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Journal of Virology, November 2000, p. 9828-9835, Vol. 74, No. 21
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Human T-Lymphotropic Virus Type 1 Open Reading Frame I p12I Is Required for Efficient Viral Infectivity in Primary Lymphocytes

Björn Albrecht,1 Nathaniel D. Collins,1,dagger Mark T. Burniston,1,Dagger John W. Nisbet,1 Lee Ratner,2 Patrick L. Green,1,3,4 and Michael D. Lairmore1,3,4,*

Center for Retrovirus Research and Department of Veterinary Biosciences,1 Comprehensive Cancer Center, The Arthur G. James Cancer Hospital and Research Institute,3 and Department of Molecular Virology, Immunology and Medical Genetics,4 The Ohio State University, Columbus, Ohio 43210, and Departments of Medicine, Pathology, and Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri 631102

Received 22 May 2000/Accepted 27 July 2000

Human T-lymphotropic virus type 1 (HTLV-1) is a complex retrovirus encoding regulatory and accessory genes in four open reading frames (ORF I to IV) of the pX region. Emerging evidence indicates an important role for the pX ORF I-encoded accessory protein p12I in viral replication, but its contribution to viral pathogenesis remains to be defined. p12I is a conserved, membrane-associated protein containing four SH3-binding motifs (PXXP). Its interaction with the interleukin-2 (IL-2) receptor beta - and gamma -chains implies an involvement of p12I in intracellular signaling pathways. In addition, we have demonstrated that expression of pX ORF I p12I is essential for persistent infection in rabbits. In contrast, standard in vitro systems have thus far failed to demonstrate a contribution of p12I to viral infectivity and ultimately cellular transformation. In this study we developed multiple in vitro coculture assays to evaluate the role of p12I in viral infectivity in quiescent peripheral blood mononuclear cells to more accurately reflect the virus-cell interactions as they occur in vivo. Using these assays, we demonstrate a dramatic reduction in viral infectivity in quiescent T lymphocytes for a p12 mutant viral clone (ACH.p12) in comparison to the wild-type clone ACH. Moreover, addition of IL-2 and phytohemagglutinin during the infection completely rescued the ability of ACH.p12 to infect primary lymphocytes. When newly infected primary lymphocytes are used to passage virus, ACH.p12 also exhibited a reduced ability to productively infect activated lymphocytes. Our data are the first to demonstrate a functional role for pX ORF I in the infection of primary lymphocytes and suggest a role for p12I in activation of host cells during early stages of infection.

* Corresponding author. Mailing address: Center for Retrovirus Research and Department of Veterinary Biosciences, The Ohio State University, 1925 Coffey Road, Columbus, OH, 43210-1092. Phone: (614) 292-4819. Fax: (614) 292-6473. E-mail: lairmore.1{at}osu.edu.

dagger Present address: Schering-Plough Research Institute, Lafayette, NJ 07848-0032.

Dagger Present address: Medical College of Ohio, Toledo, OH 43614.

Journal of Virology, November 2000, p. 9828-9835, Vol. 74, No. 21
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.


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