academy of Sciences of the United States of America, 2001, 98(19): 10954-10959.[45]Yuan Z C, Liu P, Saenkham P, Kerr K, Nester E W. Transcriptome profiling and functional analysis of Agrobacterium tumefaciens reveals a general conserved response to acidic conditions (pH 5.5) and a complex acid-mediated signaling involved in Agrobacterium-plant interactions. Journal of Bacteriology, 2008, 190(2): 494-507.[46]Ballas N, Citovsky V. Nuclear localization signal binding protein from Arabidopsis mediates nuclear import of Agrobacterium VirD2 protein. Proceedings of the National Academy of Sciences of the United States of America, 1997, 94(20): 10723-10728.[47]Tao Y, Rao P K, Bhattacharjee S, Gelvin S B. Expression of plant protein phosphatase 2C interferes with nuclear import of the Agrobacterium T-complex protein VirD2. Proceedings of the National Academy of Sciences of the United States of America, 2004, 101(14): 5164-5169.[48]Bako L, Umeda M, Tiburcio A F, Schell J, Koncz C. The VirD2 pilot protein of Agrobacterium-transferred DNA interacts with the TATA box-binding protein and a nuclear protein kinase in plants. Proceedings of the National Academy of Sciences of the United States of America, 2003, 100(17): 10108-10113.[49]Tzfira T, Vaidya M, Citovsky V. VIP1, an Arabidopsis protein that interacts with Agrobacterium VirE2, is involved in VirE2 nuclear import and Agrobacterium infectivity. The EMBO Journal, 2001, 20(13): 3596-3607. [50]Tzfira T, Vaidya M, Citovsky V. Increasing plant susceptibility to Agrobacterium infection by overexpression of the Arabidopsis nuclear protein VIP1. Proceedings of the National Academy of Sciences of the United States of America, 2002, 99(16): 10435-10440.[51]Anand A, Krichevsky A, Schornack S, Lahaye T, Tzfira T, Tang Y, Citovsky V, Mysore K S. Arabidopsis VIRE2 interacting protein 2 is required for Agrobacterium T-DNA integration in plants. The Plant Cell, 2007, 19(5): 1695-1708.[52]Hoff De P L, Brill L M, Hirsch A M. Plant lectins: The ties that bind in root symbiosis and plant defense. Molecular Genetics and Genomics, 2009, 282(1): 1-15.[53]Hamblin J, Kent S P. Possible role of phytohaemagglutinin in Phaseolus vulgaris L.. Nature New Biology, 1973, 245(140): 28-30.[54]Lerouge P, Roche P, Faucher C, Maillet F, Truchet G, Promé J C, Dénarié J. Symbiotic host-specificity of Rhizobium meliloti is determined by a sulphated and acylated glucosamine oligosaccharide signal. Nature, 1990, 344(6268): 781-784.[55]van de Wiel C, Scheres B, Franssen H, van Lierop M J, van Lammeren A, van Kammen A, Bisseling T. The early nodulin transcript ENOD2 is located in the nodule parenchyma (inner cortex) of pea and soybean root nodules. The EMBO Journal, 1990, 9(1): 1-7.[56]Csanadi G, Szecsi J, Kalo P, Kiss P, Endre G, Kondorosi A, Kondorosi E, Kiss G B. ENOD12, an early nodulin gene, is not required for nodule formation and efficient nitrogen fixation in alfalfa. The Plant Cell, 1994, 6(2): 201-213.