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J Gen Virol 76 (1995), 167-173; DOI 10.1099/0022-1317-76-1-167
© 1995 Society for General Microbiology

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Cell-mediated transmission of human T cell lymphotropic virus type I to human malignant trophoblastic cells results in long-term persistent infection

Xiangdong Liu1, Vladimir Zachar1,2,, Niels Nørskov-Lauritsen1, George Aboagye-Mathiesen1, Milan Zdravkovic1, Peter Mosborg-Peterson1, Anne Mette Dalsgaard1, Henrik Hager1 and Peter Ebbesen1,*

1 Department of Virus and Cancer, Danish Cancer Society, Gustav Wieds Vej 10, DK-8000 Åarhus C, Denmark
and2 Institute of Virology, Slovak Academy of Sciences, Bratislava, Slovak Republic

We investigated permissiveness of the malignantly transformed trophoblast (choriocarcinoma) cell lines JAR, BeWo and JEG-3 to the human T cell lymphotropic virus type I (HTLV-I). After co-culture with the productively infected cell line MT-2 the choriocarcinoma cell lines were analysed for infection over a period of three months. The presence of HTLV-I viral DNA was examined by PCR using primers targeting the gag, pol, env and pX specific sequences. All amplified segments were found consistently in the cell cultures throughout the period of study. Further analysis that aimed to characterize the size variation of the integrated proviral DNA by Southern blotting revealed the presence of integrated proviral sequences which consisted, for the most part, of incomplete genomes. The presence of the full-length HTLV-I genome, however, was unequivocally confirmed in clonally expanded cell cultures derived from the originally infected parental cells. In order to analyse virus expression at the transcriptional level, we used reverse transcriptase (RT)-mediated PCR that was targeted at intra-exon regions (gag, pol, env and pX), and the splicing sites of the env and pX-tax/rex mRNAs. When compared with MT-2 cells, substantially lower levels of all transcripts were found in all the cell lines analysed. We were unsuccessful in attempts to detect viral protein expression using polyvalent or Tax- and Gag-specific monoclonal antibodies by Western blot analysis or immunoprecipitation, and we could not detect any RT activity released into the supernatant of the infected cells either. Collectively, these data suggest that the trophoblastic cells may become persistently but essentially non-productively infected with HTLV-I.

* Author for correspondence. Fax +45 86195415. e-mail Ebbesen@virus.aau.dk

Received 14 June 1994; accepted 1 September 1994.


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P. Bhat and D. A. Anderson
Hepatitis B Virus Translocates across a Trophoblastic Barrier
J. Virol., July 1, 2007; 81(13): 7200 - 7207.
[Abstract] [Full Text] [PDF]




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