Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, USA.
mSphere. 2022 Dec 21;7(6):e0033122. doi: 10.1128/msphere.00331-22. Epub 2022 Nov 21.
Nasopharyngeal swabs are considered the gold-standard sample type for the detection of Streptococcus pneumoniae carriage, but recent studies have demonstrated the utility of saliva in improving the detection of carriage in adults. Saliva is generally collected in its raw, unsupplemented state, unlike nasopharyngeal swabs, which are collected into stabilizing transport media. Few data exist regarding the stability of pneumococci in unsupplemented saliva during transport and laboratory storage. We therefore evaluated the effect of storage conditions on the detection of pneumococci in saliva samples using strains representing eight pneumococcal serotypes. The bacteria were spiked into raw saliva from asymptomatic individuals, and we assessed sample viability after storage at 4°C, room temperature, and 30°C for up to 72 h; at 40°C for 24 h; and following three freeze-thaw cycles. We observed little decrease in pneumococcal detection following culture enrichment and quantitative PCR (qPCR) detection of the and genes compared to testing fresh samples, indicating the prolonged viability of pneumococci in neat saliva samples. This sample stability makes saliva a viable sample type for pneumococcal carriage studies conducted in remote or low-resource settings and provides insight into the effect of the storage of saliva samples in the laboratory. For pneumococcal carriage studies, saliva is a sample type that can overcome some of the issues typically seen with nasopharyngeal and oropharyngeal swabs. Understanding the limitations of saliva as a sample type is important for maximizing its use. This study sought to better understand how different storage conditions and freeze-thaw cycles affect pneumococcal survival over time. These findings support the use of saliva as an alternative sample type for pneumococcal carriage studies, particularly in remote or low-resource settings with reduced access to health care facilities.
鼻咽拭子被认为是检测肺炎链球菌携带的金标准样本类型,但最近的研究表明,唾液在提高成人携带检测方面具有实用性。与鼻咽拭子不同,唾液通常以未添加任何物质的原始状态收集,而鼻咽拭子则收集到稳定的运输介质中。关于未添加物质的唾液中肺炎链球菌在运输和实验室储存过程中的稳定性的数据很少。因此,我们使用代表八种肺炎链球菌血清型的菌株来评估储存条件对唾液样本中肺炎链球菌检测的影响。将细菌掺入来自无症状个体的原始唾液中,然后在 4°C、室温下和 30°C 下储存 72 小时;在 40°C 下储存 24 小时;并进行三个冻融循环。我们观察到,与测试新鲜样本相比,在培养富集和定量 PCR(qPCR)检测 和 基因后,肺炎链球菌的检测几乎没有减少,这表明肺炎链球菌在未稀释的唾液样本中具有较长的存活能力。这种样本稳定性使唾液成为在偏远或资源匮乏环境中进行肺炎链球菌携带研究的可行样本类型,并深入了解实验室中唾液样本储存的影响。对于肺炎链球菌携带研究,唾液是一种可以克服鼻咽和口咽拭子通常存在的一些问题的样本类型。了解唾液作为样本类型的局限性对于最大限度地利用它非常重要。本研究旨在更好地了解不同储存条件和冻融循环如何随时间影响肺炎链球菌的存活。这些发现支持将唾液作为肺炎链球菌携带研究的替代样本类型,特别是在偏远或资源匮乏环境中,这些地方的医疗设施较少。