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Abstract

This Technical Resource presents genome sequence data for three strains of the bacterial pathogen pv. () collected in Serbia. We isolated these strains from pepper crops showing bacterial spot symptoms in 2016 at the municipality of Irig, in the Srem district. The presented data comprise raw sequencing reads and annotated, contig-level genome assemblies. We checked for the presence of sequences of known type-3 secretion system (T3SS) effector genes and plasmid-like sequences. Phylogenomic reconstruction revealed that the three strains fell in the same clade within . Strain X13 is most closely related to strain 66b, collected in Bulgaria in 2012. Strains X22 and X31 are most closely related to Tu-10 collected in the Southeastern Anatolia region of Türkiye in 2020. In common with other members of the clade, all three strains share a 75 kb plasmid that carries T3SS effector genes , , and . Additionally, strain X13 shares extensive sequence similarity to the pXCV183 plasmid, including T3SS effector gene , and shares extensive sequence similarity with plasmid pXap41, including T3SS effector gene . This difference in plasmid content might contribute to the observed difference in virulence among the Serbian strains. The three Serbian strains lack a 31 kb plasmid, pLMG730.4, that is seen in several Vietnamese and Canadian strains within this clade of . The data presented will be a useful resource for future molecular epidemiology and genomic surveillance of this pathogen in the Balkan region, augmenting the previously available draft genome sequences of strains 66b (Bulgaria) and 83M (North Macedonia).

Funding
This study was supported by the:
  • UK Research and Innovation (Award BB/T010916/1)
    • Principal Award Recipient: DavidStudholme
  • Biotechnology and Biological Sciences Research Council (Award BB/W018853/1)
    • Principal Award Recipient: MurrayGrant
  • Wellcome Trust (Award 218247/Z/19/Z)
    • Principal Award Recipient: NotApplicable
  • Innovation Fund of the Republic of Serbia (Award 451-03-136/2025-03/200010)
    • Principal Award Recipient: TatjanaPopovic Milovanovic
  • Innovation Fund of the Republic of Serbia (Award 451-03-136/2025-03/200053)
    • Principal Award Recipient: TatjanaPopovic Milovanovic
  • Innovation Fund of the Republic of Serbia (Award 451-03-136/2025-03/200117)
    • Principal Award Recipient: TatjanaPopovic Milovanovic
  • This is an open-access article distributed under the terms of the Creative Commons Attribution License. This article was made open access via a Publish and Read agreement between the Microbiology Society and the corresponding author’s institution.
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2026-02-04
2026-02-09

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References

  1. Petrović M, Savić B, Cvijanović V. Financial aspects of pepper (Capsicum annuum L) production on family farms in Serbia. Ekon poljopr 2021; 68:1015–1028 [View Article]
    [Google Scholar]
  2. Abrahamian P, Klein-Gordon JM, Jones JB, Vallad GE. Epidemiology, diversity, and management of bacterial spot of tomato caused by Xanthomonas perforans. Appl Microbiol Biotechnol 2021; 105:6143–6158 [View Article]
    [Google Scholar]
  3. Obradovic A, Mavridis A, Rudolph K, Arsenijevic M, Mijatovic M. In De Boer SH. eds Plant Pathogenic Bacteria Dordrecht: Springer Netherlands; 2001 pp 255–258 [View Article]
    [Google Scholar]
