Zijian Wang , Jiao Yang, Lihua Yang, Youhong Zhong, Peng Wang
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Various methods including continuous passage lysogenic tests, in vitro lysis tests, comparative genomic assays, fluorescence quantitative PCR and receptor identification tests were employed to demonstrate that the lysogenic life cycle of this phage is applicable to wild <em>Y. pestis</em> strains; its lysogeny is pseudolysogenic (carrying but not integrating), allowing it to replicate and proliferate within <em>Y. pestis</em>. Furthermore, we have identified the outer membrane protein OmpA of <em>Y. pestis</em> as the receptor for phage infection. In conclusion, our research provides insight into the characteristics and receptors of a novel <em>Y. pestis</em> phage infection with a pseudolysogenic cycle. The findings of this study enhance our understanding of <em>Y. pestis</em> phages and plague microecology, offering valuable insights for future studies on the conservation and genetic evolution of <em>Y. pestis</em> in nature.</p></div>","PeriodicalId":23483,"journal":{"name":"Virus research","volume":null,"pages":null},"PeriodicalIF":2.5000,"publicationDate":"2024-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0168170224000881/pdfft?md5=ffe49070c8e66a86001137b0fe86aa37&pid=1-s2.0-S0168170224000881-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Characteristics of a pseudolysogenic phage vB_YpM_HQ103 infecting Yersinia pestis\",\"authors\":\"Zijian Wang , Jiao Yang, Lihua Yang, Youhong Zhong, Peng Wang\",\"doi\":\"10.1016/j.virusres.2024.199395\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The plague, caused by <em>Yersinia pestis</em>, is a natural focal disease and the presence of <em>Y. pestis</em> in the environment is a critical ecological concern worldwide. 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引用次数: 0
摘要
由鼠疫耶尔森氏菌引起的鼠疫是一种自然疫源性疾病,鼠疫耶尔森氏菌在环境中的存在是世界范围内一个重要的生态问题。鼠疫耶尔森菌噬菌体在鼠疫生态生命周期中的作用至关重要。此前,一种名为 vB_YpM_HQ103 的对温度敏感的噬菌体从中国云南省的鼠疫病灶中分离出来。感染鼠疫噬菌体 EV76 菌株后,vB_YpM_HQ103 在 21 °C 时表现出溶菌行为,在 37 °C 时表现出溶解行为。通过连续通过溶菌试验、体外溶菌试验、基因组比较试验、荧光定量 PCR 和受体鉴定试验等多种方法证明,该噬菌体的溶菌生命周期适用于野生鼠疫酵母菌株;其溶菌作用为假溶菌(携带但不整合),可在鼠疫酵母菌内复制和增殖。此外,我们还发现鼠疫耶氏菌的外膜蛋白 OmpA 是噬菌体感染的受体。总之,我们的研究深入揭示了一种新型鼠疫噬菌体感染假溶解周期的特征和受体。本研究的发现加深了我们对鼠疫噬菌体和鼠疫微生态学的理解,为今后研究鼠疫噬菌体在自然界中的保存和遗传进化提供了宝贵的见解。
Characteristics of a pseudolysogenic phage vB_YpM_HQ103 infecting Yersinia pestis
The plague, caused by Yersinia pestis, is a natural focal disease and the presence of Y. pestis in the environment is a critical ecological concern worldwide. The role of Y. pestis phages in the ecological life cycle of the plague is crucial. Previously, a temperature-sensitive phage named vB_YpM_HQ103 was isolated from plague foci in Yunnan province, China. Upon infecting the EV76 strain of Y. pestis, vB_YpM_HQ103 exhibits lysogenic behavior at 21 °C and lytic behavior at 37 °C. Various methods including continuous passage lysogenic tests, in vitro lysis tests, comparative genomic assays, fluorescence quantitative PCR and receptor identification tests were employed to demonstrate that the lysogenic life cycle of this phage is applicable to wild Y. pestis strains; its lysogeny is pseudolysogenic (carrying but not integrating), allowing it to replicate and proliferate within Y. pestis. Furthermore, we have identified the outer membrane protein OmpA of Y. pestis as the receptor for phage infection. In conclusion, our research provides insight into the characteristics and receptors of a novel Y. pestis phage infection with a pseudolysogenic cycle. The findings of this study enhance our understanding of Y. pestis phages and plague microecology, offering valuable insights for future studies on the conservation and genetic evolution of Y. pestis in nature.
期刊介绍:
Virus Research provides a means of fast publication for original papers on fundamental research in virology. Contributions on new developments concerning virus structure, replication, pathogenesis and evolution are encouraged. These include reports describing virus morphology, the function and antigenic analysis of virus structural components, virus genome structure and expression, analysis on virus replication processes, virus evolution in connection with antiviral interventions, effects of viruses on their host cells, particularly on the immune system, and the pathogenesis of virus infections, including oncogene activation and transduction.