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Fidaxomicin reduces early toxin A and B production and sporulation in Clostridium difficile in vitro
Author(s) -
Michael J. Aldape,
Aaron Eugene Packham,
Dustin Heeney,
Savannah Nicole Rice,
Amy E. Bryant,
Dennis L. Stevens
Publication year - 2017
Publication title -
journal of medical microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.91
H-Index - 117
eISSN - 1473-5644
pISSN - 0022-2615
DOI - 10.1099/jmm.0.000580
Subject(s) - fidaxomicin , clostridium difficile , microbiology and biotechnology , biology , antibiotics , spore , virulence , clostridium difficile toxin a , toxin , vancomycin , bacteria , staphylococcus aureus , gene , biochemistry , genetics
Fidaxomicin, a macrocyclic antibiotic, has been approved for the treatment of Clostridium difficile infection (CDI). Previous work by our group has demonstrated that some antibiotics at sub-inhibitory concentrations stimulate early toxin production and sporulation by C. difficile. Prior studies revealed that fidaxomicin, when added to late stationary-phase organisms, reduced exotoxin production and spore formation by C. difficile. However, the ability of fidaxomicin to trigger early virulence factor production and spore formation has never been investigated.

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