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1.
ACS Infect Dis ; 6(7): 1807-1815, 2020 07 10.
Article in English | MEDLINE | ID: mdl-32374586

ABSTRACT

The leading animal model of experimental Chagas disease, the mouse, plays a significant role in studies for vaccine development, diagnosis, and human therapies. Humans, along with Old World primates, alone among mammals, cannot make the terminal carbohydrate linkage of the α-Gal trisaccharide. It has been established that the anti-α-Gal immune response is likely to be a critical factor for protection against Trypanosoma cruzi (T. cruzi) infection in humans. However, the mice customarily employed for the study of T. cruzi infection naturally express the α-Gal epitope and therefore do not produce anti-α-Gal antibodies. Here, we used the C57BL/6 α-1,3-galactosyltransferase knockout (α-GalT-KO) mouse, which does not express the α-Gal epitope as a model for experimental Chagas disease. We found the anti-α-Gal IgG antibody response to an increase in α-GalT-KO mice infected with Arequipa and Colombiana strains of T. cruzi, leading to fewer parasite nests, lower parasitemia, and an increase of INF-γ, TNF-α, and IL-12 cytokines in the heart of α-GalT-KO mice compared with α-GalT-WT mice on days 60 and 120 postinfection. We therefore agree that the C57BL/6 α-GalT-KO mouse represents a useful model for initial testing of therapeutic and immunological approaches against different strains of T. cruzi.


Subject(s)
Chagas Disease , Trypanosoma cruzi , Animals , Galactosyltransferases/genetics , Mice , Mice, Inbred C57BL , Mice, Knockout
2.
ACS Infect Dis ; 2(12): 917-922, 2016 12 09.
Article in English | MEDLINE | ID: mdl-27696820

ABSTRACT

The α-Gal antigen [Galα(1,3)Galß(1,4)GlcNAcα] is an immunodominant epitope displayed by infective trypomastigote forms of Trypanosoma cruzi, the causative agent of Chagas disease. A virus-like particle displaying a high density of α-Gal was found to be a superior reagent for the ELISA-based serological diagnosis of Chagas disease and the assessment of treatment effectiveness. A panel of sera from patients chronically infected with T. cruzi, both untreated and benznidazole-treated, was compared with sera from patients with leishmaniasis and from healthy donors. The nanoparticle-α-Gal construct allowed for perfect discrimination between Chagas patients and the others, avoiding false negative and false positive results obtained with current state-of-the-art reagents. As previously reported with purified α-Gal-containing glycosylphosphatidylinositol-anchored mucins, the current study also showed concentrations of anti-α-Gal IgG to decrease substantially in patients receiving treatment with benznidazole, suggesting that the semiquantitative assessment of serum levels of this highly abundant type of antibody can report on disease status in individual patients.


Subject(s)
Chagas Disease/diagnosis , Trisaccharides/analysis , Trypanosoma cruzi/isolation & purification , Antibodies, Protozoan/analysis , Antibodies, Protozoan/immunology , Antigens, Protozoan/analysis , Antigens, Protozoan/immunology , Chagas Disease/parasitology , Enzyme-Linked Immunosorbent Assay , Humans , Trisaccharides/immunology , Trypanosoma cruzi/genetics , Trypanosoma cruzi/immunology , Viruses/genetics , Viruses/metabolism
3.
Int J Parasitol ; 46(3): 213-220, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26812026

ABSTRACT

The anaphylaxis response is frequently associated with food allergies, representing a significant public health hazard. Recently, exposure to tick bites and production of specific IgE against α-galactosyl (α-Gal)-containing epitopes has been correlated to red meat allergy. However, this association and the source of terminal, non-reducing α-Gal-containing epitopes have not previously been established in Brazil. Here, we employed the α-1,3-galactosyltransferase knockout mouse (α1,3-GalT-KO) model and bacteriophage Qß-virus like particles (Qß-VLPs) displaying Galα1,3Galß1,4GlcNAc (Galα3LN) epitopes to investigate the presence of α-Gal-containing epitopes in the saliva of Amblyomma sculptum, a species of the Amblyomma cajennense complex, which represents the main tick that infests humans in Brazil. We confirmed that the α-1,3-galactosyltransferase knockout animals produce significant levels of anti-α-Gal antibodies against the Galα1,3Galß1,4GlcNAc epitopes displayed on Qß-virus like particles. The injection of A. sculptum saliva or exposure to feeding ticks was also found to induce both IgG and IgE anti-α-Gal antibodies in α-1,3-galactosyltransferase knockout mice, thus indicating the presence of α-Gal-containing epitopes in the tick saliva. The presence of α-Gal-containing epitopes was confirmed by ELISA and immunoblotting following removal of terminal α-Gal epitopes by α-galactosidase treatment. These results suggest for the first known time that bites from the A. sculptum tick may be associated with the unknown etiology of allergic reactions to red meat in Brazil.


Subject(s)
Food Hypersensitivity/immunology , Red Meat/adverse effects , Saliva/immunology , Ticks/immunology , Animals , Brazil , Epitope Mapping , Epitopes/chemistry , Epitopes/immunology , Female , Food Hypersensitivity/etiology , Galactosyltransferases/genetics , Galactosyltransferases/immunology , Humans , Immunoglobulin E/immunology , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Red Meat/analysis , Saliva/chemistry , Ticks/chemistry
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