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猪肺炎支原体脂蛋白Mhp390作为纤溶酶原受体,介导细胞外基质降解和呼吸道上皮细胞损伤。

Mesomycoplasma hyopneumoniae lipoprotein Mhp390 serves as a plasminogen receptor mediating extracellular matrix degradation and respiratory epithelial cells injury.

作者信息

Liu Wei, Ye Liying, Yang Keli, Yan Xingyu, Gao Ting, Yuan Fangyan, Guo Rui, Liu Zewen, Li Chang, Wu Qiong, Zhu Jiajia, Tian Yongxiang, Tang Bo, Song Qiqi, Zhou Danna

机构信息

Key Laboratory of Prevention and Control Agents for Animal Bacteriosis (Ministry of Agriculture and Rural Affairs), Hubei Provincial Key Laboratory of Animal Pathogenic Microbiology, Institute of Animal Husbandry and Veterinary, Hubei Academy of Agricultural Sciences, Wuhan, 430070, China.

Tianjin Key Laboratory of Agricultural Animal Breeding and Healthy Husbandry, College of Animal Science and Veterinary Medicine, Tianjin Agricultural University, Tianjin, 300384, China.

出版信息

Vet Res. 2025 Jun 21;56(1):124. doi: 10.1186/s13567-025-01551-7.

DOI:10.1186/s13567-025-01551-7
PMID:40544247
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12182672/
Abstract

The destruction of the respiratory barrier caused by Mesomycoplasma (Mycoplasma) hyopneumoniae plays a pivotal role in facilitating secondary infections by other respiratory pathogens. However, the pathogenesis of M. hyopneumoniae breaching the respiratory barrier to establish infection remains largely elusive. In this study, the role of Mhp390 encoded by M. hyopneumoniae in invasion of the respiratory tract barrier, including extracellular matrix and tracheal epithelial cells, were investigated through the Transwell assay. Our finding indicated that M. hyopneumoniae may exploit the host fibrinolytic system via Mhp390 to accumulate activated plasmin outside its membrane, thereby breaching the respiratory tract barrier and facilitating the progression of infection. Furthermore, the key functional domains within Mhp390 involved in its interaction with host plasminogen were determined by using truncated mutation techniques. Collectively, these findings will enhance our understanding of the mechanism underlying respiratory barrier invasion by M. hyopneumoniae thereby providing new theoretical basis for the development of novel vaccines and effective control strategies against secondary infection.

摘要

猪肺炎支原体(Mesomycoplasma (Mycoplasma) hyopneumoniae)引起的呼吸屏障破坏在促进其他呼吸道病原体的继发感染中起关键作用。然而,猪肺炎支原体突破呼吸屏障以建立感染的发病机制在很大程度上仍不清楚。在本研究中,通过Transwell试验研究了猪肺炎支原体编码的Mhp390在侵袭包括细胞外基质和气管上皮细胞在内的呼吸道屏障中的作用。我们的研究结果表明,猪肺炎支原体可能通过Mhp390利用宿主纤维蛋白溶解系统在其膜外积累活化的纤溶酶,从而突破呼吸道屏障并促进感染进展。此外,通过使用截短突变技术确定了Mhp390内参与其与宿主纤溶酶原相互作用的关键功能域。总的来说,这些发现将增进我们对猪肺炎支原体侵袭呼吸屏障机制的理解,从而为开发新型疫苗和针对继发感染的有效控制策略提供新的理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f977/12182672/d7ef73853119/13567_2025_1551_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f977/12182672/5eaae8429a99/13567_2025_1551_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f977/12182672/cf43f05f221f/13567_2025_1551_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f977/12182672/f135e5d7eac8/13567_2025_1551_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f977/12182672/b6dc627c7192/13567_2025_1551_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f977/12182672/18d9e21bb2e0/13567_2025_1551_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f977/12182672/d7ef73853119/13567_2025_1551_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f977/12182672/5eaae8429a99/13567_2025_1551_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f977/12182672/cf43f05f221f/13567_2025_1551_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f977/12182672/f135e5d7eac8/13567_2025_1551_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f977/12182672/b6dc627c7192/13567_2025_1551_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f977/12182672/18d9e21bb2e0/13567_2025_1551_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f977/12182672/d7ef73853119/13567_2025_1551_Fig6_HTML.jpg

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本文引用的文献

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Microbial evasion of the complement system: a continuous and evolving story.微生物逃避补体系统:一个持续不断的演变故事。
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A Recombinant Chimera Vaccine Composed of LTB and Antigens P97R1, mhp390 and P46 Elicits Cellular Immunologic Response in Mice.一种由LTB与抗原P97R1、mhp390和P46组成的重组嵌合疫苗在小鼠中引发细胞免疫反应。
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