Evidence map›Paper›PMID 40108131›Full record

ArticleNature communications2025

Staphylococcus aureus ST764-SCCmecII high-risk clone in bloodstream infections revealed through national genomic surveillance integrating clinical data.

Junzo Hisatsune, Shoko Kutsuno, Yasuhisa Iwao, Kasumi Ishida-Kuroki, Koji Yahara, Norikazu Kitamura, Toshiki Kajihara, Shizuo Kayama, Yo Sugawara, Hiroki Kitagawa and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
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  5. Article
  6. Article
  7. Infection and immunity · 2025
    Review
  8. Article
  9. 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

16 authors.

Junzo HisatsuneAntimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan. hisatune@niid.go.jp.
Shoko KutsunoAntimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Yasuhisa IwaoAntimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Kasumi Ishida-KurokiAntimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Koji YaharaAntimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan.ORCID http://orcid.org/0000-0003-4289-1115
Norikazu KitamuraAntimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Toshiki KajiharaAntimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Shizuo KayamaAntimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan.ORCID http://orcid.org/0000-0003-2420-3542
Yo SugawaraAntimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan.ORCID http://orcid.org/0000-0002-9897-3905
Hiroki KitagawaProject Research Center for Nosocomial Infectious Diseases, Hiroshima University, Hiroshima, Japan.
Hiroki OhgeProject Research Center for Nosocomial Infectious Diseases, Hiroshima University, Hiroshima, Japan.
Tomoyuki MizukamiNational Hospital Organization Kumamoto Medical Center, Kumamoto, Japan.
JARBS-SA Consortium
Takeshi TakahashiNational Hospital Organization Kumamoto Medical Center, Kumamoto, Japan.
Fumio KawanoNational Hospital Organization Kumamoto Medical Center, Kumamoto, Japan.
Motoyuki SugaiAntimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan. sugai@niid.go.jp.ORCID http://orcid.org/0000-0001-9252-7739

Funding

Japan Agency for Medical Research and Development (AMED) 21fk0108604
6 · The paper itself

Abstract

Antimicrobial resistance is a global health concern, and methicillin-resistant Staphylococcus aureus (MRSA) is one of the highest-priority organisms exhibiting this phenotype. Here, we performed a national surveillance integrating patient clinical data of S. aureus isolated from bloodstream infections. We performed genome sequencing, standardized antimicrobial susceptibility testing, and collected clinical metadata of 580 S. aureus isolates collected during 2019-2020. We focused on three predominant clonal complexes (CC1, CC5, and CC8) and assesses their microbiological and clinical significance, as well as their distribution across eastern and western Japan. Furthermore, we conducted a genomic comparison of the isolates of 2019-2000 with those of 1994-2000 and investigated the evolutionary trajectory of emerging clones from the three dominant clonal complexes. We revealed that the emerging MRSA ST764-SCCmecII showed the highest mortality rate within 30 days of hospitalization. This high-risk clone diverged from the New York/Japan clone (ST5-SCCmecII), which was inferred to have undergone repeated infections with phages carrying superantigen toxin genes and acquired antimicrobial resistance genes via mobile genetic elements, leading to its emergence around 1994. Overall, we provide a blueprint for a national genomic surveillance study that integrates clinical data and enables the identification and evolutionary characterization of a high-risk clone.

Indexed as

BacteremiaMethicillin-Resistant Staphylococcus aureusStaphylococcal InfectionsStaphylococcus aureusAdultAgedAnti-Bacterial AgentsFemaleGenome, BacterialGenomicsHumansJapanMaleMicrobial Sensitivity TestsMiddle AgedPhylogenyAnti-Bacterial Agents

Identifiers

PMID40108131
PMCPMC11923158

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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.