ABSTRACT
Small populations of Virginia opossum (Didelphis virginiana) in western Mexico are endangered by hunting and natural predators as well as by different kinds of diseases. After two serological analyses using Serodia® latex particle agglutination and indirect haemagglutination (IHA) tests, 35 (53.03%) of 66 collected opossums in two small towns in western Mexico were positive for the presence of Trypanosoma cruzi. Twenty-eight of the 35 seropositive opossums had pathological lesions: 11 had changes in only one organ, 13 in two organs, and four had pathological changes in three organs. Splenomegaly was the most common finding in the examined opossums, followed by hepatomegaly. These potentially fatal pathological changes could contribute to the scarcity of the opossum population, even leading to the extinction of this species in western Mexico.
Subject(s)
Didelphis/parasitology , Trypanosoma cruzi/isolation & purification , Trypanosomiasis/veterinary , Animals , Cardiomegaly/epidemiology , Cardiomegaly/parasitology , Cardiomegaly/veterinary , Esophageal Achalasia/epidemiology , Esophageal Achalasia/parasitology , Esophageal Achalasia/veterinary , Hepatomegaly/epidemiology , Hepatomegaly/parasitology , Hepatomegaly/veterinary , Mexico/epidemiology , Splenomegaly/epidemiology , Splenomegaly/parasitology , Splenomegaly/veterinary , Trypanosomiasis/epidemiology , Trypanosomiasis/pathologyABSTRACT
A systematic study following infection by various strains of the protozoan parasite, Trypanosoma cruzi, and the simultaneous monitoring of the humoral immune response together with the elicited cellular response, could add greatly to our understanding of differences between strains of this important human pathogen. In that sense, acute and chronic infections with distinct T. cruzi strains (Y, Berenice-78 and ABC) in Beagle dogs were studied through a longitudinal evaluation of immunoglobulin G (IgG), IgG1 and IgG2 isotypes (by ELISA and flow cytometry (FC)), as well as measurements of peripheral blood mononuclear cell (PBMC) proliferation over a 100-week period, and their correlation with cardiomegaly. Our results show that infected animals presenting cardiomegaly showed lower or absent levels of IgG1 during the chronic phase of the infection, when compared to those that did not show an increase in heart weight. In that manner, our results suggest that IgG1 could be used as a marker for cardiac pathogenicity in Chagas disease.
Subject(s)
Cardiomegaly/immunology , Cardiomegaly/parasitology , Chagas Disease/veterinary , Dog Diseases/immunology , Dog Diseases/parasitology , Immunoglobulin G/immunology , Trypanosoma cruzi/immunology , Animals , Antibodies, Protozoan/blood , Cell Growth Processes/immunology , Chagas Disease/immunology , Chagas Disease/parasitology , Dogs , Enzyme-Linked Immunosorbent Assay/veterinary , Flow Cytometry/veterinary , Immunoglobulin G/blood , Kinetics , Leukocytes, Mononuclear/immunology , Organ Size , Regression AnalysisSubject(s)
Cardiac Surgical Procedures , Cardiomyopathies/parasitology , Echinococcosis/complications , Echocardiography, Transesophageal/methods , Heart Diseases/diagnosis , Heart Diseases/parasitology , Heart Ventricles , Multidetector Computed Tomography , Adolescent , Cardiomegaly/diagnostic imaging , Cardiomegaly/parasitology , Computer Systems , Female , Heart Diseases/surgery , Humans , Radiography, ThoracicABSTRACT
Dilated cardiomyopathy (degeneration of heart muscle and heart enlargement) is an important cause of heart failure among young adults. Dilated cardiomyopathy may be a complication during or after various viral, bacterial, or parasitic diseases. Substance P (SP) is a neurotransmitter that is involved in the pathogenesis of various diseases. To determine whether SP is associated with cardiac changes in murine cysticercosis, we compared heart-weight to body-weight ratio, cardiac pathology, cardiomyocyte size, and cardiac-apoptosis (TUNEL assay) in hearts from Taenia crassiceps-infected (wild-type vs. SP-knockout) mice. We noted that, as compared with control uninfected wild-type mice, elevated protein levels of SP and its receptor as studied by ELISA or immunohistochemistry, respectively, were elevated in the hearts of parasite-infected wild-type mice. The heart-weight to body-weight ratios were significantly higher in the parasite-infected wild-type mice versus those of the infected SP-knockout mice. Furthermore, wild-type infected mice developed dilated cardiomyopathy with increased chamber size of both ventricles, decreased ventricular wall thickness, compensatory cardiomyocyte hypertrophy, and increased cardiac apoptosis. This cardiac pathology did not develop in mice lacking SP activity (i.e., in infected SP knockout mice) or in uninfected mice. These data indicate that SP is associated with cardiac changes in an animal model of parasitic dilated cardiomyopathy.
