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231224s2013 xx |||||o 00| ||eng c |
| 024 |
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|a 10.1111/nph.12408
|2 doi
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|a pubmed24n1342.xml
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|a (DE-627)NLM229266134
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|a (NLM)23865782
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|a DE-627
|b ger
|c DE-627
|e rakwb
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| 041 |
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|a eng
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| 100 |
1 |
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|a Clarke, Christopher R
|e verfasserin
|4 aut
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| 245 |
1 |
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|a Allelic variation in two distinct Pseudomonas syringae flagellin epitopes modulates the strength of plant immune responses but not bacterial motility
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|c 2013
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| 336 |
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|a Text
|b txt
|2 rdacontent
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| 337 |
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|a ƒaComputermedien
|b c
|2 rdamedia
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| 338 |
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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| 500 |
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|a Date Completed 29.04.2014
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| 500 |
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|a Date Revised 23.03.2024
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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| 520 |
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|a © 2013 The Authors. New Phytologist © 2013 New Phytologist Trust.
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|a The bacterial flagellin (FliC) epitopes flg22 and flgII-28 are microbe-associated molecular patterns (MAMPs). Although flg22 is recognized by many plant species via the pattern recognition receptor FLS2, neither the flgII-28 receptor nor the extent of flgII-28 recognition by different plant families is known. Here, we tested the significance of flgII-28 as a MAMP and the importance of allelic diversity in flg22 and flgII-28 in plant-pathogen interactions using purified peptides and a Pseudomonas syringae ∆fliC mutant complemented with different fliC alleles. The plant genotype and allelic diversity in flg22 and flgII-28 were found to significantly affect the plant immune response, but not bacterial motility. The recognition of flgII-28 is restricted to a number of solanaceous species. Although the flgII-28 peptide does not trigger any immune response in Arabidopsis, mutations in both flg22 and flgII-28 have FLS2-dependent effects on virulence. However, the expression of a tomato allele of FLS2 does not confer to Nicotiana benthamiana the ability to detect flgII-28, and tomato plants silenced for FLS2 are not altered in flgII-28 recognition. Therefore, MAMP diversification is an effective pathogen virulence strategy, and flgII-28 appears to be perceived by an as yet unidentified receptor in the Solanaceae, although it has an FLS2-dependent virulence effect in Arabidopsis
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| 650 |
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4 |
|a Journal Article
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| 650 |
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|a Research Support, N.I.H., Extramural
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| 650 |
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4 |
|a Research Support, Non-U.S. Gov't
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| 650 |
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4 |
|a Research Support, U.S. Gov't, Non-P.H.S.
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| 650 |
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4 |
|a FLS2
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|a flagellin
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|a flg22
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4 |
|a flgII-28
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| 650 |
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|a microbe-associated molecular pattern (MAMP)
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| 650 |
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4 |
|a pathogen-associated molecular pattern (PAMP)
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| 650 |
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4 |
|a pattern-triggered immunity (PTI)
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| 650 |
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7 |
|a Arabidopsis Proteins
|2 NLM
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| 650 |
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7 |
|a Flagellin
|2 NLM
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| 650 |
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7 |
|a 12777-81-0
|2 NLM
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| 650 |
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7 |
|a Protein Kinases
|2 NLM
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| 650 |
|
7 |
|a EC 2.7.-
|2 NLM
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| 650 |
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7 |
|a FLS2 protein, Arabidopsis
|2 NLM
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| 650 |
|
7 |
|a EC 2.7.1.-
|2 NLM
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| 700 |
1 |
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|a Chinchilla, Delphine
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Hind, Sarah R
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Taguchi, Fumiko
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Miki, Ryuji
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Ichinose, Yuki
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Martin, Gregory B
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Leman, Scotland
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Felix, Georg
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Vinatzer, Boris A
|e verfasserin
|4 aut
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| 773 |
0 |
8 |
|i Enthalten in
|t The New phytologist
|d 1979
|g 200(2013), 3 vom: 18. Nov., Seite 847-860
|w (DE-627)NLM09818248X
|x 1469-8137
|7 nnns
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| 773 |
1 |
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|g volume:200
|g year:2013
|g number:3
|g day:18
|g month:11
|g pages:847-860
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| 856 |
4 |
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|u http://dx.doi.org/10.1111/nph.12408
|3 Volltext
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|a GBV_USEFLAG_A
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|a SYSFLAG_A
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|a GBV_ILN_350
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|a AR
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| 952 |
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|d 200
|j 2013
|e 3
|b 18
|c 11
|h 847-860
|