M
Maryse Gibert
Researcher at Pasteur Institute
Publications - 42
Citations - 4364
Maryse Gibert is an academic researcher from Pasteur Institute. The author has contributed to research in topics: Clostridium perfringens & Actin cytoskeleton. The author has an hindex of 31, co-authored 42 publications receiving 4103 citations.
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Journal ArticleDOI
Clostridium perfringens: toxinotype and genotype
TL;DR: Toxin genotyping is more reliable than the classical toxinotyping for identifying pathovars involved in a specific disease and to define vaccine requirements.
Journal ArticleDOI
Comparative genome and phenotypic analysis of Clostridium difficile 027 strains provides insight into the evolution of a hypervirulent bacterium
Richard A. Stabler,Miao-Xia He,Lisa F. Dawson,Melissa J. Martin,Esmeralda Valiente,Craig Corton,Trevor D. Lawley,Mohammed Sebaihia,Michael A. Quail,Graham Rose,Dale N. Gerding,Maryse Gibert,Michel R. Popoff,Julian Parkhill,Gordon Dougan,Brendan W. Wren +15 more
TL;DR: This study provides genetic markers for the identification of 027 strains and offers a unique opportunity to explain the recent emergence of a hypervirulent bacterium.
Journal ArticleDOI
Production of actin‐specific ADP‐ribosyltransferase (binary toxin) by strains of Clostridium difficile
Simon L. J. Stubbs,Maja Rupnik,Maryse Gibert,Jon S. Brazier,Brian I. Duerden,Michel R. Popoff +5 more
TL;DR: Results indicate that 6.4% of toxigenic isolates of C. difficile referred to the Anaerobe Reference Unit from UK hospitals have cdtA and cdtB genes.
Journal ArticleDOI
Production of a complete binary toxin (actin-specific ADP-ribosyltransferase) by Clostridium difficile CD196.
TL;DR: The results indicate that some C. difficile strains synthesize a binary toxin that could be an additional virulence factor, similar to other clostridial binary toxins.
Journal ArticleDOI
Beta2 toxin, a novel toxin produced by Clostridium perfringens.
TL;DR: A novel toxin (Beta2) and its gene were characterized from a Clostridium perfringens strain isolated from a piglet with necrotic enteritis, and sequence homology with alpha-toxin, gamma-t toxin, and leukocidin of Staphylococcus aureus is revealed.