Literature DB >> 26668374

Global divergence of the human follicle mite Demodex folliculorum: Persistent associations between host ancestry and mite lineages.

Michael F Palopoli1, Daniel J Fergus2, Samuel Minot3, Dorothy T Pei3, W Brian Simison4, Iria Fernandez-Silva5, Megan S Thoemmes6, Robert R Dunn7, Michelle Trautwein4.   

Abstract

Microscopic mites of the genus Demodex live within the hair follicles of mammals and are ubiquitous symbionts of humans, but little molecular work has been done to understand their genetic diversity or transmission. Here we sampled mite DNA from 70 human hosts of diverse geographic ancestries and analyzed 241 sequences from the mitochondrial genome of the species Demodex folliculorum. Phylogenetic analyses recovered multiple deep lineages including a globally distributed lineage common among hosts of European ancestry and three lineages that primarily include hosts of Asian, African, and Latin American ancestry. To a great extent, the ancestral geography of hosts predicted the lineages of mites found on them; 27% of the total molecular variance segregated according to the regional ancestries of hosts. We found that D. folliculorum populations are stable on an individual over the course of years and that some Asian and African American hosts maintain specific mite lineages over the course of years or generations outside their geographic region of birth or ancestry. D. folliculorum haplotypes were much more likely to be shared within families and between spouses than between unrelated individuals, indicating that transmission requires close contact. Dating analyses indicated that D. folliculorum origins may predate modern humans. Overall, D. folliculorum evolution reflects ancient human population divergences, is consistent with an out-of-Africa dispersal hypothesis, and presents an excellent model system for further understanding the history of human movement.

Entities:  

Keywords:  Demodex; coevolution; phylogeography; symbiosis

Mesh:

Substances:

Year:  2015        PMID: 26668374      PMCID: PMC4703014          DOI: 10.1073/pnas.1512609112

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


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