Department of Biophysics, University of Delhi South Campus, New Delhi, 110021, India.
Sci Rep. 2020 Feb 20;10(1):3036. doi: 10.1038/s41598-020-59924-1.
Yersinia pseudotuberculosis is one of the three pathogenic species of the genus Yersinia. Most studies regarding pathogenesis of Y. pseudotuberculosis are based on the proteins related to Type III secretion system, which is a well-known primary virulence factor in pathogenic Gram-negative bacteria, including Y. pseudotuberculosis. Information related to the factors involved in Y. pseudotuberculosis granuloma formation is scarce. In the present study we have used a computational approach to identify proteins that might be potentially involved in formation of Y. pseudotuberculosis granuloma. A comparative proteome analysis and conserved orthologous protein identification was performed between two different genera of bacteria - Mycobacterium and Yersinia, their only common pathogenic trait being ability to form necrotizing granuloma. Comprehensive analysis of orthologous proteins was performed in proteomes of seven bacterial species. This included M. tuberculosis, M. bovis and M. avium paratuberculosis - the known granuloma forming Mycobacterium species, Y. pestis and Y. frederiksenii - the non-granuloma forming Yersinia species and, Y. enterocolitica - that forms micro-granuloma and, Y. pseudotuberculosis - a prominent granuloma forming Yersinia species. In silico proteome analysis indicated that seven proteins (UniProt id A0A0U1QT64, A0A0U1QTE0, A0A0U1QWK3, A0A0U1R1R0, A0A0U1R1Z2, A0A0U1R2S7, A7FMD4) might play some role in Y. pseudotuberculosis granuloma. Validation of the probable involvement of the seven proposed Y. pseudotuberculosis granuloma proteins was done using transcriptome data analysis and, by mapping on a composite protein-protein interaction map of experimentally proved M. tuberculosis granuloma proteins (RD1 locus proteins, ESAT-6 secretion system proteins and intra-macrophage secreted proteins). Though, additional experiments involving knocking out of each of these seven proteins are required to confirm their role in Y. pseudotuberculosis granuloma our study can serve as a basis for further studies on Y. pseudotuberculosis granuloma.
假结核耶尔森菌是耶尔森氏菌属的三种致病菌之一。大多数关于假结核耶尔森氏菌发病机制的研究都是基于与 III 型分泌系统相关的蛋白质,III 型分泌系统是一种著名的革兰氏阴性致病菌主要毒力因子,包括假结核耶尔森氏菌。关于假结核耶尔森氏菌肉芽肿形成相关因子的信息很少。在本研究中,我们使用计算方法来鉴定可能参与假结核耶尔森氏菌肉芽肿形成的蛋白质。在两种不同的细菌——分枝杆菌和耶尔森氏菌之间进行了比较蛋白质组分析和保守直系同源蛋白鉴定,它们唯一的共同致病特征是能够形成坏死性肉芽肿。在七种细菌的蛋白质组中进行了同源蛋白的综合分析。这包括结核分枝杆菌、牛分枝杆菌和副结核分枝杆菌——已知的形成肉芽肿的分枝杆菌种,鼠疫耶尔森氏菌和弗氏耶尔森氏菌——非形成肉芽肿的耶尔森氏菌种,以及形成微肉芽肿的肠炎耶尔森氏菌和形成显著肉芽肿的假结核耶尔森氏菌。计算机蛋白质组学分析表明,有七种蛋白质(UniProt id A0A0U1QT64、A0A0U1QTE0、A0A0U1QWK3、A0A0U1R1R0、A0A0U1R1Z2、A0A0U1R2S7、A7FMD4)可能在假结核耶尔森氏菌肉芽肿中发挥一定作用。通过转录组数据分析和在已证实的结核分枝杆菌肉芽肿蛋白(RD1 基因座蛋白、ESAT-6 分泌系统蛋白和巨噬细胞内分泌蛋白)的复合蛋白质-蛋白质相互作用图谱上进行映射,验证了这七种假结核耶尔森氏菌肉芽肿蛋白的可能参与。尽管需要进行敲除这七种蛋白质中的每一种的额外实验来确认它们在假结核耶尔森氏菌肉芽肿中的作用,但我们的研究可以作为进一步研究假结核耶尔森氏菌肉芽肿的基础。