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亚种HN019活益生菌和后生元:潜在治疗特性的生产策略及生物活性评估

subsp. HN019 live probiotics and postbiotics: production strategies and bioactivity evaluation for potential therapeutic properties.

作者信息

D'ambrosio Sergio, Dabous Azza, Sadiq Saba, Casillo Angela, Schiraldi Chiara, Cassese Elisabetta, Bedini Emiliano, Corsaro Maria Michela, Cimini Donatella

机构信息

Department of Environmental, Biological and Pharmaceutical Sciences and Technologies, University of Campania Luigi Vanvitelli, Caserta, Italy.

Department of Experimental Medicine, University of Campania "L.Vanvitelli", Naples, Italy.

出版信息

Front Bioeng Biotechnol. 2024 Jul 9;12:1379574. doi: 10.3389/fbioe.2024.1379574. eCollection 2024.

Abstract

subsp. HN019 is a commercially available well-characterized probiotic with documented effects on human health, such as the ability to enhance the immune function and to balance the intestinal microbiome. Therefore, optimizing the manufacturing process to improve sustainability, increasing biomass yields and viability, and avoiding animal -derived nutrients in the medium to meet vegan consumer's needs, is currently of interest. Besides the established use of live probiotic cells, alternative supplements indicated as postbiotics, like non-viable cells and/or probiotics derived bioactive molecules might be considered as potential next generation biotherapeutics. In fact, advantages of postbiotics include fewer technological limitations, such as easier production processes and scale-up, and even higher specificity. In this work, medium design together with different fermentation strategies such as batch, fed-batch and in situ product removal on lab-scale bioreactors were combined. Medium pretreatment by ultrafiltration and protease digestion was performed to reduce polysaccharidic contaminants and facilitate the purification of secreted exopolysaccharides (EPS). The latter were isolated from the fermentation broth and characterized through NMR, GC-MS and SEC-TDA analyses. The expression of TLR-4, NF-kb and IL-6 in LPS challenged differentiated CaCo-2 cells treated with EPS, live and heat-killed cells/broth, was evaluated by western blotting and ELISA. Zonulin was also assessed by immunofluorescence assays. The titer of viable HN019 was increased up to 2.9 ± 0.1 x 10 on an animal-free semidefined medium by applying an ISPR fermentation strategy. Medium pre-treatment and a simple downstream procedure enriched the representativity of the EPS recovered (87%), the composition of which revealed the presence of mannuronic acid among other sugars typically present in polysaccharides produced by bifidobacteria. The isolated EPS, live cells and whole heat inactivated broth were compared for the first up to date for their immunomodulatory and anti-inflammatory properties and for their ability to promote intestinal barrier integrity. Interestingly, EPS and live cells samples demonstrated immune-stimulating properties by downregulating the expression of TLR-4 and NF-kb, and the ability to promote restoring the integrity of the intestinal barrier by up-regulating the expression of zonulin, one of the tight junctions forming proteins. Postbiotics in the form of heat killed broth only reduced NF-kb expression, whereas they did not seem effective in the other tested conditions.

摘要

亚种HN019是一种市面上可买到的、特性明确的益生菌,对人体健康有诸多已被证实的作用,比如增强免疫功能和平衡肠道微生物群的能力。因此,目前人们感兴趣的是优化生产工艺以提高可持续性、提高生物量产量和活力,并避免培养基中使用动物源性营养成分以满足纯素消费者的需求。除了已确立的活益生菌细胞的用途外,作为后生元的替代补充剂,如无活力细胞和/或源自益生菌的生物活性分子,可能被视为潜在的下一代生物治疗剂。事实上,后生元的优势包括技术限制较少,如生产过程和扩大规模更容易,以及特异性更高。在这项工作中,将培养基设计与不同的发酵策略(如分批发酵、补料分批发酵和实验室规模生物反应器中的原位产物去除)相结合。通过超滤和蛋白酶消化进行培养基预处理,以减少多糖污染物并促进分泌型胞外多糖(EPS)的纯化。从发酵液中分离出后者,并通过核磁共振、气相色谱-质谱联用和尺寸排阻色谱-多角度光散射分析进行表征。通过蛋白质印迹法和酶联免疫吸附测定法评估了用EPS、活细胞和热灭活细胞/肉汤处理的脂多糖刺激的分化Caco-2细胞中TLR-4、NF-κB和IL-6的表达。还通过免疫荧光测定法评估了闭合蛋白。通过应用原位产物去除发酵策略,在无动物来源的半限定培养基上,HN019的活菌滴度提高到了2.9±0.1×10。培养基预处理和简单的下游程序提高了回收的EPS的代表性(87%),其组成显示除了双歧杆菌产生的多糖中通常存在的其他糖类外,还存在甘露糖醛酸。首次对分离出的EPS、活细胞和全热灭活肉汤的免疫调节和抗炎特性以及促进肠道屏障完整性的能力进行了比较。有趣的是,EPS和活细胞样本通过下调TLR-4和NF-κB的表达表现出免疫刺激特性,并通过上调闭合蛋白(一种形成紧密连接的蛋白质)的表达来促进恢复肠道屏障的完整性。热灭活肉汤形式的后生元仅降低了NF-κB的表达,而在其他测试条件下似乎没有效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6886/11270027/8a7498702ca7/fbioe-12-1379574-g001.jpg

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