Back to Search Start Over

Recombinant HBsAg-S and RFRP-3 DNA vaccine promotes reproduction hormone secretion in sheep.

Authors :
Ding, Yi
Jiang, Xunping
Jing, Haijing
Liu, Guiqiong
Cheng, Junjun
Source :
Theriogenology. Apr2023, Vol. 201, p68-75. 8p.
Publication Year :
2023

Abstract

RF-amide related peptides (RFRP) have been proposed as critical regulators of gonadotropin secretion in mammals. This study was designed to construct a DNA vaccine and investigate the effect of vaccine encoding RFRP-3 on reproduction physiology in ewe. A recombinant vaccine was constructed using two copies of the RFRP-3 gene and HBsAg-S that generate a fusion protein to induce an immunology response. Results showed this recombinant vaccine could produce a significant antibody titer in the treated animals (P < 0.05). The specific RFRP-3 antibody response induced by the vaccine was detected at week 2 with a peak at week 6 after the initial immunization. Furthermore, we found that ewes inoculated with pVAX-tPA-HBsAg-S-2RFRP-asd vaccine significantly raised the concentration of GnRH, LH and E 2 in serum compared to the control group. LH and E2 concentration in the treated ewes (Group T) was significantly higher than that in control ewes (Group C) at weeks 10, 12 and 14 after the initial immunization, respectively (P < 0.05). Therefore, RFRP-3 can be used as a target for DNA immunization to promote reproductive hormone secretion in ewes and RFRP-3 gene immunization might be a candidate tool to regulate mammal reproduction. • The recombinant HBsAg-S and RFRP-3 DNA bivalent vaccine induces powerful anti-RFRP-3 antibody response. • The vaccine increased the secretion of reproductive hormones in the HPG axis in sheep. • RFRP-3 can be used as a target for DNA immunization to promote the reproductive hormones in ewes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0093691X
Volume :
201
Database :
Academic Search Index
Journal :
Theriogenology
Publication Type :
Academic Journal
Accession number :
162437110
Full Text :
https://doi.org/10.1016/j.theriogenology.2023.02.008