# Silent Outbreaks of Candida duobushaemulonii in a Pediatric Ward in Brazil

**Authors:** Daniel Wagner de Castro Lima Santos, Bram Spruijtenburg, Eelco F. J. Meijer, Dayse Azevedo Coelho de Souza, Conceição de Maria Pedrozo e Silva de Azevedo, Jacques F. Meis

PMC · DOI: 10.3390/antibiotics15030237 · Antibiotics · 2026-02-25

## TL;DR

A rare yeast, Candida duobushaemulonii, caused two silent outbreaks in a Brazilian pediatric ward, highlighting its potential as an opportunistic pathogen.

## Contribution

The second documented outbreak of Candida duobushaemulonii is reported, with detailed genomic and antifungal susceptibility analysis.

## Key findings

- Genomic analysis confirmed two distinct clusters of C. duobushaemulonii infections in a Brazilian pediatric ward.
- All isolates were susceptible to azoles and echinocandins but showed resistance to amphotericin B.
- The outbreaks occurred in 2022 and 2024, with no prior documentation of such events for this species.

## Abstract

Background: While Candida auris is well known to cause hospital outbreaks, other species in the C. haemulonii complex are less well documented but gained attention as opportunistic pathogens. Only one documented outbreak has been published. We describe the second, silent, fungemia outbreak due to antifungal-susceptible C. duobushaemulonii. Methods: We retrospectively genotyped six C. duobushaemulonii bloodstream isolates, collected in a 4-month-period in 2022 (n = 4) and during a week in 2024 (n = 2) in pediatric patients in Brazil. Whole genome sequencing (WGS) was done and compared to n = 33 publicly available genomes, including four cases from an outbreak in Panama. Antifungal susceptibility was performed with the reference CLSI method. Results: MALDI-TOF-MS identified isolates as either C. pseudohaemulonii or C. duobushaemulonii albeit with low scores. ITS sequence analyses confirmed all isolates as C. duobushaemulonii. WGS proved the presence of an outbreak among four pediatric patients in 2022 and a genetically distinct cluster of two cases in 2024. All six isolates were susceptible to azoles and echinocandins and were interpreted as being resistant to amphotericin B with a MIC at breakpoint of 2 µg/mL. Conclusions: This study describes the second documented outbreak due to the rare yeast C. duobushaemulonii, belonging to the C. haemulonii species complex, during 2022–2024 in patients admitted to a pediatric oncology ward in a Brazilian hospital.

## Linked entities

- **Chemicals:** amphotericin B (PubChem CID 1972), azoles (PubChem CID 699591)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** Cancer (MESH:D009369), Candida duobushaemulonii infection (MESH:D002177), chills (MESH:D023341), bloodstream infection (MESH:D018805), Acute lymphoblastic leukemia (MESH:D054198), Fever (MESH:D005334), vulvovaginal candidiasis (MESH:D002181), injury to (MESH:D014947), C. duobushaemulonii (OMIM:211750), fungemia (MESH:D016469), C. duobushaemulonii infection (MESH:D007239), febrile (MESH:D000071072), bacteraemia (MESH:C531821), neutropenia (MESH:D009503), aneuploidy (MESH:D000782), wound infections (MESH:D014946), candidemia (MESH:D058387)
- **Chemicals:** anidulafungin (MESH:D000077612), isavuconazole (MESH:C508735), echinocandins (MESH:D054714), acetonitrile (MESH:C032159), ITC (MESH:C009051), POS (MESH:D011059), formic acid (MESH:C030544), voriconazole (MESH:D065819), alpha-cyano-4-hydroxycinnamic acid (MESH:C007175), Fluconazole (MESH:D015725), Micafungin (MESH:D000077551), ethanol (MESH:D000431), AF172262.1 (-), azole (MESH:D001393), trifluoroacetic acid (MESH:D014269), posaconazole (MESH:C101425), itraconazole (MESH:D017964), AMB (MESH:D000666), MgCl2 (MESH:D015636)
- **Species:** Candidozyma pseudohaemuli (species) [taxon 418784], Candidozyma auris (species) [taxon 498019], Candidozyma duobushaemuli (species) [taxon 1231522], Acinetobacter baumannii (species) [taxon 470], Candidozyma vulturna (species) [taxon 2093215], Pichia kudriavzevii (species) [taxon 4909], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Candidozyma haemuli (species) [taxon 45357], Clavispora lusitaniae (species) [taxon 36911], Candidozyma haemuli var. vulneris (varietas) [taxon 1231523], Staphylococcus epidermidis (species) [taxon 1282], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Y132F

## Full text

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## Figures

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## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC13023860/full.md

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Source: https://tomesphere.com/paper/PMC13023860