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1.
Emerg Infect Dis ; 30(3): 613-616, 2024 Mar.
Article in English | MEDLINE | ID: mdl-38407164

ABSTRACT

We report a case of Enterocytozoon bieneusi infection in a pediatric hematopoietic stem cell transplant recipient in Argentina. Spores were visualized in feces using Calcofluor White and modified trichrome stainings. PCR and sequencing identified E. bieneusi genotype D in fecal samples and liver samples, confirming extraintestinal dissemination of the parasite.


Subject(s)
Enterocytozoon , Hematopoietic Stem Cell Transplantation , Humans , Child , Argentina/epidemiology , Enterocytozoon/genetics , Transplant Recipients , Feces , Hematopoietic Stem Cell Transplantation/adverse effects
2.
J Fungi (Basel) ; 8(8)2022 Jul 28.
Article in English | MEDLINE | ID: mdl-36012781

ABSTRACT

Lung dendritic cells (DC) are powerful antigen-presenting cells constituted by various subpopulations that differ in terms of their function and origin and differentially regulate cell-mediated antifungal immunity. The lung is the primary target organ of Cryptococcus neoformans and C. gattii infections, which makes it essential in the establishment of the first line of anti-cryptococcal defense. However, the lung-specific dynamics and function of DC subsets are poorly understood in cryptococcosis. In this study, we provide evidence for the in vivo function of a conventional langerin-expressing DC1 dendritic cell (LangDC1) population during the first week of intratracheal C. neoformans infection in mice. By using conditional depletion of LangDC1 after diphtheria toxin treatment of LangDTREGFP mice, we demonstrate that these animals better control the fungal infection and produce type 1 and 17 cytokines in the context of a type 2 immune response, favoring a predominance of iNOS over arginase-1 expression by pulmonary cells. Our results suggest that LangDC1 cells play a role in impairing immune response for the clearance of C. neoformans in the early stage of pulmonary infection.

3.
Rev. argent. microbiol ; 53(2): 1-10, June 2021. graf
Article in English | LILACS | ID: biblio-1376402

ABSTRACT

Abstract Microsporidia are obligate intracellular fungi with a remarkable ability to infect a wide range of invertebrate and vertebrate hosts. Namely, Enterocytozoon bieneusi is the most frequently microsporidia reported worldwide, and mainly associated with chronic diarrea and wasting syndrome in AIDS patients. Microscopy and PCR-based detection techniques are effective for diagnosis and identification of species and genotypes; however, these methods should be standardized in each laboratory. In this study, we performed microscopy and nested PCR techniques with PCR product sequencing to detect E. bieneusi in human stool samples. These techniques, if applied together, might prove useful for diagnosis and future epidemiological studies of intestinal microsporidiosis in Argentina.


Resumen Los microsporidios son hongos intracelulares obligados con una notable capacidad para infectar una amplia gama de hospedadores invertebrados y vertebrados. Enterocytozoon bieneusi es el microsporidio más frecuentemente reportado en todo el mundo, principalmente tricrómicaasociado con diarrea crónica y síndrome debilitante en pacientes con sida. Las técnicas dedetección basadas en microscopía y PCR son útiles para el diagnóstico y la identificación deespecies y genotipos, pero estos métodos deben estar estandarizados en cada laboratorio.En este estudio evaluamos técnicas de microscopía y PCR anidada, con secuenciación de losproductos, para detectar E. bieneusi en muestras de heces humanas. Estas técnicas, usadas con-juntamente, podrían ser útiles para su aplicación en el diagnóstico de microsporidiosis intestinaly para realizar estudios epidemiológicos de esta afección en Argentina.


Subject(s)
Humans , Microsporidia , Enterocytozoon , Spores, Fungal , Polymerase Chain Reaction , Microsporidia/genetics , Enterocytozoon/genetics , Feces
4.
Rev Argent Microbiol ; 53(2): 124-128, 2021.
Article in English | MEDLINE | ID: mdl-32595002

ABSTRACT

Microsporidia are obligate intracellular fungi with a remarkable ability to infect a wide range of invertebrate and vertebrate hosts. Namely, Enterocytozoon bieneusi is the most frequently microsporidia reported worldwide, and mainly associated with chronic diarrhea and wasting syndrome in AIDS patients. Microscopy and PCR-based detection techniques are effective for diagnosis and identification of species and genotypes; however, these methods should be standardized in each laboratory. In this study, we performed microscopy and nested PCR techniques with PCR product sequencing to detect E. bieneusi in human stool samples. These techniques, if applied together, might prove useful for diagnosis and future epidemiological studies of intestinal microsporidiosis in Argentina.


