Sunil Kumar, Ayaan Ahmad, Namrata Kushwaha, Niti Shokeen, Sheetal Negi, Kamini Gautam, Anup Singh, Pavan Tiwari, Rakesh Garg, Richa Agarwal, Anant Mohan, Anjan Trikha, Alok Thakar, Vikram Saini
Selection of reference genes during real-time quantitative PCR (qRT-PCR) is critical to determine accurate and reliable mRNA expression. Nonetheless, not a single study has investigated the expression stability of candidate reference genes to determine their suitability as internal controls in SARS-CoV-2 infection or COVID-19-associated mucormycosis (CAM). Using qRT-PCR, we determined expression stability of the nine most commonly used housekeeping genes, namely, TATA-box binding protein ( TBP ), cyclophilin ( CypA ), β-2-microglobulin ( B2M ), 18S rRNA (18S), peroxisome proliferator-activated receptor gamma (PPARG) coactivator 1 alpha ( PGC-1 α), glucuronidase beta ( GUSB ), hypoxanthine phosphoribosyltransferase 1 ( HPRT-1 ), β-ACTIN , and glyceraldehyde-3-phosphate dehydrogenase ( GAPDH ) in patients with COVID-19 of various severities (asymptomatic, mild, moderate, and severe) and those with CAM...
November 15, 2022: Microbiology Spectrum