F. Cazein, J. Pillonel, L. Strat, Y. Pinget, R. et al., Découvertes de séropositivité VIH et de sida, Bull Epidémiol Hebd, pp.9-10152, 2003.

R. Kampmeier, Identification of the Gonococcus by Albert Neisser, Sexually Transmitted Diseases, vol.5, issue.2, pp.71-73, 1978.
DOI : 10.1097/00007435-197804000-00010

J. Oriel, The history of non-gonococcal urethritis., Sexually Transmitted Infections, vol.72, issue.5, pp.374-383, 1996.
DOI : 10.1136/sti.72.5.374

B. Jones, Ocular Syndromes of TRIC Virus Infection and Their Possible Genital Significance, Sexually Transmitted Infections, vol.40, issue.1, pp.3-18, 1964.
DOI : 10.1136/sti.40.1.3

J. Schachter, G. Causse, and M. Tarizzo, Chlamydiae as agents of sexually transmitted diseases, Bull World Health Organ, vol.54, issue.3, p.245, 1976.

M. Favre, Sur l'étiologie de la lymphogranulomatose inguinale subaigue (ulcère vénérien adénogène) Presse Médicale, pp.651-653, 1924.

S. Bedson, C. Barwell, E. King, and L. Bishop, The Laboratory Diagnosis of Lymphogranuloma Venereum, Journal of Clinical Pathology, vol.2, issue.4, p.241, 1949.
DOI : 10.1136/jcp.2.4.241

W. Coutts and . Lymphogranuloma-venereum, A general review):545. 10. Beeson PB, Miller ES. Epidemiological Study of Lymphogranuloma Venereum, Employing the Complement-Fixation Test, Bull World Health Organ. Am J Public Health Nations Health, vol.234, issue.410, pp.1076-82, 1944.

E. Dunlop, I. Harper, M. Hussaini, J. Garland, J. Treharne et al., Relation of TRIC agent to « non-specific genital infection » Infection of urethra by TRIC agent in men presenting because of « non-specific » urethritis, Br J Vener Dis. Lancet, vol.42285, issue.27396, pp.77-87, 1965.

L. Page, Proposal for the recognition of two species in the genus Chlamydia Jones, Rake, and Stearns, 1945, International Journal of Systematic Bacteriology, vol.18, issue.1, pp.51-66, 1945.
DOI : 10.1099/00207713-18-1-51

S. Wang, J. Grayston, T. Ripa, L. Svensson, and L. Weström, Immunologic relationship between genital TRIC, lymphogranuloma venereum, and related organisms in a new microtiter indirect immunofluorescence test Chlamydia trachomatis Infection in Patients with Acute Salpingitis, 367?74. 15. Mårdh P-A, pp.1377-1386, 1970.

J. Rowley, I. Toskin, and F. Ndowa, World Health Organization, Reproductive Health and Research. Global incidence and prevalence of selected curable sexually transmitted infections World Health Organization, 2008.

J. Wasserheit, Epidemiological Synergy, Sexually Transmitted Diseases, vol.19, issue.2, pp.61-77, 1992.
DOI : 10.1097/00007435-199219020-00001

P. Mayaud, S. Hawkes, D. Mabey, H. Grosskurth, F. Mosha et al., Advances in control of sexually transmitted diseases in developing countries Impact of improved treatment of sexually transmitted diseases on HIV infection in rural Tanzania: randomised controlled trial):530?6. 22. Nicoll A. Assessing the impact of national anti-HIV sexual health campaigns: trends in the transmission of HIV and other sexually transmitted infections in England, Mayaud P. Interventions against sexually transmitted infections (STI) to prevent HIV infection242?7. 23. Renton AM, Whitaker L. Using STD occurrence to monitor AIDS prevention, pp.29-32, 1994.

L. Meyer, V. Goulet, V. Massari, and A. Lepoutre-toulemon, Surveillance of sexually transmitted diseases in France: recent trends and incidence., 15?21. 25. Nicoll A, Hamers FF. Are trends in HIV, gonorrhoea, and syphilis worsening in western Europe, pp.1324-1331, 1994.
DOI : 10.1136/sti.70.1.15

I. Martin, C. Ison, and L. Group, Rise in gonorrhoea in London, UK, The Lancet, vol.355, issue.9204, p.623, 2000.
DOI : 10.1016/S0140-6736(99)05495-1

V. Goulet, P. Sednaoui, A. Laporte, C. Billy, and J. Desenclos, The number of gonococcal infections identified by the RENAGO network is increasing, Euro Surveill, vol.5, issue.1, pp.13-28, 2000.

