Evidence map›Paper›PMID 27741255›Full record

ArticlePloS one2016

Complete Circular Genome Sequence of Successful ST8/SCCmecIV Community-Associated Methicillin-Resistant Staphylococcus aureus (OC8) in Russia: One-Megabase Genomic Inversion, IS256's Spread, and Evolution of Russia ST8-IV.

Tsai-Wen Wan, Olga E Khokhlova, Yasuhisa Iwao, Wataru Higuchi, Wei-Chun Hung, Ivan V Reva, Olga A Singur, Vladimir V Gostev, Sergey V Sidorenko, Olga V Peryanova and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. The Pathogenicity Mechanisms ofInternational journal of molecular sciences · 2025
    Review
  3. Transposition of TnAntimicrobial agents and chemotherapy · 2025
    Article
  4. Article
  5. Characterisation of PVL-PositiveAntibiotics (Basel, Switzerland) · 2024
    Article
  6. Article
  7. Article
  8. Identification of methicillin-resistantEmerging microbes & infections · 2022
    Article
  9. Article
  10. Article
  11. Unstable chromosome rearrangements inProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  12. Fatal case of ST8/SCCNew microbes and new infections · 2018
    Article
  13. Article
  14. Influence of ISAntimicrobial agents and chemotherapy · 2017
    Article
  15. Article
  16. Article
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 6 institutions in 3 countries.

Tsai-Wen WanDepartment of Epidemiology, Genomics, and Evolution, International Medical Education and Research Center, Niigata, Japan.
Olga E KhokhlovaDepartment of Epidemiology, Genomics, and Evolution, International Medical Education and Research Center, Niigata, Japan.
Yasuhisa IwaoDepartment of Epidemiology, Genomics, and Evolution, International Medical Education and Research Center, Niigata, Japan.
Wataru HiguchiDivision of Bacteriology, Department of Infectious Disease Control and International Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Wei-Chun HungDepartment of Microbiology and Immunology, Kaohsiung Medical University, Kaohsiung, Taiwan.
Ivan V RevaDepartment of Epidemiology, Genomics, and Evolution, International Medical Education and Research Center, Niigata, Japan.
Olga A SingurDepartment of Venereal and Skin Diseases and Cosmetology, Pacific State Medical University, Vladivostok, Russia.
Vladimir V GostevDepartment of Medical Microbiology and Molecular Epidemiology, Scientific Research Institute of Children's Infections, St. Petersburg, Russia.
Sergey V SidorenkoDepartment of Medical Microbiology and Molecular Epidemiology, Scientific Research Institute of Children's Infections, St. Petersburg, Russia.
Olga V PeryanovaRussia-Japan Center of Microbiology, Metagenomics and Infectious Diseases, Krasnoyarsk State Medical University named after Professor V.F. Vojno-Yasenetsky, Krasnoyarsk, Russia.
Alla B SalminaResearch Institute of Molecular Medicine and Pathobiochemistry, Krasnoyarsk State Medical University named after Professor V.F. Vojno-Yasenetsky, Krasnoyarsk, Russia.
Galina V RevaDepartment of Clinical and Fundamental Medicine, Far Eastern Federal University School of Biomedicine, Vladivostok, Russia.
Lee-Jene TengDepartment of Clinical Laboratory Sciences and Medical Biotechnology, National Taiwan University College of Medicine, Taipei, Taiwan.
Tatsuo YamamotoDepartment of Epidemiology, Genomics, and Evolution, International Medical Education and Research Center, Niigata, Japan.
Krasnoyarsk State Medical University · RUFar Eastern Federal University · RUNational Taiwan University · TWKaohsiung Medical University · TWNiigata University · JPVladivostok State Medical University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ST8/SCCmecIV community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) has been a common threat, with large USA300 epidemics in the United States. The global geographical structure of ST8/SCCmecIV has not yet been fully elucidated. We herein determined the complete circular genome sequence of ST8/SCCmecIVc strain OC8 from Siberian Russia. We found that 36.0% of the genome was inverted relative to USA300. Two IS256, oppositely oriented, at IS256-enriched hot spots were implicated with the one-megabase genomic inversion (MbIN) and vSaβ split. The behavior of IS256 was flexible: its insertion site (att) sequences on the genome and junction sequences of extrachromosomal circular DNA were all divergent, albeit with fixed sizes. A similar multi-IS256 system was detected, even in prevalent ST239 healthcare-associated MRSA in Russia, suggesting IS256's strong transmission potential and advantage in evolution. Regarding epidemiology, all ST8/SCCmecIVc strains from European, Siberian, and Far Eastern Russia, examined had MbIN, and geographical expansion accompanied divergent spa types and resistance to fluoroquinolones, chloramphenicol, and often rifampicin. Russia ST8/SCCmecIVc has been associated with life-threatening infections such as pneumonia and sepsis in both community and hospital settings. Regarding virulence, the OC8 genome carried a series of toxin and immune evasion genes, a truncated giant surface protein gene, and IS256 insertion adjacent to a pan-regulatory gene. These results suggest that unique single ST8/spa1(t008)/SCCmecIVc CA-MRSA (clade, Russia ST8-IVc) emerged in Russia, and this was followed by large geographical expansion, with MbIN as an epidemiological marker, and fluoroquinolone resistance, multiple virulence factors, and possibly a multi-IS256 system as selective advantages.

Indexed as

Genome, BacterialBacterial ProteinsBase SequenceBiological EvolutionCommunity-Acquired InfectionsDNA, BacterialDNA, CircularElectrophoresis, Gel, Pulsed-FieldErythromycinGenotypeMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsMolecular Sequence DataRNA, MessengerRNA, Ribosomal, 16SRussiaBacterial ProteinsDNA, BacterialDNA, CircularErythromycinRNA, MessengerRNA, Ribosomal, 16S

Identifiers

PMID27741255
PMCPMC5065196
OpenAlexW2531257293

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.