Synergistic effects of toll-like receptor 1/2 and toll-like receptor 3 signaling triggering interleukin 27 gene expression in chikungunya virus-infected macrophages

Chikungunya virus (CHIKV) is the etiological agent of chikungunya fever (CHIKF), a self-limiting disease characterized by myalgia and severe acute or chronic arthralgia. CHIKF is associated with immunopathology and high levels of pro-inflammatory factors. CHIKV is known to have a wide range of tropi...

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Autores:
Valdés López, Juan Felipe
Fernández García, Geysson Javier
Urcuqui Inchima, Silvio
Tipo de recurso:
Article of investigation
Fecha de publicación:
2022
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/26090
Acceso en línea:
http://hdl.handle.net/10495/26090
Palabra clave:
Interleukin-27
Interleucina-27
Toll-like receptors
Receptores toll-like
Chikungunya virus
Virus Chikungunya
Antiviral agents
Antivirales
Inmunidad innata
Immunity, innate
Transcriptome
Transcriptoma
Respuesta anti-inflamatoria
http://id.nlm.nih.gov/mesh/D064094
http://id.nlm.nih.gov/mesh/D051193
http://id.nlm.nih.gov/mesh/D002646
http://id.nlm.nih.gov/mesh/D000998
http://id.nlm.nih.gov/mesh/D007113
http://id.nlm.nih.gov/mesh/D059467
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc/4.0/
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network_acronym_str UDEA2
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repository_id_str
dc.title.spa.fl_str_mv Synergistic effects of toll-like receptor 1/2 and toll-like receptor 3 signaling triggering interleukin 27 gene expression in chikungunya virus-infected macrophages
title Synergistic effects of toll-like receptor 1/2 and toll-like receptor 3 signaling triggering interleukin 27 gene expression in chikungunya virus-infected macrophages
spellingShingle Synergistic effects of toll-like receptor 1/2 and toll-like receptor 3 signaling triggering interleukin 27 gene expression in chikungunya virus-infected macrophages
Interleukin-27
Interleucina-27
Toll-like receptors
Receptores toll-like
Chikungunya virus
Virus Chikungunya
Antiviral agents
Antivirales
Inmunidad innata
Immunity, innate
Transcriptome
Transcriptoma
Respuesta anti-inflamatoria
http://id.nlm.nih.gov/mesh/D064094
http://id.nlm.nih.gov/mesh/D051193
http://id.nlm.nih.gov/mesh/D002646
http://id.nlm.nih.gov/mesh/D000998
http://id.nlm.nih.gov/mesh/D007113
http://id.nlm.nih.gov/mesh/D059467
title_short Synergistic effects of toll-like receptor 1/2 and toll-like receptor 3 signaling triggering interleukin 27 gene expression in chikungunya virus-infected macrophages
title_full Synergistic effects of toll-like receptor 1/2 and toll-like receptor 3 signaling triggering interleukin 27 gene expression in chikungunya virus-infected macrophages
title_fullStr Synergistic effects of toll-like receptor 1/2 and toll-like receptor 3 signaling triggering interleukin 27 gene expression in chikungunya virus-infected macrophages
title_full_unstemmed Synergistic effects of toll-like receptor 1/2 and toll-like receptor 3 signaling triggering interleukin 27 gene expression in chikungunya virus-infected macrophages
title_sort Synergistic effects of toll-like receptor 1/2 and toll-like receptor 3 signaling triggering interleukin 27 gene expression in chikungunya virus-infected macrophages
dc.creator.fl_str_mv Valdés López, Juan Felipe
Fernández García, Geysson Javier
Urcuqui Inchima, Silvio
dc.contributor.author.none.fl_str_mv Valdés López, Juan Felipe
