A case study from the interaction of strawberry and Botrytis cinerea highlights the benefits of comonitoring both partners at genomic and mRNA level

被引:29
作者
Mehli, L [1 ]
Kjellsen, TD
Dewey, FM
Hietala, AM
机构
[1] Sor Trondelag Univ Coll, Fac Food Sci & Med Technol, N-7004 Trondheim, Norway
[2] Norwegian Univ Sci & Technol, Dept Biol, N-7491 Trondheim, Norway
[3] Skogforsk, Dept Ecol & Environm, N-1432 As, Norway
[4] Univ Calif Davis, Dept Viticulture & Enol, Davis, CA 95616 USA
关键词
biomass; Botrytis cinerea; ELISA; ergosterol; PGIP (polygalacturonase-inhibiting protein); polygalacturonase; real-time PCR; strawberry (Fragaria X ananassa);
D O I
10.1111/j.1469-8137.2005.01526.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Strawberry Fragaria x ananassa (cv. Korona) was inoculated with Botrytis cinerea by dipping berries in a conidial suspension. Colonization by the pathogen was monitored using real-time PCR, ELISA and ergosterol assays, the first showing the highest sensitivity. The expression of pathogen beta-tubulin and six polygalacturonases (Bcpg1-6) and three host defence genes (polygalacturonase-inhibiting protein (FaPGIP) and two class II chitinases) were monitored using real-time RT-PCR. The maximum transcript levels of the host defence genes occurred at 16 h postinoculation (hpi) at the presumed initial penetration stage. The unique transcript profile of Bcpg2 over the 96-h incubation time and its high transcript levels relative to those of the other Bcpgs at 8-24 hpi suggest that the gene has a specific role in the penetration stage. Bcpg1 was expressed constitutively at a relatively high level in actively growing mycelia throughout the experimental period. Comparison of the transcript profiles indicated that Bcpg1 and Bcpg3-6 were coordinately regulated.
引用
收藏
页码:465 / 474
页数:10
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