Seven-year performance of a clinical metagenomic next-generation sequencing test for diagnosis of central nervous system infections

被引:6
|
作者
Benoit, Patrick [1 ]
Brazer, Noah [1 ]
de Lorenzi-Tognon, Mikael [1 ]
Kelly, Emily [1 ]
Servellita, Venice [1 ]
Oseguera, Miriam [1 ]
Nguyen, Jenny [1 ]
Tang, Jack [1 ]
Omura, Charles [1 ]
Streithorst, Jessica [1 ]
Hillberg, Melissa [1 ]
Ingebrigtsen, Danielle [1 ]
Zorn, Kelsey [2 ]
Wilson, Michael R. [3 ,4 ]
Blicharz, Tim [5 ]
Wong, Amy P. [5 ]
O'Donovan, Brian [5 ]
Murray, Brad [5 ]
Miller, Steve [1 ,5 ]
Chiu, Charles Y. [1 ,6 ,7 ]
机构
[1] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA USA
[3] Univ Calif San Francisco, Weill Inst Neurosci, San Francisco, CA USA
[4] Univ Calif San Francisco, Dept Neurol, San Francisco, CA USA
[5] Delve Bio, Boston, MA USA
[6] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[7] Chan Zuckerberg Biohub, San Francisco, CA 94158 USA
关键词
UNITED-STATES; MENINGITIS; VIRUS; ENCEPHALITIS; DELAY;
D O I
10.1038/s41591-024-03275-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Metagenomic next-generation sequencing (mNGS) of cerebrospinal fluid (CSF) is an agnostic method for broad-based diagnosis of central nervous system (CNS) infections. Here we analyzed the 7-year performance of clinical CSF mNGS testing of 4,828 samples from June 2016 to April 2023 performed by the University of California, San Francisco (UCSF) clinical microbiology laboratory. Overall, mNGS testing detected 797 organisms from 697 (14.4%) of 4,828 samples, consisting of 363 (45.5%) DNA viruses, 211 (26.4%) RNA viruses, 132 (16.6%) bacteria, 68 (8.5%) fungi and 23 (2.9%) parasites. We also extracted clinical and laboratory metadata from a subset of the samples (n = 1,164) from 1,053 UCSF patients. Among the 220 infectious diagnoses in this subset, 48 (21.8%) were identified by mNGS alone. The sensitivity, specificity and accuracy of mNGS testing for CNS infections were 63.1%, 99.6% and 92.9%, respectively. mNGS testing exhibited higher sensitivity (63.1%) than indirect serologic testing (28.8%) and direct detection testing from both CSF (45.9%) and non-CSF (15.0%) samples (P < 0.001 for all three comparisons). When only considering diagnoses made by CSF direct detection testing, the sensitivity of mNGS testing increased to 86%. These results justify the routine use of diagnostic mNGS testing for hospitalized patients with suspected CNS infection.
引用
收藏
页码:3522 / 3533
页数:17
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