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首页> 外文期刊>Microbial Pathogenesis >Intramuscular Immunization of Streptococcus pyogenes SF370 protein extract and identification of multiple virulence factors through proteomic profiling in RHD induced Balb/c mice
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Intramuscular Immunization of Streptococcus pyogenes SF370 protein extract and identification of multiple virulence factors through proteomic profiling in RHD induced Balb/c mice

机译:通过RHD诱导BALB / C小鼠蛋白质组学分析,肌内免疫链球菌的SF370蛋白提取物和多种毒力因子的鉴定

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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 TNF alpha, IFN gamma and TGF-beta 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 alpha-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.
机译:组中的链球菌(气体)和自身免疫与成年人中的心脏相关二尖瓣损伤有关。在本研究中,BALB / C小鼠用S. pyogenes SF370肌肉注射4周。在安乐死之前,记录了物体重量和心脏的电信号等生理参数。制服后,制备心脏组织匀浆,并使用SDS-PAGE和2D电泳研究蛋白质组改变。使用实时PCR定量TNFα,IFNγ和TGF-β等炎症基因的表达水平。进行Insilico分析以确定假设蛋白质和毒力因子诱导风湿性心肌炎的功能。结果表明,由于RHD,用S. py370免疫的小鼠中的体重,溃疡,炎症,心脏病变和延长的PR间隔减少。发现心脏相关蛋白,如α-肌醇素,脂肪酸结合蛋白 - 心脏,肌蛋白轻链3,血红蛋白亚基α,肌蛋白调节轻链2,(室心/心肌同种素),肌苷-6,肌钙蛋白-6,肌钙蛋白-1与对照相比上调。通过在NCBI基因组数据库中检索1696鉴定的蛋白质和653个假想蛋白序列来进行S. pyogenes(SF370)的功能诠释。保守结构域被鉴定为505个蛋白质。 PFAM数据库记录了279个序列和40个信号肽的超级系列,使不同类别的蛋白质分类为生物(20%),细胞(22%)和分子官能(36%)。推定的转录修复偶联因子和推定的赖氨酸氨肽酶N末端是由S. py370中的vicmpred鉴定的两种毒力因子。这两种鉴定的毒力因子参与改变小鼠心脏蛋白质组,从而控制细菌能细胞感染。因此,本研究结果揭示了免疫原性蛋白在诱导风湿性心动炎中的作用,并阐明了BALB / C小鼠中的自身免疫反应的分子机制。

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