Evidence map›Paper›PMID 42223843›Full record

ArticleInfection2026

Temporal trends in Group A Streptococcus epidemiology, antimicrobial susceptibility and emm-type distribution: a seven-year surveillance study from a UK district general hospital.

Pushpa Saajan, John Paul Candolesas, Shayi Shali, Uzoukwu Cyril, Anusha Karunasagar, Eldho Philip, Shikandhini Visuvanathan

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Article in Infection, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Pushpa SaajanDepartment of Microbiology, The Princess Alexandra Hospital NHS Trust, Harlow, CM20 1QX, UK. pushpa.saajan@gmail.com.
John Paul CandolesasDepartment of Infection Prevention and Control, The Princess Alexandra Hospital NHS Trust, Harlow, UK.
Shayi ShaliDepartment of Pharmacy, The Princess Alexandra Hospital NHS Trust, Harlow, UK.
Uzoukwu CyrilDepartment of Microbiology, The Princess Alexandra Hospital NHS Trust, Harlow, CM20 1QX, UK.
Anusha KarunasagarDepartment of Microbiology, The Princess Alexandra Hospital NHS Trust, Harlow, CM20 1QX, UK.
Eldho PhilipCentral Sterile Service Department, The Princess Alexandra Hospital NHS Trust, Harlow, UK.
Shikandhini VisuvanathanDepartment of Microbiology, The Princess Alexandra Hospital NHS Trust, Harlow, CM20 1QX, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGroup A Streptococcus (GAS) remains universally susceptible to penicillin; however, resistance to macrolides and clindamycin varies geographically and may affect management, particularly in patients with penicillin allergy. Recent increases in GAS incidence reported in the United Kingdom highlight the need for continued local epidemiological and antimicrobial resistance surveillance.

methodsWe conducted a retrospective laboratory-based surveillance study at a UK district general hospital between January 2017 and December 2023. All laboratory-confirmed GAS isolates were included. Isolates were classified as invasive or non-invasive based on specimen source. Antimicrobial susceptibility testing was performed using European Committee on Antimicrobial Susceptibility Testing (EUCAST) methodology, and emm typing was undertaken for available invasive isolates. Data were analysed descriptively to assess temporal trends across pre-pandemic, pandemic and post-pandemic periods.

resultsA total of 2,893 GAS isolates were identified, including 45 invasive isolates (1.6%). GAS activity demonstrated marked temporal variation during the seven-year surveillance period, with substantial suppression during 2020-2021 followed by a marked increase in 2022-2023, exceeding pre-pandemic levels. Throat swab specimens accounted for the largest proportion of isolates (59.0%), followed by wound specimens (22.8%) and genital specimens (12.4%). Penicillin susceptibility remained universal throughout the study period. Erythromycin and clindamycin susceptibility demonstrated temporal variation, with the lowest susceptibility observed in 2021 before recovery in subsequent years. Tetracycline susceptibility remained relatively stable. Among typed invasive isolates (29/45), emm1 was the predominant emm type (48.3%).

conclusionsGAS activity demonstrated marked temporal variation, with a substantial increase following the COVID-19 pandemic. Despite this, antimicrobial susceptibility patterns remained largely stable, with universal penicillin susceptibility. Variability in macrolide and clindamycin susceptibility highlights the importance of ongoing surveillance to inform empirical therapy, particularly in penicillin-allergic patients. The predominance of emm1 among invasive isolates aligns with national trends and supports continued molecular surveillance.

Indexed as

Antimicrobial resistanceemm typingEpidemiologyGroup A StreptococcusInvasive group A streptococcusStreptococcus pyogenes

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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.