Characterization of the novel Cutibacterium acnes phage KIT08 and its associated pseudolysogenic bacterial isolate

IF 2.6 3区 生物学 Q3 MICROBIOLOGY
Phuoc-Dung Nguyen, Koki Nakanishi, Chihiro Hosokawa, Nguyen Song Han, Masao Kitao, Masanao Yoshimoto, Kaeko Kamei
{"title":"Characterization of the novel Cutibacterium acnes phage KIT08 and its associated pseudolysogenic bacterial isolate","authors":"Phuoc-Dung Nguyen,&nbsp;Koki Nakanishi,&nbsp;Chihiro Hosokawa,&nbsp;Nguyen Song Han,&nbsp;Masao Kitao,&nbsp;Masanao Yoshimoto,&nbsp;Kaeko Kamei","doi":"10.1007/s00203-025-04451-8","DOIUrl":null,"url":null,"abstract":"<div><p><i>Cutibacterium acnes</i>, formerly <i>Propionibacterium</i> acnes, is a Gram-positive bacterium commonly recognized as an important factor in acne vulgaris and infections associated with prosthetic medical devices. With the rise in antibiotic resistance, phage therapy has gained renewed attention as a promising alternative to antibiotics. In addition to a strict lytic cycle, some virulent phages may enter a pseudolysogenic state and exclude superinfections, thereby significantly limiting the applicability of these potential antimicrobial agents. However, the trade-off induced by phage infection of bacterial cells during this state and its molecular mechanism are yet to be confirmed, especially for <i>C. acnes</i> phages. In this study, a novel <i>Cutibacterium acnes</i> phage, KIT08, was isolated and characterized. It demonstrated rapid infectivity and moderately strong bacteriolysis. After infection of <i>C. acnes</i> NBRC 107,605, pseudolysogenic bacteria were collected and examined for physiological tradeoffs. The pseudolysogenic isolate exhibited slower growth and downregulation of the transcriptional levels of biofilm-producing genes, such as <i>lipase 2</i> and <i>hyaluronate lyase</i>, leading to a decrease in biofilm formation. Additionally, a genomic study of phage KIT08 revealed that open reading frames 23 and 34 encode putative proteins homologous to repressor C and LTP proteins, which may play an important role in the induction of pseudolysogeny and superinfection exclusion in <i>C. acnes</i>.</p></div>","PeriodicalId":8279,"journal":{"name":"Archives of Microbiology","volume":"207 10","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00203-025-04451-8.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Microbiology","FirstCategoryId":"99","ListUrlMain":"https://link.springer.com/article/10.1007/s00203-025-04451-8","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Cutibacterium acnes, formerly Propionibacterium acnes, is a Gram-positive bacterium commonly recognized as an important factor in acne vulgaris and infections associated with prosthetic medical devices. With the rise in antibiotic resistance, phage therapy has gained renewed attention as a promising alternative to antibiotics. In addition to a strict lytic cycle, some virulent phages may enter a pseudolysogenic state and exclude superinfections, thereby significantly limiting the applicability of these potential antimicrobial agents. However, the trade-off induced by phage infection of bacterial cells during this state and its molecular mechanism are yet to be confirmed, especially for C. acnes phages. In this study, a novel Cutibacterium acnes phage, KIT08, was isolated and characterized. It demonstrated rapid infectivity and moderately strong bacteriolysis. After infection of C. acnes NBRC 107,605, pseudolysogenic bacteria were collected and examined for physiological tradeoffs. The pseudolysogenic isolate exhibited slower growth and downregulation of the transcriptional levels of biofilm-producing genes, such as lipase 2 and hyaluronate lyase, leading to a decrease in biofilm formation. Additionally, a genomic study of phage KIT08 revealed that open reading frames 23 and 34 encode putative proteins homologous to repressor C and LTP proteins, which may play an important role in the induction of pseudolysogeny and superinfection exclusion in C. acnes.

新型痤疮角质杆菌噬菌体KIT08及其相关假原性分离菌的鉴定
痤疮表皮杆菌,原名痤疮丙酸杆菌,是一种革兰氏阳性细菌,通常被认为是寻常性痤疮和与假体医疗器械相关的感染的重要因素。随着抗生素耐药性的增加,噬菌体治疗作为一种有希望的抗生素替代品重新受到关注。除了严格的裂解周期外,一些强毒噬菌体可能进入假溶原状态并排除重复感染,从而极大地限制了这些潜在抗菌剂的适用性。然而,在这种状态下,噬菌体感染细菌细胞诱导的权衡及其分子机制尚未得到证实,特别是对于C. acnes噬菌体。本研究分离并鉴定了一种新的痤疮表皮杆菌噬菌体KIT08。它表现出快速的传染性和中等强的细菌溶解能力。在感染痤疮C. NBRC 107,605后,收集假多原菌并检查生理权衡。假原分离物表现出生长缓慢和生物膜生成基因转录水平下调,如脂肪酶2和透明质酸裂解酶,导致生物膜形成减少。此外,一项对噬菌体KIT08的基因组研究显示,开放阅读框23和34编码了与阻遏物C和LTP蛋白同源的推定蛋白,这可能在诱导C. acnes假溶解和排斥重复感染中发挥重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Archives of Microbiology
Archives of Microbiology 生物-微生物学
CiteScore
4.90
自引率
3.60%
发文量
601
审稿时长
3 months
期刊介绍: Research papers must make a significant and original contribution to microbiology and be of interest to a broad readership. The results of any experimental approach that meets these objectives are welcome, particularly biochemical, molecular genetic, physiological, and/or physical investigations into microbial cells and their interactions with their environments, including their eukaryotic hosts. Mini-reviews in areas of special topical interest and papers on medical microbiology, ecology and systematics, including description of novel taxa, are also published. Theoretical papers and those that report on the analysis or ''mining'' of data are acceptable in principle if new information, interpretations, or hypotheses emerge.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信