Enhancement of protective efficacy of recombinant attenuated Salmonella typhimurium delivering H9N2 avian influenza virus hemagglutinins(HA) antigen vaccine candidate strains by C-C motif chemokine ligand 5 in chickens(chCCL5)

IF 2.4 2区 农林科学 Q3 MICROBIOLOGY Veterinary microbiology Pub Date : 2024-10-09 DOI:10.1016/j.vetmic.2024.110264
Jingwen Ma , Shunshun Xu , Zewei Li , Yu-An Li , Shifeng Wang , Huoying Shi
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Abstract

The H9N2 inactivated avian influenza vaccine cannot induce cellular and mucosal immune responses, while the attenuated Salmonella vector as an intracellular bacterium can induce dominant cellular and mucosal immune responses. However, it provides low protection against the virus when delivering viral antigens and needs further optimization. Chicken C-C motif chemokine ligand 5 (chCCL5) is an important CC chemokine associated with immune cell chemotaxis, migration, and viral infection. This study connected the sequence of chCCL5 (CCL5) with the hemagglutinin sequence of the H9N2 avian influenza virus (yH9HA), utilizing the attenuated Salmonella typhimurium vector containing the delayed lysis system MazE/F regulated by arabinose as a carrier. A vaccine strain of recombinant attenuated Salmonella typhimurium and H9N2 avian influenza virus HA, rSC0130 (pS0017-yH9HA-CCL5), was successfully constructed. The experimental results indicate that yH9HA-CCL5 can be expressed in 293 T cells; compared to the strain without CCL5, rSC0130 (pS0017-yH9HA-CCL5) can induce significantly increased cellular immune responses and provide better protective effects in H9N2 virus challenge experiments. The above results indicate that chCCL5 can significantly enhance the protective effect of Salmonella delivering H9N2 avian influenza virus HA protein vaccine against H9N2 avian influenza virus infection, providing valuable theoretical support for further improving the protective efficiency of recombinant attenuated Salmonella vectors for delivering viral antigens.
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C-C motif趋化因子配体5(chCCL5)增强重组减毒鼠伤寒沙门氏菌输送H9N2禽流感病毒血凝素(HA)抗原候选株疫苗对鸡的保护效力
H9N2 灭活禽流感疫苗不能诱导细胞和粘膜免疫反应,而作为细胞内细菌的减毒沙门氏菌载体可诱导细胞和粘膜免疫反应。然而,在传递病毒抗原时,它对病毒的保护能力较低,需要进一步优化。鸡 C-C motif 趋化因子配体 5(chCCL5)是一种重要的 CC 趋化因子,与免疫细胞趋化、迁移和病毒感染有关。本研究利用含有阿拉伯糖调控的延迟裂解系统 MazE/F 的鼠伤寒沙门氏菌减毒载体作为载体,将 chCCL5(CCL5)序列与 H9N2 禽流感病毒(yH9HA)的血凝素序列连接起来。成功构建了鼠伤寒沙门氏菌和 H9N2 禽流感病毒 HA 重组减毒疫苗株 rSC0130(pS0017-yH9HA-CCL5)。实验结果表明,yH9HA-CCL5可在293个T细胞中表达;与不含CCL5的毒株相比,rSC0130(pS0017-yH9HA-CCL5)可诱导细胞免疫反应显著增强,在H9N2病毒挑战实验中具有更好的保护作用。上述结果表明,chCCL5能显著增强沙门氏菌递送H9N2禽流感病毒HA蛋白疫苗对H9N2禽流感病毒感染的保护作用,为进一步提高重组减毒沙门氏菌载体递送病毒抗原的保护效率提供了有价值的理论支持。
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来源期刊
Veterinary microbiology
Veterinary microbiology 农林科学-兽医学
CiteScore
5.90
自引率
6.10%
发文量
221
审稿时长
52 days
期刊介绍: Veterinary Microbiology is concerned with microbial (bacterial, fungal, viral) diseases of domesticated vertebrate animals (livestock, companion animals, fur-bearing animals, game, poultry, fish) that supply food, other useful products or companionship. In addition, Microbial diseases of wild animals living in captivity, or as members of the feral fauna will also be considered if the infections are of interest because of their interrelation with humans (zoonoses) and/or domestic animals. Studies of antimicrobial resistance are also included, provided that the results represent a substantial advance in knowledge. Authors are strongly encouraged to read - prior to submission - the Editorials (''Scope or cope'' and ''Scope or cope II'') published previously in the journal. The Editors reserve the right to suggest submission to another journal for those papers which they feel would be more appropriate for consideration by that journal. Original research papers of high quality and novelty on aspects of control, host response, molecular biology, pathogenesis, prevention, and treatment of microbial diseases of animals are published. Papers dealing primarily with immunology, epidemiology, molecular biology and antiviral or microbial agents will only be considered if they demonstrate a clear impact on a disease. Papers focusing solely on diagnostic techniques (such as another PCR protocol or ELISA) will not be published - focus should be on a microorganism and not on a particular technique. Papers only reporting microbial sequences, transcriptomics data, or proteomics data will not be considered unless the results represent a substantial advance in knowledge. Drug trial papers will be considered if they have general application or significance. Papers on the identification of microorganisms will also be considered, but detailed taxonomic studies do not fall within the scope of the journal. Case reports will not be published, unless they have general application or contain novel aspects. Papers of geographically limited interest, which repeat what had been established elsewhere will not be considered. The readership of the journal is global.
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