{"title":"一种新型灭活油佐剂牛病毒性腹泻病毒疫苗预防病毒血症和临床表现：牛的免疫反应和攻击研究。","authors":"Berfin Ertürk, Gizem Aytoğu, Kadir Yeşilbağ","doi":"10.1007/s11259-025-10792-y","DOIUrl":null,"url":null,"abstract":"<p><p>Bovine viral diarrhea virus continues to threaten animal health with serious economic losses worldwide. Various killed, live-modified, or recombinant vaccine strategies are being developed for protection and control against this virus. The most important thing discovered is the choice of local and widespread strains in the vaccine content. In this study, the effectiveness of a Montanide<sup>®</sup> ISA 206 adjuvanted killed trivalent vaccine containing endemic local strains (TR-21 [BVDV-1l], TR-26 [BVDV-1f], and TR-15 [BVDV-2b]) isolated from Türkiye, was evaluated with a cattle challenge study. Experimental groups were designed as single dose vaccination (Group-I, n:11), two dose vaccination (Group-II, n:11), and unvaccinated (Group-III, n:6) with male calves aged about 6 months. Following the immunization, challenge virus (TR-72 [BVDV-1l], TCID<sub>50</sub> 10<sup>6.5</sup>) was given intranasally to each group (5 animals in Group-I and II and 4 animals in Group-III), and clinical findings, hematological changes, virus shedding, side effects, and viremia were monitored for 14 days after inoculation. Serological monitoring of the remaining animals against homologous and heterologous strains was carried out at one-month intervals between the 21st and 201st days after the first vaccination. The obtained results showed that the viremia, hematological changes, and clinical findings shown in unvaccinated animals (Group-III) were significantly suppressed (p < 0.05) in the vaccinated groups (Group-I and II). In addition, it was found that serologically monitored animals maintained protective neutralizing antibody (nAb) titers ≥ 8 log<sub>2</sub> for vaccinal and also for all reference BVDV-1 strains, which is more than three-fold protective antibody response, lasting more than 7 months after the first vaccination, whether in single or two dose application. The rise of nAbs was also detected for heterogous BVDV strains. The detected nAb titers were significantly higher (p < 0.05) in the two dose vaccination group. Based on the results, it was concluded that this trivalent- inactivated vaccine candidate can protect cattle against acute BVDV infections.</p>","PeriodicalId":23690,"journal":{"name":"Veterinary Research Communications","volume":"49 4","pages":"224"},"PeriodicalIF":1.8000,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12165897/pdf/","citationCount":"0","resultStr":"{\"title\":\"A novel killed oil adjuvanted bovine viral diarrhea virus vaccine protects from viremia and clinical manifestations: an immune response and challenge study in cattle.\",\"authors\":\"Berfin Ertürk, Gizem Aytoğu, Kadir Yeşilbağ\",\"doi\":\"10.1007/s11259-025-10792-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Bovine viral diarrhea virus continues to threaten animal health with serious economic losses worldwide. Various killed, live-modified, or recombinant vaccine strategies are being developed for protection and control against this virus. The most important thing discovered is the choice of local and widespread strains in the vaccine content. In this study, the effectiveness of a Montanide<sup>®</sup> ISA 206 adjuvanted killed trivalent vaccine containing endemic local strains (TR-21 [BVDV-1l], TR-26 [BVDV-1f], and TR-15 [BVDV-2b]) isolated from Türkiye, was evaluated with a cattle challenge study. Experimental groups were designed as single dose vaccination (Group-I, n:11), two dose vaccination (Group-II, n:11), and unvaccinated (Group-III, n:6) with male calves aged about 6 months. Following the immunization, challenge virus (TR-72 [BVDV-1l], TCID<sub>50</sub> 10<sup>6.5</sup>) was given intranasally to each group (5 animals in Group-I and II and 4 animals in Group-III), and clinical findings, hematological changes, virus shedding, side effects, and viremia were monitored for 14 days after inoculation. Serological monitoring of the remaining animals against homologous and heterologous strains was carried out at one-month intervals between the 21st and 201st days after the first vaccination. The obtained results showed that the viremia, hematological changes, and clinical findings shown in unvaccinated animals (Group-III) were significantly suppressed (p < 0.05) in the vaccinated groups (Group-I and II). In addition, it was found that serologically monitored animals maintained protective neutralizing antibody (nAb) titers ≥ 8 log<sub>2</sub> for vaccinal and also for all reference BVDV-1 strains, which is more than three-fold protective antibody response, lasting more than 7 months after the first vaccination, whether in single or two dose application. The rise of nAbs was also detected for heterogous BVDV strains. The detected nAb titers were significantly higher (p < 0.05) in the two dose vaccination group. Based on the results, it was concluded that this trivalent- inactivated vaccine candidate can protect cattle against acute BVDV infections.</p>\",\"PeriodicalId\":23690,\"journal\":{\"name\":\"Veterinary Research Communications\",\"volume\":\"49 4\",\"pages\":\"224\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2025-06-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12165897/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Veterinary Research Communications\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1007/s11259-025-10792-y\",\"RegionNum\":3,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"VETERINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Veterinary Research Communications","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1007/s11259-025-10792-y","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
A novel killed oil adjuvanted bovine viral diarrhea virus vaccine protects from viremia and clinical manifestations: an immune response and challenge study in cattle.
Bovine viral diarrhea virus continues to threaten animal health with serious economic losses worldwide. Various killed, live-modified, or recombinant vaccine strategies are being developed for protection and control against this virus. The most important thing discovered is the choice of local and widespread strains in the vaccine content. In this study, the effectiveness of a Montanide® ISA 206 adjuvanted killed trivalent vaccine containing endemic local strains (TR-21 [BVDV-1l], TR-26 [BVDV-1f], and TR-15 [BVDV-2b]) isolated from Türkiye, was evaluated with a cattle challenge study. Experimental groups were designed as single dose vaccination (Group-I, n:11), two dose vaccination (Group-II, n:11), and unvaccinated (Group-III, n:6) with male calves aged about 6 months. Following the immunization, challenge virus (TR-72 [BVDV-1l], TCID50 106.5) was given intranasally to each group (5 animals in Group-I and II and 4 animals in Group-III), and clinical findings, hematological changes, virus shedding, side effects, and viremia were monitored for 14 days after inoculation. Serological monitoring of the remaining animals against homologous and heterologous strains was carried out at one-month intervals between the 21st and 201st days after the first vaccination. The obtained results showed that the viremia, hematological changes, and clinical findings shown in unvaccinated animals (Group-III) were significantly suppressed (p < 0.05) in the vaccinated groups (Group-I and II). In addition, it was found that serologically monitored animals maintained protective neutralizing antibody (nAb) titers ≥ 8 log2 for vaccinal and also for all reference BVDV-1 strains, which is more than three-fold protective antibody response, lasting more than 7 months after the first vaccination, whether in single or two dose application. The rise of nAbs was also detected for heterogous BVDV strains. The detected nAb titers were significantly higher (p < 0.05) in the two dose vaccination group. Based on the results, it was concluded that this trivalent- inactivated vaccine candidate can protect cattle against acute BVDV infections.
期刊介绍：
Veterinary Research Communications publishes fully refereed research articles and topical reviews on all aspects of the veterinary sciences. Interdisciplinary articles are particularly encouraged, as are well argued reviews, even if they are somewhat controversial.
The journal is an appropriate medium in which to publish new methods, newly described diseases and new pathological findings, as these are applied to animals. The material should be of international rather than local interest. As it deliberately seeks a wide coverage, Veterinary Research Communications provides its readers with a means of keeping abreast of current developments in the entire field of veterinary science.
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