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Volume 22, Number 9—September 2016
Research

Enterohemorrhagic Escherichia coli Hybrid Pathotype O80:H2 as a New Therapeutic Challenge

Nurcan Soysal, Patricia Mariani-Kurkdjian, Yasmine Smail, Sandrine Liguori, Malika Gouali, Estelle Loukiadis, Patrick Fach, Mathias Bruyand, Jorge Blanco, Philippe Bidet, and Stéphane BonacorsiComments to Author 
Author affiliations: Centre Hospitalo-Universitaire Robert-Debré (AP-HP), Paris, France (N. Soysal, P. Mariani-Kurkdjian, Y. Smail, S. Liguori, P. Bidet, S. Bonacorsi); Institut National de la Santé et de la Recherche Médicale, Paris (N. Soysal, P. Mariani-Kurkdjian, P. Bidet, S. Bonacorsi); Université Paris Diderot, Paris (N. Soysal, P. Mariani-Kurkdjian, P. Bidet, S. Bonacorsi); Institut Pasteur, Paris (M. Gouali); Laboratoire National de Réference pour les Escherichia coli, Marcy l’Etoile, France (E. Loukiadis); ANSES, Maison-Alfort, France (P. Fach); Institut de Veille Sanitaire, Saint Maurice, France (M. Bruyand); Universidade de Santiago de Compostela, Lugo, Spain (J. Blanco)

Main Article

Figure 5

Relative production rate of Shiga toxin produced in 5 strains of enterohemorrhagic Escherichia coli (4 O80 strains and 1 O157 strain) at subinhibitory concentrations of azithromycin, ciprofloxacin, and ceftriaxone, compared with basal production rate (no antibiotics), France, January 2005–October 2014. A) Isolate 35344. B) Isolate 33115. C) Isolate 35431. D) Isolate 36047. E) Isolate EDL933.

Figure 5. Relative production rate of Shiga toxin produced in 5 strains of enterohemorrhagic Escherichia coli (4 O80 strains and 1 O157 strain) at subinhibitory concentrations of azithromycin, ciprofloxacin, and ceftriaxone, compared with basal production rate (no antibiotics), France, January 2005–October 2014. A) Isolate 35344. B) Isolate 33115. C) Isolate 35431. D) Isolate 36047. E) Isolate EDL933. Error bars indicate SDs.

Main Article

Page created: August 16, 2016
Page updated: August 16, 2016
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