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1.
Acta Parasitol ; 67(3): 1136-1144, 2022 Sep.
Article in English | MEDLINE | ID: mdl-35536427

ABSTRACT

PURPOSE: The aim of this study was to identify the risk factors associated with house infestation by Triatoma dimidiata as well as with Trypanosoma cruzi infection in humans and owned dogs in two rural communities from the municipality of Catemaco, Veracruz, Mexico. METHODS: One hundred and 16 human blood samples and 34 dog blood samples were collected. The presence of anti-T. cruzi antibodies was determined using four different ELISA assays. Moreover, reactive ELISA sera from humans and dogs were processed by indirect immunofluorescence (IFI) to confirm the presence of anti-T. cruzi antibodies. RESULTS: Serologic tests for T. cruzi infection showed a prevalence of 5.1% (6/116) in humans and of 50% (17/34) in owned dogs. CONCLUSION: The presence of animals (dogs, chickens and wild animals), as well as some characteristics of house construction were identified as risk factors for infestation and infection. Complementary studies must be carried out to allow a better understanding of the transmission dynamics in the state of Veracruz, Mexico, and the implementation of adequate control programs.


Subject(s)
Chagas Disease , Triatoma , Trypanosoma cruzi , Animals , Chagas Disease/epidemiology , Chagas Disease/veterinary , Chickens , Dogs , Humans , Insect Vectors , Mexico/epidemiology , Rural Population
2.
Acta Trop ; 213: 105754, 2021 Jan.
Article in English | MEDLINE | ID: mdl-33166517

ABSTRACT

The mechanisms of infection and dispersion of Trypanosoma cruzi among animals, especially in the sylvatic environment, are still not entirely clear, and various aspects of the transmission dynamics of this parasite in the sylvatic environment are still unknown. T. cruzi is a parasite with a great biological and genetic diversity that infects a wide variety of hosts, therefore, transmission cycles of this parasite are complex. The objective of this study was to determine the prevalence of T. cruzi infection and analyze the genetic variability of the discrete typing units (DTUs) of the parasite in three non-human primate species (Alouatta palliata, Alouatta pigra, and Ateles geoffroyi) in southeastern Mexico. A total of one hundred sixty-four serum samples (42 samples of A. pigra, 41 samples of A. palliata (free-ranging) and 81 samples of A. geoffroyi (hosted in care centers)) were analyzed for the detection of anti-T. cruzi antibodies by ELISA assays. The seroprevalence of infection was 23.39% in A. palliata, 21.40% in A. pigra and 16.27% in A. geoffroyi. Additionally, presence of parasite DNA was assessed by PCR, and the identification of DTUs was performed by real-time PCR coupled to High Resolution Melting (qPCR-HRM). Different DTUs (TcI, TcII, TcIII, TcV and TcVI) were found in the analyzed monkeys. In addition, infection of monkeys was not associated with age or gender, but it was associated with the species. This study reveals the risk of infection in the study area and that the different DTUs of the parasite can coexist in the same habitat, indicating that T. cruzi transmission in the study area is very complex and involves many ecological factors. However, there is a need for long-term studies of host-parasite interactions to provide a solid understanding of the ecology of these species and to understand the dispersion strategies of T. cruzi.


Subject(s)
Alouatta/parasitology , Ateles geoffroyi/parasitology , Chagas Disease/transmission , Monkey Diseases/transmission , Trypanosoma cruzi/pathogenicity , Animals , Chagas Disease/parasitology , Chagas Disease/veterinary , Genotype , Host-Parasite Interactions , Humans , Mexico , Monkey Diseases/parasitology , Seroepidemiologic Studies , Species Specificity , Trypanosoma cruzi/genetics
3.
Acta Parasitol ; 65(1): 19-26, 2020 Mar.
Article in English | MEDLINE | ID: mdl-31571142