Fernández García, Geysson Javier
Urcuqui Inchima, Silvio
dc.contributor.researchgroup.spa.fl_str_mv Inmunovirología
dc.subject.mesh.none.fl_str_mv Interleukin-27
Interleucina-27
Toll-like receptors
Receptores toll-like
Chikungunya virus
Virus Chikungunya
Antiviral agents
Antivirales
Inmunidad innata
Immunity, innate
Transcriptome
Transcriptoma
topic Interleukin-27
Interleucina-27
Toll-like receptors
Receptores toll-like
Chikungunya virus
Virus Chikungunya
Antiviral agents
Antivirales
Inmunidad innata
Immunity, innate
Transcriptome
Transcriptoma
Respuesta anti-inflamatoria
http://id.nlm.nih.gov/mesh/D064094
http://id.nlm.nih.gov/mesh/D051193
http://id.nlm.nih.gov/mesh/D002646
http://id.nlm.nih.gov/mesh/D000998
http://id.nlm.nih.gov/mesh/D007113
http://id.nlm.nih.gov/mesh/D059467
dc.subject.proposal.spa.fl_str_mv Respuesta anti-inflamatoria
dc.subject.meshuri.none.fl_str_mv http://id.nlm.nih.gov/mesh/D064094
http://id.nlm.nih.gov/mesh/D051193
http://id.nlm.nih.gov/mesh/D002646
http://id.nlm.nih.gov/mesh/D000998
http://id.nlm.nih.gov/mesh/D007113
http://id.nlm.nih.gov/mesh/D059467
description Chikungunya virus (CHIKV) is the etiological agent of chikungunya fever (CHIKF), a self-limiting disease characterized by myalgia and severe acute or chronic arthralgia. CHIKF is associated with immunopathology and high levels of pro-inflammatory factors. CHIKV is known to have a wide range of tropism in human cell types, including keratinocytes, fibroblasts, endothelial cells, monocytes, and macrophages. Previously, we reported that CHIKV-infected monocytesderived macrophages (MDMs) express high levels of interleukin 27 (IL27), a heterodimeric cytokine consisting of IL27p28 and EBI3 subunits, that triggers JAK-STAT signaling and promotes pro-inflammatory and antiviral response, in interferon (IFN)-independent manner. Based on the transcriptomic analysis, we now report that induction of IL27-dependent proinflammatory and antiviral response in CHIKV-infected MDMs relies on two signaling pathways: an early signal dependent on recognition of CHIKV-PAMPs by TLR1/2-MyD88 to activate NFκB-complex that induces the expression of EBI3 mRNA; and second signaling dependent on the recognition of intermediates of CHIKV replication (such as dsRNA) by TLR3-TRIF, to activate IRF1 and the induction of IL27p28 mRNA expression. Both signaling pathways were required to produce a functional IL27 protein involved in the induction of ISGs, including antiviral proteins, cytokines, CC- and CXC- chemokines in an IFN-independent manner in MDMs. Furthermore, we reported that activation of TLR4 by LPS, both in human MDMs and murine BMDM, results in the induction of both subunits of IL27 that trigger strong IL27-dependent pro-inflammatory and antiviral response independent of IFNs signaling. Our findings are a significant contribution to the understanding of molecular and cellular mechanisms of CHIKV infection.
publishDate 2022
dc.date.accessioned.none.fl_str_mv 2022-02-17T15:55:33Z
dc.date.available.none.fl_str_mv 2022-02-17T15:55:33Z
dc.date.issued.none.fl_str_mv 2022
dc.type.none.fl_str_mv Artículo de investigación
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dc.identifier.issn.none.fl_str_mv 2296-634X
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10495/26090
dc.identifier.doi.none.fl_str_mv 10.3389/fcell.2022.812110
identifier_str_mv 2296-634X
10.3389/fcell.2022.812110
url http://hdl.handle.net/10495/26090
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Front. Cell. Dev. Biol.
