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一种新型细胞内劳森菌灭活疫苗对猪抵抗实验性感染及在田间条件下的效力。

Efficacy of a novel inactivated Lawsonia intracellularis vaccine in pigs against experimental infection and under field conditions.

作者信息

Jacobs A A C, Harks F, Hazenberg L, Hoeijmakers M J H, Nell T, Pel S, Segers R P A M

机构信息

MSD Animal Health, PO Box 31, 5830 AA Boxmeer, the Netherlands.

出版信息

Vaccine. 2019 Apr 3;37(15):2149-2157. doi: 10.1016/j.vaccine.2019.02.067. Epub 2019 Mar 11.

Abstract

The efficacy of a novel inactivated Lawsonia intracellularis vaccine, Porcilis® Lawsonia, was compared to that of a commercially available live attenuated vaccine in three experimental vaccination-challenge studies in pigs. The efficacy of the new vaccine was further tested under field conditions on a farm with a history of acute ileitis. The novel inactivated vaccine consists of a freeze-dried antigen fraction that is dissolved just prior to use in either the adjuvant or in Porcilis® PCV M Hyo; an existing combination vaccine against porcine circovirus type 2 and Mycoplasma hyopneumoniae. The three experimental vaccination-challenge trials had a similar design and for each trial 75 piglets were used, randomly allotted to three groups of 25 piglets. The pigs were vaccinated at 4 or 5 weeks of age with either Porcilis® Lawsonia in adjuvant or in associated mixed use with Porcilis® PCV M Hyo (group 1), with the live vaccine (group 2), or left as unvaccinated controls (group 3). The pigs were challenged with virulent Lawsonia intracellularis 3, 4 or 17 weeks after vaccination. Post-challenge the pigs were evaluated for clinical signs, average daily weight gain, shedding and macroscopic as well as microscopic immuno-histological ileum lesion scores. In the field study, the mortality and key performance parameters were evaluated over a period of 8 months. The results of all three experimental vaccination-challenge trials showed that Porcilis® Lawsonia induced statistically significant protection against experimental Lawsonia intracellularis infection. This was demonstrated by lower clinical scores, improved weight gain, reduction of Lawsonia intracellularis shedding and reduction of macroscopic as well as microscopic ileum lesion scores when compared to the controls. The protection induced was superior to that of the commercially available live vaccine. In the field study, Porcilis® Lawsonia proved to be highly efficacious; reducing Lawsonia associated mortality to zero and improving key production parameters.

摘要

在三项针对猪的实验性疫苗接种-攻毒研究中,将一种新型的胞内劳森菌灭活疫苗Porcilis® Lawsonia与一种市售的减毒活疫苗的效力进行了比较。在一个有急性回肠炎病史的猪场的田间条件下,对这种新疫苗的效力进行了进一步测试。这种新型灭活疫苗由冻干的抗原组分组成,在使用前即刻溶解于佐剂或Porcilis® PCV M Hyo(一种现有的针对猪圆环病毒2型和猪肺炎支原体的联合疫苗)中。三项实验性疫苗接种-攻毒试验设计相似,每项试验使用75头仔猪,随机分为三组,每组25头仔猪。仔猪在4或5周龄时,分别用佐剂中的Porcilis® Lawsonia或与Porcilis® PCV M Hyo联合使用(第1组)、减毒活疫苗(第2组)进行接种,或作为未接种对照(第3组)。接种后3、4或17周,用强毒胞内劳森菌对猪进行攻毒。攻毒后,对猪的临床症状、平均日增重、排菌情况以及宏观和微观免疫组织学回肠病变评分进行评估。在田间研究中,在8个月的时间里对死亡率和关键生产性能参数进行了评估。所有三项实验性疫苗接种-攻毒试验的结果表明,Porcilis® Lawsonia诱导了对实验性胞内劳森菌感染具有统计学意义的保护作用。与对照组相比,临床评分更低、体重增加改善、胞内劳森菌排菌减少以及宏观和微观回肠病变评分降低,证明了这一点。诱导的保护作用优于市售的减毒活疫苗。在田间研究中,Porcilis® Lawsonia被证明具有高效力;将与劳森菌相关的死亡率降至零,并改善了关键生产参数。

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