Classical swine fever: Comparison of oronasal immunisation with CP7E2alf marker and C-strain vaccines in domestic pigs

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• 作者：Marylè ; ne Tignon ; Gá ; bor Kulcsá ; r ; Andy Haegeman ; Timea Barna ; Katalin Fá ; biá ; n ; Ré ; ka Lé ; vai ; Yves Van der Stede ; Attila Farsang ; Robert Vrancken ; Katinka Belá ; k ; Fran
• 关键词：Classical swine fever virus (CSFV) ; DIVA marker vaccine ; CP7E2alf ; C-strain ; Oronasal vaccination ; Diagnostic tests
• 刊名：Veterinary Microbiology
• 出版年：2010
• 出版时间：21 April 2010
• 年：2010
• 卷：142
• 期：1-2
• 页码：59-68
• 全文大小：585 K

文摘

Effective oronasal vaccination against classical swine fever (CSF) is essential to achieve protection in wild boar. However the currently available live CSF vaccines, e.g. C-strain, do not allow serological differentiation between infected and vaccinated animals (DIVA). A modified live marker vaccine candidate (CP7E2alf) has been recently developed (Reimann et al., 2004). This communication reports the comparison of CP7E2alf and C-strain virus vaccines during 98 days following oronasal immunisation in domestic pigs.

C-strain vaccine virus was consistently detected in tonsils of all (n = 30) animals from 3 to 77 days post vaccination (dpv) and in blood (n = 36) between 3 and 13 dpv by CSFV-specific rRT-PCR. CP7E2alf virus RNA was detected in 6 animals slaughtered between 4 and 63 dpv by a BVDV-specific rRT-PCR. The chimeric virus was not detected in blood samples.

As detected by CSFV E2-specific antibody ELISA and virus neutralisation tests, seroconversion first occurred at 11 dpv in the C-strain vaccinated group and between 11 and 15 dpv in the CP7E2alf vaccinated group. The serological response was still present at 98 dpv. The CP7E2alf serological response remained negative using the CSFV E^rns ELISA whereas seroconversion occurred in the C-strain vaccinated group.

In conclusion, the primary replication site of CP7E2alf vaccine virus was found to be the tonsils as in the C-strain and virulent field strains. Persistence of CP7E2alf in the tonsils was also demonstrated up to 63 dpv. Both vaccines showed immunogenicity after oronasal administration in domestic pigs. In contrast to the C-strain, CP7E2alf vaccine allowed the use of DIVA approaches in serological tests. This study confirms CP7E2alf as a promising marker vaccine candidate for oronasal vaccination programmes to control CSF in domestic pigs and wild boar.