Protective efficacy of Interferon-γ and β-glucan adjuvanted formalin killed vaccines in Nile tilapia against Edwardsiella tarda infection.

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Auteurs principaux: Guha, Ritam, Lakshmi, Sreeja, Wang, Tiehui, Wangkahart, Eakapol, Elumalai, Preetham
Format: Artículo científico
Langue:en
Publié: Developmental and comparative immunology 2025
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author Guha, Ritam
Lakshmi, Sreeja
Wang, Tiehui
Wangkahart, Eakapol
Elumalai, Preetham
author_facet Guha, Ritam
Lakshmi, Sreeja
Wang, Tiehui
Wangkahart, Eakapol
Elumalai, Preetham
Guha, Ritam
Lakshmi, Sreeja
Wang, Tiehui
Wangkahart, Eakapol
Elumalai, Preetham
collection PubMed - marine biology
contents Protective efficacy of Interferon-γ and β-glucan adjuvanted formalin killed vaccines in Nile tilapia against Edwardsiella tarda infection. Guha, Ritam Lakshmi, Sreeja Wang, Tiehui Wangkahart, Eakapol Elumalai, Preetham Animals beta-Glucans Enterobacteriaceae Infections Fish Diseases Interferon-gamma Vaccines, Inactivated Edwardsiella tarda Cichlids Bacterial Vaccines Adjuvants, Immunologic Formaldehyde Aquaculture Vaccination Aquaculture is a central commercial commodity for low-to middle-income countries and a promising source of economically important food and livelihood. Indian aquaculture faces challenges with the onset of several upcoming fish diseases. The antimicrobial resistance (AMR) pathogen Edwardsiella tarda infection is one of the serious threats affecting worldwide aquaculture. Replacing antibiotics, vaccines can be used as a safe treatment for multidrug-resistant E. tarda. The present study focuses on creating a formalin killed vaccine incorporated with IFN-γ and β-glucan as adjuvants, that confers protection against E. tarda infection in Nile tilapia (Oreochromis niloticus). The isolated virulent strain was cultivated in marine nutrient broth and inactivated by 0.5 % formalin treatment. To increase the immunogenicity, the bacterial suspension was mixed with IFN-γ and β-glucan. Fish were intraperitoneally immunized with IFN-γ and β-glucan -adjuvanted formalin killed vaccine (FKV), followed by sampling at a fixed time. After 28 days from the first immunization, the fish were challenged with E. tarda at a dose of 1 x 10 CFU/fish. Blood from the immunized fish was sampled weekly to measure immunochemical parameters, including sodium oxide dismutase (SOD), myeloperoxidase (MPO), lysozyme activity (LZM), and bactericidal activity. Fish serum IgM titre values were measured on the 14th and 28 day post-vaccination (d.p.v.), and both showed that the adjuvanted vaccinated groups had higher antibody levels than the control group. The vaccinated groups with IFN-γ and β-glucan showed considerably higher expressions immune genes, including IgM, TCR β, MHC II. The study emphasizes that β-glucan and IFN-γ adjuvanted inactivated vaccine is a potentially plausible approach toward novel vaccination strategies for sustainable aquaculture.
format Artículo científico
id pubmed_40553751
institution PubMed
language en
publishDate 2025
publisher Developmental and comparative immunology
record_format pubmed
spellingShingle Protective efficacy of Interferon-γ and β-glucan adjuvanted formalin killed vaccines in Nile tilapia against Edwardsiella tarda infection.
Guha, Ritam
Lakshmi, Sreeja
Wang, Tiehui
Wangkahart, Eakapol
Elumalai, Preetham
Animals
beta-Glucans
Enterobacteriaceae Infections
Fish Diseases
Interferon-gamma
Vaccines, Inactivated
Edwardsiella tarda
Cichlids
Bacterial Vaccines
Adjuvants, Immunologic
Formaldehyde
Aquaculture
Vaccination
Protective efficacy of Interferon-γ and β-glucan adjuvanted formalin killed vaccines in Nile tilapia against Edwardsiella tarda infection. Guha, Ritam Lakshmi, Sreeja Wang, Tiehui Wangkahart, Eakapol Elumalai, Preetham Animals beta-Glucans Enterobacteriaceae Infections Fish Diseases Interferon-gamma Vaccines, Inactivated Edwardsiella tarda Cichlids Bacterial Vaccines Adjuvants, Immunologic Formaldehyde Aquaculture Vaccination Aquaculture is a central commercial commodity for low-to middle-income countries and a promising source of economically important food and livelihood. Indian aquaculture faces challenges with the onset of several upcoming fish diseases. The antimicrobial resistance (AMR) pathogen Edwardsiella tarda infection is one of the serious threats affecting worldwide aquaculture. Replacing antibiotics, vaccines can be used as a safe treatment for multidrug-resistant E. tarda. The present study focuses on creating a formalin killed vaccine incorporated with IFN-γ and β-glucan as adjuvants, that confers protection against E. tarda infection in Nile tilapia (Oreochromis niloticus). The isolated virulent strain was cultivated in marine nutrient broth and inactivated by 0.5 % formalin treatment. To increase the immunogenicity, the bacterial suspension was mixed with IFN-γ and β-glucan. Fish were intraperitoneally immunized with IFN-γ and β-glucan -adjuvanted formalin killed vaccine (FKV), followed by sampling at a fixed time. After 28 days from the first immunization, the fish were challenged with E. tarda at a dose of 1 x 10 CFU/fish. Blood from the immunized fish was sampled weekly to measure immunochemical parameters, including sodium oxide dismutase (SOD), myeloperoxidase (MPO), lysozyme activity (LZM), and bactericidal activity. Fish serum IgM titre values were measured on the 14th and 28 day post-vaccination (d.p.v.), and both showed that the adjuvanted vaccinated groups had higher antibody levels than the control group. The vaccinated groups with IFN-γ and β-glucan showed considerably higher expressions immune genes, including IgM, TCR β, MHC II. The study emphasizes that β-glucan and IFN-γ adjuvanted inactivated vaccine is a potentially plausible approach toward novel vaccination strategies for sustainable aquaculture.
title Protective efficacy of Interferon-γ and β-glucan adjuvanted formalin killed vaccines in Nile tilapia against Edwardsiella tarda infection.
topic Animals
beta-Glucans
Enterobacteriaceae Infections
Fish Diseases
Interferon-gamma
Vaccines, Inactivated
Edwardsiella tarda
Cichlids
Bacterial Vaccines
Adjuvants, Immunologic
Formaldehyde
Aquaculture
Vaccination
url https://pubmed.ncbi.nlm.nih.gov/40553751/