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1.
Braz. j. microbiol ; 49(4): 919-928, Oct.-Dec. 2018. tab, graf
Article in English | LILACS | ID: biblio-974303

ABSTRACT

ABSTRACT The presence of mycotoxins or related fungi in animal feed is a major problem for animal and human health. Silage and concentrated feed samples were collected from 21 dairy farms in the Western part of Paraná state in Southern Brazil. Water activity and pH of all samples were measured, and each sample was analyzed to check for the presence of aflatoxigenic Aspergillus. Water activity was observed to be lower in the concentrated feed samples. The pH was lower in the silage samples, indicating fermentation processes. Two silage samples and four concentrated feed samples were contaminated with Aspergillus spp. Seven isolates of Aspergillus spp. were obtained and their potential to produce aflatoxins was evaluated. Four of the isolates, two from the silage samples and two from the concentrated feed samples, produced the aflatoxins B1, B2, G1, and G2 in culture media. These isolates were identified as Aspergillus parasiticus and Aspergillus nomius. The presence of aflatoxigenic isolates of Aspergillus spp. in silage and concentrated feed samples is a matter of concern, because of the risk of aflatoxin production and contamination of the animal feed.


Subject(s)
Animals , Cattle , Aspergillus/isolation & purification , Food Contamination/analysis , Aflatoxins/metabolism , Animal Feed/microbiology , Aspergillus/classification , Aspergillus/genetics , Aspergillus/metabolism , Silage/classification , Silage/microbiology , Brazil , Animal Feed/analysis
2.
Braz. j. microbiol ; 46(3): 673-682, July-Sept. 2015. tab, ilus
Article in English | LILACS | ID: lil-755832

ABSTRACT

Aflatoxin contamination of peanut, due to infection by Aspergillus flavus, is a major problem of rain-fed agriculture in India. In the present study, molecular characterisation of 187 Aspergillus flavus isolates, which were sampled from the peanut fields of Gujarat state in India, was performed using AFLP markers. On a pooled cluster analysis, the markers could successfully discriminate among the ‘A’, ‘B’ and ‘G’ group A. flavus isolates. PCoA analysis also showed equivalent results to the cluster analysis. Most of the isolates from one district could be clustered together, which indicated genetic similarity among the isolates. Further, a lot of genetic variability was observed within a district and within a group. The results of AMOVA test revealed that the variance within a population (84%) was more than that between two populations (16%). The isolates, when tested by indirect competitive ELISA, showed about 68.5% of them to be atoxigenic. Composite analysis between the aflatoxin production and AFLP data was found to be ineffective in separating the isolate types by aflatoxigenicity. Certain unique fragments, with respect to individual isolates, were also identified that may be used for development of SCAR marker to aid in rapid and precise identification of isolates.

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Subject(s)
Aspergillus flavus , Aflatoxins/metabolism , Arachis/microbiology , Agriculture , Amplified Fragment Length Polymorphism Analysis , Aspergillus flavus/classification , Aspergillus flavus/genetics , Aspergillus flavus/isolation & purification , DNA, Fungal/genetics , Enzyme-Linked Immunosorbent Assay , Genes, Fungal , Genetic Variation/genetics , India , Molecular Typing , Mycological Typing Techniques , Principal Component Analysis
3.
Braz. j. microbiol ; 45(1): 127-134, 2014. ilus, graf, tab
Article in English | LILACS | ID: lil-709465

ABSTRACT

Manganese peroxidase (MnP) was produced from white rot edible mushroom Pleurotus ostreatus on the culture filtrate. The enzyme was purified to homogeneity using (NH4)2SO4 precipitation, DEAE-Sepharose and Sephadex G-100 column chromatography. The final enzyme activity achieved 81UmL-1, specific activity 78 U mg-1 with purification fold of 130 and recovery 1.2% of the crude enzyme. SDS-PAGE indicated that the pure enzyme have a molecular mass of approximately 42 kDa. The optimum pH was between 4-5 and the optimum temperature was 25 ºC. The pure MnP activity was enhanced by Mn2+,Cu2+,Ca2+ and K+ and inhibited by Hg+2 and Cd+2.H2O2 at 5 mM enhanced MnP activity while at 10 mM inhibited it significantly. The MnP-cDNA encoding gene was sequenced and determined (GenBank accession no. AB698450.1). The MnP-cDNA was found to consist of 497 bp in an Open Reading Frame (ORF) encoding 165 amino acids. MnP from P. ostreatus could detoxify aflatoxin B1 (AFB1) depending on enzyme concentration and incubation period. The highest detoxification power (90%) was observed after 48 h incubation at 1.5 U mL-1 enzyme activities.


