Stimulation of Defense Reactions in Medicago truncatula by Antagonistic Lipopeptides from Paenibacillus sp Strain B2

被引:14
作者
Selim, Sameh [2 ]
Negrel, Jonathan [1 ]
Wendehenne, David [1 ]
Ochatt, Sergio [3 ]
Gianinazzi, Silvio [1 ]
van Tuinen, Diederik [1 ]
机构
[1] Univ Bourgogne Plante Microbe Environm CMSE INRA, CNRS 5184, UMR INRA 1088, F-21065 Dijon, France
[2] Inst Polytech LaSalle Beauvais, F-60026 Beauvais, France
[3] INRA Dijon, UMR LEG, F-21065 Dijon, France
关键词
INDUCED SYSTEMIC RESISTANCE; PLANT DEFENSE; SIGNAL-TRANSDUCTION; BACILLUS-SUBTILIS; ARABIDOPSIS-THALIANA; STRESS RESPONSES; TOBACCO CELLS; PSEUDOMONAS-FLUORESCENS; PHENYLPROPANOID PATHWAY; OXIDATIVE BURST;
D O I
10.1128/AEM.00171-10
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
With the aim of obtaining new strategies to control plant diseases, we investigated the ability of antagonistic lipopolypeptides (paenimyxin) from Paenibacillus sp. strain B2 to elicit hydrogen peroxide (H2O2) production and several defense-related genes in the model legume Medicago truncatula. For this purpose, M. truncatula cell suspensions were used and a pathosystem between M. truncatula and Fusarium acuminatum was established. In M. truncatula cell cultures, the induction of H2O2 reached a maximum 20 min after elicitation with paenimyxin, whereas concentrations higher than 20 mu M inhibited H2O2 induction and this was correlated with a lethal effect. In plant roots incubated with different concentrations of paenimyxin for 24 h before inoculation with F. acuminatum, paenimyxin at a low concentration (ca. 1 mu M) had a protective effect and suppressed 95% of the necrotic symptoms, whereas a concentration higher than 10 mu M had an inhibitory effect on plant growth. Gene responses were quantified in M. truncatula by semiquantitative reverse transcription-PCR (RT-PCR). Genes involved in the biosynthesis of phytoalexins (phenylalanine ammonia-lyase, chalcone synthase, chalcone reductase), antifungal activity (pathogenesis-related proteins, chitinase), or cell wall (invertase) were highly upregulated in roots or cells after paenimyxin treatment. The mechanisms potentially involved in plant protection are discussed.
引用
收藏
页码:7420 / 7428
页数:9
相关论文
共 57 条
[1]   Reactive oxygen species: Metabolism, oxidative stress, and signal transduction [J].
Apel, K ;
Hirt, H .
ANNUAL REVIEW OF PLANT BIOLOGY, 2004, 55 :373-399
[2]   Induction of systemic resistance to Botrytis cinerea in tomato by Pseudomonas aeruginosa 7NSK2:: Role of salicylic acid, pyochelin, and pyocyanin [J].
Audenaert, K ;
Pattery, T ;
Cornelis, P ;
Höfte, M .
MOLECULAR PLANT-MICROBE INTERACTIONS, 2002, 15 (11) :1147-1156
[3]  
Bakker PAHM, 2003, CAN J PLANT PATHOL, V25, P5
[4]   STRESS RESPONSES IN ALFALFA (MEDICAGO-SATIVA L) .16. ANTIFUNGAL ACTIVITY OF MEDICARPIN AND ITS BIOSYNTHETIC PRECURSORS - IMPLICATIONS FOR THE GENETIC MANIPULATION OF STRESS METABOLITES [J].
BLOUNT, JW ;
DIXON, RA ;
PAIVA, NL .
PHYSIOLOGICAL AND MOLECULAR PLANT PATHOLOGY, 1992, 41 (05) :333-349
[5]   Early signal transduction pathways in plant-pathogen interactions [J].
Blumwald, E ;
Aharon, GS ;
Lam, BCH .
TRENDS IN PLANT SCIENCE, 1998, 3 (09) :342-346
[6]  
Budi SW, 1999, APPL ENVIRON MICROB, V65, P5148
[7]   Relative quantitative RT-PCR to study the expression of plant nutrient transporters in arbuscular mycorrhizas [J].
Burleigh, SH .
PLANT SCIENCE, 2001, 160 (05) :899-904
[8]   Monosaccharide transporters in plants:: structure, function and physiology [J].
Büttner, M ;
Sauer, N .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2000, 1465 (1-2) :263-274
[9]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[10]   Gene expression profiling and protection of Medicago truncatula against a fungal infection in response to an elicitor from green algae Ulva spp [J].
Cluzet, S ;
Torregrosa, C ;
Jacquet, C ;
Lafitte, C ;
Fournier, J ;
Mercier, L ;
Salamagne, S ;
Briand, X ;
Esquerré-Tugayé, MT ;
Dumas, B .
PLANT CELL AND ENVIRONMENT, 2004, 27 (07) :917-928