{"id":1063,"date":"2016-12-05T20:54:50","date_gmt":"2016-12-05T20:54:50","guid":{"rendered":"http:\/\/vivid7.vetmed.illinois.edu\/wp\/inoue-lab\/?page_id=2"},"modified":"2025-12-15T15:33:42","modified_gmt":"2025-12-15T21:33:42","slug":"publications","status":"publish","type":"page","link":"https:\/\/vetmed.illinois.edu\/jarosinski-lab\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"

PUBLICATIONS<\/h2>\n<\/div>
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  1. *Akbar H<\/strong>, Ponnuraj N<\/strong>, Shuaib M,\u00a0 Spatz SJ, Jarosinski KW<\/strong>. 2025<\/strong>. Integrated transcriptomics, proteomics, and pathway enrichment analysis in the spleen and skin of chickens reveal tissue-specific roles for the Marek\u2019s disease virus conserved herpesvirus protein kinase. Poultry Sci<\/em>, 105(1):106113. https:\/\/doi.org\/10.1016\/j.psj.2025.106113<\/a><\/li>\n
  2. *Xu H<\/strong>, Vega-Rodriguez W<\/strong>, Van Etten K<\/strong>, Jarosinski KW. 2025.<\/strong> The requirement of turkey herpesvirus (HVT) glycoprotein C during natural infection in chickens and turkeys. Pathogens<\/em>, 14(6):538 https:\/\/doi.org\/10.3390\/pathogens14060538<\/a><\/li>\n
  3. *Van Etten K<\/strong>, Lundberg E<\/strong>, Zafar HS<\/strong>, Jarosinski KW<\/strong>. 2025<\/strong> Avian model systems to understand human herpesvirus replication, transformation, reactivation, and transmission. Future Virology<\/em>, 1\u201316. https:\/\/doi.org\/10.1080\/17460794.2025.2463249<\/a><\/li>\n
  4. *Akbar H<\/strong>,\u00a0Jarosinski KW.<\/strong> 2024.<\/strong> Temporal dynamics of purinergic receptor expression in the lungs of Marek\u2019s disease (MD) virus-infected chickens resistant or susceptible to MD. Viruses.<\/em> 16(7):1130. https:\/\/doi.org\/10.3390\/v16071130<\/a> (Citations = )<\/li>\n
  5. *Zafar HS<\/strong>, Akbar H<\/strong>, Xu H<\/strong>, Ponnuraj N<\/strong>, Van Etten K<\/strong>, Jarosinski KW<\/strong>. 2024<\/strong>. Oncogenic Animal Herpesviruses. Curr Opin Virol. 8(67);101424. https:\/\/doi.org\/10.1016\/j.coviro.2024.101424<\/a><\/li>\n
  6. *Xu H<\/strong>, Vega-Rodriguez W<\/strong>, Campos V<\/strong>, Jarosinski K. 2024.<\/strong> mRNA splicing of UL44 and secretion of Alphaherpesvirinae<\/em> glycoprotein C (gC) is conserved among the Mardiviruses<\/em>. Viruses<\/em>. 16(5);782. https:\/\/doi.org\/10.3390\/v16050782<\/a><\/li>\n
  7. *Volkening J, Spatz SJ, Ponnuraj N<\/strong>, Akbar H<\/strong>, Arrington JV, Jarosinski KW<\/strong>. Viral proteogenomic and expression profiling during productive replication of a skin-tropic herpesvirus in the natural host. PLoS Pathog<\/em>. 2023; 19(6): e11011204. https:\/\/journals.plos.org\/plospathogens\/article?id=10.1371\/journal.ppat.1011204<\/a><\/li>\n
  8. *Tien, YT<\/strong>, Akbar H<\/strong>,\u00a0Jarosinski KW.<\/strong> 2023. Temperature-induced reactivation of Marek\u2019s disease virus-transformed T cells ex vivo<\/em>. Front Vet Sci.<\/em> 10:1145757. https:\/\/doi.org\/10.3389\/fvets.2023.1145757<\/a><\/li>\n
