Evaluación de la flora fungica del ambiente del archivo general del Estado Sucre Venezuela / Evaluation of the fungic flora of the atmosphere of the general archives of the Sucre State Venezuela

Los agentes fúngicos son capaces de descomponer materia orgánica como madera, papel, pintura, suelo, polvo, alimentos. Pueden ocasionar deterioro de material bibliográfico , texto, mobiliario, pinturas, igualmente causan enfermedades de tipo alérgico. El Archivo General del Estado Sucre es un centro de consulta e investigación donde se encuentran documentos y otros textos que se han ido dañando a través del tiempo; las condiciones de almacenamiento de un área con deficiencias estructurales y ambientales, favorecen el desarrollo de hongos, causando el deterioro dl material bibliográfico. Se realizaó una investigación para evaluar la flora fúngica tanto del mobiliario como documentos y textos existentes, que se servirá de base para un futuro plan de conservación y restauración. Utilizando el método de sedimentación en placa conteniendo Agar Sabouraud Dextrosa, se expusieron 60 placas durante 15 minutos en diferentes secciones del área de estudio, incubándose 10 días a temperatura ambiente. Se aislaron 86 colonias que se caracterizaron macro y microcóspicamente. Los géneros aislados fueron: Aspergillus (38,46%), Fusarium (21,70%), Curcularia (16,76%), Cladosporium (12,76%), Penicillium (10,32%), los cuales han sido descritos como contaminantes habituales de libros o textos, mobiliarios, pinturas, además capaces de causar reacciones alérgicas de tipo respiratorios resultando un riesgo para el material bibliográfico, usuarios y personal de la institución.

The fungies agents are able to disturb organics material as wood, paper, paint, ground, drust, foods they can produce deterioration of bibliographycal material, texts, house-hold goods, paintings, and equally they cause disease of alergic type. The general archives of Sucre state is a consulting center and investigation where it is found historic documents and another texts which have been damaging throuth the time, the conditions of storing in an area with estructural deficiencis and environment improve the development of fungies causing the depreciation of bibliographycal material. An investigation was done to evaluate the fingis flora as the house-hold godos, as the existen documents and texts, that it would serve the base to desing the future plan of conservation and restauration. Using the method of sedimentation in plaque containing Agar Sabouraud Dextrosa, 60 plaques were exposed during 15 minutes in different sections of study area, incubating 10 days at atmosphere temperatura. 86 colonies were isolated that were characterized macro and microcospyly. The aislated fungic species were: Aspegillus (35,46%), Fusarium (21,70%), Curvalaria (16,76%), Cladosporium (12,76%), Penicillium (10,32%), which have been described as usual contaminating of book o texts, house-hold godos, paintings, in addiction to this they are able to cuse alergic rections of respiratory type, resulting a risk to the bibliographycal material, usuaries and personal of the institution.

Biomarcadores para avaliação da exposição humana às micotoxinas / Biomarkers for assessment of human exposure to mycotoxins

Atualmente, as micotoxinas representam um risco de contaminação ambiental, acarretando sérios prejuízos à saúde humana. Essas toxinas podem estar presentes em diferentes tipos de alimentos, que constituem a principal fonte de exposição para o homem. As exposições podem ser monitoradas através do uso de biomarcadores, que elucidam a relação causa/efeito e dose/efeito na avaliação de risco à saúde para fins de diagnóstico clínico e laboratorial. Realizou-se uma revisão bibliográfica do período de 1981-2005, no MEDLINE, sobre utilização e propostas de biomarcadores para a exposição a aflatoxinas, fumonisinas, desoxinivalenol e ocratoxina A. Os possíveis biomarcadores para avaliar a exposição humana às aflatoxinas foram os metabólitos urinários de aflatoxina B1, como aflatoxina M1, aflatoxina P1, aflatoxina Q1, aflatoxina livre em soro ou plasma, os adutos de AFB-N7-guanina, os adutos de albumina ou mutação no gene supressor de tumor p53, presentes em fluidos biológicos. Para as fumonisinas, os biomarcadores foram os níveis de fumonisina B1 e fumonisina B2 livres, ou de esfinganina e esfingosina em sangue e urina. O desoxinivalenol tem como biomarcadores de exposição os produtos de seu metabolismo e adutos macromoleculares (proteína/DNA) presentes nos fluidos biológicos. Para a exposição à ocratoxina A (OA) os biomarcadores se restringem à quantificação da própria toxina nos fluidos biológicos. A avaliação da exposição às micotoxinas constitui um importante aspecto para a saúde pública, tendo em vista a possibilidade de prevenir ou minimizar a incidência de doenças decorrentes da sua interação com o organismo.

Currently, mycotoxins represent a risk of environmental contamination, causing serious damages to human health. Those toxins can be found in different kinds of foods, and they constitute the main source of human exposure. The evaluation of such exposures can be monitored through the use of biomarkers, which elucidates the cause/effect and dose/effect relation in the evaluation of health risks for clinical and laboratory diagnostic purposes. The MEDLINE review about the use of biomarkers for assessment of aflatoxins, fumonisins, deoxynivalenol and ochratoxin A was carried out from 1981 to 2005. The biomarkers for assessment of human exposure to aflatoxins were the urinary metabolites of aflatoxin B1: aflatoxin M1, aflatoxin P1, aflatoxin Q1, the free aflatoxin in serum or plasma, the AFB-N7-guanine adducts and the albumin adducts or mutation in the tumour suppressor gene p53 present in human biological fluids. As far as fumonisins are concerned, levels of free fumonisin B1 and fumonisin B2, or levels of sphinganine and sphingosin, were quantified in blood and urine. As exposure biomarkers, deoxynivalenol has its own metabolism products and adducts (protein/DNA) present in human fluids. As to ochratoxin A exposure, we measure it in biological fluids, once it enables us to prevent or minimize the incidence of deaths or illnesses provoked by chemical exposure.

Mycotoxins [aflatoxins and ochratoxins] in blood of pre-eclamptic and eclamptic egyptian patients and their relation to myocotoxins in the umbliocal cord blood and the fetal outcome umblical

This study included 172 primigravid mothers, 98 had preeclampsia, 22 had eclamptic fits, and 52 were normal pregnants. Aflatoxins were detected in 70.4% and 90.9% in maternal blood samples of preeclamptic and eclamptic patients, respectively, compared with none in the control. They were detected in 67.3%, 90.95%, and 1.9% in the fetal blood of preeclamptic, eclamptic and control groups, respectively. There was no significant difference in Aflatoxins [Afs] between maternal and fetal blood. Ochratoxin A could not be detected in maternal blood of the control group or in the fetal blood samples of all groups. Aflatoxin B1 was the most abundant aflatoxin in the maternal and fetal blood samples. Aflatoxin M1 and M2 could not be detected in the umbilical cord blood samples. There was significant high level of AfB1 in the umbilical cord blood of unhealthy babies [small for date, neonatal distress and neonatal jaundice] compared with healthy babies