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噬菌体给药可显著减少受感染小鼠的定植和排菌,且无有害副作用,也不会使肠道微生物群发生畸变。

Bacteriophage administration significantly reduces colonization and shedding by -challenged mice without deleterious side effects and distortions in the gut microbiota.

作者信息

Mai Volker, Ukhanova Maria, Reinhard Mary K, Li Manrong, Sulakvelidze Alexander

机构信息

Department of Epidemiology and Emerging Pathogens Institute; University of Florida ; Gainesville, FL USA.

Department of Pathology; University of Florida ; Gainesville, FL USA.

出版信息

Bacteriophage. 2015 Aug 28;5(4):e1088124. doi: 10.1080/21597081.2015.1088124. eCollection 2015 Oct-Dec.

Abstract

We used a mouse model to establish safety and efficacy of a bacteriophage cocktail, ShigActive™, in reducing fecal counts after oral challenge with a susceptible strain. Groups of inbred C57BL/6J mice challenged with strain S43-NalAcR were treated with a phage cocktail (ShigActive™) composed of 5 lytic bacteriophages and ampicillin. The treatments were administered (i) 1 h after, (ii) 3 h after, (iii) 1 h before and after, and (iv) 1 h before bacterial challenge. The treatment regimens elicited a 10- to 100-fold reduction in the CFU's of the challenge strain in fecal and cecum specimens compared to untreated control mice, (P < 0.05). ShigActive treatment was at least as effective as treatment with ampicillin but had a significantly less impact on the gut microbiota. Long-term safety studies did not identify any side effects or distortions in overall gut microbiota associated with bacteriophage administration. phages may be therapeutically effective in a "classical phage therapy" approach, at least during the early stages after ingestion. Oral prophylactic "phagebiotic" administration of lytic bacteriophages may help to maintain a healthy gut microbiota by killing specifically targeted bacterial pathogens in the GI tract, without deleterious side effects and without altering the normal gut microbiota.

摘要

我们使用小鼠模型来确定噬菌体鸡尾酒制剂ShigActive™在口服易感菌株后减少粪便菌数方面的安全性和有效性。用菌株S43-NalAcR攻击的近交C57BL/6J小鼠组,用由5种裂解性噬菌体和氨苄青霉素组成的噬菌体鸡尾酒制剂(ShigActive™)进行治疗。治疗分别在(i)攻击后1小时、(ii)攻击后3小时、(iii)攻击前1小时和攻击后1小时以及(iv)细菌攻击前1小时进行。与未治疗的对照小鼠相比,这些治疗方案使粪便和盲肠标本中攻击菌株的CFU减少了10至100倍(P<0.05)。ShigActive治疗至少与氨苄青霉素治疗一样有效,但对肠道微生物群的影响明显较小。长期安全性研究未发现与噬菌体给药相关的任何副作用或肠道微生物群的整体扭曲。噬菌体可能在“经典噬菌体疗法”中具有治疗效果,至少在摄入后的早期阶段如此。口服预防性“噬菌生物制剂”的裂解性噬菌体可能有助于通过杀死胃肠道中特定靶向的细菌病原体来维持健康的肠道微生物群,而不会产生有害副作用,也不会改变正常的肠道微生物群。

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