  9. *Ponnuraj N<\/strong>, Akbar H<\/strong>, Arrington JV, Spatz SJ, Nagarajan B, Desai UR, Jarosinski KW.<\/strong> 2023. The alphaherpesvirus conserved pUS10 is important for natural infection and its expression is regulated by the conserved Herpesviridae <\/em>protein kinase (CHPK). PLoS Pathog.<\/em> 19(2): e1010959. https:\/\/doi.org\/10.1371\/journal.ppat.1010959<\/a><\/li>\n
  10. *Akbar H<\/strong>, Fasick JJ<\/strong>, Ponnuraj N<\/strong>, Jarosinski KW.<\/strong> 2023. Purinergic signaling during Marek\u2019s disease in chickens. Sci Rep.<\/em> 13(1);2044. https:\/\/doi.org\/10.1038\/s41598-023-29210-x<\/a><\/li>\n
  11. *Xu H<\/strong>, Krieter AL<\/strong>, Ponnuraj N<\/strong>, Tien YT<\/strong>, Kim T, Jarosinski KW.<\/strong> 2022.<\/strong> Coinfection in the host can result in functional complementation between live vaccines and virulent virus. Virulence<\/em>. 13(1);980. https:\/\/doi.org\/10.1080\/21505594.2022.2082645<\/a><\/li>\n
  12. *Krieter A<\/strong>, Xu H<\/strong>, Akbar H<\/strong>, Kim T, Jarosinski KW.<\/strong> 2022 The conserved Herpesviridae <\/em>protein kinase (CHPK) of Gallid alphaherpesvirus<\/em> 3 (GaHV3) in required for horizontal spread and natural infection in chickens. Viruses<\/em>. 14(3):586. https:\/\/doi.org\/10.3390\/v14030586<\/a><\/li>\n
  13. Gatherer D, Depledge DP, Hartley CA, Szpara ML, Vaz PK, Benk\u0151 M, Brandt CR, Bryant NA, Dastjerdi A, Doszpoly A, Gompels UA, Inoue N,\u00a0Jarosinski KW<\/strong>, Kaul R, Lacoste V, Norberg P, Origgi FC, Orton RJ, Pellett PE, Schmid DS, Spatz SJ, Stewart JP, Trimpert J, Waltzek TB, Davison AJ. 2021. ICTV virus taxonomy profile: Herpesviridae <\/em> J Gen Virol <\/em>102(10):001673. <\/em><\/strong>https:\/\/doi.org\/10.1099\/jgv.0.001673<\/a><\/li>\n
  14. *Vega-Rodriguez W<\/strong>, Ponnuraj N<\/strong>, Garcia M, Jarosinski KW<\/strong>. 2021. The requirement of glycoprotein C for interindividual spread is functionally conserved within the Alphaherpesvirus genus (Mardivirus<\/em>), but not the host (Gallid<\/em>). Viruses<\/em> 13(8):1419. https:\/\/doi.org\/10.3390\/v13081419<\/a><\/li>\n
  15. *Vega-Rodriguez W<\/strong>, Xu H<\/strong>, Ponnuraj N<\/strong>, Akbar H<\/strong>, Kim T, Jarosinski KW<\/strong>. 2021. The requirement of glycoprotein C (gC) for interindividual spread is a conserved function of gC for avian herpesviruses. Sci Rep<\/em> 11(1):7753. https:\/\/doi.org\/10.1038\/s41598-021-87400-x<\/a><\/li>\n
  16. *Krieter A<\/strong>, Ponnuraj N<\/strong>, Jarosinski KW<\/strong>. 2020. Expression of the conserved herpesvirus protein kinase (CHPK) of Marek’s disease alphaherpesvirus in the skin reveals a mechanistic importance for CHPK during interindividual spread in chickens. J Virol <\/em>94:e01522-01519. https:\/\/doi.org\/10.1128\/JVI.01522-19<\/a><\/li>\n
  17. Girsch JH, Jackson W, Carpenter JE, Moninger TO, Jarosinski KW<\/strong>, Grose C. 2020. Exocytosis of progeny infectious varicella-zoster virus particles via a mannose-6-phosphate receptor pathway without xenophagy following secondary envelopment. J Virol <\/em>94: e00800-00820. https:\/\/doi.org\/10.1128\/jvi.00800-20<\/a><\/li>\n
