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GI24裂解的候选灭活疫苗对韩国黑山羊布鲁氏菌病的保护效力

Protective efficacy of an inactivated vaccine candidate lysed by GI24 against brucellosis in Korean black goats.

作者信息

Kim Wong-Kyong, Moon Ja-Young, Cho Jeong-Sang, Ochirkhuyag Enkhsaikhan, Akanda Md Rashedunnabi, Park Byung-Yong, Hur Jin

机构信息

Veterinary Public Health, College of Veterinary Medicine, Chonbuk National University, Gobong-ro 79, Iksan, Jeollabuk-do, Republic of Korea (Kim, Moon, Cho, Ochirkhuyag, Hur); Veterinary Histology, College of Veterinary Medicine, Chonbuk National University, Gobong-ro 79, Iksan, Jeollabuk-do, Republic of Korea (Akanda, Park).

出版信息

Can J Vet Res. 2019 Jan;83(1):68-74.

PMID:30670904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6318821/
Abstract

The efficacy of GI24-lysed cells as a vaccine candidate against brucellosis in goats was evaluated on 2 groups of Korean black goats. Group A goats were immunized subcutaneously (SC) with sterile phosphate-buffered saline, whereas group B goats were immunized SC with approximately 3 × 10 lysed cells. Subcutaneous immunization with the lysed cells did not cause any negative impact on the overall clinical status, such as behavior and appetite, throughout the study period. The enzyme-linked immunosorbent assay (ELISA) optical densities values for lipopolysaccharide in serum were considerably higher in group B than those in group A. Also, the levels of the cytokines interleukin 4 (IL-4), tumor necrosis factor-alpha (TNF-α), and interferon gamma (IFN-γ) were significantly elevated in group B compared with those in group A. Following intraconjunctival challenge with strain 544, the severity of brucellosis in terms of infection index and colonization of in tissues was significantly lower in group B than in group A. The present study concluded that 3 of 5 goats immunized with GI24-lysed bacteria were completely protected against challenge. Future investigations are required to improve the protective efficacy offered by lysed cells for practical applications in small ruminants.

摘要

在两组韩国黑山羊上评估了GI24裂解细胞作为山羊布鲁氏菌病候选疫苗的效力。A组山羊皮下注射(SC)无菌磷酸盐缓冲盐水,而B组山羊皮下注射约3×10个裂解细胞。在整个研究期间,用裂解细胞进行皮下免疫对整体临床状况(如行为和食欲)没有造成任何负面影响。B组血清中脂多糖的酶联免疫吸附测定(ELISA)光密度值明显高于A组。此外,与A组相比,B组细胞因子白细胞介素4(IL-4)、肿瘤坏死因子-α(TNF-α)和干扰素γ(IFN-γ)的水平显著升高。在用544菌株进行结膜内攻毒后,B组布鲁氏菌病在感染指数和组织定植方面的严重程度明显低于A组。本研究得出结论,用GI24裂解细菌免疫的5只山羊中有3只完全受到保护,免受攻毒。未来需要进行研究,以提高裂解细胞在小型反刍动物实际应用中的保护效力。

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引用本文的文献

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Front Vet Sci. 2022 Jul 18;9:925773. doi: 10.3389/fvets.2022.925773. eCollection 2022.

本文引用的文献

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Bacterial ghosts as adjuvants: mechanisms and potential.作为佐剂的细菌幽灵:作用机制与潜力
Vet Res. 2017 Jun 24;48(1):37. doi: 10.1186/s13567-017-0442-5.
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First evaluation of an influenza viral vector based Brucella abortus vaccine in sheep and goats: Assessment of safety, immunogenicity and protective efficacy against Brucella melitensis infection.基于流感病毒载体的流产布鲁氏菌疫苗在绵羊和山羊中的首次评估:安全性、免疫原性及对羊种布鲁氏菌感染的保护效力评估
Vet Microbiol. 2016 Dec 25;197:15-20. doi: 10.1016/j.vetmic.2016.11.001. Epub 2016 Nov 3.
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Protective efficacy and immune responses by homologous prime-booster immunizations of a novel inactivated Salmonella Gallinarum vaccine candidate.新型鸡伤寒沙门氏菌灭活候选疫苗同源初免-加强免疫的保护效力和免疫反应
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Protection efficacy of the Brucella abortus ghost vaccine candidate lysed by the N-terminal 24-amino acid fragment (GI24) of the 36-amino acid peptide PMAP-36 (porcine myeloid antimicrobial peptide 36) in murine models.在小鼠模型中,由36个氨基酸的肽PMAP - 36(猪髓样抗菌肽36)的N端24个氨基酸片段(GI24)裂解的布鲁氏菌流产株候选菌苗的保护效力。
J Vet Med Sci. 2016 Nov 1;78(10):1541-1548. doi: 10.1292/jvms.16-0036. Epub 2016 Jun 25.
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Immune responses and protection induced by Brucella suis S2 bacterial ghosts in mice.猪布鲁氏菌S2菌影诱导小鼠的免疫反应及保护作用
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Characterization of culture supernatant proteins from Brucella abortus and its protection effects against murine brucellosis.流产布鲁氏菌培养上清蛋白的表征及其对小鼠布鲁氏菌病的保护作用
Comp Immunol Microbiol Infect Dis. 2014 Sep;37(4):221-8. doi: 10.1016/j.cimid.2014.06.001. Epub 2014 Jun 13.
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Identification of Brucella suis from feral swine in selected states in the USA.在美国部分州的野猪中鉴定出猪布鲁氏菌。
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Antimicrobial properties and membrane-active mechanism of a potential α-helical antimicrobial derived from cathelicidin PMAP-36.源自抗菌肽 PMAP-36 的潜在α-螺旋抗菌剂的抗菌特性和膜活性机制。
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