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马立克氏病病毒编码的 miR-M6 和 miR-M10 对于病毒在鸡体内的复制和发病机制是可有可无的。

Marek's disease virus encoded miR-M6 and miR-M10 are dispensable for virus replication and pathogenesis in chickens.

机构信息

College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, 450002, Henan, People's Republic of China; International Joint Research Center of National Animal Immunology, College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, 450002, Henan, People's Republic of China.

Division of Infectious Disease, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.

出版信息

Vet Microbiol. 2021 Nov;262:109248. doi: 10.1016/j.vetmic.2021.109248. Epub 2021 Oct 5.

Abstract

MicroRNAs (miRNAs) are a class of approximately 22 nucleotides long non-coding RNAs, and virus-encoded miRNAs play an important role in pathogenesis. Marek's disease virus (MDV) is an oncogenic avian alphaherpesvirus that causes immunosuppression and tumors in its natural host, chicken. In the MDV genome, 14 miRNA precursors and 26 mature miRNAs were identified, thus MDV has been used as a model to study the function of viral miRNAs in vivo. Recently, a cluster of miRNAs encoded by MDV, Cluster 3 miRNAs (miR-M8-M10), has been shown to restrict early cytolytic replication and pathogenesis of MDV. In this study, we further analyzed the role of miR-M6 and miR-M10, members of cluster miR-M8-M10, in MDV replication and pathogenicity. We found that, compared to parental MDV, deletion of miR-M6-5p significantly enhanced the replication of MDV in cell culture, but not in chickens. The replication of miR-M6-5p deletion MDV was restored once the deleted sequences were re-inserted. Our results also showed that deletion of miR-M10-5p did not affect the replication of MDV in vitro and in vivo. In addition, our animal study results showed that deletion of miR-M6-5p or miR-M10-5p did not alter the pathogenesis of MDV. In conclusion, our study shows that both miR-M6 and miR-M10 are dispensable for MDV replication and pathogenesis in chickens, while also suggests a repressive role of miR-M6 in MDV replication in cell culture.

摘要

微小 RNA(miRNA)是一类约 22 个核苷酸长的非编码 RNA,病毒编码的 miRNA 在发病机制中起着重要作用。马立克氏病病毒(MDV)是一种致瘤性禽α疱疹病毒,在其自然宿主鸡中引起免疫抑制和肿瘤。在 MDV 基因组中,鉴定出 14 个 miRNA 前体和 26 个成熟 miRNA,因此 MDV 已被用作研究病毒 miRNA 在体内功能的模型。最近,MDV 编码的一组 miRNA,簇 3 miRNA(miR-M8-M10),已被证明限制 MDV 的早期细胞溶解性复制和发病机制。在这项研究中,我们进一步分析了簇 miR-M8-M10 成员 miR-M6 和 miR-M10 在 MDV 复制和致病性中的作用。我们发现,与亲本 MDV 相比,miR-M6-5p 的缺失显著增强了 MDV 在细胞培养中的复制,但在鸡中并非如此。一旦重新插入缺失的序列,miR-M6-5p 缺失 MDV 的复制就会恢复。我们的结果还表明,miR-M10-5p 的缺失不影响 MDV 在体外和体内的复制。此外,我们的动物研究结果表明,miR-M6-5p 或 miR-M10-5p 的缺失不会改变 MDV 的发病机制。总之,我们的研究表明,miR-M6 和 miR-M10 对于鸡 MDV 的复制和发病机制都是可有可无的,而 miR-M6 在细胞培养中对 MDV 复制具有抑制作用。

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