Centre for Biotechnology, Maharshi Dayanand University, Rohtak, 124001, India.
Special Centre for Nano Science and Advanced Instrumentation Research Facility, Jawaharlal Nehru University, New Delhi, 110067, India.
Sci Rep. 2023 Jul 18;13(1):11560. doi: 10.1038/s41598-023-38740-3.
We detected a cocktail of Mycobacterium tuberculosis lipoarabinomannan (LAM) and MPT-64 biomarkers within urine extracellular vesicles (EVs) of genitourinary TB (GUTB) patients by nano-based immuno-PCR (I-PCR) assay, i.e., magnetic bead-coupled gold nanoparticle-based I-PCR (MB-AuNP-I-PCR) and compared the results with I-PCR and Magneto-ELISA. The size (s) of urine EVs ranged between 52.6 and 220.4 nm as analyzed by transmission electron microscopy (TEM) and nanoparticle tracking analysis. Functionalized AuNPs (coupled with detection antibodies/oligonucleotides) were characterized by UV-vis spectroscopy, TEM, ELISA, PCR, Atomic Force Microscopy and Fourier Transform Infrared spectroscopy, while conjugation of capture antibodies with MBs was validated by UV-vis spectroscopy and Magneto-ELISA. Our MB-AuNP-I-PCR exhibited sensitivities of 85% and 87.2% in clinically suspected (n = 40) and total (n = 47) GUTB cases, respectively, with 97.1% specificity in non-TB controls (n = 35). These results were further authenticated by the quantitative SYBR Green MB-AuNP-real-time I-PCR (MB-AuNP-RT-I-PCR). Concurrently, I-PCR and Magneto-ELISA showed sensitivities of 68.1% and 61.7%, respectively in total GUTB cases, which were significantly lower (p < 0.05-0.01) than MB-AuNP-I-PCR. Markedly, a wide range (400 fg/mL-11 ng/mL) of LAM+MPT-64 was quantified within urine EVs of GUTB cases by SYBR Green MB-AuNP-RT-I-PCR, which can assess the disease dynamics. This study will certainly improve the current algorithms used in GUTB diagnostics.
我们通过基于纳米的免疫聚合酶链反应(I-PCR)检测试剂盒,即在磁珠偶联的金纳米颗粒 I-PCR(MB-AuNP-I-PCR)中,检测到泌尿生殖系结核(GUTB)患者尿液细胞外囊泡(EVs)中分枝杆菌结核阿拉伯甘露聚糖(LAM)和 MPT-64 生物标志物的混合物,并与 I-PCR 和磁酶联免疫吸附试验(Magneto-ELISA)进行了比较。通过透射电子显微镜(TEM)和纳米颗粒跟踪分析,分析出尿液 EVs 的大小(s)范围在 52.6nm 至 220.4nm 之间。功能化的 AuNPs(与检测抗体/寡核苷酸偶联)通过紫外-可见光谱、TEM、ELISA、PCR、原子力显微镜和傅里叶变换红外光谱进行了表征,而捕获抗体与 MB 的偶联通过紫外-可见光谱和 Magneto-ELISA 进行了验证。在临床上疑似(n=40)和所有(n=47)GUTB 病例中,我们的 MB-AuNP-I-PCR 的灵敏度分别为 85%和 87.2%,在非结核对照(n=35)中特异性为 97.1%。这些结果通过定量 SYBR Green MB-AuNP 实时 I-PCR(MB-AuNP-RT-I-PCR)进一步得到了证实。同时,I-PCR 和 Magneto-ELISA 在所有 GUTB 病例中的灵敏度分别为 68.1%和 61.7%,明显低于 MB-AuNP-I-PCR(p<0.05-0.01)。值得注意的是,通过 SYBR Green MB-AuNP-RT-I-PCR 在 GUTB 患者的尿液 EVs 中定量检测到 LAM+MPT-64 的范围很广(400 fg/mL-11 ng/mL),这可以评估疾病的动态。这项研究肯定会改善目前用于 GUTB 诊断的算法。