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源自 Kayvirus S25-3 的溶菌素在葡萄球菌性脓疱疮治疗中的潜力。

Therapeutic Potential of an Endolysin Derived from Kayvirus S25-3 for Staphylococcal Impetigo.

机构信息

Laboratory of Veterinary Internal Medicine, Division of Animal Life Science, Institute of Agriculture, Graduate School, Tokyo University of Agriculture and Technology, 3-5-8 Saiwai-cho, Fuchu, Tokyo 183-8509, Japan.

Laboratory of Veterinary Microbiology I, School of Veterinary Medicine, Azabu University, 1-17-71 Fuchinobe, Chuo-ku, Sagamihara, Kanagawa 252-5201, Japan.

出版信息

Viruses. 2019 Aug 22;11(9):769. doi: 10.3390/v11090769.

Abstract

Impetigo is a contagious skin infection predominantly caused by . Decontamination of from the skin is becoming more difficult because of the emergence of antibiotic-resistant strains. Bacteriophage endolysins are less likely to invoke resistance and can eliminate the target bacteria without disturbance of the normal microflora. In this study, we investigated the therapeutic potential of a recombinant endolysin derived from kayvirus S25-3 against staphylococcal impetigo in an experimental setting. First, the recombinant S25-3 endolysin required an incubation period of over 15 minutes to exhibit efficient bactericidal effects against . Second, topical application of the recombinant S25-3 endolysin decreased the number of intraepidermal staphylococci and the size of pustules in an experimental mouse model of impetigo. Third, treatment with the recombinant S25-3 endolysin increased the diversity of the skin microbiota in the same mice. Finally, we revealed the genus-specific bacteriolytic effect of recombinant S25-3 endolysin against staphylococci, particularly , among human skin commensal bacteria. Therefore, topical treatment with recombinant S25-3 endolysin can be a promising disease management procedure for staphylococcal impetigo by efficient bacteriolysis of while improving the cutaneous bacterial microflora.

摘要

脓疱疮是一种传染性皮肤感染,主要由 引起。由于抗生素耐药株的出现,从皮肤中去除 变得更加困难。噬菌体裂解酶不太可能引起耐药性,并且可以在不干扰正常菌群的情况下消除靶细菌。在这项研究中,我们研究了源自 kayvirus S25-3 的重组内溶素在实验条件下对葡萄球菌性脓疱疮的治疗潜力。首先,重组 S25-3 内溶素需要超过 15 分钟的孵育期才能对 表现出有效的杀菌作用。其次,在脓疱疮实验小鼠模型中,局部应用重组 S25-3 内溶素可减少表皮内葡萄球菌的数量和脓疱的大小。第三,用重组 S25-3 内溶素治疗可增加同一小鼠皮肤微生物群的多样性。最后,我们揭示了重组 S25-3 内溶素对葡萄球菌,特别是 ,在人类皮肤共生菌中的种特异性溶菌作用。因此,局部应用重组 S25-3 内溶素可以通过有效裂解 来改善皮肤细菌微生物群,从而成为治疗葡萄球菌性脓疱疮的有前途的疾病管理程序。

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