James Hogg Research Centre, Providence Heart-Lung Institute at St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
Pediatr Infect Dis J. 2011 Feb;30(2):e18-23. doi: 10.1097/INF.0b013e3181ff2fac.
respiratory viral infections account for a considerable proportion of pediatric emergency room visits. Illnesses range in severity from mild upper respiratory tract infections to serious lower respiratory tract infections (LRTI). The relationship between viral load and specific viruses to clinical diagnosis made by physicians in this setting is poorly understood.
we applied a real-time, quantitative polymerase chain reaction (qPCR) panel for 13 common respiratory viruses to 195 frozen, archival nasopharyngeal aspirate specimens obtained from symptomatic children ≤ 4 months of age presenting to the emergency room. Mean total viral load and number of viruses per archival nasopharyngeal aspirate specimen were compared between LRTI (n = 70) and non-LRTI (1 or more of upper respiratory tract infection, fever, or cough) (n = 125), as were yield and concordance of qPCR results to viral culture/direct fluorescence assay (DFA).
children with LRTI had significantly increased total viral load and harbored more viruses than the non-LRTI group. Respiratory syncytial virus-A and -B were significantly associated with LRTI, and parainfluenza virus-1 with non-LRTI. Individual loads of parainfluenza virus-2 and human rhinovirus were increased in LRTI versus non-LRTI. Quantitative PCR yielded more viruses (including coinfections, where a "dominant virus" was typically identified) than viral culture/DFA and documented nucleic acid from pathogens not tested by culture/DFA including human rhinovirus; coronaviruses -OC43, -229E, and -NL63; and metapneumovirus.
in symptomatic children presenting to the emergency room, total viral load is related to clinical diagnosis; specific viruses are associated with particular clinical diagnoses, and qPCR has a higher yield than other viral diagnostic methods.
呼吸道病毒感染占儿科急诊就诊的相当大比例。疾病的严重程度从轻度上呼吸道感染到严重的下呼吸道感染(LRTI)不等。在这种情况下,病毒载量与特定病毒与医生临床诊断之间的关系尚未得到很好的理解。
我们应用了一种实时定量聚合酶链反应(qPCR)面板,对 195 份来自急诊科就诊的≤4 个月有症状儿童的冷冻存档鼻咽抽吸物标本进行了 13 种常见呼吸道病毒检测。将 LRTI(n = 70)和非 LRTI(1 种或多种上呼吸道感染、发热或咳嗽)(n = 125)患者的鼻咽抽吸物标本的平均总病毒载量和病毒数进行比较,比较 qPCR 结果与病毒培养/直接荧光抗体检测(DFA)的产量和一致性。
LRTI 患儿的总病毒载量显著增加,且携带的病毒数量多于非 LRTI 组。呼吸道合胞病毒-A 和-B 与 LRTI 显著相关,副流感病毒-1 与非 LRTI 相关。与非 LRTI 相比,副流感病毒-2 和人鼻病毒的个体负荷增加。与病毒培养/DFA 相比,定量 PCR 可检测到更多病毒(包括合并感染,其中通常可识别“优势病毒”),并可检测到培养/DFA 未检测到的病原体的核酸,包括人鼻病毒;冠状病毒-OC43、-229E 和-NL63;和肺炎支原体。
在急诊科就诊的有症状儿童中,总病毒载量与临床诊断有关;特定病毒与特定临床诊断有关,qPCR 的产量高于其他病毒诊断方法。