State Key Laboratory of Emerging Infectious Diseases, Hong Kong.
J Clin Virol. 2010 Mar;47(3):282-5. doi: 10.1016/j.jcv.2009.12.014. Epub 2010 Jan 13.
Although high-density resequencing microarray is useful for detection and tracking the evolution of viruses associated with respiratory tract infections, no report on using this technology for the detection of viruses in patients with conjunctivitis is available.
To test if high-density resequencing microarray can be applied to detection of viruses in conjunctival swabs for patients with conjunctivitis.
In this prospective proof-of-concept study, every 4 or 5 bacterial culture-negative conjunctival swab samples were pooled and subject to viral detection using TessArray Resequencing Pathogen Microarrays-Flu 3.1 (RPM-Flu-3.1). Results were compared with human adenovirus (HAdV) hexon gene PCR sequencing and viral culture.
Thirty-two of the 38 conjunctival swab samples were bacterial culture-negative. Four of the 7 pooled samples were positive for HAdV using RPM-Flu-3.1. Hexon gene PCR sequencing on the 38 original individual samples showed that 3 and 4 samples contained HAdVs species D and B respectively. All the 6 samples that were positive for hexon gene PCR but negative for bacterial culture were also positive by the resequencing microarray. Viral culture was positive for HAdV type 3 in 1 sample, which was also positive by PCR and resequencing microarray.
Resequencing microarray is as sensitive as PCR for detection of HAdV in conjunctival swabs. Unlike viral culture and hexon gene PCR sequencing, resequencing microarray was not able to differentiate the type and species of HAdV. Development of microarrays for conjunctivitis can be performed for rapid diagnosis of the viral cause of conjunctivitis.
高密度重测序微阵列对于检测和跟踪与呼吸道感染相关的病毒进化非常有用,但目前尚无关于使用该技术检测结膜炎患者病毒的报道。
测试高密度重测序微阵列是否可用于检测结膜炎患者结膜拭子中的病毒。
在这项前瞻性概念验证研究中,每 4 或 5 个细菌培养阴性的结膜拭子样本被混合,并使用 TessArray 重测序病原体微阵列-流感 3.1(RPM-Flu-3.1)进行病毒检测。结果与人类腺病毒(HAdV)六邻体基因 PCR 测序和病毒培养进行比较。
38 个结膜拭子样本中有 32 个为细菌培养阴性。7 个混合样本中有 4 个使用 RPM-Flu-3.1 检测到 HAdV 呈阳性。对 38 个原始个体样本的六邻体基因 PCR 测序显示,3 个和 4 个样本分别含有 HAdV 种 D 和 B。所有 6 个六邻体基因 PCR 阳性但细菌培养阴性的样本均通过重测序微阵列呈阳性。病毒培养对 1 个样本中的 HAdV 型 3 呈阳性,该样本也通过 PCR 和重测序微阵列呈阳性。
重测序微阵列与 PCR 一样,可用于检测结膜拭子中的 HAdV。与病毒培养和六邻体基因 PCR 测序不同,重测序微阵列无法区分 HAdV 的型和种。开发结膜炎微阵列可用于快速诊断结膜炎的病毒病因。