Muñoz-González Sara, Pérez-Simó Marta, Colom-Cadena Andreu, Cabezón Oscar, Bohórquez José Alejandro, Rosell Rosa, Pérez Lester Josué, Marco Ignasi, Lavín Santiago, Domingo Mariano, Ganges Llilianne
IRTA, Centre de Recerca en Sanitat Animal (CReSA, IRTA-UAB), Campus de la Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain.
Servei d'Ecopatologia de Fauna Salvatge, Departament de Medicina i Cirurgia Animals, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain.
PLoS One. 2016 Feb 26;11(2):e0149469. doi: 10.1371/journal.pone.0149469. eCollection 2016.
Two groups with three wild boars each were used: Group A (animals 1 to 3) served as the control, and Group B (animals 4 to 6) was postnatally persistently infected with the Cat01 strain of CSFV (primary virus). The animals, six weeks old and clinically healthy, were inoculated with the virulent strain Margarita (secondary virus). For exclusive detection of the Margarita strain, a specific qRT-PCR assay was designed, which proved not to have cross-reactivity with the Cat01 strain. The wild boars persistently infected with CSFV were protected from superinfection by the virulent CSFV Margarita strain, as evidenced by the absence of clinical signs and the absence of Margarita RNA detection in serum, swabs and tissue samples. Additionally, in PBMCs, a well-known target for CSFV viral replication, only the primary infecting virus RNA (Cat01 strain) could be detected, even after the isolation in ST cells, demonstrating SIE at the tissue level in vivo. Furthermore, the data analysis of the Margarita qRT-PCR, by means of calculated ΔCt values, supported that PBMCs from persistently infected animals were substantially protected from superinfection after in vitro inoculation with the Margarita virus strain, while this virus was able to infect naive PBMCs efficiently. In parallel, IFN-α values were undetectable in the sera from animals in Group B after inoculation with the CSFV Margarita strain. Furthermore, these animals were unable to elicit adaptive humoral (no E2-specific or neutralising antibodies) or cellular immune responses (in terms of IFN-γ-producing cells) after inoculation with the second virus. Finally, a sequence analysis could not detect CSFV Margarita RNA in the samples tested from Group B. Our results suggested that the SIE phenomenon might be involved in the evolution and phylogeny of the virus, as well as in CSFV control by vaccination. To the best of our knowledge, this study was one of the first showing efficient suppression of superinfection in animals, especially in the absence of IFN-α, which might be associated with the lack of innate immune mechanisms.
使用了两组,每组三只野猪:A组(动物1至3)作为对照,B组(动物4至6)在出生后持续感染猪瘟病毒(CSFV)的Cat01毒株(原始病毒)。这些六周龄且临床健康的动物接种了强毒株玛格丽塔(Margarita)(继发病毒)。为了专门检测玛格丽塔毒株,设计了一种特异性qRT-PCR检测方法,该方法被证明与Cat01毒株无交叉反应。持续感染CSFV的野猪受到强毒CSFV玛格丽塔毒株的超感染保护,血清、拭子和组织样本中没有临床症状且未检测到玛格丽塔RNA即可证明。此外,在PBMC中,这是CSFV病毒复制的一个众所周知的靶点,即使在ST细胞中分离后,也只能检测到最初感染的病毒RNA(Cat01毒株),这证明了体内组织水平的超感染免疫。此外,通过计算ΔCt值对玛格丽塔qRT-PCR进行的数据分析支持,持续感染动物的PBMC在体外接种玛格丽塔病毒株后基本上受到超感染保护,而这种病毒能够有效感染未感染的PBMC。同时,接种CSFV玛格丽塔毒株后,B组动物血清中未检测到IFN-α值。此外,这些动物在接种第二种病毒后无法引发适应性体液免疫(无E2特异性或中和抗体)或细胞免疫反应(就产生IFN-γ的细胞而言)。最后,序列分析在B组测试的样本中未检测到CSFV玛格丽塔RNA。我们的结果表明,超感染免疫现象可能与病毒的进化和系统发育有关,也与通过疫苗接种控制CSFV有关。据我们所知,这项研究是最早显示动物中超感染有效抑制的研究之一,特别是在没有IFN-α的情况下,这可能与缺乏先天免疫机制有关。