[57]Khan J A, Wang Q, Sjolund R D, Schulz A, and Thompson G A. An early nodulin-like protein accumulates in the sieve element plasma membrane of Arabidopsis. Plant Physiology, 2007, 143(4): 1576-1589.[58]Radutoiu S, Madsen L H, Madsen E B, Felle H H, Umehara Y, Gronlund M, Sato S, Nakamura Y, Tabata S, Sandal N, Stougaard J. Plant recognition of symbiotic bacteria requires two LysM receptor-like kinases. Nature, 2003, 425(6958): 585-592.[59]Ke D, Fang Q, Chen C, Zhu H, Chen T, Chang X, Yuan S, Ma L, Hong Z, Zhang Z. The small GTPase ROP6 interacts with NFR5 and is involved in nodule formation in Lotus japonicus. Plant Physiology, 2012, 159: 131-143.[60]Ane J M, Kiss G B, Riely B K, Penmetsa R V, Oldroyd G E, Ayax C, Levy J, Debelle F, Baek J M, Kalo P, Rosenberg C, Roe B A, Long S R, Denarie J, Cook D R. Medicago truncatula DMI1 required for bacterial and fungal symbioses in legumes. Science, 2004, 303(5662): 1364-1367.[61]Riely B K, Lougnon G, Ane J M, Cook D R. The symbiotic ion channel homolog DMI1 is localized in the nuclear membrane of Medicago truncatula roots. The Plant Journal, 2007, 49(2): 208-216.[62]Limpens E, Mirabella R, Fedorova E, Franken C, Franssen H, Bisseling T, Geurts R. Formation of organelle-like N2-fixing symbiosomes in legume root nodules is controlled by DMI2. Proceedings of the National Academy of Sciences of the United States of America, 2005, 102(29): 10375-10380.[63]Gleason C, Chaudhuri S, Yang T, Munoz A, Poovaiah B W, Oldroyd G E. Nodulation independent of Rhizobia induced by a calcium- activated kinase lacking autoinhibition. Nature, 2006, 441(7097): 1149-1152.[64]Maekawa T, Maekawa-Yoshikawa M, Takeda N, Imaizumi-Anraku H, Murooka Y, and Hayashi M. Gibberellin controls the nodulation signaling pathway in Lotus japonicus. The Plant Journal, 2009, 58(2): 183-194.[65] Shrawat A K, Lorz H. Agrobacterium-mediated transformation of cereals: A promising approach crossing barriers. Plant Biotechnology Journal, 2006, 4(6): 575-603.[66]Gould J, Devey M, Hasegawa O, Ulian E C, Peterson G, Smith R H. Transformation of Zea mays L. using Agrobacterium tumefaciens and the shoot apex. Plant Physiology, 1991, 95(2): 426-434.[67]Philippe V. Thirty years of plant transformation technology development. Plant Biotechnology Journal, 2007, 5(2): 221-229.[68]James C. 2011年全球生物技术/转基因作物商业化发展态势. 中国生物工程杂志, 2012, 32(1): 1-14James C. The commercial development situation of global biological technology/gm crops in 2011. China Biotechnology, 2012, 32(1): 1-14. (in Chinese)[69]Abuodeh R O, Orbach M J, Mandel M A, Das A, Galgiani J N. Genetic transformation of Coccidioides immitis facilitated by Agrobacterium tumefaciens. The Journal of Infectious Diseases, 2000, 181(6): 2106-2110.[70]Kunik T, Tzfira T, Kapulnik Y, Gafni Y, Dingwall C, Citovsky V. Genetic transformation of HeLa cells by Agrobacterium. Proceedings of the National Academy of Sciences of the United States of America, 2001, 98(4): 1871-1876.