2019
DOI: 10.3201/eid2509.181234
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Disseminated Emergomycosis in a Person with HIV Infection, Uganda

Abstract: We describe emergomycosis in a patient in Uganda with HIV infection. We tested a formalin-fixed, paraffin-embedded skin biopsy to identify Emergomyces pasteurianus or a closely related pathogen by sequencing broad-range fungal PCR amplicons. Results suggest that emergomycosis is more widespread and genetically diverse than previously documented. PCR on tissue blocks may help clarify emergomycosis epidemiology.

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Cited by 22 publications
(15 citation statements)
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(12 reference statements)
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“…DNA extracts were stored at -80°C until polymerase chain reaction (PCR) amplification for clinically important fungi. Fungal DNA was amplified using a broad-range fungal PCR targeting the 28S rRNA gene (primer 28S10f: ; 28S12r: ) using Eva Green with melt curve analysis in an ABI 7500 qPCR machine as described previously [ 10 ]. Samples were tested in duplicate.…”
Section: Methodsmentioning
confidence: 99%
“…DNA extracts were stored at -80°C until polymerase chain reaction (PCR) amplification for clinically important fungi. Fungal DNA was amplified using a broad-range fungal PCR targeting the 28S rRNA gene (primer 28S10f: ; 28S12r: ) using Eva Green with melt curve analysis in an ABI 7500 qPCR machine as described previously [ 10 ]. Samples were tested in duplicate.…”
Section: Methodsmentioning
confidence: 99%
“…In such cases, fungal DNA can be extracted from FFPE tissue biopsy sections and amplified by PCR targeting ITS region of the fungal ribosomal RNA genes. Rooms et al(38) diagnosed a case of disseminated emergomycosis caused by Es. pasteurianus in Uganda by using two broad-range fungal PCR assays targeting a region of the 28S and the ITS2 region, which was confirmed by phylogenetic analysis.…”
mentioning
confidence: 99%
“…DNA extracts were stored at -80 °C until polymerase chain reaction (PCR) amplification for clinically important fungi. Fungal DNA was amplified using a broad-range fungal PCR targeting the 28S rRNA gene using Eva Green with melt curve analysis in an ABI 7500 qPCR machine as described previously [10]. Samples were tested in duplicate.…”
Section: Fungal Detection and Identificationmentioning
confidence: 99%