Localisation of antigens in the gut post-challenge with Streptococcus iniae in vaccinated and non-vaccinated red hybrid tilapia (Oreochromis sp.)

This study was conducted to determine the localisation of antigen in the gut of vaccinated and non-vaccinated red hybrid tilapia post-challenge via immunohistochemistry and scanning electron microscopy. All groups (1, 2, 3, and 4) were vaccinated orally with feed-based killed whole-cells of Streptoc...

Full description

Saved in:
Bibliographic Details
Main Authors: M., Hayat, M. Y., Sabri, Abdul Razak, Intan Shameha, Md Yasin, Ina Salwany, Thompson, Kim D.
Format: Article
Language:English
Published: Springer 2020
Online Access:http://psasir.upm.edu.my/id/eprint/86587/1/Localisation%20of%20antigens%20.pdf
http://psasir.upm.edu.my/id/eprint/86587/
https://link.springer.com/article/10.1007/s10499-020-00554-9
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:This study was conducted to determine the localisation of antigen in the gut of vaccinated and non-vaccinated red hybrid tilapia post-challenge via immunohistochemistry and scanning electron microscopy. All groups (1, 2, 3, and 4) were vaccinated orally with feed-based killed whole-cells of Streptococcus iniae (FKV). Group 1 was fed with the FKV for 3 days consecutively only on day 0; group 2 was fed with the FKV for 3 days consecutively on day 0 and booster on day 14; group 3 was fed with the FKV for 3 days consecutively on day 0, followed by a booster on day 14 and 21; and group 4 was fed with the FKV for 5 days consecutively on day 0, followed by a booster on day 14 and 21. The remaining groups, group 5 (negative control group) and group 6 (positive control group), only fed with a commercial feed. Five fish from each group were sacrificed on a weekly basis for the entire 6 weeks for a collection of fresh small intestinal samples including post-challenge starting from 4 to 72 h. Immunohistochemical staining was conducted using the avidin-biotin-peroxidase complex method. Scanning electron microscopy was also used to view the hindgut samples from each group. Positive control group recorded significantly the highest (p < 0.05) antigen positivity, followed by groups 1 and 2, meanwhile, lowest positivity in groups 3 and 4 at 12 h, 24 h, and 72 h, respectively. Immunohistochemistry and scanning electron microscopy showed the presence of antigens in red hybrid tilapia hindgut, protruding in goblet cells, gut-associated lymphoid tissues, and villi dome epithelium in different hours of post-challenge. Significantly, boosted group 4 with a low number of antigens in 72 h showed the stimulation and irregular projection of M-cells with variable morphology and antigen distribution pattern.