PMCNA_RS00975通过TLR2激活NF-κB和ERK1/2,有助于增强多杀性巴氏杆菌的毒力。

IF 4.6 2区 医学 Q2 IMMUNOLOGY Frontiers in Cellular and Infection Microbiology Pub Date : 2024-10-15 eCollection Date: 2024-01-01 DOI:10.3389/fcimb.2024.1469304
Tenglin Xu, Mingxing Kou, Peili Cao, Benjin Liu, Yating Zheng, Qian Jiang, Jiasen Liu, Hongtao Kang, Mingfa Yang, Dongchun Guo, Liandong Qu
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To further explore the impact of the PMCNA_RS00975 protein on pathogenicity, a <i>PMCNA_RS00975</i> gene mutant of <i>P. multocida</i> strain <i>C48-1</i> was constructed using positive selection technology. Subcellular localization was performed to determine the location of the PMCNA_RS00975 protein within <i>P. multocida.</i> The recombinant protein PMCNA_RS00975 of <i>P. multocida</i> was soluble expressed, purified, and its role in pro-inflammatory cytokines was investigated.</p><p><strong>Results: </strong>The mutant exhibited significantly reduced pathogenicity in the mice model. 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引用次数: 0

摘要

导言:多杀性巴氏杆菌是一种病原菌,可导致家禽出血性败血症和肺炎。有报告表明,某些蛋白质直接参与或调节铁代谢,是多杀性巴氏杆菌的重要毒力因子。因此,了解致病因子并分析促炎细胞因子的作用有助于我们阐明潜在的发病机制:本研究对 PMCNA_RS00975 蛋白进行了研究,该蛋白是由多杀菌球菌致病菌株 C48-1 的一个特定噬菌体岛的基因编码的一种假定的封装蛋白。为了进一步探究 PMCNA_RS00975 蛋白对致病性的影响,研究人员利用阳性选择技术构建了多杀菌素菌株 C48-1 的 PMCNA_RS00975 基因突变体。为了确定 PMCNA_RS00975 蛋白在多杀菌杆菌中的位置,对其进行了亚细胞定位。对多杀菌杆菌重组蛋白 PMCNA_RS00975 进行可溶性表达、纯化,并研究其在促炎细胞因子中的作用:结果:突变体在小鼠模型中的致病性明显降低。此外,亚细胞定位表明 PMCNA_RS00975 蛋白位于外膜,并在多杀菌素感染过程中表达。此外,我们的实验还发现,重组 PMCNA_RS00975 蛋白可通过巨噬细胞中的 NF-κB 和 ERK1/2 信号通路,促进由 TLR2 受体引发的 IL-6 促炎细胞因子的分泌:本研究在C48-1菌株中发现了一种新的毒力因子,为了解其致病机理提供了依据,也为开发针对多杀霉素的减毒疫苗指明了方向。
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PMCNA_RS00975 activates NF-κB and ERK1/2 through TLR2 and contributes to the virulence of Pasteurella multocida.

Introduction: Pasteurella multocida is a pathogenic bacterium known to cause hemorrhagic septicemia and pneumonia in poultry. Reports have indicated that certain proteins, either directly involved in or regulating iron metabolism, are important virulence factors of P. multocida. Therefore, understanding virulent factors and analyzing the role of pro-inflammatory cytokines can help us elucidate the underlying pathogenesis.

Methods: In this study, the PMCNA_RS00975 protein, a putative encapsuling protein encoded by a gene from a specific prophage island of the pathogenic strain C48-1 of P. multocida, was investigated. To further explore the impact of the PMCNA_RS00975 protein on pathogenicity, a PMCNA_RS00975 gene mutant of P. multocida strain C48-1 was constructed using positive selection technology. Subcellular localization was performed to determine the location of the PMCNA_RS00975 protein within P. multocida. The recombinant protein PMCNA_RS00975 of P. multocida was soluble expressed, purified, and its role in pro-inflammatory cytokines was investigated.

Results: The mutant exhibited significantly reduced pathogenicity in the mice model. Furthermore, subcellular localization indicated that the PMCNA_RS00975 protein was located at the outer membrane and expressed during infection of P. multocida. Additionally, our experiments revealed that recombinant PMCNA_RS00975 protein promotes the secretion of the IL-6 pro-inflammatory cytokines triggered by the TLR2 receptor via NF-κB and ERK1/2 signaling pathways in the macrophages.

Discussion: This study identified a novel virulence factor in the C48-1 strain, providing a basis for understanding the pathogenesis and directions for the development of attenuated vaccines against P. multocida.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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