Department of Crop Sciences
Youfu 'Frank' Zhao
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Youfu 'Frank' Zhao

Assistant Professor
288 E R Madigan Laboratory
1201 W. Gregory Dr.
Urbana, IL 61801
(217) 265-9822

Research Areas

1. Transcriptome of Erwinia amylovora signal transduction networks

Fire blight, caused by Erwinia amylovora, is a particularly devastating disease for the apple and pear fruit industry, in part because of lack of effective control measures driven by the development of resistance to streptomycin in the bacterial pathogen population. Our long-term goal is to comprehensively characterize two-component signal transduction systems (TCSTs) and to reconstruct gene regulatory networks (GRNs) in E. amylovora, thus allowing a better understanding of the basic mechanisms of pathogenicity and biology of E. amylovora. We are currently studying a group of TCST genes, including HrpXY, RcsBCD, GrrSA, and EnvZ/OmpR, in E. amylovora, which play important roles in virulence and survival. We will genetically characterize these genes, identify target genes or regulon using microarray, and establish GRNs using computational modeling. Critical target genes and their functions will then be characterized and compared in both E. amylovora and Escherichia coli, thus extending our knowledge to two closely-related plant and mammalian microorganisms.

2. IGMSC Fire Blight (Integrated genomics and management systems for control of fire blight - Evaluate and assess virulence inhibitors against Erwinia amylovora)

Type III secretion system (T3SS) is a universal target for developing novel antibacterial agents -Recent advances in studying bacterial virulence factors provide mounting evidence that, the T3SS system is a potent virulence mechanism shared by a broad spectrum of pathogenic Gram negative bacteria that infect both plant and mammalian hosts by injecting effector proteins into host cells. Thus, the T3SS apparatus is essential for bacteria to evade the host immune defense. It is likely that agents that inhibit type III expression or effector secretion and translocation can result in antibacterial responses without actually killing the bacteria. Based on this hypothesis, recent publications have described screening of small molecular inhibitors targeting T3SSs. These screens have identified several classes of synthetic compounds as well as natural products as active T3SS inhibitors in a wide range Gram-negative bacterial pathogens, including E. coli, Salmonella, Yersinia, Shigella, and Chlamydia. We are currently evaluating and assessing virulence inhibitors against Erwinia amylovora. Project website: http://fireblight.nres.uiuc.edu/index.html

3. Genome sequencing and comparative genomics of Pseudomonas savastanoi pv. glycinea, and identification of new resistance sources of soybean against race 4

Soybean(Glycine max (L.)), one of the world’s largest providers of protein and oil, is a major crop in the United States, which accounts for about 40% of the soybeans produced in the world. Bacterial blight, caused by Pseudomonas savastanoi pv. glycinea (Psg), is a common bacterial disease of soybean and occurs in most soybean grown areas. Yield losses due to bacterial blight disease of soybean estimated at 4 to 40% in the U.S. Our recent studies have shown that field isolates of Psg are predominantly race 4, which infect all cultivars currently available. However, resistant cultivars have not been identified for Psg race 4. Identification of new resistance sources for breeding against Psg race 4 will provide us another means of control. Furthermore, genomic sequences of bacterial pathogens have greatly increased the understanding of host-pathogen interactions. Elucidation of molecular mechanisms of disease and resistance interactions between microbial plant pathogens and their host plants will lead to the development of improved disease management strategies. We are sequencing genomes of two Psg strains, race 4 and B076, using next generation sequencing technology. In silico subtractive hybridization-based comparative genomic analyses with other sequenced phytopathogenic pseudomonads will also be conducted. Genome link: http://www.ncbi.nlm.nih.gov/nuccore/320326756; http://www.ncbi.nlm.nih.gov/nuccore/320332072; and http://www.pseudomonas-syringae.org/

Journal Articles

Khan, M.A., Zhao, Y.F., and Korban, S.S. 2012. Molecular mechanisms of pathogenesis and resistance to the bacterial pathogen Erwinia amylovora, causal agent of fire blight disease in Rosaceae. Plant Mol. Biol. Rep. 30:247-260. (invited review)

McNally, R., Toth, I., Cock, P., Pritchard, L., Hedley, P., Morris, R., Zhao, Y. F., and Sundin, G. W. 2012. Genetic characterization of the HrpL regulon of the fire blight pathogen Erwinia amylovora reveals novel virulence factors. Mol. Plant Pathol. 13:160-173.

Wang, D. P., Qi, M. S., Calla, B., Korban, S. S., Clough, S. J., Cock, P., Sundin, G. W., Toth, I., and Zhao, Y. F. 2012. Genome-wide identification of genes regulated by the Rcs phosphorelay system in Erwinia amylovora. Mol. Plant-Microbe Interact. 25:6-17.

