Koo Sophia, Thomas Horatio R, Daniels S David, Lynch Robert C, Fortier Sean M, Shea Margaret M, Rearden Preshious, Comolli James C, Baden Lindsey R, Marty Francisco M
Division of Infectious Diseases, Brigham and Women's Hospital Dana-Farber Cancer Institute Harvard Medical School, Boston.
Division of Infectious Diseases, Brigham and Women's Hospital Harvard Medical School, Boston.
Clin Infect Dis. 2014 Dec 15;59(12):1733-40. doi: 10.1093/cid/ciu725. Epub 2014 Oct 22.
Invasive aspergillosis (IA) remains a leading cause of mortality in immunocompromised patients, in part due to the difficulty of diagnosing this infection.
Using thermal desorption-gas chromatography/mass spectrometry, we characterized the in vitro volatile metabolite profile of Aspergillus fumigatus, the most common cause of IA, and other pathogenic aspergilli. We prospectively collected breath samples from patients with suspected invasive fungal pneumonia from 2011 to 2013, and assessed whether we could discriminate patients with proven or probable IA from patients without aspergillosis, as determined by European Organization for Research and Treatment of Cancer/Mycoses Study Group consensus definitions, by direct detection of fungal volatile metabolites in these breath samples.
The monoterpenes camphene, α- and β-pinene, and limonene, and the sesquiterpene compounds α- and β-trans-bergamotene were distinctive volatile metabolites of A. fumigatus in vitro, distinguishing it from other pathogenic aspergilli. Of 64 patients with suspected invasive fungal pneumonia based on host risk factors, clinical symptoms, and radiologic findings, 34 were diagnosed with IA, whereas 30 were ultimately diagnosed with other causes of pneumonia, including other invasive mycoses. Detection of α-trans-bergamotene, β-trans-bergamotene, a β-vatirenene-like sesquiterpene, or trans-geranylacetone identified IA patients with 94% sensitivity (95% confidence interval [CI], 81%-98%) and 93% specificity (95% CI, 79%-98%).
In patients with suspected fungal pneumonia, an Aspergillus secondary metabolite signature in breath can identify individuals with IA. These results provide proof-of-concept that direct detection of exogenous fungal metabolites in breath can be used as a novel, noninvasive, pathogen-specific approach to identifying the precise microbial cause of pneumonia.
侵袭性曲霉病(IA)仍是免疫功能低下患者死亡的主要原因之一,部分原因是这种感染的诊断存在困难。
我们使用热脱附-气相色谱/质谱法对烟曲霉(IA最常见的病因)及其他致病性曲霉的体外挥发性代谢产物谱进行了表征。我们在2011年至2013年期间前瞻性收集了疑似侵袭性真菌性肺炎患者的呼吸样本,并通过直接检测这些呼吸样本中的真菌挥发性代谢产物,评估我们是否能够根据欧洲癌症研究与治疗组织/真菌病研究组的共识定义,将确诊或疑似IA的患者与无曲霉病的患者区分开来。
单萜类的莰烯、α-蒎烯和β-蒎烯以及柠檬烯,以及倍半萜类化合物α-和β-反式佛手柑油烯是烟曲霉体外独特的挥发性代谢产物,使其与其他致病性曲霉区分开来。在64例基于宿主危险因素、临床症状和影像学表现疑似侵袭性真菌性肺炎的患者中,34例被诊断为IA,而30例最终被诊断为其他肺炎病因,包括其他侵袭性真菌病。检测α-反式佛手柑油烯、β-反式佛手柑油烯、一种类似β-瓦伦烯的倍半萜或反式香叶基丙酮可识别IA患者,灵敏度为94%(95%置信区间[CI],81%-98%),特异性为93%(95%CI,79%-98%)。
在疑似真菌性肺炎的患者中,呼吸中的曲霉次生代谢产物特征可识别IA患者。这些结果提供了概念验证,即直接检测呼吸中的外源性真菌代谢产物可作为一种新颖的、非侵入性且针对病原体的方法来确定肺炎的确切微生物病因。