  4. Obradović A, Mavridis A, Rudolph K, Arsenijević M. Bacterial spot of capsicum and tomato in Yugoslavia. EPPO Bulletin 2000; 30:333–336 [View Article]
    [Google Scholar]
  5. Potnis N, Timilsina S, Strayer A, Shantharaj D, Barak JD et al. Bacterial spot of tomato and pepper: diverse Xanthomonas species with a wide variety of virulence factors posing a worldwide challenge. Mol Plant Pathol 2015; 16:907–920 [View Article] [PubMed]
    [Google Scholar]
  6. EPPO Global Database Xanthomonas euvesicatoria pv. euvesicatoria (XANTEU); 2012 https://gd.eppo.int/taxon/XANTEU accessed 29 September 2025
  7. Jones JB, Lacy GH, Bouzar H, Stall RE, Schaad NW. Reclassification of the xanthomonads associated with bacterial spot disease of tomato and pepper. Syst Appl Microbiol 2004; 27:755–762 [View Article] [PubMed]
    [Google Scholar]
  8. Jones JB, Stall RE, Bouzar H. Diversity among xanthomonads pathogenic on pepper and tomato. Annu Rev Phytopathol 1998; 36:41–58 [View Article] [PubMed]
    [Google Scholar]
  9. Aysan Y, Sahin F. Occurrence of bacterial spot disease, caused by Xanthomonas axonopodis pv. vesicatoria, on pepper in the eastern Mediterranean region of Turkey. Plant Pathol 2003; 52:781 [View Article]
    [Google Scholar]
  10. Popović T, Menković J, Pantelić M, Obradović A. First report of xanthomonas euvesicatoria causing bacterial leaf spot of pepper (capsicum annuum) in montenegro. Plant Dis 2022; 106:1514 [View Article]
    [Google Scholar]
  11. Vancheva T, Bogatzevska N, Moncheva P, Mitrev S, Vernière C et al. Molecular epidemiology of Xanthomonas euvesicatoria strains from the Balkan Peninsula revealed by a new multiple-locus variable-number tandem-repeat analysis scheme. Microorganisms 2021; 9:536 [View Article] [PubMed]
    [Google Scholar]
  12. Xhemali B, Bellameche F, Gjinovci G, Modica F, Biondi E et al. First report of Xanthomonas euvesicatoria pv. euvesicatoria causing bacterial leaf spot of pepper in Kosovo. J Plant Pathol 2024; 107:779–780 [View Article]
    [Google Scholar]
  13. Arsenijević M. Bakterioze Biljaka Naučna knjiga; 1988
    [Google Scholar]
  14. Balaž J. Pegavost lišća paprike prouzrokovana bakterijom xanthomonas campestris pv. vesicatoria. Savrem Poljopr Vanred Broj 1994; 42:341–345 [View Article]
    [Google Scholar]
  15. EFSA Panel on Plant Health (PLH) Scientific Opinion on the pest categorisation of Xanthomonas campestris pv. vesicatoria (Doidge) Dye. EFS2 2014; 12: [View Article]
    [Google Scholar]
  16. Bianco MI, Ponso MA, Garita-Cambronero J, Conforte VP, Galván TE et al. Genomic and phenotypic insight into Xanthomonas vesicatoria strains with different aggressiveness on tomato. Front Microbiol 2023; 14:1185368 [View Article] [PubMed]
    [Google Scholar]
  17. Jones JB, Bouzar H, Stall RE, Almira EC, Roberts PD et al. Systematic analysis of xanthomonads (Xanthomonas spp.) associated with pepper and tomato lesions. Int J Syst Evol Microbiol 2000; 50:1211–1219 [View Article] [PubMed]
    [Google Scholar]
  18. Potnis N, Krasileva K, Chow V, Almeida NF, Patil PB et al. Comparative genomics reveals diversity among xanthomonads infecting tomato and pepper. BMC Genom 2011; 12:146 [View Article] [PubMed]
    [Google Scholar]
  19. Preangtong Y, Patarapuwadol S, Phiriyangkul P, Kanhayart T, Kositcharoenkul N et al. Characterisation and genomic diversity of Xanthomonas species causing bacterial spot disease of tomato and pepper in Thailand. Plant Pathol 2025; 74:1315–1334 [View Article]
    [Google Scholar]
  20. Subedi A, Barrera LBT de la, Ivey ML, Egel DS, Kebede M et al. Population genomics reveals an emerging lineage of Xanthomonas perforans on pepper. Phytopathology 2024; 114:241–250 [View Article] [PubMed]
