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噬菌体抗性降低了 pv. 在水稻上的致病性。

Phage Resistance Reduced the Pathogenicity of pv. on Rice.

机构信息

State Key Laboratory of Rice Biology, and Ministry of Agriculture Key Laboratory of Molecular Biology of Crop Pathogens and Insects, and Key Laboratory of Biology of Crop Pathogens and Insects of Zhejiang Province, Institute of Biotechnology, Zhejiang University, Hangzhou 310058, China.

Horticulture Department, Faculty of Agriculture, Minia University, El-Minia 61517, Egypt.

出版信息

Viruses. 2022 Aug 13;14(8):1770. doi: 10.3390/v14081770.

DOI:10.3390/v14081770
PMID:36016392
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9416502/
Abstract

Plants grow together with microbes that have both negative and positive impacts on the host, while prokaryotes are in turn also hosts for viruses, co-evolving together in a complex interrelationship. Most research focuses on the interaction of either bacterial pathogens interacting with the plant host, or the impact on viruses on their pathogenic bacterial hosts. Few studies have investigated the co-evolution of bacterial pathogens with their host plants as well as with their bacterial viruses. In this work, we aimed to identify the genes that were associated with both phage sensitivity and host pathogenicity of the bacterium pv. (Xoo), which is the most important bacterial rice pathogen. Using the Tn5 transposon mutation technology, we created a library of Xoo strain C2 comprising 4524 mutants, which were subsequently tested for phage infectability. The phage infection tests showed that less than 1% of the mutants ( = 36) were resistant to phage infection, which was attributed to the Tn5 insertion in 19 genes. Interestingly, three out of 19 genes that conveyed resistance to the phage resulted in reduced pathogenicity to rice seedlings compared to the wild type. We identified three genes involved in both phage infection and bacterial virulence, which were studied by knockout mutants and complementation experiments. All of the three knockout mutants were resistant to infection by phage X2, while the complemented strains restored the susceptibility to the bacterial virus. Surprisingly, the genes are also essential for pathogenicity, which we confirmed by single knockout mutants corresponding to the Tn5 mutants. All three genes are involved in lipopolysaccharide synthesis, thus changing the cell envelope surface molecule composition. Our work shows a possible balance in terms of the connection between bacterial virulence and phage resistance, supporting the deployment of phages for the biocontrol of plant pathogens.

摘要

植物与对宿主既有负面影响又有积极影响的微生物共同生长,而原核生物反过来也是病毒的宿主,它们在复杂的相互关系中共进化。大多数研究都集中在细菌病原体与植物宿主相互作用上,或者病毒对其致病性细菌宿主的影响上。很少有研究调查细菌病原体与其宿主植物以及与其细菌病毒的共同进化。在这项工作中,我们旨在鉴定与细菌 pv 相关的基因。(Xoo),这是最重要的细菌性水稻病原体。使用 Tn5 转座子突变技术,我们创建了一个包含 4524 个突变体的 Xoo 菌株 C2 文库,随后对这些突变体进行了噬菌体感染性测试。噬菌体感染测试表明,不到 1%的突变体(=36)对噬菌体感染具有抗性,这归因于 Tn5 在 19 个基因中的插入。有趣的是,在这 19 个赋予噬菌体抗性的基因中,有三个基因导致对水稻幼苗的致病性降低,与野生型相比。我们鉴定了三个参与噬菌体感染和细菌毒力的基因,通过敲除突变体和互补实验进行了研究。所有三个敲除突变体都对噬菌体 X2 的感染具有抗性,而互补菌株恢复了对细菌病毒的敏感性。令人惊讶的是,这些基因对于致病性也是必需的,我们通过对应于 Tn5 突变体的单敲除突变体证实了这一点。这三个基因都参与了脂多糖的合成,从而改变了细胞包膜表面分子的组成。我们的工作表明,在细菌毒力和噬菌体抗性之间的连接方面存在一种可能的平衡,这支持了噬菌体在植物病原体生物防治中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/d90734a7e864/viruses-14-01770-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/f61cfa20e76f/viruses-14-01770-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/847088320470/viruses-14-01770-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/950a12de743b/viruses-14-01770-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/73c2a760059b/viruses-14-01770-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/2a8697a13631/viruses-14-01770-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/cfaf92ca5c91/viruses-14-01770-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/0352b0a39550/viruses-14-01770-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/a9849edb2444/viruses-14-01770-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/92c9493bc125/viruses-14-01770-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/d90734a7e864/viruses-14-01770-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/f61cfa20e76f/viruses-14-01770-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/847088320470/viruses-14-01770-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/950a12de743b/viruses-14-01770-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/73c2a760059b/viruses-14-01770-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/2a8697a13631/viruses-14-01770-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/cfaf92ca5c91/viruses-14-01770-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/0352b0a39550/viruses-14-01770-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/a9849edb2444/viruses-14-01770-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/92c9493bc125/viruses-14-01770-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4689/9416502/d90734a7e864/viruses-14-01770-g010.jpg

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