Subject(s)
Enterocytozoon , Microsporidia , Enterocytozoon/genetics , Feces , Humans , Microsporidia/genetics , Polymerase Chain Reaction , Spores, Fungal
5.
Front Immunol ; 11: 605644, 2020.
Article in English | MEDLINE | ID: mdl-33343578

ABSTRACT

Dermatophytoses (ringworms) are among the most frequent skin infections and are a highly prevalent cause of human disease worldwide. Despite the incidence of these superficial mycoses in healthy people and the compelling evidence on chronic and deep infections in immunocompromised individuals, the mechanisms controlling dermatophyte invasion in the skin are scarcely known. In the last years, the association between certain primary immunodeficiencies and the susceptibility to severe dermatophytosis as well as the evidence provided by novel experimental models mimicking human disease have significantly contributed to deciphering the basic immunological mechanisms against dermatophytes. In this review, we outline the current knowledge on fungal virulence factors involved in the pathogenesis of dermatophytoses and recent evidence from human infections and experimental models that shed light on the cells and molecules involved in the antifungal cutaneous immune response. The latest highlights emphasize the contribution of C-type lectin receptors signaling and the cellular immune response mediated by IL-17 and IFN-γ in the anti-dermatophytic defense and skin inflammation control.


Subject(s)
Adaptive Immunity , Arthrodermataceae/pathogenicity , Immunity, Innate , Skin/microbiology , Tinea/microbiology , Animals , Arthrodermataceae/immunology , Host-Pathogen Interactions , Humans , Immunity, Cellular , Signal Transduction , Skin/immunology , Tinea/immunology , Virulence
6.
Immunobiology ; 223(12): 834-838, 2018 12.
Article in English | MEDLINE | ID: mdl-30197196

ABSTRACT

Fasciolosis is a zoonotic disease of increasing importance due to its worldwide distribution and elevated economic losses. Previously, we demonstrated that Fasciola hepatica excretory-secretory products (FhESP) induce immunomodulatory effects on peritoneal macrophages in a Dectin-1 dependent manner. In this study, we observed that peritoneal macrophages from naive BALB/c mice stimulated in vitro with FhESP presented increased expression levels of phosphorylated extracellular-signal-regulated kinase (ERK), and this effect was dependent on Syk, protein kinase C (PKC) and Dectin-1. In this sense, we observed increased levels of arginase activity, IL-10 and TGF-ß in macrophages stimulated with FhESP, which were dependent on PKC and ERK. Furthermore, we observed that the increased arginase activity, as well as in TGF-ß and IL-10 levels, was partially dependent on IL-10 receptor signaling in macrophages that were pre-incubated with anti-IL10R before being stimulated with FhESP. Taken together, these results suggest the participation of Dectin-1 and Syk in FhESP interaction with peritoneal macrophages and the possible role of ERK and IL-10 in downstream signaling pathways involved in the immunomodulatory effects induced by Fasciola hepatica products.


Subject(s)
Fasciola hepatica/immunology , Fascioliasis/immunology , Fascioliasis/parasitology , Immunomodulation , Lectins, C-Type/metabolism , MAP Kinase Signaling System , Macrophages/immunology , Macrophages/metabolism , Animals , Arginase/metabolism , Cytokines/biosynthesis , Enzyme Activation/drug effects , Extracellular Signal-Regulated MAP Kinases/metabolism , Fascioliasis/metabolism , Female , Mice , Phosphorylation
7.
J Invest Dermatol ; 138(8): 1744-1753, 2018 08.
Article in English | MEDLINE | ID: mdl-29571944

ABSTRACT

Despite worldwide prevalence of superficial mycoses, the immune response in dermatophytosis has scarcely been investigated. In this study, we developed a model of superficial skin infection in C57BL/6 mice with Microsporum canis, a highly prevalent human pathogen. This model mimics mild inflammatory human dermatophytosis, characterized by neutrophil recruitment and fungal invasion limited to the epidermis and exhibits the establishment of a specific T helper type 17 immune response during infection. By using IL-17RA- or IL-17A/F-deficient mice we showed that, in the absence of a functional IL-17 pathway, M. canis extensively colonizes the epidermis and promotes an exaggerated skin inflammation and a shift to an IFN-γ-mediated (T helper type 1) response. IL-17 signaling was not involved in neutrophil influx to skin or fungal invasion to deeper tissues. Finally, this study shows that skin langerin-expressing cells contribute to the antifungal T helper type 17 response in vivo. In conclusion, these data directly show a dual function of IL-17 cytokines in dermatophytosis by controlling superficial infection and down-modulating a T helper type 1 antifungal response.


Subject(s)
Host-Pathogen Interactions/immunology , Microsporum/immunology , Signal Transduction/immunology , Th17 Cells/immunology , Tinea/immunology , Animals , Disease Models, Animal , Epidermis/immunology , Epidermis/microbiology , Epidermis/pathology , Humans , Interleukin-17/genetics , Interleukin-17/immunology , Interleukin-17/metabolism , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Microsporum/pathogenicity , Neutrophil Infiltration/immunology , Receptors, Interleukin-17/genetics , Receptors, Interleukin-17/immunology , Receptors, Interleukin-17/metabolism , Th17 Cells/metabolism , Tinea/microbiology , Tinea/pathology
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