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Edwardsiella tarda DnaK: Expression, activity, and the basis for the construction of a bivalent live vaccine against E. tarda and Streptococcus iniae
Hu, Yong-hua1; Dang, Wei1,2,3; Deng, Tian1; Sun, Li1; Sun, L (reprint author), Chinese Acad Sci, Inst Oceanol, Key Lab Expt Marine Biol, 7 Nanhai Rd, Qingdao 266071, Peoples R China.
2012-04-01
发表期刊FISH & SHELLFISH IMMUNOLOGY
ISSN1050-4648
卷号32期号:4页码:616-620
文章类型Article
摘要Edwardsiella tarda and Streptococcus iniae are important aquaculture pathogens that affect many species of farmed fish. In this study, we analyzed the expression, activity, and immunoprotective potential of E. tarda heat shock protein DnaK. We found that dnaK expression was upregulated under conditions of heat shock, oxidative stress, and infection of host cells. Recombinant DnaK (rDnaK) purified from Escherichia coli exhibited ATPase activity and induced protection in Japanese flounder (Paralichthys olivaceus) against lethal E. tarda challenge. On the basis of these results and our previous observation that a protective S. iniae antigen Sia10 which, when expressed heterogeneously in E. coli DH5 alpha, is secreted into the extracellular milieu, we constructed a chimeric antigen by fusing DnaK to Sia10. The resulting fusion protein Sia10-DnaK was expressed in DH5 alpha via the plasmid pTDK. Western blot analysis indicated that Sia10-DnaK was detected in the culture supernatant of DH5 alpha/pTDK. When flounder were vaccinated with live DH5 alpha/pTDK, strong protection was observed against both E. tarda and S. iniae. ELISA analysis detected specific serum antibody production in fish vaccinated with rDnaK and DH5 alpha/pTDK. Taken together, these results indicate that rDnaK is an intrinsic ATPase with immunoprotective property and that Sia10-DnaK delivered by a live bacterial host is an effective bivalent vaccine candidate against E. tarda and S. iniae infection. (C) 2012 Elsevier Ltd. All rights reserved.
关键词Dnak Edwardsiella Tarda Streptococcus Iniae Vaccine
学科领域Fisheries ; Immunology ; Marine & Freshwater Biology ; Veterinary Sciences
DOI10.1016/j.fsi.2012.01.011
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收录类别SCI
语种英语
WOS记录号WOS:000301827100014
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被引频次:7[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.qdio.ac.cn/handle/337002/12314
专题实验海洋生物学重点实验室
通讯作者Sun, L (reprint author), Chinese Acad Sci, Inst Oceanol, Key Lab Expt Marine Biol, 7 Nanhai Rd, Qingdao 266071, Peoples R China.
作者单位1.Chinese Acad Sci, Inst Oceanol, Key Lab Expt Marine Biol, Qingdao 266071, Peoples R China
2.Hangzhou Normal Univ, Coll Life & Environm Sci, Hangzhou Key Lab Anim Adaptat & Evolut, Hangzhou 310036, Zhejiang, Peoples R China
3.Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
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Hu, Yong-hua,Dang, Wei,Deng, Tian,et al. Edwardsiella tarda DnaK: Expression, activity, and the basis for the construction of a bivalent live vaccine against E. tarda and Streptococcus iniae[J]. FISH & SHELLFISH IMMUNOLOGY,2012,32(4):616-620.
APA Hu, Yong-hua,Dang, Wei,Deng, Tian,Sun, Li,&Sun, L .(2012).Edwardsiella tarda DnaK: Expression, activity, and the basis for the construction of a bivalent live vaccine against E. tarda and Streptococcus iniae.FISH & SHELLFISH IMMUNOLOGY,32(4),616-620.
MLA Hu, Yong-hua,et al."Edwardsiella tarda DnaK: Expression, activity, and the basis for the construction of a bivalent live vaccine against E. tarda and Streptococcus iniae".FISH & SHELLFISH IMMUNOLOGY 32.4(2012):616-620.
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