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[Bio-Speedy脑膜炎/脑炎检测板在中枢神经系统感染诊断中的评估]

[Evaluation of the Bio-Speedy Meningitis/Encephalitis Panel in the Diagnosis of Central Nervous System Infections].

作者信息

Merdan Osman, Sağlık İmran, Aksoy Fatma Dilşad, Önal Uğur, Özakın Cüneyt, Hacımustafaoğlu Mustafa Kemal, Çelebi Solmaz, Ağca Harun, Tekinsoy Mehmet, Ener Beyza

机构信息

Bursa Uludağ University Faculty of Medicine, Department of Medical Microbiology, Bursa, Türkiye.

Bursa Uludağ University Faculty of Medicine, Department of Pediatrics, Bursa, Türkiye.

出版信息

Mikrobiyol Bul. 2024 Jul;58(3):270-283. doi: 10.5578/mb.202497189.

Abstract

Infections of the central nervous system (CNS) can lead to severe outcomes if not accurately diagnosed and treated. The broad spectrum of pathogens involved in CNS infections can make diagnosis challenging. Polymerase chain reaction (PCR) -based multiplex molecular diagnostic panels can rapidly and simultaneously detect multiple neuropathogens in cerebrospinal fluid (CSF). This study was aimed to assess the Bio-Speedy Meningitis/Encephalitis RT-PCR MX-17 panel (Bioeksen, İstanbul, Türkiye), a novel multiplex PCR test, in diagnosing CNS infections. The panel can detect a range of pathogens, including Escherichia coli K1, Haemophilus influenzae, Listeria monocytogenes, Neisseria meningitidis, Streptococcus pneumoniae, Streptococcus agalactiae, enterovirus (EV), herpes simplex virus (HSV) 1 and 2, HHV-6, HHV-7, HHV-8, human parechovirus (HPeV), varicella zoster virus (VZV), cytomegalovirus (CMV) and Cryptococcus gatti/neoformans in CSF samples. This retrospective study included 128 CSF samples from 128 patients sent to Bursa Uludağ University Health Application and Research Center Microbiology Laboratory between June 2022 and July 2023 to search for CNS infectious agents. Patient clinical, radiological and laboratory data were collected from the Hospital Information Record System (HIRS). Bacterial pathogens were identified through culture, while viral pathogens were detected in CSF samples using the Fast Track Diagnostics (FTD) multiplex RT-PCR panel (Fast Track Diagnostics Ltd., Luxembourg) for HSV-1, HSV-2, VZV, EV, mumps virus and HPeV. The stored CSF samples were then tested using the BioSpeedy panel and the results were compared with those of the culture and the FTD panel. Pathogens that were detected were considered positive if they were consistent with the patient's symptoms and CSF characteristics according to infectious disease and pediatric infectious disease specialists. Pathogens detected but not supported by the patient's symptoms and CSF characteristics were classified as uncertain clinical relevance (UCR). Out of the 128 patients tested for CNS infectious agents, 44 (34.4%) were diagnosed with a CNS infection. The overall pathogen detection rate with all methods was 43.2% (19/44). The Bio-Speedy panel identified pathogens in 29.5% (13/44) of the patients, followed by the FTD panel (20.5%, 9/44) and culture (9.1%, 4/44). Four bacteria were identified with culture, three of which were also detected by the Bio-Speedy panel. Additionally, six bacteria were identified with Bio-Speedy panel, that were not identified by culture. The FTD panel identified nine viruses, four of which were also identified by Bio-Speedy. In total, the Bio-Speedy panel detected 13 of the 19 positive pathogens (nine bacteria and four viruses: [S.pneumoniae (n= 3), VZV (n= 3), N.meningitidis (n= 2), H.influenzae (n= 2), L.monocytogenes (n= 1), E.coli (n= 1) ve EV (n= 1)]. However, the Bio-Speedy panel identified 15 pathogens [S.pneumoniae (n= 1), E.coli (n= 1), C.gatti/neoformans (n= 1), CMV (n= 8), HHV-6 (n= 3) ve HHV-7 (n= 1)] considered as UCR. The Bio-Speedy identified the causative pathogens in the highest percentage (29.5%) of patients with confirmed CNS infections. Nevertheless, test results should be interpreted based on patient characteristics to ensure appropriate patient management. Using multiple methods and multiplex tests may improve diagnostic accuracy for CNS infections.

