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