“…The ITS primers, ITS1 and ITS4 [ 86 ] were originally designed for fungi and found useful to detect fungal contamination in herbal plant samples [ 87 , 88 , 89 , 90 ].Sequences of 18S, 5.8S and 26S rDNA are highly conserved from bacteria, fungi and higher plants, enabling the design of the sequence-complemented universal primers for PCR amplification of ITS [ 91 ] across the kingdoms. To improve the quality of ITS sequence information in DNA-barcoding, there are plant-specific ITS primers that can avoid preferential amplification of fungal contaminants or non-plants templates [ 59 , 88 , 92 , 93 ]. Due to the decreased length of the ITS2 sequence (<300 bp), it has been proposed as a suitable for DNA barcoding applications in plants [ 68 , 94 , 95 , 96 , 97 ].There are issues, such as paralogy and polymorphic sites, with the ITS repeats [ 61 , 98 ] that make some taxonomists wary of using them, but for authentication purposes, ITS (and particularly ITS2) have advantages that tend to outweigh these issues.…”