RESUMEN
OBJECTIVES: Nutritional aggression in critical periods may lead to epigenetic changes that affect gene expression. The aim of this study was to assess the effect of neonatal malnutrition on the expression of toll-like receptor (TLR)-2, TLR-4, and NLRP3 receptors, caspase-1 enzyme, and interleukin (IL)-1 ß production in macrophages infected with methicillin-resistant (MRSA) and methicillin-sensitive (MSSA) Staphylococcus aureus. METHODS: Wistar rats (N = 24) were divided in two distinct groups: nourished (17% casein) and malnourished (8% casein). Four systems were established after the isolation of mononuclear cells: negative control, positive control, MRSA, and MSSA. The plates were incubated at 37°C for 24 h in humidified atmosphere and 5% carbon dioxide. Tests were performed after this period to analyze the expression of standard recognition receptors, caspase-1 enzyme, and the production of IL-1 ß. Student's t test and analysis of variance were used in the statistical analysis; P < 0.05 was statistically significant. RESULTS: Malnutrition reduced animal growth and the expression of TLR-2, TLR-4, and NLRP3 receptors, the caspase-1 enzyme, and the IL-1 ß levels in macrophages infected with lipopolysaccharides in the present study. However, the interaction between the S. aureus and the macrophages promoted greater gene expression of receptors and enzymes. CONCLUSION: The neonatal malnutrition model compromised the expression of standard recognition receptors, of the caspase-1 enzyme as well as the production of IL-1 ß. However, the S. aureus and neonatal malnutrition combination led to intense transcription of such innate immunity components. Therefore, the deregulation in the expression of TLR and NLRP3 receptors and of the caspase-1 enzyme may induce extensive tissue injury and favor the permanence and spread of these bacteria, especially those that are methicillin resistant.
Asunto(s)
Epigénesis Genética , Regulación de la Expresión Génica , Inmunidad Innata , Inflamasomas/metabolismo , Macrófagos Alveolares/metabolismo , Desnutrición/complicaciones , Infecciones Estafilocócicas/complicaciones , Animales , Animales Recién Nacidos , Caspasa 1/genética , Caspasa 1/metabolismo , Células Cultivadas , Dieta con Restricción de Proteínas/efectos adversos , Femenino , Interleucina-1beta/genética , Interleucina-1beta/metabolismo , Lactancia , Macrófagos Alveolares/inmunología , Macrófagos Alveolares/microbiología , Macrófagos Alveolares/patología , Masculino , Desnutrición/dietoterapia , Desnutrición/etiología , Fenómenos Fisiologicos Nutricionales Maternos , Staphylococcus aureus Resistente a Meticilina/inmunología , Proteína con Dominio Pirina 3 de la Familia NLR/genética , Proteína con Dominio Pirina 3 de la Familia NLR/metabolismo , Ratas Wistar , Infecciones Estafilocócicas/inmunología , Infecciones Estafilocócicas/metabolismo , Infecciones Estafilocócicas/microbiología , Receptor Toll-Like 2/genética , Receptor Toll-Like 2/metabolismo , Receptor Toll-Like 4/genética , Receptor Toll-Like 4/metabolismoRESUMEN
The aim of the study was to compare the innate immune system of severely malnourished children admitted to the Instituto de Medicina Integral Professor Fernando Figueira and treated according to the protocol of the World Health Organization (WHO) at admission and discharge. An experimental study was conducted with 20 children under two years of age. Ten of them had severe malnutrition and ten were a control group. The malnourished group consisted of hospitalized infants and it was submitted to WHO's protocol. Children with HIV and re-admitted during the study period were excluded. A blood sample was taken at admission and at discharge. Later, an analysis of blood leukocytes, adherence index, phagocytic capacity, production of free radicals superoxide and nitric oxide was performed. Patients with severe malnutrition at hospital discharge showed improved phagocytic function, release of oxygen radicals and reduction of the number of lymphocytes when compared to the time of admission. When compared to the control group, patients at hospital discharge had lower lymphocyte values and lower production of free radicals. Thus, it can be concluded that the duration of hospitalization was insufficient to restore cell-mediated immunity and microbicide activity.
El objetivo del estudio fue comparar el sistema inmune innato de niños con malnutrición grave ingresados en el Instituto de Medicina Integral Professor Fernando Figueira, tratados de acuerdo con el protocolo de la Organización Mundial de la Salud (OMS), al ingreso y al alta hospitalaria. Se llevó a cabo un estudio experimental con 20 niños menores de dos años de edad, 10 con malnutrición grave y 10 niños del grupo de control. El grupo de malnutridos se compuso de lactantes hospitalizados y sometidos al protocolo de la OMS. Se excluyeron los niños afectados por el HIV y los readmitidos durante el período del estudio. Se recogió una muestra de sangre al ingreso y otra al alta, y posterioriormente se realizó el análisis del perfil leucocitario, y el índice de adherencia, la capacidad fagocítica y la producción de los radicales libres superóxido y óxido nítrico. Los pacientes con malnutrición grave en el alta hospitalaria mostraron mejoría de la función fagocítica, la liberación de radicales oxidantes y la reducción del número de linfocitos en comparación con el ingreso hospitalario. En comparación con el grupo de control, los pacientes en el alta hospitalario presentaron valores más bajos de linfocitos y de producción de radicales libres. Por lo tanto, se puede concluir que el tiempo de hospitalización fue insuficiente para restablecer la inmunidad mediada por células, así como para restaurar la actividad microbicida.
