Institute of Genomics, Estonian Genome Centre, University of Tartu, 51010, Tartu, Estonia.
Department of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.
Sci Rep. 2021 Oct 1;11(1):19603. doi: 10.1038/s41598-021-99046-w.
Colorectal cancer (CRC) is a challenging public health problem which successful treatment depends on the stage at diagnosis. Recently, CRC-specific microbiome signatures have been proposed as a marker for CRC detection. Since many countries have initiated CRC screening programs, it would be useful to analyze the microbiome in the samples collected in fecal immunochemical test (FIT) tubes for fecal occult blood testing. Therefore, we investigated the impact of FIT tubes and stabilization buffer on the microbial community structure evaluated in stool samples from 30 volunteers and compared the detected communities to those of fresh-frozen samples, highlighting previously published cancer-specific communities. Altogether, 214 samples were analyzed by 16S rRNA gene sequencing, including positive and negative controls. Our results indicated that the variation between individuals was greater than the differences introduced by the collection strategy. The vast majority of the genera were stable for up to 7 days. None of the changes observed between fresh-frozen samples and FIT tube specimens were related to previously identified CRC-specific bacteria. Overall, we show that FIT tubes can be used for profiling the microbiota in CRC screening programs. This circumvents the need to collect additional samples and can possibly improve the sensitivity of CRC detection.
结直肠癌(CRC)是一个具有挑战性的公共卫生问题,成功的治疗取决于诊断时的阶段。最近,CRC 特异性微生物组特征已被提议作为 CRC 检测的标志物。由于许多国家已经启动了 CRC 筛查计划,因此分析粪便免疫化学试验(FIT)管中收集的样本中的微生物组对于粪便潜血检测将是有用的。因此,我们研究了 FIT 管和稳定缓冲液对 30 名志愿者粪便样本中微生物群落结构的影响,并将检测到的群落与新鲜冷冻样本进行了比较,突出了先前发表的癌症特异性群落。总共通过 16S rRNA 基因测序分析了 214 个样本,包括阳性和阴性对照。我们的结果表明,个体之间的变异大于收集策略引入的差异。多达 7 天的绝大多数属是稳定的。在新鲜冷冻样本和 FIT 管标本之间观察到的变化均与先前鉴定的 CRC 特异性细菌无关。总体而言,我们表明 FIT 管可用于 CRC 筛查计划中对微生物组进行分析。这避免了收集额外样本的需要,并可能提高 CRC 检测的敏感性。