Zeqi Zhou, Xiuzhen Wu, Yaonan Lin, Ying Wang, Yuan Zhang, He Wang, Yan Su, Shigui Liu
{"title":"基于快速细胞生长的A-327型酵母药敏快速检测系统","authors":"Zeqi Zhou, Xiuzhen Wu, Yaonan Lin, Ying Wang, Yuan Zhang, He Wang, Yan Su, Shigui Liu","doi":"10.1093/clinchem/hvaf086.315","DOIUrl":null,"url":null,"abstract":"Background Due to the growing burden of fungal infections and a recent rise in antifungal resistance, antifungal susceptibility testing (AFST) is of increasing importance. The common methods of AFST for yeasts have turnaround times of 24 to 48 h. Given the urgency of adequate antifungal treatment in invasive mycoses, rapid antifungal susceptibility testing is urgently needed in clinics to treat invasive fungal infections with the appropriate antifungal drugs and to slow the emergence of antifungal resistance. Methods Here, we demonstrate a rapid AFST by measuring the metabolism in fungal cells using resazurin and a medium that promotes the growth and metabolism of fungal cells (Fig). A total of 32 clinical fungal strains were randomly analyzed from the Peking Union Medical College Hospital. Species of these strains were commonly found in patients with systemic infections, including 9 Candida albicans, 5 Candida krusei, 3 Candida tropicalis, 3 Candida parapsilosis, 3 Candida lusitaniae, 7 Candida glabrata, and 2 Candida guilliermondii. The Sensititre YeastOne panel was performed according to the manufacturer*s instructions as reference methods. For the rapid AFST method, MICs were determined at 6 h of incubation. MICs for the YeastOne panel were read at 24 h of incubation. The overall agreement within +/- 2 dilutions by both methods was calculated against ten antifungal agents. Results Considering the Sensititre YeastOne Colorimetric Broth method as a comparator method, ten antifungal agents (?uconazole, itraconazole, voriconazole, posaconazole, isavuconazole, caspofungin, micafungin, anidulafungin, amphotericin B, and 5-flucytosine) showed an essential agreement of > 90%. Conclusion Therefore, this rapid AFST can be considered as an optional method that can obtain results and interpretations faster than previous methods. This method overcomes the limitation of slow growth in conventional methods and has the potential for the rapid diagnosis of candidemia and other clinical fungal infections.","PeriodicalId":10690,"journal":{"name":"Clinical chemistry","volume":"19 1","pages":""},"PeriodicalIF":6.3000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A-327 Rapid Antifungal Susceptibility Testing System for Yeasts Based on Fast Cell Growth\",\"authors\":\"Zeqi Zhou, Xiuzhen Wu, Yaonan Lin, Ying Wang, Yuan Zhang, He Wang, Yan Su, Shigui Liu\",\"doi\":\"10.1093/clinchem/hvaf086.315\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background Due to the growing burden of fungal infections and a recent rise in antifungal resistance, antifungal susceptibility testing (AFST) is of increasing importance. The common methods of AFST for yeasts have turnaround times of 24 to 48 h. Given the urgency of adequate antifungal treatment in invasive mycoses, rapid antifungal susceptibility testing is urgently needed in clinics to treat invasive fungal infections with the appropriate antifungal drugs and to slow the emergence of antifungal resistance. Methods Here, we demonstrate a rapid AFST by measuring the metabolism in fungal cells using resazurin and a medium that promotes the growth and metabolism of fungal cells (Fig). A total of 32 clinical fungal strains were randomly analyzed from the Peking Union Medical College Hospital. Species of these strains were commonly found in patients with systemic infections, including 9 Candida albicans, 5 Candida krusei, 3 Candida tropicalis, 3 Candida parapsilosis, 3 Candida lusitaniae, 7 Candida glabrata, and 2 Candida guilliermondii. The Sensititre YeastOne panel was performed according to the manufacturer*s instructions as reference methods. For the rapid AFST method, MICs were determined at 6 h of incubation. MICs for the YeastOne panel were read at 24 h of incubation. The overall agreement within +/- 2 dilutions by both methods was calculated against ten antifungal agents. Results Considering the Sensititre YeastOne Colorimetric Broth method as a comparator method, ten antifungal agents (?uconazole, itraconazole, voriconazole, posaconazole, isavuconazole, caspofungin, micafungin, anidulafungin, amphotericin B, and 5-flucytosine) showed an essential agreement of > 90%. Conclusion Therefore, this rapid AFST can be considered as an optional method that can obtain results and interpretations faster than previous methods. This method overcomes the limitation of slow growth in conventional methods and has the potential for the rapid diagnosis of candidemia and other clinical fungal infections.