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Reducing Feline Immunodeficiency Viral Loads Using CRISPR: a Proof of Concept Tatiana Wolf, Brian G

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Reducing Feline Immunodeficiency Viral Loads Using CRISPR: a Proof of Concept Tatiana Wolf, Brian G Reducing Feline Immunodeficiency Viral Loads Using CRISPR: A Proof of Concept Tatiana Wolf, Brian G. Murphy DVM, PhD. School of Veterinary Medicine, University of California, Davis Department of Pathology, Microbiology and Immunology • Feline Immunodeficiency Virus (FIV) infection is a common and incurable 1 Integrated FIV Provirus • A recombinant lentivirus was designed to deliver the anti-FIV CRISPR infectious disease of domestic cats and invariably results in death once it components (Figure 2). progresses to the stage of feline acquired immunodeficiency syndrome Cat Genome 5’ LTR 3’ LTR Cat Genome • The CRISPR lentivirus integrates into a cell’s genome as DNA to express two (FAIDS). guide RNA sequences (Thing 1 & Thing 2) specific to the FIV U3 LTR proviral U3 R U5 gag pol env • FIV is a lentivirus, a type of retrovirus with a tropism for CD4+T cells. U3 R U5 sequence. Additionally, the CRISPR lentivirus codes for the Cas9 • FIV is capable of integrating into the cell’s genome and persist as a permanent endonuclease, which is co-transcribed with a Puromycin resistance gene. proviral DNA reservoir. • Two main experiments were conducted and performed in triplicates. • FIV infected cells are capable of evading the immune system resulting in Simplified models outlined by Figures 3 and 4. chronic lifelong infections, referred to as latency. 2 CRISPR/Cas9 • Experiments performed on MCH5-4 cells (immortalized feline CD4+ T-cells). • There are no current medical therapies that consistently and efficiently Mediated Cut • FIV clade C virus was utilized to infect cells. eliminate lentiviral reservoirs from infected latent cells. • Integration of proviral DNA was quantitated using real-time PCR to measure • CRISPR (clustered, regularly interspaced, short palindromic repeats) is a FIV gag DNA copies normalized to copies of feline GAPDH. molecular technique based on a bacterial antiviral defense mechanism to 3 Excised FIV Provirus • Isolated FIV viral RNA from cell-free culture media was quantitated by RT locate and excise integrated viral genes. real-time PCR measuring gag copies normalized to volume. • Proviral FIV is flanked by LTR sequences containing regions with compatible sites for CRISPR applications (Figure 1). FIV Cells + CRISPR EXPERIMENT #1 4 Host Mediated FIV-C Lentivirus CRISPR Lentivirus DNA Repair HYPOTHESIS: INFECTION Feline cells infectedTREATMENT in vitro with FIV and treated with the FIGURE 2: Plasmid Design for anti-FIV CRISPR gene editing tool will demonstrate reduced proviral loads Recombinant CRISPR Lentivirus and virus production20 Day relative to non-CRISPR treated FIV-infected felineCell cells. DNA FIGURE 1: Proposed Non-functional Incubation 7 Day anti-FIV CRISPR Mechanism LTR Reminant Incubation Isolate + Naive FIV MCH5-4 Cells Infected Cells Viral RNA FIV Infected Cells EXPERIMENT#1: FIV Infected Cells Treated witCONTROLh anti #1 -FIV CRISPR A • Real-time PCR results from Experiment #1 and #2 are supportive of our hypothesis that CRISPR treatments have an effect on reducing viral loads. FIV Cells + CRISPR EXPERIMENT #1 • Graph 2 and Graph 4 demonstrate significantly lower viral loads in FIV-C Lentivirus CRISPR Lentivirus INFECTION TREATMENT Experiment #1 & 2 CRISPR treatment groups when compared to controls. • Copies of GAPDH of Copies Higher FIV titers correspond with higher cell infectivity. 