Literature DB >> 9709034

Toxoplasma gondii: kinetics of the dissemination in the host tissues during the acute phase of infection of mice and rats.

L Zenner1, F Darcy, A Capron, M F Cesbron-Delauw.   

Abstract

Mice and rats differ in their susceptibility to Toxoplasma gondii infection. Here we have compared the parasitological parameters of acute infection in both mice and rats infected either orally with cysts of Prugniaud strain or intraperitoneally (ip) with tachyzoites of the RH strain. The animals were killed at regular interval during the acute phase, and the parasitic burden in mesenteric lymph nodes, spleen, liver, diaphragm, heart, lungs, brain, and blood was assessed by a tissue culture method in MRC5 fibroblast cells. Mice infected with the RH strain showed a drastic increase of the parasitic load in all organs (up to 10 (8) parasites / g of organs), and then died. When mice were infected with 50 cysts of Prugniaud strain, parasites were first observed in mesenteric lymph nodes, spleen, and lungs and then in other organs. In rats, infection with 1200 cysts of the same strain led to a similar pattern; however, the chronology of the infected organs changed when they were infected with RH strain tachyzoites. These results suggest that the parasites, present first in the peritoneal cavity in the case of RH ip infection, infect all the adjacent organs and then the blood which disseminates the tachyzoites all over the organism. In contrast, after an oral infection, the parasite crosses the intestinal barrier to reach the mesenteric lymph nodes and then the spleen and are finally distributed by the blood throughout the organism. We also showed that following infection with a lethal or a sublethal doses of the Prugniaud strain, the parasitic burden in the studied organs was similar and therefore does not directly correlate with the death of the mice. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9709034     DOI: 10.1006/expr.1998.4301

Source DB:  PubMed          Journal:  Exp Parasitol        ISSN: 0014-4894            Impact factor:   2.011


  19 in total

1.  Externally triggered egress is the major fate of Toxoplasma gondii during acute infection.

Authors:  Tadakimi Tomita; Tatsuya Yamada; Louis M Weiss; Amos Orlofsky
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2.  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

3.  Localized multigene expression patterns support an evolving Th1/Th2-like paradigm in response to infections with Toxoplasma gondii and Ascaris suum.

Authors:  Harry D Dawson; Ethiopia Beshah; Sandra Nishi; Gloria Solano-Aguilar; Motoko Morimoto; Aiping Zhao; Kathleen B Madden; Tonya K Ledbetter; J P Dubey; Terez Shea-Donohue; Joan K Lunney; Joseph F Urban
Journal:  Infect Immun       Date:  2005-02       Impact factor: 3.441

4.  T cell phenotype and intracellular IFN-gamma production in peritoneal exudate cells and gut intraepithelial lymphocytes during acute Toxoplasma gondii infection in mice.

Authors:  Young-Ha Lee; Dae-Whan Shin
Journal:  Korean J Parasitol       Date:  2002-09       Impact factor: 1.341

5.  The Toxoplasma gondii-shuttling function of dendritic cells is linked to the parasite genotype.

Authors:  Henrik Lambert; Polya P Vutova; William C Adams; Karin Loré; Antonio Barragan
Journal:  Infect Immun       Date:  2009-02-09       Impact factor: 3.441

6.  Blood-brain barrier-restricted translocation of Toxoplasma gondii from cortical capillaries.

Authors:  Gabriela C Olivera; Emily C Ross; Christiane Peuckert; Antonio Barragan
Journal:  Elife       Date:  2021-12-08       Impact factor: 8.140

7.  Differences in iNOS and arginase expression and activity in the macrophages of rats are responsible for the resistance against T. gondii infection.

Authors:  Zhi Li; Zhi-Jun Zhao; Xing-Quan Zhu; Qing-Shi Ren; Fang-Fang Nie; Jiang-Mei Gao; Xiao-Jie Gao; Ting-Bao Yang; Wen-Liang Zhou; Ji-Long Shen; Yong Wang; Fang-Li Lu; Xiao-Guang Chen; Geoff Hide; Francisco J Ayala; Zhao-Rong Lun
Journal:  PLoS One       Date:  2012-04-25       Impact factor: 3.240

8.  Toxoplasma MIC2 is a major determinant of invasion and virulence.

Authors:  My-Hang Huynh; Vern B Carruthers
Journal:  PLoS Pathog       Date:  2006-08       Impact factor: 6.823

9.  Reduction of Foxp3+ cells by depletion with the PC61 mAb induces mortality in resistant BALB/c mice infected with Toxoplasma gondii.

Authors:  Eda Patricia Tenorio; Jonadab Efraín Olguín; Jacquelina Fernández; Pablo Vieyra; Rafael Saavedra
Journal:  J Biomed Biotechnol       Date:  2009-12-13

10.  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

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