, Center for Diseases Control. Listeria outbreaks, 2017.

J. Thomas, N. Govender, and K. M. Mccarthy, Outbreak of listeriosis in South Africa Associated with processed meat, N Engl J Med, vol.382, issue.7, pp.632-643, 2020.
URL : https://hal.archives-ouvertes.fr/pasteur-02586017

E. Mylonakis, M. Paliou, and E. L. Hohmann, Listeriosis during pregnancy: a case series and review of 222 cases, Medicine (Baltimore), vol.81, pp.260-269, 2002.

J. Mclauchlin, Human listeriosis in Britain, 1967-85, a summary of 722 cases. 1. Listeriosis during pregnancy and in the newborn, Epidemiol Infect, vol.104, pp.181-189, 1990.

C. Charlier, E. Perrodeau, and A. Leclercq, Clinical features and prognostic factors of listeriosis: the MONALISA national prospective cohort study, Lancet Infect Dis, vol.17, pp.510-519, 2017.
URL : https://hal.archives-ouvertes.fr/pasteur-01475849

O. Disson, S. Grayo, and E. Huillet, Conjugated action of two species-specific invasion proteins for fetoplacental listeriosis, Nature, vol.455, issue.7216, pp.1114-1118, 2008.
URL : https://hal.archives-ouvertes.fr/pasteur-02456680

M. Lecuit, S. Vandormael-pournin, and J. Lefort, A transgenic model for listeriosis: role of internalin in crossing the intestinal barrier, Science, vol.292, pp.1722-1725, 2001.
URL : https://hal.archives-ouvertes.fr/pasteur-02456808

H. De-valk, C. Jacquet, and V. Goulet, Surveillance of listeria infections in Europe, Euro Surveill, vol.10, pp.251-255, 2005.

V. Goulet, H. De-valk, and O. Pierre, Effect of prevention measures on incidence of human listeriosis, Emerg Infect Dis, vol.7, pp.983-989, 1987.

D. Girard, A. Leclercq, and E. Laurent, Pregnancyrelated listeriosis in France, Euro Surveill, vol.9, issue.38, p.20909, 1984.
URL : https://hal.archives-ouvertes.fr/pasteur-02391783

H. De-valk, M. Tourdjman, and A. Leclercq, Changes in epidemiology and surveillance of listeriosis in France, International Symposium On Problems of Listeriosis

. Paris, Institut Pasteur, 2016.

B. J. Silk, K. A. Date, and K. A. Jackson, Invasive listeriosis in the Foodborne Diseases Active Surveillance Network (FoodNet), 2004-2009: further targeted prevention needed for higher-risk groups, Clin Infect Dis, vol.54, issue.5, pp.396-404, 2012.

Z. Herrador, A. Gherasim, and R. Lopez-velez, Listeriosis in Spain based on hospitalisation records, 1997 to 2015: need for greater awareness, Euro Surveill, p.24, 2019.

B. Alonso, E. Santamaria-del-tio, J. , F. Aizpuru, and E. M. , Listeriosis during the period 2003-2016, Rev Esp Enferm Dig, vol.110, pp.411-412, 2018.

P. J. Salama, P. Embarek, and J. Bagaria, Learning from listeria: safer food for all, Lancet, vol.391, pp.2305-2306, 2018.

, National Institute for communicable diseases, 2018.

H. Elinav, A. Hershko-klement, and I. Solt, Pregnancyassociated listeriosis: many beliefs, few facts, Lancet Infect Dis, vol.15, issue.10, pp.1128-1130, 2015.

H. Elinav, A. Hershko-klement, and L. Valinsky, Pregnancy-associated listeriosis: clinical characteristics and geospatial analysis of a 10-year period in Israel, Clin Infect Dis, vol.59, issue.7, pp.953-961, 2014.

R. Pouillot, K. Hoelzer, and K. A. Jackson, Relative risk of listeriosis in Foodborne Diseases Active Surveillance Network (FoodNet) sites according to age, pregnancy, and ethnicity, Clin Infect Dis, vol.54, issue.5, pp.405-415, 2012.

V. Goulet, M. Hebert, and C. Hedberg, Incidence of listeriosis and related mortality among groups at risk of acquiring listeriosis, Clin Infect Dis, vol.54, issue.5, pp.652-660, 2012.

I. A. Gillespie, P. Mook, and C. L. Little, association with neighbourhood deprivation, Euro Surveill, vol.15, issue.27, pp.7-16, 2001.

P. Mook, K. A. Grant, and C. L. Little, Emergence of pregnancy-related listeriosis amongst ethnic minorities in England and Wales, Euro Surveill, vol.15, issue.27, pp.17-23, 2010.