Subject(s)
Cardiomegaly/physiopathology , Cardiomyopathy, Dilated/physiopathology , Cysticercosis/physiopathology , Myocardium/pathology , Neurotransmitter Agents/metabolism , Substance P/metabolism , Taenia/pathogenicity , Animals , Apoptosis , Cardiomegaly/parasitology , Cardiomegaly/pathology , Cardiomyopathy, Dilated/parasitology , Cardiomyopathy, Dilated/pathology , Cysticercosis/parasitology , Cysticercosis/pathology , Disease Models, Animal , Female , Humans , Mice , Mice, Inbred C57BL , Mice, Knockout , Neurotransmitter Agents/genetics , Substance P/genetics , Taeniasis/parasitology , Taeniasis/pathology , Taeniasis/physiopathologyABSTRACT
Three patients who underwent successful surgical treatment of cardiac hydatid disease are discussed. The nonspecificity of diagnostic measures and the importance of keeping this diagnosis in mind when faced with a patient coming from an area where hydatidosis is endemic are stressed. We propose the use of cardiopulmonary bypass in the surgical treatment of this problem.
Subject(s)
Cardiomyopathies/parasitology , Echinococcosis/surgery , Adolescent , Adult , Angiocardiography , Cardiomegaly/parasitology , Cardiomyopathies/diagnostic imaging , Cardiomyopathies/surgery , Cardiopulmonary Bypass , Echinococcosis/diagnostic imaging , Electrocardiography , Female , Fluoroscopy , Humans , Male , Pericardium/parasitology , Pericardium/surgeryABSTRACT
When infected with Trypanosoma cruzi, Beagle dogs develop symptoms similar to those of Chagas disease in human beings, and could be an important experimental model for a better understanding of the immunopathogenic mechanisms involved in chronic chagasic infection. This study evaluates IL-10, IFN-gamma and TNF-alpha production in the sera, culture supernatant, heart and cervical lymph nodes and their correlation with cardiomegaly, cardiac inflammation and fibrosis in Beagle dogs infected with T. cruzi. Pathological analysis showed severe splenomegaly, lymphadenopathy and myocarditis in all infected dogs during the acute phase of the disease, with cardiomegaly, inflammation and fibrosis observed in 83% of the animals infected by T. cruzi during the chronic phase. The data indicate that infected animals producing IL-10 in the heart during the chronic phase and showing high IL-10 production in the culture supernatant and serum during the acute phase had lower cardiac alterations (myocarditis, fibrosis and cardiomegaly) than those with high IFN-gamma and TNF-alpha levels. These animals produced low IL-10 levels in the culture supernatant and serum during the acute phase and did not produce IL-10 in the heart during the chronic phase of the disease. Our findings showed that Beagle dogs are a good model for studying the immunopathogenic mechanism of Chagas disease, since they reproduce the clinical and immunological findings described in chagasic patients. The data suggest that the development of the chronic cardiac form of the disease is related to a strong Th1 response during the acute phase of the disease, while the development of the indeterminate form results from a blend of Th1 and Th2 responses soon after infection, suggesting that the acute phase immune response is important for the genesis of chronic cardiac lesions.
Subject(s)
Chagas Cardiomyopathy/veterinary , Dog Diseases/parasitology , Interferon-gamma/biosynthesis , Interleukin-10/biosynthesis , Trypanosoma cruzi/immunology , Tumor Necrosis Factor-alpha/biosynthesis , Animals , Cardiomegaly/immunology , Cardiomegaly/parasitology , Chagas Cardiomyopathy/immunology , Chagas Cardiomyopathy/parasitology , Chagas Cardiomyopathy/pathology , Disease Models, Animal , Dog Diseases/immunology , Dog Diseases/pathology , Dogs , Enzyme-Linked Immunosorbent Assay/veterinary , Fibrosis/immunology , Fibrosis/parasitology , Histocytochemistry/veterinary , Interferon-gamma/blood , Interferon-gamma/genetics , Interferon-gamma/immunology , Interleukin-10/blood , Interleukin-10/genetics , Interleukin-10/immunology , Reverse Transcriptase Polymerase Chain Reaction/veterinary , Splenomegaly/immunology , Splenomegaly/parasitology , Tumor Necrosis Factor-alpha/blood , Tumor Necrosis Factor-alpha/genetics , Tumor Necrosis Factor-alpha/immunologyABSTRACT
A case of disseminated S stercoralis is an immunosuppressed patient manifested with diarrhea, a rash, and progressive respiratory insufficiency. The parasites were eradicated with thiabendazole despite continued steroid therapy, and the patient survived the hospitalization. The characteristics of S stercoralis allow it to be harbored within a host for prolonged periods of time, only to disseminate once cell-mediated immunity is suppressed. A diagnosis of strongyloidiasis should be considered in an immunocompromised patient with a petechial rash. Prompt diagnosis and initiation of thiabendazole therapy provides the greatest opportunity for patient survival. Secondary bacterial infections should be aggressively sought. Mortality from disseminated strongyloidiasis approaches 80%.