Abstract
Background: Several European countries have reported a rise in invasive Group A Streptococcus (GAS) infections, particularly linked to the toxigenic emm1 sublineage M1UK. In Germany, historical molecular data are limited due to the absence of systematic molecular surveillance. Methods: We performed whole-genome sequencing (WGS) on 189 invasive Streptococcus pyogenes isolates collected between January 1, 2015, and May 31, 2023, at University Medical Center Carl Gustav Carus, TU Dresden. Clinical data were extracted from patient records. M1UK sublineage identification was based on 27 characteristic single nucleotide polymorphisms (SNPs). A Bayesian coalescent analysis estimated the evolutionary timescales of the M1UK clade in Germany. Results: The most common emm type was emm1 (34%, 64/189), followed by emm12, emm4, and emm89. Of the 64 emm1 isolates, 31 (48%) were M1UK. No significant associations were found between clinical outcomes and M1UK or M1global genotypes. Although a post-pandemic shift favouring M1UK was observed, our analysis indicates that M1UK had already been circulating in Germany by 2017. The estimated most recent common ancestor dates to 2012 (95% highest posterior density: 2009–2015), with a stable effective population size over time. Conclusion: Our findings confirm the pre-pandemic circulation of M1UK in Germany. While the clinical impact of M1UK remains unclear, integrating clinical data with high-resolution molecular surveillance may improve early detection of emerging high-risk clones.
| Originalsprache | Englisch |
|---|---|
| Aufsatznummer | 2576587 |
| Zeitschrift | Emerging Microbes and Infections |
| Jahrgang | 14 |
| Ausgabenummer | 1 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 2025 |
Fördermittel
The study was funded by institutional funding. The Dresden GAS Study Group: Stefan Richard Bornstein1, Roland Aschoff2, Martin Bornhäuser3, Andreas Güldner4, Florian Gunzer5, Johannes Herold6, Jurek Schultz7, Pauline Wimberger8 and Thomas Zahnert9. Affiliations of study group members: 1Department of Internal Medicine III, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany; 2Department of Dermatology, University Hospital Carl Gustav Carus, Technical University Dresden, Dresden, Germany; 3Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany; 4Department of Anesthesiology and Intensive Care Medicine, University Hospital Carl Gustav Carus at the Technische Universität Dresden, Dresden, Germany; 5Institute for Medical Microbiology and Virology, Faculty of Medicine and University Hospital Carl Gustav Carus, TUD Dresden University of Technology, Dresden, Germany; 6University Center of Orthopaedic, Trauma and Plastic Surgery, University Hospital Carl Gustav Carus at Technische Universität Dresden, Dresden, Germany; 7Department of Pediatric Surgery, University Hospital Carl Gustav Carus, Dresden, Germany; 8Department of Gynecology and Obstetrics, Technische Universität Dresden; 9Department of Otorhinolaryngology, Head and Neck Surgery, Technische Universität Dresden, Carl Gustav Carus Faculty of Medicine, Dresden, Germany.
| Träger | Trägernummer |
|---|---|
| 5Institute for Medical Microbiology and Virology | |
| Technische Universität Dresden | |
| Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden | |
| 8Department of Gynecology and Obstetrics |
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 3 – Gesundheit und Wohlergehen
Strategische Forschungsbereiche und Zentren
- Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)
DFG-Fachsystematik
- 2.21-03 Medizinische Mikrobiologie und Mykologie, Hygiene, Molekulare Infektionsbiologie
- 2.21-05 Immunologie
- 2.22-31 Klinische Infektiologie und Tropenmedizin
- 2.21-02 Mikrobielle Ökologie und Angewandte Mikrobiologie
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