dc.contributor.author | Ünal, Can Murat | |
dc.contributor.author | Steinert, Michael | |
dc.date.accessioned | 2021-01-08T21:51:27Z | |
dc.date.available | 2021-01-08T21:51:27Z | |
dc.date.issued | 2016 | |
dc.identifier.issn | 1472-8222 | |
dc.identifier.issn | 1744-7631 | |
dc.identifier.uri | http://doi.org/10.1517/14728222.2016.1090428 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12846/270 | |
dc.description | Unal, Can/0000-0003-4710-9567 | en_US |
dc.description | WOS:000370162800001 | en_US |
dc.description | PubMed: 26565670 | en_US |
dc.description.abstract | 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. | en_US |
dc.description.sponsorship | Federal State of Lower Saxony, Niedersachsisches Vorab [VWZN2889] | en_US |
dc.description.sponsorship | CM Unal and M Steinert were supported in this work by the Federal State of Lower Saxony, Niedersachsisches Vorab (VWZN2889). The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Taylor & Francis Ltd | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Alternative Drug Targets | en_US |
dc.subject | Antibiotic Resistance | en_US |
dc.subject | Cdad | en_US |
dc.subject | C. Difficile Infection | en_US |
dc.subject | Clostridium Difficile | en_US |
dc.subject | Small Inhibitors | en_US |
dc.subject | Therapeutics | en_US |
dc.subject | Toxins | en_US |
dc.subject | Virulence Factors | en_US |
dc.title | Novel therapeutic strategies for Clostridium difficile infections | en_US |
dc.type | Review | en_US |
dc.relation.journal | Expert Opinion On Therapeutic Targets | en_US |
dc.identifier.volume | 20 | en_US |
dc.identifier.issue | 3 | en_US |
dc.relation.publicationcategory | other | en_US |
dc.contributor.department | TAÜ, Fen Fakültesi, Moleküler Biyoteknoloji Bölümü | en_US |
dc.contributor.institutionauthor | Ünal, Can Murat | |
dc.identifier.doi | 10.1517/14728222.2016.1090428 | |
dc.identifier.startpage | 269 | en_US |
dc.identifier.endpage | 285 | en_US |
dc.identifier.wosquality | Q1 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.wos | WOS:000370162800001 | en_US |