Garvey P, Fitzgerald G F, Hill C
Department of Microbiology, University College, Cork, Ireland.
Appl Environ Microbiol. 1995 Dec;61(12):4321-8. doi: 10.1128/aem.61.12.4321-4328.1995.
The lactococcal plasmid pNP40, from Lactococcus lactis subsp. lactis biovar diacetylactis DRC3, confers complete resistance to the prolate-headed phage phi c2 and the small isometric-headed phage phi 712 in L. lactis subsp. lactis MG1614. A 6.0-kb NcoI fragment of pNP40 cloned in the lactococcal Escherichia coli shuttle vector pAM401 was found to confer partial resistance to phi 712. Subcloning and deletion analysis of the recombinant plasmid pPG01 defined a 2.5-kb ScaIHpaI fragment as conferring phage insensitivity. Sequence analysis of this region confirmed the presence of two overlapping open reading frames (ORFs). Further subcloning of pNP40 to characterize the resistance determinant active against phi c2 identified a 5.6-kb EcoRV fragment of pNP40 which, when cloned in pAM401, conferred partial resistance to both phi c2 and phi 712. Subcloning and deletion analysis of the recombinant plasmid pCG1 defined a 3.7-kb EcoRV-XbaI fragment as encoding phage insensitivity. DNA sequence analysis of this region revealed the presence of a single complete ORF. The introduction of a frameshift mutation at the unique BglII site within this ORF disrupted the phage resistance phenotype, confirming that this ORF is responsible for the observed phage insensitivity. The mechanisms encoded by pPG01 and pCG1 in L. lactis subsp. lactis MG1614 conformed to the criteria defining abortive infection and were designated AbiE and AbiF, respectively. Analysis of the phage DNA content of phi 712-infected hosts containing AbiF demonstrated that it inhibited the rate of phage DNA replication, while AbiE had little effect on phage DNA replication, suggesting a later target of inhibition. The predicted protein product of abiF shows significant homology to the products of two other lactococcal abortive infection genes, abiD and abiD1.
来自乳酸乳球菌乳亚种双乙酰乳酸亚种DRC3的乳球菌质粒pNP40,赋予乳酸乳球菌乳亚种MG1614对长头噬菌体φc2和小等轴头噬菌体φ712的完全抗性。在乳球菌-大肠杆菌穿梭载体pAM401中克隆的pNP40的一个6.0 kb NcoI片段被发现赋予对φ712的部分抗性。重组质粒pPG01的亚克隆和缺失分析确定一个2.5 kb ScaI-HpaI片段赋予噬菌体不敏感性。该区域的序列分析证实存在两个重叠的开放阅读框(ORF)。为了表征对φc2有活性的抗性决定簇而对pNP40进行的进一步亚克隆鉴定出pNP40的一个5.6 kb EcoRV片段,当将其克隆到pAM401中时,赋予对φc2和φ712的部分抗性。重组质粒pCG1的亚克隆和缺失分析确定一个3.7 kb EcoRV-XbaI片段编码噬菌体不敏感性。该区域的DNA序列分析揭示存在一个单一的完整ORF。在该ORF内独特的BglII位点引入移码突变破坏了噬菌体抗性表型,证实该ORF负责观察到的噬菌体不敏感性。pPG01和pCG1在乳酸乳球菌乳亚种MG1614中编码的机制符合定义流产感染的标准,分别被命名为AbiE和AbiF。对含有AbiF的φ712感染宿主的噬菌体DNA含量分析表明,它抑制噬菌体DNA复制速率,而AbiE对噬菌体DNA复制几乎没有影响,提示其抑制作用的靶点较晚。abiF的预测蛋白质产物与另外两个乳球菌流产感染基因abiD和abiD1的产物具有显著同源性。