Literature DB >> 10448664

Infection with Toxoplasma gondii RH and Prugniaud strains in mice, rats and nude rats: kinetics of infection in blood and tissues related to pathology in acute and chronic infection.

L Zenner1, A Foulet, Y Caudrelier, F Darcy, B Gosselin, A Capron, M F Cesbron-Delauw.   

Abstract

Since mice and rats are the most studied models of experimental toxoplasmosis, the aim of this work was to analyze the outcome of Toxoplasma infection in mice, rats and congenitally athymic nude rats; for this purpose, the parasitic load in different organs and the anatomic-pathological characteristics of infection were investigated in these animals. The data obtained after infection with two different strains and stages of Toxoplasma gondii (RH tachyzoites and Prugniaud cysts) concerned the following organs: brain, mesenteric lymph nodes, blood, spleen, heart, lungs, diaphragm and liver. In Fischer rats, the infection with either the Prugniaud or the RH strains displayed similar characteristics: after a peak in the parasite load, a complete disappearance of parasites was observed, except in the brain of Prugniaud strain-infected rats where toxoplasmas were evidenced throughout the experiment. In OF1 mice, where infection by the RH tachyzoites was lethal, infection with the Prugniaud strain led to survival; the parasitic burden peaked in the different organs and was then undetectable, except in the brain where toxoplasmas were still present during the chronic phase. Like mice, nude rats did not survive to the RH infection. Interestingly, for all the animals the observed histopathological changes in the infected organs, although more or less obvious in the acute phase, were not very severe in almost all cases. For instance, mice, although more susceptible to infection than rats, did not present more severe lesions. They consisted in a discrete inflammation with some focal areas of necrosis in some organs such as brain, liver and heart. Our results support the assumption that rats and nude rats constitute interesting experimental models relevant to either human acute toxoplasmosis, chronic toxoplasmosis, or disseminated toxoplasmosis in AIDS patients.

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Year:  1999        PMID: 10448664     DOI: 10.1016/S0344-0338(99)80051-X

Source DB:  PubMed          Journal:  Pathol Res Pract        ISSN: 0344-0338            Impact factor:   3.250


  17 in total

1.  The common parasite Toxoplasma gondii induces prostatic inflammation and microglandular hyperplasia in a mouse model.

Authors:  Darrelle L Colinot; Tamila Garbuz; Maarten C Bosland; Liang Wang; Susan E Rice; William J Sullivan; Gustavo Arrizabalaga; Travis J Jerde
Journal:  Prostate       Date:  2017-05-12       Impact factor: 4.104

Review 2.  Is Toxoplasma gondii type related to clinical outcome in human congenital infection? Systematic and critical review.

Authors:  C P Rico-Torres; J A Vargas-Villavicencio; D Correa
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2016-05-04       Impact factor: 3.267

3.  Innate refractoriness of the Lewis rat to toxoplasmosis is a dominant trait that is intrinsic to bone marrow-derived cells.

Authors:  Véronique Sergent; Bastien Cautain; Jamal Khalife; Didier Deslée; Patrick Bastien; Anne Dao; Jean-François Dubremetz; Gilbert J Fournié; Abdelhadi Saoudi; Marie-France Cesbron-Delauw
Journal:  Infect Immun       Date:  2005-10       Impact factor: 3.441

4.  Immune-mediated regression of established B16F10 melanoma by intratumoral injection of attenuated Toxoplasma gondii protects against rechallenge.

Authors:  Jason R Baird; Katelyn T Byrne; Patrick H Lizotte; Seiko Toraya-Brown; Uciane K Scarlett; Matthew P Alexander; Mee Rie Sheen; Barbara A Fox; David J Bzik; Marcus Bosenberg; David W Mullins; Mary Jo Turk; Steven Fiering
Journal:  J Immunol       Date:  2012-12-07       Impact factor: 5.422

5.  Temporal distribution and parasite load kinetics in blood and tissues during Neospora caninum infection in mice.

Authors:  Esther Collantes-Fernández; Inmaculada López-Pérez; Gema Alvarez-García; Luis M Ortega-Mora
Journal:  Infect Immun       Date:  2006-04       Impact factor: 3.441

Review 6.  Toxoplasma gondii and cognitive deficits in schizophrenia: an animal model perspective.

Authors:  Geetha Kannan; Mikhail V Pletnikov
Journal:  Schizophr Bull       Date:  2012-09-01       Impact factor: 9.306

7.  Identification of the moving junction complex of Toxoplasma gondii: a collaboration between distinct secretory organelles.

Authors:  David L Alexander; Jeffrey Mital; Gary E Ward; Peter Bradley; John C Boothroyd
Journal:  PLoS Pathog       Date:  2005-10-21       Impact factor: 6.823

8.  Changes in the expression of human cell division autoantigen-1 influence Toxoplasma gondii growth and development.

Authors:  Jay R Radke; Robert G Donald; Amy Eibs; Maria E Jerome; Michael S Behnke; Paul Liberator; Michael W White
Journal:  PLoS Pathog       Date:  2006-10       Impact factor: 6.823

9.  Lower expression of inducible nitric oxide synthase and higher expression of arginase in rat alveolar macrophages are linked to their susceptibility to Toxoplasma gondii infection.

Authors:  Zhi-Jun Zhao; Jia Zhang; Jun Wei; Zhi Li; Tao Wang; Si-Qi Yi; Ji-Long Shen; Ting-Bao Yang; Geoff Hide; Zhao-Rong Lun
Journal:  PLoS One       Date:  2013-05-15       Impact factor: 3.240

Review 10.  Impairment of T cell function in parasitic infections.

Authors:  Vasco Rodrigues; Anabela Cordeiro-da-Silva; Mireille Laforge; Ali Ouaissi; Khadija Akharid; Ricardo Silvestre; Jérôme Estaquier
Journal:  PLoS Negl Trop Dis       Date:  2014-02-13
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