Evaluation of Vaccination Programs in Layer Pullets Using Recombinant Fowl-Pox Mycoplasma gallisepticum Vaccine in Comparison to Commercially Available F-Strain Live Vaccines.

IF 1.3
Amro Hashish, Maria Chaves, Onyekachukwu Osemeke, Yuko Sato, Mohamed El-Gazzar
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Abstract

Over the last few decades, recombinant vaccines have been increasingly used for disease control in commercial poultry production. This study assesses the efficacy of a recombinant fowl-pox virus-based vector vaccine (rFP-MG) in conferring protection against Mycoplasma gallisepticum (MG) in different prime-boost combinations with or without the live modified F-strain vaccine. Four different vaccination programs were evaluated using Hy-line W-36 layer pullets. Group 1 served as unvaccinated controls (n = 57). Group 2 (n = 30) received a single dose of rFP-MG at 8 wk of age, and group 3 (n = 31) received two doses of rFP-MG, one at 1 day of age and again at 8 wk. Group 4 (n = 30) received a single dose of F strain at 8 wk, and group 5 (n = 32) received rFP-MG at 1 day of age and F strain at 8 wk. Four weeks after the second vaccination, all groups, including the negative control group, were divided into two (challenged and unchallenged) subgroups. All challenged groups were then inoculated with the MG Rlow strain at a dose of 3.11 × 108 CCU/bird via the fine spray route. Unchallenged groups included the unvaccinated/unchallenged and four vaccinated/unchallenged control groups. Clinical scoring, air sac scoring, and tracheal mucosal thickness at 21 days postchallenge were used as the main parameters for the evaluation of each vaccination program. No mortalities were observed in any of the study groups after the challenge; however, challenged groups that received only rFP-MG showed clinical signs (ranged from a few snicks to some gurgling sounds) as early as 7 days postchallenge, while the F-strain-vaccinated/challenged groups did not show any clinical signs. Birds from all groups exhibited varying degrees of air sac lesions (ranging from air sacs with suds or small flecks of caseous exudate to cloudy and thickened air sacs), with a higher percentage of birds in the rFP-MG groups being affected. The tracheal mucosal thickness of the F-strain-vaccinated groups was not significantly higher than that of the unvaccinated/unchallenged (negative control) group. However, the tracheal mucosal thickness of the rFP-MG-vaccinated group was significantly lower (P < 0.05) than that of the unvaccinated/ challenged (positive control) group. Results from this trial showed that rFP-MG vaccine provided partial protection against the clinical signs compared to the unvaccinated/challenged positive control; however, it was less protective than the F-strain vaccine.

鸡痘支原体重组鸡痘支原体疫苗与市售f株活疫苗接种方案的比较
在过去的几十年里,重组疫苗越来越多地用于商业家禽生产中的疾病控制。本研究评估了重组鸡痘病毒载体疫苗(rFP-MG)在与或不含改性f株活疫苗的不同初始-增强组合中对鸡败支原体(MG)的保护作用。使用hyline W-36蛋鸡对四种不同的疫苗接种方案进行了评估。第1组为未接种疫苗的对照组(n = 57)。第2组(n = 30)在8周龄时接受单剂量rFP-MG治疗,第3组(n = 31)在1日龄和8周龄时接受两剂量rFP-MG治疗。第4组(n = 30)在8周时给予单剂量F菌株,第5组(n = 32)在1日龄时给予rFP-MG, 8周时给予F菌株。第二次接种4周后,包括阴性对照组在内的所有组分为两个亚组(攻毒组和未攻毒组)。所有攻毒组均采用细喷法接种MG Rlow菌株,接种剂量为3.11 × 108 CCU/只。未挑战组包括未接种疫苗/未挑战组和四个接种疫苗/未挑战组。临床评分、气囊评分和攻毒后21天气管粘膜厚度作为评价各疫苗接种方案的主要参数。挑战后,在任何研究组中均未观察到死亡;然而,仅接受rFP-MG的攻毒组早在攻毒后7天就出现了临床症状(从轻微的咯咯声到一些咯咯声),而接种f菌株/攻毒组则没有出现任何临床症状。所有组的鸟类都表现出不同程度的气囊病变(从带有泡沫或小斑点的干酪样渗出物的气囊到浑浊和增厚的气囊),rFP-MG组的鸟类受到影响的比例更高。接种f菌组气管黏膜厚度不显著高于未接种/未攻毒(阴性对照)组。rfp - mg接种组气管黏膜厚度显著低于未接种/攻毒(阳性对照)组(P < 0.05)。该试验结果显示,与未接种疫苗/挑战阳性对照相比,rFP-MG疫苗对临床症状提供了部分保护;然而,它的保护作用不如f株疫苗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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