Human follicular mites: ectoparasites becoming symbionts

[thumbnail of Open Access]
Text (Open Access) - Published Version
· Restricted to Repository staff only
· The Copyright of this document has not been checked yet. This may affect its availability.
· Available under License Creative Commons Attribution.
Restricted to Repository staff only
Available under license: Creative Commons Attribution

Please see our End User Agreement.

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

Add to AnyAdd to TwitterAdd to FacebookAdd to LinkedinAdd to PinterestAdd to Email

Smith, G., Manzano-Marín, A. orcid id iconORCID: https://orcid.org/0000-0002-0707-9052, Reyes-Prieto, M., Antunes, C. S. R., Ashworth, V., Goselle, O. N., Jan, A. A. A., Moya, A., Latorre, A., Perotti, M. A. orcid id iconORCID: https://orcid.org/0000-0002-3769-7126 and Braig, H. R. (2022) Human follicular mites: ectoparasites becoming symbionts. Molecular Biology and Evolution, 39 (6). ISSN 1537-1719 doi: 10.1093/molbev/msac125

Abstract/Summary

Most humans carry mites in the hair follicles of their skin for their entire lives. Follicular mites are the only metazoans that continuously live on humans. We propose that Demodex folliculorum (Acari) represents a transitional stage from a host-injuring obligate parasite to an obligate symbiont. Here, we describe the profound impact of this transition on the genome and physiology of the mite. Genome sequencing revealed that the permanent host association of D. folliculorum led to an extensive genome reduction through relaxed selection and genetic drift, resulting in the smallest number of protein-coding genes yet identified among panarthropods. Confocal microscopy revealed that this gene loss coincided with an extreme reduction in the number of cells. Single uninucleate muscle cells are sufficient to operate each of the three segments that form each walking leg. While it has been assumed that the reduction of the cell number in parasites starts early in development, we identified a greater total number of cells in the last developmental stage (nymph) than in the terminal adult stage, suggesting that reduction starts at the adult or ultimate stage of development. This is the first evolutionary step in an arthropod species adopting a reductive, parasitic, or endosymbiotic lifestyle. Somatic nuclei show under-replication at the diploid stage. Novel eye structures or photoreceptors as well as a unique human host melatonin-guided day/night rhythm are proposed for the first time. The loss of DNA repair genes coupled with extreme endogamy might have set this mite species on an evolutionary dead-end trajectory.

Altmetric Badge

Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/105850
Identification Number/DOI 10.1093/molbev/msac125
Refereed Yes
Divisions Life Sciences > School of Biological Sciences > Ecology and Evolutionary Biology
Publisher Oxford University Press
Download/View statistics View download statistics for this item

University Staff: Request a correction | Centaur Editors: Update this record

Search Google Scholar