1. HIV GENOTYPE ASSAY Anabelia Perez, MLT (ASCP) Molecular Technologist August 6, 2008

2. CLINICAL REASON The ViroSeq HIV-1 Genotype Assay is clinically used:  Detect HIV genomic mutations that confer resistance to specific types of antiretroviral drugs  To aid in monitoring and treating HIV infections.

3. PRINICPLE The ViroSeq HIV-1 Genotyping System is based on six major processes:  Sample Preparation  Reverse Transcription (RT)  Polymerase Chain Reaction (PCR)  Cycle Sequencing  Automated Sequence Detection  Software Analysis

4. SAMPLE PREPARATION  Isolate HIV-1 viral RNA from 0.5mL of EDTA human plasma  1 hour centrifuge at 4°C  HIV virus particles in pellet are disrupted with Viral Lysis Buffer  Precipitation with Isopropanol  Purification with 70% Ethanol  RNA is dried and resuspended with Diluent

5. REVERSE TRANSCRIPTION The ViroSeq HIV-1 Genotype Assay amplifies 1.8 Kb region of the HIV-1 pol gene that spans the entire protease gene and approximately two-thirds of the reverse transcriptase (RT) gene. Single-stranded complementary DNA is generated.

6. POLYMERASE CHAIN REACTION PCR Reaction (40 cycles for PCR step)  1 st step: 93°C for 20 sec to denature DNA into single strands  2 nd step: 64°C for 45 sec to anneal primer  3 rd step: 66°C for 3 min to extend primer to create double-stranded DNA Amplicons are created and heated to 72° C for 10 min to allow final extension and then cooled down to 4°C infinity for next procedure

7. CYCLE SEQUENCING Cycle Sequencing has 4 steps:  PCR purification- removes unincorporated dNTPs & primers  DNA quantitation- gel electrophoresis  Cycle sequencing- 7 primers (4 forward & 3 reverse) to sequence entire region Protease (codon 1-99) and two-thirds RT region (1- 335). Big Dye Terminator chemistry is used to permit a resolution of 600 bases on the 3100 Genetic Analyzer  Sequence Purification-removes unincorporated Big terminators from samples so they do not interfere with sample sequencing & analysis. Method: Centri-Sep 96 column spin plates are used at CPL. (Cost effective). Purified cycle sequence reactions are resuspensed in Hi Hi formamide.

8. AUTOMATED SEQUENCE DETECTION 3100 Genetic Analyzer- ABI Prism automated sequencers detect fluorescence from different dye terminators that are used to identify the A C G T bases. Each dye emits light at a different wavelength when excited by an argon ion laser. All four bases are then detected & distinguished in a single capillary. Sequencing involves creating an electrical flow of ions from negative to positive thru POP-6 medium which involves smaller-size fragments migrating faster than larger-size fragments thru field. Each fragment passes by the laser read region & it is excited by the laser Fluorescence is detected by a CCD camera & converted to a sequence basecall by the Sequence Analysis software Resulting File contains the sequence information for each of the 7 primers in each sample

9. SUMMARY & EXPLANATION The ViroSeq HIV-1 Genotyping System detects mutations in the RT and protease regions of the pol gene and provides the physician with a report indicating genetic evidence of viral resistance. It is a complete system that provides reagents for viral RNA isolation from plasma, RT-PCR, and sequencing. The entire protease gene and two-thirds of the Rt gene are amplified to generate a 1.8 kb amplicon. The amplicon is used as a sequencing template for seven primers that generate an approx. 1.3 kb consensus sequence. The software compares the consensus sequence with a reference, HXB-2, to determine mutations present In the sample. Finally, the ViroSeq software uses a proprietary algorithm to analyze the mutations and generate a drug resistance report.