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Evaluation of the immune response of layer chickens to Newcastle disease virus vaccines using the new vaccination regimens
Background The study aimed to evaluate the immunological response of layer chickens to live Newcastle disease virus vaccine using a newly developed vaccine schedule administered via the ocular route, as well as assess the persistence of passive antibodies in layer chickens and the effectiveness of p...
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description | Background
The study aimed to evaluate the immunological response of layer chickens to live Newcastle disease virus vaccine using a newly developed vaccine schedule administered via the ocular route, as well as assess the persistence of passive antibodies in layer chickens and the effectiveness of protection against strains of the virus.
Methods
A total of 140‐day‐old Lohmann Brown chicks were randomly divided into seven groups, 20 chicks each. Groups 1–3 received a single eye instillation of the vaccine at ages 5, 26 and 54 days, respectively, whereas groups 4–6 received a double eye instillation. Group 7 served as non‐vaccinated control group. Ten days after immunization, samples were taken from hens that had received the vaccine at ages 15, 36 and 64, as well as from control chickens that had not received the vaccine at ages 5, 15, 21 and 31.
Results
A total of 10 serum samples from all chickens exhibited protective antibodies, and booster doses resulted in the highest haemagglutination inhibition titre. No significant change in antibody production was observed among layer hens (p > 0.05). The study found that the La Sota (GMT ± SD: 6.71 ± 4.96), La Sota (GMT ± SD: 8.00 ± 0.00) and thermostable I2 (GMT ± SD: 7.60 ± 6.02), vaccination schedules provided the maximum immune response in single eye instillation, whereas the HB1 (GMT ± SD: 7.11 ± 4.77), La Sota (GMT ± SD: 7.83 ± 5.76) and La Sota (GMT ± SD: 7.60 ± 6.02), combination was the second‐best vaccination schedule in double eye instillation. Furthermore, maternally‐derived antibodies were maintained up to 31 days of age, indicating the level of passive immunity prior to vaccination. Characteristic lesions, such as edematous and diphtheria mucosal membranes of the trachea, along with petechial and necrotic haemorrhages of the proventriculus, were observed during the necropsy of the birds that died from the challenged virus.
Conclusion
This study suggests that subsequent live virus vaccine by ocular route immunization is required to effectively protect against velogenic viscerotropic Newcastle disease infection. The results also highlight the importance of developing effective vaccination schedules and routes to enhance immunity against ND in layer chickens.
Graphical : This study examined layer immune responses of chickens to Newcastle disease virus vaccines via a novel ocular route. One hundred forty Lohmann Brown chicks were divided into seven groups, receiving single or double eye instillations at |
doi_str_mv | 10.1002/vms3.1428 |
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The study aimed to evaluate the immunological response of layer chickens to live Newcastle disease virus vaccine using a newly developed vaccine schedule administered via the ocular route, as well as assess the persistence of passive antibodies in layer chickens and the effectiveness of protection against strains of the virus.
Methods
A total of 140‐day‐old Lohmann Brown chicks were randomly divided into seven groups, 20 chicks each. Groups 1–3 received a single eye instillation of the vaccine at ages 5, 26 and 54 days, respectively, whereas groups 4–6 received a double eye instillation. Group 7 served as non‐vaccinated control group. Ten days after immunization, samples were taken from hens that had received the vaccine at ages 15, 36 and 64, as well as from control chickens that had not received the vaccine at ages 5, 15, 21 and 31.
Results
A total of 10 serum samples from all chickens exhibited protective antibodies, and booster doses resulted in the highest haemagglutination inhibition titre. No significant change in antibody production was observed among layer hens (p > 0.05). The study found that the La Sota (GMT ± SD: 6.71 ± 4.96), La Sota (GMT ± SD: 8.00 ± 0.00) and thermostable I2 (GMT ± SD: 7.60 ± 6.02), vaccination schedules provided the maximum immune response in single eye instillation, whereas the HB1 (GMT ± SD: 7.11 ± 4.77), La Sota (GMT ± SD: 7.83 ± 5.76) and La Sota (GMT ± SD: 7.60 ± 6.02), combination was the second‐best vaccination schedule in double eye instillation. Furthermore, maternally‐derived antibodies were maintained up to 31 days of age, indicating the level of passive immunity prior to vaccination. Characteristic lesions, such as edematous and diphtheria mucosal membranes of the trachea, along with petechial and necrotic haemorrhages of the proventriculus, were observed during the necropsy of the birds that died from the challenged virus.