  18. Burrell CE, Anchor C, Ahmed N, Landolfi J, Jarosinski KW<\/strong>, Terio KA. 2020. Characterization and comparison of SLAM\/CD150 in free-ranging coyotes, raccoons, and Skunks in Illinois for Elucidation of Canine Distemper Virus Disease. Pathogens<\/em> 9:e510. https:\/\/doi.org\/10.3390\/pathogens9060510<\/a><\/li>\n
  19. *Vega-Rodriguez W<\/strong>, Ponnuraj N<\/strong>, Jarosinski KW<\/strong>. 2019. Marek’s disease alphaherpesvirus (MDV) RLORF4 is not required for expression of glycoprotein C and interindividual spread. Virology <\/em>534:108-113. https:\/\/doi.org\/10.1016\/j.virol.2019.06.008<\/a><\/li>\n
  20. *Ponnuraj N<\/strong>, Tien YT<\/strong>, Vega-Rodriguez W<\/strong>, Krieter A<\/strong>, Jarosinski KW<\/strong>. 2019. The Herpesviridae conserved multifunctional infected-cell protein 27 (ICP27) is important but not required for replication and oncogenicity of Marek’s disease alphaherpesvirus. J Virol <\/em>93:e01903-01918. https:\/\/doi.org\/10.1128\/jvi.01903-18<\/a><\/li>\n
  21. Jarosinski KW<\/strong>, Carpenter JE, Buckingham EM, Jackson W, Knudtson K, Moffat JF, Kita H, Grose C. 2018. Cellular stress response to varicella-zoster virus infection of human skin includes highly elevated interleukin-6 expression. Open Forum Infect Dis<\/em> 5:ofy118. https:\/\/doi.org\/10.1093\/ofid\/ofy118<\/a><\/li>\n
  22. *Jarosinski KW. <\/strong> Interindividual Spread of Herpesviruses. In: Cell Biology of Herpes Viruses<\/em>, Adv Anat Embryol Cell Biol<\/em> 223:195-224. https:\/\/doi.org\/10.1007\/978-3-319-53168-7_9<\/a><\/li>\n
  23. Buckingham EM, Jarosinski KW<\/strong>, Jackson W, Carpenter JE, Grose C. 2016. Exocytosis of varicella-zoster virus virions involves a convergence of endosomal and autophagy pathways. J Virol <\/em>90:8673-8685. https:\/\/doi.org\/10.1128\/jvi.00915-16<\/a><\/li>\n
  24. Schippers T, Jarosinski K<\/strong>, Osterrieder N. 2015. The ORF012 gene of Marek’s disease virus type 1 produces a spliced transcript and encodes a novel nuclear phosphoprotein essential for virus growth. J Virol<\/em> 89:1348-1363. https:\/\/doi.org\/10.1128\/jvi.02687-14<\/a><\/li>\n
  25. *Jarosinski KW<\/strong>, Vautherot JF. 2015. Differential expression of Marek’s disease virus (MDV) late proteins during in vitro and in situ replication: role for pUL47 in regulation of the MDV UL46-UL49 gene locus. Virology<\/em> 484:213-226. https:\/\/doi.org\/10.1016\/j.virol.2015.06.012<\/a><\/li>\n
  26. *Jarosinski KW<\/strong>, Donovan KM, Du G. 2015. Expression of fluorescent proteins within the repeat long region of the Marek’s disease virus genome allows direct identification of infected cells while retaining full pathogenicity. Virus Res<\/em> 201:50-60. https:\/\/doi.org\/10.1016\/j.virusres.2015.02.012<\/a><\/li>\n
  27. *Veiga IB, Jarosinski KW<\/strong>, Kaufer BB, Osterrieder N. 2013. Marek’s disease virus (MDV) ubiquitin-specific protease (USP) performs critical functions beyond its enzymatic activity during virus replication. Virology<\/em> 437:110-117. https:\/\/doi.org\/10.1016\/j.virol.2013.01.003<\/a><\/li>\n
