T2 Magnetic Resonance Enables Nanoparticle-Mediated Rapid Detection of Candidemia in Whole Blood

被引:209
作者
Neely, Lori A. [1 ]
Audeh, Mark [1 ]
Nu Ai Phung [1 ]
Min, Michael [1 ]
Suchocki, Adam [1 ]
Plourde, Daniella [1 ]
Blanco, Matthew [1 ]
Demas, Vasiliki [1 ]
Skewis, Lynell R. [1 ]
Anagnostou, Theodora [2 ]
Coleman, Jeffrey J. [2 ,3 ,4 ]
Wellman, Parris [1 ]
Mylonakis, Eleftherios [2 ,3 ,4 ]
Lowery, Thomas J. [1 ]
机构
[1] T2 Biosyst, Lexington, MA 02421 USA
[2] Brown Univ, Div Infect Dis, Providence, RI 02906 USA
[3] Massachusetts Gen Hosp, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Boston, MA 02114 USA
关键词
PCR AMPLIFICATION; FUNGAL PATHOGENS; IDENTIFICATION; DIAGNOSIS; SYSTEM; CANDIDIASIS; GUIDELINES; INITIATION; RESISTANT; CELLS;
D O I
10.1126/scitranslmed.3005377
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Candida spp. cause both local and disseminated infections in immunocompromised patients. Bloodstream infections of Candida spp., known as "candidemia," are associated with a high mortality rate (40%), which is mainly attributed to the long diagnostic time required by blood culture. We introduce a diagnostic platform based on T2 magnetic resonance (T2MR), which is capable of sensitive and rapid detection of fungal targets in whole blood. In our approach, blood-compatible polymerase chain reaction is followed by hybridization of the amplified pathogen DNA to capture probe-decorated nanoparticles. Hybridization yields nanoparticle microclusters that cause large changes in the sample's T2MR signal. With this T2MR-based method, Candida spp. can be detected directly in whole blood, thus eliminating the need for analyte purification. Using a small, portable T2MR detection device, we were able to rapidly, accurately, and reproducibly detect five Candida species within human whole blood with a limit of detection of 1 colony-forming unit/ml and a time to result of < 3 hours. Spiked blood samples showed 98% positive agreement and 100% negative agreement between T2MR and blood culture. Additionally, performance of the assay was evaluated on 21 blinded clinical specimens collected serially. This study shows that the nanoparticle-and T2MR-based detection method is rapid and amenable to automation and offers clinicians the opportunity to detect and identify multiple human pathogens within hours of sample collection.
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