Failure to detect the novel retrovirus XMRV in chronic fatigue syndrome

Otto Erlwein1, Steve Kaye, Myra O McClure

  • 1Jefferiss Research Trust Laboratories, Section of Infectious Diseases, Wright-Fleming Institute, Faculty of Medicine, Imperial College London, St Mary's Campus, Norfolk Place, London, United Kingdom.

Plos One
|January 13, 2010
PubMed
Abstract

Insights

Researchers investigated if UK chronic fatigue syndrome (CFS) patients carry xenotropic murine leukaemia virus-related virus (XMRV). No XMRV or MLV sequences were detected in UK CFS patients, suggesting no association in this population.

Area of Science:

  • Virology
  • Immunology
  • Epidemiology

Background:

  • A 2009 report linked xenotropic murine leukaemia virus-related virus (XMRV) to chronic fatigue syndrome (CFS) in US patients.
  • XMRV, a gamma retrovirus, was also previously associated with prostate cancer.
  • This potential link necessitated further investigation into XMRV's role in CFS.

Purpose of the Study:

  • To investigate the presence of XMRV in patients diagnosed with CFS in the United Kingdom.
  • To determine if XMRV or related murine leukaemia virus (MLV) sequences are detectable in UK CFS patient DNA.

Main Methods:

  • Screened 186 UK CFS patients meeting CDC criteria and medically screened for organic illness.
  • Used nested PCR to detect XMRV and MLV proviral DNA in extracted blood samples.
  • Included controls for DNA integrity (beta-globin) and PCR accuracy (positive/negative controls).

Main Results:

  • The cellular beta-globin gene was successfully amplified in all 186 patient samples, confirming DNA integrity.
  • No XMRV or MLV sequences were detected in any of the DNA samples from UK CFS patients.
  • Nested PCR analysis yielded negative results for both viruses.

Conclusions:

  • Xenotropic murine leukaemia virus-related virus (XMRV) or murine leukaemia virus (MLV) sequences were not found in UK chronic fatigue syndrome (CFS) patients.
  • This study found no evidence of XMRV association with CFS in the UK cohort.
  • Observed differences may stem from geographical variations in XMRV prevalence or reporting discrepancies between North American and European studies.

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