Evidence map›Paper›PMID 27677796›Full record

ArticlemBio2016

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 and 4 more

Open access · goldAbstract read
In one paragraph

Article in mBio, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.9field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 100 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Jason W SahlCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, USA.
Talima PearsonCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, USA.
Richard OkinakaCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, USA.
James M SchuppDivision of Pathogen Genomics, The Translational Genomics Research Institute, Flagstaff, Arizona, USA.
John D GilleceDivision of Pathogen Genomics, The Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Hannah HeatonDivision of Pathogen Genomics, The Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Dawn BirdsellCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, USA.
Crystal HeppCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, USA School of Informatics, Computing and Cyber Systems, Northern Arizona University, Flagstaff, Arizona, USA.
Viacheslav FofanovCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, USA School of Informatics, Computing and Cyber Systems, Northern Arizona University, Flagstaff, Arizona, USA.
Ramón NosedaLaboratorio Azul, Azul, Buenos Aires. Argentina.
Antonio FasanellaIstituto Zooprofilattico Sperimentale of Puglia and Basilicata, Foggia, Italy.
Alex HoffmasterCenters for Disease Control and Prevention, Atlanta, Georgia, USA.
David M WagnerCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, USA.
Paul KeimCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, USA Division of Pathogen Genomics, The Translational Genomics Research Institute, Flagstaff, Arizona, USA PaulKeim@nau.edu.ORCID http://orcid.org/0000-0003-0089-5820
Northern Arizona University · USTranslational Genomics Research Institute · USCenters for Disease Control and Prevention · USIstituto Zooprofilattico Sperimentale della Puglia e della Basilicata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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. A Soviet industrial production facility in Sverdlovsk, USSR, proved deficient in 1979 when a plume of spores was accidentally released and resulted in one of the largest known human anthrax outbreaks. In order to understand this outbreak and others, we generated a Bacillus anthracis population genetic database based upon whole-genome analysis to identify all single-nucleotide polymorphisms (SNPs) across a reference genome. Phylogenetic analysis has defined three major clades (A, B, and C), 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, with many contemporary populations having resulted from a large spatial dispersal of spores from a single source. Two autopsy specimens from the Sverdlovsk outbreak were deep 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. 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. 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.

Identifiers

PMID27677796
PMCPMC5050339
OpenAlexW2524621763

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.