In vivo study of toxoplasmic parasitemia using interferon-gamma-deficient mice: absolute cell number of leukocytes, parasite load and cell susceptibility
- PMID: 18585475
- DOI: 10.1016/j.parint.2008.05.007
In vivo study of toxoplasmic parasitemia using interferon-gamma-deficient mice: absolute cell number of leukocytes, parasite load and cell susceptibility
Abstract
Toxoplasma gondii infection was induced in wild type (WT) C57BL/6 and BALB/c mice and same-background interferon-gamma knockout (GKO) mice by peroral inoculation of Fukaya strain cysts. We studied parasitemia, absolute cell number of leukocytes, and cell susceptibility in peripheral blood leukocyte (PBL) subsets in vivo. Parasitemia was observed in both WT and GKO mice, although the pattern of the parasite load was totally different among them. After infection, the absolute number of neutrophils in peripheral blood increased in both GKO C57BL/6 and GKO BALB/c mice with statistical significance, while it rose up slightly in susceptible WT C57BL/6 mice, but declined moderately in resistant WT BALB/c mice. The absolute number of lymphocytes in both WT and GKO mice decreased significantly after infection. Although leukocyte number per mul decreased significantly in both strains of WT mice, it increased in GKO BALB/c mice. There were no differences in susceptibility of PBL subsets to T. gondii infection as assessed by quantitative competitive polymerase chain reaction in both WT and GKO mice. These results indicate that each of the PBL subsets was infected in vivo. The increase of neutrophils only among immunocompromised or susceptible strains suggests that the neutrophil may be involved in the lethal process of T. gondii infection. The lack of any difference in cell susceptibility per mug gDNA among the PBL subsets examined implies that the neutrophil may contribute to the whole body dissemination process of the parasite in vivo more than other PBL subsets through the increase in number.
Similar articles
-
Effects of sulfamethoxazole on murine ocular toxoplasmosis in interferon-gamma knockout mice.Invest Ophthalmol Vis Sci. 2006 Jan;47(1):265-71. doi: 10.1167/iovs.05-0751. Invest Ophthalmol Vis Sci. 2006. PMID: 16384972
-
Maternal-fetal transmission of Toxoplasma gondii in interferon-gamma deficient pregnant mice.Parasitol Int. 2007 Jun;56(2):141-8. doi: 10.1016/j.parint.2007.01.008. Epub 2007 Jan 24. Parasitol Int. 2007. PMID: 17307382
-
In the absence of endogenous IFN-gamma, mice develop unimpaired IL-12 responses to Toxoplasma gondii while failing to control acute infection.J Immunol. 1996 Nov 1;157(9):4045-54. J Immunol. 1996. PMID: 8892638
-
Oral infection of C57BL/6 mice with Toxoplasma gondii: a new model of inflammatory bowel disease?J Infect Dis. 2002 Feb 15;185 Suppl 1:S96-101. doi: 10.1086/338006. J Infect Dis. 2002. PMID: 11865446 Review.
-
Ocular toxoplasmosis: in the storm of the eye.Parasite Immunol. 2006 Dec;28(12):635-42. doi: 10.1111/j.1365-3024.2006.00874.x. Parasite Immunol. 2006. PMID: 17096642 Review.
Cited by
-
Toxoplasma Infection Induces Sustained Up-Regulation of Complement Factor B and C5a Receptor in the Mouse Brain via Microglial Activation: Implication for the Alternative Complement Pathway Activation and Anaphylatoxin Signaling in Cerebral Toxoplasmosis.Front Immunol. 2021 Feb 5;11:603924. doi: 10.3389/fimmu.2020.603924. eCollection 2020. Front Immunol. 2021. PMID: 33613523 Free PMC article.
-
Experimental infection with the Toxoplasma gondii ME-49 strain in the Brazilian BR-1 mini pig is a suitable animal model for human toxoplasmosis.Mem Inst Oswaldo Cruz. 2015 Feb;110(1):95-100. doi: 10.1590/0074-02760140318. Epub 2015 Feb 3. Mem Inst Oswaldo Cruz. 2015. PMID: 25742268 Free PMC article.
-
CD40 in Endothelial Cells Restricts Neural Tissue Invasion by Toxoplasma gondii.Infect Immun. 2019 Jul 23;87(8):e00868-18. doi: 10.1128/IAI.00868-18. Print 2019 Aug. Infect Immun. 2019. PMID: 31109947 Free PMC article.
-
Calling in the CaValry-Toxoplasma gondii Hijacks GABAergic Signaling and Voltage-Dependent Calcium Channel Signaling for Trojan horse-Mediated Dissemination.Front Cell Infect Microbiol. 2019 Mar 20;9:61. doi: 10.3389/fcimb.2019.00061. eCollection 2019. Front Cell Infect Microbiol. 2019. PMID: 30949456 Free PMC article. Review.
-
Neutrophil Homeostasis and Emergency Granulopoiesis: The Example of Systemic Juvenile Idiopathic Arthritis.Front Immunol. 2021 Dec 13;12:766620. doi: 10.3389/fimmu.2021.766620. eCollection 2021. Front Immunol. 2021. PMID: 34966386 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources