Huang Yunfei, Zhang Yongqi, Yang Shuangshuang, Lu Hongling, Yu Hanbing, Wang Xingyue, Jia Xiaojiong, Tang Dijiao, Wu Linhong, Huang Shifeng, Yang Ping
Department of Clinical Laboratory Medicine, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Department of Laboratory Medicine, Fujian Key Clinical Specialty of Laboratory Medicine, Women and Children's Hospital, School of Medicine, Xiamen University, Xiamen, China.
Microbiol Spectr. 2024 Aug 6;12(8):e0072524. doi: 10.1128/spectrum.00725-24. Epub 2024 Jul 15.
Cryptococcal meningitis (CM), a common and serious opportunistic infection mostly caused by , is primarily treated with fluconazole. Nevertheless, strains that undergo repeated exposure to azoles can gradually acquire heteroresistance to fluconazole. The management of this specific CM infection poses a substantial challenge. Determining a globally accepted definition for fluconazole heteroresistance and developing effective and prompt methods for identifying heteroresistance is of utmost importance. We collected data on the clinical and epidemiological characteristics of patients diagnosed with CM. All the available strains isolated from these patients were collected and subjected to antifungal susceptibility testing and evaluation of fluconazole heteroresistance. AIDS was present in 40.5% of the patients, whereas 24.1% did not have any underlying diseases. Patients with chronic diseases or impaired immune systems are susceptible to infection by , a fungus that frequently (39.6%, 19/48) shows heteroresistance to fluconazole, as confirmed by population analysis profile (PAP).IMPORTANCEFluconazole heteroresistance poses a significant threat to the efficacy of fluconazole in treating cryptococcal meningitis (CM). Unfortunately, the standard broth microdilution method often misses the subtle percentages of subpopulations exhibiting heteroresistance. While the population analysis profile (PAP) method is esteemed as the gold standard, its time-consuming and labor-intensive nature makes it impractical for routine clinical use. In contrast, the Kirby-Bauer (KB) disk diffusion method offers a simple and effective screening solution. Our study highlights the value of KB over PAP and minimum inhibitory concentration (MIC) by demonstrating that when adjusting the inoculum concentration to 1.0 McFarland and subjecting samples to a 72-hour incubation period at 35°C, the KB method closely mirrors the outcomes of the PAP approach in detecting fluconazole heteroresistance. This optimization of the KB method not only enhances assay efficiency but also provides a blueprint for developing a timely and effective strategy for identifying heteroresistance.
隐球菌性脑膜炎(CM)是一种常见且严重的机会性感染,主要由[隐球菌]引起,主要用氟康唑治疗。然而,反复接触唑类药物的[隐球菌]菌株可逐渐获得对氟康唑的异质性耐药。这种特定的CM感染的管理带来了重大挑战。确定全球公认的氟康唑异质性耐药定义并开发有效且快速的异质性耐药鉴定方法至关重要。我们收集了被诊断为CM的患者的临床和流行病学特征数据。从这些患者中分离出的所有可用[隐球菌]菌株均被收集,并进行抗真菌药敏试验和氟康唑异质性耐药评估。40.5%的患者患有艾滋病,而24.1%的患者没有任何基础疾病。患有慢性疾病或免疫系统受损的患者易受[隐球菌]感染,通过群体分析谱(PAP)证实,这种真菌对氟康唑经常(39.6%,19/48)表现出异质性耐药。
重要性
氟康唑异质性耐药对氟康唑治疗隐球菌性脑膜炎(CM)的疗效构成重大威胁。不幸的是,标准肉汤微量稀释法常常遗漏表现出异质性耐药的亚群的细微百分比。虽然群体分析谱(PAP)方法被视为金标准,但其耗时且费力的性质使其在常规临床应用中不切实际。相比之下, Kirby-Bauer(KB)纸片扩散法提供了一种简单有效的筛选解决方案。我们的研究通过证明当将接种物浓度调整为1.0麦氏单位并在35°C下将样品孵育72小时时,KB方法在检测氟康唑异质性耐药方面与PAP方法的结果密切相似,突出了KB方法相对于PAP方法和最低抑菌浓度(MIC)的价值。KB方法的这种优化不仅提高了检测效率,还为制定及时有效的异质性耐药鉴定策略提供了蓝图。