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A Bacillus anthracis Genome Sequence from the Sverdlovsk 1979 Autopsy Specimens

Jason W. Sahl, Talima Pearson, Richard Okinaka, James M. Schupp, John D. Gillece, Hannah Heaton, Dawn Birdsell, Crystal Hepp, Viacheslav Fofanov, Ramón Noseda, Antonio Fasanella, Alex Hoffmaster, David M. Wagner, Paul Keim
doi: https://doi.org/10.1101/069914
Jason W. Sahl
aCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff AZ 86011-4073
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Talima Pearson
aCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff AZ 86011-4073
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Richard Okinaka
aCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff AZ 86011-4073
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James M. Schupp
bDivision of Pathogen Genomics, 3051 W. Shamrell Blvd., Ste 106 The Translational Genomics Research Institute, Flagstaff, AZ 86001
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John D. Gillece
bDivision of Pathogen Genomics, 3051 W. Shamrell Blvd., Ste 106 The Translational Genomics Research Institute, Flagstaff, AZ 86001
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Hannah Heaton
bDivision of Pathogen Genomics, 3051 W. Shamrell Blvd., Ste 106 The Translational Genomics Research Institute, Flagstaff, AZ 86001
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Dawn Birdsell
aCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff AZ 86011-4073
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Crystal Hepp
aCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff AZ 86011-4073
cSchool of Informatics, Computing, and Cyber Systems, Northern Arizona University, Flagstaff AZ 86011-5693
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Viacheslav Fofanov
aCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff AZ 86011-4073
cSchool of Informatics, Computing, and Cyber Systems, Northern Arizona University, Flagstaff AZ 86011-5693
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Ramón Noseda
dLaboratorio Azul, Av.25 de Mayo No: 485 Azul (7300) Bs.As.Argentina
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Antonio Fasanella
eIstituto Zooprofilattico Sperimentale of Puglia and Basilicata Via Manfredonia 20, 71100 Foggia, Italy
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Alex Hoffmaster
fThe Centers for Disease Control and Prevention, Atlanta GA, USA
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David M. Wagner
aCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff AZ 86011-4073
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Paul Keim
aCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff AZ 86011-4073
bDivision of Pathogen Genomics, 3051 W. Shamrell Blvd., Ste 106 The Translational Genomics Research Institute, Flagstaff, AZ 86001
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Abstract

Anthrax is a zoonotic disease that occurs naturally in wild and domestic animals but has been used by both state-sponsored programs and terrorists as a biological weapon. The 2001 anthrax letter attacks involved less than gram quantities of Bacillus anthracis spores while the earlier Soviet weapons program produced tons. A Soviet industrial production facility in Sverdlovsk proved deficient in 1979 when a plume of spores was accidentally released and resulted in one of the largest known human anthrax outbreak. In order to understand this outbreak and others, we have generated a B. anthracis population genetic database based upon whole genome analysis to identify all SNPs across a reference genome. Only ~12,000 SNPs were identified in this low diversity species and represents the breadth of its known global diversity. Phylogenetic analysis has defined three major clades (A, B and C) with B and C being relatively rare compared to A. The A clade has numerous subclades including a major polytomy named the Trans-Eurasian (TEA) group. The TEA radiation is a dominant evolutionary feature of B. anthracis, many contemporary populations, and must have resulted from large-scale dispersal of spores from a single source. Two autopsy specimens from the Sverdlovsk outbreak were deeply sequenced to produce draft B. anthracis genomes. This allowed the phylogenetic placement of the Sverdlovsk strain into a clade with two Asian live vaccine strains, including the Russian Tsiankovskii strain. The genome was examined for evidence of drug resistance manipulation or other genetic engineering, but none was found. Only 13 SNPs differentiated the virulent Sverdlovsk strain from its common ancestor with two vaccine strains. The Soviet Sverdlovsk strain genome is consistent with a wild type strain from Russia that had no evidence of genetic manipulation during its industrial production. This work provides insights into the world's largest biological weapons program and provides an extensive B. anthracis phylogenetic reference valuable for future anthrax investigations.

Importance The 1979 Russian anthrax outbreak resulted from an industrial accident at the Soviet anthrax spore production facility in the city of Sverdlovsk. Deep genomic sequencing of two autopsy specimens generated a draft genome and phylogenetic placement of the Soviet Sverdlovsk anthrax strain. While it is known that Soviet scientists had genetically manipulated Bacillus anthracis, with the potential to evade vaccine prophylaxis and antibiotic therapeutics, there was no genomic evidence of this from the Sverdlovsk production strain genome. The whole genome SNP genotype of the Sverdlovsk strain was used to precisely identify it and its close relatives in the context of an extensive global B. anthracis strain collection. This genomic identity can now be used for forensic tracking of this weapons material on a global scale and for future anthrax investigations.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted August 16, 2016.
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A Bacillus anthracis Genome Sequence from the Sverdlovsk 1979 Autopsy Specimens
Jason W. Sahl, Talima Pearson, Richard Okinaka, James M. Schupp, John D. Gillece, Hannah Heaton, Dawn Birdsell, Crystal Hepp, Viacheslav Fofanov, Ramón Noseda, Antonio Fasanella, Alex Hoffmaster, David M. Wagner, Paul Keim
bioRxiv 069914; doi: https://doi.org/10.1101/069914
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A Bacillus anthracis Genome Sequence from the Sverdlovsk 1979 Autopsy Specimens
Jason W. Sahl, Talima Pearson, Richard Okinaka, James M. Schupp, John D. Gillece, Hannah Heaton, Dawn Birdsell, Crystal Hepp, Viacheslav Fofanov, Ramón Noseda, Antonio Fasanella, Alex Hoffmaster, David M. Wagner, Paul Keim
bioRxiv 069914; doi: https://doi.org/10.1101/069914

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