  28. Shaikh SA, Katneni UK, Dong H, Gaddamanugu S, Tavlarides-Hontz P, Jarosinski KW<\/strong>, Osterrieder N, Parcells MS. 2013. A deletion in the glycoprotein L (gL) gene of U.S. Marek’s disease virus (MDV) field strains is insufficient to confer increased pathogenicity to the bacterial artificial chromosome (BAC)-based strain, RB-1B. Avian Dis<\/em> 57:509-518. https:\/\/doi.org\/10.1637\/10450-112012-reg.1<\/a><\/li>\n
  29. Schat KA, Piepenbrink MS, Buckles EL, Schukken YH, Jarosinski KW<\/strong>. 2013. Importance of differential expression of Marek’s disease virus gene pp38 for the pathogenesis of Marek’s disease. Avian Dis<\/em> 57:503-508. https:\/\/doi.org\/10.1637\/10414-100612-Reg.1<\/a><\/li>\n
  30. *Jarosinski KW<\/strong>, Osterrieder N. 2012. Marek’s disease virus expresses multiple UL44 (gC) variants through mRNA splicing that are all required for efficient horizontal transmission. J Virol<\/em> 86:7896-7906. https:\/\/doi.org\/10.1128\/jvi.00908-12<\/a><\/li>\n
  31. *Jarosinski KW<\/strong>, Arndt S, Kaufer BB, Osterrieder N. 2012. Fluorescently tagged pUL47 of Marek’s disease virus reveals differential tissue expression of the tegument protein in vivo. J Virol<\/em> 86:2428-2436. https:\/\/doi.org\/10.1128\/jvi.06719-11<\/a><\/li>\n
  32. *Jarosinski KW<\/strong>. 2012. Marek’s disease virus late protein expression in feather follicle epithelial cells as early as 8 days postinfection. Avian Dis<\/em> 56:725-731. https:\/\/doi.org\/10.1637\/10252-052212-reg.1<\/a><\/li>\n
  33. *Jarosinski KW<\/strong>. 2012. Dual infection and superinfection inhibition of epithelial skin cells by two alphaherpesviruses co-occur in the natural host. PLoS One<\/em> 7:e37428. https:\/\/doi.org\/10.1371\/journal.pone.0037428<\/a><\/li>\n
  34. Kaufer BB, Jarosinski KW<\/strong>, Osterrieder N. 2011. Herpesvirus telomeric repeats facilitate genomic integration into host telomeres and mobilization of viral DNA during reactivation. J Exp Med <\/em>208:605-615. https:\/\/doi.org\/10.1084\/jem.20101402<\/a><\/li>\n
  35. *Kaufer BB, Arndt S, Trapp S, Osterrieder N, Jarosinski KW<\/strong>. Herpesvirus telomerase RNA (vTR) with a mutated template sequence abrogates herpesvirus-induced lymphomagenesis. PLoS Pathog<\/em> 7:<\/strong>e1002333. https:\/\/doi.org\/10.1371\/journal.ppat.1002333<\/a><\/li>\n
  36. Kaufer BB, Trapp S, Jarosinski KW<\/strong>, Osterrieder N. 2010. Herpesvirus telomerase RNA(vTR)-dependent lymphoma formation does not require interaction of vTR with telomerase reverse transcriptase (TERT). PLoS Pathog <\/em>6:e1001073. https:\/\/doi.org\/10.1371\/journal.ppat.1001073<\/a><\/li>\n
  37. *Jarosinski KW<\/strong>, Osterrieder N. 2010. Further analysis of Marek’s disease virus horizontal transmission confirms that U(L)44 (gC) and U(L)13 protein kinase activity are essential, while U(S)2 is nonessential. J Virol<\/em> 84:7911-7916. https:\/\/doi.org\/10.1128\/jvi.00433-10<\/a><\/li>\n
  38. *Jarosinski KW<\/strong>, Hunt HD, Osterrieder N. 2010. Down-regulation of MHC class I by the Marek’s disease virus (MDV) UL49.5 gene product mildly affects virulence in a haplotype-specific fashion. Virology<\/em> 405:457-463. https:\/\/doi.org\/10.1016\/j.virol.2010.06.041<\/a><\/li>\n
