Spyridon Stavrou PhD

Spyridon Stavrou

Spyridon Stavrou
PhD

Assistant Professor

Department of Microbiology and Immunology

Jacobs School of Medicine & Biomedical Sciences


Specialty/Research Focus

Infectious Disease; Molecular and Cellular Biology; Transgenic organisms; Viral Pathogenesis; Virology

Contact Information
955 Main Street, Rm 5228
Buffalo, New York 14203
Phone: (716)-829-2994
stavrou2@buffalo.edu



Professional Summary:

Retroviruses comprise a large and diverse family of RNA viruses that can infect a variety of hosts and can lead to immune system dysfunction and cancer. The most well known member of this family is HIV (Human Immunodeficiency Virus), which is responsible for millions of deaths every year. Immune cells, such as CD4+ T cells, are the targets of HIV infection resulting in their subsequent destruction and the overall impairment of the immune system. As a result of the deterioration of the immune system, the host is unable to fight effectively infections and some other diseases. Opportunistic infections or cancers take advantage of the weakened host, which can prove to be lethal. Other members of the retrovirus family, Murine Leukemia Virus (MLV) and Mouse Mammary Tumor Virus (MMTV) are common pathogens of mice that are used in research to study the interplay between the host and retroviruses and have served as models for HIV and other human retroviruses.

In the context of the constant struggle between host cells and pathogens, cells have developed early innate immune and cell-intrinsic strategies to counteract retroviruses. Therefore, retroviruses have developed a variety of sophisticated mechanisms to counteract cellular responses and allow for productive infections to occur. Due to the complexity of the antiviral immune response, a full understanding of host-pathogen interactions requires the integration of in vitro and in vivo data, where the role of cellular restriction factors and the innate immune response are examined in a living organism. Infections in mouse models have provided important and at times surprising insights into the relationship between hosts and pathogens. Thus one of the areas of focus for our lab will be the integration of in vivo and in vitro models to study the interaction of novel cellular host factors and retroviruses.

HIV and other lentiviruses devote a relatively large portion of their genome to accessory proteins that counteract those cellular host factors. Understanding the function of these accessory proteins has provided insight into the intrinsic defenses utilized by the cell to block viral infections, as well as generated potential targets for antiviral interventions. However, there is no currently tractable in vivo model for studying cell host restriction factor/accessory protein interactions. Hence, the second major focus of our lab will be the development of in vivo models to examine the interplay between HIV accessory proteins and host cell intrinsic immunity.

Education and Training:

  • PhD, Microbiology, University of Chicago (2009)
  • MS, Molecular Biology, University of Pennsylvania (2003)
  • BA, Biology and Classical Studies, University of Pennsylvania (2001)

Employment:

  • Assistant Professor, Microbiology and Immunology, State University of New York at Buffalo Jacobs School of Medicine & Biomedical Sciences (2018-present)
  • Research Assistant Professor, Microbiology and Immunology, University of Illinois at Chicago, College of Medicine (2016–2018)
  • Post Doctoral Fellow, Microbiology, University of Pennsylvania, Perelman School of Medicine (2011–2016)
  • Graduate Student, Microbiology, University of Chicago (2003–2010)

Research Expertise:

  • Cell intrinsic immunity
  • Host cellular factors
  • Host-pathogens interactions
  • In vivo models of infection
  • Innate immunity
  • Retroviruses
  • Transgenic mice
  • Viral pathogenesis

Research Centers:

  • Witebsky Center for Microbial Pathogenesis and Immunology

UB 2020 Strategic Strengths:

  • Health and Wellness Across the Lifespan
  • Molecular Recognition in Biological Systems and Bioinformatics

Grants and Sponsored Research:

