Iron-dependent mechanisms in Acinetobacter baumannii: pathogenicity and resistance

被引:3
作者
Zhang, Rong [1 ,2 ]
Li, Dan [1 ,2 ]
Fang, Hong [2 ]
Xie, Qian [2 ]
Tang, Huan [2 ]
Chen, Lin [1 ,2 ]
机构
[1] Southwest Med Univ, Dept Pulm & Crit Care Med, Luzhou, Peoples R China
[2] Univ Elect Sci & Technol China, Sichuan Prov Peoples Hosp, Sch Med, Dept Pulm & Crit Care Med, Chengdu, Peoples R China
来源
JAC-ANTIMICROBIAL RESISTANCE | 2025年 / 7卷 / 02期
关键词
ENERGY TRANSDUCTION; SIDEROPHORE; TONB; CARBAPENEM; CEFIDEROCOL; ACQUISITION; INFECTIONS; STRESS; FHUA;
D O I
10.1093/jacamr/dlaf039
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Acinetobacter baumannii is a Gram-negative opportunistic pathogen that poses a significant challenge in healthcare settings, particularly in ICUs, due to its MDR and high mortality rates, especially among critically ill coronavirus disease 2019 patients. Iron is crucial for the survival, growth and pathogenicity of A. baumannii, and the bacterium has developed multiple iron acquisition systems, including siderophore production, haem uptake and TonB-dependent transport mechanisms, to adapt to the iron-limited environment within the host. Although specific studies on A. baumannii are limited, mechanisms from other bacterial species suggest that similar iron acquisition strategies may play a key role in its virulence. Therapeutic approaches targeting these iron-dependent systems, such as the siderophore-conjugated cephalosporin cefiderocol, have shown potential in overcoming MDR A. baumannii infections. Additionally, strategies such as synthetic siderophores, TonB receptor inhibitors and iron chelators are under investigation to enhance treatment outcomes. Future research should prioritize validating these mechanisms in A. baumannii, advancing clinical trials for these therapies and exploring combination treatments to mitigate resistance and improve clinical outcomes in severely affected patients.
引用
收藏
页数:13
相关论文
共 77 条
[41]  
Nakashige TG, 2015, NAT CHEM BIOL, V11, P765, DOI [10.1038/nchembio.1891, 10.1038/NCHEMBIO.1891]
[42]   Hepcidin-Ferroportin Interaction Controls Systemic Iron Homeostasis [J].
Nemeth, Elizabeta ;
Ganz, Tomas .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (12)
[43]   Iron Metabolism and Immune Regulation [J].
Ni, Shuo ;
Yuan, Yin ;
Kuang, Yanbin ;
Li, Xiaolin .
FRONTIERS IN IMMUNOLOGY, 2022, 13
[44]   Deciphering the iron response in Acinetobacter baumannii: A proteomics approach [J].
Nwugo, Chika C. ;
Gaddy, Jennifer A. ;
Zimbler, Daniel L. ;
Actis, Luis A. .
JOURNAL OF PROTEOMICS, 2011, 74 (01) :44-58
[45]   Bacterial Responses to Iron Withholding by Calprotectin [J].
Obisesan, Adunoluwa O. ;
Zygiel, Emily M. ;
Nolan, Elizabeth M. .
BIOCHEMISTRY, 2021, 60 (45) :3337-3346
[46]   Cefiderocol: A New Cephalosporin Stratagem Against Multidrug-Resistant Gram-Negative Bacteria [J].
Ong'uti, Sharon ;
Czech, Mary ;
Robilotti, Elizabeth ;
Holubar, Marisa .
CLINICAL INFECTIOUS DISEASES, 2022, 74 (07) :1303-1312
[47]   Transition Metals and Virulence in Bacteria [J].
Palmer, Lauren D. ;
Skaar, Eric P. .
ANNUAL REVIEW OF GENETICS, VOL 50, 2016, 50 :67-91
[48]   Effect of Hcp Iron Ion Regulation on the Interaction Between Acinetobacter baumannii With Human Pulmonary Alveolar Epithelial Cells and Biofilm Formation [J].
Pan, Ping ;
Wang, Xiaolei ;
Chen, Yi ;
Chen, Qiong ;
Yang, Yunxing ;
Wei, Chenxing ;
Cheng, Tongtong ;
Wan, Haitong ;
Yu, Daojun .
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2022, 12
[49]   Structure of TonB in complex with FhuA, E-coli outer membrane receptor [J].
Pawelek, Peter D. ;
Croteau, Nathalie ;
Ng-Thow-Hing, Christopher ;
Khursigara, Cezar M. ;
Moiseeva, Natalia ;
Allaire, Marc ;
Coulton, James W. .
SCIENCE, 2006, 312 (5778) :1399-1402
[50]   Genome-Wide Characterization of the Fur Regulatory Network Reveals a Link between Catechol Degradation and Bacillibactin Metabolism in Bacillus subtilis [J].
Pi, Hualiang ;
Helmann, John D. .
MBIO, 2018, 9 (05)