Rapid and efficient methods for the determination of cured pulmonary tuberculosis (TB) are lacking. We screened serum miRNAs using the Solexa sequencing method among untreated TB patients, two‐month treated TB patients, cured TB patients, and healthy controls. A total of 100 differentially expressed miRNAs were identified in cured TB patients, including 37 up‐regulated (fold change >1.50, P<0.05) and 63 down‐regulated (fold change <0.60, P<0.05) miRNAs. Gene ontology (GO) enrichment analysis revealed that most of the predicted genes were present in the nucleus with a strong protein binding function. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis strongly suggested alterations in the metabolic pathways. Following quantitative real time chain reaction (qRT‐PCR), significantly reduced expression levels of miR‐21‐5p (0.59, P=0.039), miR‐92a‐3p (0.46, P=0.038), and miR‐148b‐3p (0.96, P=0.049) were found in the cured TB patients compared with the untreated TB patients. Also, significantly increased expression levels of miR‐92a‐3p (2.82, P<0.001), miR‐125a‐5p (5.09, P<0.001), and miR‐148b‐3p (4.25, P<0.001) were found in the untreated TB patients compared with the healthy controls. We established a cured TB model with 73.08% accuracy by four miRNAs (miR‐21‐5p, miR‐92a‐3p, miR‐148b‐3p, and miR‐125a‐5p), and also established a diagnostic model with 71.43% accuracy. Our study provides experimental data for establishing objective indicators of cured TB, and also provides a new experimental basis to understand the pathogenesis and prognosis of TB.Support or Funding InformationThis work was supported by grants from the National Natural Science Foundation of China (No. 81573709), the Zhejiang Provincial Natural Science Foundation of China (No. LQ18H040009), and Zhejiang Provincial Medical Science and Technology Foundation of China (2017KY550).This abstract is from the Experimental Biology 2018 Meeting. There is no full text article associated with this abstract published in The FASEB Journal.
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