A genome-wide association study reveals that epistasis underlies the pathogenicity of Pectobacterium

ABSTRACT Pectobacterium spp. are important bacterial pathogens that cause soft rot symptoms in various crops. However, their mechanism of pathogenicity requires clarity to help control their infections. Here, genome-wide association studies (GWAS) were conducted by integrating genomic data and measurements of two phenotypes (virulence and cellulase activity) for 120 various Pectobacterium strains in order to identify the genetic basis of their pathogenicity. An artificial intelligence-based software program was developed to automatically measure lesion areas on Chinese cabbage, thereby facilitating accurate and rapid data collection for virulence phenotypes for use in GWAS analysis. The analysis discovered 428 and 158 loci significantly associated with Pectobacterium virulence (lesion area) and cellulase activity, respectively. In addition, 1,229 and 586 epistasis loci pairs were identified for the virulence and cellulase activity phenotypes, respectively. Among them, the AraC transcriptional regulator exerted epistasis effects with another three nutrient transport-related genes in pairs contributing to the virulence phenotype, and their epistatic effects were experimentally confirmed for one pair with knockout mutants of each single gene and double gene. This study consequently provides valuable insights into the genetic mechanism underlying Pectobacterium spp. pathogenicity. Importance Plant diseases and pests are responsible for the loss of up to 40% of food crops, and annual economic losses caused by plant diseases reach more than $220 billion. Fighting against plant diseases requires an understanding of the pathogenic mechanisms of pathogens. This study adopted an advanced approach using population genomics integrated with virulence-related phenotype data to investigate the genetic basis of Pectobacterium spp., which causes serious crop losses worldwide. An automated software program based on artificial intelligence was developed to measure the virulence phenotype (lesion area), which greatly facilitated this research. The analysis predicted key genomic loci that were highly associated with virulence phenotypes, exhibited epistasis effects, and were further confirmed as critical for virulence with mutant gene deletion experiments. The present study provides new insights into the genetic determinants associated with Pectobacterium pathogenicity and provides a valuable new software resource that can be adapted to improve plant infection measurements. Plant diseases and pests are responsible for the loss of up to 40% of food crops, and annual economic losses caused by plant diseases reach more than $220 billion. Fighting against plant diseases requires an understanding of the pathogenic mechanisms of pathogens. This study adopted an advanced approach using population genomics integrated with virulence-related phenotype data to investigate the genetic basis of Pectobacterium spp., which causes serious crop losses worldwide. An automated software program based on artificial intelligence was developed to measure the virulence phenotype (lesion area), which greatly facilitated this research. The analysis predicted key genomic loci that were highly associated with virulence phenotypes, exhibited epistasis effects, and were further confirmed as critical for virulence with mutant gene deletion experiments. The present study provides new insights into the genetic determinants associated with Pectobacterium pathogenicity and provides a valuable new software resource that can be adapted to improve plant infection measurements.

[1]  E. Denamur,et al.  Epistatic interactions between the high pathogenicity island and other iron uptake systems shape Escherichia coli extra-intestinal virulence , 2023, Nature communications.

[2]  Debiao Li,et al.  Impact of Measurement Imprecision on Genetic Association Studies of Cardiac Function , 2023, medRxiv.

[3]  J. Erdmann,et al.  Genome-wide association studies of cardiovascular disease. , 2023, Physiological reviews.

[4]  F. Roux,et al.  Genome-wide association studies in plant pathosystems: success or failure? , 2022, Trends in plant science.

[5]  Q. Gao,et al.  The mutational signatures of poor treatment outcomes on the drug-susceptible Mycobacterium tuberculosis genome , 2022, bioRxiv.

[6]  L. Knodler,et al.  FoxR is an AraC‐like transcriptional regulator of ferrioxamine uptake in Salmonella enterica , 2022, Molecular microbiology.

[7]  F. Xia,et al.  A Novel Computational Framework for Precision Diagnosis and Subtype Discovery of Plant With Lesion , 2022, Frontiers in Plant Science.

[8]  P. Taheri,et al.  The Arac‐like transcriptional regulator YqhC is involved in pathogenicity of Erwinia amylovora , 2021, Journal of applied microbiology.

[9]  Q. Du,et al.  Genetic architecture of the metabolic pathway of salicylic acid biosynthesis in Populus. , 2021, Tree physiology.

[10]  R. Ma,et al.  Jasmonic acid and ethylene signaling pathways participate in the defense response of Chinese cabbage to Pectobacterium carotovorum infection , 2021 .

[11]  S. Kanaujia,et al.  Structural and thermodynamic insights into the novel dinucleotide‐binding protein of ABC transporter unveils its moonlighting function , 2021, The FEBS journal.

[12]  Baishi Hu,et al.  Transcriptome of Pectobacterium carotovorum subsp. carotovorum PccS1 infected in calla plants in vivo highlights a spatiotemporal expression pattern of genes related to virulence, adaptation, and host response , 2020, Molecular plant pathology.

[13]  Hua Xie,et al.  Characteristics and Rapid Diagnosis of Pectobacterium carotovorum ssp. Associated With Bacterial Soft Rot of Vegetables in China. , 2020, Plant disease.

