Literature DB >> 8384625

Presumptive diagnostic differentiation of hog cholera virus from bovine viral diarrhea and border disease viruses by using a cDNA nested-amplification approach.

J B Katz1, J F Ridpath, S R Bolin.   

Abstract

Hog cholera virus (HCV), bovine viral diarrhea virus (BVDV), and border disease virus (BDV) are closely related pestiviruses. BVDV and BDV are found worldwide but seldom cause disease in swine. In contrast, HCV has been successfully eradicated from swine in several nations but poses a potentially devastating threat to them because of its great virulence. Rapid differential diagnosis of HCV from BVDV and BDV infections in swine is vital for detection of the possible reintroduction of HCV into national herds from which it has been eradicated. Nested polymerase chain reactions (PCRs) for each of two pestiviral genomic segments are described. Amplification of the relatively conserved 5' genomic terminus identified 59 of 61 HCV, BVDV, and BDV isolates generically as pestiviruses. Nested amplification of the second region was designed to differentiate HCV from BVDV and BDV by exploiting relatively conserved differences in the nucleotide sequences that encode the major envelope glycoprotein. This second PCR correctly identified 36 of 36 diverse HCV isolates while failing to recognize any of 25 BVDV and BDV isolates. Multiple restriction fragment length analyses confirmed the identities of both external and nested PCR products. The two sets of PCRs may help confirm the generic identity of most pestiviruses and may permit presumptive differential diagnosis of HCV from BVDV and BDV.

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Year:  1993        PMID: 8384625      PMCID: PMC262820          DOI: 10.1128/jcm.31.3.565-568.1993

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


  21 in total

Review 1.  Molecular genetics of pestiviruses.

Authors:  M S Collett
Journal:  Comp Immunol Microbiol Infect Dis       Date:  1992-07       Impact factor: 2.268

Review 2.  The pestiviruses.

Authors:  V Moennig; P G Plagemann
Journal:  Adv Virus Res       Date:  1992       Impact factor: 9.937

3.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.

Authors:  P Chomczynski; N Sacchi
Journal:  Anal Biochem       Date:  1987-04       Impact factor: 3.365

4.  Molecular cloning of the bovine viral diarrhea virus genomic RNA.

Authors:  A Renard; D Schmetz; C Guiot; S Brown-Shimmer; L Dagenais; P P Pastoret; D Dina; J A Martial
Journal:  Ann Rech Vet       Date:  1987

5.  Rapid detection of bovine viral diarrhea virus by polymerase chain reaction.

Authors:  O J Lopez; F A Osorio; R O Donis
Journal:  J Clin Microbiol       Date:  1991-03       Impact factor: 5.948

6.  Detection of bovine viral diarrhea virus, using degenerate oligonucleotide primers and the polymerase chain reaction.

Authors:  P Ward; V Misra
Journal:  Am J Vet Res       Date:  1991-08       Impact factor: 1.156

7.  Specific sequence amplification of bovine virus diarrhea virus (BVDV) and hog cholera virus and sequencing of BVDV nucleic acid.

Authors:  M Boye; S Kamstrup; K Dalsgaard
Journal:  Vet Microbiol       Date:  1991-09       Impact factor: 3.293

Review 8.  The hog cholera virus.

Authors:  V Moennig
Journal:  Comp Immunol Microbiol Infect Dis       Date:  1992-07       Impact factor: 2.268

9.  Detection of BVD viruses using synthetic oligonucleotides.

Authors:  T L Lewis; J F Ridpath; S R Bolin; E S Berry
Journal:  Arch Virol       Date:  1991       Impact factor: 2.574

10.  Rapid detection of hog cholera virus in tissues by the polymerase chain reaction.

Authors:  S T Liu; S N Li; D C Wang; S F Chang; S C Chiang; W C Ho; Y S Chang; S S Lai
Journal:  J Virol Methods       Date:  1991 Nov-Dec       Impact factor: 2.014

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  16 in total

1.  Characterization of cytopathogenicity of classical swine fever virus isolate induced by Newcastle disease virus.

Authors:  S D Raut; K K Rajak; R Kumar; V K Singh; A Saxena; D Chaudhary; D Muthuchelvan; A B Pandey
Journal:  Virusdisease       Date:  2015-05-23

2.  Diagnostic evaluation of a real-time reverse transcriptase PCR assay for detection of classical swine fever virus.

Authors:  G Risatti; L Holinka; Z Lu; G Kutish; J D Callahan; W M Nelson; E Brea Tió; M V Borca
Journal:  J Clin Microbiol       Date:  2005-01       Impact factor: 5.948

3.  A universal 'one-tube' RT-PCR protocol for amplifying isolates of bovine viral diarrhoea virus.

Authors:  M Pfeffer; M V Freyburg; O R Kaaden; M Beer
Journal:  Vet Res Commun       Date:  2000-11       Impact factor: 2.459

4.  Organization and diversity of the 3'-noncoding region of classical swine fever virus genome.

Authors:  S Vilcek; S Belák
Journal:  Virus Genes       Date:  1997       Impact factor: 2.332

5.  Pestiviruses isolated from pigs, cattle and sheep can be allocated into at least three genogroups using polymerase chain reaction and restriction endonuclease analysis.

Authors:  S Vilcek; A J Herring; J A Herring; P F Nettleton; J P Lowings; D J Paton
Journal:  Arch Virol       Date:  1994       Impact factor: 2.574

6.  Rapid detection of bovine viral diarrhea virus by using RNA extracted directly from assorted specimens and a one-tube reverse transcription PCR assay.

Authors:  A L Hamel; M D Wasylyshen; G P Nayar
Journal:  J Clin Microbiol       Date:  1995-02       Impact factor: 5.948

7.  Rapid detection of classical swine fever virus by a portable real-time reverse transcriptase PCR assay.

Authors:  G R Risatti; J D Callahan; W M Nelson; M V Borca
Journal:  J Clin Microbiol       Date:  2003-01       Impact factor: 5.948

8.  Reverse transcriptase-PCR assay for detection of hog cholera virus.

Authors:  M Harding; C Lutze-Wallace; I Prud'Homme; X Zhong; J Rola
Journal:  J Clin Microbiol       Date:  1994-10       Impact factor: 5.948

9.  Rapid characterization of new pestivirus strains by direct sequencing of PCR-amplified cDNA from the 5' noncoding region.

Authors:  M A Hofmann; K Brechtbühl; N Stäuber
Journal:  Arch Virol       Date:  1994       Impact factor: 2.574

10.  Screwworms, Cochliomyia hominivorax, reared for mass release do not carry and spread foot-and-mouth disease virus and classical swine fever virus.

Authors:  M F Chaudhury; G B Ward; S R Skoda; M Y Deng; J B Welch; T S McKenna
Journal:  J Insect Sci       Date:  2008       Impact factor: 1.857

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