Cefiderocol in Combating Carbapenem-Resistant Acinetobacter baumannii: Action and Resistance

被引:1
|
作者
Yousefi, Bahman [1 ]
Kashanipoor, Setayesh [1 ]
Mazaheri, Payman [1 ]
Alibabaei, Farnaz [1 ]
Babaeizad, Ali [1 ]
Asli, Shima [1 ]
Mohammadi, Sina [2 ]
Gorgin, Amir Hosein [2 ]
Alipour, Tahereh [3 ]
Oksenych, Valentyn [4 ]
Eslami, Majid [5 ]
机构
[1] Semnan Univ Med Sci, Canc Res Ctr, Fac Med, Semnan 3514799442, Iran
[2] Semnan Univ Med Sci, Sch Med, Student Res Comm, Semnan 3514799442, Iran
[3] Semnan Univ Med Sci, Nervous Syst Stem Cell Res Ctr, Semnan 3514799442, Iran
[4] Univ Bergen, Dept Clin Sci, N-5020 Bergen, Norway
[5] Semnan Univ Med Sci, Fac Med, Dept Bacteriol & Virol, Semnan 3514799442, Iran
关键词
<italic>Acinetobacter baumannii</italic>; beta-lactamase; carbapenem; cefiderocol; PBP; PSEUDOMONAS-AERUGINOSA;
D O I
10.3390/biomedicines12112532
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Acinetobacter baumannii (A. baumannii) has emerged as a prominent multidrug-resistant (MDR) pathogen, significantly complicating treatment strategies due to its formidable resistance mechanisms, particularly against carbapenems. Reduced membrane permeability, active antibiotic efflux, and enzymatic hydrolysis via different beta-lactamases are the main resistance mechanisms displayed by A. baumannii, and they are all effective against successful treatment approaches. This means that alternate treatment approaches, such as combination therapy that incorporates beta-lactams, beta-lactamase inhibitors, and novel antibiotics like cefiderocol, must be investigated immediately. Cefiderocol, a new catechol-substituted siderophore cephalosporin, improves antibacterial activity by allowing for better bacterial membrane penetration. Due to its unique structure, cefiderocol can more efficiently target and destroy resistant bacteria by using iron transport systems. Through its inhibition of peptidoglycan formation through binding to penicillin-binding proteins (PBPs), cefiderocol avoids conventional resistance pathways and induces bacterial cell lysis. The possibility of resistance development due to beta-lactamase synthesis and mutations in PBPs, however, emphasizes the need for continued investigation into cefiderocol's efficacy in combination treatment regimes. Cefiderocol's siderophore mimic mechanism is especially important in iron-limited conditions because it can use ferric-siderophore transporters to enter cells. Additionally, its passive diffusion through bacterial porins increases its intracellular concentrations, making it a good option for treating carbapenem-resistant A. baumannii, especially in cases of severe infections and ventilator-associated diseases (IVACs). Cefiderocol may reduce MDR infection morbidity and mortality when combined with customized antimicrobial treatments, but further investigation is needed to improve patient outcomes and address A. baumannii resistance issues.
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页数:17
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