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纳米结构脂质载体包裹的益生菌无细胞上清液的代谢组学分析及其对犬多药耐药菌的抗菌效果

Metabolomic profiling and antibacterial efficacy of probiotic-derived cell-free supernatant encapsulated in nanostructured lipid carriers against canine multidrug-resistant bacteria.

作者信息

Myo Nay Zin, Kamwa Ratchnida, Jamnong Thitirat, Swasdipisal Busaba, Somrak Papavarin, Rattanamalakorn Phanchompoo, Neatsawang Vipada, Apiwatsiri Prasert, Yata Teerapong, Hampson David J, Prapasarakul Nuvee

机构信息

Department of Veterinary Microbiology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.

The International Graduate Course of Veterinary Science and Technology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.

出版信息

Front Vet Sci. 2025 Jan 3;11:1525897. doi: 10.3389/fvets.2024.1525897. eCollection 2024.

Abstract

AIM

This study aimed to investigate the antibacterial efficacy of probiotic-derived cell-free supernatants (CFS) encapsulated within nanostructured lipid carriers (NLCs) against multidrug-resistant and . Additionally, it aimed to identify specific bioactive compounds that contribute to the reported antibacterial properties by characterizing the metabolite substances present in the CFS using a metabolomic analysis technique.

METHODS

Eight strains of lactic acid bacteria including (L22F and L25F), (P72N, BF9, BF 14, BYF 20 and BYF 26) and (BF 12) were selected as probiotic candidates. The inhibitory activity of their cell free supernatant (CFS) was tested against clinical strains of and isolated from skin wounds of dogs and cats. An untargeted metabolomic approach based on liquid chromatography-mass spectrometry (LC-MS) identified potential antibacterial metabolites in the CFS. Cell-Free Supernatants-Nanostructured Lipid Carriers (CFS-NLCs) were developed, and their antibacterial activity and minimum bactericidal concentration (MBC) were analysed.

RESULTS

Despite the strong multidrug-resistant nature of the pathogens, CFS displayed a moderate antibacterial activity against most tested strains. The acidic nature of the CFS, combined with bioactive antibacterial metabolites like Kanzonol V and 1-Hexanol, likely contributed to its inhibitory effects against pathogenic bacteria; notably, Kanzonol V was abundant in the CFS of L22F, BF12 and BYF26 (L22F_CFS, BF12_CFS and BYF26_CFS), while 1-Hexanol was particularly enriched in CFS of P72N (P72N_CFS), with both compounds effectively targeting bacterial cell membranes to disrupt cell integrity, leading to bacterial cell death. Other beneficial compounds such as Pyroglutamylleucine, Trigoneoside VIII and 18-Nor-4(19),8,11,13-abietatetraene which are likely to have anti-inflammatory, antimicrobial and antioxidant activities, were also detected in the CFS. The CFS-NLCs maintained their antibacterial activity and 30-60% dilutions of product completely inhibited the growth of pathogen strains even after three-months storage at room temperature.

CONCLUSION

These findings suggest that CFS-NLCs could be a promising biotic therapy for treating hospital infections such as canine dermatitis and otitis caused by multidrug-resistant and .

摘要

目的

本研究旨在调查封装在纳米结构脂质载体(NLCs)中的益生菌源无细胞上清液(CFS)对多重耐药菌的抗菌效果。此外,通过使用代谢组学分析技术对CFS中存在的代谢物进行表征,旨在确定有助于所报道抗菌特性的特定生物活性化合物。

方法

选择8株乳酸菌作为益生菌候选菌株,包括嗜酸乳杆菌(L22F和L25F)、植物乳杆菌(P72N、BF9、BF 14、BYF 20和BYF 26)和干酪乳杆菌(BF 12)。测试了它们的无细胞上清液(CFS)对从狗和猫的皮肤伤口分离的临床金黄色葡萄球菌和大肠杆菌菌株的抑制活性。基于液相色谱 - 质谱联用(LC - MS)的非靶向代谢组学方法鉴定了CFS中潜在的抗菌代谢物。制备了无细胞上清液 - 纳米结构脂质载体(CFS - NLCs),并分析了它们的抗菌活性和最低杀菌浓度(MBC)。

结果

尽管病原体具有很强的多重耐药性,但CFS对大多数测试菌株表现出中等抗菌活性。CFS的酸性性质,与如坎宗醇V和1 - 己醇等生物活性抗菌代谢物相结合,可能有助于其对病原菌的抑制作用;值得注意的是,坎宗醇V在L22F、BF12和BYF26的CFS(L22F_CFS、BF12_CFS和BYF26_CFS)中含量丰富,而1 - 己醇在P72N的CFS(P72N_CFS)中特别富集,这两种化合物均有效地靶向细菌细胞膜以破坏细胞完整性,导致细菌细胞死亡。在CFS中还检测到其他可能具有抗炎、抗菌和抗氧化活性的有益化合物,如焦谷氨酰亮氨酸、三角皂苷VIII和18 - 降 - 4(19),8,11,13 - 松香四烯。CFS - NLCs保持其抗菌活性,即使在室温下储存三个月后,产品30 - 60%的稀释液仍能完全抑制病原菌菌株的生长。

结论

这些发现表明,CFS - NLCs可能是一种有前景的生物疗法,用于治疗由多重耐药金黄色葡萄球菌和大肠杆菌引起的医院感染,如犬皮炎和中耳炎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ce1/11739306/fb6e518f546f/fvets-11-1525897-g001.jpg

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