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PLoS Pathog ; 17(4): e1009186, 2021 04.
Artículo en Inglés | MEDLINE | ID: mdl-33826679

RESUMEN

Pathogenic mycobacteria actively dysregulate protective host immune signalling pathways during infection to drive the formation of permissive granuloma microenvironments. Dynamic regulation of host microRNA (miRNA) expression is a conserved feature of mycobacterial infections across host-pathogen pairings. Here we examine the role of miR-206 in the zebrafish model of Mycobacterium marinum infection, which allows investigation of the early stages of granuloma formation. We find miR-206 is upregulated following infection by pathogenic M. marinum and that antagomir-mediated knockdown of miR-206 is protective against infection. We observed striking upregulation of cxcl12a and cxcr4b in infected miR-206 knockdown zebrafish embryos and live imaging revealed enhanced recruitment of neutrophils to sites of infection. We used CRISPR/Cas9-mediated knockdown of cxcl12a and cxcr4b expression and AMD3100 inhibition of Cxcr4 to show that the enhanced neutrophil response and reduced bacterial burden caused by miR-206 knockdown was dependent on the Cxcl12/Cxcr4 signalling axis. Together, our data illustrate a pathway through which pathogenic mycobacteria induce host miR-206 expression to suppress Cxcl12/Cxcr4 signalling and prevent protective neutrophil recruitment to granulomas.


Asunto(s)
Quimiocina CXCL12/metabolismo , MicroARNs/genética , Infiltración Neutrófila/inmunología , Receptores CXCR4/metabolismo , Animales , Quimiocina CXCL12/inmunología , Técnicas de Silenciamiento del Gen/métodos , Infecciones por Mycobacterium no Tuberculosas/genética , Infecciones por Mycobacterium no Tuberculosas/inmunología , Mycobacterium marinum/metabolismo , Receptores CXCR4/inmunología , Transducción de Señal/genética , Transducción de Señal/inmunología , Pez Cebra/inmunología
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