Evaluation of Potato virus X mild mutants for cross protection against severe infection in China

Virology Journal

Volumn 16, Issue 1, 2019, Pages

  Cong, Q Q ^a,b,c   Wang, Y ^a   Liu, J ^a   Lan, Y F ^c   Guo, Z K ^d   Yang, J G ^b   Li, X D ^a   Tian, Y P ^a  

^a SHANDONG AGRICULTURAL UNIVERSITY   (China)

^b Tobacco Pest Integrated Management Key Laboratory of China Tobacco   (China)

^c Tai'an Academy of Agricultural Science   (China)

^d HEILONGJIANG ACADEMY OF AGRICULTURAL SCIENCES   (China)

Author keywords

Cross protection; Potato virus X; RNA dependent RNA polymerase; Virulence

Indexed keywords

ALANINE; ASPARAGINE; COAT PROTEIN; GLUTAMINE; VIRUS RNA; RNA DIRECTED RNA POLYMERASE; VIRAL PROTEIN;

AMINO ACID SUBSTITUTION; ARTICLE; CHINA; CONTROLLED STUDY; CROSS PROTECTION; DISEASE SEVERITY; GENE MUTATION; NICOTIANA BENTHAMIANA; NONHUMAN; POTATO VIRUS X; RDRP GENE; REVERTANT; SITE DIRECTED MUTAGENESIS; TOMATO; VIRAL PLANT DISEASE; VIRUS GENE; VIRUS MUTANT; ENZYMOLOGY; EVALUATION STUDY; GENETICS; MUTATION; PHYSIOLOGY; PLANT DISEASE; PLANT LEAF; POTEXVIRUS; REVERSE GENETICS; TOBACCO; VIROLOGY; VIRULENCE; VIRUS GENOME;

CHINA; CROSS PROTECTION; GENOME, VIRAL; LYCOPERSICON ESCULENTUM; MUTAGENESIS, SITE-DIRECTED; MUTATION; PLANT DISEASES; PLANT LEAVES; POTEXVIRUS; REVERSE GENETICS; RNA REPLICASE; RNA, VIRAL; TOBACCO; VIRAL PROTEINS; VIRULENCE;

EID: 85063273858     PISSN: None     EISSN: 1743422X     Source Type: Journal    
DOI: 10.1186/s12985-019-1143-7     Document Type: Article

References (60)

