Andre Giovanni, Yin-Ze Shi, Pei-Chi Wang, Ming-An Tsai, Shih-Chu Chen
{"title":"口服生物膜疫苗和灭活细胞疫苗对四指带鱼的免疫反应和保护效果比较","authors":"Andre Giovanni, Yin-Ze Shi, Pei-Chi Wang, Ming-An Tsai, Shih-Chu Chen","doi":"10.1111/jfd.70062","DOIUrl":null,"url":null,"abstract":"<p><p>Mariculture, a significant component of the maritime industry that focuses on marine food production, faces challenges in maintaining productivity during bacterial disease outbreaks, particularly in high-value aquaculture such as the four-finger threadfin fish in Taiwan. Streptococcosis, caused by Streptococcus iniae, is a major contributor to the mortality of the four-finger threadfin (Eleutheronema tetradactylum). Recurrent streptococcosis outbreaks have highlighted the pressing need for highly effective vaccination strategies. Given its safety, environmental friendliness, and protective effects, vaccination is widely acknowledged as an effective means of preventing aquatic diseases. An innovative approach involves using biofilm-forming S. iniae as vaccine candidates for aquaculture. This study presents an effective approach for developing a biofilm-based vaccine by cultivating S. iniae on chitosan particles, facilitating robust biofilm formation and enhancing immune responses in four-finger threadfin fish. For comparison, a formalin-killed cell (FKC) vaccine, prepared from whole-cell S. iniae, was evaluated. Immune responses were examined in the blood, mucus, and gut lavage from both the vaccinated and control groups. These responses include immune-related gene expression, antibody titers, and lysozyme activity. At 30 days post-vaccination, the biofilm vaccine group exhibited elevated antibody titers, with values of 0.23 ± 0.02 in serum, 0.09 ± 0.01 in mucus, and 0.16 ± 0.01 in gut lavage. Following vaccination, both the FKC and biofilm vaccines significantly upregulated the expression of key proinflammatory cytokines (tumour necrosis factor-α, interleukin [IL]-10, IL-12) in the spleen and kidney, indicating robust activation of the innate immune response. However, the biofilm vaccine induced markedly higher expression of these cytokines, highlighting its stronger stimulation of innate immune responses. These results suggest that the biofilm-based formulation stimulates early immune signalling pathways that are critical for protection against S. iniae infection. In the challenge experiments, the relative percent survival was of 22.85% for the biofilm and 42.8% for the FKC vaccine groups. This study demonstrates that while both FKC and biofilm vaccines activated innate and adaptive immunity, the FKC vaccine provided higher protection (RPS 42.8% vs. 22.85%), indicating that strong immunogenicity does not always translate into effective protection and that oral vaccine strategies require further refinement. Further optimisation of oral vaccine formulations is required to improve the protective efficacy of biofilm-based vaccines in aquaculture.</p>","PeriodicalId":15849,"journal":{"name":"Journal of fish diseases","volume":" ","pages":"e70062"},"PeriodicalIF":2.2000,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comparative Evaluation of Oral Biofilm and Killed Cell Vaccines Against Streptococcus iniae in Four-Finger Threadfin Fish (Eleutheronema tetradactylum): Immune Response and Protection Efficacy.\",\"authors\":\"Andre Giovanni, Yin-Ze Shi, Pei-Chi Wang, Ming-An Tsai, Shih-Chu Chen\",\"doi\":\"10.1111/jfd.70062\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Mariculture, a significant component of the maritime industry that focuses on marine food production, faces challenges in maintaining productivity during bacterial disease outbreaks, particularly in high-value aquaculture such as the four-finger threadfin fish in Taiwan. Streptococcosis, caused by Streptococcus iniae, is a major contributor to the mortality of the four-finger threadfin (Eleutheronema tetradactylum). Recurrent streptococcosis outbreaks have highlighted the pressing need for highly effective vaccination strategies. Given its safety, environmental friendliness, and protective effects, vaccination is widely acknowledged as an effective means of preventing aquatic diseases. An innovative approach involves using biofilm-forming S. iniae as vaccine candidates for aquaculture. This study presents an effective approach for developing a biofilm-based vaccine by cultivating S. iniae on chitosan particles, facilitating robust biofilm formation and enhancing immune responses in four-finger threadfin fish. For comparison, a formalin-killed cell (FKC) vaccine, prepared from whole-cell S. iniae, was evaluated. Immune responses were examined in the blood, mucus, and gut lavage from both the vaccinated and control groups. These responses include immune-related gene expression, antibody titers, and lysozyme activity. At 30 days post-vaccination, the biofilm vaccine group exhibited elevated antibody titers, with values of 0.23 ± 0.02 in serum, 0.09 ± 0.01 in mucus, and 0.16 ± 0.01 in gut lavage. Following vaccination, both the FKC and biofilm vaccines significantly upregulated