Horizontal gene transfer and gene loss drove the divergent evolution of host dependency in Micrarchaeota

The DPANN superphylum is a deep-branching radiation of archaea with small cell and genome sizes. Most DPANN lineages are predicted or validated to be host-dependent. However, certain lineages have substantial biosynthetic capacities and are potentially less dependent on hosts, or even free-living. Here, we reconstructed 163 Micrarchaeota genomes, comprising 48 assigned to previously undescribed orders and 115 affiliated with known orders. Investigation of their genetic repertoire revealed substantial metabolic capacity in Norongarragalinales-, Anstonellales- and the newly proposed Wunengiarchaeales-associated lineages, including complete or near-complete glycolysis and <i>de novo</i> biosynthetic pathways for nucleotides, amino acids, cofactors and cell envelopes. We classified genes related to the central metabolism but which are uncommon in DPANN archaea as putative free-living associated genes (pFLAGs). The extensive presence of pFLAGs in Norongarragalinales suggests a potential host-independent lifestyle. Reconstruction of evolutionary history revealed that these pFLAGs were not ancestral within the DPANN superphylum. Instead, we suggest that less-host-dependent organisms evolved from symbionts through the gradual acquisition of pFLAGs through horizontal gene transfer, whereas other Micrarchaeota lineages with streamlined genomes experienced reductive evolution due to thermal adaptation. Our analyses demonstrate that host dependency is not always an evolutionary dead end, but can be reversed through the acquisition of new metabolic capabilities by horizontal transfer.

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Journal
National Science Review
Published
2025-11-27
DOI
https://doi.org/10.1093/nsr/nwaf542
Primary Topic
Genomics and Phylogenetic Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Horizontal gene transfer and gene loss drove the divergent evolution of host dependency in Micrarchaeota

Zheng‐Shuang Hua, Yan-Ni Qu, Ze-Wei Li, Brian P. Hedlund et al.
National Science Review
Genomics and Phylogenetic Studies
article

Horizontal gene transfer and gene loss drove the divergent evolution of host dependency in Micrarchaeota

Zheng‐Shuang Hua, Yan-Ni Qu, Ze-Wei Li, Brian P. Hedlund, Qijun Xie, Yang-Zhi Rao, Yuanqi Zhang, Hongchen Jiang, Wen‐Jun Li, Tom A. Williams, Mǎng Shī, Yan-Ling Qi, Yu-Xian Li, Hailong Yang, Wen-Sheng Shu, Marike Palmer
article en

Abstract

The DPANN superphylum is a deep-branching radiation of archaea with small cell and genome sizes. Most DPANN lineages are predicted or validated to be host-dependent. However, certain lineages have substantial biosynthetic capacities and are potentially less dependent on hosts, or even free-living. Here, we reconstructed 163 Micrarchaeota genomes, comprising 48 assigned to previously undescribed orders and 115 affiliated with known orders. Investigation of their genetic repertoire revealed substantial metabolic capacity in Norongarragalinales-, Anstonellales- and the newly proposed Wunengiarchaeales-associated lineages, including complete or near-complete glycolysis and <i>de novo</i> biosynthetic pathways for nucleotides, amino acids, cofactors and cell envelopes. We classified genes related to the central metabolism but which are uncommon in DPANN archaea as putative free-living associated genes (pFLAGs). The extensive presence of pFLAGs in Norongarragalinales suggests a potential host-independent lifestyle. Reconstruction of evolutionary history revealed that these pFLAGs were not ancestral within the DPANN superphylum. Instead, we suggest that less-host-dependent organisms evolved from symbionts through the gradual acquisition of pFLAGs through horizontal gene transfer, whereas other Micrarchaeota lineages with streamlined genomes experienced reductive evolution due to thermal adaptation. Our analyses demonstrate that host dependency is not always an evolutionary dead end, but can be reversed through the acquisition of new metabolic capabilities by horizontal transfer.

National Science ReviewVol. 13(4)
University of Science and Technology of China (CN), University of Nevada, Las Vegas (US), Hefei University of Technology (CN), South China Normal University (CN), China University of Geosciences (Beijing) (CN), Institute of Ecology and Geography (MD), Xinjiang Institute of Ecology and Geography (CN), Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) (CN), Institute of Infection and Immunity (CA), Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai) (CN), University of Manitoba (CA), University of Bath (GB)
National Science Foundation, John Templeton Foundation, National Natural Science Foundation of China
Openalex Percentile: Top 66%
Genomics and Phylogenetic Studies
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