Stefan Marek, Brajerova Marie, Prasad Suhanya, Bebrova Eliska, Berousek Jan, Pozniak Jiri, Jarosciakova Silvia, Rennerova Andrea, Milota Tomas, Nyc Otakar, Drevinek Pavel, Krutova Marcela, Trojanek Milan
Department of Infectious Diseases and Travel Medicine, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Department of Medical Microbiology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Virulence. 2025 Dec;16(1):2563765. doi: 10.1080/21505594.2025.2563765. Epub 2025 Sep 29.
Since late 2022, an increase in (Group A , 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 1.3 (M1) 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 89.0 carrying T4SS and GAS 12.37 with a frameshift in the 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 12.0 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.
自2022年底以来,全球报告A组链球菌(GAS)感染(包括非侵袭性和侵袭性iGAS)有所增加。本研究调查了并发复发性感染(rGAS)的iGAS病例。2023年1月至9月,4例患有严重iGAS的成人出现了rGAS。对临床和全基因组测序数据进行了分析。所有患者在初次iGAS感染期间均需要入住重症监护病房并接受手术清创。初次iGAS感染与rGAS之间的中位间隔时间为25.5天,抗生素治疗的中位持续时间分别为25天和17.5天。患者A(女性,69岁)和患者B(男性,46岁)患有上肢坏死性筋膜炎,随后在同一确切位置并发蜂窝织炎。两名患者均分离出GAS 1.3(M1),但患者A的分离株携带IV型分泌系统(T4SS),该患者的感染病程更严重。患者C(男性,66岁)有两次菌血症发作,分别由携带T4SS的GAS 89.0和基因发生移码突变的GAS 12.37引起。患者D(女性,69岁)在初次iGAS感染期间患有上肢蜂窝织炎伴菌血症,rGAS的两种并发表现为上肢蜂窝织炎伴脓性膝关节炎。所有三个分离株均相同,属于12.0,并且在SclA中有79个氨基酸的缺失。患者B和C的补体凝集素途径功能降低且存在CD19+淋巴细胞缺乏。菌株毒力因子和宿主免疫缺陷的组合可能使iGAS患者易复发。