Production of antibacterial substances by bifidobacterial isolates from infant stool active against Listeria monocytogenes

被引:112
作者
Touré, R
Kheadr, E
Lacroix, C
Moroni, O
Fliss, I
机构
[1] Univ Laval, Dairy Res Ctr STELA, Quebec City, PQ G1K 7P4, Canada
[2] Univ Alexandria, Fac Agr, Dept Dairy Sci & Technol, Alexandria, Egypt
[3] ETH Zentrum, Swiss Fed Inst Technol, Inst Food Sci & Nutr, Zurich, Switzerland
关键词
antagonism; bifidobacteria; infant faeces; Listeria monocytogenes; probiotics;
D O I
10.1046/j.1365-2672.2003.02085.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: This study aimed to characterize new isolates of human bifidobacteria, evaluate some of their probiotic potential and to screen these isolates for their effectiveness at inhibiting Listeria monocytogenes in vitro. Methods and Results: Thirty-four Bifidobacterium isolates from infant faeces were identified by fructose-6-phosphate phosphoketolase and PCR. Six isolates, coded RBL67, RBL68, RBL69, RBL70, RBL85 and RBL86, showed higher antagonistic activity against L. monocytogenes. Neutralized culture supernatants of these strains did not inhibit L. monocytogenes when tested by agar diffusion method. However, the concentration of supernatant by speed-vac resulted in the formation of an inhibitory effect with supernatants from strains RBL67, RBL68 and RBL70. This effect was shown to be related to heat-stable proteinaceous compound(s) which were resistant to heating at 100degreesC for 5 min but not to pronase-E, proteinase-K or trypsin. The extraction of the inhibitory compounds by methanol-acetone extraction procedure indicated that four strains (RBL67, RBL68, RBL69 and RBL70) were mostly soluble in acetone. However, strain RBL85 produced inhibitory substances that were soluble in methanol. Conclusion: Infant bifidobacterial isolates produce heat-stable proteinaceous compounds active against L. monocytogenes. Significance and Impact of the Study: Production of antibacterial substances by bifidobacteria would improve intestinal bacterial ecology and inhibit intestinal pathogens.
引用
收藏
页码:1058 / 1069
页数:12
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