Aleshkin A V, Ershova O N, Volozhantsev N V, Svetoch E A, Popova A V, Rubalskii E O, Borzilov A I, Aleshkin V A, Afanas'ev S S, Karaulov A V, Galimzyanov K M, Rubalsky O V, Bochkareva S S
G. N. Gabrichevsky Research Institute for Epidemiology and Microbiology, Moscow, Russia; Bphage LLC, Moscow, Russia.
N. N. Burdenko Research Institute for Neurosurgery , Moscow, Russia.
Bacteriophage. 2016 Oct 21;6(4):e1251379. doi: 10.1080/21597081.2016.1251379. eCollection 2016.
We have developed a phagebiotic composition using 8 virulent bacteriophages (2 strains of each species) which are able to lyse , , and . The unique character of the developed composition is ensured by particular properties of each bacteriophage comprising the preparation, including their range of lytic activity toward specific bacterial pathogens, morphology of their plaques, cycle of their development, restriction profile of their DNAs, specificity of their genomes (based on complete genome sequencing), and other properties. The preparation did not produce any signs of acute or chronic intoxication in the experimental animals. Therapeutic and prophylactic efficiency of the phagebiotic composition was demonstrated in the prevention and treatment of the experimental acute infection in mice. The investigations have shown that the preparation possesses a high therapeutic efficiency and is highly competitive with ciprofloxacin which is very effective against the infective strain . Our small-scale clinical trial was aimed to evaluate therapeutic effectiveness of the phagebiotic composition in an epidemiological emergency situation in an intensive care unit, caused by multi-resistant strains of , and . Seventy nine per cent of the initial samples from 14 patients' endotracheal aspirate, blood and urine were contaminated. Twenty-four hours after the 3-day phage therapy (20 ml of cocktail at a titer for each phage 10 pfu/ml were introduced intragastrically through a tube once a day) contamination level dropped to 21%. Hence the obtained results enabled us to create a new phagebiotic composition that may be used as an alternative to antibiotics to treat these healthcare-associated infections.
我们研发出了一种噬菌生物制剂,它由8种烈性噬菌体(每种噬菌体有2个菌株)组成,能够裂解[多种细菌名称未给出]。所研发制剂的独特特性由构成该制剂的每种噬菌体的特殊性质所确保,这些性质包括它们对特定细菌病原体的裂解活性范围、噬菌斑形态、发育周期、DNA的限制性图谱、基因组特异性(基于全基因组测序)以及其他性质。该制剂在实验动物身上未产生任何急性或慢性中毒迹象。噬菌生物制剂的治疗和预防效果在小鼠实验性急性[感染细菌名称未给出]感染的预防和治疗中得到了证实。研究表明,该制剂具有很高的治疗效果,并且与对感染菌株非常有效的环丙沙星相比具有很强的竞争力。我们的小规模临床试验旨在评估噬菌生物制剂在重症监护病房由[多种细菌名称未给出]多重耐药菌株引起的流行病学紧急情况下的治疗效果。14名患者气管内吸出物、血液和尿液的初始样本中有79%被污染。在进行为期3天的噬菌体治疗(每天通过管子经胃内注入20毫升每种噬菌体滴度为10⁸ pfu/ml的混合液)24小时后,污染水平降至21%。因此,所获得的结果使我们能够创建一种新的噬菌生物制剂,可作为抗生素的替代品用于治疗这些医疗相关感染。