Literature DB >> 9442943

Analysis of infectious laryngotracheitis virus isolates from Ontario and New Brunswick by the polymerase chain reaction.

H S Alexander1, D W Key, E Nagy.   

Abstract

The polymerase chain reaction (PCR) was used to amplify DNA of infectious laryngotracheitis virus (ILTV) isolates obtained from field specimens. The examined 47 samples included 37 isolates representing 35 cases of infectious laryngotracheitis from Ontario and 10 isolates originating from 10 field cases in New Brunswick. The viruses were grown in either embryonated chicken eggs or cell culture, the DNA extracted and amplified using primers designed from the sequence information of a 1.1 kb BamHI fragment of the Ontario 1598 ILTV strain. Thirty-four of the Ontario isolates and all of the New Brunswick isolates were amplified successfully. This suggests that the selected primers would be useful for the majority of the isolates encountered in outbreaks of ILTV.

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Year:  1998        PMID: 9442943      PMCID: PMC1189445     

Source DB:  PubMed          Journal:  Can J Vet Res        ISSN: 0830-9000            Impact factor:   1.310


  20 in total

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Authors:  H S Alexander; E Nagy
Journal:  Avian Dis       Date:  1997 Jul-Sep       Impact factor: 1.577

2.  Variability occurs in the inverted repeat region of genomic DNA from bovine herpesvirus 1 respiratory, genital and bovine herpesvirus 5 encephalitic isolates.

Authors:  C A Whetstone; B S Seal; J M Miller
Journal:  Vet Microbiol       Date:  1993-12       Impact factor: 3.293

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Authors:  P E Curtis; A S Wallis
Journal:  Vet Rec       Date:  1983-05-14       Impact factor: 2.695

4.  Development of a polymerase chain reaction and a nonradioactive DNA probe for infectious laryngotracheitis virus.

Authors:  F Abbas; J R Andreasen; M W Jackwood
Journal:  Avian Dis       Date:  1996 Jan-Mar       Impact factor: 1.577

5.  Restriction endonuclease analysis of infectious laryngotracheitis viruses: comparison of modified-live vaccine viruses and North Carolina field isolates.

Authors:  J S Guy; H J Barnes; L L Munger; L Rose
Journal:  Avian Dis       Date:  1989 Apr-Jun       Impact factor: 1.577

6.  Differential diagnosis of infectious laryngotracheitis from other avian respiratory diseases by a simplified PCR procedure.

Authors:  E Scholz; R E Porter; P Guo
Journal:  J Virol Methods       Date:  1994-12       Impact factor: 2.014

7.  Nucleotide sequence of infectious laryngotracheitis virus (gallid herpesvirus 1) ICP4 gene.

Authors:  M A Johnson; S G Tyack; C Prideaux; K Kongsuwan; M Sheppard
Journal:  Virus Res       Date:  1995-02       Impact factor: 3.303

8.  Development and evaluation of a non-isotopically labeled DNA probe for the diagnosis of infectious laryngotracheitis.

Authors:  D W Key; B C Gough; J B Derbyshire; E Nagy
Journal:  Avian Dis       Date:  1994 Jul-Sep       Impact factor: 1.577

9.  Detection of DNA from infectious laryngotracheitis virus by colourimetric analyses of polymerase chain reactions.

Authors:  M W Shirley; D J Kemp; M Sheppard; K J Fahey
Journal:  J Virol Methods       Date:  1990-12       Impact factor: 2.014

Review 10.  Nucleic acid amplification in vitro: detection of sequences with low copy numbers and application to diagnosis of human immunodeficiency virus type 1 infection.

Authors:  J C Guatelli; T R Gingeras; D D Richman
Journal:  Clin Microbiol Rev       Date:  1989-04       Impact factor: 26.132

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  1 in total

Review 1.  Infectious laryngotracheitis virus in chickens.

Authors:  Shan-Chia Ou; Joseph J Giambrone
Journal:  World J Virol       Date:  2012-10-12
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