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Originally published In Press as doi:10.1074/jbc.M004796200 on August 1, 2000

J. Biol. Chem., Vol. 275, Issue 41, 32347-32356, October 13, 2000
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Flagellin from an Incompatible Strain of Pseudomonas avenae Induces a Resistance Response in Cultured Rice Cells*

Fang-Sik CheDagger §, Yoshihiro NakajimaDagger , Noriko Tanaka, Megumi Iwano, Tomomi Yoshida, Seiji Takayama, Ikuo Kadota, and Akira Isogai

From the Graduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5, Takayama Ikoma, Nara 630-0101, Japan and the  National Institute of Agro-Environmental Sciences, Tsukuba, Ibaraki 305-8602, Japan

The host range of Pseudomonas avenae is wide among monocotyledonous plants, but individual strains can infect only one or a few host species. The resistance response of rice cells to pathogens has been previously shown to be induced by a rice-incompatible strain, N1141, but not by a rice-compatible strain, H8301. To clarify the molecular mechanism of the host specificity in P. avenae, a strain-specific antibody that was raised against N1141 cells and then absorbed with H8301 cells was prepared. When a cell extract of strain N1141 was separated by SDS-polyacrylamide gel electrophoresis and immunostained with the N1141 strain-specific antibody, only a flagellin protein was detected. Purified N1141 flagellin induced the hypersensitive cell death in cultured rice cells within 6 h of treatment, whereas the H8301 flagellin did not. The hypersensitive cell death could be blocked by pretreatment with anti-N1141 flagellin antibody. Furthermore, a flagellin-deficient N1141 strain lost not only the induction ability of hypersensitive cell death but also the expression ability of the EL2 gene, which is thought to be one of the defense-related genes. These results demonstrated that the resistance response in cultured rice cells is induced by the flagellin existing in the incompatible strain of P. avenae but not in the flagellin of the compatible strain.


* This work was supported by "Research for the Future" Program of the Japan Society for the Promotion of Science (JSPS-RFTF96R16001).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

The nucleotide sequence(s) reported in this paper has been submitted to the DDBJ/GenBankTM/EBI Data Bank with acession number(s) AB040139.

Dagger The first two authors contributed equally to this work.

§ To whom correspondence should be addressed. Tel.: 81-743-72-5452; Fax: 81-743-72-5459; E-mail: fsche@bs.aist-nara.ac.jp.


Copyright © 2000 by The American Society for Biochemistry and Molecular Biology, Inc.
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