Discovery of Early-Branching Reveals Functional Enrichment on Horizontally Transferred Genes.

is a widespread endosymbiont of insects and filarial nematodes that profoundly influences host biology. has also been reported in rhizosphere hosts, where its diversity and function remain poorly characterized. The discovery that plant-parasitic nematodes (PPNs) host strains with unknown roles is of interest evolutionarily, ecologically, and for agriculture as a potential target for developing new biological controls. The goal of this study was to screen communities for PPN endosymbionts and analyze genes and genomic patterns that might indicate their role. Genome assemblies revealed 1 out of 16 sampled sites had nematode communities hosting a strain, designated Tex, that has highly diverged as one of the early supergroup L strains. Genome features, gene repertoires, and absence of known genes for cytoplasmic incompatibility, riboflavin, biotin, and other biosynthetic functions placed Tex between mutualist C + D strains and reproductive parasite A + B strains. Functional terms enriched in group L included protoporphyrinogen IX, thiamine, lysine, fatty acid, and cellular amino acid biosynthesis, while dN/dS analysis suggested the strongest purifying selection on arginine and lysine metabolism, and vitamin B6, heme, and zinc ion binding, suggesting these as candidate roles in PPN . Higher dN/dS pathways between group L, Pni from aphids, Fol from springtails, and CfeT from cat fleas suggested distinct functional changes characterizing these early host transitions. PPN had several putative horizontally transferred genes, including a lysine biosynthesis operon like that of the mitochondrial symbiont , a spirochete-like thiamine synthesis operon shared only with CfeT, an ATP/ADP carrier important in , and a eukaryote-like gene that may mediate plant systemic acquired resistance through the lysine-to-pipecolic acid system. The Discovery of group L-like variants from global rhizosphere databases suggests diverse PPN strains remain to be discovered. These findings support the hypothesis of plant-specialization as key to shaping early evolution and present new functional hypotheses, demonstrating promise for future genomics-based rhizosphere screens.