    [Google Scholar]
  21. Popov G, Fraiture M, Brunner F, Sessa G. Multiple Xanthomonas euvesicatoria type III effectors inhibit flg22-triggered immunity. Mol Plant-Microbe Interactions 2016; 29:651–660 [View Article]
    [Google Scholar]
  22. Roden JA, Belt B, Ross JB, Tachibana T, Vargas J et al. A genetic screen to isolate type III effectors translocated into pepper cells during Xanthomonas infection. Proc Natl Acad Sci U S A 2004; 101:16624–16629 [View Article] [PubMed]
    [Google Scholar]
  23. Teper D, Burstein D, Salomon D, Gershovitz M, Pupko T et al. Identification of novel Xanthomonas euvesicatoria type III effector proteins by a machine-learning approach. Mol Plant Pathol 2016; 17:398–411 [View Article] [PubMed]
    [Google Scholar]
  24. Thieme F, Szczesny R, Urban A, Kirchner O, Hause G et al. New type III effectors from Xanthomonas campestris pv. vesicatoria trigger plant reactions dependent on a conserved N-myristoylation motif. Mol Plant Microbe Interact 2007; 20:1250–1261 [View Article] [PubMed]
    [Google Scholar]
  25. Galán JE, Lara-Tejero M, Marlovits TC, Wagner S. Bacterial type III secretion systems: specialized nanomachines for protein delivery into target cells. Annu Rev Microbiol 2014; 68:415–438 [View Article] [PubMed]
    [Google Scholar]
  26. Schreiber KJ, Chau-Ly IJ, Lewis JD. What the wild things do: mechanisms of plant host manipulation by bacterial type III-secreted effector proteins. Microorganisms 2021; 9:1029 [View Article] [PubMed]
    [Google Scholar]
  27. An S-Q, Potnis N, Dow M, Vorhölter F-J, He Y-Q et al. Mechanistic insights into host adaptation, virulence and epidemiology of the phytopathogen Xanthomonas. FEMS Microbiol Rev 2020; 44:1–32 [View Article] [PubMed]
    [Google Scholar]
  28. Catara V, Cubero J, Pothier JF, Bosis E, Bragard C et al. Trends in molecular diagnosis and diversity studies for phytosanitary regulated Xanthomonas. Microorganisms 2021; 9:862 [View Article] [PubMed]
    [Google Scholar]
  29. Jacques M-A, Arlat M, Boulanger A, Boureau T, Carrère S et al. Using ecology, physiology, and genomics to understand host specificity in Xanthomonas. Annu Rev Phytopathol 2016; 54:163–187 [View Article] [PubMed]
    [Google Scholar]
  30. Timilsina S, Potnis N, Newberry EA, Liyanapathiranage P, Iruegas-Bocardo F et al. Xanthomonas diversity, virulence and plant-pathogen interactions. Nat Rev Microbiol 2020; 18:415–427 [View Article] [PubMed]
    [Google Scholar]
  31. Vancheva T, Lefeuvre P, Bogatzevska N, Moncheva P, Koebnik R. Draft genome sequences of two Xanthomonas euvesicatoria strains from the Balkan Peninsula. Genome Announc 2015; 3:6–7 [View Article] [PubMed]
    [Google Scholar]
  32. Popović Milovanović T, Jelušić A, Iličić R, Trkulja N, Damnjanović J et al. Biocontrol potential of indigenous pepper seed bacillus strains against Xanthomonas euvesicatoria. Pest Manag Sci 2025; 81:4875–4885 [View Article]
    [Google Scholar]
  33. Koenraadt H, van Betteray B, Germain R, Hiddink G, Jones JB et al. Development of specific primers for the molecular detection of bacterial spot of pepper and tomato. Acta Hortic 200999–102 [View Article]
    [Google Scholar]
  34. R Core TeamR: a language and environment for statistical computing 2025 https://www.R-project.org
  35. Wickham H, Vaughan D, Girlich M. tidyr: tidy messy data; 2025 https://CRAN.R-project.org/package=tidyr
  36. Wickham H. ggplot2: elegant graphics for data analysis. Springer-Verlag New York; 2016 https://ggplot2.tidyverse.org
