The Coevolution of Plants and Viruses: Resistance and Pathogenicity

被引:75
作者
Fraile, Aurora [1 ]
Garcia-Arenal, Fernando
机构
[1] Univ Politecn Madrid, Ctr Biotecnol & Genom Plantas UPM INIA, Madrid, Spain
来源
NATURAL AND ENGINEERED RESISTANCE TO PLANT VIRUSES, PT II | 2010年 / 76卷
关键词
TURNIP-MOSAIC-VIRUS; GENE-FOR-GENE; INITIATION-FACTOR EIF4E; YELLOW-MOTTLE-VIRUS; TOBACCO ETCH VIRUS; DISEASE-RESISTANCE; RECESSIVE RESISTANCE; HYPERSENSITIVE RESPONSE; COAT PROTEIN; MOLECULAR CHARACTERIZATION;
D O I
10.1016/S0065-3527(10)76001-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Virus infection may damage the plant, and plant defenses are effective against viruses; thus, it is currently assumed that plants and viruses coevolve. However, and despite huge advances in understanding the mechanisms of pathogenicity and virulence in viruses and the mechanisms of virus resistance in plants, evidence in support of this hypothesis is surprisingly scant, and refers almost only to the virus partner. Most evidence for coevolution derives from the study of highly virulent viruses in agricultural systems, in which humans manipulate host genetic structure, what determines genetic changes in the virus population. Studies have focused on virus responses to qualitative resistance, either dominant or recessive but, even within this restricted scenario, population genetic analyses of pathogenicity and resistance factors are still scarce. Analyses of quantitative resistance or tolerance, which could be relevant for plant virus coevolution, lag far behind. A major limitation is the lack of information on systems in which the host might evolve in response to virus infection, that is, wild hosts in natural ecosystems. It is presently unknown if, or under which circumstances, viruses do exert a selection pressure on wild plants, if qualitative resistance is a major defense strategy to viruses in nature, or even if characterized genes determining qualitative resistance to viruses did indeed evolve in response to virus infection. Here, we review evidence supporting plant virus coevolution and point to areas in need of attention to understand the role of viruses in plant ecosystem dynamics, and the factors that determine virus emergence in crops.
引用
收藏
页码:1 / 32
页数:32
相关论文
共 165 条
[41]   Mechanisms of genetic robustness in RNA viruses [J].
Elena, SF ;
Carrasco, P ;
Daròs, JA ;
Sanjuán, R .
EMBO REPORTS, 2006, 7 (02) :168-173
[42]   Transmissibility of Cucumber mosaic virus by Aphis gossypii correlates with viral accumulation and is affected by the presence of its satellite RNA [J].
Escriu, F ;
Perry, KL ;
García-Arenal, F .
PHYTOPATHOLOGY, 2000, 90 (10) :1068-1072
[43]   Constraints to genetic exchange support gene coadaptation in a tripartite RNA virus [J].
Escriu, Fernando ;
Fraile, Aurora ;
Garcia-Arenal, Fernando .
PLOS PATHOGENS, 2007, 3 (01) :67-74
[44]   Diversification of Rice yellow mottle virus and related viruses spans the history of agriculture from the Neolithic to the present [J].
Fargette, Denis ;
Pinel-Galzi, Agnes ;
Sereme, Drissa ;
Lacombe, Severine ;
Hebrard, Eugenie ;
Traore, Oumar ;
Konate, Gnissa .
PLOS PATHOGENS, 2008, 4 (08)
[45]   Artificial evolution extends the spectrum of viruses that are targeted by a disease-resistance gene from potato [J].
Farnham, Garry ;
Baulcombe, David C. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (49) :18828-18833
[46]   INHERITANCE OF RESISTANCE TO POTYVIRUSES IN PHASEOLUS-VULGARIS L .3. COSEGREGATION OF PHENOTYPICALLY SIMILAR DOMINANT RESPONSES TO 9 POTYVIRUSES [J].
FISHER, ML ;
KYLE, MM .
THEORETICAL AND APPLIED GENETICS, 1994, 89 (7-8) :818-823
[47]   CURRENT STATUS OF GENE-FOR-GENE CONCEPT [J].
FLOR, HH .
ANNUAL REVIEW OF PHYTOPATHOLOGY, 1971, 9 :275-+
[48]  
FLOR HH, 1955, PHYTOPATHOLOGY, V45, P680
[49]   IMPORTANCE OF VIRUS SOURCE LEAVES IN VECTOR SPECIFICITY OF BARLEY YELLOW DWARF VIRUS [J].
FOXE, MJ ;
ROCHOW, WF .
PHYTOPATHOLOGY, 1975, 65 (10) :1124-1129
[50]  
FRAILE A, 2010, HIGH FITNES IN PRESS