China-Japan Friendship Institute of Clinical Medical Sciences, China-Japan Friendship Hospital, Beijing, China.
Laboratory of Clinical Microbiology and Infectious Diseases, Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, National Clinical Research Center for Respiratory Diseases, National Center for Respiratory Medicine, China-Japan Friendship Hospital, Beijing, China.
Ann Clin Microbiol Antimicrob. 2024 Nov 8;23(1):99. doi: 10.1186/s12941-024-00743-x.
Carbapenem-resistant Klebsiella pneumoniae (CRKP) poses a significant threat to immunocompromised populations, including lung transplant recipients. This study investigates mixed CRKP strains carrying either bla or bla following ceftazidime-avibactam (CAZ/AVI) exposure, particularly in the context of lung transplantation. Mixed CRKP strains with shifting resistance phenotypes were frequently identified in patients exposed to CAZ/AVI. We aimed to elucidate the transitional state of bla variants by selecting CAZ/AVI-sensitive and -resistant CRKP strains from a lung transplantation patient.
The bla-variant-carrying CRKP strains were collected from lung transplant recipients exposed to CAZ/AVI in less than two years. Antibiotic susceptibility testing (AST) was conducted using microbroth dilution, and whole-genome sequencing (WGS) was used to identify genotypes and resistance mechanisms. Limiting dilution, drop-plate, and in vitro induction experiments determined bla-variant changes during CAZ/AVI administration. qPCR primers/probes were designed to identify bla mutations.
Among 104 lung transplant recipients infected by bla-harboring CRKP strains and receiving CAZ/AVI, 10 (9.6%) experienced changing resistance phenotypes. The limiting dilution method found that Patient 10's CRKP strains carried either bla or bla. The drop-plate experiment showed differing growth patterns on CAZ/AVI mediums. The in vitro induction experiment demonstrated shifting from bla to bla.
The study identified a "transitional state" of the mixed CRKP strains carrying either bla or bla in CAZ/AVI-exposed patients. Molecular diagnostics are crucial for identifying mixed strains and the transitional state of bla variants, guiding treatment decisions in this complex landscape.
耐碳青霉烯肺炎克雷伯菌(CRKP)对包括肺移植受者在内的免疫功能低下人群构成重大威胁。本研究调查了在接触头孢他啶-阿维巴坦(CAZ/AVI)后携带 bla 或 bla 的混合 CRKP 菌株,特别是在肺移植背景下。在接触 CAZ/AVI 的患者中,经常发现具有耐药表型变化的混合 CRKP 菌株。我们旨在通过从肺移植患者中选择 CAZ/AVI 敏感和耐药的 CRKP 菌株来阐明 bla 变异体的过渡状态。
从在不到两年内接触 CAZ/AVI 的肺移植受者中收集携带 bla-变体的 CRKP 菌株。使用微量肉汤稀释法进行抗生素敏感性试验(AST),并使用全基因组测序(WGS)鉴定基因型和耐药机制。通过限制稀释、滴板和体外诱导实验确定 CAZ/AVI 给药期间 bla 变体的变化。设计 qPCR 引物/探针以鉴定 bla 突变。
在 104 例感染 bla 携带 CRKP 菌株并接受 CAZ/AVI 治疗的肺移植受者中,有 10 例(9.6%)出现耐药表型变化。限制稀释法发现,患者 10 的 CRKP 菌株携带 bla 或 bla。滴板实验显示在 CAZ/AVI 培养基上有不同的生长模式。体外诱导实验表明 bla 向 bla 的转变。
本研究在接触 CAZ/AVI 的患者中发现了携带 bla 或 bla 的混合 CRKP 菌株的“过渡状态”。分子诊断对于识别混合菌株和 bla 变异体的过渡状态至关重要,这有助于在这种复杂环境下指导治疗决策。