Asunto(s)
Trastornos de la Nutrición del Niño/inmunología , Trastornos de la Nutrición del Niño/terapia , Inmunidad , Biomarcadores , Adhesión Celular , Trastornos de la Nutrición del Niño/diagnóstico , Preescolar , Humanos , Lactante , Recién Nacido , Recuento de Leucocitos , Óxido Nítrico , Fagocitosis , Guías de Práctica Clínica como Asunto , Índice de Severidad de la Enfermedad , Organización Mundial de la SaludRESUMEN
Patients infected with human immunodeficiency virus (HIV) are a risk group for onychomycosis, fungal infections caused mainly by dermatophytes and yeast. However, non-dermatohytic moulds are becoming common agents for nail infections in this population of patients. We report four cases of onychomycosis caused by non-dermatophytic moulds (Aspergillus niger, Scytalidium hyalinum, Scytalidium dimidiatum and Fusarium solani) in patients infected with HIV from Recife, Pernambuco, Brazil. Onychomicosis by non-dermatophytic species in HIV-positive patients requires special attention in the clinical and the laboratory. A proper diagnosis is necessary to establish the specific and adequate treatment, preventing fungal invasion.
Asunto(s)
Infecciones Oportunistas Relacionadas con el SIDA/microbiología , Ascomicetos/aislamiento & purificación , Aspergilosis/microbiología , Aspergillus niger/aislamiento & purificación , Fusarium/aislamiento & purificación , Onicomicosis/microbiología , Adulto , Terapia Antirretroviral Altamente Activa , Femenino , Humanos , Masculino , Persona de Mediana EdadRESUMEN
La infección causada por el virus de la inmunodeficiencia humana (VIH) es unfactor de riesgo para el desarrollo de las onicomicosis, infecciones micóticascausadas principalmente por dermatofitos y levaduras. Los hongos filamentososno dermatofitos están emergiendo como agentes de lesiones ungueales eninmunodeprimidos. Presentamos cuatro casos de onicomicosis por hongosfilamentosos no dermatofitos (Aspergillus niger, Scytalidium hyalinum,Scytalidium dimidiatum y Fusarium solani) en pacientes portadores del VIH,residentes en la ciudad de Recife, Pernambuco - Brasil. Las onicomicosis porespecies no dermatofíticas en pacientes VIH-positivos requieren mayor atenciónen relación a los aspectos clínicos y de laboratorio con la finalidad deestablecer el diagnóstico etiológico correcto e indicar el tratamiento específico yadecuado, previniendo invasiones por hongos en otros sitios(AU)
Patients infected with human immunodeficiency virus (HIV) are a risk group foronychomycosis, fungal infections caused mainly by dermatophytes and yeast.However, non-dermatohytic moulds are becoming common agents for nailinfections in this population of patients. We report four cases of onychomycosiscaused by non-dermatophytic moulds (Aspergillus niger, Scytalidium hyalinum,Scytalidium dimidiatum and Fusarium solani) in patients infected with HIV fromRecife, Pernambuco, Brazil. Onychomicosis by non-dermatophytic species inHIV-positive patients requires special attention in the clinical and the laboratory.A proper diagnosis is necessary to establish the specific and adequatetreatment, preventing fungal invasion(AU)
Asunto(s)
Humanos , Masculino , Adulto , Hongos/patogenicidad , Onicomicosis/microbiología , Infecciones por VIH/complicaciones , Infecciones Oportunistas Relacionadas con el SIDA/microbiología , Aspergillus/aislamiento & purificación , Fusarium/aislamiento & purificaciónRESUMEN
BACKGROUND/AIMS: Neonatal malnutrition induces metabolic and endocrine changes that have beneficial effects on the neonatal in the short term but, in the longer term, these alterations lead to maladaptations. We investigated the effect of neonatal malnutrition on immune responses in adult rats submitted or not to an aggressiveness test. METHODS: Male Wistar rats were distributed to one of two groups according to their mothers' diet during lactation: the well-nourished group (group C, n = 42, receiving 23% of protein) and the malnourished group (group MN, n = 42, receiving 8% of protein). After weaning, all rats received normoproteic diet. Ninety days after birth, each group was subdivided into three subgroups: control rats (n = 14, respectively), aggressive rats (n = 14, respectively) and rats receiving foot shock (FS; n = 14, respectively). Plasma corticosterone concentration was measured after FS sessions. Leukocyte counts and humoral immunity were evaluated. RESULTS: In neonatal malnourished animals, FS-induced stress reduced plasma corticosterone concentration. Intraspecific aggressiveness induced alterations in leukocyte counts and antibody titers 7 and 15 days after immunization. Neonatal malnourished animals showed no changes in the immune parameters evaluated. CONCLUSIONS: Expression of intraspecific aggressiveness activates the immune system. Neonatal malnutrition seems to have a long-lasting effect on components of both neuroendocrine and immune functions.