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基因缺失突变对青海牦牛出血性败血症的免疫保护作用

The Immunoprotection of Gene Deletion Mutation of on Hemorrhagic Sepsis in Qinghai Yak.

作者信息

Jia Jianlei, Zhao Meng, Ma Kairu, Zhang Hongjian, Gui Linsheng, Sun Huzhi, Ren Huiying, Okabayashi Tamaki, Zhao Jing

机构信息

College of Agriculture and Animal Husbandry, Qinghai University, Xining 810016, China.

School of Life Sciences, Qilu Normal University, Jinan 250200, China.

出版信息

Vet Sci. 2023 Mar 14;10(3):221. doi: 10.3390/vetsci10030221.

Abstract

is among the most important virulence factors of , which mediates septicemia in yaks ( I) after infection with the bacteria. In the present study, yaks were infected with wild-type (WT) (P0910) and OmpH-deficient (ΔOmpH) strains. The mutant strain was generated through the reverse genetic operation system of pathogens and proteomics technology. The live-cell bacterial count and clinical manifestations of infection in Qinghai yak tissues (thymus, lung, spleen, lymph node, liver, kidney, and heart) were analyzed. The expression of differential proteins in the yak spleen under different treatments was analyzed using the marker-free method. We found that compared with the mutant strain, the titer of wild-type strains was significantly higher in tissues. Additionally, compared with other organs, the bacteria titer was significantly higher in the spleen. Compared with the WT p0910 strain, the mutant strain generated milder pathological changes in the tissues of yak. Proteomics analysis revealed that 57 of the 773 proteins expressed in were significantly differentially expressed between the ΔOmpH and P0910 groups. Of the 57, 14 were over-expressed, whereas 43 were under-expressed. The differentially expressed proteins in the ΔompH group regulated the ABC transporter (ATP-powered translocation of many substrates across membranes) system, the two-component system, RNA degradation, RNA transcription, glycolysis/gluconeogenesis, biosynthesis of ubiquinone and other terpenoid-quinones, oxidative phosphorylation (citrate cycle) as well as fructose and mannose metabolism. The relationship among 54 significantly regulated proteins was analyzed using STRING. We found that WT P0910 and ΔOmpH of infection activated the expression of ropE, HSPBP1, FERH, ATP10A, ABCA13, RRP7A, IL-10, IFN-γ, IL-17A, EGFR, and dnaJ. Overall, deletion of the gene weakened the virulence but maintained the immunogenicity of in yak. The findings of this study provide a strong foundation for the pathogenesis of and the management of related septicemia in yaks.

摘要

是最重要的毒力因子之一,在牦牛感染该细菌后介导牦牛败血症(I型)。在本研究中,用野生型(WT)(P0910)和OmpH缺陷型(ΔOmpH)菌株感染牦牛。突变菌株是通过病原体的反向遗传操作系统和蛋白质组学技术产生的。分析了青海牦牛组织(胸腺、肺、脾、淋巴结、肝、肾和心脏)中活细胞细菌计数及感染的临床表现。采用无标记方法分析不同处理下牦牛脾脏中差异蛋白的表达。我们发现,与突变菌株相比,野生型菌株在组织中的滴度显著更高。此外,与其他器官相比,脾脏中的细菌滴度显著更高。与WT p0910菌株相比,突变菌株在牦牛组织中产生的病理变化较轻。蛋白质组学分析显示,在ΔOmpH组和P0910组之间,该菌表达的773种蛋白质中有57种存在显著差异表达。在这57种蛋白质中,14种过表达,43种低表达。ΔompH组中差异表达的蛋白质调节ABC转运蛋白(许多底物通过膜的ATP驱动转运)系统、双组分系统、RNA降解、RNA转录、糖酵解/糖异生、泛醌和其他萜类醌的生物合成、氧化磷酸化(柠檬酸循环)以及果糖和甘露糖代谢。使用STRING分析了54种显著调节的蛋白质之间的关系。我们发现该菌感染的WT P0910和ΔOmpH激活了ropE、HSPBP1、FERH、ATP10A、ABCA13、RRP7A、IL-10、IFN-γ、IL-17A、EGFR和dnaJ的表达。总体而言,该基因的缺失减弱了该菌在牦牛中的毒力,但保留了其免疫原性。本研究结果为该菌的发病机制及牦牛相关败血症的管理提供了有力依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4bc/10055848/43d46f812d11/vetsci-10-00221-g001.jpg

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