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Isolation and Proteomic Analysis of Extracellular Vesicles from Lactobacillus salivarius SNK-6.
Huang, Jiwen; Zhao, Ayong; He, Daqian; Wu, Xiao; Yan, Huaxiang; Zhu, Lihui.
Afiliação
  • Huang J; College of Animal Science and Technology, Zhejiang Agriculture and Forestry University, Hangzhou 311300, P.R. China.
  • Zhao A; Institute of Animal Husbandry and Veterinary Science, Shanghai Academy of Agricultural Sciences, Shanghai 201106, P.R. China.
  • He D; College of Animal Science and Technology, Zhejiang Agriculture and Forestry University, Hangzhou 311300, P.R. China.
  • Wu X; Institute of Animal Husbandry and Veterinary Science, Shanghai Academy of Agricultural Sciences, Shanghai 201106, P.R. China.
  • Yan H; Key Laboratory of Agricultural Genetics and Breeding, Biotechnology Research Institute, Shanghai Academy of Agricultural Sciences, Shanghai 201106, P.R. China.
  • Zhu L; Institute of Animal Husbandry and Veterinary Science, Shanghai Academy of Agricultural Sciences, Shanghai 201106, P.R. China.
J Microbiol Biotechnol ; 34(1): 224-231, 2024 Jan 28.
Article em En | MEDLINE | ID: mdl-38282412
ABSTRACT
The proteins carried by the extracellular vesicles of Lactobacillus salivarius SNK-6 (LsEVs) were identified to provide a foundation for further explorations of the probiotic activities of L. salivarius SNK-6. LsEVs were isolated from the culture media of L. salivarius SNK-6 and morphological analysis was conducted by scanning electron microscopy. Subsequent transmission electron microscopy and nanoparticle tracking analysis were performed to assess the morphology and particle size of the LsEVs. In addition, the protein composition of LsEVs was analyzed using silver staining and protein mass spectrometry. Finally, internalization of the identified LsEVs was confirmed using a confocal microscope, and enzyme-linked immunosorbent assay was employed to analyze the levels of inflammatory cytokines in LPS-challenged RAW264.7 cells. The results revealed that the membrane-enclosed LsEVs were spherical, with diameters ranging from 100-250 nm. The LsEVs with diameters of 111-256 nm contained the greatest amount of cargo. In total, 320 proteins (10-38 kD) were identified in the LsEVs and included anti-inflammatory molecules, such as PrtP proteinase, co-chaperones, and elongation factor Tu, as well as some proteins involved in glycolysis/gluconeogenesis, such as fructose-1,6-bisphosphate aldolase. Enrichment analysis showed these proteins to be related to the terms "metabolic pathway," "ribosome," "glycolysis/gluconeogenesis," "carbohydrate metabolism," and "amino acid metabolism." Furthermore, the LsEVs were internalized by host liver cells and can regulate inflammation. These findings confirm that LsEVs contain various functional proteins that play important roles in energy metabolism, signal transduction, and biosynthesis.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vesículas Extracelulares / Ligilactobacillus salivarius Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vesículas Extracelulares / Ligilactobacillus salivarius Idioma: En Ano de publicação: 2024 Tipo de documento: Article