Department of Biological Sciences, University of Delaware, 328 Wolf Hall, Newark, DE, 19716, USA.
BMC Genomics. 2019 Feb 4;20(1):105. doi: 10.1186/s12864-019-5439-1.
Bacteria are prey for many viruses that hijack the bacterial cell in order to propagate, which can result in bacterial cell lysis and death. Bacteria have developed diverse strategies to counteract virus predation, one of which is the clustered regularly interspaced short palindromic repeat (CRISPR) and CRISPR associated (Cas) proteins immune defense system. Species within the bacterial family Vibrionaceae are marine organisms that encounter large numbers of phages. Our goal was to determine the significance of CRISPR-Cas systems as a mechanism of defense in this group by investigating their prevalence, phylogenetic distribution, and genome context.
Herein, we describe all the CRISPR-Cas system types and their distribution within the family Vibrionaceae. In Vibrio cholerae genomes, we identified multiple variant type I-F systems, which were also present in 41 additional species. In a large number of Vibrio species, we identified a mini type I-F system comprised of tniQcas5cas7cas6f, which was always associated with Tn7-like transposons. The Tn7-like elements, in addition to the CRISPR-Cas system, also contained additional cargo genes such as restriction modification systems and type three secretion systems. A putative hybrid CRISPR-Cas system was identified containing type III-B genes followed by a type I-F cas6f and a type I-F CRISPR that was associated with a prophage in V. cholerae and V. metoecus strains. Our analysis identified CRISPR-Cas types I-C, I-E, I-F, II-B, III-A, III-B, III-D, and the rare type IV systems as well as cas loci architectural variants among 70 species. All systems described contained a CRISPR array that ranged in size from 3 to 179 spacers. The systems identified were present predominantly within mobile genetic elements (MGEs) such as genomic islands, plasmids, and transposon-like elements. Phylogenetic analysis of Cas proteins indicated that the CRISPR-Cas systems were acquired by horizontal gene transfer.
Our data show that CRISPR-Cas systems are phylogenetically widespread but sporadic in occurrence, actively evolving, and present on MGEs within Vibrionaceae.
细菌是许多病毒的猎物,这些病毒劫持细菌细胞以进行繁殖,这可能导致细菌细胞裂解和死亡。细菌已经发展出多种策略来对抗病毒的捕食,其中之一是成簇规律间隔短回文重复(CRISPR)和 CRISPR 相关(Cas)蛋白免疫防御系统。弧菌科内的细菌物种是生活在海洋中的生物体,它们会遇到大量噬菌体。我们的目标是通过研究 CRISPR-Cas 系统的普遍性、系统发生分布和基因组背景,确定该系统在该群体中作为防御机制的重要性。
在此,我们描述了弧菌科内所有的 CRISPR-Cas 系统类型及其分布。在霍乱弧菌基因组中,我们鉴定了多个变体 I-F 系统,该系统也存在于 41 个其他物种中。在大量弧菌物种中,我们鉴定了一个由 tniQcas5cas7cas6f 组成的小型 I-F 系统,该系统总是与 Tn7 样转座子相关。除了 CRISPR-Cas 系统外,Tn7 样元件还包含其他货物基因,如限制修饰系统和 III 型分泌系统。在霍乱弧菌和 V. metoecus 菌株中,我们发现了一个假定的混合 CRISPR-Cas 系统,其中包含 III-B 基因,随后是一个 I-F cas6f 和一个与噬菌体相关的 I-F CRISPR。我们的分析鉴定了 CRISPR-Cas 类型 I-C、I-E、I-F、II-B、III-A、III-B、III-D 和罕见的 IV 系统以及 70 个物种中的 cas 基因座结构变体。所有描述的系统都包含一个大小为 3 至 179 个间隔区的 CRISPR 数组。这些系统主要存在于移动遗传元件(MGEs)中,如基因组岛、质粒和转座子样元件。Cas 蛋白的系统发育分析表明,CRISPR-Cas 系统是通过水平基因转移获得的。
我们的数据表明,CRISPR-Cas 系统在系统发生上广泛分布,但发生频率较低,积极进化,并存在于弧菌科的 MGEs 中。