Panahi Bahman, Majidi Mohammad, Hejazi Mohammad Amin
Department of Genomics, Branch for Northwest and West Region, Agricultural Biotechnology Research Institute of Iran (ABRII), Agricultural Research, Education and Extension Organization (AREEO), Tabriz, Iran.
Department of Biotechnology, Faculty of Agriculture, Azarbaijan Shahid Madani University, Tabriz, Iran.
Front Microbiol. 2022 Jun 3;13:911706. doi: 10.3389/fmicb.2022.911706. eCollection 2022.
Clustered regularly interspaced short palindromic repeats (CRISPR) together with their CRISPR-associated (Cas) genes are widely distributed in prokaryotes that provide an adaptive defense mechanism against foreign invasive DNA. There is relatively little knowledge about the CRISPR-Cas diversity and evolution in strains. Therefore, in this study, a genome-mining approach was employed to investigate the diversity and occurrence of the CRISPR-Cas system in 83 strains. Moreover, trans-activating CRISPR RNA (tracrRNA) and protospacer adjacent motif (PAM) as pivotal elements for the successful targeting and inference of phages by the subtype II CRISPR-Cas systems were surveyed. Finally, evolutionary paths of strains under selective pressure from foreign invasive DNA such as plasmids and phages of studied strains were surveyed using acquisition and deletion events analysis of spacers. A total of 127 confirmed CRISPRs were identified, which were distributed in 69 strains. Among strains with confirmed CRISPRs, 35 strains only contained one CRISPR locus, 23 strains contained two CRISPR loci, and 12 strains contained three to six CRISPR loci. strains frequently harbor more than one CRISPR system. Analysis of confirmed CRISPR arrays showed that 31 out of 127 confirmed CRISPRs included Cas genes which were categorized as one of the II-A, II-C, and I-E subtypes. Analysis of subtype II-A spacers reflected divergent evolution for 18 strains into 16 unique groups. Additional analysis of spacer sequences also confirmed the implication of characterizing CRISPR-Cas systems in targeting of phages and plasmids. The current study highlighted the potential of utilizing CRISPR spacer polymorphism in genotyping lactobacillus strains. Moreover, it provides deep insights into the occurrence, diversity, and functional impacts of the CRISPR-Cas system in strains.
成簇规律间隔短回文重复序列(CRISPR)及其相关(Cas)基因广泛分布于原核生物中,为抵御外来入侵DNA提供了一种适应性防御机制。关于菌株中CRISPR-Cas的多样性和进化,人们了解相对较少。因此,在本研究中,采用基因组挖掘方法来研究83株菌株中CRISPR-Cas系统的多样性和存在情况。此外,还对反式激活CRISPR RNA(tracrRNA)和原间隔相邻基序(PAM)进行了调查,它们是II型CRISPR-Cas系统成功靶向和推断噬菌体的关键元件。最后,通过对间隔序列的获得和缺失事件分析,研究了所研究菌株在质粒和噬菌体等外来入侵DNA的选择压力下的进化路径。共鉴定出127个已确认的CRISPR,分布于69株菌株中。在有已确认CRISPR的菌株中,35株仅含有一个CRISPR位点,23株含有两个CRISPR位点,12株含有三到六个CRISPR位点。菌株经常含有不止一个CRISPR系统。对已确认的CRISPR阵列分析表明,127个已确认的CRISPR中有31个包含Cas基因,这些基因被归类为II-A、II-C和I-E亚型之一。对II-A亚型间隔序列的分析反映了18株菌株分化为16个独特的组。对间隔序列的进一步分析也证实了CRISPR-Cas系统在靶向噬菌体和质粒方面的作用。本研究突出了利用CRISPR间隔多态性对乳酸杆菌菌株进行基因分型的潜力。此外,它还深入了解了CRISPR-Cas系统在菌株中的存在、多样性和功能影响。