OG716: Designing a fit-for-purpose lantibiotic for the treatment of Clostridium difficile infections.

Lantibiotics continue to offer an untapped pipeline for the development of novel antibiotics. We report here the discovery of a novel lantibiotic for the treatment of C. difficile infection (CDI). The leads were selected from a library of over 300 multiple substitution variants of the lantibiotic Mu...

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Main Authors: Johan A Kers, Anthony W DeFusco, Jae H Park, Jin Xu, Mark E Pulse, William J Weiss, Martin Handfield
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5997364?pdf=render
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spelling doaj-8576e0e2154a45a69a25cf4db2f4e4892020-11-25T01:48:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01136e019746710.1371/journal.pone.0197467OG716: Designing a fit-for-purpose lantibiotic for the treatment of Clostridium difficile infections.Johan A KersAnthony W DeFuscoJae H ParkJin XuMark E PulseWilliam J WeissMartin HandfieldLantibiotics continue to offer an untapped pipeline for the development of novel antibiotics. We report here the discovery of a novel lantibiotic for the treatment of C. difficile infection (CDI). The leads were selected from a library of over 300 multiple substitution variants of the lantibiotic Mutacin 1140 (MU1140). Top performers were selected based on testing for superior potency, solubility, manufacturability, and physicochemical and/or metabolic stability in biologically-relevant systems. The best performers in vitro were further evaluated orally in the Golden Syrian hamster model of CDAD. In vivo testing ultimately identified OG716 as the lead compound, which conferred 100% survival and no relapse at 3 weeks post infection. MU1140-derived variants are particularly attractive for further clinical development considering their novel mechanism of action.http://europepmc.org/articles/PMC5997364?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Johan A Kers
Anthony W DeFusco
Jae H Park
Jin Xu
Mark E Pulse
William J Weiss
Martin Handfield
spellingShingle Johan A Kers
Anthony W DeFusco
Jae H Park
Jin Xu
Mark E Pulse
William J Weiss
Martin Handfield
OG716: Designing a fit-for-purpose lantibiotic for the treatment of Clostridium difficile infections.
PLoS ONE
author_facet Johan A Kers
Anthony W DeFusco
Jae H Park
Jin Xu
Mark E Pulse
William J Weiss
Martin Handfield
author_sort Johan A Kers
title OG716: Designing a fit-for-purpose lantibiotic for the treatment of Clostridium difficile infections.
title_short OG716: Designing a fit-for-purpose lantibiotic for the treatment of Clostridium difficile infections.
title_full OG716: Designing a fit-for-purpose lantibiotic for the treatment of Clostridium difficile infections.
title_fullStr OG716: Designing a fit-for-purpose lantibiotic for the treatment of Clostridium difficile infections.
title_full_unstemmed OG716: Designing a fit-for-purpose lantibiotic for the treatment of Clostridium difficile infections.
title_sort og716: designing a fit-for-purpose lantibiotic for the treatment of clostridium difficile infections.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description Lantibiotics continue to offer an untapped pipeline for the development of novel antibiotics. We report here the discovery of a novel lantibiotic for the treatment of C. difficile infection (CDI). The leads were selected from a library of over 300 multiple substitution variants of the lantibiotic Mutacin 1140 (MU1140). Top performers were selected based on testing for superior potency, solubility, manufacturability, and physicochemical and/or metabolic stability in biologically-relevant systems. The best performers in vitro were further evaluated orally in the Golden Syrian hamster model of CDAD. In vivo testing ultimately identified OG716 as the lead compound, which conferred 100% survival and no relapse at 3 weeks post infection. MU1140-derived variants are particularly attractive for further clinical development considering their novel mechanism of action.
url http://europepmc.org/articles/PMC5997364?pdf=render
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