Identifying and characterizing recently transmitted viruses

被引:37
作者
Keele, Brandon F. [1 ]
机构
[1] NCI, SAIC Frederick Inc, AIDS & Canc Virus Program, Frederick, MD 21701 USA
基金
美国国家卫生研究院;
关键词
acute infection; HIV; simian immunodeficiency virus; transmitted virus; viral evolution; T-CELL RESPONSES; SELECTIVE TRANSMISSION; HIV-1; DIVERSITY; TYPE-1; VARIANTS; IMMUNE ESCAPE; INFECTION; GAG; POPULATIONS; ANTIBODIES; MUTATIONS;
D O I
10.1097/COH.0b013e32833a0b9b
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose of review Improvements in sequencing approaches and robust mathematical modeling have dramatically increased information on viral genetics during acute infection with HIV and simian immunodeficiency virus, providing unprecedented insight into viral transmission and viral/immune interactions. Recent findings Overall viral genetic diversity is reduced significantly during mucosal transmission. Remarkably, in the vast majority of sexual transmissions, this diversity is reduced to a single viral variant that establishes the initial productive clinical infection. By identifying and enumerating transmitted/founder viruses, researchers can begin to define the characteristics that are necessary and sufficient for successful viral replication within a new host. Summary Acute HIV infection is a critical window of opportunity for vaccine and therapeutic intervention. New sequencing technologies and mathematical modeling of transmission and early evolution have provided a clearer understanding of the number of founder viruses that establish infection, the rapid generation of diversity in these viruses and the subsequent evasion of host immunity. The information gained by identifying transmitted viruses, monitoring the initial host responses to these viruses and then identifying mechanisms of viral escape could provide better strategies for vaccine development, preexposure prophylaxis, microbicides, or other therapeutic interventions.
引用
收藏
页码:327 / 334
页数:8
相关论文
共 65 条
[1]   Quantitating the Multiplicity of Infection with Human Immunodeficiency Virus Type 1 Subtype C Reveals a Non-Poisson Distribution of Transmitted Variants [J].
Abrahams, M. -R. ;
Anderson, J. A. ;
Giorgi, E. E. ;
Seoighe, C. ;
Mlisana, K. ;
Ping, L. -H. ;
Athreya, G. S. ;
Treurnicht, F. K. ;
Keele, B. F. ;
Wood, N. ;
Salazar-Gonzalez, J. F. ;
Bhattacharya, T. ;
Chu, H. ;
Hoffman, I. ;
Galvin, S. ;
Mapanje, C. ;
Kazembe, P. ;
Thebus, R. ;
Fiscus, S. ;
Hide, W. ;
Cohen, M. S. ;
Karim, S. Abdool ;
Haynes, B. F. ;
Shaw, G. M. ;
Hahn, B. H. ;
Korber, B. T. ;
Swanstrom, R. ;
Williamson, C. .
JOURNAL OF VIROLOGY, 2009, 83 (08) :3556-3567
[2]  
[Anonymous], 2008, REP GLOB AIDS EP
[3]   Ultradeep Pyrosequencing Detects Complex Patterns of CD8+ T-Lymphocyte Escape in Simian Immunodeficiency Virus-Infected Macaques [J].
Bimber, Benjamin N. ;
Burwitz, Benjamin J. ;
O'Connor, Shelby ;
Detmer, Ann ;
Gostick, Emma ;
Lank, Simon M. ;
Price, David A. ;
Hughes, Austin ;
O'Connor, David .
JOURNAL OF VIROLOGY, 2009, 83 (16) :8247-8253
[4]   Nef gene evolution from a single transmitted strain in acute SIV infection [J].
Bimber, Benjamin N. ;
Chugh, Pauline ;
Giorgi, Elena E. ;
Kim, Baek ;
Almudevar, Anthony L. ;
Dewhurst, Stephen ;
O'Connor, David H. ;
Lee, Ha Youn .
RETROVIROLOGY, 2009, 6
[5]   Heterosexual risk of HIV-1 infection per sexual act: systematic review and meta-analysis of observational studies [J].
Boily, Marie-Claude ;
Baggaley, Rebecca F. ;
Wang, Lei ;
Masse, Benoit ;
White, Richard G. ;
Hayes, Richard J. ;
Alary, Michel .
LANCET INFECTIOUS DISEASES, 2009, 9 (02) :118-129
[6]   Global genomic analysis reveals rapid control of a robust innate response in SIV-infected sooty mangabeys [J].
Bosinger, Steven E. ;
Li, Qingsheng ;
Gordon, Shari N. ;
Klatt, Nichole R. ;
Duan, Lijie ;
Xu, Luoling ;
Francella, Nicholas ;
Sidahmed, Abubaker ;
Smith, Anthony J. ;
Cramer, Elizabeth M. ;
Zeng, Ming ;
Masopust, David ;
Carlis, John V. ;
Ran, Longsi ;
Vanderford, Thomas H. ;
Paiardini, Mirko ;
Isett, R. Benjamin ;
Baldwin, Don A. ;
Else, James G. ;
Staprans, Silvija I. ;
Silvestri, Guido ;
Haase, Ashley T. ;
Kelvin, David J. .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (12) :3556-3572
[7]   Escape and compensation from early HLA-B57-Mediated cytotoxic T-lymphocyte pressure on human immunodeficiency virus type 1 Gag alter capsid interactions with cyclophilin A [J].
Brockman, Mark A. ;
Schneidewind, Arne ;
Lahaie, Matthew ;
Schmidt, Aaron ;
Miura, Toshiyuki ;
DeSouza, Ivna ;
Ryvkin, Faina ;
Derdeyn, Cynthia A. ;
Allen, Susan ;
Hunter, Eric ;
Mulenga, Joseph ;
Goepfert, Paul A. ;
Walker, Bruce D. ;
Allen, Todd M. .
JOURNAL OF VIROLOGY, 2007, 81 (22) :12608-12618
[8]   HLA-Associated Immune Escape Pathways in HIV-1 Subtype B Gag, Pol and Nef Proteins [J].
Brumme, Zabrina L. ;
John, Mina ;
Carlson, Jonathan M. ;
Brumme, Chanson J. ;
Chan, Dennison ;
Brockman, Mark A. ;
Swenson, Luke C. ;
Tao, Iris ;
Szeto, Sharon ;
Rosato, Pamela ;
Sela, Jennifer ;
Kadie, Carl M. ;
Frahm, Nicole ;
Brander, Christian ;
Haas, David W. ;
Riddler, Sharon A. ;
Haubrich, Richard ;
Walker, Bruce D. ;
Harrigan, P. Richard ;
Heckerman, David ;
Mallal, Simon .
PLOS ONE, 2009, 4 (08)
[9]   The efficiency of single genome amplification and sequencing is improved by quantitation and use of a bioinformatics tool [J].
Butler, David M. ;
Pacold, Mary E. ;
Jordan, Parris S. ;
Richman, Douglas D. ;
Smith, Davey M. .
JOURNAL OF VIROLOGICAL METHODS, 2009, 162 (1-2) :280-283
[10]   Viral fitness implications of variation within an immunodominant CD8+T-cell epitope of HIV-1 [J].
Christie, N. M. ;
Willer, D. O. ;
Lobritz, M. A. ;
Chan, J. K. ;
Arts, E. J. ;
Ostrowski, M. A. ;
Cochrane, A. ;
Luscher, M. A. ;
MacDonald, K. S. .
VIROLOGY, 2009, 388 (01) :137-146