Zeng Ximin, Xu Fuzhou, Lin Jun
Department of Animal Science, The University of Tennessee, Knoxville, Tennessee 37996-4574, USA.
Infect Immun. 2009 Dec;77(12):5437-48. doi: 10.1128/IAI.00666-09. Epub 2009 Sep 8.
The ferric enterobactin receptor CfrA not only is responsible for high-affinity iron acquisition in Campylobacter jejuni but also is essential for C. jejuni colonization in animal intestines. In this study, we determined the feasibility of targeting the iron-regulated outer membrane protein CfrA for immune protection against Campylobacter colonization. Alignment of complete CfrA sequences from 15 Campylobacter isolates showed that the levels of amino acid identity for CfrA range from 89% to 98%. Immunoblotting analysis using CfrA-specific antibodies demonstrated that CfrA was dramatically induced under iron-restricted conditions and was widespread and produced in 32 Campylobacter primary strains from various sources and from geographically diverse areas. The immunoblotting survey results were highly correlated with the results of an enterobactin growth promotion assay and a PCR analysis using cfrA-specific primers. Inactivation of the cfrA gene also impaired norepinephrine-mediated growth promotion, suggesting that CfrA is required for C. jejuni to sense intestinal stress hormones during colonization. Complementation of the cfrA mutant with a wild-type cfrA allele in trans fully restored the production and function of CfrA. A growth assay using purified anti-CfrA immunoglobulin G demonstrated that specific CfrA antibodies could block the function of CfrA, which diminished ferric enterobactin-mediated growth promotion under iron-restricted conditions. The inhibitory effect of CfrA antibodies was dose dependent. Immunoblotting analysis also indicated that CfrA was expressed and immunogenic in chickens experimentally infected with C. jejuni. Amino acid substitution mutagenesis demonstrated that R327, a basic amino acid that is highly conserved in CfrA, plays a critical role in ferric enterobactin acquisition in C. jejuni. Together, these findings strongly suggest that CfrA is a promising vaccine candidate for preventing and controlling Campylobacter infection in humans and animal reservoirs.
铁载体肠杆菌素受体CfrA不仅负责空肠弯曲菌中高亲和力铁的获取,而且对空肠弯曲菌在动物肠道中的定殖至关重要。在本研究中,我们确定了靶向铁调节外膜蛋白CfrA以免疫保护抵抗弯曲菌定殖的可行性。对15株弯曲菌分离株的完整CfrA序列进行比对,结果显示CfrA的氨基酸同一性水平在89%至98%之间。使用CfrA特异性抗体的免疫印迹分析表明,CfrA在铁限制条件下被显著诱导,并且广泛存在于来自不同来源和不同地理区域的32株弯曲菌原代菌株中并产生。免疫印迹调查结果与肠杆菌素生长促进试验以及使用cfrA特异性引物的PCR分析结果高度相关。cfrA基因的失活也损害了去甲肾上腺素介导的生长促进作用,这表明CfrA是空肠弯曲菌在定殖过程中感知肠道应激激素所必需的。用野生型cfrA等位基因对cfrA突变体进行反式互补完全恢复了CfrA的产生和功能。使用纯化的抗CfrA免疫球蛋白G进行的生长试验表明,特异性CfrA抗体可以阻断CfrA的功能,这在铁限制条件下减少了铁载体肠杆菌素介导的生长促进作用。CfrA抗体的抑制作用是剂量依赖性的。免疫印迹分析还表明,CfrA在实验感染空肠弯曲菌的鸡中表达且具有免疫原性。氨基酸替代诱变表明,R327是CfrA中高度保守的碱性氨基酸,在空肠弯曲菌获取铁载体肠杆菌素中起关键作用。总之,这些发现强烈表明CfrA是预防和控制人类和动物宿主中弯曲菌感染的有前景的疫苗候选物。