| pubmed-article:9212421 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9212421 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:9212421 | lifeskim:mentions | umls-concept:C0022939 | lld:lifeskim |
| pubmed-article:9212421 | lifeskim:mentions | umls-concept:C0439861 | lld:lifeskim |
| pubmed-article:9212421 | lifeskim:mentions | umls-concept:C0080194 | lld:lifeskim |
| pubmed-article:9212421 | lifeskim:mentions | umls-concept:C0279516 | lld:lifeskim |
| pubmed-article:9212421 | lifeskim:mentions | umls-concept:C0205177 | lld:lifeskim |
| pubmed-article:9212421 | lifeskim:mentions | umls-concept:C1533691 | lld:lifeskim |
| pubmed-article:9212421 | lifeskim:mentions | umls-concept:C1515655 | lld:lifeskim |
| pubmed-article:9212421 | pubmed:issue | 7 | lld:pubmed |
| pubmed-article:9212421 | pubmed:dateCreated | 1997-8-12 | lld:pubmed |
| pubmed-article:9212421 | pubmed:abstractText | The adhering human Lactobacillus acidophilus strain LA1 inhibits the cell association and cell invasion of enteropathogens in cultured human intestinal Caco-2 cells (M. F. Bernet, D. Brassard, J. R. Neeser, and A. L. Servin, Gut 35:483-489, 1994). Here, we demonstrate that strain LA1 developed its antibacterial activity in conventional or germ-free mouse models orally infected by Salmonella typhimurium. We present evidence that the spent culture supernatant of strain LA1 (LA1-SCS) contained antibacterial components active against S. typhimurium infecting the cultured human intestinal Caco-2 cells. The LA1-SCS antibacterial activity was observed in vitro against a wide range of gram-negative and gram-positive pathogens, such as Staphylococcus aureus, Listeria monocytogenes, S. typhimurium, Shigella flexneri, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Enterobacter cloacae. By contrast, no activity was observed against species of the normal gut flora, such as lactobacilli and bifidobacteria. The LA1-SCS antibacterial activity was insensitive to proteases and independent of lactic acid production. | lld:pubmed |
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| pubmed-article:9212421 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9212421 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9212421 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:9212421 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:9212421 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9212421 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:9212421 | pubmed:issn | 0099-2240 | lld:pubmed |
| pubmed-article:9212421 | pubmed:author | pubmed-author:HudaultSS | lld:pubmed |
| pubmed-article:9212421 | pubmed:author | pubmed-author:ServinA LAL | lld:pubmed |
| pubmed-article:9212421 | pubmed:author | pubmed-author:NeeserJ RJR | lld:pubmed |
| pubmed-article:9212421 | pubmed:author | pubmed-author:BrassartDD | lld:pubmed |
| pubmed-article:9212421 | pubmed:author | pubmed-author:Bernet-Camard... | lld:pubmed |
| pubmed-article:9212421 | pubmed:author | pubmed-author:LiévinVV | lld:pubmed |
| pubmed-article:9212421 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9212421 | pubmed:volume | 63 | lld:pubmed |
| pubmed-article:9212421 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9212421 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9212421 | pubmed:pagination | 2747-53 | lld:pubmed |
| pubmed-article:9212421 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:9212421 | pubmed:meshHeading | pubmed-meshheading:9212421-... | lld:pubmed |
| pubmed-article:9212421 | pubmed:meshHeading | pubmed-meshheading:9212421-... | lld:pubmed |
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| pubmed-article:9212421 | pubmed:meshHeading | pubmed-meshheading:9212421-... | lld:pubmed |
| pubmed-article:9212421 | pubmed:year | 1997 | lld:pubmed |
| pubmed-article:9212421 | pubmed:articleTitle | The human Lactobacillus acidophilus strain LA1 secretes a nonbacteriocin antibacterial substance(s) active in vitro and in vivo. | lld:pubmed |
| pubmed-article:9212421 | pubmed:affiliation | CJF 94.07 INSERM, UFR de Pharmacie, Université Paris XI, F-92296 Châtenay-Malabry, France. | lld:pubmed |
| pubmed-article:9212421 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9212421 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
