ABSTRACT
The obtainment of monoclonal antibodies for adenovirus species 4(Ad4) is described. The specificities of selected monoclonal antibodies were determined by means of viral neutralization test in cell culture, immunofluorescence and Enzyme-Linked Immunosorbent Assay (ELISA), in the presence of the following species of human adenovirus: 1, 2, 5 (subgenus C), 4 (subgenus E), 7 and 16 (subgenus B) and 9 (subgenus D). Two monoclonal antibodies species specific to adenovirus 4 (1CIII and 3DIII) and one monoclonal antibody that cross reacted with adenovirus species 4 and 7 (2HIII) were obtained.
Subject(s)
Humans , Animals , Female , Infant , Child , Adult , Mice , Adenoviruses, Human , Antibodies, Monoclonal , Adenoviruses, Human , Antibodies, Monoclonal , Antibody Specificity , Enzyme-Linked Immunosorbent Assay , Epitopes , Species Specificity , Fluorescent Antibody Technique , Mice, Inbred BALB C , Neutralization TestsABSTRACT
In September 1987 an outbreak of exanthematous illness ressembling erythma infectiosum occurres at an elementary school of Säo Paulo city. Attempts to isolate virus from the nasofaryngeal secretion and urine and serum samples collected from the ill children in acute phase of illness resulted negative. Nevertheless, parvovirus-like particles of about 24 nm in diameter were observed by negative staining electron microscopy in concentraded urine of seven out of eight ill patients and in nasopharyngeal secretion of one out of four patients. No similar viral particle was observed in concentred urine samples collected on the same occasion from their classmates without evident signs of illness. This is a proposal of an alternative test for a rapid and sensitive presumptive diagnosis of human parvovirus infection
Subject(s)
Parvoviridae Infections , ErythemaABSTRACT
Cultura de células de linhagem contínua de rim de hamster (BHK-21) demonstrou ser um sistema mais sensível e mais rápido para o isolamento do vírus da caxumba, quando comparado com o de ovos embrionados de galinha. Estas células podem ser cultivadas sem dificuldade, em laboratório, ao contrário das células primárias de rim de macaco, igualmente sensíveis mas que são de difícil obtenção. A utilização de células BHK-21 para o isolamento do vírus da caxumba, do material biológico, constitui uma boa alternativa no diagnóstico das infecções causadas por esse vírus (AU).