Differential preservation of endogenous human and microbial DNA in dental calculus and dentin
Mann AEPapers in this archive, Sabin SPapers in this archive, Ziesemer KPapers in this archive, Vågene ÅJPapers in this archive, Schroeder HPapers in this archive, Ozga ATPapers in this archive, Sankaranarayanan KPapers in this archive, Hofman CAPapers in this archive, Fellows Yates JAPapers in this archive, Salazar-García DCPapers in this archive, Frohlich BPapers in this archive, Aldenderfer MPapers in this archive, Hoogland MPapers in this archive, Read CPapers in this archive, Milner GRPapers in this archive, Stone ACPapers in this archive, Lewis CMPapers in this archive, Krause JPapers in this archive, Hofman CPapers in this archive, Bos KIPapers in this archive, Warinner CPapers in this archive
Abstract
Dental calculus (calcified dental plaque) is prevalent in archaeological skeletal collections and is a rich source of oral microbiome and host-derived ancient biomolecules. Recently, it has been proposed that dental calculus may provide a more robust environment for DNA preservation than other skeletal remains, but this has not been systematically tested. In this study, shotgun-sequenced data from paired dental calculus and dentin samples from 48 globally distributed individuals are compared using a metagenomic approach. Overall, we find DNA from dental calculus is consistently more abundant and less contaminated than DNA from dentin. The majority of DNA in dental calculus is microbial and originates from the oral microbiome; however, a small but consistent proportion of DNA (mean 0.08 ± 0.08%, range 0.007–0.47%) derives from the host genome. Host DNA content within dentin is variable (mean 13.70 ± 18.62%, range 0.003–70.14%), and for a subset of dentin samples (15.21%), oral bacteria contribute > 20% of total DNA. Human DNA in dental calculus is highly fragmented, and is consistently shorter than both microbial DNA in dental calculus and human DNA in paired dentin samples. Finally, we find that microbial DNA fragmentation patterns are associated with guanine-cytosine (GC) content, but not aspects of cellular structure.
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