“…16S PCR is the earliest and most widely used in PJI pathogenic microorganism isolation, which could simply and quickly amplify the genes or fragments by specific or non-specific primers, and the amplified products could be sequenced, then the species of pathogenic bacteria could be obtained (Saglani et al, 2005;Fida et al, 2021). This was an effective tool for detecting Mycoplasma and widely used in recent years (Jensen et al, 2003;McAuliffe et al, 2005;Kim et al, 2022). However, this method could not effectively detect true pathogenic bacteria when there was mixed infection, and it could not distinguish contaminated bacteria from true pathogenic bacteria.…”