Abstract
Candida famata has been associated with the identifiable Candida infections that takes place in human and the identification error of this species possibly will result in misinterpretation of antifungal susceptibility and improper diagnosis; which will have a major effect on the prognosis and therapy of patients. Our objective is to correctly identify Candida spp. collected from patients at the intensive care units, New Cairo University teaching hospital in Cairo-Egypt using matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF MS). Hundred clinically isolated yeast strains were identified using API 20C AUX obtained from patients receiving care at intensive care units. ATB FUNGUS 3 strips were used to detect the minimum inhibitory concentration. Thirty-three non duplicate strains identified as C. famata were subjected to re-identification by MALDI-TOF MS. Our results revealed that isolates were initially identified as C. famata 33%, C. tropicalis 15%, C. albicans 12% and C. parapsillosis 10% using the phenotypic techniques. MALDI-TOF MS analyses results showed that the 33 C. famata isolates are C. tropicalis (n = 29), Trichosporon asahii (n = 2), C. parapsilosis (n = 1), and Aeromonas sobria (n = 1). Antifungal resistance was low in the Candida species, except for reduced susceptibility to itraconazole among C. krusei strains. This report shows that misidentification of C. famata is frequent when using conventional phenotypic methods of identification which result in challenges in treating fungal infections. MALDI-TOF MS is an accurate convenient substitute to classical approaches for fungal identification. In general, antifungal multidrug resistance is uncommon in our studied Candida species and yeast isolates.
Similar content being viewed by others
Data Availability
Data available within the article or its supplementary materials.
References
Delavy M, Dos Santos AR, Heiman CM, Coste AT (2019) Investigating antifungal susceptibility in candida species with MALDI-TOF MS-based assays. Front Cell Infect Microbiol 9:19
Miceli MH, Diaz JA, Lee SA (2011) Emerging opportunistic yeast infections. Lancet Infect Dis 11:142–151
Diekema D, Arbefeville S, Boyken L, Kroeger J, Pfaller M (2012) The changing epidemiology of healthcare-associated candidemia over three decades. Diagn Microbiol Infect Dis 73:45–48
Pfaller MA, Diekema DJ, Gibbs DL, Newell VA, Ellis D, Tullio V et al (2010) Results from the artemis disk global antifungal surveillance study, 1997 to 2007: a 10.5-year analysis of susceptibilities of Candida species to fluconazole and voriconazole as determined by CLSI standardized disk diffusion. J Clin Microbiol 48:1366–1377
Castanheira M, Woosley LN, Diekema DJ, Jones RN, Pfaller MA (2013) Candida guilliermondii and other species of Candida misidentified as Candidafamata: assessment by Vitek 2, DNA sequencing analysis, and matrix-assisted laser desorption ionization-time of flight mass spectrometry in two global antifungal surveillance programs. J Clin Microbiol 51:117–124
Kim HY, Huh HJ, Choi R, Ki CS, Lee NY (2015) Three cases of candidiasis misidentified as Candidafamata by the Vitek 2 system. Ann Lab Med 35:175–177
Kim SH, Shin JH, Mok JH, Kim SY, Song SA, Kim HR et al (2014) Misidentification of Candidaguilliermondii as C. famata among strains isolated from blood cultures by the VITEK 2 system. Biomed Res Int. https://doi.org/10.1155/2014/250408
Kim TH, Kweon OJ, Kim HR, Lee MK (2016) Identification of uncommon Candida species using commercial identification systems. J Microbiol Biotechnol 26(12):2206–2213
Jamal WY, Ahmad S, Khan ZU, Rotimi VO (2014) Comparative evaluation of two matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) systems for the identification of clinically significant yeasts. Int J Infect Dis 26:167–170
Freydiere AM, Guinet R, Boiron P (2001) Yeast identification in the clinical microbiology laboratory: phenotypical methods. Med Mycol 39:9–33
Clinical and Laboratory Standards Institute (2008) Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeast; Approved Standard-Third Edition. CLSI document M27–A3. Clinical and Laboratory Standards Institute, Wayne
Iriart X, Lavergne RA, Fillaux J, Valentin A, Magnaval JF, Berry A, Cassaing S (2012) Routine identification of medical fungi by the new Vitek MS matrix-assisted laser desorption ionization-time of flight system with a new time-effective strategy. J Clin Microbiol 50:2107–2110
