Department of Pediatrics, Chang Bing Show Chwan Memorial Hospital, Changhua, Taiwan; Institute of Clinical Medicine, National Yang-Ming University, Taipei, Taiwan.
J Med Virol. 2014 Dec;86(12):2128-33. doi: 10.1002/jmv.23940. Epub 2014 Jun 11.
Human adenoviruses (HADVs) comprise at least 54 types and cause a wide spectrum of respiratory tract infections; early diagnosis and epidemiological monitoring of HADV infections requires a rapid and sensitive assay. The use of a real-time polymerase chain reaction (PCR) assay was evaluated with one set of in-house designed primers for respiratory adenoviral infections. The assay was first validated by detecting successfully 6 representative types and 100 clinical isolates. A concomitant prospective surveillance of viral aetiology using conventional cultures and PCR assays in 160 febrile children with acute respiratory tract symptoms was conducted between May 2010 and July 2011. Viral aetiologies were confirmed in 72 (45%) cases using conventional cultures, including 51 adenoviral infections. The concordance between the real-time PCR and culture was good (Kappa = 0.94), and two additional culture-negative adenovirus infections were identified. During the study period (January 2011), an adenoviral community epidemic occurred. Adenovirus B3 was the predominant type in this epidemic (69.8%), followed by C2 (5.7%), C1 (5.7%), C5 (1.9%), E4 (1.9%), C6 (1.9%), F41 (1.9%), and 4 unclassified species C (7.5%). Significantly prolonged duration of fever (>5 days), higher leukocyte counts, higher neutrophil counts, and higher C-reactive protein levels were in the adenoviral infected group (n = 53, P < 0.001), compared with the non-adenoviral infected group (n = 107). In conclusion, this in-house real-time PCR is capable of detecting adenoviral respiratory infections of various types in children; and patients with adenoviral aetiology suffered from more severe clinical manifestations.
人腺病毒(HADV)至少包含 54 种类型,可引起广泛的呼吸道感染;早期诊断和 HADV 感染的流行病学监测需要快速和敏感的检测方法。我们评估了使用一套内部设计的引物进行呼吸道腺病毒感染的实时聚合酶链反应(PCR)检测方法。该方法首先通过成功检测 6 种代表性类型和 100 种临床分离株进行了验证。2010 年 5 月至 2011 年 7 月,我们对 160 例急性呼吸道症状发热儿童进行了常规培养和 PCR 检测病毒病原学的前瞻性监测。通过常规培养证实了 72 例(45%)病毒病因,其中包括 51 例腺病毒感染。实时 PCR 和培养之间的一致性很好(Kappa = 0.94),并确定了另外 2 例培养阴性的腺病毒感染。在研究期间(2011 年 1 月),腺病毒社区爆发。在这次流行中,腺病毒 B3 是主要类型(69.8%),其次是 C2(5.7%)、C1(5.7%)、C5(1.9%)、E4(1.9%)、C6(1.9%)、F41(1.9%)和 4 种未分类的 C 型(7.5%)。与非腺病毒感染组(n=107)相比,腺病毒感染组(n=53)的发热持续时间明显延长(>5 天)、白细胞计数更高、中性粒细胞计数更高、C 反应蛋白水平更高(P<0.001)。总之,这种内部实时 PCR 能够检测儿童各种类型的腺病毒呼吸道感染;腺病毒感染的患者临床表现更严重。