Evidence map›Paper›PMID 39223407›Full record

ArticleCurrent microbiology2024

A Cluster of Diutina catenulata Funguria in Patients with Coronavirus Disease 2019 (COVID-19) Hospitalized in a Tertiary Reference Hospital from Rio de Janeiro, Brazil.

Rodrigo Almeida-Paes, Marcus de Melo Teixeira, Fernanda Alves de Oliveira, Marcos de Abreu Almeida, Fernando Almeida-Silva, Kim Mattos Geraldo, Estevão Portela Nunes, Bridget M Baker, Jason E Stajich, Beatriz Grinsztejn and 3 more

Abstract read
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In one paragraph

Article in Current microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Decoding resistance inFrontiers in cellular and infection microbiology · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Rodrigo Almeida-Paes *Laboratório de Micologia, Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Fiocruz, Av. Brazil 4365 - Manguinhos, Rio de Janeiro, RJ, 21045-900, Brazil.ORCID http://orcid.org/0000-0002-6639-6058
Marcus de Melo Teixeira *The Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ, USA.ORCID http://orcid.org/0000-0003-1763-3464
Fernanda Alves de OliveiraLaboratório de Micologia, Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Fiocruz, Av. Brazil 4365 - Manguinhos, Rio de Janeiro, RJ, 21045-900, Brazil.ORCID http://orcid.org/0000-0002-0793-2631
Marcos de Abreu AlmeidaLaboratório de Micologia, Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Fiocruz, Av. Brazil 4365 - Manguinhos, Rio de Janeiro, RJ, 21045-900, Brazil.ORCID http://orcid.org/0000-0002-5581-631X
Fernando Almeida-SilvaLaboratório de Micologia, Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Fiocruz, Av. Brazil 4365 - Manguinhos, Rio de Janeiro, RJ, 21045-900, Brazil.
Kim Mattos GeraldoLaboratório de Pesquisa Clínica em IST e Aids, Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, RJ, Brazil.
Estevão Portela NunesLaboratório de Pesquisa Clínica em IST e Aids, Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, RJ, Brazil.
Bridget M BakerThe Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ, USA.ORCID http://orcid.org/0000-0002-3439-4517
Jason E StajichDepartment of Microbiology and Plant Pathology, University of California-Riverside, Riverside, CA, USA.ORCID http://orcid.org/0000-0002-7591-0020
Beatriz GrinsztejnLaboratório de Pesquisa Clínica em IST e Aids, Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0003-3692-5155
Valdilea Gonçalves VelosoLaboratório de Pesquisa Clínica em IST e Aids, Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0002-6622-3165
Andrea d'Avila FreitasLaboratório de Micologia, Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Fiocruz, Av. Brazil 4365 - Manguinhos, Rio de Janeiro, RJ, 21045-900, Brazil.
Rosely Maria Zancopé-OliveiraLaboratório de Micologia, Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Fiocruz, Av. Brazil 4365 - Manguinhos, Rio de Janeiro, RJ, 21045-900, Brazil. rosely.zancope@ini.fiocruz.br.ORCID http://orcid.org/0000-0001-7619-1921

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 308315/2021-9Conselho Nacional de Desenvolvimento Científico e Tecnológico 314119/2023-0Conselho Nacional de Desenvolvimento Científico e Tecnológico 316067/2021-0Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/200.381/2023
6 · The paper itself

Abstract

During the COVID-19 pandemic, fungal infections, especially pulmonary aspergillosis, mucormycosis, and invasive candidiasis, have emerged as a significant health concern. Beyond Candida albicans, the most common cause of invasive candidiasis, other rare ascomycetous yeast species have been described in tertiary care units, potentially posing a broader health threat. We have isolated, from September 2020 to June 2021, nine Diutina catenulata strains from urine samples of six patients. This was intriguing as this fungus had not been previously identified in our institution, nor after June 2021. Therefore, we decided to outline the clinical features of the patients with this rare pathogen, to describe phenotypic characteristics, including antifungal susceptibility profiles, of this yeast species and to identify the genetic makeup through whole-genome sequencing analysis to evaluate if this was a cluster of genetically similar D. catenulata isolates in our institution. The strains were identified through MALDI-TOF MS analyses and Sanger sequencing of two rDNA regions. All patients yielding D. catenulata from urine samples needed ventilator support and used urinary catheters during hospitalization for treatment of COVID-19. None of them had received COVID-19 vaccines. Morphological and biochemical profiles of the nine strains were largely consistent, although fluconazole susceptibility varied, ranging from 4 to 32 μg/mL. Phylogenomic analysis revealed minimal genetic variation among the isolates, with low intrapopulation variation, supported by the identification of only 84 SNPs across all strains. Therefore, we propose that the yeast strains isolated were part of a cluster of D. catenulata funguria in the context of COVID-19.

Indexed as

Antifungal AgentsCOVID-19SARS-CoV-2Tertiary Care CentersAdultAgedBrazilFemaleHumansMaleMicrobial Sensitivity TestsMiddle AgedPhylogenySaccharomycetalesWhole Genome SequencingAntifungal Agents

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.