Department of Microbiology and Immunology, University of Michigan, Ann Arbor, MI 48109, USA.
Mol Microbiol. 2011 Nov;82(3):567-77. doi: 10.1111/j.1365-2958.2011.07847.x. Epub 2011 Oct 10.
Bacteria in their struggle for survival have evolved or acquired defences against attacking phage. However, phage often contribute to this defence through mechanisms in which a prophage protects the bacterial population from attack by another, often unrelated, phage. The 933W prophage, which carries Shiga toxin genes that enhance pathogenicity of enterohaemorrhagic Escherichia coli strain O157:H7, also carries the stk gene encoding a eukaryotic-like tyrosine kinase that excludes (aborts) infection by phage HK97. This exclusion requires the kinase activity of Stk. Little, if any, protein tyrosine phosphorylation can be detected in a 933W lysogen prior to infection with HK97, while extensive Stk-mediated tyrosine phosphorylation is evident following infection. This includes autophosphorylation that stabilizes Stk protein from degradation. Although increased levels of Stk are found following HK97 infection, these higher levels are not necessary or sufficient for exclusion or protein phosphorylation. An HK97 open reading frame, orf41, is necessary for exclusion and Stk kinase activity. We hypothesize that interaction with gp41 stimulates Stk kinase activity. Exclusion of HK97 appears to be specific since other phages tested, λ, φ80, H-19B, λ-P22dis and T4rII, were not excluded. Infection of the 933W lysogen with a non-excluded phage fails to induce Stk-determined phosphorylation.
细菌在为生存而斗争的过程中,已经进化或获得了抵御攻击噬菌体的防御机制。然而,噬菌体通常通过以下机制有助于这种防御:原噬菌体保护细菌群体免受另一种噬菌体的攻击,而这种噬菌体通常与原噬菌体无关。933W 原噬菌体携带志贺毒素基因,增强了产肠出血性大肠杆菌 O157:H7 菌株的致病性,还携带 stk 基因,该基因编码一种类似真核的酪氨酸激酶,可排除(中止)噬菌体 HK97 的感染。这种排除需要 Stk 的激酶活性。在感染 HK97 之前,933W 溶原菌中几乎检测不到任何蛋白质酪氨酸磷酸化,但在感染后,Stk 介导的广泛酪氨酸磷酸化是显而易见的。这包括自磷酸化,可稳定 Stk 蛋白免受降解。尽管在 HK97 感染后发现 Stk 水平升高,但这些更高水平对于排除或蛋白质磷酸化既不是必需的也不是充分的。HK97 的一个开放阅读框(orf41)对于排除和 Stk 激酶活性是必要的。我们假设与 gp41 的相互作用刺激了 Stk 激酶活性。排除 HK97 似乎是特异性的,因为测试的其他噬菌体,λ、φ80、H-19B、λ-P22dis 和 T4rII,都没有被排除。感染 933W 溶原菌的非排除噬菌体未能诱导 Stk 决定的磷酸化。