College of Medicine, Veterinary and Life Sciences, Institute of Cardiovascular and Medical Sciences, University of Glasgow, Scotland, UK.
Int J Obes (Lond). 2011 Apr;35 Suppl 1:S113-8. doi: 10.1038/ijo.2011.43.
To evaluate two saliva collection methods for DNA yield and quality as applied to a large, integrated, multicentre, European project involving the collection of biological material from children.
Cross-sectional multicentre comparative study in young children.
Saliva samples were collected from 14,019 children aged 2-9 years from eight European countries participating in the IDEFICS (Identification and prevention of dietary- and lifestyle-induced health effects in children and infants) study. This involved either the collection of 2 ml of saliva from children who were able to spit, or using a sponge to collect whole saliva and buccal mucosal cells from the inside of the mouth of younger children unable to spit. Samples were assembled centrally in each participating centre and subsequently despatched for DNA extraction and biobanking to the University of Glasgow. A subgroup of 4678 samples (∼33% of sampled individuals) were chosen for DNA extraction before genotyping.
The whole-saliva collection method resulted in a higher DNA yield than the sponge collection method (mean±s.d.; saliva: 20.95±2.35 μg, sponge: 9.13±2.25 μg; P<0.001). DNA quality as measured by A (260)/A (280) was similar for the two collection methods. A minimum genotype calling success rate of 95% showed that both methods provide good-quality DNA for genotyping using TaqMan allelic discrimination assays.
Our results showed higher DNA yield from the whole-saliva collection method compared with the assisted sponge collection. However, both collection methods provided DNA of sufficient quantity and quality for large-scale genetic epidemiological studies.
评估两种唾液采集方法的 DNA 产量和质量,这些方法适用于一个大型的、综合的、多中心的欧洲项目,该项目涉及从儿童中收集生物材料。
在幼儿中进行的横断面多中心比较研究。
从参与 IDEFICS(儿童和婴儿饮食和生活方式诱导的健康影响的识别和预防)研究的 8 个欧洲国家的 14019 名 2-9 岁儿童中收集唾液样本。这涉及到能够吐口水的儿童采集 2ml 唾液,或者使用海绵从不能吐口水的年幼儿童的口腔内采集全唾液和颊粘膜细胞。样本在每个参与中心集中收集,然后送往格拉斯哥大学进行 DNA 提取和生物样本库储存。选择了 4678 个样本(约占采样个体的 33%)进行 DNA 提取和基因分型。
全唾液采集法的 DNA 产量高于海绵采集法(均值±标准差;唾液:20.95±2.35μg,海绵:9.13±2.25μg;P<0.001)。两种采集方法的 A(260)/A(280)值相似,表明 DNA 质量相当。最低基因型调用成功率为 95%,表明两种方法均能为 TaqMan 等位基因区分检测提供高质量的 DNA 用于基因分型。
与辅助海绵采集法相比,全唾液采集法的 DNA 产量更高。然而,两种采集方法都提供了足够数量和质量的 DNA,适用于大规模的遗传流行病学研究。