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Dog vaccination with EgM proteins against Echinococcus granulosus

文献类型: 外文期刊

作者: Zhang, Zhuang-Zhi 1 ; Guo, Gang 2 ; Li, Jun 2 ; Shi, Bao-Xin 1 ; Zhao, Li 1 ; Guo, Bao-Ping 2 ; Zhang, Xu 1 ; Wang, Jun-W 1 ;

作者机构: 1.Xinjiang Acad Anim Sci, Xinjiang Vet Res Inst, 726 Dongrong St, Urumqi 830011, Xinjiang, Peoples R China

2.Xinjiang Med Univ, State Key Lab Pathogenesis Prevent & Treatment Hi, Inst Clin Med, Affiliated Hosp 1, Urumqi 830054, Xinjiang, Peoples R China

3.Xinjiang Med Univ, State Key Lab Pathogenesis Prevent &

关键词: Echinococcus granulosus; EgM proteins; Dog vaccine; Adjuvant

期刊名称:INFECTIOUS DISEASES OF POVERTY ( 影响因子:4.52; 五年影响因子:4.307 )

ISSN: 2095-5162

年卷期: 2018 年 7 卷

页码:

收录情况: SCI

摘要: Background: Dogs play a pivotal role in the transmission of cystic echinococcosis (CE), a zoonosis caused by the tapeworm Echinococcus granulosus. We showed previously that dogs vaccinated with two E granulosus adult-worm specific proteins, EgM9 and EgM123, emulsified with Freund's adjuvants induced significant protective efficacy in terms of reduction in worm burden and egg production after 45 days post-infection. It was not known whether this protection can be sustained using adjuvants suitable for use in dogs. Methods: Recombinant EgM9 and EgM123 were mixed with Quil A or ISCOMs for vaccinating dogs. After three vaccine injections, all the dogs were orally challenge-infected with 200 000 protoscoleces of E granulosus. After 45 days of infection, all the dogs were euthanized and necropsied for collecting and counting E. granulosus worms. Immunoglobins, including the IgG subclasses IgG1 and IgG2, were detected in the sera of vaccinated dogs by ELISA. To determine whether the protection efficacy could be maintained after 45 days post-infection, we implemented a longevity trial to count eggs in dog faeces for 170 days after infection. Results: The dogs vaccinated with EgM9 and EgM123 mixed with Quil A and ISCOMs showed similar protective efficacy as the proteins emulsified with Freund's adjuvants in our previous study in terms of reduction of worms and eggs at 45 days post-infection. The longevity trial showed that EgM9 protein-vaccinated group released lower number of eggs per gram compared with the egg counts in the control dogs during the dog trial study. Conclusion: EgM9 and EgM123 are thus suitable vaccine candidates against E granulosus infection in dogs.

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