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针对高毒力碳青霉烯耐药菌的噬菌体Kpph1和Kpph9的特性及基因组分析

Characterization and genomic insights into bacteriophages Kpph1 and Kpph9 against hypervirulent carbapenem-resistant .

作者信息

Huang Ye, Huang Yuan, Wu Zhiping, Fan Ziyue, Zheng Fanglin, Liu Yang, Xu Xinping

机构信息

Jiangxi Institute of Respiratory Disease, Jiangxi Clinical Research Center for Respiratory Diseases, The Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, P.R. China.

Jiangxi Hospital of China-Japan Friendship Hospital, Jiangxi, P.R. China.

出版信息

Virulence. 2025 Dec;16(1):2450462. doi: 10.1080/21505594.2025.2450462. Epub 2025 Jan 13.

Abstract

The increasing incidence of infections attributed to hypervirulent carbapenem-resistant (Hv-CRKp) is of considerable concern. Bacteriophages, also known as phages, are viruses that specifically infect bacteria; thus, phage-based therapies offer promising alternatives to antibiotic treatments targeting Hv-CRKp infections. In this study, two isolated bacteriophages, Kpph1 and Kpph9, were characterized for their specificity against the Hv-CRKp NUHL30457 strain that possesses a K2 capsule serotype. Both phages exhibit remarkable environmental tolerance, displaying stability over a range of pH values (4-11) and temperatures (up to 50°C). The phages demonstrate potent antibacterial and antibiofilm efficacy, as indicated by their capacity to inhibit biofilm formation and to disrupt established biofilms of Hv-CRKp. Through phylogenetic analysis, it has been revealed that Kpph1 belongs to the new species of genus, and Kpph9 to the genus. Comparative genomic analysis suggests that the tail fiber protein region exhibits the greatest diversity in the genomes of phages within the same genus, which implies distinct co-evolution histories between phages and their corresponding hosts. Interestingly, both phages have been found to contain two tail fiber proteins that may exhibit potential depolymerase activities. However, the exact role of depolymerase in the interaction between phages and their hosts warrants further investigation. In summary, our findings emphasize the therapeutic promise of phages Kpph1 and Kpph9, as well as their encoded proteins, in the context of research on phage therapy targeting hypervirulent carbapenem-resistant .

摘要

由高毒力耐碳青霉烯类(Hv-CRKp)引起的感染发病率不断上升,令人深感担忧。噬菌体,也被称为 phages,是专门感染细菌的病毒;因此,基于噬菌体的疗法为针对 Hv-CRKp 感染的抗生素治疗提供了有前景的替代方案。在本研究中,对分离出的两种噬菌体 Kpph1 和 Kpph9 针对具有 K2 荚膜血清型的 Hv-CRKp NUHL30457 菌株的特异性进行了表征。两种噬菌体均表现出显著的环境耐受性,在一系列 pH 值(4 - 11)和温度(高达 50°C)范围内都具有稳定性。这些噬菌体显示出强大的抗菌和抗生物膜功效,其抑制生物膜形成以及破坏 Hv-CRKp 已形成的生物膜的能力表明了这一点。通过系统发育分析发现,Kpph1 属于该属的新物种,Kpph9 属于该属。比较基因组分析表明,尾丝蛋白区域在同一属噬菌体的基因组中表现出最大的多样性,这意味着噬菌体与其相应宿主之间存在不同的共同进化历史。有趣的是,已发现两种噬菌体都含有两种可能具有潜在解聚酶活性的尾丝蛋白。然而,解聚酶在噬菌体与其宿主相互作用中的确切作用有待进一步研究。总之,我们的研究结果强调了噬菌体 Kpph1 和 Kpph9 及其编码蛋白在针对高毒力耐碳青霉烯类噬菌体疗法研究中的治疗前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3756/11730680/87f2097ce2b0/KVIR_A_2450462_F0001_B.jpg

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