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Differential Immune-Modulating Activities of Cell Walls and Secreted Metabolites from Probiotic Bacillus coagulans JBI-YZ6.3 under Normal versus Inflamed Culture Conditions
Spore-forming probiotic bacteria, including Bacillus coagulans, are resilient and produce a variety of beneficial metabolites. We evaluated the immune-modulating effects of the novel probiotic strain Bacillus coagulans JBI-YZ6.3, where the germinated spores, metabolite fraction, and cell wall fracti...
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Published in: | Microorganisms (Basel) 2023-10, Vol.11 (10), p.2564 |
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description | Spore-forming probiotic bacteria, including Bacillus coagulans, are resilient and produce a variety of beneficial metabolites. We evaluated the immune-modulating effects of the novel probiotic strain Bacillus coagulans JBI-YZ6.3, where the germinated spores, metabolite fraction, and cell wall fraction were tested in parallel using human peripheral blood mononuclear cell cultures under both normal and lipopolysaccharide-induced inflamed culture conditions. The expression of CD25 and CD69 activation markers was evaluated via flow cytometry. Supernatants were tested for cytokines, interferons, chemokines, and growth factors using Luminex arrays. The germinated spores were highly immunogenic; both the cell wall and metabolite fractions contributed significantly. Under normal culture conditions, increased levels of immune activation were observed as increased expressions of CD25 and CD69 relative to natural killer cells, suggesting an increased ability to attack virus-infected target cells. On monocytes, a complex effect was observed, where the expression of CD25 increased under normal conditions but decreased under inflamed conditions. This, in combination with increased interleukin-10 (IL-10) and decreased monocyte chemoattractant protein-1 (MCP-1) production under inflamed conditions, points to anti-inflammatory effects. The production of the stem cell-related growth factor granulocyte colony-stimulating Factor (G-CSF) was enhanced. Further research is warranted to characterize the composition of the postbiotic metabolite fraction and document the characteristics of immunomodulating agents secreted by this probiotic strain. |
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We evaluated the immune-modulating effects of the novel probiotic strain Bacillus coagulans JBI-YZ6.3, where the germinated spores, metabolite fraction, and cell wall fraction were tested in parallel using human peripheral blood mononuclear cell cultures under both normal and lipopolysaccharide-induced inflamed culture conditions. The expression of CD25 and CD69 activation markers was evaluated via flow cytometry. Supernatants were tested for cytokines, interferons, chemokines, and growth factors using Luminex arrays. The germinated spores were highly immunogenic; both the cell wall and metabolite fractions contributed significantly. Under normal culture conditions, increased levels of immune activation were observed as increased expressions of CD25 and CD69 relative to natural killer cells, suggesting an increased ability to attack virus-infected target cells. On monocytes, a complex effect was observed, where the expression of CD25 increased under normal conditions but decreased under inflamed conditions. This, in combination with increased interleukin-10 (IL-10) and decreased monocyte chemoattractant protein-1 (MCP-1) production under inflamed conditions, points to anti-inflammatory effects. The production of the stem cell-related growth factor granulocyte colony-stimulating Factor (G-CSF) was enhanced. Further research is warranted to characterize the composition of the postbiotic metabolite fraction and document the characteristics of immunomodulating agents secreted by this probiotic strain.</description><identifier>ISSN: 2076-2607</identifier><identifier>EISSN: 2076-2607</identifier><identifier>DOI: 10.3390/microorganisms11102564</identifier><identifier>PMID: 37894222</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Amino acids ; anti-inflammatory ; Antibiotics ; Antimicrobial agents ; Bacillus coagulans ; Bacteria ; Cancer ; CD25 antigen ; CD69 antigen ; Cell culture ; Cell walls ; Chemokines ; Cloning ; Colony-stimulating factor ; Cytokines ; Drug resistance ; Enzymes ; Fatty acids ; Fermentation ; Flow cytometry ; Genes ; Gram-positive bacteria ; Granulocyte colony-stimulating factor ; granulocyte colony-stimulating factor (G-CSF) ; Growth factors ; Immune response ; Immune system ; Immunogenicity ; Immunomodulation ; Inflammation ; Interleukin 10 ; Leukocytes (granulocytic) ; Lipopolysaccharides ; Membranes ; Metabolism ; Metabolites ; Monocyte chemoattractant protein ; Monocyte chemoattractant protein 1 ; Monocytes ; natural killer (NK) cells ; Natural killer cells ; Pathogens ; Peripheral blood ; Probiotics ; Spores ; Stem cells</subject><ispartof>Microorganisms (Basel), 2023-10, Vol.11 (10), p.2564</ispartof><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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We evaluated the immune-modulating effects of the novel probiotic strain Bacillus coagulans JBI-YZ6.3, where the germinated spores, metabolite fraction, and cell wall fraction were tested in parallel using human peripheral blood mononuclear cell cultures under both normal and lipopolysaccharide-induced inflamed culture conditions. The expression of CD25 and CD69 activation markers was evaluated via flow cytometry. Supernatants were tested for cytokines, interferons, chemokines, and growth factors using Luminex arrays. The germinated spores were highly immunogenic; both the cell wall and metabolite fractions contributed significantly. Under normal culture conditions, increased levels of immune activation were observed as increased expressions of CD25 and CD69 relative to natural killer cells, suggesting an increased ability to attack virus-infected target cells. On monocytes, a complex effect was observed, where the expression of CD25 increased under normal conditions but decreased under inflamed conditions. This, in combination with increased interleukin-10 (IL-10) and decreased monocyte chemoattractant protein-1 (MCP-1) production under inflamed conditions, points to anti-inflammatory effects. The production of the stem cell-related growth factor granulocyte colony-stimulating Factor (G-CSF) was enhanced. Further research is warranted to characterize the composition of the postbiotic metabolite fraction and document the characteristics of immunomodulating agents secreted by this probiotic strain.</description><subject>Amino acids</subject><subject>anti-inflammatory</subject><subject>Antibiotics</subject><subject>Antimicrobial agents</subject><subject>Bacillus coagulans</subject><subject>Bacteria</subject><subject>Cancer</subject><subject>CD25 antigen</subject><subject>CD69 antigen</subject><subject>Cell culture</subject><subject>Cell walls</subject><subject>Chemokines</subject><subject>Cloning</subject><subject>Colony-stimulating factor</subject><subject>Cytokines</subject><subject>Drug resistance</subject><subject>Enzymes</subject><subject>Fatty acids</subject><subject>Fermentation</subject><subject>Flow cytometry</subject><subject>Genes</subject><subject>Gram-positive bacteria</subject><subject>Granulocyte colony-stimulating factor</subject><subject>granulocyte colony-stimulating factor (G-CSF)</subject><subject>Growth factors</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immunogenicity</subject><subject>Immunomodulation</subject><subject>Inflammation</subject><subject>Interleukin 10</subject><subject>Leukocytes (granulocytic)</subject><subject>Lipopolysaccharides</subject><subject>Membranes</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Monocyte chemoattractant protein</subject><subject>Monocyte chemoattractant protein 1</subject><subject>Monocytes</subject><subject>natural killer (NK) cells</subject><subject>Natural killer cells</subject><subject>Pathogens</subject><subject>Peripheral blood</subject><subject>Probiotics</subject><subject>Spores</subject><subject>Stem cells</subject><issn>2076-2607</issn><issn>2076-2607</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkttqFDEYgAdRbKl9BQl4483UHGeSK2m3aldaFVREb0Im82fNkklqMrPgO_UhTd0iVsxNQvLx5T81zVOCTxhT-MXkbU4pb0z0ZSqEEExFxx80hxT3XUs73D_863zQHJeyxXUpwqQgj5sD1kvFKaWHzc25dw4yxNmbgNbTtERor9K4BDP7uEGndvY7P3soKDm0ghDQFxNCQSaO6CPYDDOM6ApmM6Tg54q5nCb0IafBp9lbdGasD2EpyCazqdZY0Nuzdfv1W3fC0BJHyOhdylP9fAe5VG4dXTBTla6WMC8Z0CrFsUaQYnnSPHImFDi-24-az69ffVpdtJfv36xXp5et5bKbW0GYolw66YgTgksMFtgosBCWDcYSUIJjOw496bkZjHAM7Gh7poTDbFQDO2rWe--YzFZfZz-Z_FMn4_Xvi1p5bXJNLoDm0hI3SEOV5FwCKGqFGiQ3ghnC7FhdL_eu62WoWdla6WzCPen9l-i_603aaYK72jDRVcPzO0NOPxYos558sbUTJkJaiqZSMiEF47yiz_5Bt2nJsdbqlqJCya6jler2VJ2iUjK4P9EQrG8HTP9_wNgvbpfKLQ</recordid><startdate>20231015</startdate><enddate>20231015</enddate><creator>Iloba, Ifeanyi</creator><creator>McGarry, Sage V.</creator><creator>Yu, Liu</creator><creator>Cruickshank, Dina</creator><creator>Jensen, Gitte S.</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7T7</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>P64</scope><scope>PATMY</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-9179-8369</orcidid><orcidid>https://orcid.org/0000-0003-3204-2259</orcidid><orcidid>https://orcid.org/0000-0003-4382-2605</orcidid><orcidid>https://orcid.org/0000-0002-9497-1750</orcidid></search><sort><creationdate>20231015</creationdate><title>Differential Immune-Modulating Activities of Cell Walls and Secreted Metabolites from Probiotic Bacillus coagulans JBI-YZ6.3 under Normal versus Inflamed Culture Conditions</title><author>Iloba, Ifeanyi ; McGarry, Sage V. ; Yu, Liu ; Cruickshank, Dina ; Jensen, Gitte S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-5139248f8f1f55480ece3d5055c3bac1e9540cdb7174aba5f3ecdc7395f03d9b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Amino acids</topic><topic>anti-inflammatory</topic><topic>Antibiotics</topic><topic>Antimicrobial agents</topic><topic>Bacillus coagulans</topic><topic>Bacteria</topic><topic>Cancer</topic><topic>CD25 