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通过减基因组分析牛种布鲁氏菌 2308 鉴定人类新的药物靶点和潜在的疫苗靶点。

Identification of novel drug targets for humans and potential vaccine targets for cattle by subtractive genomic analysis of Brucella abortus strain 2308.

机构信息

Department of Genetic Engineering and Biotechnology, Shahjalal University of Science and Technology, Sylhet, 3114, Bangladesh.

出版信息

Microb Pathog. 2019 Dec;137:103731. doi: 10.1016/j.micpath.2019.103731. Epub 2019 Sep 8.

Abstract

Brucella abortus is the causative agent of brucellosis, a neglected endemic zoonotic disease. It causes devastating economic losses in low income and developing countries. Clinical symptoms of infected cows include abortion, poor weight, reduced fertility gain and reduction in milk production. Transmission of the zoonotic disease from cattle to human can occur through direct contact with infected cows, their tissues (e.g. placenta or aborted tissues), or their products (e.g. dairy) whereas human-to-human transmission can occur transplacentally or via breastfeeding. Malaise, fatigue, fever, arthritis are some clinical symptom of the disease in humans. Recent studies have revealed that Brucella abortus show resistance to several antibiotics. There are worldwide concerns about rising levels of antibiotic resistance resulting in the treatment failure as well as the reduced usefulness of older broad-spectrum antibiotics. Hence, a rather novel method has been in use to combat resistant pathogens since the last decade. To overcome this challenge, subtractive genomic analysis has been successfully carried out with the whole proteome of Brucella abortus strain 2308 using various bioinformatic tools and servers. Proteins nonhomologous to cattle and human were selected for metabolic analysis. Only three membrane proteins (ABC transporter permease, acriflavine resistance protein B, penicillin-binding protein 2) were found to be potential novel vaccine candidates with cattle as the host whereas one membrane protein (ABC transporter permease) was selected as novel drug target with human as the host. Development of novel vaccines and therapeutics through targeting inhibition of the functions of any of these essential proteins can lead to disruption of pathogen-specific metabolic pathways and thereby to the destruction and the eradication of this pathogen from respective hosts. The results of this study could facilitate the discovery and release of new and effective drugs and help in designing and producing potent vaccines against Brucella abortus strain 2308.

摘要

流产布鲁氏菌是布鲁氏菌病的病原体,一种被忽视的地方性人畜共患传染病。它在低收入和发展中国家造成了巨大的经济损失。受感染奶牛的临床症状包括流产、体重下降、繁殖力下降和产奶量减少。该人畜共患病从牛传播到人可以通过直接接触受感染的牛、它们的组织(如胎盘或流产组织)或它们的产品(如奶制品)而发生,而人与人之间的传播可以通过胎盘或通过母乳喂养发生。不适、疲劳、发烧、关节炎是人类疾病的一些临床症状。最近的研究表明,流产布鲁氏菌对几种抗生素表现出耐药性。全世界都担心抗生素耐药性水平上升导致治疗失败以及旧的广谱抗生素的效用降低。因此,自十年前以来,一种相当新颖的方法一直被用于对抗耐药病原体。为了克服这一挑战,使用各种生物信息学工具和服务器对流产布鲁氏菌 2308 菌株的整个蛋白质组进行了消减基因组分析。选择与牛和人非同源的蛋白质进行代谢分析。只有三种膜蛋白(ABC 转运体渗透酶、吖啶黄素耐药蛋白 B、青霉素结合蛋白 2)被发现是宿主为牛的潜在新型疫苗候选物,而一种膜蛋白(ABC 转运体渗透酶)被选为宿主为人的新型药物靶点。通过靶向抑制这些必需蛋白中的任何一种的功能来开发新型疫苗和疗法,可以导致破坏病原体特异性代谢途径,从而从各自的宿主中破坏和根除这种病原体。这项研究的结果可以促进新的有效药物的发现和释放,并有助于设计和生产针对流产布鲁氏菌 2308 株的有效疫苗。

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