Victor L. Boyartchuk PHD
Title Assistant Professor
Institution University of Massachusetts Medical School
Department Microbiology & Physiological Systems
Address University of Massachusetts Medical School
364 Plantation Street, LRB-523
Worcester MA 01605
Telephone 508-856-4353
Email
Other Positions
Institution UMMS - School of Medicine
Department Program in Gene Function & Expression

Institution UMMS - School of Medicine
Department Program in Molecular Medicine

Institution UMMS - Graduate School of Biomedical Sciences
Department Immunology & Virology

Institution UMMS - Graduate School of Biomedical Sciences
Department Interdisciplinary Graduate Program

Institution UMMS - Graduate School of Biomedical Sciences
Department Molecular Genetics & Microbiology

Institution UMMS - Programs, Centers & Institutes
Department Center for AIDS Research
Narrative

Academic Background

Victor Boyartchuk received his M.S. in 1989 from the Kiev National University in Kiev, Ukraine, and his Ph.D. in 1998 from the University of California at Berkeley. From 1998 to 2002, he was a post-doctoral fellow in the Department of Genetics at Harvard Medical School, where his work was supported by a fellowship from the Irvington Institute for Immunological Research. Dr. Boyartchuck joined the Program in Gene Function and Expression at the University of Massachusetts Medical School as an Assistant Professor of Molecular Genetics and Microbiology in the spring of 2003.

Studies of the Genetic Factors Controlling Susceptibility to Infectious Diseases using Animal Model Systems

Photo: Victor L. Boyartchuk, PhDInnate immunity plays a critical role in the host's initial defense against infectious agents. My lab is interested in investigating the genetic basis that underlies differences in susceptibility to infectious diseases. Towards this goal, we are identifying and characterizing the variability in host genes which directly contribute to disease susceptibility. Analyzing the functional consequences of such polymorphisms will allow us to understand more fully the workings of the immune system.

Studies using inbred mouse strains have revealed a number of genetic differences in strain-specific immune responses to infectious diseases. One pathogen eliciting such a differential response is Listeria monocytogenes, a Gram positive facultative intracellular bacterium. Resistance to Listeria infection requires the participation of virtually all components of innate immunity, making this bacterium an ideal tool for studying innate immune functions. Using genetic analysis of differentially susceptible mouse strains, we have identified two major loci in the mouse genome that are likely to harbor genes controlling the course of Listeria infection. Systematic analysis of the expression of genes contained in these regions has identified several promising candidates. Our current work is directed towards identifying mutations that cause differential expression of these genes, and testing of the nature of their effect of the outcome of the infection.

Differences in host immune function usually result in very pleiotropic effects. Therefore, genes shown to affect susceptibility to one infectious disease are likely to play a role in determining the course of other infections. One of our future goals is to identify and characterize the range of pathogen responses that are controlled by each of the genes we are studying. Ultimately, we hope to apply the knowledge we have gained in our studies of disease susceptibility in animal models to customizing the management and treatment of infections in humans.

Publications
1. Zou T, Garifulin O, Berland R, Boyartchuk VL. Listeria monocytogenes Infection Induces Prosurvival Metabolic Signaling in Macrophages. Infect Immun. 2011 Apr; 79(4):1526-35.
  View in: PubMed
 
2. Lopes da Rosa J, Boyartchuk VL, Zhu LJ, Kaufman PD. Histone acetyltransferase Rtt109 is required for Candida albicans pathogenesis. Proc Natl Acad Sci U S A. 2010 Jan 26; 107(4):1594-9.
  View in: PubMed
 
3. Benoit VM, Petrich A, Alugupalli KR, Marty-Roix R, Moter A, Leong JM, Boyartchuk VL. Genetic control of the innate immune response to Borrelia hermsii influences the course of relapsing fever in inbred strains of mice. Infect Immun. 2010 Feb; 78(2):586-94.
  View in: PubMed
 
4. Chen YW, Boyartchuk V, Lewis BC. Differential roles of insulin-like growth factor receptor- and insulin receptor-mediated signaling in the phenotypes of hepatocellular carcinoma cells. Neoplasia. 2009 Sep; 11(9):835-45.
  View in: PubMed
 
5. Harrington JC, Wong SM, Rosadini CV, Garifulin O, Boyartchuk V, Akerley BJ. Resistance of Haemophilus influenzae to reactive nitrogen donors and gamma interferon-stimulated macrophages requires the formate-dependent nitrite reductase regulator-activated ytfE gene. Infect Immun. 2009 May; 77(5):1945-58.
  View in: PubMed
 
6. Chen YW, Klimstra DS, Mongeau ME, Tatem JL, Boyartchuk V, Lewis BC. Loss of p53 and Ink4a/Arf cooperate in a cell autonomous fashion to induce metastasis of hepatocellular carcinoma cells. Cancer Res. 2007 Aug 15; 67(16):7589-96.
  View in: PubMed
 
