Literature DB >> 16105721

Genetic and biologic characteristics of Toxoplasma gondii isolates in free-range chickens from Colombia, South America.

J P Dubey1, Jorge E Gomez-Marin, Angela Bedoya, Fabiana Lora, M C B Vianna, D Hill, O C H Kwok, S K Shen, P L Marcet, T Lehmann.   

Abstract

The prevalence of Toxoplasma gondii in free-ranging chickens is a good indicator of the prevalence of T. gondii oocysts in the soil because chickens feed from the ground. The prevalence of T. gondii in 77 free-range chickens (Gallus domesticus) from Colombia, South America was determined. Antibodies to T. gondii were assayed by the modified agglutination test (MAT), and found in 32 (44.4%) of 72 chickens with titers of 1:5 in 4, 1:10 in 3, 1:20 in 1, 1:40 in 1, 1:80 in 8, 1:160 in 8, 1:320 in 3, and 1:640 or higher in 4. Hearts and brains of 31 seropositive chickens were pooled and bioassayed in mice. Tissues from 32 (16+16) seronegative chickens were pooled and fed to two, T. gondii-free cats, and tissues from nine chickens without matching sera were fed to one T. gondii-free cat. Feces of cats were examined for oocysts. T. gondii oocysts were excreted by a cat that was fed tissues of 16 seronegative chickens. T. gondii was isolated by bioassay in mice from 23 chickens with MAT titers of 1:20 or higher. All infected mice from 16 of the 23 isolates died of toxoplasmosis. Overall, 82 (81.1%) of 101 mice that became infected after inoculation with chicken tissues died of toxoplasmosis. Genotyping of these 24 isolates using polymorphisms at the SAG2 locus indicated that seven T. gondii isolates were Type I, 17 were Type III, and none was Type II. Phenotypically, T. gondii isolates from chickens from Colombia were similar to isolates from Brazil but different from the isolates from North America; most isolates from chickens from Brazil and Colombia were lethal for mice whereas isolates from North America did not kill inoculated mice. Genetically, none of the T. gondii isolates from Colombia and Brazil was SAG2 Type II, whereas most isolates from chickens from North America were Type II. This is the first report of genetic characterization of T. gondii isolates from Colombia, South America.

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Year:  2005        PMID: 16105721     DOI: 10.1016/j.vetpar.2005.07.013

Source DB:  PubMed          Journal:  Vet Parasitol        ISSN: 0304-4017            Impact factor:   2.738


  10 in total

1.  A new perspective on and re-assessment of SAG2 locus as the tool for genetic analysis of Toxoplasma gondii isolates.

Authors:  A Fazaeli; A Ebrahimzadeh
Journal:  Parasitol Res       Date:  2007-02-13       Impact factor: 2.289

2.  Analysis of Toxoplasma gondii surface antigen 2 gene (SAG2). Relevance of genotype I in clinical toxoplasmosis.

Authors:  Valeria Sabaj; Mario Galindo; Daniela Silva; Lea Sandoval; Juan C Rodríguez
Journal:  Mol Biol Rep       Date:  2009-10-20       Impact factor: 2.316

3.  Detection of Toxoplasma gondii in water by an immunomagnetic separation method targeting the sporocysts.

Authors:  Aurélien Dumètre; Marie-Laure Dardé
Journal:  Parasitol Res       Date:  2007-05-26       Impact factor: 2.289

Review 4.  Genetic diversity of Toxoplasma gondii in animals and humans.

Authors:  L David Sibley; Asis Khan; James W Ajioka; Benjamin M Rosenthal
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2009-09-27       Impact factor: 6.237

5.  Genetic divergence of Toxoplasma gondii strains associated with ocular toxoplasmosis, Brazil.

Authors:  Asis Khan; Catherine Jordan; Cristina Muccioli; Adriana L Vallochi; Luiz V Rizzo; Rubens Belfort; Ricardo W A Vitor; Claudio Silveira; L David Sibley
Journal:  Emerg Infect Dis       Date:  2006-06       Impact factor: 6.883

6.  Pathogenicity of Five Strains of Toxoplasma gondii from Different Animals to Chickens.

Authors:  Shuai Wang; Guang-Wei Zhao; Wang Wang; Zhen-Chao Zhang; Bo Shen; I A Hassan; Qing Xie; Ruo-Feng Yan; Xiao-Kai Song; Li-Xin Xu; Xiang-Rui Li
Journal:  Korean J Parasitol       Date:  2015-04-22       Impact factor: 1.341

Review 7.  An overview of seventy years of research (1944-2014) on toxoplasmosis in Colombia, South America.

Authors:  William Alberto Cañón-Franco; Natalia López-Orozco; Jorge Enrique Gómez-Marín; Jitender P Dubey
Journal:  Parasit Vectors       Date:  2014-09-04       Impact factor: 3.876

8.  Detection of Toxoplasma gondii in chicken and soil of chicken farms in Nanjing region, China.

Authors:  Xin-Chao Liu; Yu He; Deng-Ge Han; Zhen-Chao Zhang; Ke Li; Shuai Wang; Li-Xin Xu; Ruo-Feng Yan; Xiang-Rui Li
Journal:  Infect Dis Poverty       Date:  2017-05-09       Impact factor: 4.520

9.  Detection of Giardia duodenalis and Toxoplasma gondii in soil and water samples in the Quindío River basin, Colombia.

Authors:  Valeria Alejandra Pinto-Duarte; Natalia Marcela Hérnandez-Arango; Benyi Juliana Marin-Gallego; Paola Andrea Toloza-Beltrán; Fabiana María Lora-Suarez; Jorge Enrique Gómez-Marín
Journal:  Food Waterborne Parasitol       Date:  2022-08-09

10.  Majority of T. gondii seropositive chickens (Gallus domesticus) in Central Ethiopia carries the infective parasite.

Authors:  Endrias Zewdu Gebremedhin; Gebregergs Tesfamaryam; Reta Duguma; Getachew Tilahun; Vincenzo Di Marco; Maria Vitale
Journal:  Acta Vet Scand       Date:  2014-09-24       Impact factor: 1.695

  10 in total

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