I. Stolte, N. Dukers, J. De-wit, J. Fennema, R. Coutinho et al., Increase in sexually transmitted infections among homosexual men in Amsterdam in relation to HAART HIV treatments optimism and sexual behaviour among gay men in Sydney and Melbourne, 184?6. 29. Van de Ven P, pp.2289-94, 1999.

C. Scieux, R. Barnes, A. Bianchi, I. Casin, P. Morel et al., Lymphogranuloma venereum: 27 cases in Paris Infection with Chlamydia trachomatis Lymphogranuloma Venereum Serovar L1 in Homosexual Men with Proctitis: Molecular Analysis of an Unusual Case Cluster, J Infect Dis. Clin Infect Dis, vol.16020, issue.43, pp.576-81, 1989.

R. Nieuwenhuis, J. Ossewaarde, W. Van-der-meijden, H. Neumann, J. Ossewaarde et al., Unusual presentation of early lymphogranuloma venereum in an HIV-1 infected patient: effective treatment with 1 g azithromycin Resurgence of Lymphogranuloma Venereum in Western Europe: An Outbreak of Chlamydia trachomatis Serovar L2 Proctitis in The Netherlands among Men Who Have Sex with Men, Sex Transm Infect. Clin Infect Dis, vol.7939, issue.67, pp.996-1003, 2003.

M. De-laar, K. Fenton, C. Ison, M. Herida, B. De-barbeyrac et al., European Surveillance of Sexually Transmitted Infections (ESSTI) Update on the European lymphogranuloma venereum epidemic among men who have sex with men Rectal lymphogranuloma venereum surveillance in France, Preliminary report of an outbreak of lymphogranuloma venereum in homosexual men in the Netherlands, pp.2367-2402, 2004.

J. Spaargaren, H. Fennema, S. Morré, H. De-vries, and R. Coutinho, New lymphogranuloma venereum Chlamydia trachomatis variant, Amsterdam. Emerg Infect Dis. juill, vol.11, issue.7, pp.1090-1092, 2005.

J. Spaargaren, J. Schachter, J. Moncada, D. Vries, H. Fennema et al., Slow Epidemic of Lymphogranuloma Venereum L2b Strain, Emerging Infectious Diseases, vol.11, issue.11, 2005.
DOI : 10.3201/eid1111.050821

URL : http://doi.org/10.3201/eid1111.050821

. Institut-de-veille-sanitaire, Lutte contre le VIH/sida et les infections sexuellement transmissibles en France ? 10 ans de surveillance, 1996.

. Institut-de-veille-sanitaire, Comment surveiller les IST ? Disponible sur: http://www.invs.sante.fr/Dossiers-thematiques/Maladies- infectieuses/VIH-sida-IST/Infections-sexuellement-transmissibles-IST, 2009.

. Institut-de-veille-sanitaire, Bulletins des réseaux de surveillance des IST -Données au 31, 2014.

]. Internet, Disponible surBilan-R%C3%A9seau-LGV-Ann%C3%A9e-20142.pdf 44 Réseau de surveillance des infections ano-rectales à Chlamydia trachomatis (CT) Résultats en France, 2010.

O. Peuchant, C. Baldit, L. Roy, C. Trombert-paolantoni, S. Clerc et al., First case of Chlamydia trachomatis L2b proctitis in a woman Évolution du nombre de lymphogranulomatoses vénériennes rectales et d'infections rectales à Chlamydia trachomatis à souches non L en France Did L Strains Responsible for Lymphogranuloma Venereum Proctitis Spread Among People With Genital Chlamydia trachomatis Infection in France in 2013, E21?3. 46. Clerc M374?6. 48. Nunes A, Gomes JP. Evolution, phylogeny, and molecular epidemiology of Chlamydia, pp.49-64, 2002.

Y. Abdel-rahman, R. Belland, C. Elwell, J. Engel, and R. Valdivia, The chlamydial developmental cycle New insights into Chlamydia intracellular survival mechanisms, ):949?59. 50. Bastidas RJ):a010256?a010256. 51. Cocchiaro JL, pp.1571-1579, 2005.

R. Stephens, S. Kalman, C. Lammel, J. Fan, R. Marathe et al., Genome sequence of an obligate intracellular pathogen of humans: Chlamydia trachomatis Interstrain Gene Transfer in Chlamydia trachomatis In Vitro: Mechanism and Significance Chlamydia cell biology and pathogenesis All subtypes of the Pmp adhesin family are implicated in chlamydial virulence and show species-specific function Making connections: snapshots of chlamydial type III secretion systems in contact with host membranes, Schoborg RV. Chlamydia persistence ? a tool to dissect chlamydia?host interactions. Microbes Infect754?9. 54. DeMars R544?56. 57. Dumoux M, Nans A,1?7. 58. Tang L, pp.649-62, 1998.

