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. 2012 Aug 28;6(8):e1756. doi: 10.1371/journal.pntd.0001756

Table 2. Specificity of 16S rRNA and IS2404 qPCR assays.

Bacterial Species Sourcea Originb 16S rRNAd IS2404 e
M. abscessus NRZ Human isolatep
M. africanum NRZ Human isolatep
M. avium NRZ Human isolatep
M. bovis NRZ Cattle isolatep
M. chelonae NRZ Human isolatep
M. fortuitum NRZ Human isolatec
M. gordonae NRZ Human isolatec
M. gordonae DITM Human isolatec
M. kansasii NRZ Human isolatep
M. leprae DITM Human isolatep
M. malmoense NRZ Human isolatec
M. marinum NRZ Human isolatep +
M. microti NRZ Mouse isolatep
M. scrofulaceum NRZ Human isolatep
M. smegmatis NRZ Human isolatep
M. szulgai NRZ Human isolatep
M. tuberculosis NRZ Human isolatep
M. ulcerans DITM Human isolatep + +
M. xenopi NRZ Human isolatec
E. coli MVP Human isolatec
P. acnes MVP Human isolatep
Staph. aureus MVP Human isolatec
Staph. epidermidis MVP Human isolatec
Str. pyogenes MVP Human isolatep

Table 2 shows DNA extracts from closely related mycobacterial species and bacteria potentially contaminating the human skin subjected to the combined 16S rRNA RT/IS2404 qPCR viability assay and the corresponding test results. Mycobacterial species were selected according to their respective genetic contiguousness to M. ulcerans Agy99 (GenBank accession no. CP000325.1) within the 16S rRNA gene sequences as determined by BLASTN analysis (GenBank, NCBI) [13]. M., Mycobacterium; E., Escherichia; P., Propionibacterium; Staph., Staphylococcus; Str., Streptococcus. While in-silico analysis revealed that the combined 16S rRNA RT/IS2404 assay will also amplify mycolactone-producing mycobacteria (MPM) other than M. ulcerans (e.g., M. pseudoshottsii, M. liflandii, and the environmental M. marinum [GenBank accession No. NR_042988.1, AY500838.1, and AF456241.1, respectively]), these MPM species were not included in specificity testing.

a

DNA extracts that were not available at the DITM were provided by the National Reference Center (NRZ) for Mycobacteria, Borstel, Germany, and the Max von Pettenkofer-Institute (MVP), Ludwig-Maximilians University, Munich, Germany.

b

The respective primary patient isolates were considered as ppathogenic bacteria or as ccommensals/contaminants of clinical samples.

d

Results of the 16S rRNA RT-qPCR of DNA extracts; “+” indicates a positive and “–” a negative test result.

e

Results of the IS2404 qPCR of DNA extracts; “+” indicates a positive and “–” a negative test result.