Shin Gee-Wook, Nho Seong-Won, Park Seong-Bin, Jang Ho-Bin, Cha In-Seok, Ha Mi-Ae, Kim Young-Rim, Dalvi Rishikesh S, Joh Seong-Joon, Jung Tae-Sung
Laboratory of Aquatic Animal Diseases, Research Institute of Life Science, College of Veterinary Medicine, Gyeongsang National University, Jinju, Gyeongnam 660-701, Republic of Korea.
Vet Microbiol. 2009 Oct 20;139(1-2):113-20. doi: 10.1016/j.vetmic.2009.05.007. Epub 2009 Jun 6.
Lactococcus garvieae is an important etiological agent of lactococcosis in various fish species including olive flounder (Paralichthys olivaceus). In this study, proteomic and immunoproteomic analyses were employed to compare the antigenic profiles of strains KG9408, MS93003, and NSS9310 strains of L. garvieae. Proteomic analysis using two-dimensional gel electrophoresis (2-DE) revealed differences in five protein spots among the different L. garvieae strains. In immunoproteomic analysis, there was a significant difference in the 2-DE immunoblot profiles of the L. garvieae strains using sera collected from fish surviving infection with either L. garvieae strains KG9408 or NSS9310. These sera reacted with 8 and 7 unique antigenic protein spots, respectively. Heat shock protein (HSP) 70 and DNA-directed RNA polymerase were among the specific antigens recognized by the anti-NSS9310 serum. In addition, the anti-NSS9310 and anti-KG9408 olive flounder sera reacted with 25 common antigenic protein spots of all the L. garvieae strains, which included elongation factor (EF)-Tu, arginine deiminase (AD), inosine-5'-monophosphate dehydrogenase (IMPD), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), phosphomannomutase (PMM), L-lactate dehydrogenase (L-LDH), 6-phosphofructokinase and UDP-galactose 4-epimerase (UDP-galactose). Based on the present results, the 8 antigens recognized by the anti-KG9408 serum and the 25 common antigens recognized by both sera may serve as potential markers for developing an effective vaccine against this bacterium.
加氏乳球菌是包括牙鲆(Paralichthys olivaceus)在内的多种鱼类发生乳球菌病的重要病原体。在本研究中,采用蛋白质组学和免疫蛋白质组学分析方法比较加氏乳球菌KG9408、MS93003和NSS9310菌株的抗原谱。使用二维凝胶电泳(2-DE)进行的蛋白质组学分析揭示了不同加氏乳球菌菌株之间在5个蛋白点上存在差异。在免疫蛋白质组学分析中,用感染加氏乳球菌KG9408或NSS9310菌株后存活的鱼血清进行检测,加氏乳球菌菌株的2-DE免疫印迹图谱存在显著差异。这些血清分别与8个和7个独特的抗原性蛋白点发生反应。热休克蛋白(HSP)70和DNA指导的RNA聚合酶是抗NSS9310血清识别的特异性抗原。此外,抗NSS9310和抗KG9408牙鲆血清与所有加氏乳球菌菌株的25个共同抗原性蛋白点发生反应,其中包括延伸因子(EF)-Tu、精氨酸脱亚氨酶(AD)、肌苷-5'-单磷酸脱氢酶(IMPD)、甘油醛-3-磷酸脱氢酶(GAPDH)、磷酸甘露糖变位酶(PMM)、L-乳酸脱氢酶(L-LDH)、6-磷酸果糖激酶和UDP-半乳糖4-表异构酶(UDP-半乳糖)。基于目前的结果,抗KG9408血清识别的8种抗原和两种血清共同识别的25种抗原可能作为开发针对该细菌的有效疫苗的潜在标志物。