Electropherotypes of rotaviruses in children less than 5 years old in Abidjan, Côte d'Ivoire in 1997

Rotaviruses Are associated with gastroenteritis in human infants and the young of many species. In this study, we analysed the circulating strains of human rotavirus isolated from young children in Abidjan by electrophoresis of the viral RNA genome in agarose gels. Rotavirus strains were identified in 33 children less than two years of age in the Yopougon district of Abidjan, Cote d'lvoire. Viral RNA was extracted from the stools by phenol-chloroform treatment at 56 degrees C, followed by centrifugation at 12 OOOrpm. The electrophoresis was performed in 1.5 % agarose gels stained with 5 % ethidium bromide and Tris-acetate as the running buffer. Ten ul of each sample was loaded onto the gels which were run at lOOv for 30min. In total, 17 of the 33 specimens yielded an RNA electropherotype. Seven different RNA profiles were observed with 14 (82.4% ) long profiles and 3 (17%) short profiles. These RNA profiles represented the group A rotavirus pattern. No mixed infections were seen. There was no correlation between the age and sex of the patient with the RNA electropherotype. Serogroup A rotaviruses were the principle strains circulating in this study. Further characterization of these strains at the subgroup and serotype level will be conducted

One-Stage Polymerase Chain Reaction for the Comprehensive Detection of Type D Retrovirus Provial DNA

To develop the polymerase chain reaction (PCR) for the detection of type D simian retrovirus (SRV) infection, an oligonucleotide primer pair was designed to hybridize to the sequences within euv gene of SRV subtype 1 (SRV-1). The 3'proximal env sequences annealing to the primers had been rather conserved among three different subtypes of SRV, SRV-1, SRV-2, and SRV-3 (Mason-Pfizer Monkey Virus: MPMV). The PCR using the primer pair targetingan an env region the successfully detected and amplified all three subtypes of SRV with excellent specificity after single round of reaction. The tests with peripheral blood mononuclear cells infected either with simian immunodeficiency virus or simian T-lymphotropic virus type 1, maior immunosuppressive viral agents together with SRV in simian, verified the specificity of the PCR by excluding any cross reactivity. Semiquantitative titration PCR, amplifying serially diluted plasmid DNA of each subtype, was performed to evaluate sensitivity limits of the reaction. Based on molecular weight of each cloned SRV genome, the PCR should be able to detect one SRV-infected cell per more than 5-7x104 uninfected cells after simple ethidium bromide staining of resulting products. The PCR must be very efficient screening sisters with its quickness, certainty, and sensitivity for SRV-infected animals used in human AIDS research model. Second round amplification of the reaction products from the first PCR, or Southern hybridization by radiolabeled probes shall render to compete its efficacy to ELISA which has been the most sensitive technique to screen SRV infection but with frequent ambiguity problem.

Conceptos actuales sobre hepatitis viral / Current concepts on viral hepatitis

Contiene:Serologia de la hepatitis viral,metotos de diagnostico laboratorial en las hepatitis virales, nuevos metodos de diagnostico para el virus de la hepatitis B y C, estado actual de la hepatitis A, mutantes del virus B de la hepatitis y sus implicociones clinicas, infeccion por virus C, hepatitis E, manual de diagnostico y tratamiento de las hepatotias virales