J. K. Haase, X. Didelot, and M. Lecuit, The ubiquitous nature of listeria monocytogenes clones: a large-scale multilocus sequence typing study, Environ Microbiol, vol.16, issue.2, pp.405-416, 2014.

M. Ragon, T. Wirth, and F. Hollandt, A new perspective on Listeria monocytogenes evolution, PLoS Pathog, vol.4, issue.9, p.1000146, 2008.

A. Moura, A. Criscuolo, and H. Pouseele, Whole genome-based population biology and epidemiological surveillance of Listeria monocytogenes, Nat Microbiol, vol.2, p.16185, 2016.
URL : https://hal.archives-ouvertes.fr/pasteur-01415883

M. M. Maury, H. Bracq-dieye, and L. Huang, Hypervirulent Listeria monocytogenes clones' adaption to mammalian gut accounts for their association with dairy products, Nat Commun, vol.10, issue.1, p.2488, 2019.
URL : https://hal.archives-ouvertes.fr/pasteur-02170796

M. M. Maury, Y. H. Tsai, and C. Charlier, Uncovering Listeria monocytogenes hypervirulence by harnessing its biodiversity, Nat Genet, vol.48, issue.3, pp.308-313, 2016.
URL : https://hal.archives-ouvertes.fr/pasteur-02170775

W. Li, L. Bai, and X. Ma, Sentinel listeriosis surveillance in selected hospitals, Emerg Infect Dis, vol.25, pp.2274-2277, 2019.

Z. Fan, J. Xie, and Y. Li, Listeriosis in mainland China: A systematic review, Int J Infect Dis, vol.81, pp.17-24, 2019.

E. Perez-trallero, C. Zigorraga, and J. Artieda, Two outbreaks of Listeria monocytogenes infection, Northern Spain. Emerg Infect Dis, vol.20, pp.2155-2157, 2014.

L. Luo, X. Chen, and M. Payne, Case report: whole genome sequencing based investigation of maternal-neonatal listeriosis in Sichuan, China, BMC Infect Dis, vol.19, p.893, 2019.

K. M. Angelo, K. A. Jackson, and K. K. Wong, Assessment of the Incubation Period for Invasive Listeriosis, Clin Infect Dis, vol.63, pp.1487-1489, 2016.

V. Goulet, L. A. King, and V. Vaillant, What is the incubation period for listeriosis?, BMC Infect Dis, vol.13, p.11, 2013.

K. S. Adriani, M. C. Brouwer, and A. Van-der-ende, Bacterial meningitis in pregnancy: report of six cases and review of the literature, Clin Microbiol Infect, vol.18, pp.345-351, 2012.

J. R. Robbins, K. M. Skrzypczynska, and V. B. Zeldovich, Placental syncytiotrophoblast constitutes a major barrier to vertical transmission of Listeria monocytogenes, PLoS Pathog, vol.6, p.1000732, 2010.

M. Lecuit, D. M. Nelson, and S. D. Smith, Targeting and crossing of the human maternofetal barrier by Listeria monocytogenes: role of internalin interaction with trophoblast E-cadherin, Proc Natl Acad Sci U S A, vol.101, pp.6152-6157, 2004.
URL : https://hal.archives-ouvertes.fr/pasteur-02456710

D. J. Platt, A. M. Smith, and N. Arora, Zika virus-related neurotropic flaviviruses infect human placental explants and cause fetal demise in mice, Sci Transl Med, vol.10, issue.426, p.7090, 2018.

M. Lecuit, S. Dramsi, and C. Gottardi, A single amino acid in E-cadherin responsible for host specificity towards the human pathogen Listeria monocytogenes, Embo J, vol.18, pp.3956-3963, 1999.
URL : https://hal.archives-ouvertes.fr/pasteur-02456831

N. Khelef, M. Lecuit, and H. Bierne, Species specificity of the Listeria monocytogenes InlB protein, Cell Microbiol, vol.8, pp.457-470, 2006.

A. M. Carter, Sources for comparative studies of placentation I. embryological collections, Placenta, vol.29, issue.1, pp.95-98, 2008.

D. E. Lowe, J. R. Robbins, and A. I. Bakardjiev, Animal and human tissue models of vertical listeria monocytogenes transmission and implications for other pregnancy-associated infections, Infect Immun, vol.86, issue.6, pp.801-818, 2018.

M. A. Smith, K. Takeuchi, and R. E. Brackett, Nonhuman primate model for Listeria monocytogenes-induced stillbirths, Infect Immun, vol.71, issue.3, pp.1574-1579, 2003.

M. A. Smith, K. Takeuchi, and G. Anderson, Dose-response model for Listeria monocytogenes-induced stillbirths in nonhuman primates, Infect Immun, vol.76, issue.2, pp.726-731, 2008.

