Single cell analysis of HIV replication capacity and drug resistance
A novel single-cell-level phenotypic assay is described, which can simultaneously analyze HIV-1 drug susceptibility and intrinsic replication capacity. This allows quantitative dissection of the functions of antiretroviral drugs into suppression of viral replication and selection of resistant viruses with diminished replication capacities. The disclosed assay provides a tool for the rational evaluation of treatment decisions for patients failing antiretroviral therapy and is expected to be an important part in clinical management of HIV.
1. A human immunodeficiency virus (HIV) vector comprising in frame gag-pol and an endoplasmic reticulum (ER) retained fluorescent protein/C-terminal signal sequence in frame with a stop codon inserted into the HIV env at a position about 125 bp from the env N-terminus replacing an env restriction fragment deletion.
2. The vector of claim 1 wherein the restriction fragment deletion is a KpmI-NheI deletion.
3. The vector of claim 1 wherein the HIV is HIV-1.
4. The vector of claim 1 wherein the stop codon is selected from the group consisting of TAA, TAG and TGA.
5. The vector of claim 1 wherein the fluorescent protein is selected from the group consisting of reef coral fluorescent proteins, Aequorea victoria fluorescent proteins, green fluorescent protein and variants thereof.
6. The vector of claim 1 wherein the fluorescent protein is green fluorescent protein (GFP).
7. The vector of claim 1 wherein the C-terminal signal sequence is KDEL (SEQ ID NO: 14) or HIEL (SEQ ID NO: 15).
8. The vector of claim 1 wherein the C-terminal signal sequence is KDEL (SEQ ID NO: 14).
9. The vector of claim 1 wherein the gag-pol is a heterologous gag-pol obtained from a human HIV patient.
10. The vector of claim 9 wherein the heterologous gag-pol is obtained from a human HIV patient treated with highly active anti-retroviral therapy (HAART).
11. A cell transformed with the vector of claim 1 .
12. A cell line prepared from the vector of claim 1 .
13. The vector of claim 10 wherein the HAART comprises a cocktail of drugs selected from the group consisting of zalcitabine (ddC), didanosine (ddI), amprenavir (AVP), Ritonavir (RTV), abacavir (ABC), tenofovir disoproxil fumarate, (TDF), nelfinavir (NFV), saquinavir (SQV), lopinavir (LPV) and indinavir (IDV)
14. A pseudotyped human immunodeficiency virus (HIV) comprising VSV-G that incorporates the vector of claim 1 .
15. A tool for evaluation of human immunodeficiency virus (HIV-1) drug treatment regimens, said tool comprising a vesicular stomatitis virus glycoprotein (VSV-G)-pseudotyped HIV-1 comprising a fluorescent fusion protein/C-terminal signal sequence inserted at an env deletion which is positioned within 125 bp of the env N-terminus, wherein said terminal signal prevents secretion of expressed fluorescent fusion protein from the endoplasmic reticulum of a cell infected with the pseudotyped HIV-1.
16. The tool of claim 15 wherein the C-terminal signal sequence is selected from the group consisting of KDEL (SEQ ID NO: 14) and HIEL (SEQ ID NO: 15).
17. The tool of claim 15 wherein the env deletion is a 1.5 kb ApaI-AgeI fragment.
18. A kit comprising in packaged or container form a human immunodeficiency virus (HIV) vector in acordance with claim 1 , a vector harboring vesicular stomatitis virus glycoprotein, and directions for preparation of pseudotyped HIV.
19. The kit of claim 18 further comprising a population of viral producing cells selected from the group consisting of 293T, Jurkat and CD4+ cells.
20. The kit of claim 18 further comprising directions for determining HIV replication capacity.
21. The kit of claim 20 further comprising directions for assessing antiretroviral drug susceptibility in HIV-1 infected patients.