4.5 Article

Assessment of an Enterobactin Conjugate Vaccine in Layers to Protect Their Offspring from Colibacillosis

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PATHOGENS
卷 12, 期 8, 页码 -

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MDPI
DOI: 10.3390/pathogens12081002

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enterobactin; maternal immunization; immunoglobulin Y; avian pathogenic E. coli

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Colibacillosis, caused by avian pathogenic Escherichia coli (APEC), is a significant infectious disease in chickens and protecting young chickens from this disease is important. A novel enterobactin (Ent) conjugate vaccine was developed to induce high levels of anti-Ent immunoglobulin Y (IgY) in chicken serum, but the maternal immunity from the vaccinated hens did not provide significant protection against APEC challenge in the young chicks. Therefore, further optimization of the APEC infection model and improvement of the maternal immunization regimen are needed.
Colibacillosis, caused by avian pathogenic Escherichia coli (APEC), is an important infectious disease in chickens and a major cause of mortality in young chicks. Therefore, protecting young chickens from colibacillosis is important for improving welfare and productivity in the poultry industry. Recently, we developed a novel enterobactin (Ent) conjugate vaccine that could induce high titers of anti-Ent immunoglobulin Y (IgY) in chicken serum and consequently mitigate the organ lesions caused by APEC infection. Considering that maternal immunization is a practical approach to confer instant immune protection to the hatchlings, in this study, we immunized breeder hens with the Ent conjugate vaccine and evaluated the maternal immune protection on the progenies challenged with APEC. Three doses of the vaccine induced high titers of anti-Ent IgY in the hens (about 16-and 64-fold higher than the control group in the sera and egg yolks, respectively), resulting in an eight-fold of increase in anti-Ent IgY in the sera of progenies. However, the anti-Ent maternal immunity did not display significant protection against APEC challenge in the young chicks as there was no significant difference in APEC load (in liver, lung, and spleen) or organ lesions (in heart, liver, spleen, lung, and air sac) between the vaccinated and control groups. In future studies, the APEC infection model needs to be optimized to exhibit proper pathogenicity of APEC, and the maternal immunization regimen can be further improved to boost the maternally derived anti-Ent IgY in the hatchlings.

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