Literature DB >> 310738

The use of a continuous cell line for the isolation of influenza viruses.

H W Davies, G Appleyard, P Cunningham, M S Pereira.   

Abstract

Cultures of MDCK cells exposed to trypsin were as efficient as cultures of rhesus monkey kidney cells for detecting influenza virus, both in dilutions of infected allantoic fluids and in nose and throat swabs. We suggest that the MDCK cell/trypsin system provides a satisfactory alternative to monkey kidney cultures for the isolation of influenza viruses from clinical specimens.

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Year:  1978        PMID： 310738      PMCID： PMC2395698     

Source DB:  PubMed          Journal:  Bull World Health Organ        ISSN： 0042-9686            Impact factor:   9.408


  8 in total

1.  Enhancement of the infectivity of influenza A and B viruses by proteolytic cleavage of the hemagglutinin polypeptide.

Authors:  S G Lazarowitz; P W Choppin
Journal:  Virology       Date:  1975-12       Impact factor: 3.616

2.  Activation of influenza A viruses by trypsin treatment.

Authors:  H D Klenk; R Rott; M Orlich; J Blödorn
Journal:  Virology       Date:  1975-12       Impact factor: 3.616

3.  Plaque formation by influenza viruses in the presence of trypsin.

Authors:  G Appleyard; H B Maber
Journal:  J Gen Virol       Date:  1974-12       Impact factor: 3.891

4.  Genetic recombination for antigenic markers of antigenically different strains of influenza B virus.

Authors:  K Tobita; E D Kilbourne
Journal:  J Virol       Date:  1974-02       Impact factor: 5.103

5.  Permanent canine kidney (MDCK) cells for isolation and plaque assay of influenza B viruses.

Authors:  K Tobita
Journal:  Med Microbiol Immunol       Date:  1975-12-30       Impact factor: 3.402

6.  Plaque assay and primary isolation of influenza A viruses in an established line of canine kidney cells (MDCK) in the presence of trypsin.

Authors:  K Tobita; A Sugiura; C Enomote; M Furuyama
Journal:  Med Microbiol Immunol       Date:  1975-12-30       Impact factor: 3.402

7.  The multiplication of an influenza C virus in an established line of canine kidney (MDCK) cells.

Authors:  K Nerome; M Ishida
Journal:  J Gen Virol       Date:  1978-04       Impact factor: 3.891

8.  Replication and plaque assay of influenza virus in an established line of canine kidney cells.

Authors:  C R Gaush; T F Smith
Journal:  Appl Microbiol       Date:  1968-04
  8 in total
  7 in total

1.  A new influenza surveillance system in France: the Ile-de-France "GROG". 1. Principles and methodology.

Authors:  C Hannoun; W Dab; J M Cohen
Journal:  Eur J Epidemiol       Date:  1989-09       Impact factor: 8.082

2.  Influenza A virus isolation, culture and identification.

Authors:  Amie J Eisfeld; Gabriele Neumann; Yoshihiro Kawaoka
Journal:  Nat Protoc       Date:  2014-10-16       Impact factor: 13.491

3.  Interferon production by leukocytes infiltrating the lungs of mice during primary influenza virus infection.

Authors:  P R Wyde; M R Wilson; T R Cate
Journal:  Infect Immun       Date:  1982-12       Impact factor: 3.441

Review 4.  Selected laboratory aspects of influenza surveillance.

Authors:  A L Frank
Journal:  Yale J Biol Med       Date:  1982 May-Aug

5.  Madin-Darby canine kidney cell sialic acid receptor modulation induced by culture medium conditions: Implications for the isolation of influenza A virus.

Authors:  Sarah W Nelson; Joshua N Lorbach; Jacqueline M Nolting; Jason W Stull; Daral J Jackwood; Ian C Davis; Andrew S Bowman
Journal:  Influenza Other Respir Viruses       Date:  2019-08-07       Impact factor: 4.380

6.  Rapid diagnostic methods for influenza virus in clinical specimens: a comparative study.

Authors:  A S Evans; B Olson
Journal:  Yale J Biol Med       Date:  1982 Sep-Dec

7.  Genic amplification of the entire coding region of the HEF RNA segment of influenza C virus.

Authors:  J C Manuguerra; C Hannoun; C Nicolson; J S Robertson
Journal:  J Virol Methods       Date:  1993-01       Impact factor: 2.014
  7 in total

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