首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >Unraveling novel broad-spectrum antibacterial targets in food and waterborne pathogens using comparative genomics and protein interaction network analysis
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Unraveling novel broad-spectrum antibacterial targets in food and waterborne pathogens using comparative genomics and protein interaction network analysis

机译:使用比较基因组学和蛋白质相互作用网络分析方法,揭示食品和水生病原体中的新型广谱抗菌目标

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Food and waterborne diseases are a growing concern in terms of human morbidity and mortality world-wide, even in the 21st century, emphasizing the need for new therapeutic interventions for these diseases. The current study aims at prioritizing broad-spectrum antibacterial targets, present in multiple food and waterborne bacterial pathogens, through a comparative genomics strategy coupled with a protein interaction network analysis. The pathways unique and common to all the pathogens under study (viz., methane metabolism, D-alanine metabolism, peptidoglycan biosynthesis, bacterial secretion system, two-component system, C5-branched dibasic acid metabolism), identified by comparative metabolic pathway analysis, were considered for the analysis. The proteins/enzymes involved in these pathways were prioritized following host non-homology analysis, essentiality analysis, gut flora non-homology analysis and protein interaction network analysis. The analyses revealed a set of promising broad-spectrum antibacterial targets, present in multiple food and waterborne pathogens, which are essential for bacterial survival, non-homologous to host and gut flora, and functionally important in the metabolic network. The identified broad-spectrum candidates, namely, integral membrane protein/virulence factor (MviN), preprotein translocase subunits SecB and SecG, carbon storage regulator (CsrA), and nitrogen regulatory protein P-II 1 (GlnB), contributed by the peptidoglycan pathway, bacterial secretion systems and two-component systems, were also found to be present in a wide range of other disease-causing bacteria. Cytoplasmic proteins SecG, CsrA and GlnB were considered as drug targets, while membrane proteins MviN and SecB were classified as vaccine targets. The identified broad-spectrum targets can aid in the design and development of antibacterial agents not only against food and waterborne pathogens but also against other pathogens
机译:就全世界的人类发病率和死亡率而言,即使在21世纪,食源性和水传播疾病也日益引起人们的关注,强调需要对这些疾病采取新的治疗措施。本研究旨在通过比较基因组策略和蛋白质相互作用网络分析,对存在于多种食物和水生细菌病原体中的广谱抗菌目标进行优先排序。通过比较性代谢途径分析确定了所研究的所有病原体独特且共有的途径(即甲烷代谢,D-丙氨酸代谢,肽聚糖生物合成,细菌分泌系统,两组分系统,C5支链二元酸代谢),被考虑进行分析。在宿主非同源性分析,必需性分析,肠道菌群非同源性分析和蛋白质相互作用网络分析之后,优先考虑这些途径中涉及的蛋白质/酶。分析揭示了一组有前景的广谱抗菌靶标,存在于多种食物和水生病原体中,这些靶标对于细菌存活至关重要,对宿主和肠道菌群而言是非同源的,并且在代谢网络中具有重要的功能。肽聚糖途径促成的广谱候选物,即完整的膜蛋白/毒力因子(MviN),前蛋白转位酶亚基SecB和SecG,碳存储调节剂(CsrA)和氮调节蛋白P-II 1(GlnB)。细菌分泌系统和两组分系统也被发现存在于多种其他致病细菌中。细胞质蛋白SecG,CsrA和GlnB被视为药物靶标,而膜蛋白MviN和SecB被分类为疫苗靶标。确定的广谱目标可以帮助设计和开发不仅针对食品和水生病原体而且还针对其他病原体的抗菌剂

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