The ecological concept of costs of induced systemic resistance (ISR)

被引:81
作者
Heil, M [1 ]
机构
[1] Biozentrum, Lehrstuhl Zool 3, D-97074 Wurzburg, Germany
[2] CNRS, Ctr Ecol Fonct & Evolut, F-34293 Montpellier 5, France
关键词
growth differentiation balance-hypothesis; fitness costs; induced defence; plant-pathogen interaction; SAR; systemic acquired resistance;
D O I
10.1023/A:1008793009517
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Plant defence is thought to provide benefits for the defended plants. Theoretical concepts must, therefore, explain why there is variation in defensive traits, which naively might be assumed to be present constitutively in fixed high amounts. Explanations are mainly based on the assumption of fitness costs. Investment in defence is thought to reduce the fitness of plants in enemy-free environments. Fitness costs often result from allocation costs, i.e. allocation of limited resources to defence, which then cannot be used for growth or other fitness-relevant processes. This theoretical concept can provide a useful tool for the interpretation of induced plant responses against pathogens, named induced systemic (or systemic acquired) resistance (ISR or SAR). Phenotypic plasticity, leading to induced responses, might have evolved mainly to reduce costs, since investment in defence is restricted to situations actually requiring defence. ISR can incur allocation costs and other, indirect costs, which ultimately may lead to fitness costs. Evolution of any defensive trait depends on both what a plant ideally 'should do' and what it actually 'is able to do'. Costs of defence constrain its expression. This might have important influences on the evolution of plant defensive traits, as well as on the exploitation of natural defences in agricultural crop protection.
引用
收藏
页码:137 / 146
页数:10
相关论文
共 108 条
[91]  
Stadnik MJ, 1999, Z PFLANZENK PFLANZEN, V106, P466
[92]   Signal interactions in pathogen and insect attack:: systemic plant-mediated interactions between pathogens and herbivores of the tomato, Lycopersicon esculentum [J].
Stout, MJ ;
Fidantsef, AL ;
Duffey, SS ;
Bostock, RM .
PHYSIOLOGICAL AND MOLECULAR PLANT PATHOLOGY, 1999, 54 (3-4) :115-130
[93]   Effect of nitrogen availability on expression of constitutive and inducible chemical defenses in tomato, Lycopersicon esculentum [J].
Stout, MJ ;
Brovont, RA ;
Duffey, SS .
JOURNAL OF CHEMICAL ECOLOGY, 1998, 24 (06) :945-963
[94]   Specificity of induced resistance in the tomato, Lycopersicon esculentum [J].
Stout M.J. ;
Workman K.V. ;
Bostock R.M. ;
Duffey S.S. .
Oecologia, 1997, 113 (1) :74-81
[95]  
Stout MJ, 1998, ENTOMOL EXP APPL, V86, P267, DOI 10.1023/A:1003199023355
[96]   Trade-offs in plant defense against pathogens and herbivores: A field demonstration of chemical elicitors of induced resistance [J].
Thaler, JS ;
Fidantsef, AL ;
Duffey, SS ;
Bostock, RM .
JOURNAL OF CHEMICAL ECOLOGY, 1999, 25 (07) :1597-1609
[97]  
Thaler JS, 1999, INDUCED PLANT DEFENSES AGAINST PATHOGENS AND HERBIVORES, P319
[98]  
Tollrian R., 1999, ECOLOGY EVOLUTION IN, DOI DOI 10.1515/9780691228198
[99]   Systemic resistance induced by rhizosphere bacteria [J].
van Loon, LC ;
Bakker, PAHM ;
Pieterse, CMJ .
ANNUAL REVIEW OF PHYTOPATHOLOGY, 1998, 36 :453-483
[100]   Induced resistance in plants and the role of pathogenesis-related proteins [J].
Van Loon, LC .
EUROPEAN JOURNAL OF PLANT PATHOLOGY, 1997, 103 (09) :753-765