dc.creatorCampos, Viviane Souza de
dc.creatorCalaza, Karin C.
dc.creatorAdesse, Daniel
dc.date2020-12-28T18:12:02Z
dc.date2020-12-28T18:12:02Z
dc.date2020
dc.date.accessioned2023-09-26T20:27:51Z
dc.date.available2023-09-26T20:27:51Z
dc.identifierCAMPOS, Viviane Souza de; CALAZA, Karin C.; ADESSE, Daniel. Implications of TORCH Diseases in Retinal Development—Special Focus on Congenital Toxoplasmosis. Frontiers in cellular and infection microbiology, v. 10, Article 585727, p. 1-17, Oct. 2020.
dc.identifier2235-2988
dc.identifierhttps://www.arca.fiocruz.br/handle/icict/45450
dc.identifier10.3389/fcimb.2020.585727
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8857488
dc.descriptionThere are certain critical periods during pregnancy when the fetus is at high risk for exposure to teratogens. Some microorganisms, including Toxoplasma gondii, are known to exhibit teratogenic effects, interfering with fetal development and causing irreversible disturbances. T. gondii is an obligate intracellular parasite and the etiological agent of Toxoplasmosis, a zoonosis that affects one third of the world's population. Although congenital infection can cause severe fetal damage, the injury extension depends on the gestational period of infection, among other factors, like parasite genotype and host immunity. This parasite invades the Central Nervous System (CNS), forming tissue cysts, and can interfere with neurodevelopment, leading to frequent neurological abnormalities associated with T. gondii infection. Therefore, T. gondii is included in the TORCH complex of infectious diseases that may lead to neurological malformations (Toxoplasmosis, Others, Rubella, Cytomegalovirus, and Herpes). The retina is part of CNS, as it is derived from the diencephalon. Except for astrocytes and microglia, retinal cells originate from multipotent neural progenitors. After cell cycle exit, cells migrate to specific layers, undergo morphological and neurochemical differentiation, form synapses and establish their circuits. The retina is organized in nuclear layers intercalated by plexus, responsible for translating and preprocessing light stimuli and for sending this information to the brain visual nuclei for image perception. Ocular toxoplasmosis (OT) is a very debilitating condition and may present high severity in areas in which virulent strains are found. However, little is known about the effect of congenital infection on the biology of retinal progenitors/ immature cells and how this infection may affect the development of this tissue. In this context, this study reviews the effects that congenital infections may cause to the developing retina and the cellular and molecular aspects of these diseases, with special focus on congenital OT.
dc.formatapplication/pdf
dc.languageeng
dc.publisherFrontiers Media
dc.rightsopen access
dc.subjectToxoplasmose congênita
dc.subjectToxoplasmose
dc.subjectDesenvolvimento da retina
dc.subjectToxoplasma gondii
dc.subjectInfecções congênitas
dc.subjectTeratogênese
dc.subjectTORCH
dc.subjectCongenital toxoplasmosis
dc.subjectToxoplasmosis
dc.subjectTORCH
dc.subjectRetinal development
dc.subjectToxoplasma gondii
dc.subjectCongenital infections
dc.subjectTeratogenesis
dc.titleImplications of TORCH Diseases in Retinal Development—Special Focus on Congenital Toxoplasmosis
dc.typeArticle


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