Author
Listed:
- Junzo Hisatsune
(National Institute of Infectious Diseases
Hiroshima University)
- Shoko Kutsuno
(National Institute of Infectious Diseases)
- Yasuhisa Iwao
(National Institute of Infectious Diseases)
- Kasumi Ishida-Kuroki
(National Institute of Infectious Diseases)
- Koji Yahara
(National Institute of Infectious Diseases)
- Norikazu Kitamura
(National Institute of Infectious Diseases)
- Toshiki Kajihara
(National Institute of Infectious Diseases)
- Shizuo Kayama
(National Institute of Infectious Diseases
Hiroshima University)
- Yo Sugawara
(National Institute of Infectious Diseases)
- Hiroki Kitagawa
(Hiroshima University
Hiroshima University Hospital
Hiroshima University)
- Hiroki Ohge
(Hiroshima University
Hiroshima University Hospital
Hiroshima University)
- Tomoyuki Mizukami
(National Hospital Organization Kumamoto Medical Center)
- Takeshi Takahashi
(National Hospital Organization Kumamoto Medical Center)
- Fumio Kawano
(National Hospital Organization Kumamoto Medical Center)
- Motoyuki Sugai
(National Institute of Infectious Diseases
Hiroshima University
Hiroshima University)
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.
Suggested Citation
Junzo Hisatsune & Shoko Kutsuno & Yasuhisa Iwao & Kasumi Ishida-Kuroki & Koji Yahara & Norikazu Kitamura & Toshiki Kajihara & Shizuo Kayama & Yo Sugawara & Hiroki Kitagawa & Hiroki Ohge & Tomoyuki Miz, 2025.
"Staphylococcus aureus ST764-SCCmecII high-risk clone in bloodstream infections revealed through national genomic surveillance integrating clinical data,"
Nature Communications, Nature, vol. 16(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-57575-2
DOI: 10.1038/s41467-025-57575-2
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