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dc.rights.licenseopenen_US
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorBITEAU, Nicolas
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorASENCIO, Corinne
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorIZOTTE, Julien
dc.contributor.authorROUSSEAU, Benoit
dc.contributor.authorFÈVRE, Muriel
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorPILLAY, Davita
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorBALTZ, Théo
dc.date.accessioned2024-10-31T08:43:15Z
dc.date.available2024-10-31T08:43:15Z
dc.date.issued2016-01-01
dc.identifier.issn1935-2735en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/203069
dc.description.abstractEnTrypanosoma brucei gambiense, transmitted by the tsetse fly, is the main causative agent of Human African trypanosomosis in West Africa and poses a significant health risk to 70 million people. Disease progression varies depending on host immunity, but usually begins with a haemo-lymphatic phase, followed by parasite invasion of the central nervous system. In the current study, the tropism of T. b. gambiense 1135, causing a low level chronic 'silent' infection, was monitored in a murine model using bioluminescence imaging and PCR. A tropism to the reproductive organs, in addition to the central nervous system, after 12-18 months of infection was observed. Bioluminescent analysis of healthy females crossed with infected males showed that 50%, 62.5% and 37.5% of the female mice were subsequently positive for parasites in their ovaries, uteri and brain respectively. Although PCR confirmed the presence of parasites in the uterus of one of these mice, the blood of all mice was negative by PCR and LAMP. Subsequently, bioluminescent imaging of the offspring of infected female mice crossed with healthy males indicated parasites were present in the reproductive organs of both male (80%) and female (60%) offspring. These findings imply that transmission of T. b. gambiense 1135 occurs horizontally, most probably via sexual contact, and vertically in a murine model, which raises the possibility of a similar transmission in humans. This has wide reaching implications. Firstly, the observations made in this study are likely to be valid for wild animals acting as a reservoir for T. b. gambiense. Also, the reproductive organs may act as a refuge for parasites during drug treatment in a similar manner to the central nervous system. This could leave patients at risk of a relapse, ultimately allowing them to act as a reservoir for subsequent transmission by tsetse and possibly, horizontally and vertically.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enAnimals
dc.subject.enFemale
dc.subject.enGonads
dc.subject.enHumans
dc.subject.enInfectious Disease Transmission
dc.subject.enVertical
dc.subject.enMale
dc.subject.enMice
dc.subject.enSexually Transmitted Diseases
dc.subject.enTrypanosoma brucei gambiense
dc.subject.enTrypanosomiasis
dc.subject.enAfrican
dc.title.enTrypanosoma brucei gambiense Infections in Mice Lead to Tropism to the Reproductive Organs, and Horizontal and Vertical Transmission.
dc.title.alternativePLoS Negl Trop Disen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1371/journal.pntd.0004350en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed26735855en_US
bordeaux.journalPLoS Neglected Tropical Diseasesen_US
bordeaux.pagee0004350en_US
bordeaux.volume10en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue1en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04761367
hal.version1
hal.date.transferred2024-10-31T08:43:18Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLoS%20Neglected%20Tropical%20Diseases&rft.date=2016-01-01&rft.volume=10&rft.issue=1&rft.spage=e0004350&rft.epage=e0004350&rft.eissn=1935-2735&rft.issn=1935-2735&rft.au=BITEAU,%20Nicolas&ASENCIO,%20Corinne&IZOTTE,%20Julien&ROUSSEAU,%20Benoit&F%C3%88VRE,%20Muriel&rft.genre=article


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