“…As one of the differences of gene numbers, it may be attributed to the sequencing depth of the PG transcriptomes, such as A. yunnanensis (47,632,610 clean reads), E. cautella (231, 851, 937 clean reads) ( Antony et al, 2015 ), S. litura (63,209,172 clean reads) ( Zhang et al, 2015 ), Maruca vitrata (119,454,916 clean reads) ( Cha et al, 2017 ) and A. segetum (53,235,252 clean reads) ( Ding & Lofstedt, 2015 ). In addition to that, the transcriptome sequencing and assembly of multi-tissues also facilitated the identification of the pheromone biosynthesis and degradation genes in the PGs, further supported by a broad tissue distribution of the pheromone biosynthesis genes in A. yunnanensis and other moth species ( Zhang et al, 2014b ; Xia et al, 2015 ; Yang, Tao & Zong, 2020 ). Except for the possible reasons mentioned above, we cannot exclude other possibilities such as the difference of sex pheromone components among species.…”