K. Moelleken and J. Hegemann, The Chlamydia outer membrane protein OmcB is required for adhesion and exhibits biovar-specific differences in glycosaminoglycan binding, Molecular Microbiology, vol.69, issue.Suppl. 3, pp.403-422, 2007.
DOI : 10.1111/j.1365-2958.2007.06050.x

F. Almeida, V. Borges, R. Ferreira, M. Borrego, J. Gomes et al., Polymorphisms in Inc Proteins and Differential Expression of inc Genes among Chlamydia trachomatis Strains Correlate with Invasiveness and Tropism of Lymphogranuloma Venereum Isolates Assessment of the load and transcriptional dynamics of Chlamydia trachomatis plasmid according to strains' tissue tropism, 6574?85. 63, pp.333-342, 2012.

J. Schachter, J. Moncada, . Lymphogranuloma-venereum, V. Borges, J. Gomes et al., How to Turn an Endemic Disease Into an Outbreak of a New Disease? Start Looking Deep comparative genomics among Chlamydia trachomatis lymphogranuloma venereum isolates highlights genes potentially involved in pathoadaptation Genital Chlamydia trachomatis: Understanding the Roles of Innate and Adaptive Immunity in Vaccine Research, ):331?2. 65, pp.346-70, 2005.

K. Redgrove, E. Mclaughlin, I. Simms, A. S. Eastick, K. Hughes et al., The Role of the Immune Response in Chlamydia trachomatis Infection of the Male Genital Tract: A Double-Edged Sword 68. de Vrieze NHN, van Rooijen M, Schim van der Loeff MF, de Vries HJC. Anorectal and inguinal lymphogranuloma venereum among men who have sex with men in Amsterdam, The Netherlands: trends over time, symptomatology and concurrent infections Rapid increase in lymphogranuloma venereum in men who have sex with men, Front Immunol. Sex Transm Infect. Euro Surveill, vol.58920, issue.748, 2003.

A. Broadbent, P. Horner, G. Wills, A. Ling, R. Carzaniga et al., HIV-1 does not significantly influence Chlamydia trachomatis serovar L2 replication in vitro, 575?84. 71. de Leng WWJ, Jansen M, 2011.
DOI : 10.1016/j.micinf.2011.01.019

J. Schachter and A. Osoba, LYMPHOGRANULOMA VENEREUM, British Medical Bulletin, vol.39, issue.2, pp.151-155, 1983.
DOI : 10.1093/oxfordjournals.bmb.a071807

D. Mabey and R. Peeling, Lymphogranuloma venereum, Sexually Transmitted Infections, vol.78, issue.2, pp.90-92, 2002.
DOI : 10.1136/sti.78.2.90

W. Stamm, Chlamydial infections -Lymphogranuloma Venereum In: Harrison's Principles of Internal Medicine. 17th éd. Mc Graw Hill, pp.1073-1077, 2008.

B. Malisiewicz, H. Schöfer, . Diagnostik-und-behandlung-genitoanaler-ulzera-infektiöser-genese, J. Nougué, S. Gupta et al., Lymphogranulomatose vénérienne : nouveau sérovariant L2b et ancien « signe de la poulie Genital elephantiasis and sexually transmitted infections?revisited, 19?29. 76. de Lavaissière M153?5. 77, pp.157-66, 2006.

A. Grace and . Anorectal-lymphogranuloma-venereum, ):74. 79. de Vrieze NHN, de Vries HJC. Lymphogranuloma venereum among men who have sex with men. An epidemiological and clinical review, J Am Med Assoc. Expert Rev Anti Infect Ther, vol.12212, issue.26, pp.697-704, 1943.

J. Hechtman, C. Dimaio, J. Matloff, N. Harpaz, H. Zhu et al., Rectal lymphogranuloma venereum mimicking cancer Rectal Lymphogranuloma Venereum in HIV-infected Patients Can Mimic Lymphoma A Case of Late-Stage Lymphogranuloma Venereum in a Woman in Europe Spontaneous pharyngeal Chlamydia trachomatis RNA clearance. A cross-sectional study followed by a cohort study of untreated STI clinic patients in Amsterdam, The Netherlands, ):414?6. 82. Lázaro MJ,792?3. 83. van Rooijen MS180?1. 85. CEDEF. Ulcération ou érosion des muqueuses orales et/ou génitales, p.24, 2009.

