Fig. 2. Pathogenicity assays of Burkholderia glumae BGR1 wild-type, PVF11 defective mutant, and PVF11C complemented mutant in rice plants at different growth stages (seedling, vegetative, and reproductive). (A) Photographs from the seedling assay showing a clear deleterious effect of wild-type BGR1 treatment and reduced virulence in the ΔPVF11 mutant-treated seedlings. The complemented mutant, PVF11C, apparently recovered the wild-type virulence. (B) Bar graphs represent the shoot and root lengths as a measure of the bacterial virulence to the seedlings. The different uppercase and lowercase letters on the error bars represent significant differences between shoot and root lengths, respectively, with P < 0.05, according to least significant difference test (LSD). (C) Photographs of rice stems at the vegetative stage showing the typical blight symptoms of infected rice stems. Treatment with the ΔPVF11 mutant resulted in reduced virulence as limited symptomatic lesions were observed, compared to plants infected with wild-type BGR1 or the complemented mutant PVF11C. Red arrows show the spread of symptomatic lesions away from the inoculation sites. (D) Bar graphs showing the bacterial populations in treated stems 8 days after inoculation, expressed as log colony forming units (cfu)/g rice stem. The different letters on the error bars indicate significant differences according to LSD test (P < 0.05). (E) Photographs from the reproductive stage assay on rice panicles showing the typical blight symptoms on the rice grains after treatment with BGR1, ΔPVF11, and PVF11C. (F) Stacked bar graphs representing disease severity distribution pattern on the harvested grains. There was no difference in disease severity between the wild-type, ΔPVF11, and PVF11C mutants. Sterile distilled water was used as negative control in all assays.
Fig. 1. Yeast two hybrid (Y2H) assays for Burkholderia glumae PVF11 interaction with rice defense-related proteins. (A) Positive Y2H interaction between PVF11, as prey, and WRKY transcriptional factors, as baits. The empty bait vector was used as a negative control. (B) Positive Y2H interaction between PVF11, as bait, and rice cDNA libraries (Y28, Y29 and Y34) as prey. In both Y2H assays, positive interactions are indicated by hybridized yeast cell survival on LTH- (SD/-His/-Leu/-Trp) and LTHA-(SD/-Ade/-His/-Leu/-Trp) agar plates.
Table 1. Putative encoded products and ontology of genes from infected rice that showed positive interaction with PVF11
참고문헌
- Birkenbihl, R. P., Diezel, C. and Somssich, I. E. 2012. Arabidopsis WRKY33 is a key transcriptional regulator of hormonal and metabolic responses toward Botrytis cinerea infection. Plant Physiol. 159:266-285. https://doi.org/10.1104/pp.111.192641
- Cao, S. and Yan, L. 2013. Construction of a high-quality yeast two-hybrid (Y2H) library and its application in identification of interacting proteins with key vernalization regulator TaVRN-A1 in wheat. BMC Res. Notes 6:81. https://doi.org/10.1186/1756-0500-6-81
- Chun, H., Choi, O., Goo, E., Kim, N., Kim, H., Kang, Y., Kim, J., Moon, J. S. and Hwang, I. 2009. The quorum sensingdependent gene katG of Burkholderia glumae is important for protection from visible light. J. Bacteriol. 191:4152-4157. https://doi.org/10.1128/JB.00227-09
- Cui, Z.-Q., Zhu, B., Xie, G.-L., Li, B. and Huang, S.-W. 2016. Research status and prospect of Burkholderia glumae, the pathogen causing bacterial panicle blight. Rice Sci. 23:111-118. https://doi.org/10.1016/j.rsci.2016.01.007
- Fields, S. and Song, O. 1989. A novel genetic system to detect protein-protein interactions. Nature 340:245-246. https://doi.org/10.1038/340245a0
- Gao, J. X., Jing, J., Yu, C. J. and Chen, J. 2015. Construction of a high-quality yeast two-hybrid library and its application in identification of interacting proteins with Brn1 in Curvularia lunata. Plant Pathol. J. 31:108-114. https://doi.org/10.5423/PPJ.OA.01.2015.0001
- Goto, K. and Ohata, K. 1956. New bacterial diseases of rice (brown stripe and grain rot). Ann. Phytopathol. Soc. Jpn. 21:46-47.