  39. Chbab N, Egerer A, Veiga I, Jarosinski KW<\/strong>, Osterrieder N. 2010. Viral control of vTR expression is critical for efficient formation and dissemination of lymphoma induced by Marek’s disease virus (MDV). Vet Res<\/em> 41:56. https:\/\/doi.org\/10.1051\/vetres\/2010026<\/a><\/li>\n
  40. Fulton A, Peters ST, Perkins GA, Jarosinski KW<\/strong>, Damiani A, Brosnahan M, Buckles EL, Osterrieder N, Van de Walle GR. 2009. Effective treatment of respiratory alphaherpesvirus infection using RNA interference. PLoS One<\/em> 4:e4118. https:\/\/doi.org\/10.1371\/journal.pone.0004118<\/a><\/li>\n
  41. Buscaglia C, O’Connell PH, Jarosinski KW<\/strong>, Pevzner I, Schat KA. 2009. Selection for increased nitric oxide production does not increase resistance to Marek’s disease in a primary broiler breeder line. Avian Dis<\/em> 53:336-340. https:\/\/doi.org\/10.1637\/8536-113008-reg.1<\/a><\/li>\n
  42. Van de Walle GR, Jarosinski KW<\/strong>, Osterrieder N. Alphaherpesviruses and chemokines: pas de deux not yet brought to perfection. J Virol<\/em> 82:<\/strong>6090-6097. https:\/\/doi.org\/10.1128\/jvi.00098-08<\/a><\/li>\n
  43. Miller MM, Jarosinski KW<\/strong>, Schat KA. 2008. Negative modulation of the chicken infectious anemia virus promoter by COUP-TF1 and an E box-like element at the transcription start site binding deltaEF1. J Gen Virol<\/em> 89:2998-3003. https:\/\/doi.org\/10.1099\/vir.0.2008\/003103-0<\/a><\/li>\n
  44. *Jarosinski KW<\/strong>, Schat KA. 2007. Multiple alternative splicing to exons II and III of viral interleukin-8 (vIL-8) in the Marek’s disease virus genome: the importance of vIL-8 exon I. Virus Genes<\/em> 34:9-22. https:\/\/doi.org\/10.1007\/s11262-006-0004-9<\/a><\/li>\n
  45. *Jarosinski KW<\/strong>, Margulis NG, Kamil JP, Spatz SJ, Nair VK, Osterrieder N. 2007. Horizontal transmission of Marek’s disease virus requires US2, the UL13 protein kinase, and gC. J Virol<\/em> 81:10575-10587. https:\/\/doi.org\/10.1128\/jvi.01065-07<\/a><\/li>\n
  46. Jarosinski K<\/strong>, Kattenhorn L, Kaufer B, Ploegh H, Osterrieder N. 2007. A herpesvirus ubiquitin-specific protease is critical for efficient T cell lymphoma formation. Proc Natl Acad Sci USA<\/em> 104:20025-20030. https:\/\/doi.org\/10.1073\/pnas.0706295104<\/a><\/li>\n
  47. *Jarosinski KW<\/strong>, Tischer BK, Trapp S, Osterrieder N. Marek’s disease virus: lytic replication, oncogenesis and control. Expert Rev Vaccines<\/em> 5:761-772. https:\/\/doi.org\/10.1586\/14760584.5.6.761<\/a><\/li>\n
  48. Poonia B, Dunn PA, Lu H, Jarosinski KW<\/strong>, Schat KA. 2006. Isolation and molecular characterization of a new Muscovy duck parvovirus from Muscovy ducks in the USA. Avian Pathol<\/em> 35:435-441. https:\/\/doi.org\/10.1080\/03079450601009563<\/a><\/li>\n
  49. Li X, Jarosinski KW<\/strong>, Schat KA. Expression of Marek’s disease virus phosphorylated polypeptide pp38 produces splice variants and enhances metabolic activity. Vet Microbiol<\/em> 117:<\/strong>154-168. https:\/\/doi.org\/10.1016\/j.vetmic.2006.06.019<\/a><\/li>\n
  50. Miller MM, Jarosinski KW<\/strong>, Schat KA. 2005. Positive and negative regulation of chicken anemia virus transcription. J Virol 79:2859-2868 https:\/\/doi.org\/10.1128\/jvi.79.5.2859-2868.2005<\/a><\/li>\n
