Comparing the Ex Vivo Fitness of CCR5-Tropic Human Immunodeficiency Virus Type 1 Isolates of Subtypes B and C
- Sarah C. Ball1,
- Awet Abraha1,
- Kalonji R. Collins2,
- Andre J. Marozsan3,
- Heather Baird3,
- Miguel E. Quiñones-Mateu4,
- Adam Penn-Nicholson1,
- Michael Murray1,
- Nathalie Richard1,
- Michael Lobritz1,
- Peter A. Zimmerman5,
- Tatsuyoshi Kawamura6,
- Andrew Blauvelt6, and
- Eric J. Arts1,2,3,*
- 1Division of Infectious Diseases, Department of Medicine
- 2Molecular Virology Program
- 3Department of Pharmacology
- 5Division of Geographical Medicine, Department of Medicine, Case Western Reserve University
- 4Department of Virology, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio
- 6Dermatology Branch, National Cancer Institute, Bethesda, Maryland
ABSTRACT
Continual human immunodeficiency virus type 1 (HIV-1) evolution and expansion within the human population have led to unequal distribution of HIV-1 group M subtypes. In particular, recent outgrowth of subtype C in southern Africa, India, and China has fueled speculation that subtype C isolates may be more fit in vivo. In this study, nine subtype B and six subtype C HIV-1 isolates were added to peripheral blood mononuclear cell cultures for a complete pairwise competition experiment. All subtype C HIV-1 isolates were less fit than subtype B isolates (P < 0.0001), but intrasubtype variations in HIV-1 fitness were not significant. Increased fitness of subtype B over subtype C was also observed in primary CD4+ T cells and macrophages from different human donors but not in skin-derived human Langerhans cells. Detailed analysis of the retroviral life cycle during several B and C virus competitions indicated that the efficiency of host cell entry may have a significant impact on relative fitness. Furthermore, phyletic analyses of fitness differences suggested that, for a recombined subtype B/C HIV-1 isolate, higher fitness mapped to the subtype B env gene rather than the subtype C gag and pol genes. These results suggest that subtype B and C HIV-1 may be transmitted with equal efficiency (Langerhans cell data) but that subtype C isolates may be less fit following initial infection (T-cell and macrophage data) and may lead to slower disease progression.
FOOTNOTES
- Received 30 July 2002.
- Accepted 22 October 2002.
- ↵*Corresponding author. Mailing address: Division of Infectious Diseases, BRB 1029, Case Western Reserve University, 10900 Euclid Ave., Cleveland, OH 44106. Phone: (216) 368-8904. Fax (216)-368 2034. E-mail: eja3{at}po.cwru.edu.
- American Society for Microbiology











