Literature DB >> 1321166

Development of a biotin-streptavidin-enhanced enzyme-linked immunosorbent assay which uses monoclonal antibodies for detection of group C rotaviruses.

C K Ojeh1, H Tsunemitsu, R A Simkins, L J Saif.   

Abstract

A biotin-streptavidin-enhanced enzyme-linked immunosorbent assay (ELISA) which uses monoclonal antibodies (MAbs) for the detection of group C rotaviruses was developed. An assay in which plates were coated with three pooled MAbs and biotinylated polyclonal immunoglobulin G (IgG) (polyclonal antibody [PAb]) was used as the detector (MAb capture-PAb detector) was found to be the most sensitive and specific of the assays when it was compared with assays in which plates were coated with polyclonal antiserum and detection was done with either biotinylated polyclonal antiserum (PAb capture-PAb detector) or biotinylated pooled MAbs (PAb capture-MAb detector). The MAb capture-PAb detector ELISA detected 83% of samples confirmed to be positive for group C rotaviruses, whereas the PAb capture-PAb detector assay detected 63% of positive samples and the PAb capture-MAb detector assay detected 65% of positive samples. All three procedures detected both of the bovine and the two human group C rotaviruses, but none of the three procedures detected fecal samples containing group A and B rotaviruses or fecal samples negative for group C rotaviruses used in this study. The sensitivity of the MAb capture-PAb detector ELISA was determined by serially diluting fecal group C rotaviruses; antigens were detected in maximal positive dilution ranges of 1:1,000 to 1:3,000 for the samples tested. On the basis of the cell culture immunofluorescence assay infectivity titer of semipurified cell culture-passaged Cowden group C rotavirus, the sensitivity of the MAb capture-PAb detection ELISA for detection of homologous group C rotavirus was 53 fluorescent focus units per ml. Epitope mapping by use of the biotinylated MAbs in competition assay suggested that our MAbs may bind to three different but overlapping epitopes. These results suggest that the MAb capture-PAb detector ELISA can be used to study the epidemiology of group C rotaviruses in humans and animals.

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Year:  1992        PMID: 1321166      PMCID: PMC265361          DOI: 10.1128/jcm.30.7.1667-1673.1992

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  33 in total

1.  Comparison of human and porcine group C rotaviruses by northern blot hybridization analysis.

Authors:  Y Qian; L J Saif; A Z Kapikian; S Y Kang; B Jiang; Y Ishimaru; Y Yamashita; M Oseto; K Y Green
Journal:  Arch Virol       Date:  1991       Impact factor: 2.574

2.  Biochemical characterization of the structural and nonstructural polypeptides of a porcine group C rotavirus.

Authors:  B M Jiang; L J Saif; S Y Kang; J H Kim
Journal:  J Virol       Date:  1990-07       Impact factor: 5.103

3.  An outbreak of gastroenteritis associated with acute rotaviral infection in schoolchildren.

Authors:  K Matsumoto; M Hatano; K Kobayashi; A Hasegawa; S Yamazaki; S Nakata; S Chiba; Y Kimura
Journal:  J Infect Dis       Date:  1989-10       Impact factor: 5.226

Review 4.  Rotavirus gene structure and function.

Authors:  M K Estes; J Cohen
Journal:  Microbiol Rev       Date:  1989-12

5.  Characterization of monoclonal antibodies to human group B rotavirus and their use in an antigen detection enzyme-linked immunosorbent assay.

Authors:  J W Burns; S K Welch; S Nakata; M K Estes
Journal:  J Clin Microbiol       Date:  1989-02       Impact factor: 5.948

6.  Atypical rotaviruses in Australian pigs.

Authors:  H S Nagesha; C P Hum; J C Bridger; I H Holmes
Journal:  Arch Virol       Date:  1988       Impact factor: 2.574

7.  Isolation, characterization, and serial propagation of a bovine group C rotavirus in a monkey kidney cell line (MA104).

Authors:  H Tsunemitsu; L J Saif; B M Jiang; M Shimizu; M Hiro; H Yamaguchi; T Ishiyama; T Hirai
Journal:  J Clin Microbiol       Date:  1991-11       Impact factor: 5.948

8.  Sequence analysis of the gene (6) encoding the major capsid protein (VP6) of group C rotavirus: higher than expected homology to the corresponding protein from group A virus.

Authors:  M Bremont; D Chabanne-Vautherot; P Vannier; M A McCrae; J Cohen
Journal:  Virology       Date:  1990-10       Impact factor: 3.616

9.  Group C rotavirus associated with fatal enteritis in a family outbreak.

Authors:  E O Caul; C R Ashley; J M Darville; J C Bridger
Journal:  J Med Virol       Date:  1990-03       Impact factor: 2.327

10.  The four subclasses of IgG can be isolated from mouse serum by using Protein A-Sepharose.

Authors:  I Seppälä; H Sarvas; F Péterfy; O Mäkelä
Journal:  Scand J Immunol       Date:  1981-10       Impact factor: 3.487

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  3 in total

1.  Comparison of monoclonal antibody-based sandwich enzyme-linked immunosorbent assay and virus isolation for detection of peste des petits ruminants virus in goat tissues and secretions.

Authors:  J T Saliki; J A House; C A Mebus; E J Dubovi
Journal:  J Clin Microbiol       Date:  1994-05       Impact factor: 5.948

2.  Detection of group C rotavirus antigens and antibodies in animals and humans by enzyme-linked immunosorbent assays.

Authors:  H Tsunemitsu; B Jiang; L J Saif
Journal:  J Clin Microbiol       Date:  1992-08       Impact factor: 5.948

3.  A longitudinal cohort study in calves evaluated for rotavirus infections from 1 to 12 months of age by sequential serological assays.

Authors:  Dianjun Cao; Blessing Igboeli; Lijuan Yuan; Albert Z Kapikian; Jess L Ayers; Francis R Abinanti; Yasutaka Hoshino
Journal:  Arch Virol       Date:  2009-04-03       Impact factor: 2.574

  3 in total

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