Literature DB >> 3310377

Inhibition of virus replication in the tonsils of pigs previously vaccinated with a Chinese strain vaccine and challenged oronasally with a virulent strain of classical swine fever virus.

P Biront1, J Leunen, J Vandeputte.   

Abstract

After an oronasal (O.N.) infection with classical swine fever (C.S.F.) virus, virus multiplication can be detected in the tonsils from Day 2 post infection (p.i.) till death. The course of viral replication during the first 10 days after O.N. challenge exposure of pigs, previously vaccinated with a Chinese strain vaccine in the presence or absence of maternal antibodies, was studied using direct immunofluorescence techniques on cryostat sections and virus isolations. When piglets were challenged O.N. in the presence of maternal antibodies, virus replication in the tonsils still occurred. The multiplication period and the localization of the virus, however, were directly correlated to the maternal antibody levels. The maternal antibody level also seems responsible for the efficacy of the vaccination to prevent challenge virus replication in the tonsils: vaccination in the presence of low maternal antibody titers completely inhibited virus replication; vaccination in the presence of high maternal antibody titers only reduced the multiplication period of the O.N.-administered virulent virus. In both cases, animals were challenged 1 week post vaccination. Vaccination of seronegative animals resulted in an almost complete inhibition of the virus replication in the tonsils during a full fattening period: cryostat sections revealed a limited virus replication in three out of 20 animals. In one of these animals, virus replication was probably so negligible that virus isolation remained negative.

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Year:  1987        PMID: 3310377     DOI: 10.1016/0378-1135(87)90002-2

Source DB:  PubMed          Journal:  Vet Microbiol        ISSN: 0378-1135            Impact factor:   3.293


  5 in total

1.  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

2.  Challenge of pigs with classical swine fever viruses after C-strain vaccination reveals remarkably rapid protection and insights into early immunity.

Authors:  Simon P Graham; Helen E Everett; Felicity J Haines; Helen L Johns; Olubukola A Sosan; Francisco J Salguero; Derek J Clifford; Falko Steinbach; Trevor W Drew; Helen R Crooke
Journal:  PLoS One       Date:  2012-01-03       Impact factor: 3.240

3.  Early protection events in swine immunized with an experimental live attenuated classical swine fever marker vaccine, FlagT4G.

Authors:  Lauren G Holinka; Vivian O'Donnell; Guillermo R Risatti; Paul Azzinaro; Jonathan Arzt; Carolina Stenfeldt; Lauro Velazquez-Salinas; Jolene Carlson; Douglas P Gladue; Manuel V Borca
Journal:  PLoS One       Date:  2017-05-24       Impact factor: 3.240

4.  Validation of a real time PCR for classical Swine Fever diagnosis.

Authors:  Natanael Lamas Dias; Antônio Augusto Fonseca Júnior; Anapolino Macedo Oliveira; Erica Bravo Sales; Bruna Rios Coelho Alves; Fernanda Alves Dorella; Marcelo Fernandes Camargos
Journal:  Vet Med Int       Date:  2014-04-09

5.  Generation and efficacy evaluation of recombinant classical swine fever virus E2 glycoprotein expressed in stable transgenic mammalian cell line.

Authors:  Rong-Hong Hua; Hong Huo; Ye-Nan Li; Yao Xue; Xiao-Lei Wang; Li-Ping Guo; Bin Zhou; Yong Song; Zhi-Gao Bu
Journal:  PLoS One       Date:  2014-09-08       Impact factor: 3.240

  5 in total

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