Mycoplasma gallisepticum escapes the host immune response via gga-miR-365-3p/SOCS5/STATs axis

被引:11
|
作者
Wang, Yingjie [1 ]
Han, Yun [1 ]
Wang, Lulu [1 ]
Zou, Mengyun [1 ]
Sun, Yingfei [1 ]
Sun, Huanling [1 ]
Guo, Qiao [1 ]
Peng, Xiuli [1 ]
机构
[1] Huazhong Agr Univ, Key Lab Agr Anim Genet Breeding & Reprod, Minist Educ, Wuhan 430070, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Mycoplasma gallisepticum; Gga-miR-365-3p; SOCS5; immune escape; JAK/STAT; CHICKEN; SUPPRESSOR; IDENTIFICATION; EXPRESSION; MICRORNAS; INFECTION; GENES; ROLES; SOCS; JAK;
D O I
10.1186/s13567-022-01117-x
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
A disruption in the expression of gga-miR-365-3p was confirmed in the Mycoplasma gallisepticum (MG)-infected Chicken primary alveolar type II epithelial (CP-II) cells based on previous sequencing results, but the role it plays in the infection was unclear. In the present study, we demonstrate that MG evaded cellular host immunity via a gga-miR-365-3p/SOCS5-JAK/STATs negative feedback loop. Specifically, we found that at the initial stage of MG infection in cells, gga-miR-365-3p was rapidly increased and activated the JAK/STAT signaling pathway by inhibiting SOCS5, which induced the secretion of inflammatory factors and triggered immune response against MG infection. Over time, though, the infection progressed, MG gradually destroyed the immune defences of CP-II cells. In late stages of infection, MG escaped host immunity by reducing intracellular gga-miR-365-3p and inhibiting the JAK/STAT pathway to suppress the secretion of inflammatory factors and promote MG adhesion or invasion. These results revealed the game between MG and host cell interactions, providing a new perspective to gain insight into the pathogenic mechanisms of MG or other pathogens. Meanwhile, they also contributed to novel thoughts on the prevention and control of MG and other pathogenic infections, shedding light on the immune modulating response triggered by pathogen invasion and their molecular targeting.
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页数:14
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