- Ham, J. H., Melanson, R. A. and Rush, M. C. 2011. Burkholderia glumae: next major pathogen of rice?. Mol. Plant Pathol. 12:329-339. https://doi.org/10.1111/j.1364-3703.2010.00676.x
- James, P., Halladay, J. and Craig, E. A. 1996. Genomic libraries and a host strain designed for highly efficient two-hybrid selection in yeast. Genetics 144:1425-1436. https://doi.org/10.1093/genetics/144.4.1425
- Jung, B., Park, J., Kim, N., Li, T., Kim, S., Bartley, L. E., Kim, J., Kim, I. Y., Kang, Y. H., Yun, K., Choi, Y., Lee, H. H., Ji, S., Lee, K. S., Kim, B. Y., Shon, J. C., Kim, W. C., Liu, K. H., Yoon, D., Kim, S., Seo, Y. S. and Lee, J. 2018. Cooperative interactions between seed-borne bacterial and air-borne fungal pathogens on rice. Nat. Commun. 9:31. https://doi.org/10.1038/s41467-017-02430-2
- Kalogeraki, V. S. and Winans, S. C. 1997. Suicide plasmids containing promoterless reporter genes can simultaneously disrupt and create fusions to target genes of diverse bacteria. Gene 188:69-75. https://doi.org/10.1016/S0378-1119(96)00778-0
- Keen, N. T., Tamaki, S., Kobayashi, D. and Trollinger, D. 1988. Improved broad-host-range plasmids for DNA cloning in gram-negative bacteria. Gene 70:191-197. https://doi.org/10.1016/0378-1119(88)90117-5
- Kim, S., Park, J., Lee, J., Shin, D., Park, D. S., Lim, J. S., Choi, I. Y. and Seo, Y. S. 2014. Understanding pathogenic Burkholderia glumae metabolic and signaling pathways within rice tissues through in vivo transcriptome analyses. Gene 547:77-85. https://doi.org/10.1016/j.gene.2014.06.029
- Kolonin, M. G., Zhong, J. and Finley Jr, R. L. 2000. Interaction mating methods in two-hybrid systems. Methods Enzymol. 328:26-46. https://doi.org/10.1016/S0076-6879(00)28388-2
- Lin, J. S. and Lai, E. M. 2017. Protein-protein interactions: Yeast two-hybrid system. Methods Mol. Biol. 1615:177-187. https://doi.org/10.1007/978-1-4939-7033-9_14
- Maier, R. H., Brandner, C. J., Hintner, H., Bauer, J. W. and Onder, K. 2008. Construction of a reading frame-independent yeast two-hybrid vector system for site-specific recombinational cloning and protein interaction screening. Biotechniques 45:235-244. https://doi.org/10.2144/000112897
- Mannaa, M., Park, I. and Seo, Y. S. 2019. Genomic features and insights into the taxonomy, virulence, and benevolence of plant-associated Burkholderia species. Int. J. Mol. Sci. 20:121. https://doi.org/10.3390/ijms20010121
- Mukhtar, M. S., Carvunis, A. R., Dreze, M., Epple, P., Steinbrenner, J., Moore, J., Tasan, M., Galli, M., Hao, T., Nishimura, M. T., Pevzner, S. J., Donovan, S. E., Ghamsari, L., Santhanam, B., Romero, V., Poulin, M. M., Gebreab, F., Gutierrez, B. J., Tam, S., Monachello, D., Boxem, M., Harbort, C. J., McDonald, N., Gai, L., Chen, H., He, Y., Vandenhaute, J., Roth, F. P., Hill, D. E., Ecker, J. R., Vidal, M., Beynon, J., Braun, P. and Dangl, J. L. 2011. Independently evolved virulence effectors converge onto hubs in a plant immune system network. Science 333:596-601. https://doi.org/10.1126/science.1203659
- Ryu, H. S., Han, M., Lee, S. K., Cho, J. I., Ryoo, N., Heu, S., Lee, Y. H., Bhoo, S. H., Wang, G. L., Hahn, T. R. and Jeon, J. S. 2006. A comprehensive expression analysis of the WRKY gene superfamily in rice plants during defense response. Plant Cell Rep. 25:836-847. https://doi.org/10.1007/s00299-006-0138-1
- Sambrook, J., Fritsch, E. F. and Maniatis, T. 1989. Molecular cloning: A laboratory manual. 2nd ed. Cold Spring Harbor Laboratory Press, NY, USA. 1546 pp.
- Sarris, P. F., Duxbury, Z., Huh, S. U., Ma, Y., Segonzac, C., Sklenar, J., Derbyshire, P., Cevik, V., Rallapalli, G., Saucet, S. B., Wirthmueller, L., Menke, F. L. H., Sohn, K. H. and Jones, J. D. G. 2015. A plant immune receptor detects pathogen effectors that target WRKY transcription factors. Cell 161:1089-1100. https://doi.org/10.1016/j.cell.2015.04.024
- Seo, Y. S., Lim, J. Y., Park, J., Kim, S., Lee, H. H., Cheong, H., Kim, S. M., Moon, J. S. and Hwang, I. 2015. Comparative genome analysis of rice-pathogenic Burkholderia provides insight into capacity to adapt to different environments and hosts. BMC Genomics 16:349. https://doi.org/10.1186/s12864-015-1558-5
- Trung, H. M., Van, N. V., Vien, N. V., Lam, D. T. and Lien, M. 1993. Occurrence of rice grain rot disease in Vietnam. Int. Rice Res. Notes 18:30.