Natural antisense transcripts are detected in different cell lines and tissues of cats infected with feline immunodeficiency virus

Gene ◽  
2001 ◽  
Vol 267 (2) ◽  
pp. 157-164 ◽  
Author(s):  
Sylvie Briquet ◽  
Jennifer Richardson ◽  
Christine Vanhée-Brossollet ◽  
Catherine Vaquero
1994 ◽  
Vol 56 (1) ◽  
pp. 199-201 ◽  
Author(s):  
Keizo TOMONAGA ◽  
Takayuki MIYAZAWA ◽  
Yasushi KAWAGUCHI ◽  
Mariko KOHMOTO ◽  
Yasuo INOSHIMA ◽  
...  

1999 ◽  
Vol 73 (3) ◽  
pp. 2491-2498 ◽  
Author(s):  
James Johnston ◽  
Christopher Power

ABSTRACT Feline immunodeficiency virus (FIV) is a lentivirus causing immune suppression and neurological disease in cats. Like primate lentiviruses, FIV utilizes the chemokine receptor CXCR4 for infection. In addition, FIV gene expression has been demonstrated in immortalized human cell lines. To investigate the extent and mechanism by which FIV infected primary and immortalized human cell lines, we compared the infectivity of two FIV strains, V1CSF and Petaluma, after cell-free infection. FIV genome was detected in infected human peripheral blood mononuclear cells (PBMC) and macrophages at 21 and 14 days postinfection, respectively. Flow cytometry analysis of FIV-infected human PBMC indicated that antibodies to FIV p24 recognized 12% of the cells. Antibodies binding the CCR3 chemokine receptor maximally inhibited infection of human PBMC by both FIV strains compared to antibodies to CXCR4 or CCR5. Reverse transcriptase levels increased in FIV-infected human PBMC, with detection of viral titers of 101.3 to 102.1 50% tissue culture infective doses/106 cells depending on the FIV strain examined. Cell death in human PBMC infected with either FIV strain was significantly elevated relative to uninfected control cultures. These findings indicate that FIV can productively infect primary human cell lines and that viral strain specificity should be considered in the development of an FIV vector for gene therapy.


2005 ◽  
Vol 79 (24) ◽  
pp. 15175-15188 ◽  
Author(s):  
Dyana T. Saenz ◽  
Wulin Teo ◽  
John C. Olsen ◽  
Eric M. Poeschla

ABSTRACT The Ref1 and Lv1 postentry restrictions in human and monkey cells have been analyzed for lentiviruses in the primate and ungulate groups, but no data exist for the third (feline) group. We compared feline immunodeficiency virus (FIV) to other restricted (human immunodeficiency virus type 1 [HIV-1], equine infectious anemia virus [EIAV]) and unrestricted (NB-tropic murine leukemia virus [NB-MLV]) retroviruses across wide ranges of viral inputs in cells from multiple primate and nonprimate species. We also characterized restrictions conferred to permissive feline and canine cells engineered to express rhesus and human TRIM5α proteins and performed RNA interference (RNAi) against endogenous TRIM5α. We find that expression of rhesus or human TRIM5α proteins in feline cells restricts FIV, impairing pseudotyped vector transduction and viral replication, but rhesus TRIM5α is more restricting than human TRIM5α. Notably, however, canine cells did not support restriction by human TRIM5α and supported minimal restriction by rhesus TRIM5α, suggesting that these proteins may not function autonomously or that a canine factor interferes. Stable RNAi knockdown of endogenous rhesus TRIM5α resulted in marked increases in FIV and HIV-1 infectivities while having no effect on NB-MLV. A panel of nonprimate cell lines varied widely in susceptibility to lentiviral vector transduction, but normalized FIV and HIV-1 vectors varied concordantly. In contrast, in human and monkey cells, relative restriction of FIV compared to HIV-1 varied from none to substantial, with the greatest relative infectivity deficit for FIV vectors observed in human T-cell lines. Endogenous and introduced TRIM5α restrictions of FIV could be titrated by coinfections with FIV, HIV-1, or EIAV virus-like particles. Arsenic trioxide had complex and TRIM5α-independent enhancing effects on lentiviral but not NB-MLV infection. Implications for human gene therapy are discussed.


2008 ◽  
Vol 70 (8) ◽  
pp. 777-783 ◽  
Author(s):  
Kenji BABA ◽  
Yuko GOTO-KOSHINO ◽  
Fuminori MIZUKOSHI ◽  
Asuka SETOGUCHI-MUKAI ◽  
Yasuhito FUJINO ◽  
...  

2005 ◽  
Vol 7 (2) ◽  
pp. 233-239 ◽  
Author(s):  
Farah Mustafa ◽  
Preethi Jayanth ◽  
Pretty S. Phillip ◽  
Akela Ghazawi ◽  
Russell D. Schmidt ◽  
...  

1999 ◽  
Vol 73 (9) ◽  
pp. 7916-7921 ◽  
Author(s):  
Yoshiaki Nishimura ◽  
Yuko Goto ◽  
Kumiko Yoneda ◽  
Yasuyuki Endo ◽  
Takuya Mizuno ◽  
...  

ABSTRACT Feline immunodeficiency virus (FIV) was isolated from a wild-caught Tsushima cat (Felis bengalensis euptilura), an endangered Japanese nondomestic subspecies of leopard cat (F. bengalensis). Phylogenetic analysis of the env gene sequences indicated that the FIV from the Tsushima cat belonged to a cluster of subtype D FIVs from domestic cats. FIVs from both the Tsushima cat and the domestic cat showed similar levels of replication and cytopathicity in lymphoid cell lines derived from these two species. The results indicated the occurrence of interspecies transmission of FIV from the domestic cat to the Tsushima cat in the wild.


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