Marmaras Nektarios, Xirogianni Athanasia, Papandreou Anastasia, Petinaki Efthymia, Papaevangelou Vana, Tsolia Maria, Tzanakaki Georgina
National Meningitis Reference Laboratory, Department of Public Health Policy, School of Public Health, University of West Attica, 115 21 Athens, Greece.
Department of Microbiology, Medical School, University of Thessaly, 411 10 Larissa, Greece.
Diagnostics (Basel). 2021 Dec 14;11(12):2353. doi: 10.3390/diagnostics11122353.
As almost 60-70% of Invasive Pneumococcal Disease (IPD) is identified by nonculture methods in Greece, serotyping is of high importance for the better monitoring of pneumococcal serotypes due to the availability of conjugate vaccines. The aim of the study was the modification and direct application of the Capsular Sequence Typing (CST) assay in clinical samples in order to serotype culture-negative, Polymerase Chain Reaction (PCR_-positive samples, followed by CST group specific single-tube PCR assays. A two-step PCR modified assay was applied on a total of 306 samples (such as CSF, blood, pleural and middle ear fluids, isolates) obtained from 283 patients with IPD. The overall performance permits a rapid, accurate and cost-effective method for nonculture pneumococcal serotyping. As the management of IPD is closely related to the continuous monitoring of pneumococcal serotypes, the proposed approach proved to be a valuable tool for the typing and epidemiological monitoring of , for the evaluation of the overall impact of vaccination programs in the era of pneumococcal conjugate vaccines, in order to initiate the appropriate vaccination strategy.
在希腊,近60%-70%的侵袭性肺炎球菌疾病(IPD)通过非培养方法得以确诊,由于有结合疫苗可用,血清分型对于更好地监测肺炎球菌血清型具有高度重要性。本研究的目的是对临床样本中的荚膜序列分型(CST)检测方法进行改良并直接应用,以便对培养阴性、聚合酶链反应(PCR)阳性的样本进行血清分型,随后进行CST组特异性单管PCR检测。对从283例IPD患者获得的总共306份样本(如脑脊液、血液、胸腔和中耳液、分离株)应用了两步PCR改良检测方法。总体性能允许采用一种快速、准确且经济高效的非培养肺炎球菌血清分型方法。由于IPD的管理与肺炎球菌血清型的持续监测密切相关,所提出的方法被证明是用于肺炎球菌血清分型和流行病学监测、评估肺炎球菌结合疫苗时代疫苗接种计划的总体影响以及启动适当疫苗接种策略的宝贵工具。