Abstract

Mycobacterium ulcerans is the causative agent of Buruli ulcer (BU), a WHO-defined neglected tropical disease. All Japanese BU causative isolates have shown distinct differences from the prototype and are categorized as M. ulcerans subspecies shinshuense. During repeated sub-culture, we found that some M. shinshuense colonies were non-pigmented whereas others were pigmented. Whole genome sequence analysis revealed that non-pigmented colonies did not harbor a giant plasmid, which encodes elements needed for mycolactone toxin biosynthesis. Moreover, mycolactone was not detected in sterile filtrates of non-pigmented colonies. Mice inoculated with suspensions of pigmented colonies died within 5 weeks whereas those infected with suspensions of non-pigmented colonies had significantly prolonged survival (>8 weeks). This study suggests that mycolactone is a critical M. shinshuense virulence factor and that the lack of a mycolactone-producing giant plasmid makes the strain non-pathogenic. We made an avirulent mycolactone-deletion mutant strain directly from the virulent original.

Highlights

  • Mycobacterium ulcerans is the causative agent of Buruli ulcer (BU), a World Health Organization (WHO)-defined neglected tropical disease

  • The results were in accordance with those of a previous report on M. ulcerans, except for the positive urease activity of the “M. shinshuense” isolates[2]

  • The open reading frames (ORFs) required for synthesis of this polyketide toxin are carried on a giant plasmid found in many strains of M. ulcerans[22]

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Summary

Introduction

Mycobacterium ulcerans is the causative agent of Buruli ulcer (BU), a WHO-defined neglected tropical disease. Whole genome sequence analysis revealed that non-pigmented colonies did not harbor a giant plasmid, which encodes elements needed for mycolactone toxin biosynthesis. “M. shinshuense” is considered to be an M. ulcerans subspecies, a recent whole genome sequence (WGS) analysis, which included a giant plasmid from the reference strain, revealed significant genetic differences between them[8]. Both M. ulcerans and “M. shinshuense” carry the giant plasmid (pMUM001) that www.nature.com/scientificreports/. The macrolide mycolactone is a lipid-like exotoxin that has a structure similar to immune-suppressive agents such as cyclosporine, rapamycin, and tacrolimus[11,12] Production of this toxin is critical for M. ulcerans pathogenesis

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