Subject(s)
Aflatoxins/metabolism , Peroxidases/isolation & purification , Peroxidases/metabolism , Pleurotus/enzymology , Biotransformation , Chemical Precipitation , Chromatography, Gel , Chromatography, Ion Exchange , DNA, Fungal/chemistry , DNA, Fungal/genetics , Electrophoresis, Polyacrylamide Gel , Enzyme Activators/metabolism , Enzyme Inhibitors/metabolism , Hydrogen-Ion Concentration , Molecular Sequence Data , Molecular Weight , Metals/metabolism , Open Reading Frames , Peroxidases/chemistry , Sequence Analysis, DNA , Temperature
4.
Gastroenterol. latinoam ; 23(2): 57-62, abr.-jun. 2012. tab
Article in Spanish | LILACS | ID: lil-661596

ABSTRACT

Background/aim: High consumption of red chili pepper has been shown to be a risk factor for gallbladder cancer (GBC) in Chilean women with gallstones (GS). GS are the main cause of GBC, but not all patients with gallstones develop GBC. Since red chili pepper is a widely consumed spice among the Chilean population, the development of GBC in Chilean women cannot be completely explained by the presence of GS and red chili pepper consumption alone. Genetic factors in addition to these and other environmental factors may also be associated with an increased risk of GBC. We aimed to study whether genetic polymorphisms involved in aflatoxin metabolism are associated with the risk of GBC in Chilean women, because we detected aflatoxins B1 and B2 in red chili pepper purchased in Santiago, Chile. Methods: We conducted a hospital-based case-control study whose subjects were 57 patients with GBC, 119 patients with GS, and 70 controls. DNA was extracted from subjects’ blood or paraffin block samples using standard commercial kits. The statuses of the genetic polymorphisms of cytochrome P450 (CYP) 1A2 rs762551 and CYP3A4 rs2740574 were assayed using the TaqMan® SNP Genotyping Assay or the Custom TaqMan® SNP Genotyping Assay, respectively. Results: In the assay for the CYP1A2 polymorphism, of the 57 GBC patients, 23 (40.3 percent) had at least one minor allele (A/C or C/C). However, there were no significant differences in the genotypic or allelic frequencies among the three subject groups. In the assay for the CYP3A4 polymorphism, the minor G/G genotype was not detected in the three groups, and there were no significant differences in the genotypic or allelic frequencies among the three groups. Conclusion: These genetic polymorphisms were not related to the risk of GBC in Chilean women. Further studies including a greater number of controls and cases are needed to confirm this preliminary exploratory result.


Introducción/objetivo: El alto consumo de ají rojo ha demostrado ser un factor de riesgo de cáncer vesicular (CV) en mujeres chilenas con cálculos vesiculares. Los cálculos vesiculares son la causa principal de CV, no obstante, no todos los pacientes con cálculos vesiculares desarrollan CV. Debido a que el ají rojo es una especia ampliamente consumida entre la población chilena, el desarrollo de CV en las mujeres chilenas no puede ser explicado en su totalidad sólo por la presencia de cálculos vesiculares y consumo de ají rojo. Factores genéticos además de éstos y otros factores ambientales, también podrían estar relacionados con un aumento del riesgo de CV. Nuestro objetivo es estudiar si los polimorfismos genéticos involucrados en el metabolismo de la aflatoxina están relacionados con el riesgo de CV en mujeres chilenas, porque detectamos aflatoxinas B1 y B2 en ajíes rojos comprados en Santiago de Chile. Métodos: El estudio caso control, incluyó 57 pacientes con CV, 119 pacientes con cálculos vesiculares, y 70 controles. Se extrajo ADN de la sangre de los sujetos o de bloques de parafina, usando kits comerciales estándar. El estado de los polimorfismos genéticos del citocromo P450 (CYP) 1A2 rs762551 y CYP3A4 rs2740574 fueron estudiados usando el ensayo de genotipo SNP TaqMan® o el ensayo de genotipo SNP Custom TaqMan®, respectivamente. Resultados: En el ensayo para el polimorfismo CYP1A2, de los 57 pacientes con CV, 23 (40,3 por ciento) tuvieron al menos un alelo menor (A/C o C/C). No obstante, no hubo diferencias significativas en las frecuencias genotípicas o alélicas entre los tres grupos. En el ensayo para el polimorfismo CYP3A4, el genotipo menor G/G no fue detectado en los tres grupos, y no hubo diferencias significativas en las frecuencias genotípicas o alélicas entre los tres grupos. Conclusión: Estos polimorfismos genéticos no estaban relacionados con el riesgo de CV en mujeres chilenas...


