Cull Charley A, Singu Vijay K, Bromm Jenna J, Lechtenberg Kelly F, Amachawadi Raghavendra G, Cull Brooke J
Midwest Veterinary Services, Inc., Oakland, NE 68045, USA.
Central States Research Centre, Inc., Oakland, NE 68045, USA.
Antibiotics (Basel). 2023 Mar 16;12(3):599. doi: 10.3390/antibiotics12030599.
A total of 90 pigs, approximately one day of age, were used in a 42-day study to evaluate whether Endovac-Porci, a core antigen vaccine with an immunostimulant, provides piglets with broad-spectrum protection against the enteric and respiratory effects of Gram-negative bacteria. This study was a single-site, randomized, prospective, blinded, comparative placebo-controlled design. Individual pigs were randomly allocated to 1 of 2 treatments in a randomized design. An individual pig was considered the experimental unit for the farrowing phase (Study day 0 to 21), and the pen was considered the experimental unit for the nursery phase (Study day 21 to 42). Thus, there were 45 replications per treatment during the farrowing phase and 15 replications per treatment during the nursery phase. Treatments included a control product (saline; CP) and an investigational product (Endovac-Porci; IVP). On Study day 23, all pigs were challenged with enterotoxigenic strain expressing K88 (F4) fimbriae and . Individual pigs were weighed and feed consumption was measured to determine body weight gain, average daily gain, and feed-to-gain ratio. Clinical and fecal scores and overall health were recorded daily. Overall, administering the IVP to pigs led to an increase ( < 0.01) in body weight gain and average daily gain compared to pigs administered the CP. Pigs administered the IVP had reduced ( < 0.01) mortality compared to pigs administered the CP. There was a Study day × treatment interaction on clinical and fecal scores ( < 0.01). There was also a main effect of Study day where clinical and fecal scores increased ( < 0.01) as the Study day increased. Treatment also had an effect on clinical and fecal scores, where pigs administered the IVP had lower ( < 0.01) clinical and fecal scores compared to pigs administered the CP. In conclusion, administering pigs with the Endovac-Porci vaccination significantly improved the performance (i.e., body weight, body weight gain, and average daily gain) and health (i.e., clinical and fecal scores), while reducing the overall mortality in pigs challenged with K88 orally and intranasally post-weaning. Results from this study suggest that Endovac-Porci could provide broad-spectrum protection against enteric and respiratory effects of Gram-negative bacteria in piglets.
总共90头约1日龄的仔猪被用于一项为期42天的研究,以评估一种含有免疫刺激剂的核心抗原疫苗Endovac-Porci是否能为仔猪提供针对革兰氏阴性菌肠道和呼吸道影响的广谱保护。本研究采用单地点、随机、前瞻性、盲法、比较安慰剂对照设计。在随机设计中,将个体仔猪随机分配到2种处理中的1种。在产仔阶段(研究第0天至21天),以个体仔猪作为实验单位;在保育阶段(研究第21天至42天),以栏作为实验单位。因此,在产仔阶段每种处理有45个重复,在保育阶段每种处理有15个重复。处理包括一种对照产品(生理盐水;CP)和一种试验产品(Endovac-Porci;IVP)。在研究第23天,所有仔猪用表达K88(F4)菌毛的产肠毒素菌株进行攻毒。对个体仔猪称重并测量采食量,以确定体重增加、平均日增重和料重比。每天记录临床和粪便评分以及整体健康状况。总体而言,与接受CP的仔猪相比,给仔猪施用IVP导致体重增加和平均日增重增加(P<0.01)。与接受CP的仔猪相比,接受IVP的仔猪死亡率降低(P<0.01)。在临床和粪便评分上存在研究天数×处理的交互作用(P<0.01)。研究天数也有主效应,随着研究天数增加,临床和粪便评分升高(P<0.01)。处理对临床和粪便评分也有影响,与接受CP的仔猪相比,接受IVP的仔猪临床和粪便评分更低(P<0.01)。总之,给仔猪接种Endovac-Porci疫苗显著改善了性能(即体重、体重增加和平均日增重)和健康状况(即临床和粪便评分),同时降低了断奶后经口和鼻内接种K88攻毒仔猪的总体死亡率。本研究结果表明,Endovac-Porci可为仔猪提供针对革兰氏阴性菌肠道和呼吸道影响的广谱保护。