1. Fulton RW. Practices and precautions in the use of cross protection for plant virus disease control. Annu Rev Phytopathol. 1986;24:67-81.
2. Kurihara Y, Watanabe Y. Cross-protection in Arabidopsis against crucifer tobamovirus cg by an attenuated strain of the virus. Mol Plant Pathol. 2003;4:259-69.
3. Sherwood JL. Mechanisms of cross-protection between plant virus strains. Plant resistance to viruses. Wiley, Chichester. CIBA Found Symp. 1987;133:136-50.
4. McKinney HH. Mosaic diseases in the Canary Islands, West Africa and Gibraltar. J Agric Res. 1929;39:557-78.
5. Nakazono-Nagaoka E, Takahashi T, Shimizu T, Kosaka Y, Natsuaki T, Omura T, et al. Cross-protection against Bean yellow mosaic virus (BYMV) and Clover yellow vein virus by attenuated BYMV isolate M11. Phytopathology. 2009;99:251-7.
6. Costa AS, Muller GW. Tristeza control by cross protection: a US-Brazil cooperative success. Plant Dis. 1980;64:538-41.
7. Ieki H, Yamaguchi A, Kano T, Koizumi M, Iwanami T. Control of stem pitting disease caused by citrus tristeza virus using protective mild strains in navel orange. Ann Phytopathol Soc Jpn. 1997;63:170-5.
8. Motoyoshi F, Nishiguchi M. Control of virus diseases by attenuated virus strains, comparison between attenuated strains of cucumber green mottle mosaic virus and tobacco mosaic virus. Gamma Field Symposia. 1988;27:91-109.
9. Kosaka Y, Fukunishi T. Multiple inoculation with three attenuated viruses for the control of cucumber virus disease. Plant Dis. 1997;81:733-8.
10. Sayama H, Sato T, Kominato M, Natsuaki T, Kaper JM. Field testing of a satellite-containing attenuated strain of cucumber mosaic virus for tomato protection in Japan. Phytopathology. 1993;83:405-10.
11. Tien P, Wu GS. Satellite RNA for the biocontrol of plant disease. Adv Virus Res. 1991;39:321-39.
12. Owor B, Legg JP, Okao-Okuja G, Obonyo R, Kyamanywa S, Ogenga-Latigo MW. Field studies of cross protection with cassava mosaic geminiviruses in Uganda. J Phytopathol. 2004;152:243-9.
13. Yeh SD, Gonsalves D. Evaluation of induced mutants of Papaya ringspot virus for control by cross protection. Phytopathology. 1984;74:1086-91.
14. You BJ, Chiang CH, Chen LF, Su WC, Yeh SD. Engineered mild strains of Papaya ringspot virus for broader cross protection in cucurbits. Phytopathology. 2005;95:533-40.
15. Agüero J, Gómez-Aix C, Sempere RN, García-Villalba J, García-Núñez J, Hernando Y, et al. Stable and broad spectrum cross-protection against Pepino mosaic virus attained by mixed infection. Front Plant Sci. 2018;9:1810.
16. Yoon JY, Ahn HI, Kim M, Tsuda S, Ryu KH. Pepper mild mottle virus pathogenicity determinants and cross protection effect of attenuated mutants in pepper. Virus Res. 2006;118:23-30.
17. Kosaka Y, Fukunishi T. Attenuated isolates of soybean mosaic virus derived at a low temperature. Plant Dis. 1993;77:882-6.
18. Burgyan J, Gaborjanyi R. Cross-protection and multiplication of mild and severe strains of TMV in tomato plants. J Phytopathol. 1984;110:156-67.
19. Goto T, Nemoto M. Studies on control of plant virus diseases by interference of attenuated virus-selection of TMV attenuated strain and influence on various plants inoculated with the attenuated strain. Res Bull Hokkaido Natl Agric Exp Sta. 1971;99:67-76.
20. Oshima N. Control of tomato mosaic disease by attenuated virus. Jpn Agric Res Q. 1981;14:222-8.
21. Rast ATB. Variability of tobacco mosaic virus in relation to control of tomato mosaic in glasshouse tomato crops by resistance breeding and cross protection. Agric Res Rep. 1975;834:1-76.
22. Yang G, Qiu BS, Liu XG, Li Y, Wang XF. Nonsense mutations of replicase and movement protein genes contribute to the attenuation of an avirulent tomato mosaic virus. Virus Res. 2002;87:119-28.
23. Kosaka Y, Ryang BS, Kobori T, Shiomi H, Yasuhara H, Kataoka M. Effectiveness of an attenuated Zucchini yellow mosaic virus isolate for cross-protecting cucumber. Plant Dis. 2006;90:67-72.
24. Lin SS, Wu HW, Jan FJ, Hou RF, Yeh SD. Modifications of the helper component-protease of Zucchini yellow mosaic virus for generation of attenuated mutants for cross protection against severe infection. Phytopathology. 2007;97:287-96.
25. Bercks, R. 1970. Potato virus X. Commonwealth Mycological Institute (Kew, England)/Association of Applied Biologists Descriptions of Plant Viruses, no. 4.
26. Huisman MJ, Linthorst HJ, Bol JF, Cornelissen JC. The complete nucleotide sequence of potato virus X and its homologies at the amino acid level with various plus-stranded RNA viruses. J Gen Virol. 1988;69:1789-98.
27. Skryabin KG, Kraev AS, Morozov SY, Rozanov MN, Chernov BK, Lukasheva LI, et al. The nucleotide sequence of potato virus X RNA. Nucleic Acids Res. 1988;16:10929-30.
28. Yu XQ, Jia JL, Zhang CL, Li XD, Wang YJ. Phylogenetic analyses of an isolate obtained from potato in 1985 revealed potato virus X was introduced to China via multiple events. Virus Genes. 2010;40:447-51.
29. Yu XQ, Wang HY, Lan YF, Zhu XP, Li XD, Fan ZF, et al. Complete genome sequence of a Chinese isolate of Potato virus X and analysis of genetic diversity. J Phytopathol. 2008;156:346-51.
30. Forster RL, Bevan MW, Harbison SA, Gardner RC. The complete nucleotide sequence of the potexvirus white clover mosaic virus. Nucleic Acids Res. 1988;16:291-303.
31. Angell SM, Davies C, Baulcombe DC. Cell-to-cell movement of potato virus X is associated with a change in the size-exclusion limit of plasmodesmata in trichome cells of Nicotiana clevelandii. Virology. 1996;216:197-201.
