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Parallel Propagation of Toxoplasma gondii In Vivo, In Vitro and in Alternate Model: Towards Less Dependence on the Mice Model

dc.contributor.authorGargaté, Maria João
dc.contributor.authorVilares, Anabela
dc.contributor.authorFerreira, Idalina
dc.contributor.authorReis, Tânia
dc.contributor.authorMartins, Susana
dc.contributor.authorMendonça, Joana
dc.contributor.authorBorges, Vítor
dc.contributor.authorGomes, João Paulo
dc.date.accessioned2023-01-30T11:39:41Z
dc.date.available2023-01-30T11:39:41Z
dc.date.issued2022-09-13
dc.descriptionThis article belongs to the Special Issue Epidemiology and Management of Foodborne Parasitic Diseases.pt_PT
dc.description.abstractToxoplasma gondii is an obligate intracellular protozoan. In pregnant women, it can lead to severe birth defects or intrauterine death of the fetus. Most of what is currently know on cell biology of T. gondii comes from studies relying on the RH strain propagated in mice. According to the recommendations concerning the animal welfare, we assayed in vitro/in vivo procedures to replace, or at least reduce, the demanding animal model for strain propagation. We evaluated the genetic and phenotypic stability of the RH strain throughout its parallel continuous propagation in mice, in human foreskin fibroblasts (HFF) and in an alternate fashion of these two procedures. We also assessed the virulence impact on the RH strain after different periods of its long-term propagation strictly in cells. The RH strain completely lost its virulence after long-term passage in HFF. Nevertheless, we obtained a successful outcome with the alternate passaging of the parasite in HFF and in mice as this approach enabled T. gondii to maintain the evaluated phenotypic properties, mainly its virulence potential. Also, no genetic changes were observed in genes known to be highly polymorphic or involved in pathoadaptation. In conclusion, the alternate model seems to be a feasible method for T. gondii propagation and maintenance, strongly impacting the number of sacrificed mice.pt_PT
dc.description.sponsorshipThis research received no external funding. This study was funded by Infectious Diseases Department of National Institute of Health (NIH) Dr Ricardo Jorge, Portugal.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationPathogens. 2022 Sep 13;11(9):1038. doi: 10.3390/pathogens11091038.pt_PT
dc.identifier.doi10.3390/pathogens11091038pt_PT
dc.identifier.issn2076-0817
dc.identifier.urihttp://hdl.handle.net/10400.18/8468
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherMDPIpt_PT
dc.relation.publisherversionhttps://www.mdpi.com/2076-0817/11/9/1038pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subject3Rspt_PT
dc.subjectToxoplasma gondiipt_PT
dc.subjectIn vitro Propagationpt_PT
dc.subjectMice Modelpt_PT
dc.subjectStrain Propagationpt_PT
dc.subjectVirulencept_PT
dc.subjectInfecções Sistémicas e Zoonosespt_PT
dc.titleParallel Propagation of Toxoplasma gondii In Vivo, In Vitro and in Alternate Model: Towards Less Dependence on the Mice Modelpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue9pt_PT
oaire.citation.startPage1038pt_PT
oaire.citation.titlePathogenspt_PT
oaire.citation.volume11pt_PT
rcaap.embargofctAcesso de acordo com política editorial da revista.pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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