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Detection of Mycobacterium leprae DNA from Archaeological Skeletal Remains in Japan Using Whole Genome Amplification and Polymerase Chain Reaction

Identifieur interne : 000389 ( Pmc/Curation ); précédent : 000388; suivant : 000390

Detection of Mycobacterium leprae DNA from Archaeological Skeletal Remains in Japan Using Whole Genome Amplification and Polymerase Chain Reaction

Auteurs : Koichi Suzuki [Japon] ; Wataru Takigawa [Japon] ; Kazunari Tanigawa [Japon] ; Kazuaki Nakamura [Japon] ; Yuko Ishido [Japon] ; Akira Kawashima [Japon] ; Huhehasi Wu [Japon] ; Takeshi Akama [Japon] ; Mariko Sue [Japon] ; Aya Yoshihara [Japon] ; Shuichi Mori [Japon] ; Norihisa Ishii [Japon]

Source :

RBID : PMC:2928730

Abstract

Background

Identification of pathogen DNA from archaeological human remains is a powerful tool in demonstrating that the infectious disease existed in the past. However, it is very difficult to detect trace amounts of DNA remnants attached to the human skeleton, especially from those buried in a humid atmosphere with a relatively high environmental temperature such as in Asia.

Methodology/Principal Findings

Here we demonstrate Mycobacterium leprae DNA from archaeological skeletal remains in Japan by polymerase chain reaction, DNA sequencing and single nucleotide polymorphism (SNP) analysis. In addition, we have established a highly sensitive method of detecting DNA using a combination of whole genome amplification and polymerase chain reaction, or WGA-PCR, which provides superior sensitivity and specificity in detecting DNA from trace amounts of skeletal materials.

Conclusion/Significance

We have detected M. leprae DNA in archaeological skeletal remains for the first time in the Far East. Its SNP genotype corresponded to type 1; the first detected case worldwide of ancient M. leprae DNA. We also developed a highly sensitive method to detect ancient DNA by utilizing whole genome amplification.


