Development of an attenuated oral vaccine strain of tilapia Group B Streptococci serotype Ia by gene knockout technology

被引:6
作者
Li, Liping [1 ]
Liu, Yu [1 ]
Huang, Ting [1 ]
Liang, Wanwen [1 ]
Chen, Ming [1 ]
机构
[1] Guangxi Acad Fishery Sci, Qingshan Rd 8, Nanning 530021, Peoples R China
基金
中国国家自然科学基金;
关键词
Tilapia; Streptococcus agalactiae; Vaccine; Knock-out; Virulence; Multi-omics; SURFACE IMMUNOGENIC PROTEIN; ARGININE DEIMINASE SYSTEM; MOLECULAR CHARACTERIZATION; OREOCHROMIS-NILOTICUS; NILE TILAPIA; MYCOBACTERIUM-TUBERCULOSIS; GLUTAMINE-SYNTHETASE; RED TILAPIA; AGALACTIAE; FISH;
D O I
10.1016/j.fsi.2019.07.081
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Our previous studies demonstrated that the deletion of D2 fragment in tilapia Streptococcus agalactiae(GBS) attenuated strain YM001 is the main reason for the loss of virulence to tilapia. In this study, a Delta 2 mutant that deletion of D2 fragment in parental virulent strain HN016 was constructed, and the safety, stability, immunogenicity, and growth characteristics, as well as the virulence mechanism of Delta 2 mutant were evaluated. The results showed that Delta 2 mutant was not pathogenic to tilapia, and the virulent revertants were not observed after 50 generations of passage. The RPS reached 96.11% at 15 days and 93.05% at 30 days, respectively, after intraperitoneal injection, while RPS reached 74.80% at 15 days and 53.16% at 30 days, respectively, after oral immunization. The growth of Delta 2 mutant was significantly faster than YM001, and genes that were enriched in the nitrogen metabolism and arginine biosynthesis signaling pathway (arc, glnA, and gdhA) were identified as important candidate genes responsible for growth rate of S. agalactiae. The absence of D2 fragment affected the expression of Sip, therefore influencing the bacterial virulence. Altogether, this study demonstrated that deletion of D2 fragment in HN016 causes the loss of virulence to tilapia, and Delta 2 mutant is a promising, better attenuated oral vaccine strain of S. agalactiae compared to YM001.
引用
收藏
页码:924 / 933
页数:10
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