Ying Hua, FengYing Sun, YanHong Wu, YouMing Huang, FaYou Zhou, HongXiang Zhang, XiaoLei Tang
Vascular Disease Research Center and Basic Medical Laboratory, the Second Affiliated Hospital of Wannan Medical College, Kangfu Road 10#, Wuhu 241000, Anhui Province, PR China.
School of Nursing, Wannan Medical College, Wenchang Xi Road 22#, Wuhu 241000, Anhui Province, PR China.
Iran J Basic Med Sci. 2020 Nov;23(11):1419-1425. doi: 10.22038/ijbms.2020.44029.10324.
Tuberculosis (TB), caused by , is a widespread infectious disease around the world. Early diagnosis is always important in order to avoid spreading. At present, many studies have confirmed that microRNA (miRNA) could be a useful tool for diagnosis. This study aimed to evaluate whether miRNAs could be regarded as a noninvasive diagnosis biomarker from sputum for pulmonary tuberculosis (PTB).
The strain H37Rv was incubated and cultured with human macrophage line THP-1. The total RNA was extracted from the THP-1 cells for detection. Six increased expressions of miRNAs were selected by miRNA microarray chips and the miRNAs were confirmed by qRT-PCR in the infection cell model. At last, the efficiency of other methods was compared with using miRNA.
Only miR-155 showed a better diagnostic value for PTB than the other five miRNAs to distinguish PTB from non-PTB, including pneumonia, lung cancer, and unexplained pulmonary nodules. Next, we detected and analyzed the results of 68 PTB patients and 122 non-PTB, the sensitivity and specificity of miR-155 detection was 94.1% and 87.7%, respectively. It was higher than sputum smear detection and anti-TB antibody detection. But slightly lower than ELISpot (97%, 0.404). Interestingly, the ranking of sputum smear by Ziehl-Neelsen staining had positive correlation with the expression level of miR-155 in smear-positive sputum (R=0.8443, <0.05).
Our research suggested that miR-155 may be an efficiency biomarker for active PTB diagnosis and bacteria-loads evaluation.
由结核分枝杆菌引起的结核病是一种在全球广泛传播的传染病。为避免传播,早期诊断一直很重要。目前,许多研究已证实微小RNA(miRNA)可能是一种有用的诊断工具。本研究旨在评估miRNA是否可被视为肺结核(PTB)痰液的非侵入性诊断生物标志物。
将结核分枝杆菌H37Rv菌株与人巨噬细胞系THP-1一起孵育培养。从THP-1细胞中提取总RNA进行检测。通过miRNA微阵列芯片选择6种表达增加的miRNA,并在结核分枝杆菌感染细胞模型中通过qRT-PCR对这些miRNA进行确认。最后,将其他方法的效率与使用miRNA的方法进行比较。
与其他5种miRNA相比,只有miR-155在区分PTB与非PTB(包括肺炎、肺癌和不明原因的肺结节)方面对PTB具有更好的诊断价值。接下来,我们检测并分析了68例PTB患者和122例非PTB患者的结果,miR-155检测的敏感性和特异性分别为94.1%和87.7%。它高于痰涂片检测和抗结核抗体检测。但略低于ELISpot(97%,0.404)。有趣的是,萋-尼染色痰涂片的分级与涂片阳性痰液中miR-155的表达水平呈正相关(R=0.8443,P<0.05)。
我们的研究表明,miR-155可能是活动性PTB诊断和细菌载量评估的有效生物标志物。