  • December 2021–November 2026
    MARCH proteins, members of a host protein family that targets HIV
    NIH/NIAID
    Role: Principal Investigator
    $1,974,920
  • August 2023–June 2024
    Grand Resubmission Award, R21 90K and SARS-CoV-2
    Role: Principal Investigator
    $15,000
  • May 2022–April 2024
    Elucidating the role of SERINC5 in SARS-CoV-2 infection
    NIAID
    Role: Principal Investigator
    $438,625
  • May 2022–April 2024
    Creation and validation of cell-based screening systems for SARS-CoV-2 drug targets
    NIAID
    Role: Co-Investigator
    $438,625
  • January 2022–December 2023
    Elucidating the antiviral role of LGALS3BP against SARS-CoV-2
    American Heart Association
    Role: Contributor
    $64,072
  • July 2022–June 2023
    Grant Resubmission Award, Hpse R21
    OVPRED
    Role: Principal Investigator
    $12,000
  • January 2020–December 2021
    The role of SERINC5 during retrovirus infection in vivo
    NIH/NIAID
    Role: Principal Investigator
    $435,650
  • August 2021–November 2021
    MARCH proteins, members of a host protein family that targets HIV
    NIAID
    Role: Principal Investigator
    $391,890
  • April 2018–March 2019
    A3G induced virus evolution
    amfAR Foundation
    Role: Principal Investigator
    $50,000
  • October 2014–September 2016
    A3G induced virus evolution
    amfAR Foundation
    Role: Principal Investigator
    $130,000
  • February 2013–January 2014
    The in vivo function of APOBEC3 during retrovirus infection
    National Institute of AIlergy and Infectious Diseases
    Role: Principal Investigator
    $53,942
See all (1 more)

Journal Articles:

See all (12 more)

Abstracts:

  • Umthong S., Timilsina U., Stavrou S. (2023) MARCH2, a T cell specific factor that inhibits HIV-1 infection. 33rd International Workshop on Retroviral Pathogenesis. Trento, (Dec) Oral
  • Waxman B., Timilsina U., Umthong S., Stavrou S. (2023) Heparanase blocks retrovirus infection by targeting proviral transcription. American Society of Virology. (Jun) Oral
  • Umthong S., Timilsina U., D’Angelo M., Stavrou S. (2023) Characterization of MARCH2 protein and its anti-HIV-1 function. HIV vaccines, Immunoprophylaxis, and Drugs. (Jun) Poster
  • Timilsina U., Umthong S., D’Angelo M., Stavrou S. (2023) MARCH2 restricts HIV-1 infection as a T cell specific factor. Cold Spring Harbor Laboratory, Retroviruses. (May) Oral
  • Waxman B., Timilsina U., Umthong S., Stavrou S. (2023) Heparanase blocks retrovirus infection by targeting provirus transcription. Cold Spring Harbor, Retroviruses. (May) Poster
  • Ivey EB, Timilsina U, Stavrou S. (2022) LGALS3BP/90K restricts SARS-CoV-2 infection by targeting the Spike glycoprotein. American Society of Virology. (Jul) Oral
  • Timilsina U, Umthong S, Stavrou S,. (2022) MARCH2, a T cell specific factor that restricts HIV-1 infection. American Society of Virology. (Jul) Oral
  • Waxman B, Timilsina U, Umthong S, Stavrou S,. (2022) Heparanase (HPSE), an ISG, blocks retrovirus infection at a post-integration step. American Society of Virology. (Jul) Poster; Oral
  • Stavrou S, Timilsina U, Umthong S,. (2022) SERINC5, a novel target of SARS-CoV-2 ORF7a. Positive-strand RNA Virus Meeting. Keystone, Colorado (Jun) Poster
  • Timilsina U., Umthong S., Stavrou S.,. (2021) SERINC5 potently restricts SARS-CoV-2 entry and is counteracted by Orf7a. American Society of Virology. (Jul) Oral
  • Umthong S., Lynch B., Timilsina U., Waxman B., Ivey EB., Stavrou S. (2021) Elucidating the role of MARCH family proteins on viral envelope glycoproteins. Retroviruses. Cold Spring Harbor, New York (Jun) Oral
  • Umthong S., Timilsina U., Waxman B., Lynch B., Stavrou S. (2020) Elucidating the roles of the murine MARCH protein family on retrovirus infection. ASV. Fort Collins/Virtual, Colorado (Jun) Oral
  • Timilsina U., Umthong S., Lynch B., Stavrou S. (2020) SERINC5-mediated restriction of MLV infection in vivo is dependent on glyco-Gag and the viral envelope. Retroviruses. Cold Spring Harbor, New York (May) Oral
  • Timilsina U., Umthong S., Stablewski A., Stavrou S. (2020) SERINC5 potently restricts retrovirus infection in vivo. ASV. Fort Collins/Virtual, Colorado (Jan) Oral
  • Stavrou S., Blouch K., Agarwal N., Bass A., Ross S.R.,. (2017) Sensing of reverse transcripts is critical for the in vivo control of retrovirus infection. American Society of Virology. Madison, Wisconsin (Jun) Oral
  • Stavrou S., Blouch K., Ross S.R. (2017) The nucleic acid sensor DDX41 recognizes retroviral RNA/DNA hybrids and is critical for controlling in vivo infection. Retroviruses. Cold Spring Harbor, New York (May) Oral
  • Stavrou S., Blouch K., Ross S.R. (2016) Sensing of reverse transcripts is critical for the in vivo control of retrovirus infection. The 28th International Workshop on Retrovirus Pathogenesis. New Orleans, Louisiana (Dec) Oral
  • Stavrou S., Blouch K., Ross S.R. (2015) The cytidine deamination domains (CDAs) of mouse APOBEC3 are dispensable for retrovirus restriction. Retroviruses. Cold Spring Harbor, New York (May) Poster
  • Cadena C., Stavrou S., Iyer S., Bibollet-Ruche F., Hahn B., Browne E.P., Ross S.R. (2015) Modeling HIV VIF/APOBEC3G interactions in mice. Retroviruses. Philadelphia, Pennsylvania (May) Poster
  • Stavrou S., Blouch K., Bass A., Ross S.R. (2015) DDX41, IFI203 and CGAS synergistically detect reverse transcripts and activate the type I IFN response. Retroviruses. Cold Spring Harbor, New York (May) Oral
See all (10 more)

