Identification and evaluation of an outer membrane protein OmpU from a pathogenic Vibrio harveyi isolate as vaccine candidate in turbot (Scophthalmus maximus)
被引:37
作者:
Wang, Q.
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机构:
Ocean Univ China, Dept Marine Biol, Coll Marine Life Sci, Qingdao 266003, Peoples R ChinaOcean Univ China, Dept Marine Biol, Coll Marine Life Sci, Qingdao 266003, Peoples R China
Wang, Q.
[1
]
Chen, J.
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机构:
Ocean Univ China, Dept Marine Biol, Coll Marine Life Sci, Qingdao 266003, Peoples R ChinaOcean Univ China, Dept Marine Biol, Coll Marine Life Sci, Qingdao 266003, Peoples R China
Chen, J.
[1
]
Liu, R.
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机构:
Ocean Univ China, Dept Marine Biol, Coll Marine Life Sci, Qingdao 266003, Peoples R ChinaOcean Univ China, Dept Marine Biol, Coll Marine Life Sci, Qingdao 266003, Peoples R China
Liu, R.
[1
]
Jia, J.
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机构:
Shandong Entry Exit Inspect & Quarantine Bur, Qingdao, Peoples R ChinaOcean Univ China, Dept Marine Biol, Coll Marine Life Sci, Qingdao 266003, Peoples R China
Jia, J.
[2
]
机构:
[1] Ocean Univ China, Dept Marine Biol, Coll Marine Life Sci, Qingdao 266003, Peoples R China
[2] Shandong Entry Exit Inspect & Quarantine Bur, Qingdao, Peoples R China
Aims: The main aims of this study were to clone and express a new outer membrane protein U (OmpU) from a pathogenic Vibrio harveyi SF-1 and investigate its immune efficiency as a vaccine candidate against V. harveyi infection in turbot (Scophthalmus maximus). Methods and Results: In this study, a new gene, ompU was cloned from the genomic DNA of pathogenic V. harveyi SF-1. The ompU gene encoded a 35 kDa protein, which was purified by Ni-NTA His-Bind Resin column. A DNA vaccine was constructed by inserting ompU gene into pEGFP-N1 plasmid. Turbot were injected intramuscularly with the purified OmpU protein and the recombinant pEGFP-N1/ompU plasmid, respectively. The fish vaccinated with the purified OmpU protein were completely protected with a relative per cent of survival (RPS) of 100% against pathogenic V. harveyi infection. Efficient protection was also found in the pEGFP-N1/ompU vaccinated group, with a RPS of 51.4%. Significant specific antibody responses were detected in the vaccinated turbot by indirect enzyme-linked immunosorbent assay. Conclusions: A new OmpU was cloned and expressed. Both OmpU protein vaccine and DNA vaccine showed good immune protections in turbot. Significance and Impact of the Study: The OmpU was identified to be a new effective vaccine candidate and could be used as subunit vaccine and DNA vaccine for disease control caused by pathogenic V. harveyi.