Nian Wang

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Organization: University of Florida
Department: Department of Microbiology and Cell Science
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Co-reporter:Yunzeng Zhang, Neha Jalan, Xiaofeng Zhou, Erica Goss, Jeffrey B Jones, João C Setubal, Xiaoling Deng and Nian Wang
The ISME Journal 2015 9(10) pp:2128-2138
Publication Date(Web):February 17, 2015
DOI:10.1038/ismej.2015.15
Understanding the evolutionary history and potential of bacterial pathogens is critical to prevent the emergence of new infectious bacterial diseases. Xanthomonas axonopodis subsp. citri (Xac) (synonym X. citri subsp. citri), which causes citrus canker, is one of the hardest-fought plant bacterial pathogens in US history. Here, we sequenced 21 Xac strains (14 XacA, 3 XacA* and 4 XacAw) with different host ranges from North America and Asia and conducted comparative genomic and evolutionary analyses. Our analyses suggest that acquisition of beneficial genes and loss of detrimental genes most likely allowed XacA to infect a broader range of hosts as compared with XacAw and XacA*. Recombination was found to have occurred frequently on the relative ancient branches, but rarely on the young branches of the clonal genealogy. The ratio of recombination/mutation ρ/θ was 0.0790±0.0005, implying that the Xac population was clonal in structure. Positive selection has affected 14% (395 out of 2822) of core genes of the citrus canker-causing Xanthomonas. The genes affected are enriched in ‘carbohydrate transport and metabolism’ and ‘DNA replication, recombination and repair’ genes (P<0.05). Many genes related to virulence, especially genes involved in the type III secretion system and effectors, are affected by positive selection, further highlighting the contribution of positive selection to the evolution of citrus canker-causing Xanthomonas. Our results suggest that both metabolism and virulence genes provide advantages to endow XacA with higher virulence and a wider host range. Our analysis advances our understanding of the genomic basis of specialization by positive selection in bacterial evolution.
Co-reporter:Pankaj Trivedi and Nian Wang
The ISME Journal 2014 8(3) pp:727-731
Publication Date(Web):December 5, 2013
DOI:10.1038/ismej.2013.215
Pathogens face a hostile and often novel environment when infecting a new host, and adaptation is likely to be an important determinant of the success in colonization and establishment. We hypothesized that resistant hosts will impose stronger selection on pathogens than susceptible hosts, which should accelerate pathogen evolution through selection biased toward effector genes. To test this hypothesis, we conducted an experimental evolution study on Xanthomonas citri subsp. citri (Xcc) in a susceptible plant species and a resistant plant species. We performed 55 rounds of repeated reinoculation of Xcc through susceptible host grapefruit (isolates G1, G2, G3) and resistant host kumquat (isolates K1, K2, K3). Consequently, only K1 and K3 isolates lost their ability to elicit a hypersensitive response (HR) in kumquat. Illumina sequencing of the parental and descendant strains P, G1, G2, G3, K1, K2 and K3 revealed that fixed mutations were biased toward type three secretion system effectors in isolates K1 and K3. Parallel evolution was observed in the K1 and K3 strains, suggesting that the mutations result from selection rather than by random drift. Our results support our hypothesis and suggest that repeated infection of resistant hosts by pathogens should be prevented to avoid selecting for adaptive pathogens.
