A Mummy and Her Microbes

A recent paper in PLOS One describes the gut microbiome of an 11th century A.D. Andean mummy and found distinct gut microbiome profiles associated with the mummification process. Most surprising, they found antibiotic resistant genes, putting into question the accepted role of selective antibiotic pressure for these resistance genes.

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Nov 04, 2015
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Santiago-Rodriguez TM, Fornaciari G, Luciani S, Dowd SE, Toranzos GA, Marota I, et al. (2015) Gut Microbiome of an 11th Century A.D. Pre-Columbian Andean Mummy. PLoS ONE 10(9): e0138135. doi:10.1371/journal.pone.0138135

The process of natural mummification is a rare and unique process from which little is known about the resulting microbial community structure. In the present study, we characterized the microbiome of paleofeces, and ascending, transverse and descending colon of an 11th century A.D. pre-Columbian Andean mummy by 16S rRNA gene high-throughput sequencing and metagenomics. Firmicutes were the most abundant bacterial group, with Clostridium spp. comprising up to 96.2% of the mummified gut, while Turicibacter spp. represented 89.2% of the bacteria identified in the paleofeces. Microbiome profile of the paleofeces was unique when compared to previously characterized coprolites that did not undergo natural mummification. We identified DNA sequences homologous to Clostridium botulinum, Trypanosoma cruzi and human papillomaviruses (HPVs). Unexpectedly, putative antibiotic-resistance genes including beta-lactamases, penicillin-binding proteins, resistance to fosfomycin, chloramphenicol, aminoglycosides, macrolides, sulfa, quinolones, tetracycline and vancomycin, and multi-drug transporters, were also identified. The presence of putative antibiotic-resistance genes suggests that resistance may not necessarily be associated with a selective pressure of antibiotics or contact with European cultures. Identification of pathogens and antibiotic-resistance genes in ancient human specimens will aid in the understanding of the evolution of pathogens as a way to treat and prevent diseases caused by bacteria, microbial eukaryotes and viruses.

Go to the profile of Mary Cloud B. Ammons

Mary Cloud B. Ammons

Assistant Research Professor, Montana State University

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