Viral Pathogen Detection by Metagenomics and Pan-Viral Group Polymerase Chain Reaction in Children With Pneumonia Lacking Identifiable Etiology

被引:83
作者
Schlaberg, Robert [1 ,5 ]
Queen, Krista [6 ]
Simmon, Keith [2 ]
Tardif, Keith [5 ]
Stockmann, Chris [3 ]
Flygare, Steven [4 ]
Kennedy, Brett [4 ]
Voelkerding, Karl [1 ,5 ]
Bramley, Anna [6 ]
Zhang, Jing [6 ]
Eilbeck, Karen [2 ]
Yandell, Mark [4 ]
Jain, Seema [6 ]
Pavia, Andrew T. [3 ]
Tong, Suxiang [6 ]
Ampofo, Krow [3 ]
机构
[1] Univ Utah, Dept Pathol, Salt Lake City, UT USA
[2] Univ Utah, Dept Biomed Informat, Salt Lake City, UT USA
[3] Univ Utah, Dept Pediat, Salt Lake City, UT USA
[4] Univ Utah, Dept Human Genet, Salt Lake City, UT USA
[5] ARUP Inst Clin & Expt Pathol, Salt Lake City, UT USA
[6] Ctr Dis Control & Prevent, Atlanta, GA USA
基金
美国国家卫生研究院;
关键词
RNA sequencing (RNA-seq); metagenomics; pan-viral group polymerase chain reaction (PVG PCR); pneumonia; COMMUNITY-ACQUIRED PNEUMONIA; RESPIRATORY SYNCYTIAL VIRUS; REQUIRING HOSPITALIZATION; CLINICAL CHARACTERISTICS; HUMAN METAPNEUMOVIRUS; DISEASE SEVERITY; LOAD; PCR; INFECTION; BATS;
D O I
10.1093/infdis/jix148
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Community-acquired pneumonia (CAP) is a leading cause of pediatric hospitalization. Pathogen identification fails in approximately 20% of children but is critical for optimal treatment and prevention of hospital-acquired infections. We used two broad-spectrum detection strategies to identify pathogens in test-negative children with CAP and asymptomatic controls. Methods. Nasopharyngeal/oropharyngeal (NP/OP) swabs from 70 children <5 years with CAP of unknown etiology and 90 asymptomatic controls were tested by next-generation sequencing (RNA-seq) and pan viral group (PVG) PCR for 19 viral families. Association of viruses with CAP was assessed by adjusted odds ratios (aOR) and 95% confidence intervals controlling for season and age group. Results. RNA-seq/PVG PCR detected previously missed, putative pathogens in 34% of patients. Putative viral pathogens included human parainfluenza virus 4 (aOR 9.3, P = .12), human bocavirus (aOR 9.1, P < .01), Coxsackieviruses (aOR 5.1, P = .09), rhinovirus A (aOR 3.5, P = .34), and rhinovirus C (aOR 2.9, P = .57). RNA-seq was more sensitive for RNA viruses whereas PVG PCR detected more DNA viruses. Conclusions. RNA-seq and PVG PCR identified additional viruses, some known to be pathogenic, in NP/OP specimens from one-third of children hospitalized with CAP without a previously identified etiology. Both broad-range methods could be useful tools in future epidemiologic and diagnostic studies.
引用
收藏
页码:1407 / 1415
页数:9
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