Conclusion
This study suggests that subsequent live virus vaccine by ocular route immunization is required to effectively protect against velogenic viscerotropic Newcastle disease infection. The results also highlight the importance of developing effective vaccination schedules and routes to enhance immunity against ND in layer chickens.
Graphical : This study examined layer immune responses of chickens to Newcastle disease virus vaccines via a novel ocular route. One hundred forty Lohmann Brown chicks were divided into seven groups, receiving single or double eye instillations at various ages. Antibody titres were measured 10 days post‐immunization. The La Sota, La Sota thermostable I2 schedule showed the highest response with single instillation, whereas HB1, La Sota La Sota were effective with double instillation. Maternally‐derived antibodies persisted for 31 days, indicating passive immunity. Necropsy findings emphasized the need for tailored vaccination schedules for enhanced immunity against velogenic viscerotropic Newcastle disease in layer chickens.</description><identifier>ISSN: 2053-1095</identifier><identifier>EISSN: 2053-1095</identifier><identifier>DOI: 10.1002/vms3.1428</identifier><identifier>PMID: 38519843</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Agricultural research ; Animals ; Antibodies ; Antibodies, Viral ; Antibody Formation ; Chickens ; Diphtheria ; Eye ; Farms ; Female ; Genotype & phenotype ; Haemagglutination inhibition ; Hemagglutination inhibition ; Hemorrhage ; Immune response ; Immunity (passive) ; immunological reactions ; Juveniles ; Mortality ; Necropsy ; Newcastle disease ; Newcastle disease virus ; ocular route ; Poultry ; protective antibodies ; Rural areas ; Vaccination - veterinary ; Vaccines ; Vaccines, Attenuated ; Viral Vaccines ; Viruses</subject><ispartof>Veterinary medicine and science, 2024-05, Vol.10 (3), p.e1428-n/a</ispartof><rights>2024 The Authors. published by John Wiley & Sons Ltd.</rights><rights>2024 The Authors. Veterinary Medicine and Science published by John Wiley & Sons Ltd.</rights><rights>2024. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4818-b39512e453fe55c7d7bdb4c8b321fe4e715ad11e7d52e756d4d7ae712a362e833</cites><orcidid>0000-0002-3674-9457</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3054872108/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3054872108?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,11561,25752,27923,27924,37011,37012,44589,46051,46475,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38519843$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Geletu, Abel Sorsa</creatorcontrib><creatorcontrib>Robi, Dereje Tulu</creatorcontrib><title>Evaluation of the immune response of layer chickens to Newcastle disease virus vaccines using the new vaccination regimens</title><title>Veterinary medicine and science</title><addtitle>Vet Med Sci</addtitle><description>Background
The study aimed to evaluate the immunological response of layer chickens to live Newcastle disease virus vaccine using a newly developed vaccine schedule administered via the ocular route, as well as assess the persistence of passive antibodies in layer chickens and the effectiveness of protection against strains of the virus.
Methods
A total of 140‐day‐old Lohmann Brown chicks were randomly divided into seven groups, 20 chicks each. Groups 1–3 received a single eye instillation of the vaccine at ages 5, 26 and 54 days, respectively, whereas groups 4–6 received a double eye instillation. Group 7 served as non‐vaccinated control group. Ten days after immunization, samples were taken from hens that had received the vaccine at ages 15, 36 and 64, as well as from control chickens that had not received the vaccine at ages 5, 15, 21 and 31.
Results
A total of 10 serum samples from all chickens exhibited protective antibodies, and booster doses resulted in the highest haemagglutination inhibition titre. No significant change in antibody production was observed among layer hens (p > 0.05). The study found that the La Sota (GMT ± SD: 6.71 ± 4.96), La Sota (GMT ± SD: 8.00 ± 0.00) and thermostable I2 (GMT ± SD: 7.60 ± 6.02), vaccination schedules provided the maximum immune response in single eye instillation, whereas the HB1 (GMT ± SD: 7.11 ± 4.77), La Sota (GMT ± SD: 7.83 ± 5.76) and La Sota (GMT ± SD: 7.60 ± 6.02), combination was the second‐best vaccination schedule in double eye instillation. Furthermore, maternally‐derived antibodies were maintained up to 31 days of age, indicating the level of passive immunity prior to vaccination. Characteristic lesions, such as edematous and diphtheria mucosal membranes of the trachea, along with petechial and necrotic haemorrhages of the proventriculus, were observed during the necropsy of the birds that died from the challenged virus.