B. Wolfe, G. J. Wiepz, and M. Schotzko, Acute fetal demise with first trimester maternal infection resulting from listeria monocytogenes in a nonhuman primate model, MBio, vol.8, issue.1, pp.1938-1954, 2017.

A. H. Pirie, Rodent Ulcer, Can Med Assoc J, vol.17, pp.1326-1328, 1927.

R. M. Roulo, J. D. Fishburn, and M. Amosu, Dose response of Listeria monocytogenes invasion, fetal morbidity, and fetal mortality after oral challenge in pregnant and nonpregnant Mongolian gerbils, Infect Immun, vol.82, issue.11, pp.4834-4841, 2014.

A. I. Bakardjiev, J. A. Theriot, and D. A. Portnoy, Listeria monocytogenes traffics from maternal organs to the placenta and back, PLoS Pathog, vol.2, issue.6, p.66, 2006.

C. Jacquet, M. Doumith, and J. I. Gordon, A Molecular Marker for Evaluating the Pathogenic Potential of Foodborne Listeria monocytogenes, J Infect Dis, vol.189, issue.11, pp.2094-2100, 2004.
URL : https://hal.archives-ouvertes.fr/hal-02683027

A. I. Bakardjiev, B. A. Stacy, and S. J. Fisher, Listeriosis in the pregnant guinea pig: a model of vertical transmission, Infect Immun, vol.72, issue.1, pp.489-497, 2004.

G. Gessain, Y. H. Tsai, and L. Travier, PI3-kinase activation is critical for host barrier permissiveness to Listeria monocytogenes, J Exp Med, vol.212, issue.2, pp.165-183, 2015.
URL : https://hal.archives-ouvertes.fr/pasteur-01128770

L. Monnier, A. Autret, N. Join-lambert, and O. F. , ActA is required for crossing of the fetoplacental barrier by Listeria monocytogenes, Infect Immun, vol.75, issue.2, pp.950-957, 2007.

K. Ireton, B. Payrastre, and H. Chap, A role for phosphoinositide 3-kinase in bacterial invasion, Science, vol.274, issue.5288, pp.780-782, 1996.

K. Ireton, B. Payrastre, and P. Cossart, The listeria monocytogenes protein InlB is an agonist of mammalian phosphoinositide 3-kinase, J Biol Chem, vol.274, issue.24, pp.17025-17032, 1999.

G. Nikitas, C. Deschamps, and O. Disson, Transcytosis of Listeria monocytogenes across the intestinal barrier upon specific targeting of goblet cell accessible E-cadherin, J Exp Med, vol.208, issue.11, pp.2263-2277, 2011.
URL : https://hal.archives-ouvertes.fr/pasteur-02040395

M. A. Hamon, D. Ribet, and F. Stavru, Listeriolysin O: the Swiss army knife of Listeria, Trends Microbiol, vol.20, issue.8, pp.360-368, 2012.
URL : https://hal.archives-ouvertes.fr/hal-02650867

A. I. Bakardjiev, B. A. Stacy, and D. A. Portnoy, Growth of listeria monocytogenes in the guinea pig placenta and role of cell-to-cell spread in fetal infection, J Infect Dis, vol.191, issue.11, pp.1889-1897, 2005.

C. Faralla, G. A. Rizzuto, and D. E. Lowe, Infect Immun, vol.84, issue.12, pp.3584-3596, 2016.

C. Faralla, E. E. Bastounis, and F. E. Ortega, Listeria monocytogenes InlP interacts with afadin and facilitates basement membrane crossing, PLoS Pathog, vol.14, issue.5, p.1007094, 2018.

I. Guleria and J. W. Pollard, The trophoblast is a component of the innate immune system during pregnancy, Nat Med, vol.6, issue.5, pp.589-593, 2000.

X. Qiu, L. Zhu, and J. W. Pollard, Colony-stimulating factor-1-dependent macrophage functions regulate the maternal decidua immune responses against Listeria monocytogenes infections during early gestation in mice, Infect Immun, vol.77, issue.1, pp.85-97, 2009.

J. H. Rowe, J. M. Ertelt, and M. N. Aguilera, Foxp3+ regulatory T cell expansion required for sustaining pregnancy compromises host defense against prenatal bacterial pathogens, Cell Host Microbe, vol.10, issue.1, pp.54-64, 2011.

J. H. Rowe, J. M. Ertelt, and L. Xin, Listeria monocytogenes cytoplasmic entry induces fetal wastage by disrupting maternal Foxp3+ regulatory T cell-sustained fetal tolerance, PLoS Pathog, vol.8, issue.8, p.1002873, 2012.

V. Chaturvedi, J. M. Ertelt, and T. T. Jiang, CXCR3 blockade protects against Listeria monocytogenes infectioninduced fetal wastage, J Clin Invest, vol.125, issue.4, pp.1713-1725, 2015.