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Gut Microbiome of an 11(th) Century A.D. Pre-Columbian Andean Mummy

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 11(th) century A.D. pre-Columbian...

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Autores principales: Santiago-Rodriguez, Tasha M., Fornaciari, Gino, Luciani, Stefania, Dowd, Scot E., Toranzos, Gary A., Marota, Isolina, Cano, Raul J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589460/
https://www.ncbi.nlm.nih.gov/pubmed/26422376
http://dx.doi.org/10.1371/journal.pone.0138135
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author Santiago-Rodriguez, Tasha M.
Fornaciari, Gino
Luciani, Stefania
Dowd, Scot E.
Toranzos, Gary A.
Marota, Isolina
Cano, Raul J.
author_facet Santiago-Rodriguez, Tasha M.
Fornaciari, Gino
Luciani, Stefania
Dowd, Scot E.
Toranzos, Gary A.
Marota, Isolina
Cano, Raul J.
author_sort Santiago-Rodriguez, Tasha M.
collection PubMed
description 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 11(th) 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.
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spelling pubmed-45894602015-10-02 Gut Microbiome of an 11(th) Century A.D. Pre-Columbian Andean Mummy Santiago-Rodriguez, Tasha M. Fornaciari, Gino Luciani, Stefania Dowd, Scot E. Toranzos, Gary A. Marota, Isolina Cano, Raul J. PLoS One Research Article 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 11(th) 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. Public Library of Science 2015-09-30 /pmc/articles/PMC4589460/ /pubmed/26422376 http://dx.doi.org/10.1371/journal.pone.0138135 Text en © 2015 Santiago-Rodriguez et al http://creativecommons.org/licenses/by/4.0/ This 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 properly credited.
spellingShingle Research Article
Santiago-Rodriguez, Tasha M.
Fornaciari, Gino
Luciani, Stefania
Dowd, Scot E.
Toranzos, Gary A.
Marota, Isolina
Cano, Raul J.
Gut Microbiome of an 11(th) Century A.D. Pre-Columbian Andean Mummy
title Gut Microbiome of an 11(th) Century A.D. Pre-Columbian Andean Mummy
title_full Gut Microbiome of an 11(th) Century A.D. Pre-Columbian Andean Mummy
title_fullStr Gut Microbiome of an 11(th) Century A.D. Pre-Columbian Andean Mummy
title_full_unstemmed Gut Microbiome of an 11(th) Century A.D. Pre-Columbian Andean Mummy
title_short Gut Microbiome of an 11(th) Century A.D. Pre-Columbian Andean Mummy
title_sort gut microbiome of an 11(th) century a.d. pre-columbian andean mummy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589460/
https://www.ncbi.nlm.nih.gov/pubmed/26422376
http://dx.doi.org/10.1371/journal.pone.0138135
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