Subject(s)
Humans , Female , Middle Aged , Aflatoxins/metabolism , Gallbladder Neoplasms/genetics , Gallbladder Neoplasms/metabolism , Polymorphism, Genetic , Chile , Case-Control Studies , Risk Assessment , Genetic Predisposition to Disease
5.
GEN ; 49(1): 36-41, ene.-mar. 1995. tab
Article in Spanish | LILACS | ID: lil-163515

ABSTRACT

Está reconocido el valor de las aflatoxinas como agentes carcinogénicos, mutagénicos, teratogénico y su asociación con el virus de la hepatitis B. Por otra parte es asociada la incidencia del carcinoma hepatocelular en dicha infección viral, en vista de lo cual se realizó estudio de los niveles de aductos albúmina-aflatoxina en suero determinado por método de ELISA en niños entre 3 y 15 años del servicio de gastroenterología pediátrica del instituto nacional de gastoenterología de Cuba. Nuestra muestra estuvo constituida por 70 niños: 40 con diagnóstico de hepatitis crónica activa (HCA), 10 portadores de antígeno de superficie positivo del virus de la hepatitis B y 20 controles. En el grupo de HCA se obtuvieron un 32.5 por ciento de positivos con nivel máximo del 25 pg de lisina-aflatoxina/mg de albúmina, los portadores con un 20 por ciento (12.3 pg de lisina-AF/mg de albúmina) y los controles con 15 por ciento (5pg de lisina-AF/mg albúmina). Podemos observar que los niveles de aductos albúmina-aflatoxina de los pacientes de HCA presentaron valores de hasta 5 veces por encima de los controles. Este estudio sugiere la validez de los aductos de albúmina-aflatoxina como un marcador de exposición crónica a este cancerígeno y su importancia en relación con el virus de la hepatitis B


Subject(s)
Child, Preschool , Child , Adolescent , Humans , Male , Female , Aflatoxins/blood , Aflatoxins/immunology , Aflatoxins/metabolism , Albumins/immunology , Hepatitis B/immunology , Carcinogens/supply & distribution , Carcinogens/toxicity
6.
Acta cient. venez ; 37(3): 325-6, 1986.
Article in English | LILACS | ID: lil-44497

ABSTRACT

Una muestra de hígado humano fue obtenida de la autopsia practicada a un paciente admitido en el Hospital Universitario de Los Andes, Mérida, Venezuela. El paciente quien parecía sufrir una enfermedad la cual fue referida al Síndrome de Reye, presentó entre otros hallazgos: degeneración grasa y en largamiento del hígado, encefalopatía y hemorragia de la tráquea, de la mucosa del ileum y del ciego. Este reporte presenta evidencia de la presencia de Aflatoxina B1 en el tejido hepático. Ningún otro metabolito fue detectado. Un número de reportes han sido asociados con el Síndrome de Reye y la presencia de Aflatoxina B1 en tejido, pero hasta ahora, ésta es la primera evidencia reportada en nuestro país


Subject(s)
Adolescent , Humans , Male , Aflatoxins/metabolism , Liver/metabolism , Reye Syndrome/etiology , Liver/pathology
9.
Indian J Exp Biol ; 1979 Jan; 17(1): 97-8
Article in English | IMSEAR | ID: sea-56150
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