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血清对猪原代单核细胞非洲猪瘟病毒感染力的中和和增强作用。

Serum Neutralizing and Enhancing Effects on African Swine Fever Virus Infectivity in Adherent Pig PBMC.

机构信息

Foreign Animal Disease Research Unit, Plum Island Animal Disease Center, Agricultural Research Service, United States Department of Agriculture, Orient, NY 11957, USA.

Plum Island Animal Disease Center, Oak Ridge Institute for Science and Education, Oak Ridge, TN 37830, USA.

出版信息

Viruses. 2022 Jun 9;14(6):1249. doi: 10.3390/v14061249.

Abstract

African swine fever virus (ASFV) causes hemorrhagic fever with mortality rates of up to 100% in domestic pigs. Currently, there are no commercial vaccines for the disease. Only some live-attenuated viruses have been able to protect pigs from ASFV infection. The immune mechanisms involved in the protection are unclear. Immune sera can neutralize ASFV but incompletely. The mechanisms involved are not fully understood. Currently, there is no standardized protocol for ASFV neutralization assays. In this study, a flow cytometry-based ASFV neutralization assay was developed and tested in pig adherent PBMC using a virulent ASFV containing a fluorescent protein gene as a substrate for neutralization. As with previous studies, the percentage of infected macrophages was approximately five time higher than that of infected monocytes, and nearly all infected cells displayed no staining with anti-CD16 antibodies. Sera from naïve pigs and pigs immunized with a live-attenuated ASFV and fully protected against parental virus were used in the assay. The sera displayed incomplete neutralization with MOI-dependent neutralizing efficacies. Extracellular, but not intracellular, virions suspended in naïve serum were more infectious than those in the culture medium, as reported for some enveloped viruses, suggesting a novel mechanism of ASFV infection in macrophages. Both the intracellular and extracellular virions could not be completely neutralized.

摘要

非洲猪瘟病毒(ASFV)可引起家猪出血性发热,死亡率高达 100%。目前,该病尚无商业疫苗。只有一些减毒活病毒能够保护猪免受 ASFV 感染。涉及的免疫机制尚不清楚。免疫血清可以中和 ASFV,但不完全。其涉及的机制尚未完全阐明。目前,尚无 ASFV 中和测定的标准化方案。在这项研究中,开发了一种基于流式细胞术的 ASFV 中和测定法,并使用含有荧光蛋白基因的强毒 ASFV 作为中和的底物,在猪贴壁 PBMC 中进行了测试。与先前的研究一样,感染巨噬细胞的比例约比感染单核细胞的比例高五倍,几乎所有感染的细胞均未显示与抗 CD16 抗体的染色。在测定中使用了来自未接种猪和接种了减毒 ASFV 并完全免受亲本病毒感染的猪的血清。血清显示出与 MOI 相关的中和功效不完全中和。与一些包膜病毒一样,悬浮在未接种血清中的细胞外而不是细胞内病毒比在培养基中更具传染性,这表明了巨噬细胞中 ASFV 感染的一种新机制。细胞内和细胞外的病毒均不能完全中和。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f72/9229155/1d73098663ec/viruses-14-01249-g001.jpg

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