Literature DB >> 7019340

Visualization of minute centers of viral infection in unfixed cell cultures by an enzyme-linked antibody assay.

K O Smith, W L Kennell, D L Lamm.   

Abstract

Enzyme-linked antibody was used to treat unfixed herpesvirus-infected human fetal lung cell cultures in a mode which permitted the visualizing of local sites of infection. Foci containing as few as 20 herpesvirus-infected cells produced sufficient viral mass to be easily detectable by this method. 'Clouds' or 'plumes' of colored reaction product diffused into the substrate overlay, accumulated above and around each focus of infection and allowed quantitation of the number of foci in a culture. The number of minute centers of viral infection determined by the enzyme-linked antibody method corresponded almost exactly with values obtained by fluorescence microscopy. Quantitation of herpes simplex infectivity by focus assay was possible within only 17 h after culture inoculation, well before cytopathic effects were visible macroscopically. The technique was also applied to demonstrate measles and mumpsvirus plaques (infectious centers) in Vero cell cultures.

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Year:  1981        PMID: 7019340     DOI: 10.1016/0022-1759(81)90361-6

Source DB:  PubMed          Journal:  J Immunol Methods        ISSN: 0022-1759            Impact factor:   2.303


  13 in total

1.  The attenuated pseudorabies virus strain Bartha fails to package the tegument proteins Us3 and VP22.

Authors:  Mathew G Lyman; Gretchen L Demmin; Bruce W Banfield
Journal:  J Virol       Date:  2003-01       Impact factor: 5.103

2.  Site-specific insertion of DNA into a pseudorabies virus vector.

Authors:  B Sauer; M Whealy; A Robbins; L Enquist
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

3.  Mutations in the C-terminal hydrophobic domain of pseudorabies virus gIII affect both membrane anchoring and protein export.

Authors:  K A Solomon; A K Robbins; L W Enquist
Journal:  J Virol       Date:  1991-11       Impact factor: 5.103

4.  The putative cytoplasmic domain of the pseudorabies virus envelope protein gIII, the herpes simplex virus type 1 glycoprotein C homolog, is not required for normal export and localization.

Authors:  K A Solomon; A K Robbins; M E Whealy; L W Enquist
Journal:  J Virol       Date:  1990-07       Impact factor: 5.103

5.  The export pathway of the pseudorabies virus gB homolog gII involves oligomer formation in the endoplasmic reticulum and protease processing in the Golgi apparatus.

Authors:  M E Whealy; A K Robbins; L W Enquist
Journal:  J Virol       Date:  1990-05       Impact factor: 5.103

6.  An amino-terminal deletion mutation of pseudorabies virus glycoprotein gIII affects protein localization and RNA accumulation.

Authors:  L W Enquist; C L Keeler; A K Robbins; J P Ryan; M E Whealy
Journal:  J Virol       Date:  1988-10       Impact factor: 5.103

7.  An enzyme immunoassay for identification and quantification of infectious murine parvovirus in cultured cells.

Authors:  A L Smith
Journal:  J Virol Methods       Date:  1985-08       Impact factor: 2.014

8.  Physical mapping of the mutation in an antigenic variant of herpes simplex virus type 1 by use of an immunoreactive plaque assay.

Authors:  T C Holland; R M Sandri-Goldin; L E Holland; S D Marlin; M Levine; J C Glorioso
Journal:  J Virol       Date:  1983-05       Impact factor: 5.103

9.  Analysis of pseudorabies virus glycoprotein gIII localization and modification by using novel infectious viral mutants carrying unique EcoRI sites.

Authors:  J P Ryan; M E Whealy; A K Robbins; L W Enquist
Journal:  J Virol       Date:  1987-10       Impact factor: 5.103

10.  Pseudorabies virus gene encoding glycoprotein gIII is not essential for growth in tissue culture.

Authors:  A K Robbins; M E Whealy; R J Watson; L W Enquist
Journal:  J Virol       Date:  1986-09       Impact factor: 5.103

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