Dynamics of Antibody Response to Yersinia pestis Proteins in Plague Affected Guinea Pigs

Q3 Medicine
T. V. Gapel’chenkova, R. Z. Shaikhutdinova, A. Trunyakova, T. E. Svetoch, T. I. Kombarova, M. E. Platonov, A. Borzilov, P. Kopylov, S. V. Dentovskaya
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Abstract

Designing of new means for the specific prevention of plague, especially protein subunit vaccines, is impossible without studying the role of individual antigens in the manifestation of the pathogenic and immunogenic properties of Yersinia pestis. The aim of the present study was to determine the antibody levels to Y. pestis antigens in guinea pigs that survived infection with sub-lethal doses of virulent plague agent strains using enzyme immunoassay (ELISA). Materials and methods. Guinea pigs were inoculated subcutaneously with 30 CFU of the wild type Y. pestis subsp. Pestis strain 231 or non-capsular Y. pestis subsp. pestis Caf1-negative strain 358/12. Blood samples from sick or recovered guinea pigs were collected on day 15, 30, 60, and 90 after infection. The antibody response was assessed by 18 recombinant Y. pestis proteins in ELISA. Results and discussion. Heterogeneity of the antibody responses to the majority of the antigens with variation of IgG titers from animal to animal has been revealed. We observed increase in antibody titers by day 90 for the most analyzed antigens in the sera of the guinea pigs injected with wild type Y. pestis 231. On the contrary we found reduction in antibody titers by day 90 in case of inoculation with Y. pestis 358/12. The preservation of antibodies to Y. pestis proteins of different localization in the organism of the guinea pigs, as well functional activity, and the degree of representation on the surface of bacterial cell for a prolonged period of time indicates the multiplex nature of the plague immunity formation. Our findings are significant for the future design and development of effective vaccines against plague and the search for new targets for diagnostics of this disease.
鼠疫感染豚鼠对鼠疫耶尔森菌蛋白的抗体反应动态
如果不研究个体抗原在鼠疫杆菌致病性和免疫原性表现中的作用,就不可能设计出特异性预防鼠疫的新方法,特别是蛋白质亚单位疫苗。本研究的目的是使用酶免疫测定法(ELISA)测定在感染亚致死剂量的强毒株后存活的豚鼠中对鼠疫杆菌抗原的抗体水平。材料和方法。豚鼠皮下接种30CFU的野生型鼠疫杆菌亚种。鼠疫杆菌菌株231或非荚膜鼠疫杆菌亚种。鼠疫Caf1阴性菌株358/12。在感染后第15、30、60和90天采集患病或康复豚鼠的血样。在ELISA中用18种重组鼠疫杆菌蛋白评估抗体反应。结果和讨论。已经揭示了抗体对大多数抗原的反应的异质性,以及不同动物的IgG滴度的变化。在注射了野生型鼠疫杆菌231的豚鼠的血清中,我们观察到在第90天抗体滴度对于大多数分析抗原的增加。相反,我们发现在接种鼠疫杆菌358/12的情况下,到第90天抗体滴度降低。在豚鼠体内不同定位的鼠疫杆菌蛋白抗体的长期保存,以及功能活性和在细菌细胞表面的表现程度,表明鼠疫免疫形成的多重性。我们的发现对未来设计和开发有效的鼠疫疫苗以及寻找诊断该疾病的新靶点具有重要意义。
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来源期刊
Problemy Osobo Opasnykh Infektsii
Problemy Osobo Opasnykh Infektsii Medicine-Infectious Diseases
CiteScore
1.90
自引率
0.00%
发文量
79
审稿时长
12 weeks
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