Classical swine fever (CSF) marker vaccine - Trial II. Challenge study in pregnant sows

被引:68
作者
Depner, KR
Bouma, A
Koenen, F
Klinkenberg, D
Lange, E
de Smit, H
Vanderhallen, H
机构
[1] Fed Res Ctr Virus Dis Anim, Inst Diagnost Virol, D-17498 Insel Riems, Germany
[2] Inst Anim Sci & Hlth ID Lelystad, NL-8200 AB Lelystad, Netherlands
[3] VAR, CERVA, CODA, Vet & Agrochem Res Ctr, B-1180 Uccle, Belgium
关键词
pig-viruses; classical swine fever virus; transplacental transmission; marker vaccination;
D O I
10.1016/S0378-1135(01)00410-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The efficacy of two marker vaccines against classical swine fever (CSF) was tested in a large scale laboratory trial in several National Swine Fever Laboratories (NSFL) of the EU member states. The vaccines were: BAYOVAC CSF Marker (Vaccine A) from Bayer, Leverkusen, Germany and PORCILIS PESTI (Vaccine B) from Intervet, Boxmccr, The Netherlands. At the NSFL of Belgium, The Netherlands and Germany experiments were carried out to examine the ability of the vaccines to prevent transplacental transmission of CSF virus. In Belgium and The Netherlands pregnant sows were vaccinated once and challenged with virulent CSF virus 14 days later, which was around day 60 of gestation. At the NSFL in Germany sows were vaccinated twice, on days 25 and 46 of pregnancy and were challenged fourteen days after booster vaccination (day 60 of gestation). Apart from minor inflammatory reactions in some sows, no reactions post vaccination were noticed in either vaccine group. Sows vaccinated with Vaccine A were better protected against clinical CSF than sows vaccinated with Vaccine B. The antibody response after vaccination with Vaccine A was more pronounced than after vaccination with Vaccine B. After single vaccination six out of eight sows vaccinated with Vaccine A and all eight sows vaccinated with Vaccine B had viraemic piglets. After double vaccination one out of four litters from sows vaccinated with Vaccine A and four out of five litters from sows vaccinated with Vaccine B were found to be viraemic. However, both vaccines reduced the transmission probability significantly (Vaccine A: P = 0.004, Vaccine B: P = 0.024) after booster vaccination. However, Vaccine A appeared in this regard more potent as the estimated probability of fetal infections was lower. Nevertheless the risk of virus spreading after vaccination via transplacental transmission is still present and has to be addressed from an epidemiological point of view. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
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页码:107 / 120
页数:14
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