Cheng Xueqin, Dou Zhiqian, Yang Jing, Liu Dexi, Gu Yulong, Cai Fenglin, Li Xiaobing, Wang Meifang, Tang Yijun
Department of Respiratory and Critical Medical, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, China.
Hubei Key Laboratory of Embryonic Stem Cell Research, Tai-He Hospital, Hubei University of Medicine, Shiyan, China.
AMB Express. 2021 Jan 6;11(1):9. doi: 10.1186/s13568-020-01168-3.
Streptococcus agalactiae (S. agalactiae) is an important pathogen that can lead to neonatus and mother infection. The current existing techniques for the identification of S. agalactiae are limited by accuracy, speed and high-cost. Therefore, a new multiple cross displacement amplification (MCDA) assay was developed for test of the target pathogen immediately from vaginal and rectal swabs. MCDA primers screening were conducted targeting S. agalactiae pcsB gene, and one set of MCDA primers with better rapidity and efficiency was selected for establishing the S. agalactiae-MCDA assay. As a result, the MCDA method could be completed at a constant temperature of 61 °C, without the requirement of special equipment. The detection limit is 250 fg (31.5 copies) per reaction, all S. agalactiae strains displayed positive results, but not for non-S. agalactiae strains. The visual MCDA assay detected 16 positive samples from 200 clinical specimen, which were also detected positive by enrichment/qPCR. While the CHROMagar culture detected 6 positive samples. Thus, the MCDA assay is prefer to enrichment/qPCR and culture for detecting S. agalactiae from clinical specimen. Particularly, the whole test of MCDA takes about 63.1 min, including sample collection (3 min), DNA preparation (15 min), MCDA reaction (45 min) and result reporting (6 s). In addition, the cost was very economic, with only US$ 4.9. These results indicated that our S. agalaciae-MCDA assay is a rapid, sensitive and cost-efficient technique for target pathogen detection, and is more suitable than conventional assays for an urgent detection, especially for 'on-site' laboratories and resource-constrained settings.
无乳链球菌是一种重要的病原体,可导致新生儿和母亲感染。目前现有的无乳链球菌鉴定技术受到准确性、速度和高成本的限制。因此,开发了一种新的多重交叉置换扩增(MCDA)检测方法,可直接从阴道和直肠拭子中检测目标病原体。针对无乳链球菌的pcsB基因进行MCDA引物筛选,选择一组具有更好快速性和效率的MCDA引物来建立无乳链球菌-MCDA检测方法。结果表明,MCDA方法可在61℃恒温下完成,无需特殊设备。检测限为每个反应250 fg(31.5个拷贝),所有无乳链球菌菌株均显示阳性结果,而非无乳链球菌菌株则为阴性。可视化MCDA检测从200份临床标本中检测出16份阳性样本,经富集/qPCR检测也呈阳性。而CHROMagar培养法检测出6份阳性样本。因此,在从临床标本中检测无乳链球菌方面,MCDA检测优于富集/qPCR和培养法。特别是,MCDA的整个检测过程约需63.1分钟,包括样本采集(3分钟)、DNA制备(15分钟)、MCDA反应(45分钟)和结果报告(6秒)。此外,成本非常经济,仅为4.9美元。这些结果表明,我们的无乳链球菌-MCDA检测方法是一种快速、灵敏且经济高效的目标病原体检测技术,比传统检测方法更适合紧急检测