Department of Microbiology, Southeast Dairy Foods Research Center, North Carolina State University, Raleigh, North Carolina 27695-7624.
Appl Environ Microbiol. 1993 Feb;59(2):365-72. doi: 10.1128/aem.59.2.365-372.1993.
A new strategy for starter culture rotations was developed for a series of phage-resistant clones genetically derived from a single strain of Lactococcus lactis subsp. lactis. Phage-resistant derivatives carrying different defense systems were constructed via conjugation with various plasmids encoding abortive infection (Abi/Hsp) and/or restriction and modification (R/M) systems of different specificity. The plasmids included pTR2030 (Hsp R/M), pTN20 (Abi R/M), pTRK11 (R/M), and pTRK68 (R/M). Selected phage-resistant transconjugants or transformants were evaluated in different rotation sequences through cycles of the Heap-Lawrence starter culture activity test in milk contaminated with phage and whey from the previous cycle. When used in consecutive sequence, derivative strains carrying the R/M systems encoded by pTN20, pTRK11, and pTRK68 retarded phage development when the initial levels of phage contamination were below 10 PFU/ml but not when levels were increased to 10 PFU/ml. Use of a derivative bearing pTR2030 (Hsp R/M) at the beginning of the rotation prevented phage development, even when the initial levels of phage contamination were high (10 PFU/ml). Alternating the type and specificity of R/M and Abi defenses through the rotation prevented phage proliferation and in some cases eliminated contaminating phages. A model rotation sequence for the phage defense rotation strategy was developed and performed successfully over nine cycles of the Heap-Lawrence starter culture activity test in the presence of high-titer commercial phage composites. This phage defense rotation strategy is designed to protect a highly specialized Lactococcus strain from phage attack during continuous and extended use in the dairy industry.
为了从单一致 lactis 亚种乳球菌的一系列噬菌体抗性克隆中开发出一种新的启动子培养物旋转策略,构建了携带不同防御系统的噬菌体抗性衍生物,这些衍生物通过与各种质粒进行共轭来实现,这些质粒编码了夭折感染(Abi/Hsp)和/或不同特异性的限制和修饰(R/M)系统。这些质粒包括 pTR2030(Hsp R/M)、pTN20(Abi R/M)、pTRK11(R/M)和 pTRK68(R/M)。在含有噬菌体的牛奶和来自前一轮的乳清污染的 Heap-Lawrence 启动培养物活性测试中,通过循环评估选择的噬菌体抗性转导子或转化子在不同旋转序列中的表现。当在连续序列中使用时,当初始噬菌体污染水平低于 10 PFU/ml 时,携带由 pTN20、pTRK11 和 pTRK68 编码的 R/M 系统的衍生菌株会延迟噬菌体的发展,但当水平增加到 10 PFU/ml 时则不会。在旋转的开始使用携带 pTR2030(Hsp R/M)的衍生菌株可以防止噬菌体的发展,即使初始噬菌体污染水平很高(10 PFU/ml)。通过旋转交替使用 R/M 和 Abi 防御的类型和特异性可以防止噬菌体增殖,并在某些情况下消除污染的噬菌体。针对噬菌体防御旋转策略开发了一个模型旋转序列,并在存在高滴度商业噬菌体复合物的情况下,在 Heap-Lawrence 启动培养物活性测试中成功地进行了九轮循环。该噬菌体防御旋转策略旨在保护高度专业化的乳球菌菌株免受噬菌体攻击,同时在乳制品行业中进行连续和扩展使用。