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CRISPR-Cas 噬菌体防御系统和假噬菌体在候选累积菌属中。

CRISPR-Cas phage defense systems and prophages in Candidatus Accumulibacter.

机构信息

School of Environment and Energy, South China University of Technology, Guangzhou 510006, China.

School of Environment and Energy, South China University of Technology, Guangzhou 510006, China; The Key Lab of Pollution Control and Ecosystem Restoration in Industry Clusters, Ministry of Education, Guangzhou 510006, China.

出版信息

Water Res. 2023 May 15;235:119906. doi: 10.1016/j.watres.2023.119906. Epub 2023 Mar 23.

Abstract

Candidatus Accumulibacter plays a major role in enhanced biological phosphorus removal (EBPR) from wastewater. Although bacteriophages have been shown to represent fatal threats to Ca. Accumulibacter organisms and thus interfere with the stability of the EBPR process, little is known about the ability of different Ca. Accumulibacter strains to resist phage infections. We conducted a systematic analysis of the occurrence and characteristics of clustered regularly interspaced short palindromic repeats and associated proteins (CRISPR-Cas) systems and prophages in Ca. Accumulibacter lineage members (43 in total, including 10 newly recovered genomes). Results indicate that 28 Ca. Accumulibacter genomes encode CRISPR-Cas systems. They were likely acquired via horizontal gene transfer, conveying a distinct adaptivity to phage predation to different Ca. Accumulibacter members. Major differences in the number of spacers show the unique phage resistance of these members. A comparison of the spacers in closely related Ca. Accumulibacter members from distinct geographical locations indicates that habitat isolation may have resulted in the acquisition of resistance to different phages by different Ca. Accumulibacter. Long-term operation of three laboratory-scale EBPR bioreactors revealed high relative abundances of Ca. Accumulibacter with CRISPSR-Cas systems. Their specific resistance to phages in these reactors was indicated by spacer analysis. Metatranscriptomic analyses showed the activation of the CRISPR-Cas system under both anaerobic and aerobic conditions. Additionally, 133 prophage regions were identified in 43 Ca. Accumulibacter genomes. Twenty-seven of them (in 19 genomes) were potentially active. Major differences in the occurrence of CRISPR-Cas systems and prophages in Ca. Accumulibacter will lead to distinct responses to phage predation. This study represents the first systematic analysis of CRISPR-Cas systems and prophages in the Ca. Accumulibacter lineage, providing new perspectives on the potential impacts of phages on Ca. Accumulibacter and EBPR systems.

摘要

钙磷球菌在废水强化生物除磷(EBPR)中起着重要作用。尽管噬菌体已被证明对钙磷球菌生物体构成致命威胁,并因此干扰 EBPR 过程的稳定性,但对于不同的钙磷球菌菌株抵抗噬菌体感染的能力知之甚少。我们对钙磷球菌谱系成员(共 43 个,包括新回收的 10 个基因组)中的聚类规则间隔短回文重复序列和相关蛋白(CRISPR-Cas)系统和噬菌体的发生和特征进行了系统分析。结果表明,28 个钙磷球菌基因组编码 CRISPR-Cas 系统。它们可能是通过水平基因转移获得的,赋予了不同钙磷球菌成员对噬菌体捕食的明显适应性。间隔物数量的主要差异显示了这些成员独特的噬菌体抗性。对来自不同地理位置的密切相关的钙磷球菌成员的间隔物进行比较表明,栖息地隔离可能导致不同的钙磷球菌获得对不同噬菌体的抗性。三个实验室规模的 EBPR 生物反应器的长期运行表明,具有 CRISPRR-Cas 系统的钙磷球菌相对丰度较高。间隔物分析表明,它们在这些反应器中对噬菌体具有特异性抗性。宏转录组分析表明,在厌氧和有氧条件下都激活了 CRISPR-Cas 系统。此外,在 43 个钙磷球菌基因组中鉴定出 133 个噬菌体区域。其中 27 个(在 19 个基因组中)可能是活跃的。钙磷球菌中 CRISPR-Cas 系统和噬菌体的发生存在显著差异,这将导致对噬菌体捕食的不同反应。本研究代表了对钙磷球菌谱系中 CRISPR-Cas 系统和噬菌体的首次系统分析,为噬菌体对钙磷球菌和 EBPR 系统的潜在影响提供了新的视角。

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