Comparison of antagonistic ability against enteropathogens by G+ and G- anaerobic dominant components of human fecal microbiota
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
16821725
DOI
10.1007/bf02932170
Knihovny.cz E-resources
- MeSH
- Anti-Bacterial Agents biosynthesis MeSH
- Bacteriological Techniques methods MeSH
- Adult MeSH
- Ecosystem MeSH
- Feces microbiology MeSH
- Gram-Negative Anaerobic Bacteria isolation & purification metabolism MeSH
- Growth Inhibitors biosynthesis isolation & purification MeSH
- Humans MeSH
- Salmonella typhimurium growth & development MeSH
- Shigella sonnei growth & development MeSH
- Intestines microbiology MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Anti-Bacterial Agents MeSH
- Growth Inhibitors MeSH
To confirm if anaerobic G+-components are those responsible for the function of colonization resistance, obligate anaerobic G+- and G- -bacteria from normal dominant microbiota of human feces were isolated from three successive collections and then used in in vitro assays for antagonism against two enteropathogenic bacteria. The production of inhibitory diffusible compounds was determined on supplemented BHI agar and MRS agar media for G- - and G+-bacteria, respectively. Salmonella enterica subsp. enterica serovar Typhimurium and Shigella sonnei were used as indicators. G+-bacteria presented a higher overall antagonistic frequency against both pathogenic bacteria (57 and 64 % for S. enterica serovar Typhimurium and S. sonnei, respectively) when compared to G+-microorganisms but with a quite elevated variation between volunteers (0-100 %) and collection samples (40-72 and 40-80 % for S. enterica sv. Typhimurium and S. sonnei, respectively). On the other hand, only three among 143 G- -isolates tested showed antagonistic activity. The results showed that, at least in vitro, obligate anaerobic G+-components of the dominant human fecal microbiota present a higher potential for antagonism against the enteropathogenic models tested than do G- -bacteria.
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Appl Environ Microbiol. 1999 Sep;65(9):4264-7 PubMed
J Clin Microbiol. 1978 May;7(5):448-53 PubMed
Infection. 1983;11 Suppl 2:S90-2 PubMed
Appl Environ Microbiol. 1996 Dec;62(12):4608-13 PubMed
Curr Opin Crit Care. 2002 Apr;8(2):139-44 PubMed
Res Microbiol. 1998 Sep;149(8):585-94 PubMed
J Med Microbiol. 2001 Feb;50(2):161-164 PubMed
FEMS Microbiol Rev. 2004 Oct;28(4):405-40 PubMed
Appl Environ Microbiol. 1993 Sep;59(9):2876-83 PubMed
Folia Microbiol (Praha). 2001;46(6):573-6 PubMed
Trends Microbiol. 1996 Nov;4(11):430-5 PubMed
Annu Rev Nutr. 2002;22:107-38 PubMed
Infect Immun. 1981 Dec;34(3):957-69 PubMed
Int J Antimicrob Agents. 2003 Apr;21(4):340-6 PubMed
J Exp Med. 1956 Sep 1;104(3):411-8 PubMed
Res Microbiol. 1994 Jan;145(1):9-16 PubMed
Gut. 2000 Nov;47(5):646-52 PubMed
FEMS Immunol Med Microbiol. 1993 Mar;6(2-3):235-40 PubMed
Appl Environ Microbiol. 1998 Oct;64(10):3854-9 PubMed
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