“…Initially, 16S rRNA gene sequencing of colonies, or alternatively specific real-time PCR assays, were successfully used for the identification of this bacterium [7,11,12,15,[17][18][19][20]22,23,25,27,30,34,44,51]. Today, MALDI-TOF using Microflex LT with the Biotyper 2.3 database (Bruker Daltonics, Bremen, Germany) of colonies is probably the most accurate and rapid method for the routine identification of A. schaalii [35,[48][49][50]. Indeed, its utilization is faster and easier than 16S rRNA gene sequencing, and several studies have shown its efficiency [14,28,35,50].…”