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细胞培养中 PDCoV 的连续传代降低了其致病性及其对仔猪肠道微生物群稳态的破坏。

Serial passage of PDCoV in cell culture reduces its pathogenicity and its damage of gut microbiota homeostasis in piglets.

机构信息

The College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, Henan, China.

Key Laboratory for Animal-derived Food Safety of Henan Province, Zhengzhou, Henan, China.

出版信息

mSystems. 2024 Mar 19;9(3):e0134623. doi: 10.1128/msystems.01346-23. Epub 2024 Feb 13.

DOI:10.1128/msystems.01346-23
PMID:38349151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10949489/
Abstract

Porcine deltacoronavirus (PDCoV) is an enteropathogenic coronavirus that mainly causes diarrhea in suckling piglets, and also has the potential for cross-species transmission. However, there are still no commercial vaccines available to prevent and control PDCoV infection. In this study, PDCoV strain HNZK-02 was serially propagated for up to 150 passages and the amino acid changes have mainly occurred in the S protein during serial passage which caused structure change. PDCoV HNZK-02-passage 5 (P5)-infected piglets exhibited acute and severe watery diarrhea, an obvious intestinal damage, while the piglets infected with PDCoV HNZK-02-P150 showed no obvious clinical signs, weak intestinal lesions, and lower viral loads in rectal swabs and various tissues. Compared with the PDCoV HNZK-02-P5 infection, HNZK-02-P150 infection resulted in a decrease in intestinal mucosal permeability and pro-inflammatory cytokines. Moreover, PDCoV HNZK-02-P5 infection had significantly reduced bacterial diversity and increased relative abundance of opportunistic pathogens, while PDCoV HNZK-02-P150 infection did not significantly affect the bacterial diversity, and the relative abundance of probiotics increased. Furthermore, the alterations of gut microbiota were closely related to the change of pro-inflammatory factor. Metagenomics prediction analysis demonstrated that HNZK-02-P150 modulated the tyrosine metabolism, Nucleotide-binding and oligomerization domain (NOD)-like receptor signaling pathway, and lipopolysaccharide biosynthesis, which coincided with lower inflammatory response and intestinal permeability in the piglets infected with HNZK-02-P150. In conclusion, the PDCoV HNZK-02 was successfully attenuated by serial passage , and the changes of S gene, metabolic function, and gut microbiota may contribute to the attenuation. The PDCoV HNZK-02-P150 may have the potential for developing live-attenuated vaccine.IMPORTANCEPorcine deltacoronavirus (PDCoV) is an enteropathogen causing severe diarrhea, dehydration, and death in nursing piglets, devastating great economic losses for the global swine industry, and has cross-species transmission and zoonotic potential. There are currently no approved treatments or vaccines available for PDCoV. In addition, gut microbiota has an important relationship with the development of many diseases. Here, the PDCoV virulent HNZK-02 strain was successfully attenuated by serial passage on cell cultures, and the pathogenesis and effects on the gut microbiota composition and metabolic function of the PDCoV HNZK-02-P5 and P150 strains were investigated in piglets. We also found the genetic changes in the S protein during passage and the gut microbiota may contribute to the pathogenesis of PDCoV, while their interaction molecular mechanism would need to be explored further.

摘要

猪德尔塔冠状病毒(PDCoV)是一种主要引起仔猪腹泻的肠致病性冠状病毒,也具有跨种传播的潜力。然而,目前还没有可用于预防和控制 PDCoV 感染的商业疫苗。在这项研究中,PDCoV 株 HNZK-02 连续传代培养了多达 150 代,在连续传代过程中 S 蛋白的氨基酸变化主要导致了结构的改变。PDCoV HNZK-02-P5 感染的仔猪表现出急性和严重的水样腹泻,明显的肠道损伤,而 PDCoV HNZK-02-P150 感染的仔猪则没有明显的临床症状,肠道病变较弱,直肠拭子和各种组织中的病毒载量较低。与 PDCoV HNZK-02-P5 感染相比,HNZK-02-P150 感染导致肠黏膜通透性和促炎细胞因子降低。此外,PDCoV HNZK-02-P5 感染显著降低了细菌多样性并增加了机会性病原体的相对丰度,而 PDCoV HNZK-02-P150 感染并没有显著影响细菌多样性,益生菌的相对丰度增加。此外,肠道微生物群的改变与促炎因子的变化密切相关。宏基因组预测分析表明,HNZK-02-P150 调节了酪氨酸代谢、核苷酸结合和寡聚化结构域(NOD)样受体信号通路和脂多糖生物合成,这与感染 HNZK-02-P150 的仔猪炎症反应和肠通透性降低相一致。总之,PDCoV HNZK-02 通过连续传代成功减毒,S 基因、代谢功能和肠道微生物群的变化可能有助于减毒。PDCoV HNZK-02-P150 可能具有开发活疫苗的潜力。

重要性

猪德尔塔冠状病毒(PDCoV)是一种肠致病性病原体,可引起哺乳仔猪严重腹泻、脱水和死亡,给全球养猪业造成巨大经济损失,具有跨种传播和人畜共患潜力。目前尚无批准的 PDCoV 治疗方法或疫苗。此外,肠道微生物群与许多疾病的发展有着重要的关系。在这里,我们通过细胞培养成功地使 PDCoV 毒力株 HNZK-02 减毒,并用仔猪研究了 PDCoV HNZK-02-P5 和 P150 株的致病机制及其对肠道微生物群组成和代谢功能的影响。我们还发现了在传代过程中 S 蛋白的遗传变化,而肠道微生物群可能有助于 PDCoV 的发病机制,但其相互作用的分子机制仍需要进一步探索。

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