[71]Broothaerts W, Mitchell H J, Weir B, Kaines S, Smith L M, Yang W, Mayer J E, Roa-Rodriguez C, Jefferson R A. Gene transfer to plants by diverse species of bacteria. Nature, 2005, 433(7026): 629-633.[72]Ma Y M, Li Y, Liu J Y, Song Y C, Tan R X. Anti-Helicobacter pylori metabolites from Rhizoctonia sp. Cy064, an endophytic fungus in Cynodon dactylon. Fitoterapia, 2004, 75(5): 451-456.[73]Pongcharoen W, Rukachaisirikul V, Phongpaichit S, Kuhn T, Pelzing M, Sakayaroj J, Taylor W C. Metabolites from the endophytic fungus Xylaria sp. PSU-D14. Phytochemistry, 2008, 69(9): 1900-1902.[74]Song Y C, Li H, Ye Y H, Shan C Y, Yang Y M, Tan R X. Endophytic naphthopyrone metabolites are co-inhibitors of xanthine oxidase, SW1116 cell and some microbial growths. FEMS Microbiology Letters, 2004, 241(1): 67-72.[75]Khan A L, Hamayun M, Kang S M, Kim Y H, Jung H Y, Lee J H, Lee I J. Endophytic fungal association via gibberellins and indole acetic acid secretion can improve plant growth potential in abiotic stress: An example of Paecilomyces formosus LHL10. BMC Microbiology, 2012, 12(1): 3.[76]Saikkonen K, Faeth S, Helander M, Sullivan T. Fungal endophytes: A continuum of interactions with host plants. Annual Review of Ecology and Systematics, 1998: 319-343.[77]Moricca S, Ragazzi A. Fungal endophytes in Mediterranean oak forests: A lesson from Discula quercina. Phytopathology, 2008, 98(4): 380-386.[78]Saikkonen K, Wali P R, Helander M. Genetic compatibility determines endophyte-grass combinations. PLoS Pathogens, 2010, 5(6): e11395.[79]Kogel K H, Franken P, Huckelhoven R. Endophyte or parasite-what decides? Current Opinion in Plant Biology, 2006, 9(4): 358-363.[80]Márquez L M, Redman R S, Rodriguez R J, Roossinck M J. A virus in a fungus in a plant: Three-way symbiosis required for thermal tolerance. Science, 2007, 315(5811): 513-515.[81]Shahollari B, Vadassery J, Varma A, Oelmüller R. A leucine-rich repeat protein is required for growth promotion and enhanced seed production mediated by the endophytic fungus Piriformospora indica in Arabidopsis thaliana. The Plant Journal, 2007, 50(1): 1-13.[82]Cunningham P, Foot J, Reed K. Perennial ryegrass (Lolium perenne) endophyte (Acremonium lolii) relationships: The Australian experience. Agriculture, Ecosystems and Environment, 1993, 44: 157-168.[83]Noh M J, Yang J G, Kim K S, Yoon Y M, Kang K, Han H Y, Shim S B, Park H J. Isolation of a novel microorganism, Pestalotia heterocornis, producing paclitaxel. Biotechnology and Bioengineering, 1999, 64(5): 620-623.[84]Krohn K, Flörke U, Rao M S, Steingröver K, Aust H J, Draeger S, Schulz B. Metabolites from fungi 15. new isocoumarins from an endophytic fungus isolated from the Canadian thistle Cirsium arvense. Natural Product Letters, 2001, 15(5): 353-361.[85]Villarreal L P. Are viruses alive? Scientific American, 2004, 291: 100-105.