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噬菌体和 CRISPR-Cas 系统在阪崎克罗诺杆菌进化中的驱动力。

The driving force of prophages and CRISPR-Cas system in the evolution of Cronobacter sakazakii.

机构信息

State Key Laboratory of Applied Microbiology, South China, Guangdong Provincial Key Laboratory of Microbiology Culture Collection and Application, Guangdong Open Laboratory of Applied Microbiology, Guangdong Institute of Microbiology, Guangzhou 510070, China.

出版信息

Sci Rep. 2017 Jan 6;7:40206. doi: 10.1038/srep40206.

Abstract

Cronobacter sakazakii is an important foodborne pathogens causing rare but life-threatening diseases in neonates and infants. CRISPR-Cas system is a new prokaryotic defense system that provides adaptive immunity against phages, latter play an vital role on the evolution and pathogenicity of host bacteria. In this study, we found that genome sizes of C. sakazakii strains had a significant positive correlation with total genome sizes of prophages. Prophages contributed to 16.57% of the genetic diversity (pan genome) of C. sakazakii, some of which maybe the potential virulence factors. Subtype I-E CRISPR-Cas system and five types of CRISPR arrays were found in the conserved site of C. sakazakii strains. CRISPR1 and CRISPR2 loci with high variable spacers were active and showed potential protection against phage attacks. The number of spacers from two active CRISPR loci in clinical strains was significant less than that of foodborne strains, it maybe a reason why clinical strains were found to have more prophages than foodborne strains. The frequently gain/loss of prophages and spacers in CRISPR loci is likely to drive the quick evolution of C. sakazakii. Our study provides a new insight into the co-evolution of phages and C. sakazakii.

摘要

阪崎克罗诺杆菌是一种重要的食源性致病菌,可导致新生儿和婴儿罕见但危及生命的疾病。CRISPR-Cas 系统是一种新的原核防御系统,可针对噬菌体提供适应性免疫,后者在宿主细菌的进化和致病性方面发挥着至关重要的作用。在本研究中,我们发现阪崎克罗诺杆菌菌株的基因组大小与噬菌体的总基因组大小呈显著正相关。噬菌体为阪崎克罗诺杆菌的遗传多样性(泛基因组)贡献了 16.57%,其中一些可能是潜在的毒力因子。在阪崎克罗诺杆菌菌株的保守位点发现了 I-E 型 CRISPR-Cas 系统和五种类型的 CRISPR 数组。CRISPR1 和 CRISPR2 位点具有高度可变的间隔区,是活跃的,显示出对噬菌体攻击的潜在保护作用。来自两个活跃 CRISPR 位点的间隔区数量在临床株中明显少于食源株,这可能是临床株比食源株拥有更多噬菌体的原因之一。CRISPR 位点中噬菌体和间隔区的频繁获得/缺失可能导致阪崎克罗诺杆菌的快速进化。我们的研究为噬菌体和阪崎克罗诺杆菌的共同进化提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a12/5216340/08e113a93845/srep40206-f1.jpg

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