Shiluli Clement, Kamath Shwetha, Kanoi Bernard N, Kimani Racheal, Maina Michael, Waweru Harrison, Kamita Moses, Ndirangu Ibrahim, Abkallo Hussein M, Oduor Bernard, Pamme Nicole, Dupaty Joshua, Klapperich Catherine M, Lolabattu Srinivasa Raju, Gitaka Jesse
Centre for Research in Infectious Diseases, College of Graduate Studies and Research, Mount Kenya University, Thika, Kenya.
Division of Research and Development, Jigsaw Bio Solutions Private Limited, Bangalore, India.
Heliyon. 2024 Mar 5;10(6):e27344. doi: 10.1016/j.heliyon.2024.e27344. eCollection 2024 Mar 30.
Curable sexually transmitted infections (STIs), such as (), are a major cause of poor pregnancy outcomes. The infection is often asymptomatic in pregnant women, and a syndrome-based approach of testing leads to a missed diagnosis. Culture followed by microscopy is inadequate and time-consuming. The gold standard nucleic acid amplification tests require advanced infrastructure settings, whereas point-of-care tests are limited to immunoassays with sensitivities and specificities insufficient to accurately diagnose asymptomatic cases. This necessitates the development and validation of assays that are fit for purpose.
We identified new diagnostic target biomarker regions for using an algorithm for genome mining of identical multi-repeat sequences (IMRS). These were then developed as DNA amplification primers to design better diagnostic assays. To test the primer pair, genomic DNA was 10-fold serially diluted (100 pg/μL to 1 × 10 pg/μL) and used as DNA template for PCR reactions. The gold standard PCR using 16S rRNA primers was also run as a comparative test, and both assay products were resolved on 1% agarose gel.
Our newly developed IMRS-PCR assay had an analytical sensitivity of 6 fg/μL representing better sensitivity than the 16S rRNA PCR assay with an analytical sensitivity of 4.3096 pg/μL. The assay was also successfully validated using clinical urethral swab samples. We further advanced this technique by developing an isothermal IMRS, which was both reliable and sensitive for detecting cultured isolates at a concentration of 38 ng/μL. Combining isothermal IMRS with a low-cost lateral flow assay, we were able to detect amplicons at a starting concentration of 100 pg/μL.
Therefore, there is a potential to implement this concept within miniaturized, isothermal, microfluidic platforms, and laboratory-on-a-chip diagnostic devices for highly reliable point-of-care testing.
可治愈的性传播感染(STIs),如(此处原文括号内内容缺失),是导致不良妊娠结局的主要原因。这种感染在孕妇中通常无症状,基于综合征的检测方法会导致漏诊。培养后镜检既不充分又耗时。金标准核酸扩增检测需要先进的基础设施,而即时检测仅限于免疫测定,其灵敏度和特异性不足以准确诊断无症状病例。这就需要开发和验证适用的检测方法。
我们使用相同多重复序列(IMRS)基因组挖掘算法确定了(此处原文缺失相关病原体名称)的新诊断靶标生物标志物区域。然后将其开发为DNA扩增引物以设计更好的诊断检测方法。为测试引物对,将基因组DNA进行10倍系列稀释(100 pg/μL至1×10 pg/μL),并用作PCR反应的DNA模板。同时进行使用16S rRNA引物的金标准PCR作为对比测试,两种检测产物在1%琼脂糖凝胶上进行分离。
我们新开发的(此处原文缺失相关病原体名称)IMRS-PCR检测方法的分析灵敏度为6 fg/μL,比分析灵敏度为4.3096 pg/μL的16S rRNA PCR检测方法灵敏度更高。该检测方法也使用临床尿道拭子样本成功进行了验证。我们通过开发等温IMRS进一步改进了这项技术,该技术在检测浓度为38 ng/μL的培养(此处原文缺失相关病原体名称)分离株时既可靠又灵敏。将等温IMRS与低成本侧向流动检测相结合,我们能够在起始浓度为100 pg/μL时检测到(此处原文缺失相关病原体名称)扩增子。
因此,有潜力在小型化、等温、微流控平台以及芯片实验室诊断设备中应用这一概念,以实现高度可靠的即时检测。