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首页> 外文期刊>Comparative Medicine >Experimental infection of baboons (Papio cynocephalus anubis) with apathogenic and neurovirulent subtypes of herpesvirus papio 2.
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Experimental infection of baboons (Papio cynocephalus anubis) with apathogenic and neurovirulent subtypes of herpesvirus papio 2.

机译:实验性感染狒狒(Papio cynocephalus anubis)的致病性和神经毒性亚型疱疹病毒papio 2。

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Cercopithecine herpesvirus 16 (Herpesvirus papio 2; HVP2) is an alpha -herpesvirus of baboons (Papio spp.) that generally causes minimal to inapparent disease in the natural host species. HVP2 is very closely related genetically and antigenically to Cercopithecine herpesvirus 1 (monkey B virus; BV) of macaques, which is well known for its extreme lethality in nonmacaque species including humans. Preliminary evidence suggests that a mouse model of HVP2 would be an excellent tool for studying zoonotic BV infections. Although the pathogenicity of different BV isolates in mice spans the full range of severity from apathogenic to extremely neurovirulent, testing of multiple HVP2 isolates revealed only two distinct phenotypes in mice regardless of route of inoculation: apathogenic (HVP2ap) and highly neurovirulent (HVP2nv). For the HVP2nv mouse model to truly reflect BV infection in both its natural host and the differential pathogenicity of BV in aberrant host species, HVP2nv should not produce severe disease in its natural host. To test this, juvenile baboons were inoculated with doses of 106 or 104 plaque-forming units of HVP2ap or HVP2nv by using an oral subdermal inoculation route. Parameters followed included the appearance of lesions, shedding of infectious virus, general health, and the immune response to the infection. Regardless of the inoculum dose used, no differences were noted between the two HVP2 subtypes in baboons in any of the parameters measured. These findings further support the use of the HVP2nv mouse system as a model to elucidate and study the viral determinants associated with cross-species BV neurovirulence..
机译:乙型小疱疹病毒疱疹病毒16(疱疹性疱疹病毒2; HVP2)是狒狒的甲型疱疹病毒(Papio spp。),通常在天然宿主物种中引起的病害很小至不明显。 HVP2在基因和抗原上与猕猴的cerpipithecine疱疹病毒1(猴B病毒; BV)密切相关,众所周知,HVP2在包括人在内的非猕猴物种中具有极高的致死性。初步证据表明,HVP2小鼠模型将是研究人畜共患性BV感染的极佳工具。尽管不同BV分离株在小鼠中的致病性涵盖了从致病性到极度神经毒性的整个严重程度,但是对多种HVP2分离株的测试显示,无论接种途径如何,小鼠中仅表现出两种不同的表型:无源性(HVP2ap)和高度神经毒性(HVP2nv)。为了使HVP2nv小鼠模型能够真正反映其自然宿主中的BV感染以及异常宿主物种中BV的致病性差异,HVP2nv不应在其自然宿主中产生严重的疾病。为了对此进行测试,通过口服皮下接种途径向幼狒狒接种了106或104个HVP2ap或HVP2nv噬菌斑形成单位。随后的参数包括病变的外观,传染性病毒的脱落,总体健康状况以及对感染的免疫反应。不管使用何种接种剂量,狒狒的两种HVP2亚型之间在任何测量参数上均未发现差异。这些发现进一步支持使用HVP2nv小鼠系统作为模型来阐明和研究与跨物种BV神经毒力相关的病毒决定因素。

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