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建立山羊伪狂犬病病毒攻毒模型及其在评估伪狂犬病疫苗效力中的应用。

Development of a PPRV challenge model in goats and its use to assess the efficacy of a PPR vaccine.

机构信息

Merial S.A.S., 29 Avenue Tony Garnier, 69007 Lyon, France; ASTRE, Univ Montpellier, CIRAD, INRA, Montpellier, France.

Merial S.A.S., 29 Avenue Tony Garnier, 69007 Lyon, France; ASTRE, Univ Montpellier, CIRAD, INRA, Montpellier, France.

出版信息

Vaccine. 2019 Mar 14;37(12):1667-1673. doi: 10.1016/j.vaccine.2019.01.057. Epub 2019 Feb 13.

Abstract

Peste des Petits Ruminants (PPR) is a severe disease of small ruminants and has high economic impacts in developing countries. Endemic in Africa, the Middle East and Asia, the disease is currently progressing with occurrences reported in North Africa, Turkey and in Georgia, and now threatens Europe. Much remains unknown about the infection dynamics, the virulence of the different strains and species/breed susceptibility. Robust experimental challenge models are needed to explore these fields and to confirm the efficacy of currently sold vaccines. We first assessed virulence of two PPR virus strains (CI89 and MA08) in Saanen goats. Whereas the MA08 strain led to classical severe clinical signs of PPR, the CI89 strain appeared to cause a mild disease in Saanen goats, highlighting the difference in virulence between strains in this animal model. We further demonstrated the importance of the inoculation route in the appearance of clinical signs and that ocular excretion is a better choice than blood for viral detection. After developing a robust challenge model, we assessed the efficacy of a vaccine (PPR-VAC®, BVI Botswana) against the MA08 strain and demonstrated that this vaccine blocked viral excretion and significantly reduced clinical signs. These results reinforce the paradigm that a strain from one lineage could protect against strains from other lineages.

摘要

小反刍兽疫(PPR)是一种严重影响小反刍动物的疾病,在发展中国家造成了重大的经济影响。该病流行于非洲、中东和亚洲,目前在北非、土耳其和格鲁吉亚有报道,现在对欧洲也构成威胁。关于感染动态、不同毒株的毒力以及物种/品种易感性,人们仍然知之甚少。需要建立稳健的实验性攻毒模型来探索这些领域,并验证当前市售疫苗的效果。

我们首先评估了两种小反刍兽疫病毒株(CI89 和 MA08)在萨能山羊中的毒力。MA08 株导致了 PPR 的典型严重临床症状,而 CI89 株在萨能山羊中似乎引起了轻度疾病,这突出了该动物模型中不同毒株之间毒力的差异。我们进一步证明了接种途径对临床症状出现的重要性,并且眼部排泄是比血液更适合用于病毒检测的选择。在建立了稳健的攻毒模型后,我们评估了针对 MA08 株的疫苗(PPR-VAC®,BVI Botswana)的效果,并证明该疫苗可阻止病毒排泄并显著减轻临床症状。这些结果强化了一个观点,即一个谱系的毒株可以预防来自其他谱系的毒株。

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