32. Beck DL, Guilford PJ, Voot DM, Andersen MT, Forster RLS. Triple gene block proteins of white clover mosaic potexvirus are required for transport. Virology. 1991;183:695-702.
33. Morozov SY, Zakhariev VM, Chernov BK, Prasolov VS, Kozlov YV, Atabekov JG, et al. The analysis of the primary structure and localization of the coat protein gene on the genomic RNA of potato virus X. Dokl Akad Nauk SSSR. 1983;271:211-5.
34. Cockerham G. Proceedings of the second conference on potato virus diseasesLisse-Wageningen; 1955. p. 89-92.
35. Moreira A, Jones RAC, Fribourg CE. Properties of a resistance- breaking strain of potato virus X. Ann Appl Biol. 1980;95:93-103.
36. Querci M, Baulcombe D, Goldbach R, Salazar L. Analysis of the resistance-breaking determinants of potato virus X (PVX) strain HB on different potato genotypes expressing extreme resistance to PVX. Phytopathology. 1995;85:1003-10.
37. Tozzini A, Ceriani M, Cramer P, Palva E, Hopp H. PVX MS, a new strain of potato virus that overcomes the extreme resistance gene Rx. J Phytopathol. 1994;141:241-8.
38. Salaman RN. Protective inoculation against a plant virus. Nature. 1933;131:468.
39. Brigneti G, Voinnet O, Li WX, Ji LH, Ding SW, Baulcombe DC. Viral pathogenicity determinants are suppressors of transgene silencing in Nicotiana benthamiana. EMBO J. 1998;17:6739-46.
40. Csorba T, Pantaleo V, Burgyán J. RNA silencing: an antiviral mechanism. Adv Virus Res. 2009;75:35-230.
41. Gal-On A. A point mutation in the FRNK motif of the potyvirus helper component-protease gene alters symptom expression in cucurbits and elicits protection against the severe homologous virus. Phytopathology. 2000;90:467-73.
42. Saenz P, Quiot L, Quiot JB, Candresse T, Garcia JA. Pathogenicity determinants in the complex virus population of a Plum pox virus isolate. Mol Plant-Microbe Interact. 2001;14:278-87.
43. Wu HW, Lin SS, Chen KC, Yeh SD, Chua NH. Discriminating mutations of HC-pro of Zucchini yellow mosaic virus with differential effects on small RNA pathways involved in viral pathogenicity and symptom development. Mol Plant-Microbe Interact. 2010;23:17-28.
44. Diveki Z, Salanki K, Balazs E. The necrotic pathotype of the Cucumber mosaic virus (CMV) ns strain is solely determined by amino acid 461 of the 1a protein. Mol Plant-Microbe Interact. 2004;17:837-45.
45. Hagiwara K, Ichiki TU, Ogawa Y, Omura T, Tsuda S. A single amino acid substitution in 126-kDa protein of Pepper mild mottle virus associates with symptom attenuation in pepper; the complete nucleotide sequence of an attenuated strain, C-1421. Arch Virol. 2002;147:833-40.
46. Lewandowski DJ, Dawson WO. A single amino acid change in Tobacco mosaic virus replicase prevents symptom production. Mol Plant-Microbe Interact. 1993;6:157-60.
47. Tsuda S, Kubota K, Kanda A, Ohki T, Meshi T. Pathogenicity of Pepper mild mottle virus is controlled by the RNA silencing suppression activity of its replication protein but not the viral accumulation. Phytopathology. 2007;97:412-20.
48. Ziebell H, Payne T, Berry JO, Walsh JA, Carr JP. A cucumber mosaic virus mutant lacking the 2b counter-defence protein gene provides protection against wild-type strains. J Gen Virol. 2007;88:2862-71.
49. Voinnet O, Lederer C, Baulcombe DC. A viral movement protein prevents spread of the gene silencing signal in Nicotiana benthamiana. Cell. 2000;103:157-67.
50. Roy A, Kucukural A, Zhang Y. I-TASSER: a unified platform for automated protein structure and function prediction. Nat Protoc. 2010;5:725-38.
51. Liu HT, Naismith JH. An efficient one-step site-directed deletion, insertion, single and multiple-site plasmid mutagenesis protocol. BMC Biotechnol. 2008;8:91.
52. Wang Y, Cong QQ, Lan YF, Geng C, Li X, Liang YC, et al. Development of new potato virus X-based vectors for gene over- expression and gene silencing assay. Virus Res. 2014;191:62-9.
53. Kagiwada S, Yamaji Y, Komatsu K, Takahashi S, Mori T, Hirata H, et al. A single amino acid residue of RNA-dependent RNA polymerase in the Potato virus X genome determines the symptoms in Nicotiana plants. Virus Res. 2005;110:177-82.
54. Kimalov B, Gal-On A, Stav R, Belausov E, Arazi T. Maintenance of coat protein N-terminal net charge and not primary sequence is essential for zucchini yellow mosaic virus systemic infectivety. J Gen Virol. 2004;85:3421-30.
55. Johansen IE, Dougherty WG, Keller KE, Wang D, Hampton RO. Multiple viral determinants affect seed transmission of pea seedborne mosaic virus in Pisum sativum. J Gen Virol. 1996;77:3149-54.
56. Gal-On A, Shiboleth YM. Cross-protection. In: Loebenstein G, Carr JP, editors. Natural resistance mechanism of plants to viruses. Berlin: Springer; 2006. p. 261-88.
57. Kung Y, Lin P, Yeh S, Hong S, Chua N, Liu L, et al. Genetic analyses of the FRNK motif function of Turnip mosaic virus uncover multiple and potentially interactive pathways of cross- protection. Mol Plant-Microbe Interact. 2014;27:944-55.
58. Baulcombe DC. Mechanisms of pathogen-derived resistance to viruses in transgenic plants. Plant Cell. 1996;8:1833-44.
59. Beachy RN. Coat-protein-mediated resistance to tobacco mosaic virus: discovery mechanisms and exploitation. Philos Trans R Soc Lond Ser B Biol Sci. 1999;354:659-64.
60. Lu B, Stubbs G, Culver JN. Coat protein interactions involved in tobacco mosaic tobamovirus cross-protection. Virology. 1998;248:188-98.