Conclusion
This study suggests that subsequent live virus vaccine by ocular route immunization is required to effectively protect against velogenic viscerotropic Newcastle disease infection. The results also highlight the importance of developing effective vaccination schedules and routes to enhance immunity against ND in layer chickens.
Graphical : This study examined layer immune responses of chickens to Newcastle disease virus vaccines via a novel ocular route. One hundred forty Lohmann Brown chicks were divided into seven groups, receiving single or double eye instillations at various ages. Antibody titres were measured 10 days post‐immunization. The La Sota, La Sota thermostable I2 schedule showed the highest response with single instillation, whereas HB1, La Sota La Sota were effective with double instillation. Maternally‐derived antibodies persisted for 31 days, indicating passive immunity. Necropsy findings emphasized the need for tailored vaccination schedules for enhanced immunity against velogenic viscerotropic Newcastle disease in layer chickens.</description><subject>Agricultural research</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Antibodies, Viral</subject><subject>Antibody Formation</subject><subject>Chickens</subject><subject>Diphtheria</subject><subject>Eye</subject><subject>Farms</subject><subject>Female</subject><subject>Genotype & phenotype</subject><subject>Haemagglutination inhibition</subject><subject>Hemagglutination inhibition</subject><subject>Hemorrhage</subject><subject>Immune response</subject><subject>Immunity (passive)</subject><subject>immunological reactions</subject><subject>Juveniles</subject><subject>Mortality</subject><subject>Necropsy</subject><subject>Newcastle disease</subject><subject>Newcastle disease virus</subject><subject>ocular route</subject><subject>Poultry</subject><subject>protective antibodies</subject><subject>Rural areas</subject><subject>Vaccination - veterinary</subject><subject>Vaccines</subject><subject>Vaccines, Attenuated</subject><subject>Viral Vaccines</subject><subject>Viruses</subject><issn>2053-1095</issn><issn>2053-1095</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kUtv1DAURiMEolXpgj-ALLGBxbR-jp0lqlpaqYUFj63lx83UQxIPdjKj4dfjTIYKIbG61qejc6_1VdVrgi8IxvRy22V2QThVz6pTigVbEFyL53-9T6rznNcYYyK4ZEK-rE6YEqRWnJ1Wv663ph3NEGKPYoOGR0Ch68YeUIK8iX2GKW7NHhJyj8H9gD6jIaJPsHMmDy0gHzKYgm1DGjPaGudCDxmNOfSrg6-H3TGe1yRYha5oXlUvGtNmOD_Os-rbzfXXq9vF_eePd1cf7heOK6IWltWCUOCCNSCEk15ab7lTllHSAAdJhPGEgPSCghRLz700JaWGLSkoxs6qu9nro1nrTQqdSXsdTdCHIKaVNmkIrgUtKcHc1rKh3nAuuJJ1Y62lhkhP6iUU17vZtUnx5wh50F3IDtrW9BDHrGktOca1XKqCvv0HXccx9eWnmuFJXXZN1PuZcinmnKB5OpBgPfWrp3711G9h3xyNo-3AP5F_2izA5QzsQgv7_5v094cv7KD8DelJr4s</recordid><startdate>202405</startdate><enddate>202405</enddate><creator>Geletu, Abel Sorsa</creator><creator>Robi, Dereje Tulu</creator><general>John Wiley & Sons, Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3674-9457</orcidid></search><sort><creationdate>202405</creationdate><title>Evaluation of the immune response of layer chickens to Newcastle disease virus vaccines using the new vaccination regimens</title><author>Geletu, Abel Sorsa ; Robi, Dereje Tulu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4818-b39512e453fe55c7d7bdb4c8b321fe4e715ad11e7d52e756d4d7ae712a362e833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Agricultural research</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Antibodies, Viral</topic><topic>Antibody Formation</topic><topic>Chickens</topic><topic>Diphtheria</topic><topic>Eye</topic><topic>Farms</topic><topic>Female</topic><topic>Genotype & phenotype</topic><topic>Haemagglutination inhibition</topic><topic>Hemagglutination inhibition</topic><topic>Hemorrhage</topic><topic>Immune response</topic><topic>Immunity (passive)</topic><topic>immunological reactions</topic><topic>Juveniles</topic><topic>Mortality</topic><topic>Necropsy</topic><topic>Newcastle disease</topic><topic>Newcastle disease virus</topic><topic>ocular route</topic><topic>Poultry</topic><topic>protective antibodies</topic><topic>Rural areas</topic><topic>Vaccination - veterinary</topic><topic>Vaccines</topic><topic>Vaccines, Attenuated</topic><topic>Viral Vaccines</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Geletu, Abel Sorsa</creatorcontrib><creatorcontrib>Robi, Dereje Tulu</creatorcontrib><collection>Wiley-Blackwell Open Access Collection</collection><collection>Wiley Free Archive</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Biological Sciences</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Veterinary medicine and science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Geletu, Abel Sorsa</au><au>Robi, Dereje Tulu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of the immune response of layer chickens to Newcastle disease virus vaccines using the new vaccination regimens</atitle><jtitle>Veterinary medicine and science</jtitle><addtitle>Vet Med Sci</addtitle><date>2024-05</date><risdate>2024</risdate><volume>10</volume><issue>3</issue><spage>e1428</spage><epage>n/a</epage><pages>e1428-n/a</pages><issn>2053-1095</issn><eissn>2053-1095</eissn><abstract>Background
The study aimed to evaluate the immunological response of layer chickens to live Newcastle disease virus vaccine using a newly developed vaccine schedule administered via the ocular route, as well as assess the persistence of passive antibodies in layer chickens and the effectiveness of protection against strains of the virus.
