Recurrence following invasive GAS infections in adults: Triumph of virulence or failure of immunity?
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, kazuistiky
PubMed
41017571
PubMed Central
PMC12482427
DOI
10.1080/21505594.2025.2563765
Knihovny.cz E-zdroje
- Klíčová slova
- CD19+ deficiency, Streptococcus pyogenes, cellulitis, lectin pathway complement deficiency, necrotizing fasciitis, sepsis,
- MeSH
- antibakteriální látky terapeutické užití MeSH
- bakteriemie mikrobiologie MeSH
- dospělí MeSH
- fasciitida nekrotizující mikrobiologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- recidiva MeSH
- sekreční systém typu IV genetika MeSH
- sekvenování celého genomu MeSH
- senioři MeSH
- Streptococcus pyogenes * patogenita genetika imunologie MeSH
- streptokokové infekce * imunologie mikrobiologie MeSH
- virulence MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- Názvy látek
- antibakteriální látky MeSH
- sekreční systém typu IV MeSH
Since late 2022, an increase in Streptococcus pyogenes (Group A Streptococcus, GAS) infections, both non-invasive and invasive (iGAS), has been reported globally. This study investigates iGAS cases complicated by recurrent infection (rGAS). From January to September 2023, four adults with severe iGAS suffered from rGAS. Clinical and whole-genome sequencing data were analysed. All patients required ICU admission and surgical debridement during their initial iGAS. The median interval between the initial iGAS and rGAS was 25.5 days, with a median duration of antibiotic treatment of 25 and 17.5 days, respectively. Patients A (female, age 69) and B (male, age 46) had upper limb necrotising fasciitis complicated by a subsequent cellulitis at the exact location. GAS emm1.3 (M1UK) was isolated in both patients, but patient A´s isolates carried a type-IV secretion system (T4SS), and this patient had a more severe course of infection. Patient C (male, age 66) had two episodes of bacteremia caused by GAS emm89.0 carrying T4SS and GAS emm12.37 with a frameshift in the rocA gene. Patient D (female, age 69) had upper limb cellulitis with bacteremia during the initial iGAS and upper limb cellulitis with septic gonitis as two concurrent manifestations of rGAS. All three isolates were identical, belonging to emm12.0 and carrying a 79 amino acid deletion in the SclA. Patients B and C had a reduced function of the complement lectin pathway and CD19+ lymphocyte deficiency. A combination of strain virulence factors and host immune deficiencies may predispose patients with iGAS to recurrence.
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