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ABSTRACT: Mycobacterium ulcerans reinfection of two patient

PROVIDER: PRJNA743744 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR16611549_1.fastq.gz	Fastqsanger.gz
	SRR16611549_2.fastq.gz	Fastqsanger.gz
	SRR16611550_1.fastq.gz	Fastqsanger.gz
	SRR16611550_2.fastq.gz	Fastqsanger.gz
	SRR16611551_1.fastq.gz	Fastqsanger.gz

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Project description:Mycolactone, a lipid-like toxin, is the major virulence factor of Mycobacterium ulcerans, the etiological agent of Buruli ulcer. Its involvement in lesions development has been widely described in early stages of the disease, through its cytotoxic and immunosuppressive activities, but less is known about later stages. Here, we revisit the role of mycolactone in disease outcome and provide the first demonstration of the pro-inflammatory potential of this toxin. We found that the mycolactone-containing mycobacterial extracellular vesicles produced by M. ulcerans induced the production of IL-1β, a potent pro-inflammatory cytokine, in a TLR2-dependent manner, targeting NLRP3/1 inflammasomes. We showed our data to be relevant in a physiological context. The in vivo injection of these mycolactone-containing vesicles induced a strong local inflammatory response and tissue damages, which were prevented by corticosteroids. Finally, several soluble pro-inflammatory factors, including IL-1β, were detected in infected tissues from mice and Buruli ulcer patients. Our results revisit Buruli ulcer pathophysiology by giving a new insight, thus paving the way for development of new therapeutic strategies, taking account the pro-inflammatory potential of mycolactone.

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