Satta G, Pruzzo C, Debbia E, Calegari L
J Virol. 1978 Dec;28(3):786-94. doi: 10.1128/JVI.28.3.786-794.1978.
We have previously described Klebsiella pneumoniae MirM7b, which, although stably lysogenic for the inducible and nondefective phages FR2 and AP3, is not immune to superinfection by these same viruses. MirA12b, a strain which is lysogenic for FR2 and AP3 and immune to superinfection, has been derived from MirM7b. The sensitivity of this strain and that of the nonimmune parent to several bacteriophages have been compared in this work. It has been found that, whereas MirM7b is sensitive to coliphages P1, T3, T7, and phiI, MirA12b is fully resistant to all of them. It is shown that phages FR2 and AP3 convert Klebsiella strains to resistance to coliphage P1 and coliphages T3, T7, and phiI, respectively, and cause loss of surface antigens in lysogenic cells. To determine such a conversion, both FR2 and AP3 require expression of immunity to superinfection. This explains the differences that exist between MirM7b and MirA12b in both phage sensitivity and surface antigens. Hypotheses are presented to explain the peculiar need for an active superinfection repressor to express lysogenic conversion.
我们之前描述过肺炎克雷伯菌MirM7b,它虽然能稳定地携带可诱导且无缺陷的噬菌体FR2和AP3进行溶源化,但对这些相同病毒的超感染并不免疫。MirA12b是一种对FR2和AP3进行溶源化且对超感染免疫的菌株,它是从MirM7b衍生而来的。在这项研究中,比较了该菌株和非免疫亲本对几种噬菌体的敏感性。结果发现,MirM7b对大肠杆菌噬菌体P1、T3、T7和phiI敏感,而MirA12b对所有这些噬菌体完全抗性。研究表明,噬菌体FR2和AP3分别使克雷伯菌菌株对大肠杆菌噬菌体P1以及噬菌体T3、T7和phiI产生抗性,并导致溶源化细胞表面抗原的丧失。为了确定这种转化,FR2和AP3都需要表达对超感染的免疫性。这就解释了MirM7b和MirA12b在噬菌体敏感性和表面抗原方面存在的差异。本文提出了一些假设来解释表达溶源化转化时对活性超感染阻遏物的特殊需求。