Ian Hogue
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Mail code: 7601Campus: Tempe
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Ian Hogue is an assistant professor in the Biodesign Center for Immunotherapy, Vaccines and Virotherapy and the School of Life Sciences at Arizona State University.
He earned a B.A. in molecular and cell biology at the University of California, Berkeley, where he performed undergraduate research on baculoviruses and worked as a laboratory technician studying alphavirus vaccine vectors at Chiron Corporation. He worked as a laboratory technician at University of Texas Southwestern Medical Center studying HIV-1 latency. He then earned his Ph.D. in microbiology and immunology at the University of Michigan, studying HIV-1 assembly. He then completed postdoctoral training at Princeton University, studying alpha herpesvirus egress and spread.
Professor Hogue’s research focuses on neurovirology, the molecular and cell biology of viruses in the nervous system. Specifically, his laboratory uses specialized live-cell fluorescence microscopy methods, cryo electron microscopy structural biology methods, and primary neuron cell culture methods to study how alpha herpesviruses interact with the molecular and cell biology of neurons.
- Postdoctoral Research, Princeton University
- Ph.D. Microbiology and Immunology, University of Michigan
- B.A. Molecular and Cell Biology, University of California-Berkeley
Neurovirology...
the study of viruses in the nervous system
Many diverse and unrelated viruses are capable of entering the nervous system, often causing severe neurological diseases. Viral neurological diseases are often acute (e.g. encephalitis), but can also cause or contribute to chronic neurodegenerative diseases. Some viruses enter the nervous system from the blood by breaching the blood-brain barrier, but others can directly infect neurons in the peripheral nervous system, and then spread from neuron to neuron via neuronal synapses. The diseases caused by rabies, polio, and herpes viruses have been known to humanity for millennia, and many newly emerging viral diseases such as West Nile and Zika viruses most recently, directly infect neurons. Most broadly, our laboratory is interested in the molecular and cellular mechanisms of how neurotropic viruses enter, transport within, and spread within the specialized cell biology of neurons.
Alpha Herpesviruses...
among the very few viruses evolved to exploit the mammalian nervous system
The herpesviruses constitute a large, ancient, and highly diverse family of viruses. There are herpesviruses of mammals, birds, reptiles, amphibians, fish, and even oysters, and for the most part, these viruses have co-evolved and co-speciated with their natural hosts for tens or hundreds of millions of years. There are nine human herpesviruses divided into three sub-families. The viruses in the alpha herpesvirus sub-family infect neurons, and are among the very few viruses that have evolved to make their living in the mammalian nervous system.
Human Alpha Herpesviruses:
- Herpes Simplex Virus 1 (HSV-1)
- Herpes Simplex Virus 2 (HSV-2)
- Varicella-Zoster Virus (VZV)
In the natural course of disease, these viruses infect the sensory and autonomic neurons of the peripheral nervous system, and establish a life-long latent infection in these neurons. Occasionally, the virus replication can reactivate, leading to asymptomatic shedding of virus, or the recurrence of herpetic lesions (e.g. oral and genital lesions in the case of HSV-1 and -2, and shingles in the case of VZV). Rarely, but most frequently in immunocompromised, newborn, and elderly patients, all three human alpha herpesviruses can spread to the central nervous system, causing severe herpes encephalitis. Critically, both the mild form of disease (herpetic lesions) and severe form of disease (herpes encephalitis) depends on the ability of virus particles to transport long distances inside infected neurons.
Major Projects
- Egress of Virus Particles from Infected Cells by Exocytosis
- Intracellular Sorting, Axonal Transport, and Egress in Primary Neurons
- Structural Biology of Viral Axonal Transport in collaboration with Dr. Wah Chiu, Stanford University.
Hogue IB, Ambrosini AE, Deshmukh N, Berry MJ, Enquist LW. Alpha Herpesvirus Egress and Spread from Neurons Uses Constitutive Secretory Mechanisms and Does Not Depend on Action Potential Firing. In preparation.
Hogue IB, Card JP, Rinaman L, Staniszewska Goraczniak H, Enquist LW. Characterization of the neuroinvasive profile of a pseudorabies virus recombinant expressing the mTurquoise2 reporter in single and multiple injection experiments. J Neurosci Methods, 308:228-239, 2018.
