Molecular Cardiology Unit, Department of Biochemistry, Center for Excellence in Genomic Sciences, School of Biological Sciences, Madurai Kamaraj University, Madurai, 625021, Tamil Nadu, India.
Government Sivagangai Medical College and Hospital, Sivagangai, Tamil Nadu, 630561, India.
Microb Pathog. 2020 Mar;140:103888. doi: 10.1016/j.micpath.2019.103888. Epub 2019 Nov 23.
Group A streptococcus (GAS) and autoimmunity are associated with heart related mitral valve damage, in adults. In this study Balb/c mice were intramuscularly immunized with S. pyogenes SF370 for 4 weeks. Prior to euthanization, physiological parameters like body weight and electrical signalling of the heart were recorded. After euthanization, the heart tissue homogenate was prepared and proteomic alterations were studied using SDS-PAGE and 2D electrophoresis. The expression levels of inflammatory genes like TNFα, IFNγ and TGF-β were quantified using real time PCR. Insilico analysis was performed to identify the functions of hypothetical proteins and virulence factors involved in the induction of rheumatic carditis. The results showed a reduction in body weight, ulceration, inflammation, cardiac lesions and prolonged PR interval in mice immunized with S. pyogenes SF370, as a result of RHD. The heart related proteins like α-actinin, fatty acid binding protein-heart, myosin light chain 3, hemoglobin subunit alpha, myoglobin regulatory light chain 2, (ventricular/cardiac muscle isoform), myosin-6, troponin-1 were found to be up-regulated when compared with the control. The functional annotation of S. pyogenes (SF370) was carried out by retrieving 1696 identified proteins and 653 hypothetical protein sequences in NCBI genome database. The conserved domain was identified for 505 proteins. The pfam database documented that the super families of 279 sequences and 40 signal peptides enabled the classification of proteins in different categories like biological (20%), cellular (22%) and molecular functions (36%). Putative transcription repair coupling factor and putative lysine aminopeptidase N terminal are the two virulence factors identified by VICMPRED in S. pyogenes SF370. The two identified virulence factors are involved in altering the mice heart proteome and thereby controlling the streptococcus pyogenes infection. Thus, the results of the present study reveals the role of immunogenic proteins in induction of rheumatic carditis and to elucidate the molecular mechanisms leading to autoimmune reactions in Balb/c mice.
A 组链球菌(GAS)和自身免疫与成人心脏相关的二尖瓣损伤有关。在这项研究中,Balb/c 小鼠通过肌肉内免疫 S. pyogenes SF370 进行了 4 周。在安乐死之前,记录了生理参数,如体重和心脏电信号。安乐死后,制备心脏组织匀浆,并使用 SDS-PAGE 和 2D 电泳研究蛋白质组学变化。使用实时 PCR 定量炎症基因(如 TNFα、IFNγ 和 TGF-β)的表达水平。进行了计算机分析,以鉴定与风湿性心脏病诱导相关的假设蛋白和毒力因子的功能。结果表明,由于 RHD,用 S. pyogenes SF370 免疫的小鼠体重减轻、溃疡、炎症、心脏病变和 PR 间期延长。与对照相比,心脏相关蛋白如α-辅肌动蛋白、脂肪酸结合蛋白-心脏、肌球蛋白轻链 3、血红蛋白亚基α、肌球蛋白调节轻链 2(心室/心肌同工型)、肌球蛋白-6、肌钙蛋白-1 上调。通过检索 NCBI 基因组数据库中的 1696 种鉴定蛋白和 653 种假设蛋白序列,对 S. pyogenes(SF370)进行了功能注释。鉴定了 505 种蛋白质的保守结构域。pfam 数据库记录了 279 个序列和 40 个信号肽的超家族,使蛋白质能够分为不同类别,如生物(20%)、细胞(22%)和分子功能(36%)。VICMPRED 在 S. pyogenes SF370 中鉴定出两种潜在的转录修复偶联因子和潜在的赖氨酸氨肽酶 N 端,这两种潜在的毒力因子参与改变小鼠心脏蛋白质组,从而控制链球菌感染。因此,本研究的结果揭示了免疫原性蛋白在诱导风湿性心脏病中的作用,并阐明了导致 Balb/c 小鼠自身免疫反应的分子机制。