Co-reporter:Hongge Jia
Plant Cell Reports 2014 Volume 33( Issue 12) pp:1993-2001
Publication Date(Web):2014 December
DOI:10.1007/s00299-014-1673-9
Xanthomonas citrisubsp. citri pretreatment before agroinfiltration could significantly promote transient expression in citrus leaves which were previously recalcitrant to agroinfiltration.Transient expression via agroinfiltration is widely used in biotechnology but remains problematic in many economically important plants. Xanthomonas citri subsp. citri (Xcc)-facilitated agroinfiltration was employed to promote transient protein expression in Valencia sweet orange leaves, which are recalcitrant to agroinfiltration. However, it is unclear whether Xcc-facilitated agroinfiltration has broad application, i.e., whether Xcc-facilitated agroinfiltration could be used on other citrus varieties. In addition, we intended to investigate whether Xcc-facilitated agroinfiltration could be used to hasten transgene function assays, e.g., Cre/lox system and Cas9/sgRNA system. In this report, Xcc-facilitated agroinfiltration was further exploited to enhance β-glucuronidase (GUS) expression in five citrus varieties. Xcc-facilitated agroinfiltration also significantly increased GFP expression in six citrus varieties tested. Both GUS and GFP assays indicated that Xcc-facilitated agroinfiltration had the best performance in grapefruit. After Xcc-facilitated agroinfiltration was carried out in grapefruit, protoplast analysis of the transformed cells indicated that there were more than 20 % leaf cells expressing GFP. In grapefruit, usefulness of Xcc-facilitated agroinfiltration was assayed in three case studies: (1) fast functional analysis of Cre/lox system, (2) the heat shock regulation of HSP70B promoter derived from Arabidopsis, and (3) Cas9/sgRNA-mediated genome modification.
Co-reporter:Nagaraju Akula, Pankaj Trivedi, Frank Q. Han, Nian Wang
European Journal of Medicinal Chemistry 2012 Volume 54() pp:919-924
Publication Date(Web):August 2012
DOI:10.1016/j.ejmech.2012.05.035
Huanglongbing is the most devastating disease of citrus caused by Candidatus Liberibacter asiaticus (Las). In the present study, we report the discovery of novel small molecule inhibitors against SecA ATPase of Las by using structure based design methods. We built the homology model of SecA protein structure of Las based on the SecA of Escherichia coli. The model was used for in-silico screening of commercially available compounds from ZINC database. Using the glide flexible molecular docking method, twenty structures were chosen for in vitro studies. Five compounds were found to inhibit the ATPase activity of SecA of Las at nano molar concentrations and showed antimicrobial activities against Agrobacterium tumefaciens with MBC ranging from 128 to 256 μg/mL. These compounds appear to be suitable as lead compounds for further development of antimicrobial compounds against Las.Graphical abstractHomology model of SecA ATPase of Candidatus Liberibacter asiaticus and Escherichia coli SecA (2FSG.pdb) were superimposed to identify the ATP binding site on SecA. The RMS deviation between these two proteins is 0.8 Å. Various domains of the protein structure were represented in different colors. The Identified ATP site on SecA is in between NBD (Nucleotide Binding Domain), IRA2-VAR (Intramolecular Regulator of ATPase) domains colored in blue and green-light green.Highlights► Homology model of SecA was built and optimized for structure based design. ► Molecular docking methods were used to identify 20 structures for activity studies. ► Five compounds were found at nano molar concentrations against SecA ATPase activity. ► Five compounds have shown antimicrobial activity against Agrobacterium tumefaciens. ► Identified small molecules could be used as leads for development of antimicrobial compounds.
Co-reporter:Nagaraju Akula, Hong Zheng, Frank Q. Han, Nian Wang
Bioorganic & Medicinal Chemistry Letters 2011 Volume 21(Issue 14) pp:4183-4188
Publication Date(Web):15 July 2011
DOI:10.1016/j.bmcl.2011.05.086
Candidatus Liberibacter asiaticus is the causal agent of Huanglongbing (HLB) disease of citrus. Current management practices have not been able to control HLB and stop the spread of HLB. The current study is focused on screening small molecule inhibitors against SecA protein of Ca. L. asiaticus. Homology modeling, structure based virtual screening and molecular docking methods have been used to find the novel inhibitory compounds against SecA activity at ATP binding region. At 20 μm 17 compounds showed >50% inhibition and four compounds had more than 65% inhibition. The most active compound has IC50 value of 2.5 μM. The differences between the activities of the compounds are explained by their inter-molecular interactions at ATP binding site.
Aureobasidin A (9CI)
(4-HYDRAZINOPHENYL)ACETONITRILE