Bannister Stephanie A, Kidd Stephen P, Kirby Elizabeth, Shah Sonal, Thomas Anvy, Vipond Richard, Elmore Michael J, Telfer Brunton Andrew, Marsh Peter, Green Steve, Silman Nigel J, Kempsell Karen E
Public Health England, Porton Down, Salisbury SP4 0JG, UK.
Department of Clinical Microbiology, Royal Cornwall Hospitals NHS Trust, Penventinnie Lane, Treliske, Truro, Cornwall TR1 3LQ, UK.
High Throughput. 2018 Oct 16;7(4):32. doi: 10.3390/ht7040032.
Meningitis is commonly caused by infection with a variety of bacterial or viral pathogens. Acute bacterial meningitis (ABM) can cause severe disease, which can progress rapidly to a critical life-threatening condition. Rapid diagnosis of ABM is critical, as this is most commonly associated with severe sequelae with associated high mortality and morbidity rates compared to viral meningitis, which is less severe and self-limiting. We have designed a microarray for detection and diagnosis of ABM. This has been validated using randomly amplified DNA targets (RADT), comparing buffers with or without formamide, in glass slide format or on the Alere ArrayTube (Alere Technologies GmbH) microarray platform. Pathogen-specific signals were observed using purified bacterial nucleic acids and to a lesser extent using patient cerebral spinal fluid (CSF) samples, with some technical issues observed using RADT and glass slides. Repurposing the array onto the Alere ArrayTube platform and using a targeted amplification system increased specific and reduced nonspecific hybridization signals using both pathogen nucleic and patient CSF DNA targets, better revealing pathogen-specific signals although sensitivity was still reduced in the latter. This diagnostic microarray is useful as a laboratory diagnostic tool for species and strain designation for ABM, rather than for primary diagnosis.
脑膜炎通常由多种细菌或病毒病原体感染引起。急性细菌性脑膜炎(ABM)可导致严重疾病,病情可迅速发展至危及生命的危急状态。ABM的快速诊断至关重要,因为与病毒性脑膜炎相比,ABM最常伴有严重后遗症,死亡率和发病率较高,而病毒性脑膜炎症状较轻且具有自限性。我们设计了一种用于检测和诊断ABM的微阵列。已使用随机扩增DNA靶标(RADT)对其进行验证,比较了含或不含甲酰胺的缓冲液,采用载玻片形式或在Alere ArrayTube(Alere Technologies GmbH)微阵列平台上进行验证。使用纯化的细菌核酸观察到病原体特异性信号,使用患者脑脊液(CSF)样本时观察到的信号较弱,使用RADT和载玻片时存在一些技术问题。将该阵列重新应用于Alere ArrayTube平台并使用靶向扩增系统,使用病原体核酸和患者CSF DNA靶标时,特异性杂交信号增加,非特异性杂交信号减少,尽管后者的灵敏度仍有所降低,但能更好地显示病原体特异性信号。这种诊断微阵列作为一种实验室诊断工具,对于ABM的菌种和菌株鉴定很有用,而不是用于初步诊断。