Literature DB >> 8141755

Newcastle disease virus passage in MDBK cells as an aid in detection of a virulent subpopulation.

D J King1.   

Abstract

Newcastle disease virus strains (NDV) La Sota, Texas GB (GB), and mixtures of the two strains were serially passaged in embryonated chicken eggs or the MDBK cell line, a more restrictive culture system than eggs for NDV. The two culture systems were compared by evaluating culture harvests for pathogenicity in inoculated chickens; the harvests were identified by hemagglutination-inhibition tests against monoclonal antibodies that can differentiate La Sota and GB cultures. Both viruses, inoculated alone or as mixtures, were propagated by passage in chicken eggs. La Sota strain failed to propagate by continuous passage in MDBK cells, and only GB was identified in culture harvests propagated in MDBK cells that had been inoculated with GB or mixtures of GB and La Sota. The results indicate that the MDBK cell line is a more selective substrate than chicken eggs and suggest that passage in MDBK cells may aid in selecting for more virulent subpopulations of NDV in a mixed culture. Other reference NDV strains, pigeon NDV isolates, and recent lentogenic NDV isolates from chickens were also passaged in MDBK cells; all strains except those that are classified as lentogens like La Sota could be serially propagated in MDBK cells.

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Year:  1993        PMID: 8141755

Source DB:  PubMed          Journal:  Avian Dis        ISSN: 0005-2086            Impact factor:   1.577


  8 in total

1.  Comparison of various diagnostic methods in characterizing Newcastle disease virus isolates from Desi chickens.

Authors:  V S Raghavan; K Kumanan; G Thirumurugan; K Nachimuthu
Journal:  Trop Anim Health Prod       Date:  1998-10       Impact factor: 1.559

2.  Complete genome sequence of highly virulent neurotropic Newcastle disease virus strain Texas GB.

Authors:  Anandan Paldurai; Sachin Kumar; Baibaswata Nayak; Siba K Samal
Journal:  Virus Genes       Date:  2010-04-30       Impact factor: 2.332

3.  Development of a cell culture method for quantal assay of strain I-2 of Newcastle disease virus.

Authors:  P Wambura; J Meers; P Spradbrow
Journal:  Vet Res Commun       Date:  2006-08       Impact factor: 2.459

4.  Use of a heteroduplex mobility assay to detect differences in the fusion protein cleavage site coding sequence among Newcastle disease virus isolates.

Authors:  A Berinstein; H S Sellers; D J King; B S Seal
Journal:  J Clin Microbiol       Date:  2001-09       Impact factor: 5.948

5.  Phylogenetic relationships among highly virulent Newcastle disease virus isolates obtained from exotic birds and poultry from 1989 to 1996.

Authors:  B S Seal; D J King; D P Locke; D A Senne; M W Jackwood
Journal:  J Clin Microbiol       Date:  1998-04       Impact factor: 5.948

6.  Nucleotide and predicted amino acid sequence analysis of the fusion protein and hemagglutinin-neuraminidase protein genes among Newcastle disease virus isolates. Phylogenetic relationships among the Paramyxovirinae based on attachment glycoprotein sequences.

Authors:  Bruce S Seal
Journal:  Funct Integr Genomics       Date:  2004-04-24       Impact factor: 3.410

7.  Characterization of Newcastle disease virus isolates by reverse transcription PCR coupled to direct nucleotide sequencing and development of sequence database for pathotype prediction and molecular epidemiological analysis.

Authors:  B S Seal; D J King; J D Bennett
Journal:  J Clin Microbiol       Date:  1995-10       Impact factor: 5.948

8.  Newcastle Disease Virus: Potential Therapeutic Application for Human and Canine Lymphoma.

Authors:  Diana Sánchez; Rosana Pelayo; Luis Alberto Medina; Eduardo Vadillo; Rogelio Sánchez; Luis Núñez; Gabriela Cesarman-Maus; Rosa Elena Sarmiento-Silva
Journal:  Viruses       Date:  2015-12-23       Impact factor: 5.048

  8 in total

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