Andrew W Tai, MD, PhD
Internal Medicine, Division of Gastroenterology and Hepatology
1150 W. Medical Center Dr, 6510E MSRB I
Ann Arbor, MI 48109
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About
Andrew W. Tai, MD, PhD is an Associate Professor in the Department of Internal Medicine and in the Department of Microbiology & Immunology. Dr. Tai obtained his bachelor's degree in biochemistry from Harvard University, followed by a combined MD-PhD training program at the Weill Medical College of Cornell University. Following a residency in internal medicine at the Brigham and Women's Hospital in Boston, he completed a clinical and research fellowship in gastroenterology and hepatology at the Massachusetts General Hospital.
Dr. Tai joined the faculty at the University of Michigan in 2009. His research work focuses on the molecular mechanisms by which cells support RNA virus infection, such as by hepatitis C virus, dengue and Zika viruses, and SARS-CoV-2. He has been awarded a Research Scholar Award by the American Gastroenterological Association and is an elected member of the American Society for Clinical Investigation (ASCI). He is the Assistant Dean for Early Medical Education at the University of Michigan Medical School and has been recognized by multiple teaching awards.
In his spare time, he enjoys running, cycling, soccer, and downhill skiing.
Qualifications
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Clinical FellowMassachusetts General Hospital, Gastroenterology and Hepatology, Boston, MA, United States
2005 - 2009
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Research FellowMassachusetts General Hospital, Gastroenterology and Hepatology, Boston, MA, United States
2006 - 2009
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ResidencyBrigham and Women's Hospital, Internal Medicine, Boston, MA, United States
2003 - 2005
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InternshipBrigham and Women's Hospital, Internal Medicine, Boston, MA, United States
2002 - 2003
Research Overview
- Specialty
Gastroenterology, Internal Medicine
Area of practice
Liver disease, including viral hepatitis B and hepatitis C, cirrhosis, metabolic associated steatotic liver disease (MASLD); liver cancer including hepatocellular carcinoma.
All viruses are parasites in that they need to infect a cell in order to replicate and produce more viruses. During viral infection, viruses hijack many cellular proteins and cellular functions. My laboratory seeks to discover these cellular proteins and to understand how they are exploited during viral infection, as they may represent targets for antiviral therapies. We focus on a large class of viruses called “positive-strand RNA viruses” that includes many medically important viruses such as hepatitis C virus, dengue virus, Zika virus, and SARS-CoV-2 (the virus that causes COVID-19).
Recent Publications
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Sarkar R, Reid W, Sutanto R, Tai AW, Tsai B. Plos Pathogens, 2026 Jul 1; 22 (7):Journal ArticleThe Sigma1 ER membrane receptor promotes structural protein folding and genome packaging of dengue virus
DOI:10.1371/journal.ppat.1014347 PMID: 42461861 -
2026 Jun 10;PresentationUpdated Standard 7 - Curriculum Content for AY27-28
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2026 Jun 10;PresentationUpdated Standard 7 - Curriculum Content for AY27-28
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Tai A. 2026 Jun 10;PresentationThe hijacked cell: how positive-strand RNA viruses exploit the ER and protein quality control
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Guo S, Li X, Xun M, He Y, Tai AW, Wang H. Plos Pathogens, 2025 Nov 1; 21 (11 NOVEMBER):Journal ArticleDisrupted glycosylphosphatidylinositol anchoring induces ER stress and restricts enterovirus infection
DOI:10.1371/journal.ppat.1013685 PMID: 41252368 -
Zhang J, Kennedy A, de Melo Jorge DM, Xing L, Reid W, Bui S, Joppich J, Rose M, Ercan S, Tang Q, Ginsburg D, Tai AW, Wang Y. Plos Pathogens, 2025 Oct 10; 21 (6 June):Journal ArticleSARS-CoV-2 remodels the Golgi apparatus to facilitate viral assembly and secretion
DOI:10.1371/journal.ppat.1013295 -
Porter SS, Gilchrist TM, Schrodel S, Tai AW. Journal of Virology, 2025 Oct 10; 99 (2):Journal ArticleDengue and Zika virus NS4B proteins differ in topology and in determinants of ER membrane protein complex dependency
DOI:10.1128/jvi.01443-24 -
Elaimy AL, El-Derany MO, James J, Wang Z, Pearson AN, Holcomb EA, Huber AK, Gijón M, Bell HN, Sanghvi VR, Frankel TL, Su GL, Tapper EB, Tai AW, Ramnath N, Centonze CP, Dobrosotskaya I, Moeller JA, Bryant AK, Elliott DA, Choi E, Evans JR, Cuneo KC, Fitzgerald TJ, Wahl DR, Morgan MA, Chang DT, Wicha MS, Lawrence TS, Shah YM, Green MD. Jci Insight, 2025 Oct 10; 9 (21):Journal ArticleSLC4A11 mediates ammonia import and promotes cancer stemness in hepatocellular carcinoma
DOI:10.1172/jci.insight.184826
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