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Treatment ofClostridium difficileinfection using SQ641, a capuramycin analogue, increases post-treatment survival and improves clinical measures of disease in a murine model
Author(s) -
John H. Moore,
Edward J. van Opstal,
Glynis L. Kolling,
Jae Hyun Shin,
Elena Bogatcheva,
B. V. Nikonenko,
Leo Einck,
Andrew J. Phipps,
Richard L. Guerrant,
Marina Protopopova,
Cirle A. Warren
Publication year - 2016
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkv479
Subject(s) - clostridium difficile , disease , microbiology and biotechnology , medicine , clostridiaceae , antibiotics , clostridium infections , immunology , biology , toxin
Clostridium difficile infection (CDI) is a primary cause of antibiotic-associated diarrhoeal illness. Current therapies are insufficient as relapse rates following antibiotic treatment range from 25% for initial treatment to 60% for treatment of recurrence. In this study, we looked at the efficacy of SQ641 in a murine model of CDI. SQ641 is an analogue of capuramycin, a naturally occurring nucleoside-based compound produced by Streptomyces griseus.

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