K. Workowski and G. Bolan, Sexually transmitted diseases treatment guidelines, 2015, Centers for Disease Control and Prevention MMWR Recomm Rep, vol.64, pp.1-137, 2015.

M. Chernesky, The laboratory diagnosis of Chlamydia trachomatis infections Diagnostic biologique de l'infection à Chlamydia trachomatis -Document d'avis [Internet]. [cité 10 juill 2016]. Disponible sur: http://www.hassante .fr/portail/upload/docs/application/pdf/2010-10/chlamydia_-_document_davis.pdf 89 Recommendations for the laboratorybased detection of Chlamydia trachomatis and Neisseria gonorrhoeae--2014, 39?44. 88, pp.21-40, 2005.

A. Costa, S. Tabrizi, D. Whiley, and J. Twin, Disponible sur: http://www.codage.ext.cnamts.fr/f_mediam/fo/nabm/DOC.pdf 91 Evaluation du dépistage des infections uro-génitales basses à Chlamydia trachomatis en France Opportunities and pitfalls of molecular testing for detecting sexually transmitted pathogens, Biologie Médicale -Nomenclature des Actes [Internet]. [cité 10 juill 2016, pp.219-245, 2015.

M. Unemo, I. Clarke, C. Kent, J. Chaw, W. Wong et al., The Swedish new variant of Chlamydia trachomatis Prevalence of rectal, urethral, and pharyngeal chlamydia and gonorrhea detected in 2 clinical settings among men who have sex with men, ):62?9. 94, pp.67-74, 2003.

J. Schachter, J. Moncada, S. Liska, C. Shayevich, and J. Klausner, Nucleic Acid Amplification Tests in the Diagnosis of Chlamydial and Gonococcal Infections of the Oropharynx and Rectum in Men Who Have Sex With Men, Sexually Transmitted Diseases, vol.35, issue.7, pp.637-679, 2008.
DOI : 10.1097/OLQ.0b013e31817bdd7e

L. Cosentino, T. Campbell, A. Jett, I. Macio, T. Zamborsky et al., Use of Nucleic Acid Amplification Testing for Diagnosis of Anorectal Sexually Transmitted Infections, Journal of Clinical Microbiology, vol.50, issue.6
DOI : 10.1128/JCM.00185-12

W. Li, D. Raoult, and P. Fournier, Bacterial strain typing in the genomic era, 892?916. 98. Harris SR, 2009.
DOI : 10.1111/j.1574-6976.2009.00182.x

P. Lnã¸, B. Herrmann, and J. Mã¸ller, Typing Chlamydia trachomatis : from egg yolk to nanotechnology, FEMS Immunol Med Microbiol, vol.55, issue.2, pp.120-150, 2009.

P. Rodriguez, A. Vekris, D. Barbeyrac, B. Dutilh, B. Bonnet et al., Typing of Chlamydia trachomatis by restriction endonuclease analysis of the amplified major outer membrane protein gene, J Clin Microbiol, vol.29, issue.6, pp.1132-1138, 1991.

S. Morré, J. Ossewaarde, J. Lan, G. Van-doornum, J. Walboomers et al., Serotyping and genotyping of genital Chlamydia trachomatis isolates reveal variants of serovars Ba, G, and J as confirmed by omp1 nucleotide sequence analysis, J Clin Microbiol, vol.36, issue.2, pp.345-51, 1998.

C. Yang, I. Maclean, and R. Brunham, DNA Sequence Polymorphism of the Chlamydia trachomatis omp1 Gene, Journal of Infectious Diseases, vol.168, issue.5, pp.1225-1255, 1993.
DOI : 10.1093/infdis/168.5.1225

S. Morré, J. Spaargaren, J. Fennema, H. De-vries, R. Coutinho et al., Real-time Polymerase Chain Reaction To Diagnose Lymphogranuloma Venereum, Emerging Infectious Diseases, vol.11, issue.8, pp.1311-1313, 2005.
DOI : 10.3201/eid1108.050535

N. Macdonald, A. Sullivan, P. French, J. White, G. Dean et al., Risk factors for rectal lymphogranuloma venereum in gay men: results of a multicentre case-control study in the UK, Sexually Transmitted Infections, vol.64, issue.4, pp.262-270, 2014.
DOI : 10.1136/sextrans-2013-051404

J. Lan, J. Ossewaarde, J. Walboomers, C. Meijer, and A. Van-den-brule, Improved PCR sensitivity for direct genotyping of Chlamydia trachomatis serovars by using a nested PCR, J Clin Microbiol, vol.32, issue.2, pp.528-558, 1994.

