Yamamoto Isato, Ishihara Kazuyuki, Muramatsu Kyotaro, Wada Yoshiyuki, Kiwaki Mayumi, Kushiro Akira, Okuda Katsuji
Department of Microbiology, Tokyo Dental College.
Bull Tokyo Dent Coll. 2013;54(4):233-41. doi: 10.2209/tdcpublication.54.233.
Porphyromonas gingivalis, a pathogen involved in the development of chronic periodontitis, has a number of major virulence factors, among which are its surface cysteine protease gingipains. The purpose of this study was to investigate the feasibility of inducing protective antibodies against P. gingivalis by means of immunization with recombinant Lactococcus lactis expressing the 44-kDa gingipain adhesion/hemagglutinin domain (Hgp44). Part of the Hgp44 sequence encoding the first 314 amino acid residues, residues 188-251, and residues 354-393 was amplified and inserted into shuttle plasmid pSGANC332, with the resulting chimeric plasmids designated as pISTY210, pCOL, and pSHGRP44A, respectively. After confirming the clone sequences, expression of recombinant proteins was investigated by immunoblot. The results revealed that while pISTY210 and pCOL both expressed the Hgp44 antigen on the surface of L. lactis, the level of expression was quite low. To enhance expression of the protein on the surface of the cells, cysteine residues were changed to serine residues by site-directed mutagenesis. Replacement of 3 out of 5 cysteine residues (pISTY213) significantly increased expression of the recombinant protein on the surface of the bacteria. Interestingly, replacement of the 4th cysteine residue (pISTY215) reduced antigenicity of the recombinant protein. These results indicate that expression of Hgp44 on the surface of L. lactis cells requires the replacement of several key cysteine residues, and that L. lactis expressing this antigen could be a promising candidate for immunization against P. gingivalis-induced periodontitis.
牙龈卟啉单胞菌是一种与慢性牙周炎发展相关的病原体,它有许多主要毒力因子,其中包括其表面的半胱氨酸蛋白酶牙龈蛋白酶。本研究的目的是探讨通过用表达44 kDa牙龈蛋白酶粘附/血凝素结构域(Hgp44)的重组乳酸乳球菌免疫来诱导针对牙龈卟啉单胞菌的保护性抗体的可行性。扩增Hgp44序列中编码前314个氨基酸残基、第188 - 251个残基和第354 - 393个残基的部分,并将其插入穿梭质粒pSGANC332,所得嵌合质粒分别命名为pISTY210、pCOL和pSHGRP44A。确认克隆序列后,通过免疫印迹研究重组蛋白的表达。结果显示,虽然pISTY210和pCOL都在乳酸乳球菌表面表达了Hgp44抗原,但表达水平相当低。为了增强该蛋白在细胞表面的表达,通过定点诱变将半胱氨酸残基变为丝氨酸残基。5个半胱氨酸残基中的3个被替换(pISTY213)显著增加了重组蛋白在细菌表面的表达。有趣的是,第4个半胱氨酸残基的替换(pISTY215)降低了重组蛋白的抗原性。这些结果表明,Hgp44在乳酸乳球菌细胞表面的表达需要替换几个关键的半胱氨酸残基,并且表达该抗原的乳酸乳球菌可能是针对牙龈卟啉单胞菌诱导的牙周炎进行免疫的有前途的候选物。