Url:
DOI: 10.1371/journal.pone.0012422
PubMed: 20865042
PubMed Central: 2928730

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PMC:2928730

Le document en format XML

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<title>Background</title>
<p>Identification of pathogen DNA from archaeological human remains is a powerful tool in demonstrating that the infectious disease existed in the past. However, it is very difficult to detect trace amounts of DNA remnants attached to the human skeleton, especially from those buried in a humid atmosphere with a relatively high environmental temperature such as in Asia.</p>
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<p>Here we demonstrate
<italic>Mycobacterium leprae</italic>
DNA from archaeological skeletal remains in Japan by polymerase chain reaction, DNA sequencing and single nucleotide polymorphism (SNP) analysis. In addition, we have established a highly sensitive method of detecting DNA using a combination of whole genome amplification and polymerase chain reaction, or WGA-PCR, which provides superior sensitivity and specificity in detecting DNA from trace amounts of skeletal materials.</p>
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<p>We have detected
<italic>M. leprae</italic>
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<italic>M. leprae</italic>
DNA. We also developed a highly sensitive method to detect ancient DNA by utilizing whole genome amplification.</p>
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</author>
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</author>
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</author>
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</TEI>
<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">PLoS One</journal-id>
<journal-id journal-id-type="publisher-id">plos</journal-id>
<journal-id journal-id-type="pmc">plosone</journal-id>
<journal-title-group>
<journal-title>PLoS ONE</journal-title>
</journal-title-group>
<issn pub-type="epub">1932-6203</issn>
<publisher>
<publisher-name>Public Library of Science</publisher-name>
<publisher-loc>San Francisco, USA</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">20865042</article-id>
<article-id pub-id-type="pmc">2928730</article-id>
<article-id pub-id-type="publisher-id">10-PONE-RA-18056R1</article-id>
<article-id pub-id-type="doi">10.1371/journal.pone.0012422</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Research Article</subject>
</subj-group>
<subj-group subj-group-type="Discipline">
<subject>Microbiology/Microbial Evolution and Genomics</subject>
<subject>Infectious Diseases/Neglected Tropical Diseases</subject>
<subject>Infectious Diseases/Skin Infections</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Detection of
<italic>Mycobacterium leprae</italic>
DNA from Archaeological Skeletal Remains in Japan Using Whole Genome Amplification and Polymerase Chain Reaction</article-title>
<alt-title alt-title-type="running-head">
<italic>M. leprae</italic>
aDNA in Asia</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Suzuki</surname>
<given-names>Koichi</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="corresp" rid="cor1">
<sup>*</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Takigawa</surname>
<given-names>Wataru</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tanigawa</surname>
<given-names>Kazunari</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Nakamura</surname>
<given-names>Kazuaki</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ishido</surname>
<given-names>Yuko</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kawashima</surname>
<given-names>Akira</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wu</surname>
<given-names>Huhehasi</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Akama</surname>
<given-names>Takeshi</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sue</surname>
<given-names>Mariko</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Yoshihara</surname>
<given-names>Aya</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mori</surname>
<given-names>Shuichi</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ishii</surname>
<given-names>Norihisa</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
</contrib>
</contrib-group>
<aff id="aff1">
<label>1</label>
<addr-line>Laboratory of Molecular Diagnostics, Department of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases, Tokyo, Japan</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>School of Rehabilitation Sciences at Fukuoka, International University of Health and Welfare, Fukuoka, Japan</addr-line>
</aff>
<aff id="aff3">
<label>3</label>
<addr-line>Department of Pharmacology, National Research Institute for Child Health and Development, Tokyo, Japan</addr-line>
</aff>
<aff id="aff4">
<label>4</label>
<addr-line>Laboratory of Molecular Epidemiology and Social Science, Leprosy Research Center, National Institute of Infectious Diseases, Tokyo, Japan</addr-line>
</aff>
<aff id="aff5">
<label>5</label>
<addr-line>Leprosy Research Center, National Institute of Infectious Diseases, Tokyo, Japan</addr-line>
</aff>
<contrib-group>
<contrib contrib-type="editor">
<name>
<surname>Hansen</surname>
<given-names>Immo A.</given-names>
</name>
<role>Editor</role>
<xref ref-type="aff" rid="edit1"></xref>
</contrib>
</contrib-group>
<aff id="edit1">New Mexico State University, United States of America</aff>
<author-notes>
<corresp id="cor1">* E-mail:
<email>koichis@nih.go.jp</email>
</corresp>
<fn fn-type="con">
<p>Conceived and designed the experiments: KS NI. Performed the experiments: KS WT KT KN YI AK HW SM. Analyzed the data: KS TA MS AY. Contributed reagents/materials/analysis tools: KS TA MS AY. Wrote the paper: KS WT NI.</p>
</fn>
</author-notes>
<pub-date pub-type="collection">
<year>2010</year>
</pub-date>
<pub-date pub-type="epub">
<day>26</day>
<month>8</month>
<year>2010</year>
</pub-date>
<volume>5</volume>
<issue>8</issue>
<elocation-id>e12422</elocation-id>
<history>
<date date-type="received">
<day>18</day>
<month>4</month>
<year>2010</year>
</date>
<date date-type="accepted">
<day>4</day>
<month>8</month>
<year>2010</year>
</date>
</history>
<permissions>
<copyright-statement>Suzuki et al. 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 credited.</copyright-statement>
</permissions>
<abstract>
<sec>
<title>Background</title>
<p>Identification of pathogen DNA from archaeological human remains is a powerful tool in demonstrating that the infectious disease existed in the past. However, it is very difficult to detect trace amounts of DNA remnants attached to the human skeleton, especially from those buried in a humid atmosphere with a relatively high environmental temperature such as in Asia.</p>
</sec>
<sec>
<title>Methodology/Principal Findings</title>
<p>Here we demonstrate
<italic>Mycobacterium leprae</italic>
DNA from archaeological skeletal remains in Japan by polymerase chain reaction, DNA sequencing and single nucleotide polymorphism (SNP) analysis. In addition, we have established a highly sensitive method of detecting DNA using a combination of whole genome amplification and polymerase chain reaction, or WGA-PCR, which provides superior sensitivity and specificity in detecting DNA from trace amounts of skeletal materials.</p>
</sec>
<sec>
<title>Conclusion/Significance</title>
<p>We have detected
<italic>M. leprae</italic>
DNA in archaeological skeletal remains for the first time in the Far East. Its SNP genotype corresponded to type 1; the first detected case worldwide of ancient
<italic>M. leprae</italic>
DNA. We also developed a highly sensitive method to detect ancient DNA by utilizing whole genome amplification.</p>
</sec>
</abstract>
<counts>
<page-count count="8"></page-count>
</counts>
</article-meta>
</front>
</pmc>
</record>

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