Corrigendum: Heterogeneous Family of Cyclomodulins: Smart Weapons That Allow Bacteria to Hijack the Eukaryotic Cell Cycle and Promote Infections

Affiliations

¹ STLO, Agrocampus Ouest Rennes, Institut National de la Recherche AgronomiqueRennes, France.
² Departamento de Biologia Geral, Laboratório de Genética Celular e Molecular, Instituto de Ciências Biológicas, Universidade Federal de Minas GeraisBelo Horizonte, Brazil.
³ HistoPathologie et Modèles Animaux/Pathogénie des Toxi-Infections Bactériennes, Institut PasteurParis, France.
⁴ CHU Purpan USC INRA 1360-CPTP, U1043 Institut National de la Santé et de la Recherche Médicale, Pathogénie Moléculaire et Cellulaire des Infections à Escherichia coliToulouse, France.
⁵ International Center for Infectiology ResearchLyon, France.
⁶ Centre National de la Recherche Scientifique, UMR5308, Institut National de la Santé et de la Recherche Médicale U1111, Ecole Normale Supérieure de Lyon, Université Lyon 1Lyon, France.
⁷ Département de Biologie, Institut des Agents Infectieux, Hospices Civils de LyonLyon, France.

Published Erratum

Rachid A El-Aouar Filho et al. Front Cell Infect Microbiol. 2017.

. 2017 Aug 14:7:364.

doi: 10.3389/fcimb.2017.00364. eCollection 2017.

¹ STLO, Agrocampus Ouest Rennes, Institut National de la Recherche AgronomiqueRennes, France.
² Departamento de Biologia Geral, Laboratório de Genética Celular e Molecular, Instituto de Ciências Biológicas, Universidade Federal de Minas GeraisBelo Horizonte, Brazil.
³ HistoPathologie et Modèles Animaux/Pathogénie des Toxi-Infections Bactériennes, Institut PasteurParis, France.
⁴ CHU Purpan USC INRA 1360-CPTP, U1043 Institut National de la Santé et de la Recherche Médicale, Pathogénie Moléculaire et Cellulaire des Infections à Escherichia coliToulouse, France.
⁵ International Center for Infectiology ResearchLyon, France.
⁶ Centre National de la Recherche Scientifique, UMR5308, Institut National de la Santé et de la Recherche Médicale U1111, Ecole Normale Supérieure de Lyon, Université Lyon 1Lyon, France.
⁷ Département de Biologie, Institut des Agents Infectieux, Hospices Civils de LyonLyon, France.

Abstract

[This corrects the article on p. 208 in vol. 7, PMID: 28589102.].

Keywords: bacterial toxins; colonization; cyclomodulins; eukaryotic cell cycle alteration; infective efficiency; invasion; reduced host response.

Heterogeneous Family of Cyclomodulins: Smart Weapons That Allow Bacteria to Hijack the Eukaryotic Cell Cycle and Promote Infections.
El-Aouar Filho RA, Nicolas A, De Paula Castro TL, Deplanche M, De Carvalho Azevedo VA, Goossens PL, Taieb F, Lina G, Le Loir Y, Berkova N. El-Aouar Filho RA, et al. Front Cell Infect Microbiol. 2017 May 23;7:208. doi: 10.3389/fcimb.2017.00208. eCollection 2017. Front Cell Infect Microbiol. 2017. PMID: 28589102 Free PMC article. Review.

1. Basler M., Masin J., Osicka R., Sebo P. (2006). Pore-forming and enzymatic activities of Bordetella pertussis adenylate cyclase toxin synergize in promoting lysis of monocytes. Infect. Immun. 74, 2207–2214. 10.1128/IAI.74.4.2207-2214.2006 - DOI - PMC - PubMed
1. Carbonetti N. H. (2010). Pertussis toxin and adenylate cyclase toxin: key virulence factors of Bordetella pertussis and cell biology tools. Future Microbiol. 5, 455–469. 10.2217/fmb.09.133 - DOI - PMC - PubMed
1. Eby J. C., Ciesla W. P., Hamman W., Donato G. M., Pickles R. J., Hewlett E. L., et al. . (2010). Selective Translocation of the Bordetella pertussis adenylate cyclase toxin across the basolateral membranes of polarized epithelial cells. J. Biol. Chem. 285, 10662–10670. 10.1074/jbc.M109.089219 - DOI - PMC - PubMed
1. Glaser P., Sakamoto H., Bellalou J., Ullmann A., Danchin A. (1988). Secretion of cyclolysin, the calmodulin-sensitive adenylate cyclase-haemolysin bifunctional protein of Bordetella pertussis. EMBO J. 7, 3997–4004. - PMC - PubMed
1. Guermonprez P., Khelef N., Blouin E., Rieu P., Ricciardi-Castagnoli P., Guiso N., et al. . (2001). The adenylate cyclase toxin of Bordetella pertussis binds to target cells via the αMβ2gf integrin (CD11b/CD18). J. Exp. Med. 193, 1035–1044. 10.1084/jem.193.9.1035 - DOI - PMC - PubMed