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Nontypeable Haemophilus influenzae challenge during gammaherpesvirus infection enhances viral reactivation and latency.
Huss, Nicholas P; Majeed, Sheikh Tahir; Wills, Brandon M; Tarakanova, Vera L; Brockman, Kenneth L; Jondle, Christopher N.
Affiliation
  • Huss NP; Department of Investigative Medicine and Center for Immunobiology, Western Michigan University Homer Stryker M.D. School of Medicine, Kalamazoo, MI, 49007, USA.
  • Majeed ST; Department of Investigative Medicine and Center for Immunobiology, Western Michigan University Homer Stryker M.D. School of Medicine, Kalamazoo, MI, 49007, USA.
  • Wills BM; Department of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
  • Tarakanova VL; Department of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI, 53226, USA; Cancer Center, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
  • Brockman KL; Department of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
  • Jondle CN; Department of Investigative Medicine and Center for Immunobiology, Western Michigan University Homer Stryker M.D. School of Medicine, Kalamazoo, MI, 49007, USA. Electronic address: christopher.jondle@wmed.edu.
Virology ; 597: 110153, 2024 Sep.
Article in En | MEDLINE | ID: mdl-38941745
ABSTRACT
Gammaherpesviruses are ubiquitous, lifelong pathogens associated with multiple cancers that infect over 95% of the adult population. Increases in viral reactivation, due to stress and other unknown factors impacting the immune response, frequently precedes lymphomagenesis. One potential stressor that could promote viral reactivation and increase viral latency would be the myriad of infections from bacterial and viral pathogens that we experience throughout our lives. Using murine gammaherpesvirus 68 (MHV68), a mouse model of gammaherpesvirus infection, we examined the impact of bacterial challenge on gammaherpesvirus infection. We challenged MHV68 infected mice during the establishment of latency with nontypeable Haemophilus influenzae (NTHi) to determine the impact of bacterial infection on viral reactivation and latency. Mice infected with MHV68 and then challenged with NTHi, saw increases in viral reactivation and viral latency. These data support the hypothesis that bacterial challenge can promote gammaherpesvirus reactivation and latency establishment, with possible consequences for viral lymphomagenesis.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virus Activation / Haemophilus influenzae / Virus Latency / Herpesviridae Infections / Haemophilus Infections Limits: Animals Language: En Journal: Virology Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virus Activation / Haemophilus influenzae / Virus Latency / Herpesviridae Infections / Haemophilus Infections Limits: Animals Language: En Journal: Virology Year: 2024 Document type: Article