Wu Zongzhi, Liu Shufeng, Ni Jinren
College of Environmental Sciences and Engineering, Peking University, Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing, People's Republic of China.
Eco-environment and Resource Efficiency Research Laboratory, School of Environment and Energy, Peking University Shenzhen Graduate School, Shenzhen, People's Republic of China.
Nat Microbiol. 2024 Dec;9(12):3362-3375. doi: 10.1038/s41564-024-01839-y. Epub 2024 Oct 24.
The archaeal superphylum DPANN (an acronym formed from the initials of the first five phyla discovered: Diapherotrites, Parvarchaeota, Aenigmarchaeota, Nanohaloarchaeota and Nanoarchaeota) is a group of ultrasmall symbionts able to survive in extreme ecosystems. The diversity and dynamics between DPANN archaea and their virome remain largely unknown. Here we use a metagenomic clustered regularly interspaced short palindromic repeats (CRISPR) screening approach to identify 97 globally distributed, non-redundant viruses and unclassified mobile genetic elements predicted to infect hosts across 8 DPANN phyla, including 7 viral groups not previously characterized. Genomic analysis suggests a diversity of viral morphologies including head-tailed, tailless icosahedral and spindle-shaped viruses with the potential to establish lytic, chronic or lysogenic infections. We also find evidence of a virally encoded Cas12f1 protein (probably originating from uncultured DPANN archaea) and a mini-CRISPR array, which could play a role in modulating host metabolism. Many metagenomes have virus-to-host ratios >10, indicating that DPANN viruses play an important role in controlling host populations. Overall, our study illuminates the underexplored diversity, functional repertoires and host interactions of the DPANN virome.
古菌超门DPANN(由最初发现的五个门的首字母组成的首字母缩写词:Diapherotrites、Parvarchaeota、Aenigmarchaeota、Nanohaloarchaeota和Nanoarchaeota)是一组能够在极端生态系统中生存的超小型共生体。DPANN古菌与其病毒群落之间的多样性和动态关系在很大程度上仍不为人所知。在这里,我们使用一种宏基因组成簇规律间隔短回文重复序列(CRISPR)筛选方法,来识别97种全球分布的、非冗余的病毒以及预测会感染8个DPANN门宿主的未分类移动遗传元件,其中包括7个以前未被表征的病毒组。基因组分析表明病毒形态具有多样性,包括有尾噬菌体、无尾二十面体病毒和纺锤形病毒,它们有可能建立裂解性、慢性或溶原性感染。我们还发现了一种病毒编码的Cas12f1蛋白(可能源自未培养的DPANN古菌)和一个小型CRISPR阵列的证据,它们可能在调节宿主代谢中发挥作用。许多宏基因组的病毒与宿主比例>10,这表明DPANN病毒在控制宿主种群方面发挥着重要作用。总体而言,我们的研究揭示了DPANN病毒群落尚未被充分探索的多样性、功能库以及宿主相互作用。