Zhang Hui, Hu Guyue, Lu Doukun, Zhao Gang, Zhang Yiqiu, Zubair Muhammad, Chen Yingyu, Hu Changmin, Chen Xi, Chen Jianguo, Chen Huanchun, Yang Liguo, Guo Aizhen
The State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China.
Front Vet Sci. 2021 Jun 18;8:666769. doi: 10.3389/fvets.2021.666769. eCollection 2021.
Mycoplasmas are successful pathogens both in humans as well as in animals. In cattle, () is known to be responsible for serious health complications, including pneumonia, mastitis, and arthritis. However, pathogenesis remains unclear. Secreted proteins of could influence infection and modify host defense signaling pathways after they enter their extracellular space in the host micro-environment. Therefore, this study was aimed to compare the secretomes of HB0801 virulent (P1) and attenuated (P150) strains and identify potential pathogenesis-related secreted proteins and biomarkers. The cells of P1 and P150 strains were grown in pleuropneumonia-like organism medium to log phase and then transferred to phosphate-buffered saline for 2 h. Then, the supernatant was analyzed by using label-free quantitative proteomics, and 477 potential secreted proteins were identified. Combined with the bioinformatics prediction, we found that 178 proteins were commonly secreted by the P1 and P150 strains, and 49 of them were encoded by mycoplasmal core genes. Additionally, 79 proteins were found to have a different abundance between the P1 and P150 strains. Among these proteins, 34 were more abundant and uniquely expressed in P1, indicating a possible association with the virulence of . Three differentially secreted proteins, MbovP0145, MbovP0725, and MbovP0174, as well as one equally secreted protein, MbovP0481, as positive control and one protein of inner membrane, MbovP0310, as negative control were, respectively, cloned, expressed, and evaluated for antigenicity, subcellular location, and the secretion nature with their mouse antisera by western blotting and colony immunoblotting assay. Among them, MbovP0145 was confirmed to be more secreted by P1 than P150 strain, highly reactive with the antisera from naturally infected and P1 experimentally infected cattle but not with the P150 vaccinated calves, indicating its potential as a diagnostic antigen. In conclusion, these findings may represent the most extensive compilation of potentially secreted proteins in mycoplasma species and the largest number of differentially secreted proteins between the virulent and attenuated strains to date and provide new insights into pathogenesis and diagnosis.
支原体是人和动物体内成功的病原体。在牛身上,已知(某种支原体)会导致严重的健康并发症,包括肺炎、乳腺炎和关节炎。然而,其发病机制仍不清楚。(该支原体)分泌的蛋白质在进入宿主微环境的细胞外空间后,可能会影响感染并改变宿主防御信号通路。因此,本研究旨在比较HB0801强毒株(P1)和弱毒株(P150)的分泌蛋白组,并鉴定潜在的与发病机制相关的分泌蛋白和生物标志物。将P1和P150菌株的细胞在类胸膜肺炎微生物培养基中培养至对数期,然后转移至磷酸盐缓冲盐水中2小时。然后,使用无标记定量蛋白质组学分析上清液,鉴定出477种潜在的分泌蛋白。结合生物信息学预测,我们发现P1和P150菌株共同分泌178种蛋白质,其中49种由支原体核心基因编码。此外,发现79种蛋白质在P1和P150菌株之间丰度不同。在这些蛋白质中,34种在P1中丰度更高且独特表达,表明可能与(该支原体的)毒力有关。分别克隆、表达三种差异分泌蛋白MbovP0145、MbovP0725和MbovP0174,以及一种等量分泌蛋白MbovP0481作为阳性对照和一种内膜蛋白MbovP0310作为阴性对照,并通过蛋白质印迹和菌落免疫印迹分析用它们的小鼠抗血清评估其抗原性、亚细胞定位和分泌性质。其中,证实MbovP0145在P1菌株中比P150菌株分泌更多,与自然感染和P1实验感染牛的抗血清反应强烈,但与P150疫苗接种小牛的抗血清无反应,表明其作为诊断抗原的潜力。总之,这些发现可能代表了支原体物种中潜在分泌蛋白的最广泛汇编,以及迄今为止强毒株和弱毒株之间差异分泌蛋白数量最多的情况,并为(该支原体的)发病机制和诊断提供了新的见解。