Chen H, Bartee M, Yaron J, Liu L, Zhang L, Zheng D, Hogue I, Bullard W, Tibbets S, Lucas A. Mouse Gamma Herpesvirus MHV-68 Induces Severe Gastrointestinal (GI) Dilatation in Interferon Gamma Receptor-Deficient Mice (IFNγR−/−) That Is Blocked by Interleukin-10. Viruses, 10(10):518, 2018.
Hogue IB, Jean J, Scherer J, Enquist LW. A Functional Carboxy-Terminal Fluorescent Protein Fusion to Pseudorabies Virus Small Capsid Protein VP26. J Virology, 92(1):e01193-17, 2018.
Koyuncu OO, MacGibeny MA, Hogue IB, Enquist LW. Compartmented neuronal cultures reveal two distinct mechanisms for alpha herpesvirus escape from genome silencing. PLOS Pathogens, 13(10):e1006608, 2017.
Hogue IB, Scherer J, Enquist LW. Exocytosis of Alphaherpesvirus Virions, Light Particles, and Glycoproteins Uses Constitutive Secretory Mechanisms. mBio, 7(3): e00820-16, 2016.
Johnson BN, Lancaster KZ, Hogue IB, Meng F, Kong YL, Enquist LW, McAlpine, MC. 3D Printed Nervous System on a Chip. Lab on a Chip, 16(8):1393-1400, 2015. Featured in: The Royal Society of Chemistry’s Lab on a Chip 3D Printing Collection, 2016.
Bosse JB, Tanneti NS, Hogue IB, Enquist LW. Open LED Illuminator: A simple and inexpensive LED illuminator for fast multicolor particle tracking in neurons. PLOS One, 10(11):e0143547, 2015.
Hogue IB, Bosse JB, Engel EA, Scherer J, Hu J-R, del Rio T, Enquist LW. Fluorescent Protein Approaches in Alpha Herpesvirus Research. Viruses, 7:5933-5961, 2015.
Bosse JB, Hogue IB, Feric M, Thiberge SY, Sodeik B, Brangwynne CP, Enquist LW. Remodeling nuclear architecture allows efficient transport of herpesvirus capsids by diffusion. PNAS, 112(42):E5725-E5733, 2015.
Hogue IB, Bosse JB, Hu J-R, Thiberge SY, Enquist LW. Cellular Mechanisms of Alpha Herpesvirus Egress: Live Cell Fluorescence Microscopy of Pseudorabies Virus Exocytosis. PLOS Pathogens, 10(12):e1004535, 2014.
Nguyen TD, Hogue IB, Cung K, Purohit PK, McAlpine MC. Tension induced neurite growth in microfluidic channels. Lab on a Chip, 13(18):3735-3740, 2013.
Sun XR, Badura A, Pacheco DA, Lynch LA, Schneider ER, Taylor MP, Hogue IB, Enquist LW, Murthy M, Wang SS-H. Fast GCaMPs for improved tracking of neuronal activity. Nature Communications, 4:2170, 2013.
Koyuncu OO, Hogue IB, Enquist LW. Virus Infections in the Nervous System. Cell Host & Microbe, 13(4):379-93, 2013.
Hogue IB, Llewellyn GN, Ono A. Dynamic Association between HIV-1 Gag and Membrane Domains. Molecular Biology International, 2012.
Hogue IB, Grover JR, Soheilian F, Nagashima K, Ono A. Gag induces the coalescence of clustered lipid rafts and tetraspanin-enriched microdomains at HIV-1 assembly sites on the plasma membrane. J Virology, 85(19):9749-66, 2011.
Llewellyn GN, Hogue IB, Grover JR, Ono A. Nucleocapsid promotes localization of HIV-1 Gag to uropods that participate in virological synapses between T Cells. PLOS Pathogens, 6(10):e1001167, 2010.
Hogue IB, Hoppe A, Ono A. Quantitative fluorescence resonance energy transfer microscopy analysis of the human immunodeficiency virus type 1 Gag-Gag interaction: relative contributions of the CA and NC domains and membrane binding. J Virology, 83(14):7322-36, 2009.
Bauer AL, Hogue IB, Marino S, Kirschner DE. The Effects of HIV-1 Infection on Latent Tuberculosis. Mathematical Modelling of Natural Phenomena, 3(7):229, 2008.
