The Virology Core will serve as a centralized source for well characterized stocks of strains of HIV-1, HIV-2, and SIV. In addition to the standard, prototypic laboratory strains, the Specimen Banking Core will provide isolates from well-characterized clinical material and the Molecular Biology Core will provide genetically defined isolates obtained by DNA transfections of infectious molecular clones. Stocks will be produced in the appropriate host cell (primary CD4+T cells, monocyte- derived macrophages, or cell lines), aliquotted, and archive at -80 C or in liquid nitrogen. The Core will standardize the characterization of theses viruses (which should enhance the quality of the participating CFAR research units) and thereby eliminate much duplication of effort. Three areas of characterization will be performed: (1) tittering of viral strains in the relevant host cells type; (2) phenotyping of viral strains (cell tropism, syncytium-inducing (SI) versus non-SI, cytopathic versus non-cytopathic, replication kinetics, drug susceptibilities, etc.); an (3) studying the effects of investigational interventions (gene therapies, antiviral compounds, antibody neutralization, etc.). In addition, the Core will supply isolated CD4+ cells and macrophages, which are technically difficult to prepare. The availability of these Core viral stocks and services should extend the experimental capabilities of the investigators who use its services.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Center Core Grants (P30)
Project #
5P30AI036214-03
Application #
5205745
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1996
Total Cost
Indirect Cost
Chaillon, Antoine; Gianella, Sara; Lada, Steven M et al. (2018) Size, Composition, and Evolution of HIV DNA Populations during Early Antiretroviral Therapy and Intensification with Maraviroc. J Virol 92:
Bengtson, Angela M; Pence, Brian W; Eaton, Ellen F et al. (2018) Patterns of efavirenz use as first-line antiretroviral therapy in the United States: 1999-2015. Antivir Ther 23:363-372
Dubé, Karine; Gianella, Sara; Concha-Garcia, Susan et al. (2018) Ethical considerations for HIV cure-related research at the end of life. BMC Med Ethics 19:83
Mittal, María Luisa; Bazzi, Angela Robertson; Rangel, María Gudelia et al. (2018) 'He's not my pimp': toward an understanding of intimate male partner involvement in female sex work at the Mexico-US border. Cult Health Sex 20:961-975
Letendre, Scott; Bharti, Ajay; Perez-Valero, Ignacio et al. (2018) Higher Anti-Cytomegalovirus Immunoglobulin G Concentrations Are Associated With Worse Neurocognitive Performance During Suppressive Antiretroviral Therapy. Clin Infect Dis 67:770-777
Basova, Liana; Najera, Julia A; Bortell, Nikki et al. (2018) Dopamine and its receptors play a role in the modulation of CCR5 expression in innate immune cells following exposure to Methamphetamine: Implications to HIV infection. PLoS One 13:e0199861
Eren, Kemal; Murrell, Ben (2018) RIFRAF: a frame-resolving consensus algorithm. Bioinformatics 34:3817-3824
de Almeida, Sérgio Monteiro; Ribeiro, Clea E; Rotta, Indianara et al. (2018) Biomarkers of neuronal injury and amyloid metabolism in the cerebrospinal fluid of patients infected with HIV-1 subtypes B and C. J Neurovirol 24:28-40
Martin, Thomas C S; Rauch, Andri; Salazar-Vizcaya, Luisa et al. (2018) Understanding and Addressing Hepatitis C Virus Reinfection Among Men Who Have Sex with Men. Infect Dis Clin North Am 32:395-405
Jenks, Jeffrey D; Hoenigl, Martin (2018) Treatment of Aspergillosis. J Fungi (Basel) 4:

Showing the most recent 10 out of 921 publications