Ruan Xuelian, Gong Zhiyu, Zeng Moqiyi, Zhong Ziqing, Chen Yongling, Wei Fangyi, Lei Chong, Zhu Yuanyuan, Qin Xue, Li Meng
Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning, Guangxi, People's Republic of China.
Guangxi Health Commission Key Laboratory of Fungi and Mycosis Research and Prevention, Nanning, Guangxi, People's Republic of China.
Infect Drug Resist. 2025 May 3;18:2243-2253. doi: 10.2147/IDR.S523498. eCollection 2025.
Carbapenem-resistant Enterobacteriaceae (CRE) presents a significant challenge due to its role in severe and multidrug-resistant infections.
This study aims to evaluate aztreonam (ATM) as a synergistic agent with ceftazidime/avibactam (CZA) for treating CRE strains with different carbapenemase phenotypes.
A total of 87 non-repeated clinical CRE strains were collected from various clinical specimens at The First Affiliated Hospital of Guangxi Medical University. Carbapenemase genotypes and phenotypes were identified using polymerase chain reaction (PCR) and NG-Test Carba 5 methods. The synergistic effect of CZA combined with ATM was assessed via the checkerboard MIC and disk stacking methods.
The clinical analysis revealed that underlying pulmonary disease, pneumonia, urinary catheter, and central intravenous catheter were associated with poor prognosis in CRE infections (p<0.05). All 87 CRE strains showed high resistance to most antibiotics, especially cefazolin, ceftriaxone, piperacillin/tazobactam, ertapenem, and meropenem, with a rate of 100.00%. For strains with a single carbapenemase gene, NG-Test Carba 5 demonstrated 100.00% accuracy. Notably, The combination of CZA and ATM showed synergy in 95.40% (83/87) of the CRE strains overall, with specific rates of 100.00% (4/4) in strains lacking detectable carbapenemase genes, 94.29% (33/35) in those with , and 100.00% (3/3) in those with plus or plus .
In conclusion, ATM significantly enhances CZA's activity against CRE strains in Guangxi, achieving a high synergy rate across diverse isolates, regardless of the carbapenemase genes present.
耐碳青霉烯类肠杆菌科细菌(CRE)因其在严重和多重耐药感染中的作用而构成重大挑战。
本研究旨在评估氨曲南(ATM)作为头孢他啶/阿维巴坦(CZA)的协同剂,用于治疗具有不同碳青霉烯酶表型的CRE菌株。
从广西医科大学第一附属医院的各种临床标本中收集了总共87株非重复的临床CRE菌株。使用聚合酶链反应(PCR)和NG-Test Carba 5方法鉴定碳青霉烯酶基因型和表型。通过棋盘微量肉汤稀释法和纸片扩散法评估CZA与ATM联合使用的协同作用。
临床分析显示,基础肺部疾病、肺炎、导尿管和中心静脉导管与CRE感染的预后不良相关(p<0.05)。所有87株CRE菌株对大多数抗生素均表现出高度耐药性,尤其是头孢唑林、头孢曲松、哌拉西林/他唑巴坦、厄他培南和美罗培南,耐药率为100.00%。对于具有单个碳青霉烯酶基因的菌株,NG-Test Carba 5的准确率为100.00%。值得注意的是,总体而言,CZA与ATM的联合在95.40%(83/87)的CRE菌株中显示出协同作用,在缺乏可检测碳青霉烯酶基因的菌株中为100.00%(4/4),在具有 的菌株中为94.29%(33/35),在具有 加 或 加 的菌株中为100.00%(3/3)。
总之,在广西,ATM显著增强了CZA对CRE菌株的活性,无论存在何种碳青霉烯酶基因,在不同分离株中均实现了高协同率。