Dabrowska K, Switała-Jeleń K, Opolski A, Górski A
Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wroclaw, Poland.
Arch Virol. 2006 Feb;151(2):209-15. doi: 10.1007/s00705-005-0641-7. Epub 2005 Sep 30.
Mammals have become "an environment" for enterobacterial phage life cycles. Therefore it could be expected that bacteriophages adapt to them. This adaptation must comprise bacteriophage proteins. Gp Hoc seems to have significance neither for phage particle structure nor for phage antibacterial activity. It is evidently not necessary for the "typical" antibacterial actions of bacteriophages. But the rules of evolution make it improbable that gp Hoc really has no function, and non-essential genes of T4-type phages are probably important for phages' adaptation to their particular lifestyle. More interesting is the eukaryotic origin of gp Hoc: a resemblance to immunoglobulin-like proteins that reflects their evolutionary relation. Substantial differences in biological activity between T4 and a mutant that lacks gp Hoc were observed in a mammalian system. Hoc protein seems to be one of the molecules predicted to interact with mammalian organisms and/or modulate these interactions.
哺乳动物已成为肠道细菌噬菌体生命周期的“一种环境”。因此,可以预期噬菌体能够适应它们。这种适应必然涉及噬菌体蛋白。Hoc基因产物(gp Hoc)似乎对噬菌体颗粒结构和噬菌体抗菌活性均无意义。显然,它对于噬菌体的“典型”抗菌作用并非必需。但进化规律表明,gp Hoc不太可能真的没有功能,T4型噬菌体的非必需基因可能对噬菌体适应其特定生活方式很重要。更有趣的是gp Hoc的真核起源:它与免疫球蛋白样蛋白相似,这反映了它们的进化关系。在哺乳动物系统中观察到T4噬菌体与缺乏gp Hoc的突变体之间存在显著的生物活性差异。Hoc蛋白似乎是预计会与哺乳动物机体相互作用和/或调节这些相互作用的分子之一。