[86]Roossinck M J. Mechanisms of plant virus evolution. Annual Reviews Phytopathology, 1997, 35: 191-209.[87]Aranda M A, Fraile A, Dopazo J, Malpica J M, Garcia-Arenal F. Contribution of mutation and RNA recombination to the evolution of a plant pathogenic RNA. Journal of Molecular Evolution, 1997, 44(1): 81-88.[88]Corona F M O, Lebas B S M, Elliott D, Tang J, Alexander B J R. New host records and new host family range for turnip mosaic virus in New Zealand. Australasian Plant Disease Notes, 2007, 2(1): 127-130.[89]Mochizuki T, Ohki S T. Cucumber mosaic virus: Viral genes as virulence determinants. Molecular Plant Pathology, 2011, 13(3): 217-225.[90]Nouri S, Falk B W, Groves R L. A new satellite RNA is associated with natural infections of cucumber mosaic virus in succulent snap bean. Archives of Virology, 2011, 157(2): 375-377.[91]Körbelin J, Willingmann P, Adam G, Heinze C. The complete sequence of tobacco mosaic virus isolate Ohio V reveals a high accumulation of silent mutations in all open reading frames. Archives of Virology, 2011, 157(2): 387-389.[92]Huh S U, Kim K J, Paek K H. Capsicum annuum basic transcription factor 3 (CaBtf3) regulates transcription of pathogenesis-related genes during hypersensitive response upon Tobacco mosaic virus infection. Biochemical and Biophysical Research Communications, 2012, 417(2): 910-917.[93]McCormick A A, Kumagai M H, Hanley K, Turpen T H, Hakim I, Grill L K, Tuse D, Levy S, Levy R. Rapid production of specific vaccines for lymphoma by expression of the tumor-derived single-chain Fv epitopes in tobacco plants. Proceedings of the National Academy of Sciences of the United States of America, 1999, 96(2): 703-708.[94]Nichols M E, Stanislaus T, Keshavarz-Moore E, Young H A. Disruption of leaves and initial extraction of wildtype CPMV virus as a basis for producing vaccines from plants. Journal of Biotechnology, 2002, 92(3): 229-235.[95]Mechtcheriakova I, Eldarov M, Nicholson L, Shanks M, Skryabin K, Lomonossoff G. The use of viral vectors to produce hepatitis B virus core particles in plants. Journal of Virological Methods, 2006, 131(1): 10-15.[96]Fernandez-Fernandez M R, Mourino M, Rivera J, Rodriguez F, Plana-Duran J, Garcia J A. Protection of rabbits against rabbit hemorrhagic disease virus by immunization with the VP60 protein expressed in plants with a potyvirus-based vector. Virology, 2001, 280(2): 283-291.[97]Yasawardene S G, Lomonossoff G P, Ramasamy R. Expression and immunogenicity of malaria merozoite peptides displayed on the small coat protein of chimaeric cowpea mosaic virus. Indian Journal of Medical Research, 2003, 118: 115-124.[98]Yusibov V, Mett V, Davidson C, Musiychuk K, Gilliam S, Farese A, Macvittie T, Mann D. Peptide-based candidate vaccine against respiratory syncytial virus. Vaccine, 2005, 23(17/18): 2261-2265.[99]Brennan F R, Gilleland L B, Staczek J, Bendig M M, Hamilton W D, Gilleland H E, Jr. A chimaeric plant virus vaccine protects mice against a bacterial infection. Microbiology, 1999, 145: 2061-2067.