dc.relation.citationvolume.spa.fl_str_mv 10
dc.relation.ispartofjournal.spa.fl_str_mv Frontiers in Cell and Developmental Biology
dc.relation.issupplementedby.spa.fl_str_mv https://www.frontiersin.org/articles/10.3389/fcell.2022.812110/full
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dc.publisher.place.spa.fl_str_mv Lausana, Suiza
publisher.none.fl_str_mv Frontiers Media
institution Universidad de Antioquia
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spelling Valdés López, Juan FelipeFernández García, Geysson JavierUrcuqui Inchima, SilvioInmunovirología2022-02-17T15:55:33Z2022-02-17T15:55:33Z20222296-634Xhttp://hdl.handle.net/10495/2609010.3389/fcell.2022.812110Chikungunya virus (CHIKV) is the etiological agent of chikungunya fever (CHIKF), a self-limiting disease characterized by myalgia and severe acute or chronic arthralgia. CHIKF is associated with immunopathology and high levels of pro-inflammatory factors. CHIKV is known to have a wide range of tropism in human cell types, including keratinocytes, fibroblasts, endothelial cells, monocytes, and macrophages. Previously, we reported that CHIKV-infected monocytesderived macrophages (MDMs) express high levels of interleukin 27 (IL27), a heterodimeric cytokine consisting of IL27p28 and EBI3 subunits, that triggers JAK-STAT signaling and promotes pro-inflammatory and antiviral response, in interferon (IFN)-independent manner. Based on the transcriptomic analysis, we now report that induction of IL27-dependent proinflammatory and antiviral response in CHIKV-infected MDMs relies on two signaling pathways: an early signal dependent on recognition of CHIKV-PAMPs by TLR1/2-MyD88 to activate NFκB-complex that induces the expression of EBI3 mRNA; and second signaling dependent on the recognition of intermediates of CHIKV replication (such as dsRNA) by TLR3-TRIF, to activate IRF1 and the induction of IL27p28 mRNA expression. Both signaling pathways were required to produce a functional IL27 protein involved in the induction of ISGs, including antiviral proteins, cytokines, CC- and CXC- chemokines in an IFN-independent manner in MDMs. Furthermore, we reported that activation of TLR4 by LPS, both in human MDMs and murine BMDM, results in the induction of both subunits of IL27 that trigger strong IL27-dependent pro-inflammatory and antiviral response independent of IFNs signaling. Our findings are a significant contribution to the understanding of molecular and cellular mechanisms of CHIKV infection.El virus chikungunya (CHIKV) es el agente etiológico de la fiebre chikungunya (CHIKF), una enfermedad autolimitada caracterizada por mialgias y artralgias agudas o crónicas graves. CHIKF está asociado con inmunopatología y altos niveles de factores proinflamatorios. Se sabe que CHIKV tiene una amplia gama de tropismo en tipos de células humanas, incluidos queratinocitos, fibroblastos, células endoteliales, monocitos y macrófagos. Anteriormente, informamos que los macrófagos derivados de monocitos (MDM) infectados con CHIKV expresan altos niveles de interleucina 27 (IL27), una citocina heterodimérica que consta de las subunidades IL27p28 y EBI3, que desencadena la señalización JAK-STAT y promueve la respuesta proinflamatoria y antiviral, en interferón (IFN) de manera independiente. Con base en el análisis transcriptómico, ahora informamos que la inducción de una respuesta proinflamatoria y antiviral dependiente de IL27 en MDM infectados con CHIKV se basa en dos vías de señalización: una señal temprana que depende del reconocimiento de CHIKV-PAMP por TLR1/2-MyD88 para activar NFκB- complejo que induce la expresión de ARNm de EBI3; y una segunda señalización dependiente del reconocimiento de intermediarios de replicación de CHIKV (como dsRNA) por parte de TLR3-TRIF, para activar IRF1 y la inducción de la expresión de mRNA de IL27p28. Se requerían ambas vías de señalización para producir una proteína IL27 funcional involucrada en la inducción de ISG, incluidas proteínas antivirales, citocinas, quimiocinas CC y CXC de manera independiente de IFN en MDM. Además, informamos que la activación de TLR4 por LPS, tanto en MDM humanos como en BMDM murino, da como resultado la inducción de ambas subunidades de IL27 que desencadenan una fuerte respuesta proinflamatoria y antiviral dependiente de IL27 independiente de la señalización de IFN. Nuestros hallazgos son una contribución significativa a la comprensión de los mecanismos moleculares y celulares de la infección por CHIKV. 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