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Exp Parasitol ; 207: 107781, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31626796

ABSTRACT

The paradigm that Toxoplasma gondii infection generates sterilizing protective immunity was broken by case studies in which reinfections were observed in immunocompetent pregnant women in the chronic phase of toxoplasmosis. Since then, several murine models have suggested that immunoprotection against a previous T. gondii infection may be violated after reinfection with strains of different genotypes. This study aimed to evaluate the dissemination of the parasite after reinfection with the virulent TgCTBr9 and EGS strains in BALB/c mice chronically infected with the avirulent TgCTBr5 strain. Three mice were euthanized at 2, 4, 8, 12, 24 and 48 h post challenge (p.c.) and at 7, 14 and 30 days p.c. Intestines, mesenteric lymph nodes, lungs and brains were collected for PCR-RFLP. Blood samples were collected to measure total IgG, IgG1 and IgG2a by ELISA. The reinfected animals survived and presented reduced morbidity after challenge with the virulent strains. Mice challenged with the TgCTBr9 strain showed a slight increase in anti-T. gondii IgG1. The spread of the TgCTBr5 strain was observed to occur earlier than the dissemination of the virulent TgCTBr9 or EGS strains. The TgCTBr9 strain was observed in the mesenteric lymph node at 7 days post challenge (d.p.c.); in the intestine and lungs at 14 d.p.c.; and in the brain at 30 d.p.c. EGS strain was demonstrated in the mesenteric lymph node and lung at 7 d.p.c and in the intestine and brain at a later time point. The immune response promoted by the primary infection with the avirulent strain (TgCTBr5) protected the animals from death after challenge with the virulent strains (TgCTBr9 or EGS).


Subject(s)
Antibodies, Protozoan/blood , Toxoplasma/physiology , Toxoplasmosis, Congenital/parasitology , Animals , Body Weight , Brain/parasitology , Brazil , Female , Genotype , Humans , Immunoglobulin G/blood , Intestines/parasitology , Lung/parasitology , Lymph Nodes/parasitology , Mesentery , Mice , Mice, Inbred BALB C , Morbidity , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Recurrence , Toxoplasma/genetics , Toxoplasma/immunology , Toxoplasma/pathogenicity , Toxoplasmosis, Congenital/immunology , Virulence
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