a Technology & Innovation , DuPont Nutrition and Health , Madison , WI , USA.
b Département de biochimie, de microbiologie, et de bioinformatique, Faculté des sciences et de génie, Groupe de recherche en écologie buccale, Faculté de médecine dentaire , Université Laval , Québec City , QC , Canada.
RNA Biol. 2019 Apr;16(4):461-468. doi: 10.1080/15476286.2018.1502589. Epub 2018 Oct 2.
CRISPR-Cas defends microbial cells against invading nucleic acids including viral genomes. Recent studies have shown that type III-A CRISPR-Cas systems target both RNA and DNA in a transcription-dependent manner. We previously found a type III-A system on a conjugative plasmid in Lactococcus lactis which provided resistance against virulent phages of the Siphoviridae family. Its naturally occurring spacers are oriented to generate crRNAs complementary to target phage mRNA, suggesting transcription-dependent targeting. Here, we show that only constructs whose spacers produce crRNAs complementary to the phage mRNA confer phage resistance in L. lactis. In vivo nucleic acid cleavage assays showed that cleavage of phage dsDNA genome was not detected within phage-infected L. lactis cells. On the other hand, Northern blots indicated that the lactococcal CRISPR-Cas cleaves phage mRNA in vivo. These results cannot exclude that single-stranded phage DNA is not being targeted, but phage DNA replication has been shown to be impaired.
CRISPR-Cas 系统防御微生物细胞免受入侵核酸的侵害,包括病毒基因组。最近的研究表明,III-A 型 CRISPR-Cas 系统以转录依赖的方式靶向 RNA 和 DNA。我们之前在乳球菌的一个接合质粒上发现了一个 III-A 型系统,该系统对 Siphoviridae 家族的毒性噬菌体具有抗性。其天然存在的间隔序列被定向生成与靶噬菌体 mRNA 互补的 crRNA,提示转录依赖性靶向。在这里,我们表明只有那些间隔序列产生与噬菌体 mRNA 互补的 crRNA 的构建体才能在乳球菌中赋予噬菌体抗性。体内核酸切割实验表明,在噬菌体感染的乳球菌细胞内未检测到噬菌体 dsDNA 基因组的切割。另一方面,Northern blot 表明乳球菌 CRISPR-Cas 在体内切割噬菌体 mRNA。这些结果不能排除单链噬菌体 DNA 未被靶向,但已表明噬菌体 DNA 复制受到损害。