Literature DB >> 16567042

Biologic and genetic characteristics of Toxoplasma gondii isolates in free-range chickens from Costa Rica, Central America.

J P Dubey1, C Su, J Oliveira, J A Morales, R V Bolaños, N Sundar, O C H Kwok, S K Shen.   

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 144 free-range chickens (Gallus domesticus) from Costa Rica was determined. Antibodies to T. gondii were assayed by the modified agglutination test (MAT), and found in 60 (40.1%) of 144 chickens with titers of 1:5 in 16, 1:10 in 5, 1:20 in 2, 1:40 in 3, 1:80 in 5, and 1:160 or higher in 29. Tissues of all chickens were bioassayed for T. gondii in mice or cats. Hearts and brains of 52 chickens with titers of 1:5 or higher and 16 chickens with doubtful titers were pooled and bioassayed in mice. Tissues from 76 chickens with MAT titers of 1:10 or less were pooled and fed to three T. gondii-free cats. Fecal floats of cats were bioassayed orally in mice but were negative for T. gondii oocysts. T. gondii was isolated by bioassay in mice from 32 chickens with MAT titers of 1:10 or higher. All infected mice from 4 of the 32 isolates died of toxoplasmosis. Genotyping of these 32 isolates using polymorphisms at the loci SAG1, SAG2, SAG3, BTUB and GRA6 revealed five genotypes. Five isolates had type I alleles and one isolate had type III alleles at all loci. The rest 26 isolates contained the combination of type I and II or I and III alleles and were divided into three genotypes. None was found to have genotype II alleles at all five loci. This is the first report of genetic characterization of T. gondii isolates from Costa Rica, Central America.

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Year:  2006        PMID: 16567042     DOI: 10.1016/j.vetpar.2006.02.031

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


  6 in total

1.  Selection of polymorphic peptides from GRA6 and GRA7 sequences of Toxoplasma gondii strains to be used in serotyping.

Authors:  Susana Sousa; Daniel Ajzenberg; Maggy Marle; Dominique Aubert; Isabelle Villena; José Correia da Costa; Marie-Laure Dardé
Journal:  Clin Vaccine Immunol       Date:  2009-06-03

2.  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 3.  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

4.  Phenotypic and genotypic characterization of two Toxoplasma gondii isolates in free-range chickens from Uberlândia, Brazil.

Authors:  C S Lopes; P S Franco; N M Silva; D A O Silva; E A V Ferro; H F J Pena; R M Soares; S M Gennari; J R Mineo
Journal:  Epidemiol Infect       Date:  2016-01-08       Impact factor: 4.434

5.  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

6.  Prevalence and genotyping of Toxoplasma gondii in stray cats in Mashhad area, Iran.

Authors:  Majid Khodaverdi; Gholamreza Razmi
Journal:  BMC Vet Res       Date:  2019-12-21       Impact factor: 2.741

  6 in total

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