ABSTRACT

PURPOSE: The state of Puebla has the social marginalization and ecological conditions for the transmission of infectious agents to be effective. Until a few years ago, the state of Puebla was considered non-endemic to the presence of Trypanosoma cruzi as there are no official reports of chronic cases. The objective of this work was to carry out a preliminary study on the prevalence of anti-T. cruzi antibodies in rural areas of the Huatlatlauca municipality in the Mixtec sierra of the state of Puebla. METHODS: A total of 196 serum samples from 12 rural localities were tested by using four tests: two enzyme-linked immunosorbent assays, an xenodiagnoses and PCR assay. RESULTS: Overall, 28 (14.2%) of 196 samples were positive for T. cruzi by ≥ 2 tests (95% CI 6.6-20.8%). Our results suggested that the municipality of Huatlatlauca in the Mixteca Sierra of the state of Puebla is an area with endemic potential for the disease with a high prevalence rate in the adult population and with cases in newborns, these high transmission rates are probably associated with problems of congenital and vector transmission. CONCLUSION: Additional studies should be conducted to generate adequate campaigns for the control of Chagas disease in this area.


Subject(s)
Antibodies, Protozoan/blood , Chagas Disease/epidemiology , Rural Population/statistics & numerical data , Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Cross-Sectional Studies , Endemic Diseases/statistics & numerical data , Female , Geography , Humans , Infant , Infant, Newborn , Male , Mexico/epidemiology , Middle Aged , Preliminary Data , Prevalence , Seroepidemiologic Studies , Trypanosoma cruzi/isolation & purification , Young Adult
4.
J Biomed Sci ; 23(1): 85, 2016 Dec 01.
Article in English | MEDLINE | ID: mdl-27903271

ABSTRACT

BACKGROUND: The dengue non-structural 3 (NS3) is a multifunctional protein, containing a serine-protease domain, located at the N-terminal portion, and helicase, NTPase and RTPase domains present in the C-terminal region. This protein is considered the main target for CD4+ and CD8+ T cell responses during dengue infection, which may be involved in protection. However, few studies have been undertaken evaluating the use of this protein as a protective antigen against dengue, as well as other flavivirus. In the present work we evaluated the potential of the NS3 (protease domain) as a protective antigen by comparing the administration of a recombinant protein versus a DNA vaccine in the mouse model. RESULTS: BALB/c mice were immunized with the recombinant protein NS3-DEN3 via intraperitoneal and with plasmid pcDNA3/NS3-DEN3 intramuscularly and the immune response was evaluated. The activity of T lymphocytes was analyzed by the MTT assay, and cells of mice immunized with the recombinant protein showed no activity when stimulated with the homologous protein. However, cells from mice immunized with DNA, responded to stimulation with the recombinant protein. When the expression (RT-PCR) and cytokine production (ELISA) was evaluated in the splenocytes, different behavior depending on the type of immunization was observed, splenocytes of mice immunized with the recombinant protein expressed cytokines such as IL-4, IL-10 and produced high concentrations of IL-1, IL-6 and TNFα. Splenocytes from mice immunized with DNA expressed IL-2 and IFNγ and did not produce IL-6. In addition, immunization with the recombinant protein induced the production of antibodies that are detected up to a dilution 1:3200 by ELISA and Western blot assays, however, the serum of mice immunized with DNA presented no detectable antibody titers. CONCLUSION: The results obtained in this study show that administration of pcDNA3/NS3-DEN3 induces a favorable response in the activation of T lymphocytes with low production of specific antibodies against NS3-DEN3.