Methods
A total of 140‐day‐old Lohmann Brown chicks were randomly divided into seven groups, 20 chicks each. Groups 1–3 received a single eye instillation of the vaccine at ages 5, 26 and 54 days, respectively, whereas groups 4–6 received a double eye instillation. Group 7 served as non‐vaccinated control group. Ten days after immunization, samples were taken from hens that had received the vaccine at ages 15, 36 and 64, as well as from control chickens that had not received the vaccine at ages 5, 15, 21 and 31.
Results
A total of 10 serum samples from all chickens exhibited protective antibodies, and booster doses resulted in the highest haemagglutination inhibition titre. No significant change in antibody production was observed among layer hens (p > 0.05). The study found that the La Sota (GMT ± SD: 6.71 ± 4.96), La Sota (GMT ± SD: 8.00 ± 0.00) and thermostable I2 (GMT ± SD: 7.60 ± 6.02), vaccination schedules provided the maximum immune response in single eye instillation, whereas the HB1 (GMT ± SD: 7.11 ± 4.77), La Sota (GMT ± SD: 7.83 ± 5.76) and La Sota (GMT ± SD: 7.60 ± 6.02), combination was the second‐best vaccination schedule in double eye instillation. Furthermore, maternally‐derived antibodies were maintained up to 31 days of age, indicating the level of passive immunity prior to vaccination. Characteristic lesions, such as edematous and diphtheria mucosal membranes of the trachea, along with petechial and necrotic haemorrhages of the proventriculus, were observed during the necropsy of the birds that died from the challenged virus.
Conclusion
This study suggests that subsequent live virus vaccine by ocular route immunization is required to effectively protect against velogenic viscerotropic Newcastle disease infection. The results also highlight the importance of developing effective vaccination schedules and routes to enhance immunity against ND in layer chickens.
Graphical : This study examined layer immune responses of chickens to Newcastle disease virus vaccines via a novel ocular route. One hundred forty Lohmann Brown chicks were divided into seven groups, receiving single or double eye instillations at various ages. Antibody titres were measured 10 days post‐immunization. The La Sota, La Sota thermostable I2 schedule showed the highest response with single instillation, whereas HB1, La Sota La Sota were effective with double instillation. Maternally‐derived antibodies persisted for 31 days, indicating passive immunity. Necropsy findings emphasized the need for tailored vaccination schedules for enhanced immunity against velogenic viscerotropic Newcastle disease in layer chickens.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>38519843</pmid><doi>10.1002/vms3.1428</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-3674-9457</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Agricultural research Animals Antibodies Antibodies, Viral Antibody Formation Chickens Diphtheria Eye Farms Female Genotype & phenotype Haemagglutination inhibition Hemagglutination inhibition Hemorrhage Immune response Immunity (passive) immunological reactions Juveniles Mortality Necropsy Newcastle disease Newcastle disease virus ocular route Poultry protective antibodies Rural areas Vaccination - veterinary Vaccines Vaccines, Attenuated Viral Vaccines Viruses |
title | Evaluation of the immune response of layer chickens to Newcastle disease virus vaccines using the new vaccination regimens |
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