Mycobacterium ulcerans and Other Mycolactone-Producing Mycobacteria Should Be Considered a Single Species 英文参考文献.docVIP
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Mycobacterium ulcerans and Other Mycolactone-Producing Mycobacteria Should Be Considered a Single Species 英文参考文献
Viewpoints
MycobacteriumulceransandOtherMycolactone-
ProducingMycobacteriaShouldBeConsideredaSingle
Species
SachaJ.Pidot1,2,KingsleyAsiedu3,MichaelKa¨ser4,5,JanetA.M.Fyfe6,TimothyP.Stinear1,2*
1Department of Microbiology and Immunology, University ofMelbourne, Melbourne, Australia, 2Department of Microbiology, Monash University, Clayton, Australia,
3World Health Organization, Geneva, Switzerland, 4Swiss Tropical and Public Health Institute,Basel, Switzerland, 5University of Basel, Basel, Switzerland, 6Victorian
InfectiousDiseasesReferenceLaboratory,NorthMelbourne,Australia
The nomenclature of Mycobacterium ul-
cerans has become confused with the
discovery that other mycobacteria that
are not necessarily associated with Buruli
ulcer also produce the lipid toxin myco-
lactone.Thesemycobacteria—collectively
known as mycolactone-producing myco-
parisons have shown that these species
over 4,000 genes with 98.3%
common M.marinum progenitor [5,11,12]
and have then diverged again into two
distinct lineages, with both lineages bear-
ing strains that cause Buruli ulcer [5,13]
(Figure1).
share
averageDNAsequenceidentity[2].How-
are also some important
ever,
there
genetic differences between them. DNA–
DNA hybridisation (DDH) analysis con-
firmed their status as distinct species, as
inter-species relative hybridisation ratios
(RBR)werelessthan40%[3,4].Thelow
RBRisexplainedbyanumberoffeatures
uniquetoM.ulcerans,suchasthepresence
of a large virulence plasmid (pMUM)
ThenewspeciesassignationsforMPM
havenotconsideredtheirgenomiccontext
and have been based on variable pheno-
typic characteristics (such as colony mor-
phology and in vitro growth rates) and
limited, monophyletic rRNA, hsp65 , or
rpoB analyses, which have shown these
mycobacteria have a few unique nucleo-
tidesequenceswhencomparedtoasmall
number of allele sequences in GenBank.
However, more complex and time-con-
suming DDH analyses, which, together
with 16S rRNA sequencing, are the
prescribed methods for defin
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