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Bifidobacteria in the Culture Collection

Bifidobacterium longum CCOS 606 Bifidobacterium longum CCOS 606

Bifidobacteria are potential health-promoting lactic acid bacteria present in the human gastrointestinal tract. In the large intestine, bifidobacteria contribute to the production of butyrate which is an important energy source for the colonic mucosa (Kleerebezem and Vaughan 2009). Selection criteria for probiotic bacteria are: human origin, GRAS (generally recognized as safe) status, suitable for large scale production, bile acid resistance, adherence to human intestinal cells and intestinal mucins, ability to modulate immune response, antimicrobial activity, efficacy and proven safety (Kolida et al. 2006; Dunne et al. 2001).

Beneficial effects associated with bifidobacteria include: reduction of duration of diarrhoea (Rerksuppaphol and Rerksuppaphol 2010), protection of intestinal cells from pathogenic bacteria (Chenoll et al. 2011), inhibition of inflammation (Philippe et al. 2011; Roselli et al. 2006), folate production (Santacruz et al. 2010; Pompei et al. 2007) and reduction of serum cholesterol levels (Lee et al. 2009).

Under the microscope, bifidobacteria show different forms: straight rods, forked or bifid rods, branched or globular swelling of rods (Husain et al. 1972).

Characterisation of Bifidobacteria

Moderately oxygen-tolerant Bifidobacterium strains were isolated from faeces of infant and adult humans by the institute for microbiology and biotechnology of the Max Rubner Institute in D-Kiel and further characterised by the CCOS. More than 60 different strains are available from CCOS.

Table 1: Properties of selected Bifidobacterium strains

Property Bifidobacterium
bifidum breve breve longum longum longum animalis
subsp. lactis
CCOS no. 571 549 586 522 527 545 594
Origin: Feces of infant infant infant adult infant infant adult
Ox bile resistance1 1% 0.5% 0% 1% 1% 1% 1%
Haemolysis on sheep blood gamma gamma beta beta gamma gamma gamma
Adherence2 +++ ++ nd +/++ +/- - ++
Ratio IL-10/IL-123 < 1 1.7 nd < 1 < 1 1.7 nd
Folate production4
µg 100g-1 DW
8000 200 nd 800 500 300 1350

1Growth on agarplate with indicated ox bile concentration
2Adherence of the strains to Caco-2 and HT-29 cells were determined using FACS analysis.
3IL-10/IL-12 cytokine ratio was determined by incubation of human peripheral blood mononuclear cells (ZEN-Bio, SER-PBMC-200) with the different strains using ELISA.
4Determination of folate production of lyophilized strains in folate-free medium using HPLC-M.
Abbreviations: DW: Dry weight; nd: not determined

Table 2: Antibiotic resistance patterns of selected Bifidobacterium strains:

Antibiotic MIC in µg mL-1 of Bifidobacterium
bifidum breve breve longum longum longum animalis subsp. lactis
CCOS no. 571 549 586 522 527 545 594
Ampicillin 0.06 0.5 nd 2 0.12 0.5 nd
Chloramphenicol 1 8 nd 1 0.5 2 0.5
Ciprofloxacin 16 0.25 1 64 8 8 4
Clindamycin 0.06 0.25 0.03 0.06 0.03 0.06 0.03
Erythromycin 0.03 0.12 0.016 0.06 0.016 0.06 0.016
Gentamycin 32 16 2 16 16 8 8
Kanamycin 256 128 4 256 128 128 nd
Linezolid 2 0.5 nd 0.5 0.5 1 0.5
Neomycin 64 64 1 64 32 32 4
Penicillin 0.12 0.5 nd 1 0.12 0.5 nd
Rifampicin 0.5 0.25 0.12 0.12 0.25 0.25 0.25
Streptomycin 32 >256 0.5 32 16 16 16
Tetracycline 1 16 0.5 0.5 0.25 1 16
Trimethoprim >64 >64 0.5 32 2 8 0.12
Vancomycin 1 0.5 0.25 0.5 0.5 0.25 0.25
Virginiamycin 0.25 0.12 0.03 0.03 0.06 0.12 nd

Antibiotic susceptibility testing was performed according to ISO 10932 using VetMIC and/or Etest systems. nd: not determined