利用生物表面活性剂生成化脓性链球菌的空细胞包膜

IF 3.4 Q2 PHARMACOLOGY & PHARMACY
Amany Abdelfattah, Heba M. Amin, Sameh Rabea, Reham Samir
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引用次数: 0

摘要

背景细菌鬼细胞(BGCs)是没有细胞质和基因内容物的细胞包膜,可用于多种用途,包括作为候选疫苗的巨大潜力以及作为药物和蛋白质递送系统的有效性。据我们所知,这是首次通过用 Tween80(TW80)或 TritonX-100 (TX100)处理化脓性链球菌(S. pyogenes)ATCC 19615 来生产革兰氏阳性 BGCs 的研究,随后在 NIH/Ola-Hsd 小鼠中对其抗原性和安全性进行了初步测试。在光学显微镜下可以看到完整的细胞,再培养时也没有生长迹象,从而确认了所生产的 BGCs。使用扫描电子显微镜可观察到跨膜隧道,随后在 BGCs 的培养上清液中检测到大量释放的 DNA 和蛋白质。通过三次鼻内免疫剂量和感染测试了所生产的 BGCs 的抗原性。结果与阳性对照组 "未免疫 ATCC 19615 的小鼠 "相比,免疫小鼠血清中的抗原性(TW80 产生的 BGC = 68%,TX100 产生的 BGC = 75%)和 IgG 水平(TW80 产生的 BGC = 增加了三倍,TX100 产生的 BGC = 增加了四倍)均有显著提高。组织病理学分析表明,与 TX100 相比,TW80 产生的 BGC 相对更安全,影响也更小。然而,还需要进一步的临床前研究来确认其有效性并确保其完全安全性,特别是在没有自身免疫和与人体心脏组织中肌球蛋白的抗体交叉反应方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Generation of empty cell envelopes of Streptococcus pyogenes using biosurfactants

Background

Bacterial ghost cells (BGCs) are cell envelopes that devoid of cytoplasmic and genetic contents in purpose of variable applications, including their great potential as vaccine candidates and their effectiveness as delivery systems for drugs and proteins. To our knowledge, this is the first study to produce Gram-positive BGCs by treating Streptococcus pyogenes (S. pyogenes) ATCC 19615 with Tween80 (TW80) or TritonX-100 (TX100), followed by preliminary testing of their antigenicity and safety in NIH/Ola-Hsd mice. The produced BGCs were confirmed by the presence of intact cells under a light microscope, the absence of growth signs upon re-cultivation. The transmembrane tunnels were visualized using a scanning electron microscope, and subsequently, considerable quantities of released DNA and protein were detected in the culture supernatant of the BGCs. The antigenicity of the produced BGCs was tested through three intra-nasal immunization doses followed by infection. Afterward, the opsonic activity and the IgG levels were measured, followed by a comprehensive histopathological examination for selected tissues and organs.

Results

The sera of immunized mice exhibited a significant rise in both opsonic activity (TW80 produced BGC = 68% and TX100 produced BGC = 75%) and IgG levels (TW80 produced BGC = a threefold increase and TX100 produced BGC = a fourfold increase) when compared to the positive control group "non-immunized challenged with ATCC 19615." Histopathological analysis revealed that the BGCs produced by TW80 are relatively safer and have a less severe impact than those produced by TX100.

Conclusion

The study's findings suggest that Sp-BGC/TW80 is initially effective and safe in vivo. However, further pre-clinical studies are necessary to confirm its effectiveness and ensure complete safety, specifically in terms of the absence of autoimmunity and antibody cross-reactivity with myosin proteins in human cardiac tissues.

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来源期刊
自引率
0.00%
发文量
44
审稿时长
23 weeks
期刊介绍: Future Journal of Pharmaceutical Sciences (FJPS) is the official journal of the Future University in Egypt. It is a peer-reviewed, open access journal which publishes original research articles, review articles and case studies on all aspects of pharmaceutical sciences and technologies, pharmacy practice and related clinical aspects, and pharmacy education. The journal publishes articles covering developments in drug absorption and metabolism, pharmacokinetics and dynamics, drug delivery systems, drug targeting and nano-technology. It also covers development of new systems, methods and techniques in pharmacy education and practice. The scope of the journal also extends to cover advancements in toxicology, cell and molecular biology, biomedical research, clinical and pharmaceutical microbiology, pharmaceutical biotechnology, medicinal chemistry, phytochemistry and nutraceuticals.
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