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利用非常规酵母马克斯克鲁维酵母高效生产猪圆环病毒样颗粒。

Efficient production of porcine circovirus virus-like particles using the nonconventional yeast Kluyveromyces marxianus.

机构信息

State Key Laboratory of Genetic Engineering, School of Life Sciences, Fudan University, Shanghai, China.

Shanghai Engineering Research Center of Industrial Microorganisms, Shanghai, 200438, China.

出版信息

Appl Microbiol Biotechnol. 2019 Jan;103(2):833-842. doi: 10.1007/s00253-018-9487-2. Epub 2018 Nov 13.

Abstract

Porcine circovirus type 2 (PCV2) is a ubiquitous virus with high pathogenicity closely associated with the postweaning multisystemic wasting syndrome (PMWS) and porcine circovirus diseases (PCVDs), which caused significant economic losses in the swine industry worldwide every year. The PCV2 virus-like particles (VLPs) are a powerful subunit vaccine that can elicit high immune response due to its native PCV2 virus morphology. The baculovirus expression system is the widely used platform for producing commercial PCV2 VLP vaccines, but its yield and cost limited the development of low-cost vaccines for veterinary applications. Here, we applied a nonconventional yeast Kluyveromyces marxianus to enhance the production of PCV2 VLPs. After codon optimization, the PCV2 Cap protein was expressed in K. marxianus and assemble spontaneously into VLPs. Using a chemically defined medium, we achieved approximately 1.91 g/L of PCV2 VLP antigen in a 5-L bioreactor after high cell density fermentation for 72 h. That yield greatly exceeded to recently reported PCV2 VLPs obtained by baculovirus-insect cell, Escherichia coli and Pichia pastoris. By the means of two-step chromatography, 652.8 mg of PCV2 VLP antigen was obtained from 1 L of the recombinant K. marxianus cell culture. The PCV2 VLPs induced high level of anti-PCV2 IgG antibody in mice serums and decreased the virus titers in both livers and spleens of the challenged mice. These results illustrated that K. marxianus is a powerful yeast for cost-effective production of PCV2 VLP vaccines.

摘要

猪圆环病毒 2 型(PCV2)是一种普遍存在的高致病性病毒,与断奶后多系统衰竭综合征(PMWS)和猪圆环病毒病(PCVDs)密切相关,每年给全球养猪业造成重大经济损失。PCV2 病毒样颗粒(VLPs)是一种强大的亚单位疫苗,由于其天然的 PCV2 病毒形态,能够引起高免疫反应。杆状病毒表达系统是生产商业 PCV2 VLP 疫苗的广泛应用平台,但由于产量和成本的限制,限制了兽医应用的低成本疫苗的发展。在这里,我们应用一种非常规酵母马克斯克鲁维酵母来提高 PCV2 VLPs 的产量。经过密码子优化后,PCV2 Cap 蛋白在马克斯克鲁维酵母中表达,并自发组装成 VLPs。使用化学定义的培养基,我们在 5L 生物反应器中进行高密度发酵 72 小时后,获得了约 1.91g/L 的 PCV2 VLP 抗原。该产量大大超过了最近报道的通过杆状病毒-昆虫细胞、大肠杆菌和毕赤酵母获得的 PCV2 VLPs。通过两步层析法,从 1L 重组马克斯克鲁维酵母细胞培养物中获得了 652.8mg 的 PCV2 VLP 抗原。PCV2 VLPs 诱导小鼠血清中高水平的抗 PCV2 IgG 抗体,并降低了攻毒小鼠肝脏和脾脏中的病毒滴度。这些结果表明马克斯克鲁维酵母是一种用于生产具有成本效益的 PCV2 VLP 疫苗的强大酵母。

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