  37. Mendiburu F de. Agricolae: statistical procedures for agricultural research CRAN 2023 https://CRAN.R-project.org/package=agricolae
    [Google Scholar]
  38. Zivkovic I, Ilicic R, Barac G, Damnjanovic J, Cvikic D et al. Influence of Xanthomonas euvesicatoria on quality parameters of pepper seed from Serbia. Pesticidi i fitomedicina 2023; 38:1–9 [View Article]
    [Google Scholar]
  39. Grant M, Greer S, Vicente J. Culturing Xanthomonas. protocols.io 2022 [View Article]
    [Google Scholar]
  40. Grant M, Greer S, Vicente J. DNA extraction using the Qiagen 67563 MagAttract HMW DNA Kit (48) v1. protocols.io 2022 [View Article]
    [Google Scholar]
  41. Studholme DJ. Davidjstudholme/xanthomonas-euvesicatoria-serbia: v1.0r Zenodo 2025 [View Article]
    [Google Scholar]
  42. Krueger F. Trim Galore!. Babraham Bioinformatics n.d http://www.bioinformatics.babraham.ac.uk/projects/trim_galore/ accessed 14 July 2020
    [Google Scholar]
  43. Martin M. Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnet j 2011; 17:10 [View Article]
    [Google Scholar]
  44. Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M et al. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol 2012; 19:455–477 [View Article]
    [Google Scholar]
  45. Benson DA, Karsch-Mizrachi I, Lipman DJ, Ostell J, Wheeler DL. GenBank. Nucleic Acids Research 2005; 33:D34–D38 [View Article]
    [Google Scholar]
  46. Wick RR, Judd LM, Gorrie CL, Holt KE. Unicycler: resolving bacterial genome assemblies from short and long sequencing reads. PLOS Comput Biol 2017; 13:e1005595 [View Article] [PubMed]
    [Google Scholar]
  47. Sayers EW, Bolton EE, Brister JR, Canese K, Chan J et al. Database resources of the national center for biotechnology information. Nucleic Acids Res 2022; 50:D20–D26 [View Article]
    [Google Scholar]
  48. Tatusova T, DiCuccio M, Badretdin A, Chetvernin V, Nawrocki EP et al. NCBI prokaryotic genome annotation pipeline. Nucleic Acids Res 2016; 44:6614–6624 [View Article]
    [Google Scholar]
  49. Chklovski A, Parks DH, Woodcroft BJ, Tyson GW. CheckM2: a rapid, scalable and accurate tool for assessing microbial genome quality using machine learning. Nat Methods 2023; 20:1203–1212 [View Article] [PubMed]
    [Google Scholar]
  50. Shakya M, Ahmed SA, Davenport KW, Flynn MC, Lo C-C et al. Standardized phylogenetic and molecular evolutionary analysis applied to species across the microbial tree of life. Sci Rep 2020; 10:1723 [View Article] [PubMed]
    [Google Scholar]
  51. Price MN, Dehal PS, Arkin AP. FastTree 2--approximately maximum-likelihood trees for large alignments. PLoS ONE 2010; 5:e9490 [View Article] [PubMed]
    [Google Scholar]
  52. Studholme DJ. Phylogenomic analysis of Xanthomonas v1. protocols.io 2022 [View Article]
    [Google Scholar]
  53. Letunic I, Bork P. Interactive Tree Of Life (iTOL) v5: an online tool for phylogenetic tree display and annotation. Nucleic Acids Res 2021; 49:W293–W296 [View Article] [PubMed]
    [Google Scholar]
  54. Grant JR, Enns E, Marinier E, Mandal A, Herman EK et al. Proksee: in-depth characterization and visualization of bacterial genomes. Nucleic Acids Res 2023; 51:W484–W492 [View Article]
    [Google Scholar]
  55. Schwengers O, Barth P, Falgenhauer L, Hain T, Chakraborty T et al. Platon: identification and characterization of bacterial plasmid contigs in short-read draft assemblies exploiting protein sequence-based replicon distribution scores. Microb Genom 2020; 6:e000398 [View Article]
    [Google Scholar]
