Evaluación del método de Petroff modificado con solución salina para el diagnóstico de micobacterias en el sistema Bact/Alert 3D / Assessment of Petroff method modified with saline solution for the diagnosis of mycobacteria in Bact/Alert 3D system

Introducción: Existen diferentes métodos de descontaminación de muestras pulmonares para el diagnóstico de micobacterias. El Programa Nacional de Control de Tuberculosis recomienda el método de Petroff modificado con solución salina, pero no existen evidencias documentadas que avalen este método. Objetivo: Evaluar el método de Petroff modificado con solución salina para el diagnóstico de micobacterias en el sistema Bact/Alert 3D. Métodos: Se realizó un estudio observacional analítico de pruebas diagnósticas utilizando 100 muestras pulmonares recibidas en el Laboratorio Nacional de Referencia e Investigaciones de Tuberculosis, Lepra y Micobacterias del Instituto Pedro Kourí, abril 2016 enero 2017. La muestra se dividió en 3 alícuotas y se descontaminaron mediante 3 métodos; luego se inocularon en los medios de cultivo sólido y líquido. Se compararon los resultados del cultivo en cuanto: tiempo de detección de crecimiento, tasa de contaminación, por ciento de positividad, además se calcularon indicadores de desempeño. Resultados: Al comparar el método Petroff modificado con solución salina con el Petroff modificado con solución fosfato en Löwenstein Jensen, el tiempo de detección de crecimiento, por ciento de positividad y la tasa de contaminación se comportaron de forma similar y la sensibilidad (93,75 por ciento), concordancia (96,47 por ciento) e índice de Youden (0,91) fueron elevadas. Al compararlo el Petroff modificado con solución salina con el N-Acetil-L-Cisteína, las variables no mostraron diferencias significativas y los Indicadores de Desempeño se comportaron por encima del 93 por ciento, para el medio sólido y líquido. Conclusiones: Los resultados avalan la continuidad del uso del Petroff modificado con solución salina como método de descontaminación de las muestras pulmonares en la red de laboratorios de Cuba y como alternativa en el pretratamiento de las muestras para el medio líquido (Bact/Alert 3D), además constituye un soporte para el Programa Nacional de Control de Tuberculosis(AU)

Introduction: There are different decontamination methods of pulmonary samples for the diagnosis of mycobacteria. The National Program for the Control of Tuberculosis recommends Petroff method modified with saline solution; but there are not documented evidences that endorse it. Objective: Assess Petroff method modified with saline solution for the diagnosis of mycobacteria in Bact / Alert 3D system. Methods: An observational analytic study of diagnostic tests was conducted; there were used 100 pulmonary samples received in the National Laboratory of References and Researches of Tuberculosis, Leprosy and Mycobacteria of Pedro Kourí Institute, from April 2016 to January 2017. The sample was divided in 3 aliquots and those were decontaminated using 3 methods; then, they were inoculated in the solid and liquid culture means. Cultures´ results were compared according to: growth's detection time, contamination rate, percent of positivity; in addition, performance indicators were calculated. Results: When comparing Petroff method modified with saline solution with Petroff method modified with phosphate solution in Löwenstein Jensen, the growth's detection time, the percent of positivity and the rate of contamination behaved similarly, and sensitivity (93,75percent), concordance (96,47percent) and Youden´s index (0,91) were high. When the Petroff method modified with saline solution was compared with N-Acetil-L- Cisteina, the variables did not show significative differences and the behaviour indicators were over 93percent for the solid and liquid mean. Conclusions: The results endorse the continuity of the use of Petroff method modified with saline solution as a decontamination method of pulmonary samples in the network of Cuban laboratories and as alternative to the pre-treatment of the samples for the liquid mean (Bact/Alert 3D); it also constitutes a support for the National Program for the Control of Tuberculosis(AU)

Antioxidants in the control of microorganism contamination and phenol oxidation in Eugenia pyriformis / Antioxidantes no controle da contaminação microbiana e da oxidação fenólica em Eugenia pyriformis