Marino S, Hogue IB, Ray CJ, Kirschner DE. A methodology for performing global uncertainty and sensitivity analysis in systems biology. J Theoretical Biology, 254(1):178-96, 2008.
Hogue IB, Bajaria SH, Fallert BA, Qin S, Reinhart TA, Kirschner DE. The dual role of dendritic cells in the immune response to human immunodeficiency virus type 1 infection. J General Virology, 89(9):2228-2239, 2008. Featured in: The Society for General Microbiology’s Microbiology Today, November 2008.
Chukkapalli V, Hogue IB, Boyko V, Hu WS, Ono A. Interaction between Gag matrix domain and phosphatidylinositol-(4,5)-bisphosphate is essential for efficient Gag-membrane binding. J Virology, 82(5):2405-17, 2008.
Lehrman G, Hogue IB, Palmer S, Jennings C, Spina CA, Wiegand A, Landay AL, Coombs RW, Richman DD, Mellors JW, Coffin JM, Bosch RJ, Margolis DM. Depletion of latent HIV-1 infection in vivo: a proof-of-concept study. Lancet, 366(9485):549-55, 2005.
Courses
2025 Spring
Course Number | Course Title |
---|---|
BCH 392 | Intro to Research Techniques |
BCH 492 | Honors Directed Study |
BCH 493 | Honors Thesis |
CHM 392 | Intro to Research Techniques |
CHM 492 | Honors Directed Study |
CHM 493 | Honors Thesis |
MIC 495 | Undergraduate Research |
MBB 495 | Undergraduate Research |
BIO 495 | Undergraduate Research |
BDE 799 | Dissertation |
BDE 792 | Research |
MIC 590 | Reading and Conference |
CHM 392 | Intro to Research Techniques |
BCH 392 | Intro to Research Techniques |
BDE 795 | Continuing Registration |
BDE 799 | Dissertation |
BCH 392 | Intro to Research Techniques |
2024 Fall
Course Number | Course Title |
---|---|
BCH 392 | Intro to Research Techniques |
BCH 492 | Honors Directed Study |
BCH 493 | Honors Thesis |
BIO 353 | Cell Biology |
CHM 392 | Intro to Research Techniques |
CHM 492 | Honors Directed Study |
MIC 495 | Undergraduate Research |
BIO 494 | Special Topics |
BIO 495 | Undergraduate Research |
CHM 493 | Honors Thesis |
BCH 392 | Intro to Research Techniques |
BIO 394 | Special Topics |
CHM 392 | Intro to Research Techniques |
MIC 598 | Special Topics |
2024 Summer
Course Number | Course Title |
---|---|
BDE 792 | Research |
BIO 495 | Undergraduate Research |
MBB 495 | Undergraduate Research |
2024 Spring
Course Number | Course Title |
---|---|
MIC 495 | Undergraduate Research |
MBB 495 | Undergraduate Research |
BIO 495 | Undergraduate Research |
BDE 799 | Dissertation |
BDE 792 | Research |
MIC 591 | Seminar |
MIC 590 | Reading and Conference |
MBB 591 | Seminar |
BDE 795 | Continuing Registration |
MIC 598 | Special Topics |
BDE 799 | Dissertation |
BIO 494 | Special Topics |
BIO 591 | Seminar |
MBB 494 | Special Topics |
MCB 591 | Seminar |
MIC 494 | Special Topics |
MIC 591 | Seminar |
NEU 591 | Seminar |
2023 Fall
Course Number | Course Title |
---|---|
BIO 353 | Cell Biology |
MIC 495 | Undergraduate Research |
BIO 494 | Special Topics |
BIO 495 | Undergraduate Research |
BIO 394 | Special Topics |
MIC 591 | Seminar |
2023 Summer
Course Number | Course Title |
---|---|
BDE 792 | Research |
2023 Spring
Course Number | Course Title |
---|---|
MIC 495 | Undergraduate Research |
BIO 495 | Undergraduate Research |
BDE 799 | Dissertation |
BDE 792 | Research |
