Evidence map›Paper›PMID 38941745›Full record

ArticleVirology2024

Nontypeable Haemophilus influenzae challenge during gammaherpesvirus infection enhances viral reactivation and latency.

Nicholas P Huss, Sheikh Tahir Majeed, Brandon M Wills, Vera L Tarakanova, Kenneth L Brockman, Christopher N Jondle

Abstract read
In one paragraph

Article in Virology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Molecular detection ofNew microbes and new infections · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Nicholas P HussDepartment of Investigative Medicine and Center for Immunobiology, Western Michigan University Homer Stryker M.D. School of Medicine, Kalamazoo, MI, 49007, USA.
Sheikh Tahir MajeedDepartment of Investigative Medicine and Center for Immunobiology, Western Michigan University Homer Stryker M.D. School of Medicine, Kalamazoo, MI, 49007, USA.
Brandon M WillsDepartment of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
Vera L TarakanovaDepartment of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI, 53226, USA; Cancer Center, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
Kenneth L BrockmanDepartment of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
Christopher N JondleDepartment 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.

Funding

Gammaherpesvirus protein kinase: a master manipulator of the host during chronic infection.R01AI165578 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI Vera L. Tarakanova · 2022 to 2026
$2.3M
From friend to foe: proviral role of IRF-3 in chronic gammaherpesvirus infectionR21AI182596 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI TARAKANOVA, VERA L. · 2024 to 2025
$440k
Gammaherpesvirus and IL-17: using host antibacterial defense to benefit chronic virus infectionR21CA263018 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI TARAKANOVA, VERA L. · 2021 to 2022
$389k
NCI NIH HHS R21 CA263018NIAID NIH HHS R01 AI165578NIAID NIH HHS R21 AI182596
6 · The paper itself

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.

Indexed as

Haemophilus InfectionsHaemophilus influenzaeHerpesviridae InfectionsVirus ActivationVirus LatencyAnimalsDisease Models, AnimalFemaleGammaherpesvirinaeMiceMice, Inbred C57BLRhadinovirusAcute bacterial infectionBacterial challengeEBVGammaherpesvirusGerminal center responseKSHVLatencyMHV68NTHiReactivation

Identifiers

PMID38941745
PMCPMC11257779

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.