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Virology. 2020 Mar;542:1-7. doi: 10.1016/j.virol.2019.12.012. Epub 2020 Jan 7.
2
Structural bases for F plasmid conjugation and F pilus biogenesis in .F 质粒接合和 F 菌毛生物发生的结构基础。
Proc Natl Acad Sci U S A. 2019 Jul 9;116(28):14222-14227. doi: 10.1073/pnas.1904428116. Epub 2019 Jun 25.
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A carrier state is established in Pseudomonas aeruginosa by phage LeviOr01, a newly isolated ssRNA levivirus.噬菌体LeviOr01(一种新分离的单链RNA微小病毒)在铜绿假单胞菌中建立了一种携带状态。
J Gen Virol. 2017 Aug;98(8):2181-2189. doi: 10.1099/jgv.0.000883. Epub 2017 Aug 4.
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Asymmetric cryo-EM structure of the canonical Allolevivirus Qβ reveals a single maturation protein and the genomic ssRNA in situ.典型的同尾病毒Qβ的不对称冷冻电镜结构揭示了单个成熟蛋白和原位基因组单链RNA。
Proc Natl Acad Sci U S A. 2016 Oct 11;113(41):11519-11524. doi: 10.1073/pnas.1609482113. Epub 2016 Sep 26.
5
Structure of the Bacterial Sex F Pilus Reveals an Assembly of a Stoichiometric Protein-Phospholipid Complex.细菌性菌毛的结构揭示了一种化学计量蛋白质-磷脂复合物的组装。
Cell. 2016 Sep 8;166(6):1436-1444.e10. doi: 10.1016/j.cell.2016.08.025.
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Asymmetric cryo-EM reconstruction of phage MS2 reveals genome structure in situ.噬菌体 MS2 的非对称低温冷冻电镜重构揭示了原位基因组结构。
Nat Commun. 2016 Aug 26;7:12524. doi: 10.1038/ncomms12524.
7
Measuring mRNA copy number in individual Escherichia coli cells using single-molecule fluorescent in situ hybridization.利用单分子荧光原位杂交技术测量单个大肠杆菌细胞中的 mRNA 拷贝数。
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F conjugation: back to the beginning.F 构型:回到起点。
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Diversity of pili-specific bacteriophages: genome sequence of IncM plasmid-dependent RNA phage M.菌毛特异性噬菌体的多样性:IncM 质粒依赖性 RNA 噬菌体 M 的基因组序列。
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10
Rethinking the evolution of single-stranded RNA (ssRNA) bacteriophages based on genomic sequences and characterizations of two R-plasmid-dependent ssRNA phages, C-1 and Hgal1.基于基因组序列和两种依赖于 R 质粒的 ssRNA 噬菌体 C-1 和 Hgal1 的特性,重新思考单链 RNA (ssRNA) 噬菌体的进化。
J Bacteriol. 2012 Sep;194(18):5073-9. doi: 10.1128/JB.00929-12. Epub 2012 Jul 20.

ssRNA 噬菌体穿透触发 F 菌毛的脱落。

ssRNA phage penetration triggers detachment of the F-pilus.

机构信息

Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843.

Center for Phage Technology, Texas A&M University, College Station, TX 77843.

出版信息

Proc Natl Acad Sci U S A. 2020 Oct 13;117(41):25751-25758. doi: 10.1073/pnas.2011901117. Epub 2020 Sep 28.

DOI:10.1073/pnas.2011901117
PMID:32989140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7568308/
Abstract

Although the F-specific ssRNA phage MS2 has long had paradigm status, little is known about penetration of the genomic RNA (gRNA) into the cell. The phage initially binds to the F-pilus using its maturation protein (Mat), and then the Mat-bound gRNA is released from the viral capsid and somehow crosses the bacterial envelope into the cytoplasm. To address the mechanics of this process, we fluorescently labeled the ssRNA phage MS2 to track F-pilus dynamics during infection. We discovered that ssRNA phage infection triggers the release of F-pili from host cells, and that higher multiplicity of infection (MOI) correlates with detachment of longer F-pili. We also report that entry of gRNA into the host cytoplasm requires the F-plasmid-encoded coupling protein, TraD, which is located at the cytoplasmic entrance of the F-encoded type IV secretion system (T4SS). However, TraD is not essential for pilus detachment, indicating that detachment is triggered by an early step of MS2 engagement with the F-pilus or T4SS. We propose a multistep model in which the ssRNA phage binds to the F-pilus and through pilus retraction engages with the distal end of the T4SS channel at the cell surface. Continued pilus retraction pulls the Mat-gRNA complex out of the virion into the T4SS channel, causing a torsional stress that breaks the mature F-pilus at the cell surface. We propose that phage-induced disruptions of F-pilus dynamics provides a selective advantage for infecting phages and thus may be prevalent among the phages specific for retractile pili.

摘要

虽然 F 特异性 ssRNA 噬菌体 MS2 长期以来一直具有范例地位,但人们对基因组 RNA (gRNA) 进入细胞的过程知之甚少。噬菌体最初使用其成熟蛋白 (Mat) 结合 F 菌毛,然后 Mat 结合的 gRNA 从病毒衣壳中释放出来,并以某种方式穿过细菌包膜进入细胞质。为了解决这个过程的机制,我们用荧光标记 ssRNA 噬菌体 MS2 来跟踪感染过程中 F 菌毛的动态。我们发现 ssRNA 噬菌体感染会触发 F 菌毛从宿主细胞中释放,并且更高的感染复数 (MOI) 与更长的 F 菌毛的脱落相关。我们还报告说,gRNA 进入宿主细胞质需要 F 质粒编码的偶联蛋白 TraD,它位于 F 编码的 IV 型分泌系统 (T4SS) 的细胞质入口处。然而,TraD 不是菌毛脱落所必需的,这表明脱落是由 MS2 与 F 菌毛或 T4SS 早期结合引发的。我们提出了一个多步骤模型,其中 ssRNA 噬菌体与 F 菌毛结合,通过菌毛回缩与细胞表面 T4SS 通道的远端结合。持续的菌毛回缩将 Mat-gRNA 复合物从病毒粒子中拉入 T4SS 通道,导致扭转应力,从而在细胞表面将成熟的 F 菌毛折断。我们提出,噬菌体诱导的 F 菌毛动力学破坏为感染噬菌体提供了选择优势,因此可能在针对回缩菌毛的噬菌体中很普遍。