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Microbiology resource announcements2026; 15(7); e0130125; doi: 10.1128/mra.01301-25

Complete genome of Bacillus anthracis strain ter21 from an infected zoo pony in Ternopil, Ukraine, 2021.

Abstract: Using rapid nanopore whole-genome sequencing, we assembled the genome of strain ter21 (5,229,480 bp), a Tsiankovskii-I group isolate cultured from a fatal case in 2021 of a pony from a zoo in Ternopil, Ukraine, identifying virulence plasmid pXO1 that encodes anthrax toxin, and pXO2.
Publication Date: 2026-06-22 PubMed ID: 42363848PubMed Central: PMC13348218DOI: 10.1128/mra.01301-25Google Scholar: Lookup
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  • Journal Article

Summary

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Overview

  • This study presents the complete genome sequencing and analysis of Bacillus anthracis strain ter21, isolated from a fatal anthrax case in a zoo pony in Ternopil, Ukraine, in 2021.
  • The researchers used rapid nanopore sequencing technology to assemble the entire bacterial genome and identify important virulence factors.

Introduction and Background

  • Bacillus anthracis is the bacterial pathogen responsible for anthrax, a serious infectious disease that can affect animals and humans.
  • The bacteria typically harbor two key virulence plasmids: pXO1 and pXO2, which are essential for its pathogenicity.
  • Understanding the genetic makeup and presence of these plasmids in specific isolates helps in epidemiological tracking and understanding outbreaks.
  • This study focuses on a particular strain, named ter21, isolated from an infected pony at a zoo in Ternopil, Ukraine.

Methods

  • The research team employed rapid nanopore whole-genome sequencing, a modern sequencing technology capable of reading long stretches of DNA quickly.
  • This method allowed for the near real-time assembly of the bacterial genome, enabling prompt analysis of the pathogen.
  • Genome assembly involved sequencing the entire chromosomal DNA plus any plasmids present within the strain.

Results

  • The complete genome of strain ter21 was successfully assembled, totaling 5,229,480 base pairs (bp).
  • Phylogenetic analysis assigned this strain to the Tsiankovskii-I group of Bacillus anthracis, contributing to strain classification and understanding of regional diversity.
  • Critically, both major virulence plasmids were identified:
    • pXO1, which carries genes encoding the anthrax toxin responsible for severe disease symptoms.
    • pXO2, which is involved in capsule formation, helping the bacteria evade the host immune system.
  • The detection of these plasmids confirms the isolate’s potential to cause severe anthrax infection.

Significance

  • This work demonstrates the utility of rapid nanopore sequencing for pathogen genome assembly directly from outbreak samples.
  • Having detailed genomic information aids in understanding anthrax outbreaks, tracking the spread, and developing targeted responses.
  • Specifically, identifying the presence of key virulence factors helps confirm the strain’s pathogenic potential and may guide public health interventions, especially in zoonotic contexts such as zoo animals.
  • The data also contribute to the global genetic database of Bacillus anthracis strains, which is valuable for epidemiological studies and vaccine development.

Cite This Article

APA
Bolotin V, Buttler J, Kravtsova O, Pishchanskyi O, Ukhovskiy V, Aliekseieva G, Arefiev V, Kovalenko G, Gerilovych A, Bortz E. (2026). Complete genome of Bacillus anthracis strain ter21 from an infected zoo pony in Ternopil, Ukraine, 2021. Microbiol Resour Announc, 15(7), e0130125. https://doi.org/10.1128/mra.01301-25

Publication

ISSN: 2576-098X
NlmUniqueID: 101728794
Country: United States
Language: English
Volume: 15
Issue: 7
Pages: e0130125
PII: e01301-25

Researcher Affiliations

Bolotin, Vitaliy
  • State Scientific and Control Institute of Biotechnology and Strains of Microorganisms (SSCIBSM), Kyiv, Ukraine.
  • National Scientific Center Institute of Experimental and Clinical Veterinary Medicine (NSC IECVM), Kharkiv, Ukraine.
  • State Scientific and Research Institute of Laboratory Diagnostics and Veterinary and Sanitary Expertise (SSRILDVSE), Kyiv, Ukraine.
Buttler, Jeremy
  • Department of Biological Sciences, University of Alaska Anchorage, Anchorage, Alaska, USA.
Kravtsova, Oksana
  • State Scientific and Research Institute of Laboratory Diagnostics and Veterinary and Sanitary Expertise (SSRILDVSE), Kyiv, Ukraine.
Pishchanskyi, Oleksandr
  • State Scientific and Research Institute of Laboratory Diagnostics and Veterinary and Sanitary Expertise (SSRILDVSE), Kyiv, Ukraine.
Ukhovskiy, Vitaliy
  • State Scientific and Research Institute of Laboratory Diagnostics and Veterinary and Sanitary Expertise (SSRILDVSE), Kyiv, Ukraine.
Aliekseieva, Galina
  • State Scientific and Research Institute of Laboratory Diagnostics and Veterinary and Sanitary Expertise (SSRILDVSE), Kyiv, Ukraine.
Arefiev, Vasyl
  • State Scientific and Research Institute of Laboratory Diagnostics and Veterinary and Sanitary Expertise (SSRILDVSE), Kyiv, Ukraine.
Kovalenko, Ganna
  • Department of Biological Sciences, University of Alaska Anchorage, Anchorage, Alaska, USA.
  • Department of Population Health and Disease Prevention, Joe C. Wen School of Population and Public Health, University of California, Irvine, California, USA.
Gerilovych, Anton
  • Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, Kharkiv, Ukraine.
  • PSI One Health Scientific and Research Institute, Kharkiv, Ukraine.
Bortz, Eric
  • Department of Biological Sciences, University of Alaska Anchorage, Anchorage, Alaska, USA.
  • Pathogenomics Lab, Department of Computer Science, Kyiv School of Economics, Kyiv, Ukraine.

Grant Funding

  • No. 2023.04/0141 / National Research Foundation of Ukraine

Conflict of Interest Statement

The authors declare no conflict of interest.

References

This article includes 8 references
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Citations

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