Evidence map›Paper›PMID 30517644›Full record

ArticleJournal of animal science2019

Tilmicosin modulates the innate immune response and preserves casein production in bovine mammary alveolar cells during Staphylococcus aureus infection.

Ismael Martínez-Cortés, Naray A Acevedo-Domínguez, Roxana Olguin-Alor, Arimelek Cortés-Hernández, Violeta Álvarez-Jiménez, Marcia Campillo-Navarro, Héctor S Sumano-López, Lilia Gutiérrez-Olvera, Daniel Martínez-Gómez, José L Maravillas-Montero and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of animal science, 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
0.7field-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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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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

13 authors at 2 institutions in 2 countries.

Ismael Martínez-CortésChemokine Biology Research Laboratory, UNAM, Ciudad de México, Mexico.
Naray A Acevedo-DomínguezChemokine Biology Research Laboratory, UNAM, Ciudad de México, Mexico.
Roxana Olguin-AlorDepartamento de Inmunología, Instituto de Investigaciones Biomédicas, UNAM, Ciudad de México, Mexico.
Arimelek Cortés-HernándezDepartamento de Inmunología, Instituto de Investigaciones Biomédicas, UNAM, Ciudad de México, Mexico.
Violeta Álvarez-JiménezChemokine Biology Research Laboratory, UNAM, Ciudad de México, Mexico.
Marcia Campillo-NavarroLaboratorio de Inmunología Integrativa-INER, Ismael Cosio Villegas. Ciudad de México, Mexico.
Héctor S Sumano-LópezFacultad de Medicina Veterinaria y Zootecnia, UNAM, Ciudad de México, Mexico.
Lilia Gutiérrez-OlveraFacultad de Medicina Veterinaria y Zootecnia, UNAM, Ciudad de México, Mexico.
Daniel Martínez-GómezLaboratorio de Microbiología Agropecuaria, UAM-Xochimilco, Ciudad de México, Mexico.
José L Maravillas-MonteroResearch Support Network, INCMNSZ-UNAM, Ciudad de México, Mexico.
Juan J LoorMammalian NutriPhysioGenomics-University of Illinois, Urbana, IL.
Eduardo A García-ZepedaChemokine Biology Research Laboratory, UNAM, Ciudad de México, Mexico.
Gloria SoldevilaDepartamento de Inmunología, Instituto de Investigaciones Biomédicas, UNAM, Ciudad de México, Mexico.
Universidad Nacional Autónoma de México · MXUniversity of Illinois Urbana-Champaign · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tilmicosin is an antimicrobial agent used to treat intramammary infections against Staphylococcus aureus and has clinical anti-inflammatory effects. However, the mechanism by which it modulates the inflammatory process in the mammary gland is unknown. We evaluated the effect of tilmicosin treatment on the modulation of the mammary innate immune response after S. aureus infection and its effect on casein production in mammary epithelial cells. To achieve this goal, we used immortalized mammary epithelial cells (MAC-T), pretreated for 12 h or treated with tilmicosin after infection with S. aureus (ATCC 27543). Our data showed that tilmicosin decreases intracellular infection (P < 0.01) and had a protective effect on MAC-T reducing apoptosis after infection by 80% (P < 0.01). Furthermore, tilmicosin reduced reactive oxygen species (ROS) (P < 0.01), IL-1β (P < 0.01), IL-6 (P < 0.01), and TNF-α (P < 0.05) production. In an attempt to investigate the signaling pathways involved in the immunomodulatory effect of tilmicosin, mitogen-activated protein kinase (MAPK) phosphorylation was measured by fluorescent-activated cell sorting. Pretreatment with tilmicosin increased ERK1/2 (P < 0.05) but decreased P38 phosphorylation (P < 0.01). In addition, the anti-inflammatory effect of tilmicosin helped to preserve casein synthesis in mammary epithelial cells (P < 0.01). This result indicates that tilmicosin could be an effective modulator inflammation in the mammary gland. Through regulation of MAPK phosphorylation, ROS production and pro-inflammatory cytokine secretion tilmicosin can provide protection from cellular damage due to S. aureus infection and help to maintain normal physiological functions of the bovine mammary epithelial cell.

Indexed as

Alveolar Epithelial CellsAnimalsAnti-Bacterial AgentsCaseinsCattleCytokinesFemaleImmunity, InnateMammary Glands, AnimalMastitis, BovineMitogen-Activated Protein KinasesSignal TransductionStaphylococcal InfectionsStaphylococcus aureusTylosinAnti-Bacterial AgentsCaseinsCytokinesMitogen-Activated Protein KinasestilmicosinTylosin

Identifiers

PMID30517644
PMCPMC6358261
OpenAlexW2903330398

What OpenQuestion holds

Textmetadata
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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.