Schlaberg Robert, Queen Krista, Simmon Keith, Tardif Keith, Stockmann Chris, Flygare Steven, Kennedy Brett, Voelkerding Karl, Bramley Anna, Zhang Jing, Eilbeck Karen, Yandell Mark, Jain Seema, Pavia Andrew T, Tong Suxiang, Ampofo Krow
Department of Pathology.
ARUP Institute for Clinical and Experimental Pathology, Salt Lake City, Utah ; and.
J Infect Dis. 2017 May 1;215(9):1407-1415. doi: 10.1093/infdis/jix148.
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.
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.
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.
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.
社区获得性肺炎(CAP)是儿童住院的主要原因。约20%的儿童无法确定病原体,但这对于优化治疗和预防医院获得性感染至关重要。我们采用两种广谱检测策略来识别检测结果为阴性的CAP儿童及无症状对照中的病原体。
对70名病因不明的5岁以下CAP儿童及90名无症状对照的鼻咽/口咽拭子进行下一代测序(RNA测序)和针对19个病毒家族的泛病毒组(PVG)PCR检测。通过调整优势比(aOR)和95%置信区间评估病毒与CAP的相关性,并对季节和年龄组进行控制。
RNA测序/PVG PCR在34%的患者中检测到了之前遗漏的推定病原体。推定的病毒病原体包括人副流感病毒4型(aOR 9.3,P = 0.12)、人博卡病毒(aOR 9.1,P < 0.01)、柯萨奇病毒(aOR 5.1,P = 0.09)、鼻病毒A(aOR 3.5,P = 0.34)和鼻病毒C(aOR 2.9,P = 0.57)。RNA测序对RNA病毒更敏感,而PVG PCR检测到更多的DNA病毒。
RNA测序和PVG PCR在三分之一病因未明的住院CAP儿童的鼻咽/口咽标本中检测到了其他病毒,其中一些已知具有致病性。这两种广谱方法可能成为未来流行病学和诊断研究的有用工具。