BIO 591 | Seminar |
BIO 494 | Special Topics |
NEU 591 | Seminar |
MCB 591 | Seminar |
MIC 591 | Seminar |
MCB 494 | Special Topics |
MIC 494 | Special Topics |
MIC 591 | Seminar |
MIC 590 | Reading and Conference |
MBB 494 | Special Topics |
MBB 591 | Seminar |
BDE 795 | Continuing Registration |
BDE 799 | Dissertation |
2022 Fall
Course Number | Course Title |
---|---|
BIO 353 | Cell Biology |
MIC 495 | Undergraduate Research |
BIO 494 | Special Topics |
BIO 495 | Undergraduate Research |
MIC 591 | Seminar |
BIO 590 | Reading and Conference |
BIO 394 | Special Topics |
2022 Summer
Course Number | Course Title |
---|---|
BDE 792 | Research |
2022 Spring
Course Number | Course Title |
---|---|
MIC 495 | Undergraduate Research |
BIO 495 | Undergraduate Research |
BDE 799 | Dissertation |
BDE 792 | Research |
MIC 591 | Seminar |
MIC 791 | Seminar |
BIO 591 | Seminar |
BIO 494 | Special Topics |
NEU 591 | Seminar |
MCB 591 | Seminar |
MIC 591 | Seminar |
NEU 494 | Special Topics |
MCB 494 | Special Topics |
MIC 494 | Special Topics |
MIC 591 | Seminar |
MIC 590 | Reading and Conference |
MBB 494 | Special Topics |
MBB 591 | Seminar |
BDE 792 | Research |
BDE 795 | Continuing Registration |
BDE 799 | Dissertation |
2021 Fall
Course Number | Course Title |
---|---|
BIO 353 | Cell Biology |
MIC 495 | Undergraduate Research |
BIO 494 | Special Topics |
BIO 495 | Undergraduate Research |
MIC 591 | Seminar |
BIO 590 | Reading and Conference |
BIO 394 | Special Topics |
2021 Summer
Course Number | Course Title |
---|---|
BDE 792 | Research |
2021 Spring
Course Number | Course Title |
---|---|
MIC 495 | Undergraduate Research |
BIO 495 | Undergraduate Research |
BDE 799 | Dissertation |
BDE 792 | Research |
MIC 591 | Seminar |
MIC 791 | Seminar |
BIO 591 | Seminar |
BIO 494 | Special Topics |
NEU 591 | Seminar |
MCB 591 | Seminar |
MIC 591 | Seminar |
NEU 494 | Special Topics |
MCB 494 | Special Topics |
MIC 494 | Special Topics |
MIC 591 | Seminar |
MIC 590 | Reading and Conference |
MBB 494 | Special Topics |
MBB 591 | Seminar |
MIC 498 | Pro-Seminar |
2020 Fall
Course Number | Course Title |
---|---|
BIO 353 | Cell Biology |
MIC 495 | Undergraduate Research |
BIO 494 | Special Topics |
MIC 591 | Seminar |
MIC 791 | Seminar |
BIO 495 | Undergraduate Research |
BIO 353 | Cell Biology |
MIC 591 | Seminar |
MIC 498 | Pro-Seminar |
BIO 353 | Cell Biology |
BIO 590 | Reading and Conference |
2020 Summer
Course Number | Course Title |
---|---|
BDE 792 | Research |
2020 Spring
Course Number | Course Title |
---|---|
MIC 495 | Undergraduate Research |
BIO 495 | Undergraduate Research |
BDE 799 | Dissertation |
BDE 792 | Research |
MIC 591 | Seminar |
MIC 791 | Seminar |
BIO 591 | Seminar |
BIO 494 | Special Topics |
NEU 591 | Seminar |
MCB 591 | Seminar |
MIC 591 | Seminar |
NEU 494 | Special Topics |
MCB 494 | Special Topics |
MIC 494 | Special Topics |
MIC 591 | Seminar |
MIC 590 | Reading and Conference |
MBB 494 | Special Topics |
MBB 591 | Seminar |
MIC 498 | Pro-Seminar |
MIC 498 | Pro-Seminar |
2019 Fall
Course Number | Course Title |
---|---|
MIC 495 | Undergraduate Research |
MIC 591 | Seminar |
MIC 791 | Seminar |
MIC 591 | Seminar |
MIC 498 | Pro-Seminar |