Criado Miguel, Silva Marta, Arteche-Villasol Noive, Zapico David, Elguezabal Natalia, Molina Elena, Espinosa José, Ferreras María Del Carmen, Benavides Julio, Pérez Valentín, Gutiérrez-Expósito Daniel
Departamento de Sanidad Animal, Instituto de Ganadería de Montaña (IGM) CSIC-ULE, León, Spain.
Departamento de Sanidad Animal, Facultad de Veterinaria, Universidad de León, Campus de Vegazana, León, Spain.
Front Vet Sci. 2024 Nov 27;11:1457849. doi: 10.3389/fvets.2024.1457849. eCollection 2024.
Paratuberculosis is a chronic granulomatous enteritis, caused by subspecies (), that affects ruminants worldwide. Vaccination has been considered the most cost-effective method for the control of this disease in infected dairy herds. However, currently available vaccines do not provide complete protection and interfere with the diagnosis of both paratuberculosis and bovine tuberculosis, limiting its use. Because of that, efforts are being made for the development of new vaccines. The primary objective of this study was to evaluate the efficacy of two whole-cell inactivated experimental vaccines against paratuberculosis in goats, administered through the oral (OV) and intradermal (IDV) routes, and compare them with that of the commercial subcutaneous vaccine Gudair (SCV). Over an 11-month period, the effect of vaccination and a subsequent challenge on the specific peripheral immune responses and DNA fecal shedding were recorded. At the end of the experiment, tissue bacterial load and lesion severity were assessed. The experimental vaccines did not induce specific humoral immune responses and only elicited mild and delayed cellular immune responses. Although the OV reduced lesion severity, neither this vaccine nor the IDV prototype was able to reduce fecal shedding or tissue bacterial load. Moreover, although the SCV did not confer sterile immunity, it outperformed both experimental vaccines in all these parameters.
副结核病是一种由亚种()引起的慢性肉芽肿性肠炎,影响着全球的反刍动物。疫苗接种被认为是控制感染奶牛群中这种疾病的最具成本效益的方法。然而,目前可用的疫苗并不能提供完全的保护,并且会干扰副结核病和牛结核病的诊断,限制了其使用。因此,人们正在努力开发新的疫苗。本研究的主要目的是评估两种全细胞灭活实验性疫苗通过口服(OV)和皮内(IDV)途径接种对山羊副结核病的疗效,并将它们与商业皮下疫苗古德艾尔(SCV)进行比较。在11个月的时间里,记录了疫苗接种及随后的攻毒对特异性外周免疫反应和粪便DNA排菌的影响。在实验结束时,评估了组织细菌载量和病变严重程度。实验性疫苗未诱导特异性体液免疫反应,仅引发了轻微且延迟的细胞免疫反应。尽管口服疫苗降低了病变严重程度,但该疫苗和皮内疫苗原型均未能减少粪便排菌或组织细菌载量。此外,尽管皮下疫苗不能提供无菌免疫,但在所有这些参数上均优于两种实验性疫苗。