Novel therapeutic strategies for Clostridium difficile infections

被引:9
|
作者
Unal, Can M. [1 ,2 ]
Steinert, Michael [1 ,3 ]
机构
[1] Tech Univ Carolo Wilhelmina Braunschweig, Inst Mikrobiol, Spielmannstr 7, D-38106 Braunschweig, Germany
[2] Turk Alman Univ, Fen Fak, Sahinkaya Cad 86, TR-34820 Istanbul, Turkey
[3] Helmholtz Ctr Infect Res, Mascheroder Weg 1, D-38124 Braunschweig, Germany
关键词
alternative drug targets; antibiotic resistance; CDAD; C. difficile infection; Clostridium difficile; small inhibitors; therapeutics; toxins; virulence factors; FECAL MICROBIOTA TRANSPLANTATION; CLINDAMYCIN-INDUCED ENTEROCOLITIS; FIBRONECTIN-BINDING PROTEIN; CELL-SURFACE PROTEIN; TOXIN-B; MEMBRANE TRANSLOCATION; MONOCLONAL-ANTIBODIES; FLAGELLAR PROTEINS; CYSTEINE PROTEASE; MUCIN DYNAMICS;
D O I
10.1517/14728222.2016.1090428
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: In recent years, Clostridium difficile has become the primary cause of antibiotic-associated diarrhea and pseudomembranous colitis, resulting in long and complicated hospital stays that represent a serious burden for patients as well as health care systems. Currently, conservative treatment of C. difficile infection (CDI) relies on the antibiotics vancomycin, metronidazole or fidaxomicin, or in case of multiple recurrences, fecal microbiota transplantation (FMT).Areas covered: The fast-spreading, epidemic nature of this pathogen urgently necessitates the search for alternative treatment strategies as well as antibiotic targets. Accordingly, in this review, we highlight the recent findings regarding virulence associated traits of C. difficile, evaluate their potential as alternative drug targets, and present current efforts in designing inhibitory compounds, with the aim of pointing out possibilities for future treatment strategies.Expert opinion: Increased attention on systematic analysis of the virulence mechanisms of C. difficile has already led to the identification of several alternative drug targets. In the future, applying state of the art omics' and the development of novel infection models that mimic the human gut, a highly complex ecological niche, will unveil the genomic and metabolic plasticity of this pathogen and will certainly help dealing with future challenges.
引用
收藏
页码:269 / 285
页数:17
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