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. 2022 Feb 2:64:e9.
doi: 10.1590/S1678-9946202264009. eCollection 2022.

Toxocara canis 30-35 kDa excretory-secretory antigen is an important marker in mice challenged by inocula containing different parasite load levels

Affiliations

Toxocara canis 30-35 kDa excretory-secretory antigen is an important marker in mice challenged by inocula containing different parasite load levels

Gabriela Rodrigues E Fonseca et al. Rev Inst Med Trop Sao Paulo. .

Abstract

The Western-blotting technique was applied to identify antigenic fractions of excretory-secretory Toxocara canis antigen recognized by IgG antibodies throughout an experimental infection in mice challenged by different inocula. Mice were inoculated with 5, 50 and 500 embryonated eggs and serum samples were collected 15, 30, 60, 90 and 120 days post-infection. Serum samples were analyzed using an excretory-secretory Toxocara antigen. Antibodies recognized antigenic fractions from 30 to 90 kDa. The protein fraction of 30-35 kDa was the most frequently recognized regardless of the size of inoculum and the stage of infection represented by the different collection times, but the antigenic recognition was more evident in groups infected with 50 and 500 eggs. This study presents an antigenic panel of the excretory-secretory antigen of T. canis and suggests that the 30-35 kDa antigenic fraction is a promising marker of the infection and should be further explored in future studies on experimental toxocariasis.

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Figures

Figure 1
Figure 1. - Dynamics of the recognition of protein fractions by anti-Toxocara IgG antibodies in serum samples of mice from groups I, II and III, at collection times corresponding to 15, 30, 60, 90 and 120 dpi. MW = molecular weight marker; NC = negative controls.

References

    1. Chieffi PP, Zevallos Lescano SA, Fonseca GR, Santos SV. Human toxocariasis: 2010 to 2020 contributions from Brazilian researchers. Res Rep Trop Med. 2021;12:81–91. - PMC - PubMed
    1. Fillaux J, Magnaval JF. Laboratory diagnosis of human toxocariasis. Vet Parasitol. 2013;193:327–336. - PubMed
    1. Macpherson CN. The epidemiology and public health importance of toxocariasis: a zoonosis of global importance. Int J Parasitol. 2013;43:999–1008. - PubMed
    1. Overgaauw PA, van Knapen F. Veterinary and public health aspects of Toxocara spp. Vet Parasitol. 2013;193:398–403. - PubMed
    1. Abo-Shehada MN, Herbert IV. The migration of larval Toxocara canis in mice II. Post-intestinal migration in primary infections. Vet Parasitol. 1984;17:75–83. - PubMed