A complete-genome view of phylum Nanobdellota and recurrent Form III RuBisCO transfer between archaea and Patescibacteriota

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This study presents a complete-genome analysis of phylum Nanobdellota and reports the recurrent horizontal gene transfer of Form III RuBisCO between archaea and Patescibacteriota.

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This study expanded the archaeal phylum Nanobdellota from four previously available complete genomes to 208 complete genomes reconstructed from Oxford Nanopore metagenomes of the Baltic Sea water column and Fennoscandian groundwater, using ORC1/Cdc6 rotation and phylogenetic analyses based on large marker supermatrices across 1,239 taxa. It finds that named GTDB orders within Nanobdellota form monophyletic clades and resolves nomenclature by retiring a placeholder order name and introducing a complete-genome-anchored SeqCode chain (Maxwellarchaeales, Maxwellarchaeaceae, Maxwellarchaeum). Metabolic capacity differs by order, with Pacearchaeales and Maxwellarchaeales retaining only Form III RuBisCO, PEP synthase, and ferredoxin, while Woesearchaeales has partial glycolysis and a V/A-type ATPase; a limitation is that the conclusions are based on metagenome-derived genome reconstructions and comparative gene phylogenies. Using a 4,262-tip rbcL phylogeny, the authors identify nine candidate archaea-to-Patescibacteriota Form III RuBisCO horizontal transfer events, and release multiple curated genome sets, marker resources, and analysis files. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract The archaeal phylum Nanobdellota (formerly Nanoarchaeota) was previously represented by four complete genomes. We present 208 complete Nanobdellota genomes from Oxford Nanopore metagenomes of the Baltic Sea water column and Fennoscandian groundwater (69–201 m below sea level), rotated to the ORC1/Cdc6 replication origin — a 52-fold expansion of complete-genome representation. Across the ar53 supermatrix and a Nanobdellota-tuned 71-marker supermatrix on 1,239 taxa, the named GTDB orders within Nanobdellota are recovered as monophyletic clades, including the three orders that dominate our environmental sampling: Woesearchaeales, Pacearchaeales, and the GTDB placeholder order SCGC-AAA011-G17. This is consistent with the existing GTDB R232 order-level circumscription. We retire the SCGC-AAA011-G17 placeholder name, replacing it with a complete-genome-anchored SeqCode nomenclatural chain (Maxwellarchaeales ord. nov., Maxwellarchaeaceae fam. nov., Maxwellarchaeum gen. nov., and Maxwellarchaeum balticum sp. nov.) without altering the order-level circumscription. Pacearchaeales and Maxwellarchaeales retain no central or energy metabolism beyond Form III RuBisCO, PEP synthase, and ferredoxin; Woesearchaeales retains partial glycolysis and a V/A-type ATPase. A 4,262-tip phylogeny of rbcL (the RuBisCO large-subunit gene) identifies nine candidate archaea-to-Patescibacteriota Form III RuBisCO transfer events — including one to a Baltic Minisyncoccia — versus two reciprocal candidates, consistent with archaea-to-CPR being the more frequently identified direction in our data. All 256 Nanobdellota genomes (208 complete + 48 high-quality non-circular), the ar71 marker set with its 1,239-taxon ML tree, 154 Nanobdellota-trained HMMs for KEGG-ortholog detection in DPANN proteomes (94 ROBUST), and the 4,262-tip rbcL reference tree are released as a community resource, alongside the full analysis archive — alignments, intermediate trees, structural predictions, and per-step scripts — at Zenodo (DOI 10.5281/zenodo.20174424; see Using the resource). Competing Interest Statement The authors have declared no competing interest.

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