Uvaia (Eugenia pyriformis) is a fruit tree of the Myrtaceae family. It has recalcitrant seeds of limited longevity, making seed propagation difficult. Micropropagation is an alternative method to obtain a large quantity of progeny plants in a short period of time, by using any part of the plant as explant. The high concentration of phenols associated with the chemical composition of the Myrtaceae, and the presence of microorganisms in the plant material or culture media, can make in vitro propagation difficult and/or impossible. The objective was to evaluate various concentrations of antioxidants affecting the control of microbial contamination and phenol oxidation in vitro in uvaia. A completely randomized design was used, with a 3 (antioxidants PVP, L-cysteine, and ascorbic acid) × 3 (antioxidant concentrations 100, 200, and 300 mg L-1) × 2 (activated charcoal at 0 and 2 g L-1) factorial arrangement + 2 additional variables (absence of antioxidants and activated charcoal; absence of antioxidants with 2 g L-1 activated charcoal), with three repetitions comprising four plants each. The percentage of bacterial and fungal contaminations, along with the number of oxidized explants, was evaluated after 7, 14 and 21 days of in vitro cultivation. It was concluded that, where bacterial and fungal contaminations were concerned, in vitro cultivation of uvaia can be performed without the use of antioxidants. PVP or ascorbic acid must, however be used in the process, at a concentration of 300 mg L-1, along with 2 g L-1 of activated charcoal. This helps to minimize phenol oxidation.

A uvaia Eugenia pyriformis é uma frutífera da família das mirtáceas cujas sementes apresentam longevidade curta e aspecto recalcitrante, fato que dificulta a propagação seminífera. A micropropagação surge como alternativa para obtenção de grande quantidade de mudas em curto período de tempo, por meio da utilização de qualquer parte da planta como explante. A elevada concentração de fenóis associados à composição química das mirtáceas e a presença de microrganismos no material vegetal ou no meio de cultura podem dificultar e/ou impossibilitar a propagação in vitro. Objetivou-se avaliar tipos e concentrações de antioxidantes no controle da contaminação microbiana e da oxidação fenólica in vitro de E. pyriformis. Utilizou-se o delineamento inteiramente casualizado em esquema fatorial 3 (antioxidantes ­ PVP, L-cisteína e ácido ascórbico) x 3 (concentrações - 100, 200 e 300 mg L-1) x 2 (carvão ativado ­ 0 e 2 g L-1) + 2 adicionais (ausência de antioxidantes e de carvão ativado; ausência de antioxidantes com 2 g L-1 de carvão ativado), com três repetições constituídas por quatro plantas. Após sete, 14 e 21 dias do cultivo in vitro foram avaliadas a porcentagem de contaminação bacteriana, fúngica e de explantes oxidados. Conclui-se que o cultivo in vitro de E. pyriformis, em relação as contaminações bacterianas e fúngicas, pode ser efetuado sem a utilização de agentes antioxidantes. Entretanto, para reduzir a oxidação fenólica deve ser utilizado o PVP ou ácido ascórbico, ambos na concentração de 300 mg L-1, associados a 2 g L-1 de carvão ativado.

Synthesis and characterization of a cysteine xyloglucan conjugate as mucoadhesive polymer

The aim of this study was to improve the mucoadhesive potential of xyloglucan polymer by the covalent attachment of cysteine as thiol moiety. The parent polymer xyloglucan was chemically modified by introducing sulphydryl bearing compound L-cysteine HCl. Different batches of xyloglucan-cysteine conjugates were prepared at varying reaction pH (2-6) and evaluated for optimum thiol incorporation, disulphide group content, swelling behavior, rheological properties and mucoadhesive properties. The obtained conjugates characterized in vitro by quantification of immobilized thiol groups; showed maximum thiol incorporation on xyloglucan (7.67 ± 0.14 %) at pH 5. The disulphide group content was found maximum (2.83 ± 0.12) at pH 6. The water uptake at end of 4 h was 5.0 for xyloglucan and was found to decrease in thiolated derivatives with increase in thiolation. Mucoadhesion studies revealed that mucoadhesion of xyloglucan-cysteine conjugate increased more than twice compared to the unmodified polymer. The viscosity of thiomer was more than that of xyloglucan because of formation of disulphide bonds.

