Department of Health Sciences, University of Genoa, Genoa, Italy; Infectious Diseases Unit, Ospedale Policlinico San Martino - IRCCS, Genoa, Italy.
Department of Health Sciences, University of Genoa, Genoa, Italy.
Clin Microbiol Infect. 2022 Aug;28(8):1154.e1-1154.e3. doi: 10.1016/j.cmi.2022.02.045. Epub 2022 Mar 10.
Serum (1,3)-beta-d-glucan (BDG) assay is a non-culture-based test recommended for the diagnosis of invasive candidiasis owing to its faster results and higher sensitivity than blood cultures. Its performance might vary for different Candida species. The aim of this study was to determine in vitro levels of BDG in Candida auris culture supernatants and evaluate BDG levels in patients with C. auris candidemia sustained by these stains.
C. auris strains were collected from blood cultures of patients who had a concomitant (-24 to +72 hours) serum BDG test (Fungitell assay). Supernatants of broth media culture of C. auris strains and two Candida albicans (controls) strains were prepared and tested for BDG.
Ten C auris strains were included. Supernatants of two C. albicans considered as controls had a mean BDG level of 1155 pg/mL (considered 100% reactivity). The median BDG level in supernatants of C. auris strains was 275 pg/mL (IQR 165-523 pg/mL), with a median reactivity of 24% (range 6%-72%). In vivo, the median BDG level was 129 pg/mL (IQR, 28-199 pg/mL). Sensitivity of BDG for C. auris candidemia was 60%. All patients received antifungal treatment with an echinocandin initiated a median of 2 days (IQR -8 to 0) before blood collection for BDG.
Our C. auris strains released lower amounts of BDG when compared to C. albicans. Clinical implications include lower sensitivity of serum BDG for the diagnosis of C. auris candidemia with a consequent impact on management protocols in settings with high prevalence of this species.
血清(1,3)-β-d-葡聚糖(BDG)检测是一种基于非培养的检测方法,由于其检测结果更快且比血培养更敏感,因此被推荐用于侵袭性念珠菌病的诊断。但其性能可能因不同的念珠菌物种而异。本研究旨在确定 C. auris 培养上清液中的 BDG 体外水平,并评估这些菌株引起的 C. auris 念珠菌血症患者的 BDG 水平。
从同期(-24 至+72 小时)进行血清 BDG 检测(Fungitell 检测)的患者血液培养物中收集 C. auris 菌株。制备 C. auris 菌株和两种 C. albicans(对照)菌株的肉汤培养基培养上清液并进行 BDG 检测。
纳入 10 株 C auris 菌株。两种作为对照的 C. albicans 菌株的上清液的平均 BDG 水平为 1155 pg/mL(被认为是 100%反应性)。C. auris 菌株上清液的中位 BDG 水平为 275 pg/mL(IQR 165-523 pg/mL),中位反应性为 24%(范围 6%-72%)。在体内,BDG 中位水平为 129 pg/mL(IQR,28-199 pg/mL)。BDG 对 C. auris 念珠菌血症的敏感性为 60%。所有患者均接受棘白菌素类抗真菌治疗,在采集血液进行 BDG 检测前中位时间为 2 天(IQR -8 至 0)。
与 C. albicans 相比,我们的 C. auris 菌株释放的 BDG 量较低。临床意义包括血清 BDG 对 C. auris 念珠菌血症的诊断敏感性较低,这可能会对该物种高发地区的管理方案产生影响。