Shigella pathogenesis: molecular and computational insights

IF 0.7 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
S. Mukhopadhyay, S. Ganguli, S. Chakrabarti
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引用次数: 2

Abstract

Shigellosis, characterized by inflammation and ulceration of the large intestine, is caused by infection with Shigella species. It is a major public health problem in developing countries where filthy sanitation practices and restricted access to clean water encourage the spread of the disease. Shigellosis is spread by means of fecal-oral route. It is one of the most common disorders specially affecting children in West Bengal, India. Disease from Shigella species accounts for 165 million cases of diarrhoea culminating in one million deaths annually worldwide. Severe dysentery is treated still with antibiotics, with limited success because of the continuous development of multi drug resistance by the bacteria. WHO has identified Shigella as a potential target pathogen against which new drugs need to be formulated and in silico approach has the potential to identify drug targets. Molecular modeling of Shigella invasion proteins using computational tools may divulge novel therapeutic targets that can be used for future pharmacological intervention. Detailed annotation of previously unknown Hypothetical Proteins using an in-silico pipeline can identify crucial proteins in pathogenesis cascade, which can be explored further as effective drug targets, which may eventually enable us to combat the menace of shigellosis.
志贺菌的发病机制:分子和计算见解
志贺菌病以大肠炎症和溃疡为特征,是由志贺菌感染引起的。在发展中国家,这是一个主要的公共卫生问题,肮脏的卫生习惯和获得清洁水的限制助长了疾病的传播。志贺菌病通过粪口途径传播。它是最常见的疾病之一,特别影响到印度西孟加拉邦的儿童。志贺氏菌引起的腹泻病例达1.65亿例,全球每年有100万人死亡。严重痢疾仍使用抗生素治疗,但由于细菌对多种药物的耐药性不断发展,成功率有限。世界卫生组织已确定志贺氏菌是一种潜在的靶向病原体,需要配制新的药物,而硅方法有可能确定药物靶点。使用计算工具对志贺菌侵袭蛋白进行分子建模可能会揭示可用于未来药物干预的新治疗靶点。使用计算机管道对以前未知的假设蛋白质进行详细注释,可以确定发病机制级联中的关键蛋白质,这些蛋白质可以作为有效的药物靶点进一步探索,最终可能使我们能够对抗志贺菌病的威胁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
AIMS Molecular Science
AIMS Molecular Science BIOCHEMISTRY & MOLECULAR BIOLOGY-
自引率
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发文量
4
审稿时长
5 weeks
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