Evidence map›Paper›PMID 41251328›Full record

ArticleJournal of evolutionary biology2026

Hidden genetic diversity among Blochmanniella endosymbionts of closely related carpenter ant populations.

Reo H Maynard, Yumary M Vasquez, Gordon M Bennett

Abstract read
In one paragraph

Article in Journal of evolutionary biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Reo H MaynardDepartment of Life and Environmental Sciences, University of California, Merced, California, United States.ORCID 0009-0008-7321-6976
Yumary M VasquezDepartment of Energy Joint Genome Institute, Berkeley, California, United States.
Gordon M BennettDepartment of Life and Environmental Sciences, University of California, Merced, California, United States.

Funding

Howard Hughes Medical Institute GT15982National Science Foundation NSF-1347116
6 · The paper itself

Abstract

Carpenter ants (Family Formicidae; Genus Camponotus) are a globally distributed, arboreal clade. They harbor an intracellular obligate bacterial endosymbiont known as "Candidatus Blochmanniella spp." (hereafter Blochmanniella). The host ant species, C. vicinus, is geographically dispersed across the western United States of America and western Canada. To investigate how Blochmanniella have differentially evolved from related host-endosymbiont lineages, we sampled a C. vicinus population from California's Sierra Nevada mountains, California, U.S.A., at an elevation of 2,300 m. Using morphological characters and Cytochrome Oxidase I markers, we determined that this population is genetically distinct from geographically distributed lineages of C. vicinus from Central California and Western North America (Arizona, U.S.A. to British Columbia, Canada). Thus, we sequenced the genome of the Blochmanniella endosymbiont from this host to understand how closely related symbiont lineages evolve. While our newly sequenced lineage is syntenic with other Blochmanniella, it has lost genes involved in membrane maintenance, bacterial cell information, and nutrition synthesis. Protein-coding genes across its genome are highly divergent as well (average sequence similarity = 93.6%). Therefore, we refer to our novel lineage as the B. vicinus Sequoia lineage (BSEQ). BSEQ can provide 7 of the 10 essential amino acids required by its insect host. It can also help break down toxic urea and repair UV radiation-induced DNA damage. Tests of selection reveal that most protein-coding genes BSEQ and related lineages are under strong or relaxed purifying selection. Taken together, our results demonstrate that while BSEQ and related Blochmanniella lineages have highly conserved content, there is considerable evolutionary diversity between them.

Indexed as

AntsGenetic VariationSymbiosisAnimalsPhylogenyBlochmanniaBlochmanniellacarpenter antendosymbiosisgenome evolutionmolecular evolutionselection

Identifiers

PMID41251328
PMCPMC12779916

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.