N. W. Charon and S. F. Goldstein, Genetics of motility and chemotaxis of a fascinating group of bacteria: the spirochetes, Annu. Rev. Genet, vol.36, pp.47-73, 2002.

F. Costa, J. E. Hagan, J. Calcagno, M. Kane, P. Torgerson et al., Global Morbidity and Mortality of Leptospirosis: a systematic Review, PLoS Negl. Trop. Dis, vol.9, p.3898, 2015.

C. Fontana, A. Lambert, N. Benaroudj, D. Gasparini, O. Gorgette et al., Analysis of a spontaneous non-motile and avirulent mutant shows that FliM is Required for full endoflagella assembly in Leptospira interrogans, PLoS ONE, vol.11, 2016.
URL : https://hal.archives-ouvertes.fr/pasteur-01435250

D. E. Fouts, M. A. Matthias, H. Adhikarla, B. Adler, D. E. Berg et al., What makes a bacterial species pathogenic? Comparative genomic analysis of the genus, Leptospira PLoS Negl. Trop. Dis, vol.10, p.4403, 2016.
URL : https://hal.archives-ouvertes.fr/pasteur-01436457

S. F. Goldstein and N. W. Charon, Motility of the spirochete Leptospira, Cell Motil. Cytoskeleton, vol.9, pp.101-110, 1988.

S. F. Goldstein and N. W. Charon, Multiple-exposure photographic analysis of a motile spirochete, Proc. Natl. Acad. Sci. U.S.A, vol.87, pp.4895-4899, 1990.

A. Lambert, M. Picardeau, D. A. Haake, R. W. Sermswan, A. Srikram et al., FlaA proteins in Leptospira interrogans are essential for motility and virulence but are not required for formation of the flagellum sheath, Infect. Immun, vol.80, pp.2019-2025, 2012.

C. Li, M. Sal, M. Marko, and N. W. Charon, Differential regulation of the multiple flagellins in spirochetes, J. Bacteriol, vol.192, pp.2596-2603, 2010.

S. Liao, A. Sun, D. M. Ojcius, S. Wu, J. Zhao et al., Inactivation of the fliY gene encoding a flagellar motor switch protein attenuates mobility and virulence of Leptospira interrogans strain Lai, BMC Microbiol, vol.9, p.253, 2009.

R. M. Macnab, How bacteria assemble flagella, Annu. Rev. Microbiol, vol.57, pp.77-100, 2003.

J. Malmström, M. Beck, A. Schmidt, V. Lange, E. W. Deutsch et al., Proteome-wide cellular protein concentrations of the human pathogen Leptospira interrogans, Nature, vol.460, pp.762-765, 2009.

D. N. Mastronarde, Automated electron microscope tomography using robust prediction of specimen movements, J. Struct. Biol, vol.152, pp.36-51, 2005.

M. J. Pallen, C. W. Penn, and R. R. Chaudhuri, Bacterial flagellar diversity in the post-genomic era, Trends Microbiol, vol.13, pp.143-149, 2005.

M. Picardeau, Conjugative transfer between Escherichia coli and Leptospira spp. as a new genetic tool, Appl. Environ. Microbiol, vol.74, pp.319-322, 2008.

M. Picardeau, Toolbox of molecular techniques for Studying Leptospira spp, Curr. Top. Microbiol. Immunol, 2017.

M. Picardeau, Virulence of the zoonotic agent of leptospirosis: still terra incognita?, Nat. Rev. Microbiol, vol.15, pp.297-307, 2017.

M. Picardeau, A. Brenot, and I. Girons, First evidence for gene replacement in Leptospira spp. Inactivation of L. biflexa flaB results in non-motile mutants deficient in endoflagella, Mol. Microbiol, vol.40, pp.189-199, 2001.

Z. Qin, W. T. Lin, S. Zhu, A. T. Franco, and J. Liu, Imaging the motility and chemotaxis machineries in Helicobacter pylori by cryo-electron tomography, J. Bacteriol, vol.199, pp.695-711, 2016.

F. San-martin, A. E. Mechaly, N. Larrieux, E. A. Wunder, A. Ko et al., Crystallization of FcpA from Leptospira, a novel flagellar protein that is essential for pathogenesis, Acta Crystallogr. F Struct. Biol. Commun, vol.73, pp.123-129, 2017.

S. H. Scheres, A Bayesian view on cryo-EM structure determination, J. Mol. Biol, vol.415, pp.406-418, 2012.

L. Slamti and M. Picardeau, Construction of a library of random mutants in the spirochete Leptospira biflexa using a mariner transposon, pp.169-176, 2012.

P. E. Stewart, J. A. Carroll, L. R. Olano, D. E. Sturdevant, and P. A. Rosa, multiple posttranslational modifications of Leptospira biflexa proteins as revealed by proteomic analysis, Appl. Environ. Microbiol, vol.82, pp.1183-1195, 2015.

K. Takabe, A. Kawamoto, H. Tahara, S. Kudo, and S. Nakamura, Implications of coordinated cell-body rotations for Leptospira motility, Biochem. Biophys. Res. Commun, vol.491, pp.1040-1046, 2017.

G. Tang, L. Peng, P. R. Baldwin, D. S. Mann, W. Jiang et al., EMAN2: an extensible image processing suite for electron microscopy, J. Struct. Biol, vol.157, pp.38-46, 2007.

P. R. Torgerson, J. E. Hagan, F. Costa, J. Calcagno, M. Kane et al., Global burden of Leptospirosis: estimated in terms of disability adjusted life years, PLoS Negl. Trop. Dis, vol.9, p.4122, 2015.

C. W. Wolgemuth, Flagellar motility of the pathogenic spirochetes, Semin. Cell Dev. Biol, vol.46, pp.104-112, 2015.

E. A. Wunder, C. P. Figueira, G. R. Santos, K. Lourdault, M. A. Matthias et al., Real-Time PCR reveals rapid dissemination of Leptospira interrogans after intraperitoneal and conjunctival inoculation of hamsters, Infect. Immun, vol.84, pp.2105-2115, 2016.

E. A. Wunder, C. P. Figueira, N. Benaroudj, B. Hu, B. A. Tong et al., A novel flagellar sheath protein, FcpA, determines filament coiling, translational motility and virulence for the Leptospira spirochete, Mol. Microbiol, vol.101, pp.457-470, 2016.

K. Yonekura, S. Maki-yonekura, and K. Namba, Complete atomic model of the bacterial flagellar filament by electron cryomicroscopy, Nature, vol.424, pp.643-650, 2003.

K. Zhang, Gctf: real-time CTF determination and correction, J. Struct. Biol, vol.193, pp.1-12, 2016.

X. Zhao, S. J. Norris, and J. Liu, Molecular architecture of the bacterial flagellar motor in cells, Biochemistry, vol.53, pp.4323-4333, 2014.

S. Zhu, T. Nishikino, B. Hu, S. Kojima, M. Homma et al., Molecular architecture of the sheathed polar flagellum in Vibrio alginolyticus, Proc. Natl. Acad. Sci. U.S.A, vol.114, pp.10966-10971, 2017.