In this current age of genome biology, the primary objective of the Genomics Core is to accelerate thestudy of HIV and opportunistic infections associated with AIDS by providing researchers with access togenomic technologies. Examining host genetics following pathogen infection can identify new targets andpathways for drug development, reveal the genetic mechanisms of disease pathogenesis, determinepredictive gene expression profiles that can guide treatment options, and identify single nucleotidepolymorphisms (SNPs) associated with disease that can be used to judge the effectiveness of differentantiviral drug therapies. To facilitate such research, the specific aims of the Genomics Core are as follows:(1) to provide researchers with a cost-effective mechanism to analyze mammalian gene expression at thewhole genome level using microarray technology, (2) to enable the more precise quantification of bothcoding and non-coding gene expression using real-time quantitative RT-PCR (qRT-PCR), (3) to screenlarge numbers of samples for specific SNPs, and (4) to offer expertise and training in bioinformaticsapplications required to process and interpret the data generated by genomic technologies. The GenomicsCore is currently outfitted with a suite of laboratory equipment to meet these aims (2 x ABI Prism 7700Sequence Detection Systems, a Bio-Rad iCycler, an Affymetrix Fluidics Station 400 and a SunMicrosystems Sunfire 250 Enterprise server). Staff at the core are highly trained and skilled in areas ofnucleic acid isolation, purification and quantification, and primer design, gene expression assays andbioinformatic analysis. In summary, the contribution of the Genomics Core to HIV- and AIDS-relatedresearch is best reflected by the numerous projects supported by the core, among which include the firstassessment of HIV-stimulated gene expression in CD4 T cells, identification of pathways resulting in HIVinduced apoptosis, the effects of methamphetamine use on HIV encephalitis, and identification of theamino acid polymorphisms that contribute to ritonavir hypersusceptibility. This proposal will allow theGenomics Core to continue bridging the gap between HIV-related research and genomic technologies in aneconomical manner. This will allow HIV research to benefit from the very latest developments in genomebiology, which will ultimately translate into a better understanding of disease pathogenesis and theevolution of better therapies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Center Core Grants (P30)
Project #
2P30AI036214-14
Application #
7278948
Study Section
Special Emphasis Panel (ZAI1-EC-A (J1))
Project Start
2007-06-01
Project End
2012-05-31
Budget Start
2007-06-01
Budget End
2008-05-31
Support Year
14
Fiscal Year
2007
Total Cost
$250,351
Indirect Cost
Name
University of California San Diego
Department
Type
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Blumenthal, Jill; Jain, Sonia; Mulvihill, Evan et al. (2018) Perceived versus calculated HIV risk: Implications for Pre-exposure prophylaxis uptake in a randomized trial of men who have sex with men. J Acquir Immune Defic Syndr :
Naticchia, Matthew R; Laubach, Logan K; Tota, Ember M et al. (2018) Embryonic Stem Cell Engineering with a Glycomimetic FGF2/BMP4 Co-Receptor Drives Mesodermal Differentiation in a Three-Dimensional Culture. ACS Chem Biol 13:2880-2887
Wagner, Karla D; Syvertsen, Jennifer L; Verdugo, Silvia R et al. (2018) A mixed methods study of the social support networks of female sex workers and their primary noncommercial male partners in Tijuana, Mexico. J Mix Methods Res 12:437-457
Bastos, Francisco I; Bastos, Leonardo Soares; Coutinho, Carolina et al. (2018) HIV, HCV, HBV, and syphilis among transgender women from Brazil: Assessing different methods to adjust infection rates of a hard-to-reach, sparse population. Medicine (Baltimore) 97:S16-S24
Kardava, Lela; Sohn, Haewon; Youn, Christine et al. (2018) IgG3 regulates tissue-like memory B cells in HIV-infected individuals. Nat Immunol 19:1001-1012
Namazi, Golnaz; Fajnzylber, Jesse M; Aga, Evgenia et al. (2018) The Control of HIV After Antiretroviral Medication Pause (CHAMP) Study: Posttreatment Controllers Identified From 14 Clinical Studies. J Infect Dis 218:1954-1963
Lada, Steven M; Huang, Karissa; VanBelzen, D Jake et al. (2018) Quantitation of Integrated HIV Provirus by Pulsed-Field Gel Electrophoresis and Droplet Digital PCR. J Clin Microbiol 56:
Cepeda, Javier A; Eritsyan, Ksenia; Vickerman, Peter et al. (2018) Potential impact of implementing and scaling up harm reduction and antiretroviral therapy on HIV prevalence and mortality and overdose deaths among people who inject drugs in two Russian cities: a modelling study. Lancet HIV 5:e578-e587
Skaathun, Britt; Voisin, Dexter R; Cornwell, Benjamin et al. (2018) A Longitudinal Examination of Factors Associated with Network Bridging Among YMSM: Implications for HIV Prevention. AIDS Behav :
Stone, Jack; Fraser, Hannah; Lim, Aaron G et al. (2018) Incarceration history and risk of HIV and hepatitis C virus acquisition among people who inject drugs: a systematic review and meta-analysis. Lancet Infect Dis 18:1397-1409

Showing the most recent 10 out of 921 publications