Evidence map›Paper›PMID 31442273›Full record

ArticlePloS one2019

Immuno-modulating properties of Tulathromycin in porcine monocyte-derived macrophages infected with porcine reproductive and respiratory syndrome virus.

D Desmonts de Lamache, R Moges, A Siddiq, T Allain, T D Feener, G P Muench, N McKenna, R M Yates, A G Buret

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Effect of EthanolicVeterinary sciences · 2021
    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

9 authors at 1 institution in 1 country.

D Desmonts de LamacheDepartment of Biological Sciences, University of Calgary, Calgary, AB, Canada.ORCID 0000-0002-0777-6958
R MogesDepartment of Biological Sciences, University of Calgary, Calgary, AB, Canada.
A SiddiqDepartment of Biological Sciences, University of Calgary, Calgary, AB, Canada.
T AllainDepartment of Biological Sciences, University of Calgary, Calgary, AB, Canada.
T D FeenerDepartment of Biological Sciences, University of Calgary, Calgary, AB, Canada.
G P MuenchFaculty of Veterinary Medicine, University of Calgary, Calgary, AB, Canada.
N McKennaDepartment of Biochemistry and Molecular Biology, University of Calgary, Calgary AB, Canada.
R M YatesFaculty of Veterinary Medicine, University of Calgary, Calgary, AB, Canada.
A G BuretDepartment of Biological Sciences, University of Calgary, Calgary, AB, Canada.
University of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Porcine reproductive and respiratory syndrome virus (PRRSV) is a positive-stranded RNA virus that grows in macrophages and causes acute pneumonia in pigs. PRRSV causes devastating losses to the porcine industry. However, due to its high antigenic variability and poorly understood immunopathogenesis, there is currently no effective vaccine or treatment to control PRRSV infection. The common occurrence of PRRSV infection with bacterial infections as well as its inflammatory-driven pathobiology raises the question of the value of antibiotics with immunomodulating properties for the treatment of the disease it causes. The macrolide antibiotic Tulathromycin (TUL) has been found to exhibit potent anti-inflammatory and immunomodulating properties in cattle and pigs. The aim of this study was to characterize the anti-viral and immunomodulating properties of TUL in PRRSV-infected porcine macrophages. Our findings indicate that blood monocyte-derived macrophages are readily infected by PRRSV and can be used as an effective cellular model to study PRRSV pathogenesis. TUL did not change intracellular or extracellular viral titers, not did it alter viral receptors (CD163 and CD169) expression on porcine macrophages. In contrast, TUL exhibited potent immunomodulating properties, which therefore occurred in the absence of any direct antiviral effects against PRRSV. TUL had an additive effect with PRRSV on the induction of macrophage apoptosis, and inhibited virus-induced necrosis. TUL significantly attenuated PRRSV-induced macrophage pro-inflammatory signaling (CXCL-8 and mitochondrial ROS production) and prevented PRRSV inhibition of non-opsonized and opsonized phagocytic function. Together, these data demonstrate that TUL inhibits PRRSV-induced inflammatory responses in porcine macrophages and protects against the phagocytic impairment caused by the virus. Research in live pigs is warranted to assess the potential clinical benefits of this antibiotic in the context of virally induced inflammation and tissue injury.

Indexed as

AnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticApoptosisCD163 AntigenCell DifferentiationCell LineCell ShapeDisaccharidesFemaleHeterocyclic CompoundsImmunologic FactorsInterleukin-10Interleukin-8Intracellular SpaceMacrolidesAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenDisaccharidesHeterocyclic CompoundsImmunologic FactorsInterleukin-10Interleukin-8MacrolidesOpsonin ProteinsReactive Oxygen SpeciesReceptors, Cell SurfaceReceptors, VirusSialic Acid Binding Ig-like Lectin 1tulathromycin

Identifiers

PMID31442273
PMCPMC6707645
OpenAlexW2969783937

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.