A nuclease domain fused to the Snf2 helicase confers antiphage defence in coral-associated Halomonas meridiana

被引:1
作者
Liu, Tianlang [1 ,2 ]
Gao, Xinyu [1 ,2 ]
Chen, Ran [1 ]
Tang, Kaihao [1 ,2 ,3 ]
Liu, Ziyao [1 ,2 ]
Wang, Pengxia [1 ,2 ,3 ]
Wang, Xiaoxue [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Key Lab Trop Marine Bioresources & Ecol, Innovat Acad South China Sea Ecol & Environm Engn, Guangdong Key Lab Marine Mat Med,South China Sea I, 164 West Xingang Rd, Guangzhou 510301, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
[3] Southern Marine Sci & Engn Guangdong Lab Guangzhou, Guangzhou, Peoples R China
来源
MICROBIAL BIOTECHNOLOGY | 2024年 / 17卷 / 07期
基金
中国国家自然科学基金;
关键词
CRISPR-CAS SYSTEMS; ABORTIVE INFECTION; PHAGE THERAPY; BACTERIAL; IDENTIFICATION; CLASSIFICATION; ENDONUCLEASE; RECOGNITION; COMPLEX; DNA;
D O I
10.1111/1751-7915.14524
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The coral reef microbiome plays a vital role in the health and resilience of reefs. Previous studies have examined phage therapy for coral pathogens and for modifying the coral reef microbiome, but defence systems against coral-associated bacteria have received limited attention. Phage defence systems play a crucial role in helping bacteria fight phage infections. In this study, we characterized a new defence system, Hma (HmaA-HmaB-HmaC), in the coral-associated Halomonas meridiana derived from the scleractinian coral Galaxea fascicularis. The Swi2/Snf2 helicase HmaA with a C-terminal nuclease domain exhibits antiviral activity against Escherichia phage T4. Mutation analysis revealed the nickase activity of the nuclease domain (belonging to PDD/EXK superfamily) of HmaA is essential in phage defence. Additionally, HmaA homologues are present in similar to 1000 bacterial and archaeal genomes. The high frequency of HmaA helicase in Halomonas strains indicates the widespread presence of these phage defence systems, while the insertion of defence genes in the hma region confirms the existence of a defence gene insertion hotspot. These findings offer insights into the diversity of phage defence systems in coral-associated bacteria and these diverse defence systems can be further applied into designing probiotics with high-phage resistance.
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页数:17
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