The conundrum of related taxa: Detection and authentication of pathogen DNA in bioarchaeological samples from the Pacific.

Miss Meriam van Os1, Dr Hugh Cross1, Ms Olga Kardailsky1, Dr  Gert-Jan  Jeunen1, Dr Catherine Collins1, Ms Kate McDonald1, Dr Rebecca Kinaston1, Dr Melandri Vlok1, Professor  Richard  Walter2,3, Professor Greg Cook4, Dr  Htin Lin Aung4, Professor Lisa Matisoo-Smith1, Professor Hallie Buckley1, Associate Professor Michael Knapp1

1Department of Anatomy, School of Biomedical Sciences, University Of Otago, Dunedin, New Zealand, 2Southern Pacific Archaeological Research, University of Otago, Dunedin, New Zealand, 3School of Social Science, University of Queensland, Brisbane, Australia, 4Department of Microbiology and Immunology, School of Biomedical Sciences, University Of Otago, Dunedin, New Zealand

 

Humans populations have co-existed with infectious diseases for millennia, but microorganisms have only been recognised as the causative agent since the 1880s. The importance of genetic analysis of extant strains has long been recognised in fields such as medicine, but the rise of drug-resistant pathogens has increased the need for further knowledge about the co-evolution of humans and pathogens, and the genetic processes involved.

With the advancement of DNA technologies and improved ancient DNA protocols, it is now possible to detect highly degraded pathogen DNA in bioarchaeological samples, providing crucial insights into the pre-antibiotic era. Recent studies focusing on pathogens in Europe, the Americas and Africa, have provided valuable knowledge into the evolutionary history of pathogens, but there are currently no publications focused on the Pacific region.

This study uses ancient DNA analysis to learn more about diseases in past Pacific populations. We focus primarily on the detection and authentication of tuberculosis (Mycobacterium tuberculosis) from bioarchaeological samples. The samples originate from several Pacific sites, and date to between one hundred and three thousand years old. Three criteria have been used to authenticate pathogen DNA, which includes evenness of coverage, percent identity and haploidy. Using a range of bioinformatic tools, results indicate the presence of species closely resembling M. tuberculosis, but the major challenge is separating the pathogenic reads from closely related non-pathogenic species.


Biography:

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