7. Garifulin O, Qi Z, Shen H, Patnala S, Green MR, Boyartchuk V. Irf3 polymorphism alters induction of interferon beta in response to Listeria monocytogenes infection. PLoS Genet. 2007 Sep; 3(9):1587-97.
  View in: PubMed
 
8. Wang F, Paradkar PN, Custodio AO, McVey Ward D, Fleming MD, Campagna D, Roberts KA, Boyartchuk V, Dietrich WF, Kaplan J, Andrews NC. Genetic variation in Mon1a affects protein trafficking and modifies macrophage iron loading in mice. Nat Genet. 2007 Aug; 39(8):1025-32.
  View in: PubMed
 
9. Garifulin O, Boyartchuk V. Listeria monocytogenes as a probe of immune function. Brief Funct Genomic Proteomic. 2005 Nov; 4(3):258-69.
  View in: PubMed
 
10. Boyartchuk V, Rojas M, Yan BS, Jobe O, Hurt N, Dorfman DM, Higgins DE, Dietrich WF, Kramnik I. The host resistance locus sst1 controls innate immunity to Listeria monocytogenes infection in immunodeficient mice. J Immunol. 2004 Oct 15; 173(8):5112-20.
  View in: PubMed
 
11. Shaw MH, Boyartchuk V, Wong S, Karaghiosoff M, Ragimbeau J, Pellegrini S, Muller M, Dietrich WF, Yap GS. A natural mutation in the Tyk2 pseudokinase domain underlies altered susceptibility of B10.Q/J mice to infection and autoimmunity. Proc Natl Acad Sci U S A. 2003 Sep 30; 100(20):11594-9.
  View in: PubMed
 
12. Laprade L, Boyartchuk VL, Dietrich WF, Winston F. Spt3 plays opposite roles in filamentous growth in Saccharomyces cerevisiae and Candida albicans and is required for C. albicans virulence. Genetics. 2002 Jun; 161(2):509-19.
  View in: PubMed
 
13. Boyartchuk V, Dietrich W. Genetic dissection of host immune response. Genes Immun. 2002 May; 3(3):119-22.
  View in: PubMed
 
14. Kramnik I, Boyartchuk V. Immunity to intracellular pathogens as a complex genetic trait. Curr Opin Microbiol. 2002 Feb; 5(1):111-7.
  View in: PubMed
 
15. Watters JW, Dewar K, Lehoczky J, Boyartchuk V, Dietrich WF. Kif1C, a kinesin-like motor protein, mediates mouse macrophage resistance to anthrax lethal factor. Curr Biol. 2001 Oct 2; 11(19):1503-11.
  View in: PubMed
 
16. Boyartchuk VL, Broman KW, Mosher RE, D'Orazio SE, Starnbach MN, Dietrich WF. Multigenic control of Listeria monocytogenes susceptibility in mice. Nat Genet. 2001 Mar; 27(3):259-60.
  View in: PubMed
 
17. Trueblood CE, Boyartchuk VL, Picologlou EA, Rozema D, Poulter CD, Rine J. The CaaX proteases, Afc1p and Rce1p, have overlapping but distinct substrate specificities. Mol Cell Biol. 2000 Jun; 20(12):4381-92.
  View in: PubMed
 
18. Boyartchuk VL, Rine J. Roles of prenyl protein proteases in maturation of Saccharomyces cerevisiae a-factor. Genetics. 1998 Sep; 150(1):95-101.
  View in: PubMed
 
19. Trueblood CE, Boyartchuk VL, Rine J. Substrate specificity determinants in the farnesyltransferase beta-subunit. Proc Natl Acad Sci U S A. 1997 Sep 30; 94(20):10774-9.
  View in: PubMed
 
20. Boyartchuk VL, Ashby MN, Rine J. Modulation of Ras and a-factor function by carboxyl-terminal proteolysis. Science. 1997 Mar 21; 275(5307):1796-800.
  View in: PubMed
 
21. Cheng JF, Boyartchuk V, Zhu Y. Isolation and mapping of human chromosome 21 cDNA: progress in constructing a chromosome 21 expression map. Genomics. 1994 Sep 1; 23(1):75-84.
  View in: PubMed
 
22. Ashby MN, Errada PR, Boyartchuk VL, Rine J. Isolation and DNA sequence of the STE14 gene encoding farnesyl cysteine: carboxyl methyltransferase. Yeast. 1993 Aug; 9(8):907-13.
  View in: PubMed
 
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Co-Authors  
Akerley, Brian
Green, Michael
Kaufman, Paul
Lewis, Brian
Zhu, Lihua
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Physical Neighbors  
He, Feng
Papavinasasundaram, Kadambavan
Ikebe, Mitsuo
Pryciak, Peter
Honeyman, Thomas

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