O objetivo deste estudo foi melhorar o potencial mucoadesivo do polímero xiloglicano pela ligação covalente de cisteína como unidade de tiol. O polímero xiloglicano foi quimicamente modificado pela introdução de cloridrato de cisteína como grupo contendo sulfidrila. Prepararam-se diferentes lotes de conjugados cisteína-xiloglicano em pH variando de 2 a 6, avaliando-se a incorporação ótima de tiol, o conteúdo de dissulfeto, o comportamento de inchamento, as propriedades reológicas e mucoadesivas. Os conjugados obtidos foram caracterizados in vitro pela quantificação de grupos tiol, mostrando máxima incorporação na xiloglicana (7.67 ± 0.14 %) em pH 5. O conteúdo de grupos dissulfeto foi máximo (2.83 ± 0.12) em pH 6. O índice de inchamento em % no fim de 4 h foi 83.87 para o xiloglicano e diminuiu para os derivados tiolados. O conteúdo foi mínimo para TH2 (78.26), aumentou pouco até TH5 (83.33) e diminuiu, posteriormente, para TH6 (80.13). Os estudos de mucoadesão revelaram que o conjugado xiloglicano-cisteína aumentou mais que duas vezes comparativamente ao polímero não modificado. A viscosidade do tiômero foi maior do que a do xiloglicano devido à formação das ligações dissulfeto.

Cuantificacion de arsenico por inyeccion en flujo-generacion de hidruros-espectrometria de absorcion atomica (IF-GH-EAA) previa derivatizacion con L-cisteina. Validacion y comparaci¨®o intermetodologica utilizando dos tecnicas de referencia / Arsenic quantitation by flow injection-hydride generation- atomic absorption spectrometry (FI-HG-AAS) after L-cysteine derivatization. Validation and inter-methodological comparison using two reference techniques

La presencia de Arsenico (As) en aguas de consumo representa una problematica para la salud publica en muchas regiones del mundo, incluida la Argentina. La cuantificacion de arsenico en agua de bebida y en orina se utiliza para evaluar la exposicion a este contaminante. El presente trabajo tuvo como objetivo la validacion metodologica de una tecnica para la cuantificacion de especies del As [AsV + AsIII + acido monometilarsonico (MMA) + acido dimetilarsinico (DMA)] por inyeccion en flujo-generacion de hidruros-espectrometria de absorcion atomica (IF-GH-EAA), previa derivatizacion con L-cisteina. Los resultados fueron comparados con los obtenidos utilizando dos metodologias de referencia, generacion de hidruros-espectrometria de absorcion atomica (GH-EAA) para muestras de aguas y orina, y cromatografia de alta resolucion ¨Cgeneracion de hidruros-espectrometr¨ªa de absorcion atomica (HPLC-GH-EAA) para muestras de orina. Ademas, se evaluo la selectividad de la cuantificacion por IF-GH-EAA, en presencia de otras especies quimicas del As, provenientes del consumo de alimentos producto de la pesca, a traves de un ensayo biologico. Los niveles de As hallados en las muestras de agua y de orina utilizando las tecnicas de referencia presentaron un rango de 6 a 176 ¦Ìg/L y de 143 a 3312 ¦Ìg/g de creatinina, respectivamente. Los coeficientes de Pearson resultantes de la comparacion de los datos obtenidos por IF-GH-EAA, con los logrados por los metodos de referencia fueron r = 0,9976 y r = 0,9422, para agua y orina, respectivamente. Los resultados de la prueba biologica indicaron un mayor nivel de As, debido al consumo de alimentos producto de la pesca, cuando las muestras de orina fueron previamente mineralizadas (GH-EAA), con la consecuente sobreestimacion del contenido de As proveniente del consumo de As inorganico. Este aumento no se observo cuando estas fueron analizadas por IF-GH-EAA ...

