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Mouse DNA contamination in human tissue tested for XMRV

BACKGROUND: We used a PCR-based approach to study the prevalence of genetic sequences related to a gammaretrovirus, xenotropic murine leukemia virus-related virus, XMRV, in human prostate cancer. This virus has been identified in the US in prostate cancer patients and in those with chronic fatigue s...

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Autores principales: Robinson, Mark J, Erlwein, Otto W, Kaye, Steve, Weber, Jonathan, Cingoz, Oya, Patel, Anup, Walker, Marjorie M, Kim, Wun-Jae, Uiprasertkul, Mongkol, Coffin, John M, McClure, Myra O
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3019155/
https://www.ncbi.nlm.nih.gov/pubmed/21171966
http://dx.doi.org/10.1186/1742-4690-7-108
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author Robinson, Mark J
Erlwein, Otto W
Kaye, Steve
Weber, Jonathan
Cingoz, Oya
Patel, Anup
Walker, Marjorie M
Kim, Wun-Jae
Uiprasertkul, Mongkol
Coffin, John M
McClure, Myra O
author_facet Robinson, Mark J
Erlwein, Otto W
Kaye, Steve
Weber, Jonathan
Cingoz, Oya
Patel, Anup
Walker, Marjorie M
Kim, Wun-Jae
Uiprasertkul, Mongkol
Coffin, John M
McClure, Myra O
author_sort Robinson, Mark J
collection PubMed
description BACKGROUND: We used a PCR-based approach to study the prevalence of genetic sequences related to a gammaretrovirus, xenotropic murine leukemia virus-related virus, XMRV, in human prostate cancer. This virus has been identified in the US in prostate cancer patients and in those with chronic fatigue syndrome. However, with the exception of two patients in Germany, XMRV has not been identified in prostate cancer tissue in Europe. Most putative associations of new or old human retroviruses with diseases have turned out to be due to contamination. We have looked for XMRV sequences in DNA extracted from formalin-fixed paraffin- embedded prostate tissues. To control for contamination, PCR assays to detect either mouse mitochondrial DNA (mtDNA) or intracisternal A particle (IAP) long terminal repeat DNA were run on all samples, owing to their very high copy number in mouse cells. RESULTS: In general agreement with the US prevalence, XMRV-like sequences were found in 4.8% of prostate cancers. However, these were also positive, as were 21.5% of XMRV-negative cases, for IAP sequences, and many, but not all were positive for mtDNA sequences. CONCLUSIONS: These results show that contamination with mouse DNA is widespread and detectable by the highly sensitive IAP assay, but not always with less sensitive assays, such as murine mtDNA PCR. This study highlights the ubiquitous presence of mouse DNA in laboratory specimens and offers a means of rigorous validation for future studies of murine retroviruses in human disease.
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spelling pubmed-30191552011-01-12 Mouse DNA contamination in human tissue tested for XMRV Robinson, Mark J Erlwein, Otto W Kaye, Steve Weber, Jonathan Cingoz, Oya Patel, Anup Walker, Marjorie M Kim, Wun-Jae Uiprasertkul, Mongkol Coffin, John M McClure, Myra O Retrovirology Research BACKGROUND: We used a PCR-based approach to study the prevalence of genetic sequences related to a gammaretrovirus, xenotropic murine leukemia virus-related virus, XMRV, in human prostate cancer. This virus has been identified in the US in prostate cancer patients and in those with chronic fatigue syndrome. However, with the exception of two patients in Germany, XMRV has not been identified in prostate cancer tissue in Europe. Most putative associations of new or old human retroviruses with diseases have turned out to be due to contamination. We have looked for XMRV sequences in DNA extracted from formalin-fixed paraffin- embedded prostate tissues. To control for contamination, PCR assays to detect either mouse mitochondrial DNA (mtDNA) or intracisternal A particle (IAP) long terminal repeat DNA were run on all samples, owing to their very high copy number in mouse cells. RESULTS: In general agreement with the US prevalence, XMRV-like sequences were found in 4.8% of prostate cancers. However, these were also positive, as were 21.5% of XMRV-negative cases, for IAP sequences, and many, but not all were positive for mtDNA sequences. CONCLUSIONS: These results show that contamination with mouse DNA is widespread and detectable by the highly sensitive IAP assay, but not always with less sensitive assays, such as murine mtDNA PCR. This study highlights the ubiquitous presence of mouse DNA in laboratory specimens and offers a means of rigorous validation for future studies of murine retroviruses in human disease. BioMed Central 2010-12-20 /pmc/articles/PMC3019155/ /pubmed/21171966 http://dx.doi.org/10.1186/1742-4690-7-108 Text en Copyright ©2010 Robinson et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Robinson, Mark J
Erlwein, Otto W
Kaye, Steve
Weber, Jonathan
Cingoz, Oya
Patel, Anup
Walker, Marjorie M
Kim, Wun-Jae
Uiprasertkul, Mongkol
Coffin, John M
McClure, Myra O
Mouse DNA contamination in human tissue tested for XMRV
title Mouse DNA contamination in human tissue tested for XMRV
title_full Mouse DNA contamination in human tissue tested for XMRV
title_fullStr Mouse DNA contamination in human tissue tested for XMRV
title_full_unstemmed Mouse DNA contamination in human tissue tested for XMRV
title_short Mouse DNA contamination in human tissue tested for XMRV
title_sort mouse dna contamination in human tissue tested for xmrv
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3019155/
https://www.ncbi.nlm.nih.gov/pubmed/21171966
http://dx.doi.org/10.1186/1742-4690-7-108
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