Chen Qiao-Guang, Zhang Yu-Ming, Chen Chen, Wang Shuang, Li Zai-Fan, Hou Zhao-Feng, Liu Dan-Dan, Tao Jian-Ping, Xu Jin-Jun
College of Veterinary Medicine, Yangzhou University, Yangzhou, China.
Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonosis, Yangzhou, China.
Front Vet Sci. 2023 Mar 17;10:1106807. doi: 10.3389/fvets.2023.1106807. eCollection 2023.
can cause histomonosis in poultry. Due to the prohibition of effective drugs, the prevention and treatment of the disease requires new strategies. Questions about its pathogenic mechanisms and virulence factors remain puzzling.
To address these issues, a tandem mass tag (TMT) comparative proteomic analysis of a virulent strain and its attenuated strain of Chinese chicken-origin was performed.
A total of 3,494 proteins were identified in the experiment, of which 745 proteins were differentially expressed (fold change ≥1.2 or ≤0.83 and < 0.05), with 192 up-regulated proteins and 553 down-regulated proteins in the virulent strain relative to the attenuated strain.
Surface protein BspA like, digestive cysteine proteinase, actin, and GH family 25 lysozyme were noted among the proteins up regulated in virulent strains, and these several proteins may be directly related to the pathogenic capacity of the histomonad. Ferredoxin, 60S ribosomal protein L6, 40S ribosomal protein S3, and NADP-dependent malic enzyme which associated with biosynthesis and metabolism were also noted, which have the potential to be new drug targets. The up-regulation of alpha-amylase, ras-like protein 1, ras-like protein 2, and involucrin in attenuated strains helps to understand how it is adapted to the long-term culture environment. The above results provide some candidate protein-coding genes for further functional verification, which will help to understand the molecular mechanism of pathogenicity and attenuation of more comprehensively.
可引起家禽组织滴虫病。由于有效药物被禁用,该病的防治需要新策略。关于其致病机制和毒力因子的问题仍然令人困惑。
为解决这些问题,对中国鸡源的强毒株及其弱毒株进行了串联质谱标签(TMT)比较蛋白质组学分析。
实验共鉴定出3494种蛋白质,其中745种蛋白质差异表达(倍数变化≥1.2或≤0.83且P<0.05),相对于弱毒株,强毒株中有192种蛋白质上调,553种蛋白质下调。
在强毒株中上调的蛋白质中有表面蛋白BspA样蛋白、消化性半胱氨酸蛋白酶、肌动蛋白和GH家族25溶菌酶,这几种蛋白质可能与组织滴虫的致病能力直接相关。还发现了与生物合成和代谢相关的铁氧化还原蛋白、60S核糖体蛋白L6、40S核糖体蛋白S3和NADP依赖性苹果酸酶,它们有可能成为新的药物靶点。弱毒株中α-淀粉酶、类Ras蛋白1、类Ras蛋白2和内披蛋白的上调有助于了解其如何适应长期培养环境。上述结果为进一步的功能验证提供了一些候选蛋白质编码基因,这将有助于更全面地了解其致病性和减毒的分子机制。