Galactinol is Involved in Induced Systemic Resistance against Bacterial Infection and Environmental Stresses

  • Cho, Song-Mi (Department of Floriculture, Chunnam Techno College) ;
  • Kim, Su-Hyun (Department of Plant Biotechnology, College of Agriculture and Life Sciences, Chonnam National University) ;
  • Kim, Young-Cheol (Department of Plant Biotechnology, College of Agriculture and Life Sciences, Chonnam National University) ;
  • Yang, Kwang-Yeol (Department of Plant Biotechnology, College of Agriculture and Life Sciences, Chonnam National University) ;
  • Kim, Kwang-Sang (Jangheunggun Mushroom Research Institute) ;
  • Choi, Yong-Soo (Department of Floriculture, Chunnam Techno College) ;
  • Cho, Baik-Ho (Department of Plant Biotechnology, College of Agriculture and Life Sciences, Chonnam National University)
  • Received : 2009.11.16
  • Accepted : 2010.03.02
  • Published : 2010.06.30

Abstract

We previously demonstrated that root colonization of the rhizobacterium, Pseudomonas chlororaphis O6, induced expression of a galactinol synthase gene (CsGolS1), and resulting galactinol conferred induced systemic resistance (ISR) against fungal and bacterial pathogens in cucumber leaves. To examine the role of galactinol on ISR, drought or high salt stress, we obtained T-DNA insertion Arabidopsis mutants at the AtGolS1 gene, an ortholog of the CsGolS1 gene. The T-DNA insertion mutant compromised resistance induced by the O6 colonization against Erwinia carotovora. Pharmaceutical application of 0.5 - 5 mM galactinol on roots was sufficient to elicit ISR in wild-type Arabidopsis against infection with E. carotovora. The involvement of jasmonic acid (JA) signaling on the ISR was validated to detect increased expression of the indicator gene PDF1.2. The T-DNA insertion mutant also compromised tolerance by increasing galactinol content in the O6-colonized plant against drought or high salt stresses. Taken together, our results indicate that primed expression of the galactinol synthase gene AtGolS1in the O6-colonized plants can play a critical role in the ISR against infection with E. carotovora, and in the tolerance to drought or high salt stresses.

Keywords

References

  1. Alonso, J.M. et al. 2003. Genome-wide insertional mutagenesis of Arabidopsis thaliana. Science 301: 653-657. https://doi.org/10.1126/science.1086391
  2. Berger, S., E. Bell, A. Sadka and J.E. Mullet. 1995. Arabidopsis thaliana AtVsp is homologous to soybean VspA and VspB, genes encoding vegetative storage protein acid phosphatases, and is regulated similarly by methyl jasmonate, wounding, sugars, light and phosphate. Plant Mol. Biol. 27: 933-942. https://doi.org/10.1007/BF00037021
  3. Conrath, U., C.M. Pieterse and B. Mauch-Mani. 2002. Priming in plant-pathogen interactions. Trends Plant Sci. 7: 210-216. https://doi.org/10.1016/S1360-1385(02)02244-6
  4. Kim, M.S., S.M. Cho, E.Y. Kang, Y.J. Im, H. Hwangbo, Y.C. Kim, C.M. Ryu, K.Y. Yang, G.C. Chung and B.H. Cho. 2008. Galactinol is a signaling component of the induced systemic resistance caused by Pseudomonas chlororaphis O6 root colonization. Mol. Plant-Microbe Interac. 21: 1643-1653. https://doi.org/10.1094/MPMI-21-12-1643
  5. Kim, M.S., Y.C. Kim and B.H. Cho. 2004. Gene expression analysis in cucumber leaves primed by root colonization with Pseudomonas chlororaphis O6 upon challenge-inoculation with Corynespora cassiicola. Plant Biol. 6: 105-108. https://doi.org/10.1055/s-2004-817803
  6. Peterbauer, T., L.B. Lahuta, A. Blöchl, J. Mucha, D.A. Jones, C.L.Hedley, R.J. Gòrecki and A. Richter. 2001. Analysis of the raffinose family oligosaccharide pathway in pea seeds with contrasting carbohydrate composition. Plant Physiol. 127: 1764-1772. https://doi.org/10.1104/pp.010534
  7. Pieterse, C.M.J., J.A. Van Pelt, J. Ton, S. Parchmann, M.J. Mueller, A.J. Buchala, J.P. Metraux and L.C. Van Loon. 2000. Rhizobacteria-mediated induced systemic resistance (ISR) in Arabidopsis requires sensitivity to jasmonate and ethylene but is not accompanied by an increase in their production. Physiol. Mol. Plant Pathol. 57: 123-134. https://doi.org/10.1006/pmpp.2000.0291
  8. Potter, S., S. Uknes, K. Lawton, A.M. Winter, D. Chandler, J. DiMaio, R. Novitzky, E. Ward and J. Ryals J. 1993. Regulation of a hevein-like gene in Arabidopsis. Mol. Plant-Microbe Interac. 6: 680-685. https://doi.org/10.1094/MPMI-6-680
  9. Spencer, M., C.M. Ryu, K.Y. Yang, Y.C. Kim, J.W. Kloepper and A. Anderson. 2003. Induced defenses in tobacco by Pseudomonas chlororaphis strain O6 involves at least the ethylene pathway. Physiol. Mol. Plant Pathol. 63: 27-34. https://doi.org/10.1016/j.pmpp.2003.09.002
  10. Sprenger, N. and F. Keller. 2000. Allocation of raffnose family oligosaccharides to transport and storage pools in Ajuga reptans: the roles of two distinct galactinol synthases. Plant J. 21: 249-258. https://doi.org/10.1046/j.1365-313x.2000.00671.x
  11. Taji, T., C. Ohsumi, S. Lnchi, M. Seki, M. Kasuga, M. Kobayashi, K. Yamaguchi-Shinozaki and K. Shinozaki. 2002. Important roles of drought- and cold-inducible genes for galactinol synthase in stress tolerance in Arabidopsis thaliana. Plant J. 29: 417-426. https://doi.org/10.1046/j.0960-7412.2001.01227.x
  12. Takahashi, H., Y. Kanayama, M.S. Zheng, T. Kusano, S. Hase, M. Ikegami and J. Shah. 2004. Antagonistic interactions between the SA and JA signaling pathways in Arabidopsis modulated expression of defense genes and gene-for-gene resistance to Cucumber mosaic virus. Plant Cell Physiol. 45: 803-809. https://doi.org/10.1093/pcp/pch085
  13. Van Loon, L.C., P.A.H.M. Bakker and C.M.J. Pieterse. 1998. Systemic resistance induced by rhizosphere bacteria. Annu. Rev. Phytopathol. 36: 453-483. https://doi.org/10.1146/annurev.phyto.36.1.453
  14. Van Wees, S.C.M., S. Van der Ent and C.M.J. Pieterse. 2008. Plant immune responses triggered by beneficial microbes. Cur. Opi. Plant Biol. 11: 443-448. https://doi.org/10.1016/j.pbi.2008.05.005