\",\"PeriodicalId\":10690,\"journal\":{\"name\":\"Clinical chemistry\",\"volume\":\"19 1\",\"pages\":\"\"},\"PeriodicalIF\":6.3000,\"publicationDate\":\"2025-10-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical chemistry\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/clinchem/hvaf086.315\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICAL LABORATORY TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/clinchem/hvaf086.315","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
A-327 Rapid Antifungal Susceptibility Testing System for Yeasts Based on Fast Cell Growth
Background Due to the growing burden of fungal infections and a recent rise in antifungal resistance, antifungal susceptibility testing (AFST) is of increasing importance. The common methods of AFST for yeasts have turnaround times of 24 to 48 h. Given the urgency of adequate antifungal treatment in invasive mycoses, rapid antifungal susceptibility testing is urgently needed in clinics to treat invasive fungal infections with the appropriate antifungal drugs and to slow the emergence of antifungal resistance. Methods Here, we demonstrate a rapid AFST by measuring the metabolism in fungal cells using resazurin and a medium that promotes the growth and metabolism of fungal cells (Fig). A total of 32 clinical fungal strains were randomly analyzed from the Peking Union Medical College Hospital. Species of these strains were commonly found in patients with systemic infections, including 9 Candida albicans, 5 Candida krusei, 3 Candida tropicalis, 3 Candida parapsilosis, 3 Candida lusitaniae, 7 Candida glabrata, and 2 Candida guilliermondii. The Sensititre YeastOne panel was performed according to the manufacturer*s instructions as reference methods. For the rapid AFST method, MICs were determined at 6 h of incubation. MICs for the YeastOne panel were read at 24 h of incubation. The overall agreement within +/- 2 dilutions by both methods was calculated against ten antifungal agents. Results Considering the Sensititre YeastOne Colorimetric Broth method as a comparator method, ten antifungal agents (?uconazole, itraconazole, voriconazole, posaconazole, isavuconazole, caspofungin, micafungin, anidulafungin, amphotericin B, and 5-flucytosine) showed an essential agreement of > 90%. Conclusion Therefore, this rapid AFST can be considered as an optional method that can obtain results and interpretations faster than previous methods. This method overcomes the limitation of slow growth in conventional methods and has the potential for the rapid diagnosis of candidemia and other clinical fungal infections.
期刊介绍:
Clinical Chemistry is a peer-reviewed scientific journal that is the premier publication for the science and practice of clinical laboratory medicine. It was established in 1955 and is associated with the Association for Diagnostics & Laboratory Medicine (ADLM).
The journal focuses on laboratory diagnosis and management of patients, and has expanded to include other clinical laboratory disciplines such as genomics, hematology, microbiology, and toxicology. It also publishes articles relevant to clinical specialties including cardiology, endocrinology, gastroenterology, genetics, immunology, infectious diseases, maternal-fetal medicine, neurology, nutrition, oncology, and pediatrics.
In addition to original research, editorials, and reviews, Clinical Chemistry features recurring sections such as clinical case studies, perspectives, podcasts, and Q&A articles. It has the highest impact factor among journals of clinical chemistry, laboratory medicine, pathology, analytical chemistry, transfusion medicine, and clinical microbiology.
The journal is indexed in databases such as MEDLINE and Web of Science.