Metagenomic sequencing and evaluation of the host response in the pediatric aerodigestive population

被引:2
|
作者
Gatcliffe, Chelsea [1 ,3 ]
Rao, Aparna [1 ]
Brigger, Matthew [2 ]
Dimmock, David [3 ]
Hansen, Christian [3 ]
Montgomery, Jesse [4 ]
Schlaberg, Robert [4 ]
Coufal, Nicole G. [3 ,5 ]
Farnaes, Lauge [3 ,6 ]
机构
[1] Univ Calif San Diego, Rady Childrens Hosp San Diego, Div Pediat Resp Med, Dept Pediat, San Diego, CA 92103 USA
[2] Rady Childrens Hosp San Diego, Rady Childrens Inst Genom Med, San Diego, CA USA
[3] Univ Calif San Diego, Rady Childrens Hosp San Diego, Div Pediat Otolaryngol, Dept Surg, San Diego, CA 92103 USA
[4] IDbyDNA Inc, Salt Lake City, UT USA
[5] Univ Calif San Diego, Rady Childrens Hosp San Diego, Dept Pediat, Pediat Crit Care, San Diego, CA 92103 USA
[6] Univ Calif San Diego, Rady Childrens Hosp San Diego, Dept Pediat, Div Pediat Infect Dis, San Diego, CA 92103 USA
关键词
aerodigestive; host response; metagenomics; next‐ generation sequencing; TROPHERYMA-WHIPPLEI; ASPIRATION; MICROBIOTA; INFECTION; DIAGNOSIS; COHORT;
D O I
10.1002/ppul.25198
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objectives To assess the diagnostic utility of metagenomic sequencing in pediatric aerodigestive clinic patients being evaluated for chronic aspiration. We hypothesize that using a metagenomics platform will aid in the identification of microbes not found on standard culture. Study Design and Methods Twenty-four children referred to an aerodigestive clinic were enrolled in a prospective, single-site, cross-sectional cohort study. At the time of clinical evaluation under anesthesia, two samples were obtained: an upper airway sample and a sample from bronchoalveolar lavage (BAL). Samples were sent for routine culture and analyzed using Explify (R) Respiratory, a CLIA Laboratory Developed Test which identifies respiratory commensals and pathogens through RNA and DNA sequencing. Since RNA was sequenced in the course of the metagenomic analysis to identify organisms (RNA viruses and bacteria), the sequencing approach also captured host derived messenger RNA during sample analysis. This incidentally obtained host transcriptomic data were analyzed to evaluate the host immune response. The results of these studies were correlated with the clinical presentation of the research subjects. Results In 10 patients, organisms primarily associated with oral flora were identified in the BAL. Standard culture was negative in three patients where clinical metagenomics led to a result with potential clinical significance. Transcriptomic data correlated with the presence or absence of dysphagia as identified on prior videofluoroscopic evaluation of swallowing. Conclusions Clinical metagenomics allows for simultaneous analysis of the microbiota and the host immune response from BAL samples. As the technologies in this field continue to advance, such testing may improve the diagnostic evaluation of patients with suspected chronic aspiration.
引用
收藏
页码:516 / 524
页数:9
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