Dutta S K, Vemulapalli R, Biswas B
Virginia-Maryland Regional College of Veterinary Medicine, University of Maryland, College Park 20742, USA.
J Clin Microbiol. 1998 Feb;36(2):506-12. doi: 10.1128/JCM.36.2.506-512.1998.
Ehrlichia risticii is the causative agent of Potomac horse fever (PHF), which continues to be an important disease of horses. Commercial inactivated whole-cell vaccines are regularly used for immunization of horses against the disease. However, PHF is occurring in large numbers of horses in spite of vaccination. In a limited study, 43 confirmed cases of PHF occurred between the 1994 and 1996 seasons; of these, 38 (89%) were in horses that had been vaccinated for the respective season, thereby clearly indicating vaccine failure. A field study of horses vaccinated with two PHF vaccines indicated a poor antibody response, as determined by immunofluorescence assay (IFA) titers. In a majority of horses, the final antibody titer ranged between 40 and 1,280, in spite of repeated vaccinations. None of the vaccinated horses developed in vitro neutralizing antibody in their sera. Similarly, one horse experimentally vaccinated three times with one of the vaccines showed a poor antibody response, with final IFA titers between 80 and 160. The horse did not develop in vitro neutralizing antibody or antibody against the 50/85-kDa strain-specific antigen (SSA), which is the protective antigen of the original strain, 25-D, and the variant strain of our laboratory, strain 90-12. Upon challenge infection with the 90-12 strain, the horse showed clinical signs of the disease. The horse developed neutralizing antibody and antibody to the 50/85-kDa SSA following the infection. Studies of the new E. risticii isolates from the field cases indicated that they were heterogeneous among themselves and showed differences from the 25-D and 90-12 strains as determined by IFA reactivity pattern, DNA amplification finger printing profile, and in vitro neutralization activity. Most importantly, the molecular sizes of the SSA of these isolates varied, ranging from 48 to 85 kDa. These studies suggest that the deficiency in the antibody response to the PHF vaccines and the heterogeneity of E. risticii isolates may be associated with the vaccine failure.
瑞氏埃立克体是波托马克马热(PHF)的病原体,该疾病仍是马匹的一种重要疾病。商业灭活全细胞疫苗经常用于马匹针对该疾病的免疫接种。然而,尽管进行了疫苗接种,大量马匹仍感染了PHF。在一项有限的研究中,1994年至1996年季节期间共出现43例确诊的PHF病例;其中38例(89%)发生在已针对相应季节接种疫苗的马匹身上,这清楚地表明了疫苗接种失败。一项对接种两种PHF疫苗的马匹的现场研究表明,通过免疫荧光测定(IFA)滴度测定,抗体反应较差。在大多数马匹中,尽管重复接种疫苗,最终抗体滴度仍在40至1280之间。接种疫苗的马匹血清中均未产生体外中和抗体。同样,一匹用其中一种疫苗进行三次实验性接种的马也表现出较差的抗体反应,最终IFA滴度在80至160之间。这匹马未产生体外中和抗体或针对50/85-kDa菌株特异性抗原(SSA)的抗体,该抗原是原始菌株25-D和我们实验室变异菌株90-12的保护性抗原。在用90-12菌株进行攻击感染后,这匹马出现了该疾病的临床症状。感染后,这匹马产生了中和抗体和针对50/85-kDa SSA的抗体。对来自现场病例的新瑞氏埃立克体分离株的研究表明,它们彼此之间存在异质性,并且通过IFA反应模式、DNA扩增指纹图谱和体外中和活性测定,与25-D和90-12菌株存在差异。最重要的是,这些分离株的SSA分子大小各不相同,范围从48至85 kDa。这些研究表明,对PHF疫苗的抗体反应不足以及瑞氏埃立克体分离株的异质性可能与疫苗接种失败有关。