F. Corpet, Multiple sequence alignment with hierarchical clustering, Nucleic Acids Research, vol.16, issue.22, pp.10881-90, 1988.
DOI : 10.1093/nar/16.22.10881

URL : http://doi.org/10.1093/nar/16.22.10881

B. Kendall, K. Tardif, and R. Schlaberg, variants, USA, Sexually Transmitted Infections, vol.16, issue.4, pp.336-336, 2014.
DOI : 10.1136/sextrans-2013-051478

M. Rodríguez-domínguez, T. Puerta, B. Menéndez, J. González-alba, C. Rodríguez et al., Clinical and epidemiological characterization of a lymphogranuloma venereum outbreak in Madrid, Spain: co-circulation of two variants, Clinical Microbiology and Infection, vol.20, issue.3, pp.219-244, 2014.
DOI : 10.1111/1469-0691.12256

F. Jin, G. Prestage, D. Templeton, I. Poynten, B. Donovan et al., The Impact of HIV Seroadaptive Behaviors on Sexually Transmissible Infections in HIV-Negative Homosexual Men in Sydney, Australia, Sexually Transmitted Diseases, vol.39, issue.3, pp.191-195, 2012.
DOI : 10.1097/OLQ.0b013e3182401a2f

H. Ward, A. S. Carder, C. Dean, G. French, P. Ivens et al., The prevalence of lymphogranuloma venereum infection in men who have sex with men: results of a multicentre case finding study, Sexually Transmitted Infections, vol.85, issue.3, pp.173-178, 2009.
DOI : 10.1136/sti.2008.035311

URL : https://hal.archives-ouvertes.fr/hal-00552809

C. Saxon, G. Hughes, C. Ison, U. For-the, and . Group, Asymptomatic Lymphogranuloma Venereum in Men who Have Sex with Men

L. Christerson, H. De-vries, B. De-barbeyrac, C. Gaydos, B. Henrich et al., Strains, Emerging Infectious Diseases, vol.16, issue.11, pp.1777-1786, 2010.
DOI : 10.3201/eid1611.100379

A. Touati, O. Peuchant, N. Hénin, C. Bébéar, and B. De-barbeyrac, The L2b real-time PCR targeting the pmpH gene of Chlamydia trachomatis used for the diagnosis of lymphogranuloma venereum is not specific to L2b strains, Clinical Microbiology and Infection, vol.22, issue.6, pp.574-581, 2016.
DOI : 10.1016/j.cmi.2016.03.018

M. Mati?i?, I. Klavs, J. Vide?nik, V. Zorman, D. Vovko et al., Confirmed inguinal lymphogranuloma venereum genovar L2c in a man who had sex with men, Slovenia, 2015, Eurosurveillance, vol.21, issue.5, p.30129, 2015.
DOI : 10.2807/1560-7917.ES.2016.21.5.30129

O. Dosekun, S. Edmonds, S. Stockwell, P. French, and J. White, Lymphogranuloma venereum detected from the pharynx in four London men who have sex with men, International Journal of STD & AIDS, vol.24, issue.6, pp.495-501, 2013.
DOI : 10.1177/0956462412472830

E. Oud, N. De-vrieze, A. De-meij, and H. De-vries, Pitfalls in the diagnosis and management of inguinal lymphogranuloma venereum: important lessons from a case series, Sexually Transmitted Infections, vol.85, issue.4, pp.279-82, 2014.
DOI : 10.1136/sextrans-2013-051427

J. Rowley, I. Toskin, and F. Ndowa, World Health Organization, Reproductive Health and Research. Global incidence and prevalence of selected curable sexually transmitted infections, World Health, 2008.

T. Hannu, Reactive arthritis, Best Practice & Research Clinical Rheumatology, vol.25, issue.3, pp.347-57, 2011.
DOI : 10.1016/j.berh.2011.01.018

N. De-vrieze and H. De-vries, Lymphogranuloma venereum among men who have sex with men. An epidemiological and clinical review, Expert Review of Anti-infective Therapy, vol.12, issue.6, pp.697-704, 2014.
DOI : 10.1586/14787210.2014.901169

H. Zeidler and A. Hudson, New insights into Chlamydia and arthritis. Promise of a cure?

J. Spaargaren, H. Fennema, S. Morré, H. De-vries, and R. Coutinho, New lymphogranuloma venereum Chlamydia trachomatis variant, Amsterdam. Emerg Infect Dis. juill, vol.11, issue.7, pp.1090-1092, 2005.

]. Internet, I. Simms, A. S. Eastick, K. Hughes, G. Field et al., Disponible sur: http://www.cnrchlamydiae.u-bordeaux2.fr/wp- content/uploads Rapid increase in lymphogranuloma venereum in men who have sex with men, 2003.