Korsten K H, Tomkiewicz C, Hausmann R
J Gen Virol. 1979 Apr;43(1):57-73. doi: 10.1099/0022-1317-43-1-57.
Five phages which are morphologically similar to coliphage T7 but attack other host bacteria have been compared to T7 and to its relative, T3, by the following criteria: (a) cross-reactivity with antisera against T7 and T3, (b) DNA base sequence homologies, as determined by the C0t technique, (c) synthesis of two phage-coded enzymes: RNA polymerase and SAMase, (d) patterns of phage-directed protein synthesis, as determined by SDS-polyacrylamide gel electrophoresis of phage coat subunits. As judged by all these criteria, Pseudomonas phage PX3 is not related to T7; thus, morphological similarity was attributed to convergent evolution. The other phages, i.e. Serratia phage IV, Psuedomonas phage gh-1, Citrobacter phage ViIII and Klebsiella phage No. 11, were considered to be related to T7 on the basis of similarities in the patterns of phage-coded proteins and because, early after infection, these phages induced, as T7 does, an RNA polymerase which specifically transcribes the DNA of thehomologous phage. Phages IV and No. 11 also induced the early synthesis of SAMase (previously only known to occur upon T3 infection). With the exception of phage IV, however, DNA base sequence homologies with T7 or T3 seem to be poor or non-existent. The tested phages, again with the exception of phage IV, did not react with antiserum against T3 or T7. It is concluded that a particular pattern of phage-directed protein synthesis (as characterized by polyacrylamide gel electrophoresis and enzyme tests) may provide evidence for phylogenetic relationships between phages, even in cases where other criteria, such as genetic recombination, serological cross-reaction, and DNA base sequence homologies, fail to indicate relatedness.
已通过以下标准,将五种形态上与大肠杆菌噬菌体T7相似但攻击其他宿主细菌的噬菌体与T7及其亲缘噬菌体T3进行了比较:(a) 与抗T7和T3抗血清的交叉反应性;(b) 通过C0t技术测定的DNA碱基序列同源性;(c) 两种噬菌体编码酶的合成:RNA聚合酶和S-腺苷甲硫氨酸酶(SAMase);(d) 噬菌体指导的蛋白质合成模式,通过噬菌体外壳亚基的SDS-聚丙烯酰胺凝胶电泳确定。根据所有这些标准判断,铜绿假单胞菌噬菌体PX3与T7无关;因此,形态相似性归因于趋同进化。其他噬菌体,即粘质沙雷氏菌噬菌体IV、铜绿假单胞菌噬菌体gh-1、柠檬酸杆菌噬菌体ViIII和肺炎克雷伯菌噬菌体11号,基于噬菌体编码蛋白质模式的相似性,并且因为在感染后早期,这些噬菌体像T7一样诱导了一种特异性转录同源噬菌体DNA的RNA聚合酶,所以被认为与T7相关。噬菌体IV和11号还诱导了SAMase的早期合成(以前只知道在T3感染时会发生)。然而,除了噬菌体IV外,与T7或T3的DNA碱基序列同源性似乎很低或不存在。除噬菌体IV外,所测试的噬菌体与抗T3或T7的抗血清均无反应。得出的结论是,即使在其他标准(如基因重组、血清学交叉反应和DNA碱基序列同源性)未能表明相关性的情况下,特定的噬菌体指导的蛋白质合成模式(以聚丙烯酰胺凝胶电泳和酶测试为特征)也可能为噬菌体之间的系统发育关系提供证据。