Show simple item record

dc.contributor.authorBeirne, Christopher
dc.contributor.authorDelahay, R
dc.contributor.authorHares, M
dc.contributor.authorYoung, AJ
dc.date.accessioned2014-10-14T15:59:41Z
dc.date.issued2014-09-30
dc.description.abstractImmunosenescence, the deterioration of immune system capability with age, may play a key role in mediating age-related declines in whole-organism performance, but the mechanisms that underpin immunosenescence are poorly understood. Biomedical research on humans and laboratory models has documented age and disease related declines in the telomere lengths of leukocytes (‘immune cells’), stimulating interest their having a potentially general role in the emergence of immunosenescent phenotypes. However, it is unknown whether such observations generalise to the immune cell populations of wild vertebrates living under ecologically realistic conditions. Here we examine longitudinal changes in the mean telomere lengths of immune cells in wild European badgers (Meles meles). Our findings provide the first evidence of within-individual age-related declines in immune cell telomere lengths in a wild vertebrate. That the rate of age-related decline in telomere length appears to be steeper within individuals than at the overall population level raises the possibility that individuals with short immune cell telomeres and/or higher rates of immune cell telomere attrition may be selectively lost from this population. We also report evidence suggestive of associations between immune cell telomere length and bovine tuberculosis infection status, with individuals detected at the most advanced stage of infection tending to have shorter immune cell telomeres than disease positive individuals. While male European badgers are larger and show higher rates of annual mortality than females, we found no evidence of a sex difference in either mean telomere length or the average rate of within-individual telomere attrition with age. Our findings lend support to the view that age-related declines in the telomere lengths of immune cells may provide one potentially general mechanism underpinning age-related declines in immunocompetence in natural populations.en_GB
dc.description.sponsorshipBiotechnology and Biological Sciences Research Council (BBSRC)en_GB
dc.description.sponsorshipThe Food and Environmental Research Agency (FERA)en_GB
dc.identifier.citationVolume 9, Issue 9, e108964en_GB
dc.identifier.doi10.1371/journal.pone.0108964
dc.identifier.urihttp://hdl.handle.net/10871/15715
dc.language.isoenen_GB
dc.publisherPublic Library of Scienceen_GB
dc.relation.urlhttp://biosciences.exeter.ac.uk/staff/index.php?web_id=andrew_youngen_GB
dc.relation.urlhttp://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0108964en_GB
dc.rightsCC-BYen_GB
dc.subjectbadgersen_GB
dc.subjectdeath ratesen_GB
dc.subjectHematopoietic stem cellsen_GB
dc.subjectImmune cellsen_GB
dc.subjectMycobacterium bovisen_GB
dc.subjectRed blood cellsen_GB
dc.subjectTelomeresen_GB
dc.subjectVertebratesen_GB
dc.titleAge-related declines and disease-associated variation in immune cell telomere length in a wild mammalen_GB
dc.typeArticleen_GB
dc.date.available2014-10-14T15:59:41Z
dc.descriptionpublication-status: Publisheden_GB
dc.descriptiontypes: Articleen_GB
dc.description© 2014 Beirne et al.en_GB
dc.descriptionThe authors confirm that all data underlying the findings are fully available without restriction. All relevant data are within the paper and its Supporting Information files.en_GB
dc.descriptionThis is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_GB
dc.identifier.journalPLoS Oneen_GB


Files in this item

This item appears in the following Collection(s)

Show simple item record