The presence of arsenic (As) in drinking water is a public health concern in many regions of the world, including Argentina. Quantification of arsenic in drinking water and urine are used to assess exposure to this pollutant. This study aimed to validate a methodology for the quantification of As species [AsV + AsIII + acid monometilarsonico (MMA) + dimetilarsinico acid (DMA)] by flow injection-hydride generation-atomic absorption spectrometry (FI-HG-AAS), after derivatization with L-cysteine. The results were compared with those obtained using two methods of reference, hydride generation-atomic absorption spectrometry (HG-AAS) for water and urine samples, and high performance liquid chromatography-hydride generation-atomic absorption spectrometry (HPLC-HG-AAS) for urine samples. In addition, the selectivity of quantification by FI-HG-AAS in the presence of other chemical species of As, from fishery products intake, was evaluated through a biological assay.The As level found in water and urine samples, using the techniques of reference, showed a range from 6 to 176 ¦Ìg/L and from 143 to 3312 ¦Ìg/g creatinine, respectively. Pearson coefficients resulting from the comparison of data obtained by FI-HG-AAS with those achieved by the reference methods were r = 0.9976 and r = 0.9422 for water and urine, respectively. The results of the biological test showed a higher level of As, due to consumption of food fishery product, when urine samples were previously mineralized (HG-AAS), with consequent overestimation of the inorganic arsenic consumption. When these samples were analyzed by FI-HG-AAS this fact was not observed, and the values were comparable to baseline level prior to consumption ...

Efecto de la suplementación con L-cisteína en la maduración in vitro de ovocitos bovinos / L-cysteine supplementation effect on the in vitro maturation of bovine oocytes

utilizada como herramienta para el estudio de diversos aspectos relacionados con la maduración de ovocitos, la fecundación y el desarrollo temprano del embrión en condiciones in vitro. La L-cisteína es un sustrato externo requerido para la síntesis del glutation en la maduración de ovocitos bovinos. Con el objetivo de evaluar el efecto de la suplementación con L-cisteína sobre la maduración in vitro de ovocitos bovinos, se llevó a cabo un experimento con ovarios obtenidos de vacas mestizas beneficiadas en una sala de matanza local. Se utilizaron tres tratamientos con diferentes concentraciones T1: 0 mM; T2: 0,1 mM y T3: 1,0 mM. Aproximadamente 400 Complejos Cumulus Ovocito (COCs) por tratamiento se maduraron en pozos de 500 µL del medio de maduración (TCM-199), distribuyéndose 50 COC por pozo en una incubadora a 5% de CO2, a 38,5°C y con humedad saturada. Los datos se analizaron por medio de un análisis de varianza (ANAVAR). No se observaron diferencias significativas entre los tratamientos en el porcentaje de ovocitos que llegaron a Metafase II (MII, T1: 72,77%, T2: 67,47% y T3: 70,43%). Los resultados indican que la suplementación con L-cisteína durante la maduración no ejerció un efecto sobre el porcentaje de ovocitos bovinos que alcanzaron el estado de MII, sin embargo se deben realizar otras investigaciones para determinar el efecto ulterior que tiene la L-cisteína adicionada en la maduración sobre la fecundación y el desarrollo embrionario in vitro.

In vitro fertilization (IVF) is now a routine technique in a number of biotechnology research laboratories worldwide. IVF is used as a tool for the study of various aspects related to oocytes maturation, fertilization and early embryo development. L-cysteine constitutes an external substrate required for synthesis of glutathione in the maturation of cattle oocytes. In order to study the effect of L-cysteine supplementation on in vitro maturation of cattle oocytes, ovaries were obtained from crossbred cows culled at a local slaughterhouse. Three different in vitro maturation treatments were utilized. Each treatment had a different concentrations of L-cysteine: T1: 0 mM, T2: 0.1 mM and T3: 1.0 mM. Approximately 400 Cumulus Oocyte Complexes (COCs) were matured in wells of 500 ìL of maturation medium (TCM-199), with 5% CO2 at 38.5°C and saturated relative humidity. Data were analyzed using analysis of variance (ANOVA). There were no significant differences between treatments in term of oocytes that arrived to Metafase II (MII, T1: 72.77%, T2: 67.47% and T3: 70.43%). Results indicate that supplementation with L-cysteine during maturation did not possitively affect the percentage of bovine oocytes that reached the M II state. Nonetheless further research should be carried out to determine the effect of L-cysteine supplementation during maturation, on fertilization and on embryonic development in vitro.