Wang, D. P., Calla, B., Vimolmangkang, S., Wu, X., Korban, S. S., Huber, S. C., Clough, S. J., and Zhao, Y. F. 2011. The orphan gene ybjN conveys pleiotropic effects on multicellular behavior and survival of Escherichia coli. PLoS ONE 6:e25293.(DOI:10.1371/journal.pone.0025293)
Sarowar, S., Zhao, Y. F., Guerra, R., Ali, S., Zheng, D., Wang, D. P., and Korban, S. S. 2011. Expression profiles of differentially regulated genes during early stages of apple flower infection with Erwinia amylovora. J. Exp. Bot. 62:4851-4861.
Zhao, Y. F., and Qi, M. S. 2011. Comparative genomics of Erwinia amylovora and related Erwinia species - what do we learn? Genes 2: 627-639 -- Special Issue [Genes and Genomes of Plant Pathogenic Bacteria]. (Invited review)
Wang, D., Korban, S. S., Pusey, L., and Zhao, Y. F. 2011. Characterization of the RcsC sensor kinase from Erwinia amylovora and other enterobacteria. Phytopathology 101:710-717.
Qi, M., Wang, D., Bradley, C., and Zhao, Y. F. 2011. Genome sequence analyses of Pseudomonas savastanoi pv. glycinea and in silico subtractive hybridization-based comparative genomics with nine phytopathogenic pseudomonads. PLoS ONE 6:e16451.(http://www.plosone.org/article/fetchObjectAttachment.action?uri=info%3Adoi%2F10.1371%2Fjournal.pone.0016451&representation=PDF)
Oh, M., Wang, X., Wu, X., Zhao, Y. F., Clouse, S. D., and Huber, S. C. 2010. Phosphorylation of Tyr-610 in the receptor kinase BAK1 plays a role in brassinosteroid signaling and affects basal defense gene expression. Proc. Natl. Acad. Sci. USA. 107: 17827-17832.
Di, C., Zhang, Q., Li. M., Hartman, G., and Zhao, Y. F. 2010. Image processing methods for quantitatively detecting soybean rust from multispectral images. Biosystems Engineering 107:186-193.
Nakka, S., Qi, M., and Zhao, Y. F. 2010. The Erwinia amylovora PhoPQ system is involved in resistance to antimicrobial peptide and suppresses gene expression of two novel type III secretion systems. Microbiol. Res. 165:665-673.
Qi, M., Sun, F., Caetano-Anolles, G., and Zhao, Y. F. 2010. Comparative genomic and phylogenetic analyses reveal the evolution of core two-component signal transduction systems in enterobacteria. J. Mol. Evol. 70: 167-180.
Wang, D., Korban, S. S., and Zhao, Y. F. 2010. Molecular signature of differential virulence in natural isolates of Erwinia amylovora. Phytopathology 100:192-198.
Nakka, S., Qi, M., and Zhao, Y. F. 2010. The PmrAB system in Erwinia amylovora renders the pathogen more susceptible to polymyxin B and more resistance to excess iron. Res. Microbiol. 161:153-157.
Koczan, J. M., McGrath, M., Zhao, Y. F., and Sundin, G. W. 2009. The contribution of the exopolysaccharide amylovoran and levan to biofilm formation: Implication in pathogenicity. Phytopathology 99:1237-1244.
Zhao, Y. F., Wang, D., Nakka, S., Sundin, G. W., and Korban, S. S. 2009. Systems level analysis of two-component signal transduction systems in Erwinia amylovora: Role in virulence, regulation of amylovoran biosynthesis and swarming motility. BMC Genomics. 10:245. (http://www.biomedcentral.com/content/pdf/1471-2164-10-245.pdf)
Li, X., Nie, J., Ward, L., Madani, M., Hsiang, T., Zhao, Y. F., De Boer, S. 2009. Comparative genomics-guided loop-mediated isothermal amplification for characterization of Pseudomonas syringae pv. phaseolicola. J. Appl. Microbiol. 107:717-726.
Zhao, Y. F., Sundin, G. W., and Wang, D. P. 2009. Construction and analysis of pathogenicity island deletion mutants in Erwinia amylovora. Can. J. Microbiol. 55:457-464.
Di, C., Zhang, Q., Li. M., Zhao, Y. F., and Hartman, G. 2009. Detection of soybean rust using a multispectral image sensor. Sensing and Instrumentation for Food Quality and Safety. 3:49-56.