the expression of key proinflammatory cytokines (tumour necrosis factor-α, interleukin [IL]-10, IL-12) in the spleen and kidney, indicating robust activation of the innate immune response. However, the biofilm vaccine induced markedly higher expression of these cytokines, highlighting its stronger stimulation of innate immune responses. These results suggest that the biofilm-based formulation stimulates early immune signalling pathways that are critical for protection against S. iniae infection. In the challenge experiments, the relative percent survival was of 22.85% for the biofilm and 42.8% for the FKC vaccine groups. This study demonstrates that while both FKC and biofilm vaccines activated innate and adaptive immunity, the FKC vaccine provided higher protection (RPS 42.8% vs. 22.85%), indicating that strong immunogenicity does not always translate into effective protection and that oral vaccine strategies require further refinement. 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引用次数: 0
摘要
海水养殖是以海洋食品生产为重点的海产业的一个重要组成部分,在细菌性疾病爆发期间,特别是在高价值水产养殖领域,如台湾的四指线鳍鱼,面临着保持生产力的挑战。由牛链球菌引起的链球菌病是导致四指线虫(四指线虫)死亡的主要原因。反复出现的链球菌病暴发突出表明迫切需要高度有效的疫苗接种战略。由于疫苗接种具有安全、环保和保护作用,被广泛认为是预防水生疾病的有效手段。一种创新的方法涉及使用生物膜形成的猪链球菌作为水产养殖的候选疫苗。本研究提出了一种利用壳聚糖在四指刺鳍鱼体内培养猪链球菌生物膜疫苗的有效方法,该方法可促进四指刺鳍鱼生物膜的形成和免疫应答的增强。为了进行比较,对由全细胞血吸虫制备的福尔马林杀伤细胞(FKC)疫苗进行了评估。在接种疫苗组和对照组的血液、粘液和肠道灌洗液中检测免疫反应。这些反应包括免疫相关基因表达、抗体滴度和溶菌酶活性。接种后30 d,生物膜疫苗组抗体滴度升高,血清抗体滴度为0.23±0.02,黏液抗体滴度为0.09±0.01,肠灌洗液抗体滴度为0.16±0.01。接种后,FKC和生物膜疫苗均显著上调脾脏和肾脏中关键促炎细胞因子(肿瘤坏死因子-α、白细胞介素[IL]-10、IL-12)的表达,表明先天免疫应答被强烈激活。然而,生物膜疫苗诱导这些细胞因子的表达明显增加,突出了其对先天免疫反应的更强刺激。这些结果表明,基于生物膜的制剂刺激了早期免疫信号通路,这对预防链球菌感染至关重要。在攻毒实验中,生物膜组相对存活率为22.85%,FKC疫苗组相对存活率为42.8%。本研究表明,虽然FKC和生物膜疫苗都能激活先天免疫和适应性免疫,但FKC疫苗提供了更高的保护(RPS为42.8% vs. 22.85%),这表明强大的免疫原性并不总是转化为有效的保护,口服疫苗策略需要进一步完善。需要进一步优化口服疫苗配方,以提高生物膜疫苗在水产养殖中的保护功效。
Comparative Evaluation of Oral Biofilm and Killed Cell Vaccines Against Streptococcus iniae in Four-Finger Threadfin Fish (Eleutheronema tetradactylum): Immune Response and Protection Efficacy.
Mariculture, a significant component of the maritime industry that focuses on marine food production, faces challenges in maintaining productivity during bacterial disease outbreaks, particularly in high-value aquaculture such as the four-finger threadfin fish in Taiwan. Streptococcosis, caused by Streptococcus iniae, is a major contributor to the mortality of the four-finger threadfin (Eleutheronema tetradactylum). Recurrent streptococcosis outbreaks have highlighted the pressing need for highly effective vaccination strategies. Given its safety, environmental friendliness, and protective effects, vaccination is widely acknowledged as an effective means of preventing aquatic diseases. An innovative approach involves using biofilm-forming S. iniae as vaccine candidates for aquaculture. This study presents an effective approach for developing a biofilm-based vaccine by cultivating S. iniae on chitosan particles, facilitating robust biofilm formation and enhancing immune responses in four-finger threadfin fish. For comparison, a formalin-killed cell (FKC) vaccine, prepared from whole-cell S. iniae, was evaluated. Immune responses were examined in the blood, mucus, and gut lavage from both the vaccinated and control groups. These responses include immune-related gene expression, antibody titers, and lysozyme activity. At 30 days post-vaccination, the biofilm vaccine group exhibited elevated antibody titers, with values of 0.23 ± 0.02 in serum, 0.09 ± 0.01 in mucus, and 0.16 ± 0.01 in gut lavage. Following vaccination, both the FKC and biofilm vaccines significantly upregulated the expression of key proinflammatory cytokines (tumour necrosis factor-α, interleukin [IL]-10, IL-12) in the spleen and kidney, indicating robust activation of the innate immune response. However, the biofilm vaccine induced markedly higher expression of these cytokines, highlighting its stronger stimulation of innate immune responses. These results suggest that the biofilm-based formulation stimulates early immune signalling pathways that are critical for protection against S. iniae infection. In the challenge experiments, the relative percent survival was of 22.85% for the biofilm and 42.8% for the FKC vaccine groups. This study demonstrates that while both FKC and biofilm vaccines activated innate and adaptive immunity, the FKC vaccine provided higher protection (RPS 42.8% vs. 22.85%), indicating that strong immunogenicity does not always translate into effective protection and that oral vaccine strategies require further refinement. Further optimisation of oral vaccine formulations is required to improve the protective efficacy of biofilm-based vaccines in aquaculture.
期刊介绍:
Journal of Fish Diseases enjoys an international reputation as the medium for the exchange of information on original research into all aspects of disease in both wild and cultured fish and shellfish. Areas of interest regularly covered by the journal include:
-host-pathogen relationships-
studies of fish pathogens-
pathophysiology-
diagnostic methods-
therapy-
epidemiology-
descriptions of new diseases