bioRxivEvolutionary BiologyPreprint
The origin and evolution of mitochondrial tropism in Midichloria bacteria
A. M. Floriano, G. Batisti Biffignandi, M. Castelli, E. Olivieri, E. Clementi, F. Comandatore, L. Rinaldi, M. Opara, O. Plantard, A. M. Palomar, V. Noel, A. Vijay, N. Lo, B. L. Makepeace, O. Duron, A. Jex, L. Guy, D. Sassera
Abstract
Midichloria are intracellular bacterial symbionts of ticks. Some representatives of this genus have the unique capability to colonize mitochondria in the cells of their hosts. Hypotheses on the nature of this interaction have proven difficult to test, partly due to a lack of data. Indeed, until now, mitochondrial tropism information and genomes were available only for symbionts of three and two tick host species, respectively. Here we analyzed the mitochondrial tropism of three additional Midichloria and sequenced nine novel genomes, showing that the tropism is pnon-monophyletic, either due to losses of the trait or multiple parallel acquisitions. Comparative genome analyses support the first hypothesis, as the genomes of non-mitochondrial symbionts appear to be reduced subsets of those capable of colonizing the organelles. We detect genomic signatures of mitochondrial tropism, showing a set of candidate genes characteristic of the strains capable of mitochondrial colonization. These include the type IV secretion system and the flagellum, which could allow the secretion of unique effectors, direct interaction with, or invasion of the mitochondria. Other genes, including putative adhesion molecules, proteins possibly involved in actin polymerization, cell wall and outer membrane proteins, are only present in mitochondrial symbionts. The bacteria could use these to manipulate host structures, including mitochondrial membranes, in order to fuse with the organelles or manipulate the mitochondrial network.
- organism: bacteria (other)
- assay: whole-genome sequencing
- research focus: phylogenetics / evolution
- research focus: gene regulatory network inference
- approach: statistical model
- approach: comparative / phylogenetic analysis
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Characterisation and genomic analysis of bacterial nutritional endosymbionts in Australian ticks from shotgun metagenomic sequencing
Laurene Leclerc, Julia Meltzer, … Nathan C. Lo·bioRxiv·Aug 14, 2026
- Population genomic insights into syntrophic symbioses between marine anaerobic ciliates and intracellular methanogens
Johana Rotterová, Corinna Breusing, … Roxanne A. Beinart·bioRxiv·Jul 30, 2025
- Detection of interphylum transfers of the magnetosome gene cluster in magnetotactic bacteria
M. Uzun, V. Koziaeva, … D. Grouzdev·bioRxiv·Mar 28, 2022
- Chlamydia trachomatis effectors target the mitochondria and alter mitochondrial protein composition
T. Hackstadt, Z. Dimond, … A. B. Carmody·bioRxiv·Aug 30, 2022
- A new Serratia taxon found in a trombidiform mite shows genomic evidence of host adaptation but is phylogenetically distinct from Serratia symbiotica
Jia Chang, Ary Hoffmann, … Joshua A Thia·bioRxiv·Nov 4, 2026
- Positive selection on mitochondria may eliminate heritable microbes from arthropod populations.
A. Fenton, F. Camus, G. D. D. Hurst·bioRxiv·Mar 26, 2021