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Microbial Volatiles as Diagnostic Biomarkers of Bacterial Lung Infection in Mechanically Ventilated Patients

催产克雷伯菌 微生物学 金黄色葡萄球菌 医学 肺炎克雷伯菌 支气管肺泡灌洗 铜绿假单胞菌 病菌 微生物培养 流感嗜血杆菌 胃肠病学 大肠杆菌 内科学 细菌 免疫学 生物 抗生素 遗传学 基因 生物化学
作者
Waqar Ahmed,Dominic Fenn,Iain R. White,Breanna Dixon,Tamara M. E. Nijsen,Hugo Knobel,Paul Brinkman,Pouline M. P. van Oort,Marcus J. Schultz,Paul Dark,Royston Goodacre,Timothy Felton,Lieuwe D. J. Bos,Stephen J. Fowler,Waqar Ahmed,Antonio Artigas Raventós,Jonathan Bannard‐Smith,Lieuwe D. J. Bos,Marta Camprubi,Luís Coelho
出处
期刊:Clinical Infectious Diseases [Oxford University Press]
卷期号:76 (6): 1059-1066 被引量:13
标识
DOI:10.1093/cid/ciac859
摘要

Abstract Background Early and accurate recognition of respiratory pathogens is crucial to prevent increased risk of mortality in critically ill patients. Microbial-derived volatile organic compounds (mVOCs) in exhaled breath could be used as noninvasive biomarkers of infection to support clinical diagnosis. Methods In this study, we investigated the diagnostic potential of in vitro–confirmed mVOCs in the exhaled breath of patients under mechanical ventilation from the BreathDx study. Samples were analyzed by thermal desorption–gas chromatography–mass spectrometry. Results Pathogens from bronchoalveolar lavage (BAL) cultures were identified in 45 of 89 patients and Staphylococcus aureus was the most commonly identified pathogen (n = 15). Of 19 mVOCs detected in the in vitro culture headspace of 4 common respiratory pathogens (S. aureus, Pseudomonas aeruginosa, Klebsiella pneumoniae, and Escherichia coli), 14 were found in exhaled breath samples. Higher concentrations of 2 mVOCs were found in the exhaled breath of patients infected with S. aureus compared to those without (3-methylbutanal: P < .01, area under the receiver operating characteristic curve [AUROC] = 0.81–0.87; and 3-methylbutanoic acid: P = .01, AUROC = 0.79–0.80). In addition, bacteria identified from BAL cultures that are known to metabolize tryptophan (E. coli, Klebsiella oxytoca, and Haemophilus influenzae) were grouped and found to produce higher concentrations of indole compared to breath samples with culture-negative (P = .034) and other pathogen-positive (P = .049) samples. Conclusions This study demonstrates the capability of using mVOCs to detect the presence of specific pathogen groups with potential to support clinical diagnosis. Although not all mVOCs were found in patient samples within this small pilot study, further targeted and qualitative investigation is warranted using multicenter clinical studies.
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