scispace - formally typeset
Journal ArticleDOI

In ovo vaccination of chicken embryos with experimental newcastle disease and avian influenza oil-emulsion vaccines

Henry D. Stone, +2 more
- 01 Oct 1997 - 
- Vol. 41, Iss: 4, pp 856-863
Reads0
Chats0
TLDR
It is demonstrated that acceptable hatchability, seroconversion rates, and protective immunity can be attained with in ovo inoculation of ND or AI OE vaccines if the vaccines are prepared with sufficient antigen and administered properly.
Abstract: 
Inactivated oil-emulsion (OE) Newcastle disease (ND) and avian influenza (AI) vaccines were injected into 18-day-old white rock (WR) and white leghorn (WL) chicken embryos to evaluate their immunologic efficacy and their effects on hatchability. Embryonating eggs were inoculated at 1.5 inches depth with various vaccine volumes and antigen concentrations. Serum hemagglutination-inhibition (HI) titers were first detected in chickens at 2 wk posthatch. Protection against morbidity and mortality was demonstrated in all of 10 chickens vaccinated as embryos and challenged with viscerotropic velogenic ND virus at 53 days of age and also in all of eight in ovo- vaccinated chickens challenged with highly pathogenic AI virus at 34 days of age. All of five unvaccinated control chickens for each respective ND- and AI-vaccinated group died. In pooled groups from successive hatches, the hatchability of WR or WL embryos injected with 100 microliters of vaccine was not significantly different (P > 0.05) from unvaccinated hatchmate controls when needle gauges of 22, 20, and 18 were used. Seroconversion rates of chickens vaccinated as embryos ranged from 27% to 100% with ND vaccination and 85% to 100% for AI vaccination. For ND, geometric mean HI titers of chickens per vaccine group ranged from 11 to 733, and in pooled groups, the range was 49 to 531. Titers for AI vaccine groups ranged from 156 to 1178. This study demonstrated that acceptable hatchability, seroconversion rates, and protective immunity can be attained with in ovo inoculation of ND or AI OE vaccines if the vaccines are prepared with sufficient antigen and administered properly.

read more

Citations
More filters
Journal ArticleDOI

Effect of Vaccine Use in the Evolution of Mexican Lineage H5N2 Avian Influenza Virus

TL;DR: Findings indicate that multilineage antigenic drift, which has not been observed in AI virus, is occurring in the Mexican lineage AI viruses and the persistence of the virus in the field is likely aided by its large antigenic difference from the vaccine strain.
Journal ArticleDOI

Strategies and challenges for eliciting immunity against avian influenza virus in birds.

TL;DR: Vaccines and vaccination have emerged during the past two decades as essential tools in avian influenza (AI) control for poultry, because they increase resistance to infection, prevent illness and death, reduce virus replication and shed from respiratory and alimentary tracts, and reduce virus transmission to birds and mammals, including humans.
Journal ArticleDOI

Generation of reassortant influenza vaccines by reverse genetics that allows utilization of a DIVA (Differentiating Infected from Vaccinated Animals) strategy for the control of avian influenza.

TL;DR: In vaccination-challenge experiments in 2-week-old specific pathogen free chickens, reassortant influenza vaccines demonstrated similar antibody profiles and comparable protection rates as vaccines prepared with parent H5N2 and H7N2 viruses.
Journal ArticleDOI

Immunity, vaccination and the avian intestinal tract.

TL;DR: Progress in understanding of this system, the location of precursor IgA B cells and antigen sampling by these sites is not as advanced as knowledge of the mammalian system, highlighting the need for ongoing research into the avian application of novel vaccination strategies.
Journal ArticleDOI

Influenza virus (A/HK/156/97) hemagglutinin expressed by an alphavirus replicon system protects chickens against lethal infection with Hong Kong-origin H5N1 viruses.

TL;DR: Venezuelan equine encephalitis virus replicon particles (VRP) containing the gene expressing hemagglutinin from the human Hong Kong Influenza A isolate (A/HK/156/97) were evaluated as vaccines in chicken embryos and young chicks.
References
More filters
Journal ArticleDOI

Preparation of inactivated oil-emulsion vaccines with avian viral or Mycoplasma antigens.

TL;DR: Oil-emulsion vaccines prepared with aqueous- and oil-phase emulsifiers had low viscosity, were stable for more than 12 weeks at 37 C, and induced a marked primary antibody response in chickens.
Journal ArticleDOI

Effect of Hatching Cabinet Sanitation Treatments on Salmonella Cross-Contamination and Hatchability of Broiler Eggs

TL;DR: It is demonstrated that the spread of bacteria can be effectively reduced in the hatching cabinet by air sanitization using UV light, ozone, and hydrogen peroxide, and the potential to reduce bacterial cross contamination in the hatcher is achievable without depressing hatchability.
Journal ArticleDOI

Evaluation of the efficacy of an oil-emulsion bacterin for protecting chickens against Salmonella enteritidis.

TL;DR: An acetone-killed oil-emulsion vaccine was prepared from a phage type 13a S. enteritidis strain and administered subcutaneously to hens in two experiments to assess the potential protective efficacy of a SalmonellaEnteritidis bacterin.
Journal Article

Immunization of chickens and turkeys against avian influenza with monovalent and polyvalent oil emulsion vaccines.

TL;DR: Data indicate that control of virulent AIV in chickens and turkeys by vaccination with inactivated vaccines may be feasible.
Related Papers (5)