{"title":"Performance of Short-Term Culture and Direct MALDI-TOF MS for Identification of Candida Species From Blood Cultures","authors":"Tugce Unalan-Altintop, Kristoffer Jansson, Volkan Özenci","doi":"10.1111/apm.70063","DOIUrl":null,"url":null,"abstract":"<p>Rapid and reliable identification of <i>Candida</i> spp. is crucial due to changing epidemiology and increasing resistance. This study aims to compare the identification rates, average Log Score (LS) values, and three different methods: short-term culture, Sepsityper kit, and an in-house method. Simulated blood culture (BC) samples with clinical <i>Candida</i> isolates and human blood from healthy donors were used. Sepsityper kit was used according to manufacturers' recommendations. An in-house protocol was designed using SDS for lysis of erythrocytes. Short-term culture was performed by inoculation of BC broth on Sabouraud Dextrose Agar (SDA) and chromogenic plates and cultured for 6 h. A total of 52 clinical <i>Candida</i> isolates were included in the study. The identification rate was highest (71.9%) for the short-term culture method, 59.6% for the Sepsityper kit, and 57.3% for the in-house method when all types of bottles were analyzed. Higher identification rates were obtained using the BD BACTEC Mycosis-IC/F bottles: 76.7% for the short-term culture method, 100% for the in-house method, and 76.9% for the Sepsityper kit. Short-term culture has high performance in the identification of <i>Candida</i> species, despite a slightly longer detection time than direct MALDI-TOF MS methods.</p>","PeriodicalId":8167,"journal":{"name":"Apmis","volume":"133 8","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/apm.70063","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Apmis","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/apm.70063","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Rapid and reliable identification of Candida spp. is crucial due to changing epidemiology and increasing resistance. This study aims to compare the identification rates, average Log Score (LS) values, and three different methods: short-term culture, Sepsityper kit, and an in-house method. Simulated blood culture (BC) samples with clinical Candida isolates and human blood from healthy donors were used. Sepsityper kit was used according to manufacturers' recommendations. An in-house protocol was designed using SDS for lysis of erythrocytes. Short-term culture was performed by inoculation of BC broth on Sabouraud Dextrose Agar (SDA) and chromogenic plates and cultured for 6 h. A total of 52 clinical Candida isolates were included in the study. The identification rate was highest (71.9%) for the short-term culture method, 59.6% for the Sepsityper kit, and 57.3% for the in-house method when all types of bottles were analyzed. Higher identification rates were obtained using the BD BACTEC Mycosis-IC/F bottles: 76.7% for the short-term culture method, 100% for the in-house method, and 76.9% for the Sepsityper kit. Short-term culture has high performance in the identification of Candida species, despite a slightly longer detection time than direct MALDI-TOF MS methods.
期刊介绍:
APMIS, formerly Acta Pathologica, Microbiologica et Immunologica Scandinavica, has been published since 1924 by the Scandinavian Societies for Medical Microbiology and Pathology as a non-profit-making scientific journal.