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Mycoplasma ovipneumoniae-derived lipid-associated membrane proteins induce cytokine secretion in mouse peritoneal macrophages through TLR2 signalling

文献类型： 外文期刊

作者： Bai, Fan 1 ; Wu, Jindi 2 ; Liu, Bo 2 ; Wang, Xiaohui 1 ; Shi, Xiaona 1 ; Lv, Tianxing 1 ; Wang, Yanfang 1 ; Hao, Yongqing 1 ;

作者机构： 1.Inner Mongolia Agr Univ, Coll Vet Med, Key Lab Microbiol & Immunol, 306 Zhaowuda Rd, Saihan Dist 010018, Hohhot, Peoples R China

2.Inner Mongolia Agr Univ, Coll Vet Med, Lab Vet Pharmacol, 306 Zhaowuda Rd, Saihan Dist 010018, Hohhot, Peoples R China

3.Inner Mongolia Agr Univ, Coll Vet Med, Key Lab Clin Diag & Treatment Tech Anim Dis, Minist Agr, 306 Zhaowuda Rd, Saihan Dist 010018, Hohhot, Peoples R China

4.Inner Mongolia Acad Agr & Anim Husb Sci, Vet Res Inst, 22 Zhaojun Rd, Yuquan Dist 010031, Hohhot, Peoples R China

关键词： Mycoplasma ovipneumoniae; TLR2; Lipid-associated membrane protein; Inflammasome; Cytokines

期刊名称：RESEARCH IN VETERINARY SCIENCE （ 影响因子：2.534； 五年影响因子：2.382 ）

ISSN： 0034-5288

年卷期： 2020 年 132 卷

页码：

收录情况： SCI

摘要： Background: Mycoplasma ovipneumoniae (M. ovi) is the causative agent of chronic non-progressive pneumonia in sheep, goats, bighorn, and wild small ruminants. However, the mechanism of infection and immune response to M. ovi remain unclear. Invading microbes express lipid-associated membrane proteins (LAMPs) on the cell surface that interact with host cells to facilitate infection, and are thus the major molecules recognised by the host immune system. Upon LAMP recognition, Toll-like receptor 2 (TLR2) and NLRP3 inflammasome sense the pathogens and signalling pathways for cytokine secretion. In this study, we investigated whether M. ovi and M. ovi-derived LAMPs are immuno-biologically active compounds capable of activating mouse peritoneal macrophages and explored the underlying mechanism. Results: After infection of wild-type mice with M. ovi, the expression of TLR2 and NLRP3 at the transcriptional and translational levels was determined with reverse transcription-polymerase chain reaction and flow cytometry. In addition, the cytokine levels and associated pathways were detected in infected wild-type, Tlr2(-/-), and Nlrp3(-/-) mice via enzyme-linked immunosorbent assays and western blotting. The nuclear factor (NF)-kappa B and mitogen-activated protein kinase (MAPK) signalling pathways were found to mediate the expression of inflammatory cytokines in M. ovi or M. ovi-derived LAMP-infected peritoneal macrophages, and cytokines were not induced in TIr2(-/-) and/or Nlrp3(-/-) macrophages. Conclusion: Host cytokine production is activated in response to M. ovi-derived LAMPs through the NF-kappa B and MAPK signalling pathway via TLR2.

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