  51. Jarosinski KW<\/strong>, Osterrieder N, Nair VK, Schat KA. 2005. Attenuation of Marek’s disease virus by deletion of open reading frame RLORF4 but not RLORF5a. J Viro<\/em>l 79:11647-11659. https:\/\/doi.org\/10.1128\/jvi.79.18.11647-11659.2005<\/a><\/li>\n
  52. Jarosinski KW<\/strong>, Njaa BL, O’Connell P H, Schat KA. 2005. Pro-inflammatory responses in chicken spleen and brain tissues after infection with very virulent plus Marek’s disease virus. Viral Immunol<\/em> 18:148-161 https:\/\/doi.org\/10.1089\/vim.2005.18.148<\/a><\/li>\n
  53. Yunis R, Jarosinski KW<\/strong>, Schat KA. 2004. Association between rate of viral genome replication and virulence of Marek’s disease herpesvirus strains. Virology<\/em> 328:142-150. https:\/\/doi.org\/10.1637\/0005-2086(2002)046[0636:iogrot]2.0.co;2<\/a><\/li>\n
  54. *Jarosinski KW<\/strong>, O’Connell PH, Schat KA. 2003. Impact of deletions within the Bam HI-L fragment of attenuated Marek’s disease virus on vIL-8 expression and the newly identified transcript of open reading frame LORF4. Virus Genes<\/em> 26:255-269. https:\/\/doi.org\/10.1023\/a:1024447230464<\/a><\/li>\n
  55. Jarosinski KW<\/strong>, Yunis R, O’Connell PH, Markowski-Grimsrud CJ, Schat KA. Influence of genetic resistance of the chicken and virulence of Marek’s disease virus (MDV) on nitric oxide responses after MDV infection. Avian Dis<\/em> 46:<\/strong>636-649. https:\/\/doi.org\/10.1637\/0005-2086(2002)046[0636:iogrot]2.0.co;2 <\/a>(P.P. Levine Award for best paper published in Avian Diseases in 2002)<\/strong><\/li>\n
  56. Jarosinski KW<\/strong>, Massa PT. 2002. Interferon regulatory factor-1 is required for interferon-gamma-induced MHC class I genes in astrocytes. J Neuroimmunol<\/em> 122:74-84. https:\/\/doi.org\/10.1016\/s0165-5728(01)00467-2<\/a><\/li>\n
  57. Jarosinski KW<\/strong>, Whitney LW, Massa PT. 2001. Specific deficiency in nuclear factor-kappaB activation in neurons of the central nervous system. Lab Invest<\/em> 81:1275-1288. https:\/\/doi.org\/10.1038\/labinvest.3780341<\/a><\/li>\n
  58. Jarosinski KW<\/strong>, Jia W, Sekellick MJ, Marcus PI, Schat KA. 2001. Cellular responses in chickens treated with IFN-alpha orally or inoculated with recombinant Marek’s disease virus expressing IFN-alpha. J Interferon Cytokine Res<\/em> 21:287-296. https:\/\/doi.org\/10.1089\/107999001300177475<\/a><\/li>\n
  59. Massa PT, Saha S, Wu C, Jarosinski KW<\/strong>. 2000. Expression and function of the protein tyrosine phosphatase SHP-1 in oligodendrocytes. Glia<\/em> 29:376-385. https:\/\/doi.org\/10.1002\/(SICI)1098-1136(20000215)29:4%3C376::AID-GLIA8%3E3.0.CO;2-S<\/a><\/li>\n
  60. Massa PT, Whitney LW, Wu C, Ropka SL, Jarosinski KW<\/strong>. 1999. A mechanism for selective induction of 2′-5′ oligoadenylate synthetase, anti-viral state, but not MHC class I genes by interferon-beta in neurons. J Neurovirol<\/em> 5:161-171. https:\/\/doi.org\/10.3109\/13550289909021998<\/a><\/li>\n
  61. <\/li>\n<\/ol>\n

    *indicates corresponding author<\/p>\n

    Full Publications List<\/a><\/p>\n<\/div>

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