Abstract
Cavities are important in clinical diagnosis of pulmonary tuberculosis (TB) infected by Mycobacterium tuberculosis. Although microRNAs (miRNAs) play a vital role in the regulation of inflammation, the relation between plasma miRNA and pulmonary tuberculosis with cavity remains unknown. In this study, plasma samples were derived from 89 cavitary pulmonary tuberculosis (CP-TB) patients, 89 non-cavitary pulmonary tuberculosis (NCP-TB) patients and 95 healthy controls. Groups were matched for age and gender. In the screening phase, Illumina high-throughput sequencing technology was employed to analyze miRNA profiles in plasma samples pooled from CP-TB patients, NCP-TB patients and healthy controls. During the training and verification phases, quantitative RT-PCR (qRT-PCR) was conducted to verify the differential expression of selected miRNAs among groups. Illumina high-throughput sequencing identified 29 differentially expressed plasma miRNAs in TB patients when compared to healthy controls. Furthermore, qRT-PCR analysis validated miR-769-5p, miR-320a and miR-22-3p as miRNAs that were differently present between TB patients and healthy controls. ROC curve analysis revealed that the potential of these 3 miRNAs to distinguish TB patients from healthy controls was high, with the area under the ROC curve (AUC) ranged from 0.692 to 0.970. Moreover, miR-320a levels were decreased in drug-resistant TB patients than pan-susceptible TB patients (AUC = 0.882). In conclusion, we identified miR-769-5p, miR-320a and miR-22-3p as potential blood-based biomarkers for TB. In addition, miR-320a may represent a biomarker for drug-resistant TB.
Highlights
According to the Global Tuberculosis Report 2016 by World Health Organization (WHO), the tuberculosis (TB) epidemic is higher than previously estimated [1]
Total RNA was extracted from healthy controls, cavitary pulmonary tuberculosis (CP-TB) patients and non-cavitary pulmonary tuberculosis (NCP-TB) patients
A total of 2,220,577; 2,230,331 and 2,768,917 reads of RNAs ranging from 18 to 30 nucleotides were obtained from pooled plasma samples of healthy controls, CP-TB patients and NCP-TB patients, respectively
Summary
According to the Global Tuberculosis Report 2016 by World Health Organization (WHO), the tuberculosis (TB) epidemic is higher than previously estimated [1]. China is still in the list of the six highest TB burden countries, and the cases in the six countries accounts for 60% of new TB cases. In 2015, the Sustainable Development Goals (SDGs) for 2030 were adopted by the United Nations and one of their main goals was to end the global TB epidemic [1]. Since 2000, the incidence of TB dropped by an average of 1.5% per year worldwide. To reach the first milestone of the “End TB Strategy”, it is essential that, by 2020, the minimum annual decline should be 4–5%. In countries with a high TB burden, the trend of multidrug-resistant TB or rifampin-resistant TB (MDR-TB/RR-TB) and mortality decline are similar to incidence. There is still a long way to go to meet the targets of the SDGs
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