Professional Memberships:

  • American Society of Virology (2018–present)
  • AAAS (2018–present)
  • American Society of Microbiology (2016–present)

Presentations:

  • "MARCH2, a host factor that inhibits HIV-1 infection in a T cell dependent manner" SUNY, University at Buffalo, Jacobs School of Medicine and Biomedical Sciences, Infectious Diseases Division (2023)
  • "Restriction factors and viral envelopes: From retroviruses to coronaviruses" Stony Brook University, Dept of Microbiology and Immunology (2023)
  • "MARCH proteins potently restrict retrovirus infection" Institut Pasteur de Montevideo (2023)
  • "SERINC5, a host factor with a broad repertoire of viral targets" University of Chicago, Dept of Microbiology (2023)
  • "SERINC5, a host factor with broad antiviral function" Oklahoma State University, Oklahoma Center for Respiratory and Infectious Diseases (OCRID) (2023)
  • "Heparanase, a novel regulator of proviral transcription" SUNY, University at Buffalo, Jacobs School of Medicine and Biomedical Sciences, Infectious Diseases Division (2022)
  • "SERINC5, an important antiviral gene, blocks SARS-CoV-2 infection and is counteracted by SARS-CoV-2 ORF7a" Chulalongkorn University, Pharmaceutical Sciences Division (2022)
  • "SERINC5, a novel target of SARS-CoV-2 ORF7a" UIC Department of Microbiology (2022)
  • "SERINC5, a potent factor of the host antiviral defense" Midwestern University, Department of Anatomy (2021)
  • "Elucidating the role of SARS-CoV-2 ORF7a" SUNY, University at Buffalo, Jacobs School of Medicine and Biomedical Sciences, Infectious Diseases Division (2021)
  • "Elucidating the antiviral role of MARCH proteins" IDI Viruses & Emerging Pathogens seminar series, Ohio State University (2021)
  • "Elucidating the antiviral role of MARCH proteins" SUNY, University at Buffalo, School of Dental Medicine, Oral Biology Department (2021)
  • "MARCH proteins potently restrict viral infections" SUNY, University at Buffalo, Jacobs School of Medicine and Biomedical Sciences, Infectious Diseases Division (2020)
  • "MARCH proteins potently restrict retrovirus infection" Annual Upstate New York Immunology Conference (2019)
  • "The role of host cell restriction factors on retrovirus infection" Roswell Park Comprehensive Cancer Center, Dept of Molecular and Cellular Biology (2019)
  • "APOBEC3 and cytosolic DNA sensors synergistically counteract retrovirus infection" University of Indiana, Dept of Microbiology and Immunology (2017)
  • "APOBEC3 and cytosolic DNA sensors synergistically counteract retrovirus infection" University of Illinois at Chicago, Dept of Microbiology and Immunology, (2016)
  • "APOBEC3 and cytosolic DNA sensors synergistically counteract retrovirus infection" University of Pennsylvania, Dept of Microbiology (2016)
  • "APOBEC3 and cytosolic DNA sensors synergistically counteract retrovirus infection" University of Texas A&M, Dept of Microbial Pathogenesis and Immunology (2016)
See all (9 more)

