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一种经典猪瘟亚单位标记疫苗及配套诊断检测方法的研发。

Development of a classical swine fever subunit marker vaccine and companion diagnostic test.

作者信息

Moormann R J, Bouma A, Kramps J A, Terpstra C, De Smit H J

机构信息

Institute of Animal Science and Health (ID-DLO), P.O. Box 65, NL-8200 AB, Lelystad, Netherlands.

出版信息

Vet Microbiol. 2000 Apr 13;73(2-3):209-19. doi: 10.1016/s0378-1135(00)00146-2.

Abstract

The development of a classical swine fever (CSF) subunit marker vaccine, based on viral envelope glycoprotein E2, and a companion diagnostic test, based on a second viral envelope glycoprotein E(RNS), will be described. Important properties of the vaccine, such as onset and duration of immunity, and prevention of horizontal and vertical transmission of virus were evaluated. A single dose of the vaccine protected pigs against clinical signs of CSF, following intranasal challenge with 100LD(50) of virulent classical swine fever virus (CSFV) at 2 weeks after vaccination. However, challenge virus transmission to unvaccinated sentinels was not always completely inhibited at this time point. From 3 weeks up to 6 months after vaccination, pigs were protected against clinical signs of CSF, and no longer transmitted challenge virus to unvaccinated sentinels. In contrast, unvaccinated control pigs died within 2 weeks after challenge. We also evaluated transmission of challenge virus in a setup enabling determination of the reproduction ratio (R value) of the virus. In such an experiment, transmission of challenge virus is determined in a fully vaccinated population at different time points after vaccination. Pigs challenged at 1 week after immunization died of CSF, whereas the vaccinated sentinels became infected, seroconverted for E(RNS) antibodies, but survived. At 2 weeks after vaccination, the challenged pigs seroconverted for E(RNS) antibodies, but none of the vaccinated sentinels did. Thus, at 1 week after vaccination, R1, and at 2 weeks, R=0, implying no control or control of an outbreak, respectively. Vertical transmission of CSFV to the immune-incompetent fetus may lead to the birth of highly viraemic, persistently infected piglets which are one of the major sources of virus spread. Protection against transplacental transmission of CSFV in vaccinated sows was, therefore, tested in once and twice vaccinated sows. Only one out of nine once-vaccinated sows transmitted challenge virus to the fetus, whereas none of the nine twice-vaccinated sows did. Finally, our data show that the E(RNS) test detects CSFV-specific antibodies in vaccinated or unvaccinated pigs as early as 14 days after infection with a virulent CSF strain. This indicates that the E2 vaccine and companion test fully comply with the marker vaccine concept. This concept implies the possibility of detecting infected animals within a vaccinated population.

摘要

本文将介绍一种基于病毒包膜糖蛋白E2的经典猪瘟(CSF)亚单位标记疫苗,以及一种基于另一种病毒包膜糖蛋白E(RNS)的配套诊断检测方法。评估了该疫苗的重要特性,如免疫的开始时间和持续时间,以及对病毒水平和垂直传播的预防效果。在接种疫苗2周后,用100LD(50)的强毒经典猪瘟病毒(CSFV)进行鼻内攻毒,单剂量疫苗可保护猪免受CSF临床症状的影响。然而,在此时间点,攻毒病毒向未接种疫苗的哨兵猪的传播并未总是被完全抑制。在接种疫苗后3周直至6个月,猪受到保护,免受CSF临床症状的影响,并且不再将攻毒病毒传播给未接种疫苗的哨兵猪。相比之下,未接种疫苗的对照猪在攻毒后2周内死亡。我们还在一个能够确定病毒繁殖率(R值)的实验装置中评估了攻毒病毒的传播情况。在这样的实验中,在接种疫苗后的不同时间点,在完全接种疫苗的猪群中确定攻毒病毒的传播情况。免疫后1周攻毒的猪死于CSF,而接种疫苗的哨兵猪被感染,产生了E(RNS)抗体,但存活下来。接种疫苗2周后,攻毒的猪产生了E(RNS)抗体,但接种疫苗的哨兵猪均未产生。因此,接种疫苗1周后,R>1,而接种疫苗2周后,R=0,分别意味着无法控制或控制了疫情爆发。CSFV向免疫功能不全的胎儿的垂直传播可能导致高病毒血症、持续感染仔猪的出生,这些仔猪是病毒传播的主要来源之一。因此,在接种一次和两次疫苗的母猪中测试了对CSFV经胎盘传播的保护作用。9头接种一次疫苗的母猪中只有1头将攻毒病毒传播给了胎儿,而9头接种两次疫苗的母猪均未传播。最后,我们的数据表明,E(RNS)检测可在感染强毒CSF毒株后14天就检测到接种或未接种疫苗的猪体内的CSFV特异性抗体。这表明E2疫苗和配套检测完全符合标记疫苗的概念。这一概念意味着有可能在接种疫苗的猪群中检测出感染动物。

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