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Published in: Comparative Clinical Pathology 1/2016

01-01-2016 | Original Article

Post challenge variability in time gap pertaining to appearance of Toxoplasma gondii DNA in blood and appearance of visible clinical signs in murine model

Authors: Vikrant Sudan, A. K. Tewari, Harkirat Singh

Published in: Comparative Clinical Pathology | Issue 1/2016

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Abstract

A marked variation, in terms of time lag gap of the depiction of visible clinical signs and the actual appearance of parasitic stages in body tissues, exists in experimental toxoplasmosis. Keeping this in mind, a study was designed to find out the time gap associated variability in appearance of tachyzoites in blood stream of infected mice. For this purpose, surface antigen 3 (SAG 3) was selected as a candidate to detect toxoplasmosis from blood samples taken at regular intervals from murine models. PCR was standardized to diagnose toxoplasmosis in ten inbred Swiss albino mice after experimental inoculation of 100 tachyzoites of laboratory maintained human RH strain of the parasite. The blood samples were subjected to PCR, in duplicates, using primers directed to the multicopy of SAG 3 gene at regular 12 -h interval post infection. The tachyzoites begin to appear between 36 h post infection and by 48 h blood of all the mice were found to be infected by tachyzoites. Alongside, other visible symptoms begin to appear after 72 h post infection. In conclusion, ample time gap was found regarding the initiation of clinical infection and actual appearance of visible clinical signs that could prove detrimental in final outcome of condition.
Literature
go back to reference Angel SO, Matrajt M, Margarit J et al (1997) Screening of active Toxoplasma in patients by DNA hybridization with ABGTg7 probe in blood samples. J Clin Microbiol 35:591–595PubMedPubMedCentral Angel SO, Matrajt M, Margarit J et al (1997) Screening of active Toxoplasma in patients by DNA hybridization with ABGTg7 probe in blood samples. J Clin Microbiol 35:591–595PubMedPubMedCentral
go back to reference Brenier-Pinchart MP, Blanc-Gonnet E, Marche PN et al (2004) Infection of human astrocytes and glioblastoma cells with Toxoplasma gondii: monocyte chemotactic protein-1 secretion and Chemokine expression in vitro. Acta Neuropathol 107:245–249CrossRefPubMed Brenier-Pinchart MP, Blanc-Gonnet E, Marche PN et al (2004) Infection of human astrocytes and glioblastoma cells with Toxoplasma gondii: monocyte chemotactic protein-1 secretion and Chemokine expression in vitro. Acta Neuropathol 107:245–249CrossRefPubMed
go back to reference Fekadu A, Shibre T, Cleare AJ (2010) Toxoplasmosis as a cause for behavior disorders—overview of evidence and mechanisms. Folia Parasitol 57:105–113CrossRefPubMed Fekadu A, Shibre T, Cleare AJ (2010) Toxoplasmosis as a cause for behavior disorders—overview of evidence and mechanisms. Folia Parasitol 57:105–113CrossRefPubMed
go back to reference Homan WL, Vercammen M, De Braekeleer J (2000) Identification of a 200- to 300-fold repetitive 529 bp DNA fragment in Toxoplasma gondii, and its use for diagnostic and quantitative PCR. Int J Parasitol 30:69–75CrossRefPubMed Homan WL, Vercammen M, De Braekeleer J (2000) Identification of a 200- to 300-fold repetitive 529 bp DNA fragment in Toxoplasma gondii, and its use for diagnostic and quantitative PCR. Int J Parasitol 30:69–75CrossRefPubMed