Subject(s)
Dengue Virus/immunology , Immunity, Cellular , Immunity, Humoral , Viral Nonstructural Proteins/immunology , Animals , Antigens, Viral/immunology , CD4-Positive T-Lymphocytes/immunology , CD8-Positive T-Lymphocytes/immunology , Dengue/prevention & control , Dengue/virology , Dengue Virus/pathogenicity , Humans , Mice , Plasmids/administration & dosage , Plasmids/immunology , RNA Helicases/administration & dosage , RNA Helicases/immunology , Recombinant Proteins/administration & dosage , Recombinant Proteins/immunology , Serine Endopeptidases/administration & dosage , Serine Endopeptidases/immunology , Vaccination , Viral Nonstructural Proteins/administration & dosage
5.
Biomed Res Int ; 2013: 281892, 2013.
Article in English | MEDLINE | ID: mdl-24069593

ABSTRACT

The aim of this study is to estimate the prevalence of Trichomonas vaginalis and Candida albicans in low-risk patients treated at a first level clinic (primary health care represents the first level of contact of individuals, families, and the community with the system national health). Using a cross-sectional study in patients treated in clinical laboratory of the Sanitary District no. 7 of the city of Orizaba during the months June-July, 252 urine samples were collected for the identification of T. vaginalis and C. albicans by PCR. Furthermore, we analyzed the sociodemographic characteristics of the studied population. We observed an overall prevalence of 23.41% (95% CI 22.10-24.72) for T. vaginalis and 38.88% (95% CI 37.73-40.03) for C. albicans. There was also presence of coinfection in 14.28% (95% CI 13.10-15.46), which was associated with the presence of pain. Most of the positive cases were observed in women house-maker (80%, 95% CI 50.36-48.98). The results of this study provide evidence that the majority of positive cases observed in the studied population are presented in an asymptomatic form and usually are not associated with any risk factor.


Subject(s)
Candida albicans/isolation & purification , Candidiasis/urine , Health Facilities , Polymerase Chain Reaction/methods , Trichomonas Vaginitis/urine , Trichomonas vaginalis/isolation & purification , Adolescent , Adult , Age Distribution , Aged , Aged, 80 and over , Candida albicans/genetics , Candidiasis/diagnosis , Candidiasis/microbiology , Female , Geography , Humans , Mexico , Middle Aged , Risk Factors , Socioeconomic Factors , Trichomonas Vaginitis/diagnosis , Trichomonas Vaginitis/parasitology , Trichomonas vaginalis/genetics , Young Adult
6.
Parasite Immunol ; 26(10): 409-18, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15752118

ABSTRACT

Acute infection with Trypanosoma cruzi is characterized by immunosuppression mediated by T cells and macrophages (Mphis). Nitric oxide (NO) production during the initial phase of acute infection might participate in the clearance of parasites by Mphis, whereas its overproduction during the late phase of acute infection would account for the immunosuppression observed. Trypanosoma cruzi molecules that might regulate the host responses have not been fully identified. Here, we demonstrate that active immunization with MBP::SSP4, a recombinant protein derived from a surface antigen specific of T. cruzi amastigotes (TcSSP4), was able to stimulate Ab production (IgG1, IgG2a, and IgG2b). On the other hand, MBP::SSP4 was able to stimulate NO production by peritoneal Mphis from BALB/c mice and Mphis from the J774 cell line. This effect was also observed at the level of inducible nitric oxide synthase (iNOS) detected by Western Blot. Furthermore, MBP::SSP4 was also shown to induce the expression of IL-1alpha, IL-6, IL-12, IFN-gamma, and TNF-alpha in normal animals, and IL-10 in immunized animals. In addition the protein MBP::SSP4 was able to bind to the surface of PMphis and J774 Mphis. These results suggest that TcSSP4 could modulate Mphi NO production and this may represent a mechanism participating in the immunoregulatory processes during Chagas' disease.


Subject(s)
Macrophages/immunology , Nitric Oxide/biosynthesis , Protozoan Proteins/immunology , Trypanosoma cruzi/immunology , Animals , Antibodies, Protozoan/blood , Antibody Formation , Blotting, Western , Cells, Cultured , Cytokines/biosynthesis , Cytokines/genetics , Immunity, Cellular , Immunoglobulin G/blood , Macrophages/metabolism , Macrophages/parasitology , Male , Mice , Mice, Inbred BALB C , Models, Animal , Nitric Oxide Synthase/metabolism , Nitric Oxide Synthase Type II , Recombinant Proteins/immunology
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