Abstract

In schistosomiasis, eggs produced by bisexual infected mature female schistosome worms (FMS) are the main cause of pathological damage to the host and the dissemination of the disease. Single-sex infected female worms (FSS) cannot completely develop to sexual maturity or produce normal eggs. In this study, isobaric tags for relative and absolute quantitation (iTRAQ)-coupled LC-MS/MS was used to explore the proteome of FSS and FMS of Schistosoma japonicum. A total of 1477 differentially expressed proteins (fold change >1.2, P < .05) between FSS and FMS were identified. Bioinformatics analysis indicated that FMS expressed more proteins related to biosynthetic processes, such as eggshell synthesis, ribosomal synthesis, protein folding, cellular detoxification, and metabolic processes such as protein metabolism and glucose metabolism, whereas more proteins related to locomotion and oxidative phosphorylation were expressed in FSS. Our identification and analysis of differentially expressed proteins between FMS and FSS provides new insights to elucidate the molecular biological mechanisms of female worm sexual maturation and reproduction. SignificanceFemale Schistosome worms must maintain constant pairing contact with male worms for differentiation of their reproductive organs. Mature female worms can produce infectious eggs, cause serious pathological damage to the host and the dissemination of the disease. Unpaired female worms remain small and sexually immature; they do not spawn normally. In this study, iTRAQ-coupled LC-MS/MS was used to explore the whole proteome of single-sex infected female worms (FSS) and bisexual infected mature female worms (FMS) of Schistosoma japonicum. 1477 differentially expressed proteins (DEPs) between FSS and FMS were identified and analyzed. Further research on DEPs’ functions in schistosome sexual maturation and reproductive development might provide theoretical bases to explore female maturation and spawning.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call