  56. Camargo AP, Roux S, Schulz F, Babinski M, Xu Y et al. Identification of mobile genetic elements with geNomad. Nat Biotechnol 2024; 42:1303–1312 [View Article] [PubMed]
    [Google Scholar]
  57. Li H. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM. arXiv 2013 [View Article]
    [Google Scholar]
  58. Jain C, Rodriguez-R LM, Phillippy AM, Konstantinidis KT, Aluru S. High throughput ANI analysis of 90K prokaryotic genomes reveals clear species boundaries. Nat Commun 2018; 9:5114 [View Article] [PubMed]
    [Google Scholar]
  59. Costa J, Pothier JF, Bosis E, Boch J, Kölliker R et al. A community-curated DokuWiki resource on diagnostics, diversity, pathogenicity, and genetic control of Xanthomonads. Mol Plant-Microbe Interactions 2024; 37:347–353 [View Article]
    [Google Scholar]
  60. Gilchrist CLM, Chooi Y-H. clinker & clustermap.js: automatic generation of gene cluster comparison figures. Bioinformatics 2021; 37:2473–2475 [View Article] [PubMed]
    [Google Scholar]
  61. Loman NJ, Pallen MJ. Twenty years of bacterial genome sequencing. Nat Rev Microbiol 2015; 13:787–794 [View Article] [PubMed]
    [Google Scholar]
  62. Kaur A, Minsavage GV, Potnis N, Jones JB, Goss EM. Evolution of copper resistance in xanthomonas euvesicatoria pv. perforans population. mSystems 2024e01427-24 [View Article]
    [Google Scholar]
  63. Tambong JT, Xu R, Cuppels D, Chapados J, Gerdis S et al. Whole-genome resources and species-level taxonomic validation of 89 plant-pathogenic Xanthomonas strains isolated from various host plants. Plant Dis 2022; 106:1558–1565 [View Article] [PubMed]
    [Google Scholar]
  64. Thieme F, Koebnik R, Bekel T, Berger C, Boch J et al. Insights into genome plasticity and pathogenicity of the plant pathogenic bacterium Xanthomonas campestris pv. vesicatoria revealed by the complete genome sequence. J Bacteriol 2005; 187:7254–7266 [View Article] [PubMed]
    [Google Scholar]
  65. Subedi A, Kara S, Aysan Y, Minsavage GV, Timilsina S et al. Draft genome sequences of 11 Xanthomonas strains associated with bacterial spot disease in Turkey. Access Microbiol 2023; 5:acmi000586.v3 [View Article] [PubMed]
    [Google Scholar]
  66. Subedi A, Nga NTT, Tien DTK, Minsavage GV, Roberts PD et al. Draft genomes announcement of Vietnamese Xanthomonas euvesicatoria strains causing bacterial spot on pepper. Access Microbiol 2024; 6:000741 [View Article] [PubMed]
    [Google Scholar]
  67. Barak JD, Vancheva T, Lefeuvre P, Jones JB, Timilsina S et al. Whole-genome sequences of Xanthomonas euvesicatoria strains clarify taxonomy and reveal a stepwise erosion of type 3 effectors. Front Plant Sci 2016; 7:1805 [View Article] [PubMed]
    [Google Scholar]
  68. Richard D, Boyer C, Lefeuvre P, Canteros BI, Beni-Madhu S et al. Complete genome sequences of six copper-resistant Xanthomonas strains causing bacterial spot of solaneous plants, belonging to X. gardneri, X. euvesicatoria, and X. vesicatoria, using long-read technology. Genome Announc 2017 [View Article]
    [Google Scholar]
  69. Pothier JF, Vorhölter F-J, Blom J, Goesmann A, Pühler A et al. The ubiquitous plasmid pXap41 in the invasive phytopathogen Xanthomonas arboricola pv. pruni: complete sequence and comparative genomic analysis. FEMS Microbiol Lett 2011; 323:52–60 [View Article] [PubMed]
    [Google Scholar]
  70. Gurevich A, Saveliev V, Vyahhi N, Tesler G. QUAST: quality assessment tool for genome assemblies. Bioinformatics 2013; 29:1072–1075 [View Article]
    [Google Scholar]
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