antigen</topic><topic>CD69 antigen</topic><topic>Cell culture</topic><topic>Cell walls</topic><topic>Chemokines</topic><topic>Cloning</topic><topic>Colony-stimulating factor</topic><topic>Cytokines</topic><topic>Drug resistance</topic><topic>Enzymes</topic><topic>Fatty acids</topic><topic>Fermentation</topic><topic>Flow cytometry</topic><topic>Genes</topic><topic>Gram-positive bacteria</topic><topic>Granulocyte colony-stimulating factor</topic><topic>granulocyte colony-stimulating factor (G-CSF)</topic><topic>Growth factors</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Immunogenicity</topic><topic>Immunomodulation</topic><topic>Inflammation</topic><topic>Interleukin 10</topic><topic>Leukocytes (granulocytic)</topic><topic>Lipopolysaccharides</topic><topic>Membranes</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Monocyte chemoattractant protein</topic><topic>Monocyte chemoattractant protein 1</topic><topic>Monocytes</topic><topic>natural killer (NK) cells</topic><topic>Natural killer cells</topic><topic>Pathogens</topic><topic>Peripheral blood</topic><topic>Probiotics</topic><topic>Spores</topic><topic>Stem cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iloba, Ifeanyi</creatorcontrib><creatorcontrib>McGarry, Sage V.</creatorcontrib><creatorcontrib>Yu, Liu</creatorcontrib><creatorcontrib>Cruickshank, Dina</creatorcontrib><creatorcontrib>Jensen, Gitte S.</creatorcontrib><collection>CrossRef</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Microorganisms (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iloba, Ifeanyi</au><au>McGarry, Sage V.</au><au>Yu, Liu</au><au>Cruickshank, Dina</au><au>Jensen, Gitte S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential Immune-Modulating Activities of Cell Walls and Secreted Metabolites from Probiotic Bacillus coagulans JBI-YZ6.3 under Normal versus Inflamed Culture Conditions</atitle><jtitle>Microorganisms (Basel)</jtitle><date>2023-10-15</date><risdate>2023</risdate><volume>11</volume><issue>10</issue><spage>2564</spage><pages>2564-</pages><issn>2076-2607</issn><eissn>2076-2607</eissn><abstract>Spore-forming probiotic bacteria, including Bacillus coagulans, are resilient and produce a variety of beneficial metabolites. We evaluated the immune-modulating effects of the novel probiotic strain Bacillus coagulans JBI-YZ6.3, where the germinated spores, metabolite fraction, and cell wall fraction were tested in parallel using human peripheral blood mononuclear cell cultures under both normal and lipopolysaccharide-induced inflamed culture conditions. The expression of CD25 and CD69 activation markers was evaluated via flow cytometry. Supernatants were tested for cytokines, interferons, chemokines, and growth factors using Luminex arrays. The germinated spores were highly immunogenic; both the cell wall and metabolite fractions contributed significantly. Under normal culture conditions, increased levels of immune activation were observed as increased expressions of CD25 and CD69 relative to natural killer cells, suggesting an increased ability to attack virus-infected target cells. On monocytes, a complex effect was observed, where the expression of CD25 increased under normal conditions but decreased under inflamed conditions. This, in combination with increased interleukin-10 (IL-10) and decreased monocyte chemoattractant protein-1 (MCP-1) production under inflamed conditions, points to anti-inflammatory effects. The production of the stem cell-related growth factor granulocyte colony-stimulating Factor (G-CSF) was enhanced. Further research is warranted to characterize the composition of the postbiotic metabolite fraction and document the characteristics of immunomodulating agents secreted by this probiotic strain.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>37894222</pmid><doi>10.3390/microorganisms11102564</doi><orcidid>https://orcid.org/0000-0001-9179-8369</orcidid><orcidid>https://orcid.org/0000-0003-3204-2259</orcidid><orcidid>https://orcid.org/0000-0003-4382-2605</orcidid><orcidid>https://orcid.org/0000-0002-9497-1750</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amino acids anti-inflammatory Antibiotics Antimicrobial agents Bacillus coagulans Bacteria Cancer CD25 antigen CD69 antigen Cell culture Cell walls Chemokines Cloning Colony-stimulating factor Cytokines Drug resistance Enzymes Fatty acids Fermentation Flow cytometry Genes Gram-positive bacteria Granulocyte colony-stimulating factor granulocyte colony-stimulating factor (G-CSF) Growth factors Immune response Immune system Immunogenicity Immunomodulation Inflammation Interleukin 10 Leukocytes (granulocytic) Lipopolysaccharides Membranes Metabolism Metabolites Monocyte chemoattractant protein Monocyte chemoattractant protein 1 Monocytes natural killer (NK) cells Natural killer cells Pathogens Peripheral blood Probiotics Spores Stem cells |
title | Differential Immune-Modulating Activities of Cell Walls and Secreted Metabolites from Probiotic Bacillus coagulans JBI-YZ6.3 under Normal versus Inflamed Culture Conditions |
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