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No Evidence of XMRV or MuLV Sequences in Prostate Cancer, Diffuse Large B-Cell Lymphoma, or the UK Blood Donor Population

Xenotropic murine leukaemia virus-related virus (XMRV) is a recently described retrovirus which has been claimed to infect humans and cause associated pathology. Initially identified in the US in patients with prostate cancer and subsequently in patients with chronic fatigue syndrome, doubt now exis...

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Autores principales: Robinson, Mark James, Tuke, Philip William, Erlwein, Otto, Tettmar, Kate I., Kaye, Steve, Naresh, Kikkeri N., Patel, Anup, Walker, Marjorie M., Kimura, Takahiro, Gopalakrishnan, Ganesh, Tedder, Richard S., McClure, Myra O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265314/
https://www.ncbi.nlm.nih.gov/pubmed/22312352
http://dx.doi.org/10.1155/2011/782353
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author Robinson, Mark James
Tuke, Philip William
Erlwein, Otto
Tettmar, Kate I.
Kaye, Steve
Naresh, Kikkeri N.
Patel, Anup
Walker, Marjorie M.
Kimura, Takahiro
Gopalakrishnan, Ganesh
Tedder, Richard S.
McClure, Myra O.
author_facet Robinson, Mark James
Tuke, Philip William
Erlwein, Otto
Tettmar, Kate I.
Kaye, Steve
Naresh, Kikkeri N.
Patel, Anup
Walker, Marjorie M.
Kimura, Takahiro
Gopalakrishnan, Ganesh
Tedder, Richard S.
McClure, Myra O.
author_sort Robinson, Mark James
collection PubMed
description Xenotropic murine leukaemia virus-related virus (XMRV) is a recently described retrovirus which has been claimed to infect humans and cause associated pathology. Initially identified in the US in patients with prostate cancer and subsequently in patients with chronic fatigue syndrome, doubt now exists that XMRV is a human pathogen. We studied the prevalence of genetic sequences of XMRV and related MuLV sequences in human prostate cancer, from B cell lymphoma patients and from UK blood donors. Nucleic acid was extracted from fresh prostate tissue biopsies, formalin-fixed paraffin-embedded (FFPE) prostate tissue and FFPE B-cell lymphoma. The presence of XMRV-specific LTR or MuLV generic gag-like sequences was investigated by nested PCR. To control for mouse DNA contamination, a PCR that detected intracisternal A-type particle (IAP) sequences was included. In addition, DNA and RNA were extracted from whole blood taken from UK blood donors and screened for XMRV sequences by real-time PCR. XMRV or MuLV-like sequences were not amplified from tissue samples. Occasionally MuLV gag and XMRV-LTR sequences were amplified from Indian prostate cancer samples, but were always detected in conjunction with contaminating murine genomic DNA. We found no evidence of XMRV or MuLV infection in the UK blood donors.
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spelling pubmed-32653142012-02-06 No Evidence of XMRV or MuLV Sequences in Prostate Cancer, Diffuse Large B-Cell Lymphoma, or the UK Blood Donor Population Robinson, Mark James Tuke, Philip William Erlwein, Otto Tettmar, Kate I. Kaye, Steve Naresh, Kikkeri N. Patel, Anup Walker, Marjorie M. Kimura, Takahiro Gopalakrishnan, Ganesh Tedder, Richard S. McClure, Myra O. Adv Virol Research Article Xenotropic murine leukaemia virus-related virus (XMRV) is a recently described retrovirus which has been claimed to infect humans and cause associated pathology. Initially identified in the US in patients with prostate cancer and subsequently in patients with chronic fatigue syndrome, doubt now exists that XMRV is a human pathogen. We studied the prevalence of genetic sequences of XMRV and related MuLV sequences in human prostate cancer, from B cell lymphoma patients and from UK blood donors. Nucleic acid was extracted from fresh prostate tissue biopsies, formalin-fixed paraffin-embedded (FFPE) prostate tissue and FFPE B-cell lymphoma. The presence of XMRV-specific LTR or MuLV generic gag-like sequences was investigated by nested PCR. To control for mouse DNA contamination, a PCR that detected intracisternal A-type particle (IAP) sequences was included. In addition, DNA and RNA were extracted from whole blood taken from UK blood donors and screened for XMRV sequences by real-time PCR. XMRV or MuLV-like sequences were not amplified from tissue samples. Occasionally MuLV gag and XMRV-LTR sequences were amplified from Indian prostate cancer samples, but were always detected in conjunction with contaminating murine genomic DNA. We found no evidence of XMRV or MuLV infection in the UK blood donors. Hindawi Publishing Corporation 2011 2011-06-09 /pmc/articles/PMC3265314/ /pubmed/22312352 http://dx.doi.org/10.1155/2011/782353 Text en Copyright © 2011 Mark James Robinson et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Robinson, Mark James
Tuke, Philip William
Erlwein, Otto
Tettmar, Kate I.
Kaye, Steve
Naresh, Kikkeri N.
Patel, Anup
Walker, Marjorie M.
Kimura, Takahiro
Gopalakrishnan, Ganesh
Tedder, Richard S.
McClure, Myra O.
No Evidence of XMRV or MuLV Sequences in Prostate Cancer, Diffuse Large B-Cell Lymphoma, or the UK Blood Donor Population
title No Evidence of XMRV or MuLV Sequences in Prostate Cancer, Diffuse Large B-Cell Lymphoma, or the UK Blood Donor Population
title_full No Evidence of XMRV or MuLV Sequences in Prostate Cancer, Diffuse Large B-Cell Lymphoma, or the UK Blood Donor Population
title_fullStr No Evidence of XMRV or MuLV Sequences in Prostate Cancer, Diffuse Large B-Cell Lymphoma, or the UK Blood Donor Population
title_full_unstemmed No Evidence of XMRV or MuLV Sequences in Prostate Cancer, Diffuse Large B-Cell Lymphoma, or the UK Blood Donor Population
title_short No Evidence of XMRV or MuLV Sequences in Prostate Cancer, Diffuse Large B-Cell Lymphoma, or the UK Blood Donor Population
title_sort no evidence of xmrv or mulv sequences in prostate cancer, diffuse large b-cell lymphoma, or the uk blood donor population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265314/
https://www.ncbi.nlm.nih.gov/pubmed/22312352
http://dx.doi.org/10.1155/2011/782353
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