摘要

如果中枢神经系统(CNS)感染未得到准确诊断和治疗,可能会导致严重后果。中枢神经系统感染涉及的病原体种类繁多,这使得诊断具有挑战性。基于聚合酶链反应(PCR)的多重分子诊断检测板可快速、同时检测脑脊液(CSF)中的多种神经病原体。本研究旨在评估新型多重PCR检测——Bio-Speedy脑膜炎/脑炎逆转录PCR MX-17检测板(Bioeksen,土耳其伊斯坦布尔)在诊断中枢神经系统感染中的应用。该检测板可检测多种病原体,包括大肠杆菌K1、流感嗜血杆菌、单核细胞增生李斯特菌、脑膜炎奈瑟菌、肺炎链球菌、无乳链球菌、肠道病毒(EV)、单纯疱疹病毒(HSV)1型和2型、HHV-6、HHV-7、HHV-8、人细小病毒(HPeV)、水痘带状疱疹病毒(VZV)、巨细胞病毒(CMV)和加氏/新生隐球菌的脑脊液样本。这项回顾性研究纳入了2022年6月至2023年7月期间送至布尔萨乌鲁达大学健康应用与研究中心微生物实验室的128例患者的128份脑脊液样本,以寻找中枢神经系统感染病原体。患者的临床、放射学和实验室数据从医院信息记录系统(HIRS)中收集。通过培养鉴定细菌病原体,而使用快速诊断(FTD)多重逆转录PCR检测板(卢森堡快速诊断有限公司)检测脑脊液样本中的病毒病原体,用于检测HSV-1、HSV-2、VZV、EV、腮腺炎病毒和HPeV。然后使用BioSpeedy检测板对储存的脑脊液样本进行检测,并将结果与培养和FTD检测板的结果进行比较。根据传染病和儿科传染病专家的意见,如果检测到的病原体与患者的症状和脑脊液特征一致,则认为其为阳性。检测到但未得到患者症状和脑脊液特征支持的病原体被归类为临床相关性不确定(UCR)。在检测中枢神经系统感染病原体的128例患者中,44例(34.4%)被诊断为中枢神经系统感染。所有方法的总体病原体检测率为43.2%(19/44)。Bio-Speedy检测板在29.5%(13/44)的患者中鉴定出病原体,其次是FTD检测板(20.5%,9/44)和培养(9.1%,4/44)。通过培养鉴定出4种细菌,其中3种也被Bio-Speedy检测板检测到。此外,Bio-Speedy检测板鉴定出6种细菌,而培养未鉴定出这些细菌。FTD检测板鉴定出9种病毒,其中4种也被Bio-Speedy检测到。总体而言,Bio-Speedy检测板检测到了19种阳性病原体中的13种(9种细菌和4种病毒:[肺炎链球菌(n = 3)、VZV(n = 3)、脑膜炎奈瑟菌(n = 2)、流感嗜血杆菌(n = 2)、单核细胞增生李斯特菌(n = 1)、大肠杆菌(n = 1)和EV(n = 1)])。然而,Bio-Speedy检测板鉴定出15种病原体[肺炎链球菌(n = 1)、大肠杆菌(n = 1)、加氏/新生隐球菌(n = 1)、CMV(n = 8)、HHV-6(n = 3)和HHV-7(n = 1)]被视为UCR。Bio-Speedy在确诊的中枢神经系统感染患者中鉴定出病原体的比例最高(29.5%)。尽管如此,应根据患者特征解释检测结果,以确保对患者进行适当管理。使用多种方法和多重检测可能会提高中枢神经系统感染的诊断准确性。

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