6 • 20 Day Cell DNA Proviral DNA loads were not significantly different between control and Incubation 7 Day B Incubation Isolate + treatment groups (Graph 1 & 3). We considered the possibility that our sample size was too small to observe a significant change or excised proviral Naive FIV DNA was not degraded and remained stable for real-time PCR gag MCH5-4 Cells Infected Cells Viral RNA amplification. Viral gag cDNA Copies per 1ml of Supernatant of 1ml per Copies cDNA gag Viral FIGURE 3 10 per Copies gag Proviral FIV • FIV Infected Cells Figure 5 were results from a preliminary experiment testing the recombinant CONTROL #1 FIGURE 5: MCH5-4 cells infected with lentivirus compatibility with MCH5-4 cells. Red fluorescence corresponded GRAPH 1 GRAPH 2 recombinant lentivirus coding for with Thing 1 & Thing 2 expression and green fluorescence corresponded Puromycin resistance. Day 2 of infection EXPERIMENT #2: anti-FIV CRISPR Treated Cells Infected by FIV (A) prior to puromycin selection. with Cas9 expression. Photo B confirmed we could select for CRISPR only Selection Day 6 (B) culture in puromycin. cells that co-transcribe Cas9 with the puromycin resistance gene. CRISPR CRISPR Cells + FIV Selected Cells EXPERIMENT #2 • Figure 6 provides evidence that MCH5-4 CRISPR treated cells contain 7 Day CRISPR Lentivirus Incubation integrated CRISPR lentivirus DNA sequences based on the presence of Thing TRANSFECTION 1 and Thing 2 gRNA. • + Puromycin GAPDH of Copies Data not shown are results from Experiment 1 and 2 using feline peripheral Selection 6 Cell DNA blood mononuclear cells (PBMC) harvested from specific pathogen free cats. 17 Day FIV-C Lentivirus Isolate + Incubation INFECTION PBMC results were mixed and inconclusive, possibly due to the mixed population of cell types and difference in FIV and/or CRISPR lentivirus Naive MCH5-4 Cells Viral RNA infectivity. Additionally, cellular RNA was collected at the end of the experiments but real-time PCR results were mixed and inconclusive. 7 Day FIGURE 4 Supernatant of 0.5ml per Copies cDNA gag Viral FIGURE 6: Gel electrophoresis image displaying FIV Proviral gag Copies per 10 per Copies gag Proviral FIV Incubation 525bp PCR amplicon of Thing 1 & Thing 2. Lane Non-CRISPR FIV Infected Cells 2 was a positive control (Figure 2). Lane 3 and 4 CONTROL #2 CONTROL Cells CRISPR Cells + FIV were DNA samples extracted from Exp #2 CRISPR GRAPH 3 GRAPH 4 treatment cells on Day 17 of Puromycin selection Selected Cells EXPERIMENT #2 (Figure 4). 7 Day • CRISPR Lentivirus Repeat experiments using a lower FIV titer and higher anti-FIV CRISPR Incubation TRANSFECTION lentivirus titer to observe effects on proviral load Supported by: This project was generously funded by the UC Davis Center for Companion Animal Heath and supported by the UC Davis Students Training in Advance Research (STAR) Program. A special thank you to Center for Companion Animal Health • Perform an infectivity assay on FIV-free cells using the cell-free virus + Puromycin Dr. Murphy and his lab members, Dr. Diego Castillo, Andre Poon, and Megan Lew. An additional recognition to the Woolard-Borjesson-Tablin Labs for sharing their equipment, guidance, and positivity. SelectionSchool of Veterinary Medicine UC Davis Cell DNA harvested at the end of the experiments 17 Day FIV-C Lentivirus Isolate + Incubation INFECTION Naive MCH5-4 Cells Viral RNA 7 Day Incubation Non-CRISPR FIV Infected Cells CONTROL Cells CONTROL #2.
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