go back to reference Hurtado A, Aduriz G, Moreno B et al (2001) Single tube nested PCR for the detection of Toxoplasma gondii in fetal tissues from naturally aborted ewes. Vet Parasitol 102:17–27CrossRefPubMed Hurtado A, Aduriz G, Moreno B et al (2001) Single tube nested PCR for the detection of Toxoplasma gondii in fetal tissues from naturally aborted ewes. Vet Parasitol 102:17–27CrossRefPubMed
go back to reference Jacquet A, Coulon L, Neve JD et al (2001) The surface antigen SAG3 mediates the attachment of Toxoplasma gondii to cell-surface proteoglycans. Mol Biochem Parasitol 116:35–44CrossRefPubMed Jacquet A, Coulon L, Neve JD et al (2001) The surface antigen SAG3 mediates the attachment of Toxoplasma gondii to cell-surface proteoglycans. Mol Biochem Parasitol 116:35–44CrossRefPubMed
go back to reference Kazemi B, Maghen L, Bandehpour M et al (2007) Gene cloning of P43 surface protein of Toxoplasma gondii tachyzoite and bradyzoite (SAG3). Gene Ther Mol Biol 11:113–116 Kazemi B, Maghen L, Bandehpour M et al (2007) Gene cloning of P43 surface protein of Toxoplasma gondii tachyzoite and bradyzoite (SAG3). Gene Ther Mol Biol 11:113–116
go back to reference Parker GA, Langloss JM, Dubey JP et al (1981) Pathogenesis of acute toxoplasmosis in specific-pathogen-free cats. Vet Pathol 18:786–803CrossRefPubMed Parker GA, Langloss JM, Dubey JP et al (1981) Pathogenesis of acute toxoplasmosis in specific-pathogen-free cats. Vet Pathol 18:786–803CrossRefPubMed
go back to reference Sreekumar C, Rao JR, Mishra AK et al (2004) Detection of toxoplasmosis in experimentally infected goats by PCR. Vet Rec 15:632–635CrossRef Sreekumar C, Rao JR, Mishra AK et al (2004) Detection of toxoplasmosis in experimentally infected goats by PCR. Vet Rec 15:632–635CrossRef
go back to reference Sudan V, Tewari AK, Singh H et al (2012) Molecular characterization of surface antigen 3 (SAG3) gene of Toxoplasma gondii RH-IVRI strain. J Parasit Dis 36(2):210–214CrossRef Sudan V, Tewari AK, Singh H et al (2012) Molecular characterization of surface antigen 3 (SAG3) gene of Toxoplasma gondii RH-IVRI strain. J Parasit Dis 36(2):210–214CrossRef
go back to reference Sudan V, Tewari AK, Singh H (2014a) An insight into the behavior, course and kinetics of acute infection of Toxoplasma gondii human RH strain in experimentally infected murine model. Iran J Parasitol 9(1):114–119PubMedPubMedCentral Sudan V, Tewari AK, Singh H (2014a) An insight into the behavior, course and kinetics of acute infection of Toxoplasma gondii human RH strain in experimentally infected murine model. Iran J Parasitol 9(1):114–119PubMedPubMedCentral
go back to reference Webster JP, Lamberton PHL, Donnelly CA et al (2006) Parasites as causative agents of human affective disorders? The impact of anti-psychotic, mood-stabilizer and anti-parasite medication on Toxoplasma gondii’s ability to alter host behaviour. Proc Biol Sci 273:1023–1030CrossRefPubMedPubMedCentral Webster JP, Lamberton PHL, Donnelly CA et al (2006) Parasites as causative agents of human affective disorders? The impact of anti-psychotic, mood-stabilizer and anti-parasite medication on Toxoplasma gondii’s ability to alter host behaviour. Proc Biol Sci 273:1023–1030CrossRefPubMedPubMedCentral
Metadata
Title
Post challenge variability in time gap pertaining to appearance of Toxoplasma gondii DNA in blood and appearance of visible clinical signs in murine model
Authors
Vikrant Sudan
A. K. Tewari
Harkirat Singh
Publication date
01-01-2016
Publisher
Springer London
Published in
Comparative Clinical Pathology / Issue 1/2016
Print ISSN: 1618-5641
Electronic ISSN: 1618-565X
DOI
https://doi.org/10.1007/s00580-015-2136-6

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