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False positives complicate ancient pathogen identifications using high-throughput shotgun sequencing
BACKGROUND: Identification of historic pathogens is challenging since false positives and negatives are a serious risk. Environmental non-pathogenic contaminants are ubiquitous. Furthermore, public genetic databases contain limited information regarding these species. High-throughput sequencing may...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938818/ https://www.ncbi.nlm.nih.gov/pubmed/24568097 http://dx.doi.org/10.1186/1756-0500-7-111 |
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author | Campana, Michael G Robles García, Nelly Rühli, Frank J Tuross, Noreen |
author_facet | Campana, Michael G Robles García, Nelly Rühli, Frank J Tuross, Noreen |
author_sort | Campana, Michael G |
collection | PubMed |
description | BACKGROUND: Identification of historic pathogens is challenging since false positives and negatives are a serious risk. Environmental non-pathogenic contaminants are ubiquitous. Furthermore, public genetic databases contain limited information regarding these species. High-throughput sequencing may help reliably detect and identify historic pathogens. RESULTS: We shotgun-sequenced 8 16th-century Mixtec individuals from the site of Teposcolula Yucundaa (Oaxaca, Mexico) who are reported to have died from the huey cocoliztli (‘Great Pestilence’ in Nahautl), an unknown disease that decimated native Mexican populations during the Spanish colonial period, in order to identify the pathogen. Comparison of these sequences with those deriving from the surrounding soil and from 4 precontact individuals from the site found a wide variety of contaminant organisms that confounded analyses. Without the comparative sequence data from the precontact individuals and soil, false positives for Yersinia pestis and rickettsiosis could have been reported. CONCLUSIONS: False positives and negatives remain problematic in ancient DNA analyses despite the application of high-throughput sequencing. Our results suggest that several studies claiming the discovery of ancient pathogens may need further verification. Additionally, true single molecule sequencing’s short read lengths, inability to sequence through DNA lesions, and limited ancient-DNA-specific technical development hinder its application to palaeopathology. |
format | Online Article Text |
id | pubmed-3938818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39388182014-03-02 False positives complicate ancient pathogen identifications using high-throughput shotgun sequencing Campana, Michael G Robles García, Nelly Rühli, Frank J Tuross, Noreen BMC Res Notes Research Article BACKGROUND: Identification of historic pathogens is challenging since false positives and negatives are a serious risk. Environmental non-pathogenic contaminants are ubiquitous. Furthermore, public genetic databases contain limited information regarding these species. High-throughput sequencing may help reliably detect and identify historic pathogens. RESULTS: We shotgun-sequenced 8 16th-century Mixtec individuals from the site of Teposcolula Yucundaa (Oaxaca, Mexico) who are reported to have died from the huey cocoliztli (‘Great Pestilence’ in Nahautl), an unknown disease that decimated native Mexican populations during the Spanish colonial period, in order to identify the pathogen. Comparison of these sequences with those deriving from the surrounding soil and from 4 precontact individuals from the site found a wide variety of contaminant organisms that confounded analyses. Without the comparative sequence data from the precontact individuals and soil, false positives for Yersinia pestis and rickettsiosis could have been reported. CONCLUSIONS: False positives and negatives remain problematic in ancient DNA analyses despite the application of high-throughput sequencing. Our results suggest that several studies claiming the discovery of ancient pathogens may need further verification. Additionally, true single molecule sequencing’s short read lengths, inability to sequence through DNA lesions, and limited ancient-DNA-specific technical development hinder its application to palaeopathology. BioMed Central 2014-02-25 /pmc/articles/PMC3938818/ /pubmed/24568097 http://dx.doi.org/10.1186/1756-0500-7-111 Text en Copyright © 2014 Campana et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Campana, Michael G Robles García, Nelly Rühli, Frank J Tuross, Noreen False positives complicate ancient pathogen identifications using high-throughput shotgun sequencing |
title | False positives complicate ancient pathogen identifications using high-throughput shotgun sequencing |
title_full | False positives complicate ancient pathogen identifications using high-throughput shotgun sequencing |
title_fullStr | False positives complicate ancient pathogen identifications using high-throughput shotgun sequencing |
title_full_unstemmed | False positives complicate ancient pathogen identifications using high-throughput shotgun sequencing |
title_short | False positives complicate ancient pathogen identifications using high-throughput shotgun sequencing |
title_sort | false positives complicate ancient pathogen identifications using high-throughput shotgun sequencing |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938818/ https://www.ncbi.nlm.nih.gov/pubmed/24568097 http://dx.doi.org/10.1186/1756-0500-7-111 |
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