噬菌体治疗细菌感染

H. Shekhar
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摘要

噬菌体治疗已被证明是控制细菌感染的有效方法[1],并已成功应用于儿童痢疾志贺菌感染的治疗。噬菌体治疗方法是控制耐多药细菌的有效方法。Félix d'Herelle在100年前发现噬菌体是一种对痢疾细菌有活性的溶解剂[2]。在印度研究霍乱时,d’Herelle观察到霍乱流行期间死亡率下降。在研究粪便噬菌体时,他将患者的死亡和疾病康复分别与患者体内是否存在毒力弧菌噬菌体联系起来[3]。志贺菌病是一种传染性腹泻病,由肠道病原体志贺菌引起。它是世界范围内的主要健康负担,每年导致近1.647亿例病例和100多万人死亡,其中大多数发生在发展中国家[4]。噬菌体是感染细菌的病毒。随着许多细菌对抗生素产生耐药性,噬菌体正重新成为一种有吸引力的替代品,并已被用于对抗各种细菌感染[5]。Felix d'Herelle于1917年发现的志贺菌噬菌体是有史以来最早分离的噬菌体之一[6,7],随后被证明可以治愈严重痢疾杆菌感染的儿童[8]。然而,从那时起,对志贺菌噬菌体的分离或表征的研究相对较少。只有~35个志贺菌噬菌体的信息保存在公共数据库中,对这些噬菌体的详细研究很少。相比之下,已有400多个埃希氏菌和沙门氏菌噬菌体,其中一些噬菌体,如φX174、P22、λ和T4,已被用作模型系统数十年。随着抗生素耐药性问题变得越来越严重,许多科学家和临床医生再次将噬菌体作为治疗细菌感染的治疗选择。
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Phage Therapy in Bacterial Infection
Phage therapy has proven to be an effective method to control bacterial infection [1] and it has been successfully applied for the treatment of Shigella dysenteriae infections in children. The phage therapy approach is an effective method for controlling multidrug-resistant bacteria. Félix d’Herelle discovered phages as a lytic agent active on dysentery bacteria exactly 100 years ago [2]. When working on cholera in India, d’Herelle observed that mortality declines during an epidemic. Studying stool phages, he linked death and recovery from disease with the absence or presence, respectively, of virulent vibriophages in the patients [3]. Shigellosis, an infectious diarrheal disease, is caused by the enteric pathogen Shigella. It is a major worldwide health burden and causes nearly 164.7 million cases and over a million deaths every year, most of them occurring in developing countries [4]. Bacteriophages (phages) are viruses that infect bacteria. With many species of bacteria becoming resistant to antibiotics, phages are reemerging as an attractive alternative and have already been used to combat a wide variety of bacterial infections [5]. One of the first bacteriophages ever isolated was a Shigella phage, discovered by Felix d’Herelle in 1917 [6,7], which was subsequently shown to cure children suffering from severe S. dysenteriae infection [8]. However, relatively few studies on the isolation or characterization of Shigella phages have been performed since then. Information for only ∼35 Shigella phages has been deposited in public databases, and detailed studies of these phages are sparse. By contrast, over 400 Escherichia and Salmonella phages are readily available, some of which, such as φX174, P22, λ, and T4, have been used as model systems for decades. As the problem of antibiotic resistance becomes ever more acute, a number of scientists and clinicians are looking again at bacteriophages as a therapeutic option in the treatment of bacterial infections.
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