Influencia de diferentes factores en el crecimiento de bacterias endófitas de caña de azúcar / Influence of different factors in the growth of endophytic bacteria of sugarcane

En Cuba, entre los esfuerzos por lograr la sostenibilidad en la agricultura se han empleado biopreparados a gran escala, los cuales han tenido un gran impacto económico, ecológico y social. La caña de azúcar constituye uno de los principales cultivos agrícolas para nuestro país y tiene gran importancia desde los puntos de vista económico y ecológico a nivel mundial. En el presente trabajo se demostró el efecto de diferentes fuentes de carbono y nitrógeno en el crecimiento de 5 cepas endófitas de caña de azúcar, 3 de Gluconacetobacter diazotrophicus, una de Bacillus licheniformis y una de Enterobacter agglomerans. De igual forma, se estudió la influencia de jugos provenientes de cinco variedades, así como diferentes concentraciones de las fitohormonas ácido 3 indolacético (AIA) y ácido giberélico (GA) en el crecimiento. Se demostró que la asparagina y el sulfato de amonio como fuentes de nitrógeno adicionadas al medio LGI posibilitan un mayor crecimiento de las bacterias endófitas estudiadas. El medio LGI suplementado con jugo de caña de azúcar favorece significativamente (p≤0,05) el crecimiento de los microorganismos endófitos y no existe relación directa entre el origen varietal del jugo y de las cepas. Por otra parte las fitohormonas en bajas concentraciones favorecieron el crecimiento, no ocurriendo así cuando se encuentran a elevadas concentraciones en el medio de cultivo. Es necesario estudiar todos los factores que pueden influir en la interacción entre la planta y los endófitos para poder utilizar sus potencialidades como promotores del crecimiento vegetal.

Among the efforts done in Cuba to the sustainability in the agricultural system, one of them is the use of bioproducts, which have a relevant economic, ecological and social impact. The sugarcane is one of main crops in our country and it has a great importance at world level. In the present work is demonstrated the effect of different carbon and nitrogen sources in the growth of 5 entophytic bacteria (three of Gluconacetobacter diazotrophicus, one of Bacillus licheniformis and one of Enterobacter agglomerans) were demonstrated. As the same form are studied the influence of juices from five varieties, as well as, different concentrations of fitohormones indole3acetic acid and giberelic acid on the growth. Was demonstrated that asparagine and ammonium sulfate as nitrogen sources added to LGI medium enhance the growth a major growth of the studied endophytic bacteria. The LGI medium supplied with juices of sugarcane enhance the growth of microorganisms (p≤0,05) and don't exist any relationships among the origin of the juice and the strains. On the other hand, the fitohormones at low concentrations don't affect the growth but at high levels of these hormones inhibit the growth. It's necessary to study the factors that have influence on the interaction between the plant and endophytes to use their potentialities as plant growth promoters.

Biological and Molecular Properties of Dengue 2 Strains Isolated during the DHF/DSS Cuban Epidemic, 1981.

To study some biological and molecular properties of nine DENV-2 strains isolated during the 1981 Cuban epidemic, temperature sensitivity, viral plaque size, the kinetic of virus replication in newborn mice inoculated by intracerebral route, the influence of pH medium on virus-cell attachment phase and the restriction enzyme pattern were studied. Strains were classified in two patterns according to temperature sensitivity, plaque size, and virus replication in mouse brain and cell culture and restriction enzymatic pattern the changes observed differentiate clearly the strains isolated at the beginning and at the end of the epidemic suggesting that viruses with different characteristics circulated.

Control externo de la calidad del diagnostico serologico del dengue en laboratorios de paises de las Americas, 1996-2001 / Quality control of the serological diagnosis of dengue in laboratories throughout the Americas, 1996-2001

Objective. To report the results from participating laboratories for four external quality control proficiency tests of dengue serological diagnosis that were carried out in the Region of the Americas in the period of 1996-2001. Methods. External quality control proficiency tests of dengue serological diagnosis were carried out in 1996-1997, 1998-1999, 2000-2001. Panels made up of 20 serum samples (12 of them positive for dengue IgM antibodies) were sent to participating laboratories in the Region. The sera were negative for HIV antibodies, hepatitis C virus antibodies, and hepatitis B surface antigen. The sera were stored at -20 degrees C until they were sent in refrigerated shipments to the participating laboratories. THe presence of IgM antibodies was determined through IgM-capture enzyme-linked immunosorbent assay (ELISA), while the IgG antibody titer was determined by hemagglutination inhibition or by IgG ELISA. The results of the IgM antibody testing that differed from those of the reference center were considered discordant. The IgG antibody titer was considered discordant when the results differed by two dilutions or more with respect to the reference center's results. Results. A total of 27 laboratories received a total of 59 serum panels over the 1996-2001 period, and the results from testing 54 of those panels (91.5 percent) were sent back in. Of the total of 1, 080 sera samples from those 54 panels, the results from 95.6 percent of the IgM antibody tests were concordant with the results from the reference center. With 47 of the 54 panels (87.0 percent) the participating laboratories' agreement with the reference center's results for the IgM antibody testing was 90.0 percent or higher. The laboratories sent back results from a total of 27 IgG antibody titer tests, and 22 of them (81.5 percent) coincided with those from the reference center. Considering the IgM antibody testing results from the four periods, the findings from 22 of the participating laboratories coincided with those from the reference center for at least 90 percent of the samples, and 13 of the laboratories were in complete concordance with the reference center. Conclusions. The majority of the participating laboratories showed an excellent level of performance in detecting dengue IgG and IgM antibodies. However, the deficiencies found in some instances confirm the need for continuing to improve laboratory diagnosis of dengue in the Region of the Americas (AU)

