Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT 06510, USA.
Department of Life Sciences and Chemistry, Utrecht University of Applied Sciences, 3584 CS Utrecht, the Netherlands.
Cell Rep Methods. 2023 Feb 21;3(2):100410. doi: 10.1016/j.crmeth.2023.100410. eCollection 2023 Feb 27.
The separation of pneumococcal serotypes from a complex polymicrobial mixture may be required for different applications. For instance, a minority strain could be present at a low frequency in a clinical sample, making it difficult to identify and isolate by traditional culture-based methods. We therefore developed an assay to separate mixed pneumococcal samples using serotype-specific antiserum and a magnetic bead-based separation method. Using qPCR and colony counting methods, we first show that serotypes (12F, 23F, 3, 14, 19A, and 15A) present at ∼0.1% of a dual serotype mixture can be enriched to between 10% and 90% of the final sample. We demonstrate two applications for this method: extraction of known pneumococcal serotypes from saliva samples and efficient purification of capsule switch variants from experimental transformation experiments. This method may have further laboratory or clinical applications when the selection of specific serotypes is required.
从复杂的多微生物混合物中分离肺炎球菌血清型可能适用于不同的应用。例如,少数菌株可能以低频率存在于临床样本中,使得通过传统的基于培养的方法难以识别和分离。因此,我们开发了一种使用血清型特异性抗血清和基于磁珠的分离方法来分离混合肺炎球菌样本的方法。我们首先使用 qPCR 和菌落计数方法表明,在双血清型混合物中以约 0.1%存在的血清型(12F、23F、3、14、19A 和 15A)可以富集到最终样本的 10%至 90%之间。我们展示了该方法的两种应用:从唾液样本中提取已知的肺炎球菌血清型和从实验转化实验中有效纯化荚膜转换变体。当需要选择特定血清型时,该方法可能在实验室或临床应用中具有进一步的应用。