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Quantification methods of Candida albicans are independent irrespective of fungal morphology

dc.contributor.authorSoares, Amanda B. [UNESP]
dc.contributor.authorde Albuquerque, Maria C. [UNESP]
dc.contributor.authorRosa, Leticia M. [UNESP]
dc.contributor.authorKlein, Marlise I.
dc.contributor.authorPavarina, Ana C. [UNESP]
dc.contributor.authorBarbugli, Paula A. [UNESP]
dc.contributor.authorDovigo, Livia N. [UNESP]
dc.contributor.authorde O Mima, Ewerton G. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.date.accessioned2025-04-29T18:49:11Z
dc.date.issued2024-01-01
dc.description.abstractThe ability of Candida albicans to switch its morphology from yeast to filaments, known as polymorphism, may bias the methods used in microbial quantification. Here, we compared the quantification methods [cell/mL, colony forming units (CFU)/mL, and the number of nuclei estimated by viability polymerase chain reaction (vPCR)] of three strains of C. albicans (one reference strain and two clinical isolates) grown as yeast, filaments, and biofilms. Metabolic activity (XTT assay) was also used for biofilms. Comparisons between the methods were evaluated by agreement analyses [Intraclass and Concordance Correlation Coefficients (ICC and CCC, respectively) and Bland-Altman Plot] and Pearson Correlation (α = 0.05). Principal Component Analysis (PCA) was employed to visualize the similarities and differences between the methods. Results demonstrated a lack of agreement between all methods irrespective of fungal morphology/growth, even when a strong correlation was observed. Bland-Altman plot also demonstrated proportional bias between all methods for all morphologies/growth, except between CFU/mL X vPCR for yeasts and biofilms. For all morphologies, the correlation between the methods were strong, but without linear relationship between them, except for yeast where vPCR showed weak correlation with cells/mL and CFU/mL. XTT moderately correlated with CFU/mL and vPCR and weakly correlated with cells/mL. For all morphologies/growth, PCA showed that CFU/mL was similar to cells/mL and vPCR was distinct from them, but for biofilms vPCR became more similar to CFU/mL and cells/mL while XTT was the most distinct method. As conclusions, our investigation demonstrated that CFU/mL underestimated cells/mL, while vPCR overestimated both cells/mL and CFU/mL, and that the methods had poor agreement and lack of linear relationship, irrespective of C. albicans morphology/growth.en
dc.description.affiliationLaboratory of Applied Microbiology Department of Dental Materials and Prosthodontics School of Dentistry São Paulo State University (UNESP), Araraquara, Araraquara
dc.description.affiliationDepartment of Oral Diagnosis Piracicaba Dental School State University of Campinas (UNICAMP), Piracicaba
dc.description.affiliationDepartment of Social Dentistry School of Dentistry São Paulo State University (UNESP), Araraquara, Araraquara
dc.description.affiliationUnespLaboratory of Applied Microbiology Department of Dental Materials and Prosthodontics School of Dentistry São Paulo State University (UNESP), Araraquara, Araraquara
dc.description.affiliationUnespDepartment of Social Dentistry School of Dentistry São Paulo State University (UNESP), Araraquara, Araraquara
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2017/24591-9
dc.description.sponsorshipIdFAPESP: 2018/02513-9
dc.description.sponsorshipIdFAPESP: 2021/08890-1
dc.description.sponsorshipIdFAPESP: RIDC 13/07276-1
dc.format.extent265-277
dc.identifierhttp://dx.doi.org/10.15698/mic2024.07.831
dc.identifier.citationMicrobial Cell, v. 11, n. 1, p. 265-277, 2024.
dc.identifier.doi10.15698/mic2024.07.831
dc.identifier.issn2311-2638
dc.identifier.scopus2-s2.0-85209719594
dc.identifier.urihttps://hdl.handle.net/11449/300294
dc.language.isoeng
dc.relation.ispartofMicrobial Cell
dc.sourceScopus
dc.subjectCandida albicans
dc.subjectcell count
dc.subjectcolony count
dc.subjecthyphae
dc.subjectmicrobial
dc.subjectpolymerase chain reaction
dc.subjectyeasts
dc.titleQuantification methods of Candida albicans are independent irrespective of fungal morphologyen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationca4c0298-cd82-48ee-a9c8-c97704bac2b0
relation.isOrgUnitOfPublication.latestForDiscoveryca4c0298-cd82-48ee-a9c8-c97704bac2b0
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt

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