No Biological Evidence of XMRV Infection in Cervical Smears from HIV/HPV Positive and Negative Kenyan Women

被引:4
|
作者
He, Xiaotong [1 ]
Walker, Thomas D. J. [1 ]
Maranga, Innocent O. [2 ,3 ]
Oliver, Anthony W. [1 ]
Hampson, Lynne [1 ]
Hampson, Ian N. [1 ]
机构
[1] Univ Manchester, St Marys Hosp, Sch Canc & Enabling Sci, Viral Oncol Labs, Manchester M13 0JH, Lancs, England
[2] Univ Nairobi, Dept Obstet, Nairobi, Kenya
[3] Univ Nairobi, Dept Gynaecol, Nairobi, Kenya
来源
PLOS ONE | 2012年 / 7卷 / 10期
关键词
VIRUS-RELATED VIRUS; GENITAL-TRACT; BLOOD-CELLS; RETROVIRUS; HOST; TRANSMISSION; EXPRESSION;
D O I
10.1371/journal.pone.0047208
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: XMRV (xenotropic murine leukaemia virus-related virus) is a gammaretrovirus first discovered in human prostate carcinomas and later linked to chronic fatigue syndrome (CFS). Emerging conflicting data and lack of reproducibility of results within the scientific community has now led to the association of XMRV with CFS being discounted. Indeed the case for an involvement with any human disease has been questioned with the suggestion that XMRV is a laboratory generated recombinant virus. The fact that not all published positive findings can be easily explained as contamination artefacts coupled with the observation that XMRV may have a sexually transmitted mode of infectivity and can be infectious for primates, where it preferential resides in cells of the reproductive tract, prompted us to look for evidence of XMRV in the cervical cells of a cohort of Kenyan women both with and without pre-existing HIV/HPV infections. Results: Using a highly sensitive and selective triplex PCR approach we analysed DNA from the liquid based cytology (LBC) cervical smears of 224 Kenyan women. There was no evidence of XMRV expression in any of the sample population irrespective of HPV and/or HIV status. Conclusions: The data presented show no indication of XMRV infection in any of the cervical samples screened in this study. Approximately 50% of the women were HIV positive but this did not influence the findings signifying that XMRV does not act as an opportunistic infection in this cohort nor is it related to HPV status. Our results therefore support the findings that XMRV is confined to the laboratory and does not currently represent an infectious agent for humans, with a cautionary adage that such potential zoonotic viruses should be carefully monitored in the future.
引用
收藏
页数:5
相关论文
共 15 条
  • [1] Analysis of the Prevalence of HTLV-1 Proviral DNA in Cervical Smears and Carcinomas from HIV Positive and Negative Kenyan Women
    He, Xiaotong
    Maranga, Innocent O.
    Oliver, Anthony W.
    Gichangi, Peter
    Hampson, Lynne
    Hampson, Ian N.
    VIRUSES-BASEL, 2016, 8 (09):
  • [2] No evidence of XMRV infection in immunocompromised patients and HIV-positive individuals from Germany
    Korn, K.
    Reil, H.
    Ensser, A.
    Knoell, A.
    INFECTION, 2012, 40 (02) : 181 - 184
  • [3] Oral HPV prevalence in women positive for cervical HPV infection and their sexual partners: a German screening study
    Ralf B. Uken
    Oliver Brummer
    Carolin von Schubert-Bayer
    Thomas Brodegger
    Ingo U. Teudt
    European Archives of Oto-Rhino-Laryngology, 2016, 273 : 1933 - 1942
  • [4] Oral HPV prevalence in women positive for cervical HPV infection and their sexual partners: a German screening study
    Uken, Ralf B.
    Brummer, Oliver
    von Schubert-Bayer, Carolin
    Brodegger, Thomas
    Teudt, Ingo U.
    EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2016, 273 (07) : 1933 - 1942
  • [5] Vaginal microbiota diversity and paucity of Lactobacillus species are associated with persistent hrHPV infection in HIV negative but not in HIV positive women
    Dareng, Eileen O.
    Ma, Bing
    Adebamowo, Sally N.
    Famooto, Ayotunde
    Ravel, Jacques
    Pharoah, Paul P.
    Adebamowo, Clement A.
    SCIENTIFIC REPORTS, 2020, 10 (01)
  • [6] Field experience with the 8-HPV-type oncoprotein test for cervical cancer screening among HPV-positive women living with and without HIV in LMICs
    Downham, Laura
    Rol, Mary Luz
    Forestier, Mathilde
    Romero, Pilar
    Mendoza, Laura
    Mongelos, Pamela
    Picconi, Maria Alejandra
    Colucci, Maria Celeste
    Padin, Valeria Mariel
    Flores, Ana Paula
    Zuniga, Michael
    Ferrera, Annabelle
    Cabrera, Yessy
    Crispin, Marcela Farfan
    Ramirez, Arianis Tatiana
    Cele, Londiwe
    Diop-Ndiaye, Halimatou
    Samate, Dianke
    Manga, Pascaline
    Thiam, Fadimatou Bintou
    Rodriguez, Maria Isabel
    DSouza, Jyoshma P.
    Nyaga, Victoria Nyawira
    Diop, Mamadou
    Sebitloane, Motshedisi
    Sanchez, Gloria Ines
    Teran, Carolina
    Calderon, Alejandro
    Wiesner, Carolina
    Murillo, Raul
    Herrero, Rolando
    Baena, Armando
    Almonte, Maribel
    INTERNATIONAL JOURNAL OF CANCER, 2024, 155 (05) : 816 - 827
  • [7] Biological factors that place women at risk for HIV: evidence from a large-scale clinical trial in Durban
    Abbai, Nathlee Samantha
    Wand, Handan
    Ramjee, Gita
    BMC WOMENS HEALTH, 2016, 16
  • [8] HPV infection-associated anogenital cyto-colpo-histological findings and molecular typing in HIV-positive women
    Tso, F. K.
    Rodrigues, C. L. L.
    Levi, J. E.
    Mattosinho de Castro Ferraz, M. G.
    Speck, N. M. G.
    Ribalta, J. C. L.
    GENETICS AND MOLECULAR RESEARCH, 2015, 14 (04) : 17630 - 17640
  • [9] Prevalence and Persistence of Cervical Human Papillomavirus Infection in HIV-Positive Women Initiating Highly Active Antiretroviral Therapy
    Fife, Kenneth H.
    Wu, Julia W.
    Squires, Kathleen E.
    Watts, D. Heather
    Andersen, Janet W.
    Brown, Darron R.
    JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2009, 51 (03) : 274 - 282
  • [10] Characterization of cervical biopsies of women with HIV and HPV co-infection using p16ink4a, ki-67 and HPV E4 immunohistochemistry and DNA methylation
    Kremer, Wieke W.
    Vink, Frederique J.
    van Zummeren, Marjolein
    Dreyer, Greta
    Rozendaal, Lawrence
    Doorbar, John
    Bleeker, Maaike C. G.
    Meijer, Chris J. L. M.
    MODERN PATHOLOGY, 2020, 33 (10) : 1968 - 1978