Update publication information. In order to identify proteins potentially act as salivary effectors, we conducted proteomic analyses in the SG of D. citri using LC−MS/MS. Two hundred pairs of SG from CLas uninfected D. citri clone were dissected out in SDT lysis buffer. LC−MS/MS analysis was conducted on a Q Exactive mass spectrometer (Thermo Fisher Scientific, MA, USA) coupled to Easy nLC (Thermo Fisher Scientific). Our results provide useful resources to identify potential functional proteins like salivary effectors and basic framework for future investigation to understand the molecular interaction between phloem sap-sucking insects and host plants.