Borst Luke B, Suyemoto M Mitsu, Chen Laura R, Barnes H John
a Department of Population Health and Pathobiology, College of Veterinary Medicine , North Carolina State University , Raleigh , NC , USA.
Avian Pathol. 2019 Feb;48(1):17-24. doi: 10.1080/03079457.2018.1536819. Epub 2018 Nov 14.
Pathogenic strains of Enterococcus cecorum cause symmetrical paralysis in broilers due to infection of the free thoracic vertebra. The disease caused by pathogenic E. cecorum, known as enterococcal spondylitis or "kinky-back" continues to be responsible for significant losses to the broiler industry worldwide. In outbreaks of pathogenic E. cecorum, gut colonization and sepsis occur in the first three weeks-of-life. Since maternal antibodies are present during this period, we postulated that vaccination of breeders with a polyvalent killed vaccine would protect chicks from challenge. To test this hypothesis, representative isolates from seven genotype groups of pathogenic E. cecorum circulating in the US were chosen to produce adjuvanted killed vaccines (bacterins) and given to broiler-breeder hens. No single strain produced high titres of antibodies to all other strains; however, the combination of serologic reactivity of pathogenic isolates (designated SA3 and SA7) was sufficient to react with all genotypes. Vaccination of commercial broiler-breeder hens with a bacterin composed of SA3 and SA7 did not have any adverse effects. Vaccinated hens developed E. cecorum specific antibodies; however, no significant difference in survival was observed in infected embryos from hens in vaccine or adjuvant only groups. Chicks from vaccinated hens also failed to resist homologous or heterologous challenge during experimental infection. In a macrophage killing assay, pathogenic E. cecorum were found to evade opsinophagocytosis with elicited antibodies. These data suggest that pathogenic strains of E. cecorum possess virulence mechanisms that confound antibody-mediated opsinophagocytosis, complicating vaccine development for this pathogen of broilers.
盲肠肠球菌的致病菌株会因感染游离胸椎而导致肉鸡出现对称性麻痹。由致病性盲肠肠球菌引起的疾病,即肠球菌性脊柱炎或“弯背病”,仍在给全球肉鸡产业造成重大损失。在致病性盲肠肠球菌的疫情爆发中,肠道定植和败血症发生在雏鸡出生后的前三周。由于在此期间存在母源抗体,我们推测用多价灭活疫苗对种鸡进行免疫接种可以保护雏鸡免受感染。为了验证这一假设,从在美国流行的七个致病性盲肠肠球菌基因型组中选择代表性菌株,制备佐剂灭活疫苗(菌苗),并接种给肉种鸡。没有单一菌株能产生针对所有其他菌株的高滴度抗体;然而,致病性菌株(命名为SA3和SA7)的血清学反应性组合足以与所有基因型发生反应。用由SA3和SA7组成的菌苗对商业肉种鸡进行免疫接种没有任何不良影响。接种疫苗的母鸡产生了盲肠肠球菌特异性抗体;然而,在疫苗组或仅接种佐剂组的母鸡所产感染胚胎中,未观察到存活率有显著差异。接种疫苗的母鸡所产雏鸡在实验性感染期间也未能抵抗同源或异源攻击。在巨噬细胞杀伤试验中,发现致病性盲肠肠球菌能够逃避由诱导抗体介导的调理吞噬作用。这些数据表明,致病性盲肠肠球菌菌株具有使抗体介导的调理吞噬作用失效的毒力机制,这使得针对这种肉鸡病原体的疫苗开发变得复杂。