Smith Adrian L, Hesketh Patricia, Archer Andrew, Shirley Martin W
Institute for Animal Health, Compton Laboratory, Compton, Newbury, Berks RG20 7NN, United Kingdom.
Infect Immun. 2002 May;70(5):2472-9. doi: 10.1128/IAI.70.5.2472-2479.2002.
Eimeria spp. are a group of highly successful intracellular protozoan parasites that develop within enterocytes. Eimeria maxima from the chicken is characterized by high immunogenicity (a small priming infection gives complete immunity to subsequent homologous challenge) and naturally occurring antigenically variant populations that do not completely cross-protect. In this study we examined the expression of antigenic diversity in E. maxima, as manifested by cross-strain protection in a series of inbred chicken lines. The IAH line of Light Sussex chickens and all lines of inbred White Leghorns were susceptible to primary infections with either of two strains (H and W) of E. maxima and were protected completely against challenge with the homologous strain of parasite. The extent of cross-protection against the heterologous parasite strain varied from 0 to almost 100% depending on host genetics. Interestingly, in one inbred line of chickens (line 15I) the cross-protective phenotype was directional and intensely influenced by the infection history of the host. The basis for the observed variation in cross-protection is not known, but our results suggest that the major histocompatibility complex is not a major genetic component of the phenotype. These results are discussed in relation to the number of protective antigens presented by complex pathogens and the development of immunoprotective responses in hosts of different genetic backgrounds.
艾美耳属原虫是一类非常成功的细胞内原生动物寄生虫,在肠上皮细胞内发育。鸡的巨型艾美耳球虫具有高免疫原性(一次小剂量的初次感染能使鸡对随后的同源攻击产生完全免疫力)以及自然存在的抗原变异群体,这些变异群体不能完全交叉保护。在本研究中,我们通过一系列近交系鸡品系中的交叉株保护来研究巨型艾美耳球虫抗原多样性的表达。轻型苏塞克斯鸡的IAH品系和所有近交白来航鸡品系对巨型艾美耳球虫的两种菌株(H和W)中的任何一种的初次感染都易感,并且对同源寄生虫菌株的攻击具有完全的抵抗力。对异源寄生虫菌株的交叉保护程度因宿主基因而异,从0到几乎100%不等。有趣的是,在一个近交系鸡(15I系)中,交叉保护表型是有方向性的,并且受到宿主感染史的强烈影响。交叉保护中观察到的变异的基础尚不清楚,但我们的结果表明,主要组织相容性复合体不是该表型的主要遗传成分。结合复杂病原体呈现的保护性抗原数量以及不同遗传背景宿主中免疫保护反应的发展对这些结果进行了讨论。