Goshia Tyler, Aralar April, Wiederhold Nathan, Jenks Jeffrey D, Mehta Sanjay R, Sinha Mridu, Karmakar Aprajita, Sharma Ankit, Shrivastava Rachit, Sun Haoxiang, White P Lewis, Hoenigl Martin, Fraley Stephanie I
Department of Bioengineering, University of California San Diego, San Diego, CA, USA.
Department of Pathology, University of Texas Health Science Center, San Antonio, TX, USA.
bioRxiv. 2023 Nov 9:2023.11.09.566457. doi: 10.1101/2023.11.09.566457.
Invasive mold infections (IMIs) such as aspergillosis, mucormycosis, fusariosis, and lomentosporiosis are associated with high morbidity and mortality, particularly in immunocompromised patients, with mortality rates as high as 40% to 80%. Outcomes could be substantially improved with early initiation of appropriate antifungal therapy, yet early diagnosis remains difficult to establish and often requires multidisciplinary teams evaluating clinical and radiological findings plus supportive mycological findings. Universal digital high resolution melting analysis (U-dHRM) may enable rapid and robust diagnosis of IMI. This technology aims to accomplish timely pathogen detection at the single genome level by conducting broad-based amplification of microbial barcoding genes in a digital polymerase chain reaction (dPCR) format, followed by high-resolution melting of the DNA amplicons in each digital reaction to generate organism-specific melt curve signatures that are identified by machine learning.
A universal fungal assay was developed for U-dHRM and used to generate a database of melt curve signatures for 19 clinically relevant fungal pathogens. A machine learning algorithm (ML) was trained to automatically classify these 19 fungal melt curves and detect novel melt curves. Performance was assessed on 73 clinical bronchoalveolar lavage (BAL) samples from patients suspected of IMI. Novel curves were identified by micropipetting U-dHRM reactions and Sanger sequencing amplicons.
U-dHRM achieved an average of 97% fungal organism identification accuracy and a turn-around-time of 4hrs. Pathogenic molds ( and were detected by U-dHRM in 73% of BALF samples suspected of IMI. Mixtures of pathogenic molds were detected in 19%. U-dHRM demonstrated good sensitivity for IMI, as defined by current diagnostic criteria, when clinical findings were also considered.
U-dHRM showed promising performance as a separate or combination diagnostic approach to standard mycological tests. The speed of U-dHRM and its ability to simultaneously identify and quantify clinically relevant mold pathogens in polymicrobial samples as well as detect emerging opportunistic pathogens may provide information that could aid in treatment decisions and improve patient outcomes.
侵袭性霉菌感染(IMIs),如曲霉病、毛霉病、镰刀菌病和罗门孢菌病,与高发病率和死亡率相关,尤其是在免疫功能低下的患者中,死亡率高达40%至80%。早期开始适当的抗真菌治疗可显著改善预后,但早期诊断仍难以确立,通常需要多学科团队评估临床和影像学检查结果以及支持性真菌学检查结果。通用数字高分辨率熔解分析(U-dHRM)可能有助于IMI的快速、可靠诊断。该技术旨在通过以数字聚合酶链反应(dPCR)形式对微生物条形码基因进行广泛扩增,在单基因组水平上及时检测病原体,随后对每个数字反应中的DNA扩增子进行高分辨率熔解,以生成通过机器学习识别的特定生物体熔解曲线特征。
开发了一种用于U-dHRM的通用真菌检测方法,并用于生成19种临床相关真菌病原体的熔解曲线特征数据库。训练了一种机器学习算法(ML)以自动分类这19种真菌熔解曲线并检测新的熔解曲线。对73份疑似IMI患者的临床支气管肺泡灌洗(BAL)样本进行了性能评估。通过微量移液U-dHRM反应和桑格测序扩增子鉴定新曲线。
U-dHRM的真菌生物体识别准确率平均达到97%,周转时间为4小时。在73%的疑似IMI的BALF样本中,U-dHRM检测到致病霉菌(和)。在19%的样本中检测到致病霉菌混合物。当同时考虑临床检查结果时,按照当前诊断标准定义,U-dHRM对IMI显示出良好的敏感性。
U-dHRM作为标准真菌学检测的单独或联合诊断方法表现出良好的性能。U-dHRM的速度及其同时识别和定量多微生物样本中临床相关霉菌病原体以及检测新出现的机会性病原体的能力可能提供有助于治疗决策和改善患者预后的信息。