Calandra T, Roberts J, Antonelli M, Bassetti M, Vincent JL (2016) Diagnosis and management of invasive candidiasis in the ICU: an updated approach to an old enemy. Crit Care 20:125
Xu J, Millar BC, Moore JE et al (2002) Comparison of API20C with molecular identification of Candida spp. isolated from bloodstream infections. J Clin Pathol 55(10):774–777
Arastehfar A, Daneshnia F, Kord M, Roudbary M, Zarrinfar H, Fang W, Hashemi SJ, Najafzadeh MJ, Khodavaisy S, Pan W, Liao W, Badali H, Rezaie S, Zomorodian K, Hagen F, Boekhout T (2019) Comparison of 21-Plex PCR and API 20C AUX, MALDI-TOF MS, and rDNA sequencing for a wide range of clinically isolated yeast species: improved identification by combining 21-Plex PCR and API 20C AUX as an alternative strategy for developing countries. Front Cell Infect Microbiol 9:21
Guo LN, Xiao M, Kong F, Chen SCA, Wang H, Sorrell TC et al (2011) Three-locus identification, genotyping, and antifungal susceptibilities of medically important Trichosporon species from China. J Clin Microbiol 49:3805–3811. https://doi.org/10.1128/JCM.00937-11
Kathuria S, Singh PK, Sharma C, Prakash A, Masih A, Kumar A et al (2015) Multidrug-resistant Candidaauris misidentified as Candidahaemulonii: characterization by matrix-assisted laser desorption ionizationtime of flight mass spectrometry and DNA sequencing and its antifungal susceptibility profile variability by vitek 2, CL. J Clin Microbiol 53:1823–1830
Svobodova L, Bednarova D, Ruzicka F, Chrenkova V, Dobias R, Mallatova N et al (2016) High frequency of Candidafabianii among clinical isolates biochemically identified as Candidapelliculosa and Candidautilis. Mycoses 59:241–246
Criseo G, Scordino F, Romeo O (2015) Current methods for identifying clinically important cryptic Candida species. J Microbiol Methods 111:50–56
Montes K, Ortiz B, Galindo C, Figueroa I, Braham S, Fontecha G (2019) Identification of Candida species from clinical samples in a Honduran Tertiary Hospital. Pathogens 8(237):1–11
Ostrosky-Zeichner L, Pappas PG (2006) Invasive candidiasis in the intensive care unit. Crit Care Med 34:857–863
Abass E, Samir S, ElKholy I, Zaki S (2019) Incidence of ICU-acquired candidemia in a tertiary care hospital in Cairo. Egypt Egypt J Microbiol 54:55–61
Fu J, Ding Y, Wei B et al (2017) Epidemiology of Candidaalbicans and non-C. albicans of neonatal candidemia at a tertiary care hospital in western China Journal List. BMC Infect Dis. 17(1):329
Hegazi M, Abdelkader A, Zaki M, El-Deek B (2014) Characteristics and risk factors of candidemia in pediatric intensive care unit of a tertiary care children’s hospital in Egypt. J Infect Dev Ctries 8(5):624–634
Dutta A, Palazzi DL (2011) Candida non-albicans versus Candida albicans fungemia in the non-neonatal pediatric population. Pediatr Infect Dis J 30(8):664–668
Tumbarello M, Fiori B, Trecarichi EM et al (2012) Risk factors and outcomes of candidemia caused by biofilm-forming isolates in a tertiary care hospital. PLoS ONE 7(3):e33705
Acknowledgements
The authors extend their appreciation to the intensive care units at new Cairo university teaching hospital, Cairo, Egypt.
Author information
Authors and Affiliations
Contributions
Dr. DG, Dr. MMZ, Dr. TH and Dr. MA contributed to the study proposal, implementation of experiments, results evaluation and writing & editing of the manuscript.
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest.
Ethical Approval
The study was approved by the Ethical committee of the clinical and chemical pathology department of Cairo University Hospital as the yeast strains described in this paper are part of routine care for hospitalized intensive care units ‘patients.
Informed Consent
No additional clinical specimens were obtained for purposes of research; therefore, informed consent was not required.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Ghaith, D., Zafer, M.M., Hosny, T. et al. MALDI-TOF MS Overcomes Misidentification of the Uncommon Human Pathogen Candida famata by Routine Phenotypic Identification Methods. Curr Microbiol 78, 1636–1642 (2021). https://doi.org/10.1007/s00284-021-02411-1
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00284-021-02411-1