Wang, D. P., Korban, S. S., and Zhao, Y. F. 2009. The Rcs phosphorelay system is essential for pathogenicity in Erwinia amylovora. Mol. Plant Pathol. 10:277-290.
Berry, M., McGhee, G. C., Zhao, Y. F., and Sundin, G. W. 2009. Effect of a waaL mutation on lipopolysaccharide composition, oxidative stress survival, and virulence in Erwinia amylovora. FEMS Microbiol. Lett. 291:80-87.
Wise, K. A., Zhao, Y. F., and Bradley, C. A. 2008. First report of pink seed of pea caused by Erwinia rhapontici in North Dakota. Plant Dis. 92:315
Perez-Martinez, I., Zhao, Y. F., Murillo, J., Sundin, G. W., and Ramos, C. 2008. Global genomic analysis of Pseudomonas savastanoi pv. savastanoi plasmids. J. Bacteriol. 190:625-635.
Ma, Z., Smith, J. J., Zhao, Y. F., Jackson, R., Arnold, D., Murillo, J., and Sundin, G. W. 2007. Phylogenetic analysis of the pPT23A plasmid family of Pseudomonas syringae. Appl. Environ. Microbiol. 73:1287-1295.
Triplett, L., Zhao, Y. F., and Sundin, G. W. 2006. Genetic differences among blight-causing Erwinia species with differing host specificities identified by suppression subtractive hybridization. Appl. Environ. Microbiol. 72:7359-7364.
Zhao, Y. F., He, S. Y., and Sundin, G. W. 2006. The Erwinia amylovora avrRpt2EA gene contributes to virulence on pear and AvrRpt2EA is recognized by Arabidopsis RPS2 when expressed in Pseudomonas syringae. Mol. Plant-Microbe Interact.9:644-654.
Zhao, Y. F., Blumer, S. E., and Sundin, G. W. 2005. Identification of Erwinia amylovora genes induced during infection of immature pear tissue. J. Bacteriol. 187:8088-8103.
Zhao, Y. F., Ma, Z., and Sundin, G. W. 2005. Comparative genomic analysis of the pPT23A plasmid family of Pseudomonas syringae. J. Bacteriol. 187:2113-2126.
Sundin, G. W., Mayfield, C. T., Zhao, Y. F., Gunasekera, T. S., Foster, G. L., and Ullrich, M. S. 2004. Complete nucleotide sequence and analysis of pPSR1 (72,601 bp), a pPT23A family plasmid from Pseudomonas syringae pv. syringae A2. Mol. Genet. Genomics. 270:462-475.
Li, L, Zhao, Y. F., McCaig, B.,Wingerd, B., Wang, J., Whalon, M., Pichersky, E., and Howe, G. A. 2004. The Tomato homolog of CORONATINE-INSENSITIVE1 is required for the maternal control of seed maturation, jasmonate-signaled defense responses, and glandular trichome development. Plant Cell 16:126-143.
Zhao, Y. F., Thilmony, R., Bender, C. L., Schaller, A., He, S. Y., and Howe, G. A. 2003.Virulence systems of Pseudomonas syringae pv. tomato promotes bacterial speck disease in tomato by targeting the jasmonate signaling pathway. Plant J. 36:485-499.
Alarcon-Chaidez, F. J., Lisa, K., Zhao, Y. F., and Bender, C. L. 2003. RpoN (σ54) is required for plasmid-encoded coronatine biosynthesis in Pseudomonas syringae. Plasmid 49:106-117.
Zhao, Y. F., Damicone, J. P., and Bender, C. 2002. Detection, survival, and sources of inoculum for bacterial diseases of leafy crucifers in Oklahoma. Plant Dis. 86:883-888.
Zhao, Y. F., Jones, W. T., Sutherland, P., Palmer, D. A., Mitchell, R. E., Reynolds, P. H. S., Damicone, J. P., and Bender, C. L. 2001. Detection of the phytotoxin coronatine by ELISA and immunolocalization in infected plant tissue. Physiol. Mol. Plant Path. 58:247-258.
Jones, W. T., Harvey, D., Zhao, Y. F., Mitchell, R., Bender, C. L., and Reynolds, P. H. S. 2001. Monoclonal antibody-based immunoassays for the phytotoxin coronatine. Food Agric. Immunol. 13:19-32.
Zhao, Y. F., Damicone, J. P., Demezas, D., Rangaswamy, V., and Bender, C. 2000. Bacterial leaf spot of leafy crucifers in Oklahoma caused by Pseudomonas syringae pv. maculicola. Plant Dis. 84:1015-1020.
Zhao, Y. F., Damicone, J. P., Demezas, D., and Bender, C. 2000. Bacterial leaf spot diseases of leafy crucifers in Oklahoma caused by pathovars of Xanthomonas campestris. Plant Dis. 84:1008-1014.