[100]Marillonnet S, Thoeringer C, Kandzia R, Klimyuk V, Gleba Y. Systemic Agrobacterium tumefaciens–mediated transfection of viral replicons for efficient transient expression in plants. Nature Biotechnology, 2005, 23(6): 718-723.[101]Hammond-Kosack K E, Staskawicz B, Jones J, Baulcombe D. Functional expression of a fungal avirulence gene from a modified potato virus X genome. Molecular Plant Microbe Interactions, 1995, 8(1): 181-185.[102]Kumagai M, Donson J, Della-Cioppa G, Harvey D, Hanley K, Grill L. Cytoplasmic inhibition of carotenoid biosynthesis with virus-derived RNA. Proceedings of the National Academy of Sciences of the United States of America, 1995, 92(5): 1679-1683.[103]Shimura H, Pantaleo V, Ishihara T, Myojo N, Inaba J, Sueda K, Burgyan J, Masuta C. A viral satellite RNA induces yellow symptoms on tobacco by targeting a gene involved in chlorophyll biosynthesis using the RNA silencing machinery. PLoS Pathogens, 2011, 7(5): 1002021.[104]Hu Q, Niu Y, Zhang K, Liu Y, Zhou X. Virus-derived transgenes expressing hairpin RNA give immunity to tobacco mosaic virus and Cucumber mosaic virus. Virology Journal, 2011, 8(1): 41-52.[105] Stafford C A, Walker G P, Ullman D E. Infection with a plant virus modifies vector feeding behavior. Proceedings of the National Academy of Sciences of the United States of America, 2011, 108(23): 9350-9355. |
[1] | 王炫栋, 宋振, 兰赫婷, 江樱姿, 齐文杰, 刘晓阳, 蒋冬花. 杨梅园土壤优势放线菌的分离及其防病促生功能[J]. 中国农业科学, 2023, 56(2): 275-286. |
[2] | 吴月,隋新华,戴良香,郑永美,张智猛,田云云,于天一,孙学武,孙棋棋,马登超,吴正锋. 慢生根瘤菌及其与花生共生机制研究进展[J]. 中国农业科学, 2022, 55(8): 1518-1528. |
[3] | 范延艮,王域,刘富浩,赵秀秀,向勤锃,张丽霞. 茶树CsHIPP26.1互作蛋白的筛选与验证[J]. 中国农业科学, 2022, 55(8): 1630-1641. |
[4] | 李世佳,吕紫敬,赵锦. 枣R2R3-MYB亚家族基因鉴定及其在果实发育中的表达分析[J]. 中国农业科学, 2022, 55(6): 1199-1212. |
[5] | 蒋琪琪,许建建,苏越,张琦,曹鹏,宋晨虎,李中安,宋震. 柑橘黄化花叶病毒侵染性克隆构建及应用[J]. 中国农业科学, 2022, 55(24): 4840-4850. |
[6] | 李扬眉,刘鑫,贾梦晗,仝宇欣. 光期湿度对植物工厂生菜干烧心及其营养品质的影响[J]. 中国农业科学, 2022, 55(20): 4011-4019. |
[7] | 刘鑫,张亚红,袁苗,党仕卓,周娟. ‘红地球’葡萄花芽分化过程中的转录组分析[J]. 中国农业科学, 2022, 55(20): 4020-4035. |
[8] | 沙月霞, 黄泽阳, 马瑞. 嗜碱假单胞菌Ej2对稻瘟病的防治效果及对水稻内源激素的影响[J]. 中国农业科学, 2022, 55(2): 320-328. |
[9] | 苏倩,杜文宣,马琳,夏亚迎,李雪,祁智,庞永珍. 紫花苜蓿MsCIPK2的克隆及功能分析[J]. 中国农业科学, 2022, 55(19): 3697-3709. |
[10] | 马雪萌,余成敏,赛小玲,刘贞,桑海洋,崔百明. PSORA:一种基于高通量测序的T-DNA插入位点分析方法[J]. 中国农业科学, 2022, 55(15): 2875-2882. |
[11] | 卞荣军,刘晓雨,郑聚锋,程琨,张旭辉,李恋卿,潘根兴. 生物质炭可溶性有机物化学组成及生物活性意义[J]. 中国农业科学, 2022, 55(11): 2174-2186. |
[12] | 宋博文,杨龙,潘云飞,李海强,李浩,冯宏祖,陆宴辉. 农田景观格局对南疆苹果园梨小食心虫成虫种群动态的影响[J]. 中国农业科学, 2022, 55(1): 85-95. |
[13] | 王冰,李慧敏,操海群,王桂荣. 挥发性化合物介导的植物-植食性昆虫-天敌三级营养级互作机制及应用[J]. 中国农业科学, 2021, 54(8): 1653-1672. |
[14] | 张锦源,李彦生,于镇华,谢志煌,刘俊杰,王光华,刘晓冰,吴俊江,Stephen J Herbert,金剑. 作物-土壤氮循环对大气CO2浓度和温度升高响应的研究进展[J]. 中国农业科学, 2021, 54(8): 1684-1701. |
[15] | 刘函西,吕浩,郭广雨,刘冬旭,石岩,孙志君,张泽鑫,张艳娇,文莹楠,王洁琦,刘春燕,陈庆山,辛大伟,王锦辉. 大豆根瘤菌HH103 rhcN突变对结瘤能力的影响[J]. 中国农业科学, 2021, 54(6): 1104-1111. |
|