Control externo de la calidad del diagnóstico serológico del dengue en laboratorios de países de las Américas, 1996-2001 / Quality control of the serological diagnosis of dengue in laboratories throughout the Americas, 1996-2001

Dar a conocer los resultados de cuatro controles externos de la calidad del diagnóstico serológico del dengue realizados en la Región de las Américas en el período de 1996- 2001 y presentar los resultados obtenidos por los laboratorios participantes. MÉTODOS: Se realizaron controles externos de la calidad del diagnóstico serológico del dengue en 1996-1997, 1998-1999, 1999-2000 y 2000-2001. Paneles compuestos por 20 sueros (12 de estos positivos a anticuerpos IgM contra el dengue) fueron enviados a laboratorios de la Región para que participaran en los controles realizados. Los sueros de los paneles eran negativos a anticuerpos contra el virus de la inmunodeficiencia humana y el virus de la hepatitis C, así como al antígeno de superficie de la hepatitis B, y fueron almacenados a -20 °C hasta su envío en refrigeración a los laboratorios participantes. La presencia de anticuerpos IgM se determinó mediante un ensayo inmunoenzimático (ELISA) de captura, mientras que el título de anticuerpos IgG se determinó por inhibición de la hemoaglutinación o ELISA de IgG. Los resultados de la determinación de anticuerpos IgM contra el dengue que no coincidían con los del centro de referencia se consideraron discordantes. El título de anticuerpos IgG se consideró discordante cuando los resultados difirieron en dos diluciones o más con respecto al resultado del centro de referencia. RESULTADOS: Un total de 27 laboratorios recibió 59 paneles de sueros de 1996 a 2001, y se recibieron los resultados del análisis de 54 de esos paneles (91,5 por ciento). De 1 080 sueros (20 X 54), 95,6 por ciento coincidieron con el laboratorio de referencia en cuanto a los resultados de la detección de anticuerpos IgM contra el dengue. Además, en 47 paneles (87 por ciento) la coincidencia con el laboratorio de referencia se observó en 90 por ciento de las muestras del panel o más. De los 27 paneles para los cuales se recibieron los resultados de los títulos de anticuerpos IgG contra el dengue, 22 (81,5 por ciento) coincidieron con el centro de referencia. Tomando en conjunto los cuatro controles realizados, 22 laboratorios coincidieron con el centro de referencia en 90 por ciento de las muestras o más y 13 en 100 por ciento de las muestras en cuanto a la presencia de IgM. CONCLUSIONES: Los resultados indican que la mayoría de los laboratorios participantes mostraron un excelente desempeño en la detección de anticuerpos IgG e IgM contra el dengue. No obstante, las deficiencias encontradas ...

Longitudinal study of herpesviruses in kidney transplant recipients in Cuba.

We compared a multiplex polymerase chain reaction assay and a shell vial assay for the detection of herpesviruses infection in 13 Cuban patients who had received kidney transplants. Cytomegalovirus and human herpesvirus 6 were detected in these patients.

[Quality control of the serological diagnosis of dengue in laboratories throughout the Americas, 1996-2001]. / Control externo de la calidad del diagnóstico serológico del dengue en laboratorios de países de las Américas, 1996-2001.

OBJECTIVE: To report the results from participating laboratories for four external quality control proficiency tests of dengue serological diagnosis that were carried out in the Region of the Americas in the period of 1996-2001. METHODS: External quality control proficiency tests of dengue serological diagnosis were carried out in 1996-1997, 1998-1999, 1999-2000, and 2000-2001. Panels made up of 20 serum samples (12 of them positive for dengue IgM antibodies) were sent to participating laboratories in the Region. The sera were negative for HIV antibodies, hepatitis C virus antibodies, and hepatitis B surface antigen. The sera were stored at -20 degrees C until they were sent in refrigerated shipments to the participating laboratories. The presence of IgM antibodies was determined through IgM-capture enzyme-linked immunosorbent assay (ELISA), while the IgG antibody titer was determined by hemagglutination inhibition or by IgG ELISA. The results of the IgM antibody testing that differed from those of the reference center were considered discordant. The IgG antibody titer was considered discordant when the results differed by two dilutions or more with respect to the reference center's results. RESULTS: A total of 27 laboratories received a total of 59 serum panels over the 1996-2001 period, and the results from testing 54 of those panels (91.5%) were sent back in. Of the total of 1 080 sera samples from those 54 panels, the results from 95.6% of the IgM antibody tests were concordant with the results from the reference center. With 47 of the 54 panels (87.0%) the participating laboratories' agreement with the reference center's results for the IgM antibody testing was 90.0% or higher. The laboratories sent back results from a total of 27 IgG antibody titer tests, and 22 of them (81.5%) coincided with those from the reference center. Considering the IgM antibody testing results from the four periods, the findings from 22 of the participating laboratories coincided with those from the reference center for at least 90% of the samples, and 13 of the laboratories were in complete concordance with the reference center. CONCLUSIONS: The majority of the participating laboratories showed an excellent level of performance in detecting dengue IgG and IgM antibodies. However, the deficiencies found in some instances confirm the need for continuing to improve laboratory diagnosis of dengue in the Region of the Americas.