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Published on: November 8, 2011
Susceptibility of human lymphoblastoid B-cell line CE to HIV1 infection
M B Valli1, G Carloni, L Bertolini
1Istituto di Medicina Sperimentale, Roma.
Insights
The CE B-lymphoblastoid cell line (LCL) is permissive to both Hepatitis C Virus and Human Immunodeficiency Virus type 1 (HIV-1). This finding suggests the CE LCL can be used to study interactions between these two viruses in co-infected cells.
Area of Science:
- Virology
- Immunology
- Cell Biology
Background:
- The human B-lymphoblastoid cell line (LCL) CE is known to be permissive to Hepatitis C Virus (HCV).
- Understanding viral permissiveness in cell lines is crucial for studying viral pathogenesis and developing antiviral strategies.
Purpose of the Study:
- To investigate whether the CE LCL is also permissive to Human Immunodeficiency Virus type 1 (HIV-1) infection.
- To establish the CE LCL as a model for studying the interactions between HCV and HIV-1 in co-infected cells.
Main Methods:
- Infection of CE LCL with HIV-1.
- Detection of HIV-1 genomes in cell supernatants.
- Detection of HIV-1 RNA transcripts and proviral DNA in cell extracts using molecular methods.
Main Results:
- HIV-1 infection was confirmed by the detection of viral genomes in cell supernatants.
- HIV-1 RNA transcripts and proviral DNA were detected in cell extracts at various time points post-infection.
- The CE LCL demonstrated permissiveness to HIV-1.
Conclusions:
- The CE LCL is permissive to both HCV and HIV-1.
- The CE LCL serves as a valuable tool for investigating the interplay between HCV and HIV-1 in a single cell environment.
- This model can facilitate research into the mutual interactions of these two significant human viruses.
Abstract:
In this preliminary report, we provide evidence that the human B-lymphoblastoid cell line (LCL) CE, bone-marrow-derived, previously reported to be permissive to hepatitis C virus, is also permissive to HIV1 infection. HIV1 genomes were detectable in cell supernatants, virus RNA transcripts and proviral DNAs in cell extracts at different times post-infection. Therefore, we propose this LCL cell line as a tool for exploring the mutual interactions of the two viruses in double-infected cells.

