School of Agricultural and Veterinarian Sciences, São Paulo State University (Unesp), Jaboticabal 14884-900, SP, Brazil.
Laboratório de Virologia Animal (LVA), Departamento de Veterinária, Universidade Federal de Viçosa, Avenida Peter Henry Rolfs s/n, Campus Universitário, Viçosa 36570-900, MG, Brazil.
Int J Mol Sci. 2023 Apr 1;24(7):6591. doi: 10.3390/ijms24076591.
is a difficult-to-control bacterium since commercial vaccines do not prevent colonization and excretion. The present study aimed to evaluate the performance of an orally administered vaccine composed of antigens extracted from and incorporated into mesoporous silica (SBA-15), which has an adjuvant-carrier function, aiming to potentiate the action of the commercial intramuscular vaccine. A total of 60 piglets were divided into four groups (n = 15) submitted to different vaccination protocols as follows, Group 1: oral SBA15 + commercial vaccine at 24 days after weaning, G2: oral vaccine on the third day of life + vaccine commercial vaccine at 24 days, G3: commercial vaccine at 24 days, and G4: commercial vaccine + oral vaccine at 24 days. On the first day, the piglets were weighed and, from the third day onwards, submitted to blood collections for the detection and quantification of anti- IgG. Nasal swabs were collected to monitor IgA by ELISA, and oropharyngeal swabs were used to assess the bacterial load by qPCR. Biological samples were collected periodically from the third day of life until the 73rd day. At 41 days of life, 15 individuals of the same age, experimentally challenged with an inoculum containing , were co-housed with the animals from groups (1 to 4) in a single pen to increase the infection pressure during the nursery period. At 73 days, all piglets were euthanized, and lungs were evaluated by collecting samples for estimation of bacterial load by qPCR. Quantitative data obtained from physical parameters and laboratory investigation were analyzed by performing parametric or non-parametric statistical tests. Results indicate that animals from G2 showed smaller affected lung areas compared to G3. Animals from G2 and G4 had a low prevalence of animals shedding at 61 days of age. Additionally, no correlation was observed between lung lesions and load in lung and BALF samples in animals that received the oral vaccine, while a strong correlation was observed in other groups. In the present study, evidence points to the effectiveness of the oral vaccine developed for controlling in pig production under field conditions.
是一种难以控制的细菌,因为商业疫苗不能预防定植和排泄。本研究旨在评估一种口服疫苗的性能,该疫苗由 中提取的抗原组成,并结合介孔硅(SBA-15),具有佐剂载体功能,旨在增强商业肌肉内疫苗的作用。总共 60 头仔猪被分为四组(n = 15),接受不同的疫苗接种方案如下,组 1:口服 SBA15 + 断奶后 24 天的商业疫苗,G2:出生后第 3 天口服疫苗+ 24 天的商业疫苗,G3:24 天的商业疫苗,G4:24 天的商业疫苗+口服疫苗。第一天,仔猪称重,从第三天开始,采集血液检测和定量抗 IgG。通过 ELISA 采集鼻拭子监测 IgA,通过 qPCR 采集口咽拭子评估细菌负荷。从出生后第三天开始,每隔一段时间收集生物样本,直到第 73 天。在第 41 天,15 名相同年龄的个体,用含有 的接种物进行实验性挑战,与来自组(1 至 4)的动物共同饲养在一个单独的围栏中,以增加保育期的感染压力。在第 73 天,所有仔猪被安乐死,采集肺部样本通过 qPCR 估计细菌负荷。通过进行参数或非参数统计检验分析来自身体参数和实验室研究的定量数据。结果表明,与 G3 相比,G2 组的动物肺部受影响的区域较小。G2 和 G4 组的动物在 61 天时的 脱落率较低。此外,在接受口服疫苗的动物中,肺部病变与肺部和 BALF 样本中的 负荷之间没有相关性,而在其他组中观察到很强的相关性。在本研究中,有证据表明,在田间条件下,针对猪生产中的 开发的口服疫苗是有效的。