Evidence map›Paper›PMID 29704667›Full record

ArticleMicrobial pathogenesis2018

Gene expression profiling of primary human type I alveolar epithelial cells exposed to Bacillus anthracis spores reveals induction of neutrophil and monocyte chemokines.

J Leland Booth, Elizabeth S Duggan, Vineet I Patel, Wenxin Wu, Dennis M Burian, David C Hutchings, Vicky L White, K Mark Coggeshall, Mikhail G Dozmorov, Jordan P Metcalf

Open access · greenAbstract read
In one paragraph

Article in Microbial pathogenesis, 2018. 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, top 96% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Local genetic adaptation to habitat in wild chimpanzees.bioRxiv : the preprint server for biology · 2024
    Article
  3. 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

10 authors at 5 institutions in 1 country.

J Leland BoothPulmonary and Critical Care Division of the Department of Internal Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA. Electronic address: john-booth@ouhsc.edu.
Elizabeth S DugganPulmonary and Critical Care Division of the Department of Internal Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA. Electronic address: elizabeth-duggan@ouhsc.edu.
Vineet I PatelPulmonary and Critical Care Division of the Department of Internal Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA; Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA. Electronic address: vineet-patel@ouhsc.edu.
Wenxin WuPulmonary and Critical Care Division of the Department of Internal Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA. Electronic address: wenxin-wu@ouhsc.edu.
Dennis M BurianCivil Aerospace Medical Institute, Office of Aviation Medicine, Federal Aviation Administration, Oklahoma City, OK 73169, USA. Electronic address: dennis.burian@faa.gov.
David C HutchingsVenesco LLC, Chantilly, VA 20151, USA. Electronic address: david.ctr.hutchings@faa.gov.
Vicky L WhiteCivil Aerospace Medical Institute, Office of Aviation Medicine, Federal Aviation Administration, Oklahoma City, OK 73169, USA. Electronic address: vicky.white@faa.gov.
K Mark CoggeshallImmunobiology and Cancer Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104, USA. Electronic address: mark-coggeshall@omrf.org.
Mikhail G DozmorovDepartment of Biostatistics, Virginia Commonwealth University, Richmond, VA 23298, USA. Electronic address: mikhail.dozmorov@vcuhealth.org.
Jordan P MetcalfPulmonary and Critical Care Division of the Department of Internal Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA; Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA. Electronic address: jordan-metcalf@ouhsc.edu.
University of Oklahoma Health Sciences Center · USFederal Aviation Administration · USOklahoma Medical Research Foundation · USVencore (United States) · USVirginia Commonwealth University · US

Funding

Translation of immunologic technologies from basic research into pre-clinical nonU19AI062629 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI COGGESHALL, KENNETH MARK · 2004 to 2023
$56.2M
ZFC3H1 Regulation of Host Defense and Influenza A Virus PathogenesisP20GM103648 · NIGMS · OKLAHOMA STATE UNIVERSITY STILLWATER · PI PATRAUCHAN, MARIANNA M. A. · 2013 to 2022
$22.3M
Antiviral Immunosuppression by Cigarette SmokeI01BX001937 · VA · OKLAHOMA CITY VA MEDICAL CENTER · PI METCALF, JORDAN PATRICK · 2015 to 2019
–
BLRD VA I01 BX001937NIAID NIH HHS U19 AI062629NIGMS NIH HHS P20 GM103648
6 · The paper itself

Abstract

The lung is the entry site for Bacillus anthracis in inhalation anthrax, the most deadly form of the disease. Spores must escape through the alveolar epithelial cell (AEC) barrier and migrate to regional lymph nodes, germinate and enter the circulatory system to cause disease. Several mechanisms to explain alveolar escape have been postulated, and all these tacitly involve the AEC barrier. In this study, we incorporate our primary human type I AEC model, microarray and gene enrichment analysis, qRT-PCR, multiplex ELISA, and neutrophil and monocyte chemotaxis assays to study the response of AEC to B. anthracis, (Sterne) spores at 4 and 24 h post-exposure. Spore exposure altered gene expression in AEC after 4 and 24 h and differentially expressed genes (±1.3 fold, p ≤ 0.05) included CCL4/MIP-1β (4 h), CXCL8/IL-8 (4 and 24 h) and CXCL5/ENA-78 (24 h). Gene enrichment analysis revealed that pathways involving cytokine or chemokine activity, receptor binding, and innate immune responses to infection were prominent. Microarray results were confirmed by qRT-PCR and multiplex ELISA assays. Chemotaxis assays demonstrated that spores induced the release of biologically active neutrophil and monocyte chemokines, and that CXCL8/IL-8 was the major neutrophil chemokine. The small or sub-chemotactic doses of CXCL5/ENA-78, CXCL2/GROβ and CCL20/MIP-3α may contribute to chemotaxis by priming effects. These data provide the first whole transcriptomic description of the human type I AEC initial response to B. anthracis spore exposure. Taken together, our findings contribute to an increased understanding of the role of AEC in the pathogenesis of inhalational anthrax.

Indexed as

Gene Expression ProfilingAlveolar Epithelial CellsAnthraxBacillus anthracisChemokine CCL20Chemokine CXCL5ChemokinesHumansInterleukin-8MonocytesNeutrophilsPlatelet Factor 4Respiratory Tract InfectionsSpores, BacterialUp-RegulationCCL20 protein, humanChemokine CCL20Chemokine CXCL5ChemokinesCXCL5 protein, humanCXCL8 protein, humanInterleukin-8PF4 protein, humanPlatelet Factor 4AnthraxBacillus anthracisChemotaxisTranscriptome microarray analysisType I alveolar epithelial cells

Identifiers

PMID29704667
PMCPMC6077097
OpenAlexW2802185736

What OpenQuestion holds

Textmetadata
LicenceTDM
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.