Clostridium difficile infections (CDI) have become more difficult to treat due to the rise of hypervirulent strains that have increased morbidity as well as mortality and the likelihood of persistence and relapse in infected patients. To address the dire need for new anti-difficile agents, we explored the premise that nature utilizes good bacteria (i.e. probiotics), including Lactobacillus spp., to suppress gut pathogens such as C. difficile by producing novel antimicrobials, which were optimized by evolution to the microenvironment of the gut. In this regard, we explored the potential for developing reutericyclin from Lactobacillus reuteri as a natural anti- difficile agent. Probiotics are emerging as alternate treatments for CDI. However, there is ongoing debate on whether live probiotics may be used treat severe CDI, especially in immunocompromised patients. We therefore hypothesize that developing the antimicrobial produced by the probiotic specie would harness one of its natural therapeutic properties for localized killing of C. difficile in the gut, providing a more reliable and efficacious treatment strategy. Application of this concept to our studies on reutericyclin revealed that it has impressive antimicrobial and pharmacological properties for treating CDI. These include: rapid killing of nongrowing, toxin- producing stationary phase C. difficile;a novel mechanism of action specific to the bacterial membrane;a narrow spectrum of activity;lack of cytotoxicity against gut epithelia;stability to proteolysis;ability to achieve high non- absorbed concentrations in gut for killing;a low molecular weight and ease of synthesis that will allow advanced chemical optimization. Importantly, the killing of toxin-producing stationary phase cells is not shown by currently prescribed antibiotics vancomycin and metronidazole, which only kill actively growing C. difficile. We believe that this proposal for developing probiotic-derived reutericylcin derivatives to treat CDI is highly innovative and will be achieved through three iterative aims: (i) Synthesis of an expanded sets of reutericyclin analogs to optimize anti-difficile activity and increase affinity for the membrane target site;(ii) Lead development and characterization involving the stepwise progression of compounds through three stages of tests that include antimicrobial assessment, pharmacokinetic testing, toxicologic and in vivo efficacy experiments. Compounds meeting the selection criteria of the tests will move onto the next stage such that a lead candidate is obtained with potent in vivo efficacy and excellent safety profile;(iii) Mode of action studies to explore the fundamental antibacterial effects of targeting the clostridial membrane. The long-term goal of this project is to develop optimized lead analogs of probiotic derived reutericyclin that exhibit novel modes of action at the membrane target and have characterized antibiotic properties that would allow their progression into advanced preclinical studies as candidates for treating CDI.
There is a need for novel treatments for Clostridium difficile infections, which are now a major cause of morbidity and mortality among elderly patients in hospital settings in the United States. To address this need, we propose to optimize and develop derivatives of the probiotic-derived reutericyclin that is obtained from Lactobacillus reuteri. Because these agents rapidly kill C. difficile they may prevent the relapse of infection.
|Cherian, Philip T; Deshpande, Aditi; Cheramie, Martin N et al. (2017) Design, synthesis and microbiological evaluation of ampicillin-tetramic acid hybrid antibiotics. J Antibiot (Tokyo) 70:65-72|
|Dang, Uyen T; Zamora, Idalia; Hevener, Kirk E et al. (2016) Rifamycin Resistance in Clostridium difficile Is Generally Associated with a Low Fitness Burden. Antimicrob Agents Chemother 60:5604-7|
|Tao, Liang; Zhang, Jie; Meraner, Paul et al. (2016) Frizzled proteins are colonic epithelial receptors for C. difficile toxin B. Nature 538:350-355|
|Cherian, Philip T; Wu, Xiaoqian; Yang, Lei et al. (2015) Gastrointestinal localization of metronidazole by a lactobacilli-inspired tetramic acid motif improves treatment outcomes in the hamster model of Clostridium difficile infection. J Antimicrob Chemother 70:3061-9|
|Kumar, Manish; Adhikari, Sudip; Hurdle, Julian G (2014) Action of nitroheterocyclic drugs against Clostridium difficile. Int J Antimicrob Agents 44:314-9|
|Feng, Li; Maddox, Marcus M; Alam, Md Zahidul et al. (2014) Synthesis, structure-activity relationship studies, and antibacterial evaluation of 4-chromanones and chalcones, as well as olympicin A and derivatives. J Med Chem 57:8398-420|
|Wu, Xiaoqian; Hurdle, Julian G (2014) The Clostridium difficile proline racemase is not essential for early logarithmic growth and infection. Can J Microbiol 60:251-4|
|Cherian, Philip T; Wu, Xiaoqian; Maddox, Marcus M et al. (2014) Chemical modulation of the biological activity of reutericyclin: a membrane-active antibiotic from Lactobacillus reuteri. Sci Rep 4:4721|
|Tsutsumi, Lissa S; Owusu, Yaw B; Hurdle, Julian G et al. (2014) Progress in the discovery of treatments for C. difficile infection: A clinical and medicinal chemistry review. Curr Top Med Chem 14:152-75|
|Castanheira, Mariana; Messer, Shawn A; Jones, Ronald N et al. (2014) Activity of echinocandins and triazoles against a contemporary (2012) worldwide collection of yeast and moulds collected from invasive infections. Int J Antimicrob Agents 44:320-6|
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