Abstract
Genes encoding for Toll-like receptors (TLRs) provide innate immunity to aquatic organisms. The function of TLRs in innate immunity has been characterized in several crustacean species; however, systematic information on TLRs is still scarce in the Pacific white shrimp (Litopenaeus vannamei). Here, we conducted a genome-wide study of TLR genes for the first time in Pacific white shrimps. A total of 11 TLR genes were recognized. Analysis of the architecture domain revealed that most TLR genes possessed three major domains: a Toll/interleukin receptor (TIR) domain, a transmembrane domain (TM), and multiple leucine-rich repeat domains (LRRs). Results revealed that all 11 TLR genes were ubiquitously expressed in all the tested tissues. Furthermore, the expression of 11 TLR genes after Vibrio parahaemolyticus infection was measured in hemocytes, hepatopancreas, and gills. The results showed that most genes were significantly up regulated at different time points, except for TLR-Tollo1 and TLR-Tollo2 in hepatopancreas, and TLR13× isoform, TLR3, TLR4, and PTL-2 in gills. Our study provided the first genome-wide systemic analysis of Pacific white shrimp and suggested that TLR genes play significant roles in the L. vannamei immune response. These findings will offer evidence for the functional study of L. vannamei TLRs and could facilitate the investigation of molecular mechanisms underlying the immune regulation of L. vannamei challenged by V. parahaemolyticus, which will consequently contribute to the sustainability of aquaculture.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.