Service Activities:

  • 33rd International Workshop on Retrovirus Pathogenesis, Chair of the Innate Immunity session; Session Chair (2023)
  • PPBS Admission; Secondary Microbiology and Immunology reviewer (2023–present)
  • Integrated Canada’s Biomedical Research Fund and Biosciences Research Infrastructure Fund (CBRF-BRIF Stage 2); Ad hoc reviewer (2023)
  • Faculty Search Committee (2023–present)
  • UB/SUNY-UWI Global Infectious Diseases (GID) Research Training Program.; Mentor (2023–present)
  • CSTEP Research Symposium (2023)
  • NIH ZRG1 70C-S (20), Virology/Mycology Fellowship study section; Ad hoc reviewer (2023)
  • STEM Career Talk at the 2023 Summer Research Program for High School Students, St Bonaventure University; Invited speaker (2023)
  • American Society of Virology 2023 meeting, “Retroviruses I” Workshop Chair; Session Chair (2023)
  • Cold Spring Harbor, Retroviruses meeting, session Chair of the RNA, transport and Assembly session; Session Chair (2023)
  • Medical School Research Forum; Poster Judge (2023)
  • Faculty Search Committee (2022–2023)
  • 12th Annual UB Postdoc Research Symposium (2022)
  • PPBS Steering Committee (2022–present)
  • ASV Program Committee; Committee member (2022–present)
  • CSTEP Research Symposium (2022)
  • American Society of Virology 2022 meeting, “Retroviruses” Workshop Chair; Session Chair (2022)
  • VIRA study section; Ad hoc reviewer (2022)
  • Nature Communications; Ad hoc reviewer (2022–present)
  • Medical School Research Forum; Poster Judge (2022)
  • Frontiers in Immunology; Ad hoc reviewer (2022–present)
  • PPBS Admission; Primary Microbiology and Immunology reviewer (2021–2023)
  • NIH VIRA study section; ad hoc (2021)
  • Member of the UB Faculty senate; member (2021–2023)
  • CSTEP Research Symposium (2021)
  • American Society of Virology 2021 meeting, “Receptors, Attachment and Entry” Workshop co-Chair; Co-chair (2021)
  • Medical School Research forum; Poster Judge (2021)
  • Faculty Council (2020–present)
  • Medical School Research Forum; Poster Judge (2020)
  • Microorganisms; Ad hoc reviewer (2020–present)
  • Cell Reports; Ad hoc reviewer (2020–present)
  • Current Research in Virological Science; Ad hoc reviewer (2020–present)
  • Small GTPases; Ad hoc reviewer (2020–present)
  • PPBS admissions; Secondary Microbiology and Immunology reviewer (2019–2021)
  • New Frontiers Distinguished Seminar; Co-Organizer (2019–present)
  • CSTEP Research Symposium (2019)
  • AmfAR Mathilde Krim Fellowship reviewer; Ad hoc reviewer (2019)
  • PPBS Admissions; Interviewer (2019)
  • mBio; Ad hoc reviewer (2019–present)
  • Plos Pathogens; Ad hoc reviewer (2019–present)
  • Netter Award Selection Committee member, Western NY ASM Chapter; Award selection Committee (2018–2019)
  • Witebsky Center Annual Buffalo Conference on Microbial Pathogenesis; Conference co-organizer and host of Virology speaker (2018–present)
  • Gorzynski Award Selection; Committee Member (2018–2019)
  • Annual UB Postdoc Research Symposium; Poster Judge (2018–2019)
  • Plos One; Academic Editor (2018–present)
  • Journal of Cellular Biochemistry; Ad hoc reviewer (2018–present)
  • Cells; Ad hoc reviewer (2017–present)
  • Viruses; Ad Hoc Reviewer (2017–present)
  • Journal of Virology; Ad Hoc Reviewer (2016–present)

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Contact Information

955 Main Street, Rm 5228
Buffalo, New York 14203
Phone: (716)-829-2994
stavrou2@buffalo.edu