Abstract
Phylogenetic diversity of symbiotic bacteria in sucking lice suggests
that lice have experienced a complex history of symbiont acquisition,
loss, and replacement during their evolution. By combining metagenomics
and amplicon screening across several populations of two louse genera
(Polyplax and Hoplopleura) we describe a novel louse
symbiont lineage related to Neisseria and Snodgrassella,
and show its independent origin within dynamic lice microbiomes. While
the genomes of these symbionts are highly similar in both lice genera,
their respective distributions and status within lice microbiomes
indicate that they have different functions and history. In
Hoplopleura acanthopus, the Neisseria-related bacterium is
a dominant obligate symbiont universally present across several host’s
populations, and seems to be replacing a presumably older and more
degenerated obligate symbiont. In contrast, the Polyplax
microbiomes are dominated by the obligate symbiont Legionella
polyplacis, with the Neisseria-related bacterium co-occurring
only in some samples and with much lower abundance.