[14]  S. Mirarab,et al.  Sequence Analysis , 2020, Encyclopedia of Bioinformatics and Computational Biology.

[15]  N. Kamimura,et al.  Publisher Correction: A TonB-dependent receptor constitutes the outer membrane transport system for a lignin-derived aromatic compound , 2019, Communications Biology.

[16]  N. Kamimura,et al.  A TonB-dependent receptor constitutes the outer membrane transport system for a lignin-derived aromatic compound , 2019, Communications Biology.

[17]  Jason G. Mezey,et al.  Identifying novel associations in GWAS by hierarchical Bayesian latent variable detection of differentially misclassified phenotypes , 2019, BMC Bioinformatics.

[18]  Sisi Xie,et al.  Comparative genomics of 84 Pectobacterium genomes reveals the variations related to a pathogenic lifestyle , 2018, BMC Genomics.

[19]  A. Charkowski The Changing Face of Bacterial Soft-Rot Diseases. , 2018, Annual review of phytopathology.

[20]  Stanford Kwenda,et al.  Transcriptome and Comparative Genomics Analyses Reveal New Functional Insights on Key Determinants of Pathogenesis and Interbacterial Competition in Pectobacterium and Dickeya spp , 2018, Applied and Environmental Microbiology.

[21]  Yunfei Xie,et al.  Hexanal as a QS inhibitor of extracellular enzyme activity of Erwinia carotovora and Pseudomonas fluorescens and its application in vegetables. , 2018, Food chemistry.

[22]  Jin Zhang,et al.  Methodological implementation of mixed linear models in multi-locus genome-wide association studies , 2017, Briefings in bioinformatics.

[23]  K. Yahara,et al.  A genome-wide association study identifies a horizontally transferred bacterial surface adhesin gene associated with antimicrobial resistant strains , 2016, Scientific Reports.

[24]  D. Falush Bacterial genomics: Microbial GWAS coming of age , 2016, Nature Microbiology.

[25]  Eduardo P C Rocha,et al.  Uncovering Listeria monocytogenes hypervirulence by harnessing its biodiversity , 2016, Nature Genetics.

[26]  S. Pethybridge,et al.  Leaf Doctor: A New Portable Application for Quantifying Plant Disease Severity. , 2015, Plant disease.

[27]  J. Corander,et al.  Erratum: Genomic signatures of human and animal disease in the zoonotic pathogen Streptococcus suis , 2015, Nature Communications.

[28]  J. Corander,et al.  Genomic signatures of human and animal disease in the zoonotic pathogen Streptococcus suis , 2015, Nature Communications.

[29]  Jayme Garcia Arnal Barbedo,et al.  An Automatic Method to Detect and Measure Leaf Disease Symptoms Using Digital Image Processing. , 2014, Plant disease.

[30]  V. Shevchik,et al.  Bacterial pectate lyases, structural and functional diversity. , 2014, Environmental microbiology reports.

[31]  Daniel J. Wilson,et al.  Predicting the virulence of MRSA from its genome sequence , 2014, Genome research.

[32]  E. Lojkowska,et al.  Characterization of Pectobacterium carotovorum subsp. odoriferum causing soft rot of stored vegetables , 2014, European Journal of Plant Pathology.

[33]  Keith A. Jolley,et al.  Genome-wide association study identifies vitamin B5 biosynthesis as a host specificity factor in Campylobacter , 2013, Proceedings of the National Academy of Sciences.

[34]  E. T. Palva,et al.  Pathogenicity of and plant immunity to soft rot pectobacteria , 2013, Front. Plant Sci..

[35]  Jason H. Moore,et al.  Chapter 11: Genome-Wide Association Studies , 2012, PLoS Comput. Biol..

[36]  L. Holm,et al.  Revised Phylogeny and Novel Horizontally Acquired Virulence Determinants of the Model Soft Rot Phytopathogen Pectobacterium wasabiae SCC3193 , 2012, PLoS pathogens.

[37]  Kevin W Eliceiri,et al.  NIH Image to ImageJ: 25 years of image analysis , 2012, Nature Methods.

[38]  Sadia Masood,et al.  Current status of post harvest soft rot in vegetables: a review. , 2010 .

[39]  Clive H. Bock,et al.  Plant Disease Severity Estimated Visually, by Digital Photography and Image Analysis, and by Hyperspectral Imaging , 2010 .

[40]  Bryan S. Biehl,et al.  Niche-specificity and the variable fraction of the Pectobacterium pan-genome. , 2008, Molecular plant-microbe interactions : MPMI.

[41]  P. Phillips Epistasis — the essential role of gene interactions in the structure and evolution of genetic systems , 2008, Nature Reviews Genetics.

[42]  David A. Baltrus,et al.  Global virulence regulation networks in phytopathogenic bacteria. , 2007, Trends in microbiology.

[43]  Thomas D. Schmittgen,et al.  Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. , 2001, Methods.

[44]  I. Toth,et al.  Characterization of Pectobacterium carotovorum proteins differentially expressed during infection of Zantedeschia elliotiana in vivo and in vitro which are essential for virulence. , 2018, Molecular plant pathology.

[45]  W. Wei-ren A Method for Measuring Relative Lesion Area on Leaves Using a Rice Chalkiness Ratio Analysis Software , 2008 .