Evidence map›Paper›PMID 26957120›Full record

ArticleBMC microbiology2016

Borrelia burgdorferi induces a type I interferon response during early stages of disseminated infection in mice.

Mary M Petzke, Radha Iyer, Andrea C Love, Zoe Spieler, Andrew Brooks, Ira Schwartz

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.3field-weighted citation impact, top 14% of its field
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

29 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Type I interferon signaling promotes early innate control ofbioRxiv : the preprint server for biology · 2026
    Article
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  9. Diversity and host specificity ofInfection and immunity · 2024
    Article
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  11. Review
  12. Article
  13. Article
  14. Article
  15. Comparative transcriptome analysis ofFrontiers in cellular and infection microbiology · 2023
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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 at 2 institutions in 1 country.

Mary M PetzkeDepartment of Microbiology and Immunology, New York Medical College, Valhalla, New York, USA. mary_petzke@nymc.edu.
Radha IyerDepartment of Microbiology and Immunology, New York Medical College, Valhalla, New York, USA. radha_iyer@nymc.edu.
Andrea C LoveDepartment of Microbiology and Immunology, New York Medical College, Valhalla, New York, USA. andreaclove@gmail.com.
Zoe SpielerDepartment of Microbiology and Immunology, New York Medical College, Valhalla, New York, USA. zospieler@gmail.com.
Andrew BrooksBionomics Research and Technology Center, Robert Wood Johnson-University of Medicine and Dentistry of New Jersey/Rutgers University, Piscataway, New Jersey, USA. brooks@dls.rutgers.edu.
Ira SchwartzDepartment of Microbiology and Immunology, New York Medical College, Valhalla, New York, USA. ira_schwartz@nymc.edu.
New York Medical College · USJohnson University · US

Funding

Lyme Disease Diagnosis with Host Gene Expression ArraysU01CI000160 · CI · NEW YORK MEDICAL COLLEGE · PI SCHWARTZ, IRA S. · 2004 to 2007
$438k
NCPDCID CDC HHS U01 CI000160NCPDCID CDC HHS U01CI000160
6 · The paper itself

Abstract

backgroundLyme borrelia genotypes differ in their capacity to cause disseminated disease. Gene array analysis was employed to profile the host transcriptome induced by Borrelia burgdorferi strains with different capacities for causing disseminated disease in the blood of C3H/HeJ mice during early infection.

resultsB. burgdorferi B515, a clinical isolate that causes disseminated infection in mice, differentially regulated 236 transcripts (P < 0.05 by ANOVA, with fold change of at least 2). The 216 significantly induced transcripts included interferon (IFN)-responsive genes and genes involved in immunity and inflammation. In contrast, B. burgdorferi B331, a clinical isolate that causes transient skin infection but does not disseminate in C3H/HeJ mice, stimulated changes in only a few genes (1 induced, 4 repressed). Transcriptional regulation of type I IFN and IFN-related genes was measured by quantitative RT-PCR in mouse skin biopsies collected from the site of infection 24 h after inoculation with B. burgdorferi. The mean values for transcripts of Ifnb, Cxcl10, Gbp1, Ifit1, Ifit3, Irf7, Mx1, and Stat2 were found to be significantly increased in B. burgdorferi strain B515-infected mice relative to the control group. In contrast, transcription of these genes was not significantly changed in response to B. burgdorferi strain B331 or B31-4, a mutant that is unable to disseminate.

conclusionsThese results establish a positive association between the disseminating capacity of B. burgdorferi and early type I IFN induction in a murine model of Lyme disease.

Indexed as

AnimalsBorrelia burgdorferiDisease Models, AnimalFemaleHumansInterferon Type ILyme DiseaseMaleMiceMice, Inbred C3HInterferon Type I

Identifiers

PMID26957120
PMCPMC4784397
OpenAlexW2297971998

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.