Evidence map›Paper›PMID 35027054›Full record

ArticleBMC biology2022

Stem cell-derived porcine macrophages as a new platform for studying host-pathogen interactions.

Stephen Meek, Tom Watson, Lel Eory, Gus McFarlane, Felicity J Wynne, Stephen McCleary, Laura E M Dunn, Emily M Charlton, Chloe Craig, Barbara Shih and 26 more

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
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

36 authors at 10 institutions in 5 countries.

Stephen MeekThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK. stephen.meek@roslin.ed.ac.uk.
Tom WatsonThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Lel EoryThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Gus McFarlaneThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Felicity J WynneVirology Department, Animal and Plant Health Agency, Addlestone, KT15 3NB, UK.
Stephen McClearyVirology Department, Animal and Plant Health Agency, Addlestone, KT15 3NB, UK.
Laura E M DunnThe Pirbright Institute, Pirbright, Surrey, UK.
Emily M CharltonThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Chloe CraigThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Barbara ShihThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Tim ReganThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Ryan TaylorThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Linda SutherlandThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Anton GossnerThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Cosmin Chintoan-UtaThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Sarah FletcherThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Philippa M BeardThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Musa A HassanThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Finn GreyThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Jayne C HopeThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Mark P StevensThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Monika Nowak-ImialekFirst Department of Medicine, Cardiology, Klinikum rechts der Isar - Technical University of Munich, Ismaninger Straße 22, 81675, Munich, Germany.
Heiner NiemannGastroenterology, Hepatology and Endocrinology Department, Hannover Medical School, Carl Neuberg Str 1, 30625, Hannover, Germany.
Pablo J RossDepartment of Animal Science, University of California, 450 Bioletti Way, Davis, CA, 95616, USA.
Christine Tait-BurkardThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Sarah M BrownThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Lucas LefevreUK Dementia Research Institute, The University of Edinburgh, Edinburgh Medical School, The Chancellor's Building, 49 Little France Crescent, Edinburgh, EH16 4SB, UK.
Gerard ThomsonCentre for Clinical Brain Sciences, University of Edinburgh, Department of Clinical Neurosciences, NHS Lothian, Edinburgh, UK.
Barry W McCollUK Dementia Research Institute, The University of Edinburgh, Edinburgh Medical School, The Chancellor's Building, 49 Little France Crescent, Edinburgh, EH16 4SB, UK.
Alistair B LawrenceThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Alan L ArchibaldThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK.
Falko SteinbachVirology Department, Animal and Plant Health Agency, Addlestone, KT15 3NB, UK.
Helen R CrookeVirology Department, Animal and Plant Health Agency, Addlestone, KT15 3NB, UK.
Xuefei GaoDepartment of Physiology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, 510515, China.
Pentao LiuThe Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
Tom BurdonThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, EH25 9RG, UK. tom.burdon@roslin.ed.ac.uk.ORCID http://orcid.org/0000-0001-6613-0519
Roslin Institute · GBAnimal and Plant Health Agency · GBThe Pirbright Institute · GBUK Dementia Research Institute · GBHong Kong Science and Technology Parks Corporation · HKMedizinische Hochschule Hannover · DENHS Lothian · GBSouthern Medical University · CNTUM Klinikum · DEUniversity of California, Davis · US

Funding

Biotechnology and Biological Sciences Research Council BB/P013732/1Biotechnology and Biological Sciences Research Council BB/S02008XBiotechnology and Biological Sciences Research Council BBS/E/D/10002070
6 · The paper itself

Abstract

backgroundInfectious diseases of farmed and wild animals pose a recurrent threat to food security and human health. The macrophage, a key component of the innate immune system, is the first line of defence against many infectious agents and plays a major role in shaping the adaptive immune response. However, this phagocyte is a target and host for many pathogens. Understanding the molecular basis of interactions between macrophages and pathogens is therefore crucial for the development of effective strategies to combat important infectious diseases.

resultsWe explored how porcine pluripotent stem cells (PSCs) can provide a limitless in vitro supply of genetically and experimentally tractable macrophages. Porcine PSC-derived macrophages (PSCdMs) exhibited molecular and functional characteristics of ex vivo primary macrophages and were productively infected by pig pathogens, including porcine reproductive and respiratory syndrome virus (PRRSV) and African swine fever virus (ASFV), two of the most economically important and devastating viruses in pig farming. Moreover, porcine PSCdMs were readily amenable to genetic modification by CRISPR/Cas9 gene editing applied either in parental stem cells or directly in the macrophages by lentiviral vector transduction.

conclusionsWe show that porcine PSCdMs exhibit key macrophage characteristics, including infection by a range of commercially relevant pig pathogens. In addition, genetic engineering of PSCs and PSCdMs affords new opportunities for functional analysis of macrophage biology in an important livestock species. PSCs and differentiated derivatives should therefore represent a useful and ethical experimental platform to investigate the genetic and molecular basis of host-pathogen interactions in pigs, and also have wider applications in livestock.

Indexed as

African Swine Fever VirusCommunicable DiseasesAnimalsHost-Pathogen InteractionsMacrophagesStem CellsSwineASFVCRISPRgene editingMacrophagePigPluripotent stem cellPRRSV

Identifiers

PMID35027054
PMCPMC8759257
OpenAlexW4206006536

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.