Cited by 13Probiotics and Fermented FoodsAntimicrobial Peptides and ActivitiesGut microbiota and health

The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.

Suppression subtractive hybridization identifies bacterial genomic regions that are possibly involved in hBD-2 regulation by enterocytes

Abstract

SCOPE: Human β-defensin 2 (hBD-2) is an inducible antimicrobial peptide synthesized by the epithelium to counteract bacterial adherence and invasion. It has been suggested that probiotic bacteria sustain gut barrier function via induction of defensins. The goals of this study were (i) to evaluate the potential immunomodulatory effects of 11 different Lactobacillus fermentum strains isolated from Kimere, an African fermented pearl millet (Pennisetum glaucum) dough, on the hBD-2 secretion by human intestinal CaCo-2 cell line and (ii) to examine genetic differences between two strains of L. fermentum (K2-Lb4 and K11-Lb3) which differed in their effect on the production of hBD-2 in this study. METHODS AND RESULTS: Totally, 46 strains of L. fermentum from Kimere were isolated and characterized using molecular biology methods including pulsed-field gel electrophoresis patterns. After performing time- and dose-experiments, CaCo-2 cells were incubated with or without bacteria for 12 h. L. fermentum PZ1162 was included as the positive control. Cell-free supernatants were analyzed for hBD-2 protein by enzyme-linked immunosorbent assay (ELISA). To identify potential bacterial genes associated with hBD-2 regulation, suppression subtractive hybridization (SSH) was used. Among the 11 strains tested, only two strains of bacteria, K11-Lb3 and K2-Lb6, significantly induced the production of hBD-2 by CaCo-2 cells. This effect was strain-specific, dose-dependent and particularly seems to be bacterial genomic-dependent as manifested by SSH. L. fermentum strains with and without hBD-2 inducing effect differed in genes encoding proteins involved in glycosylation of cell-wall proteins e.g. glycosyltransferase, UDP-N-acetylglucosamine 2-epimerase, rod shape-determining protein MreC, lipoprotein precursors, sugar ABC transporters, and glutamine ABC transporter ATP-binding protein. CONCLUSION: This study implies that certain strains of L. fermentum isolated from Kimere may stimulate the intestinal innate defense through the induction of hBD-2. The molecular basis of hBD-2 induction by L. fermentum strain K11-Lb3 may be based on glycosylated cell-surface structures synthesized with the aid of glycosyltransferase, UDP-N-acetylglucosamine 2-epimerase, and rod shape-determining protein MreC.

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Crossref · 10.1002/mnfr.201100052

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Metadata

Authors
Ghadimi, D., Hassan, M., Njeru, P. N., de Vrese, M., Geis, A., Shalabi, S. I., Abdel‐Razek, S. T., Abdel‐Khair, A. E. A., Heller, K. J., & Schrezenmeir, J.
Affiliations
  • Max Rubner Institut (DE)
  • Minia University (EG)
  • Sohag University (EG)
Corresponding author
Ghadimi, Darab
Venue
Molecular Nutrition & Food Research
Publisher
Wiley
Published
2011-06-28
Volume
55
Issue
10
Pages
1533-1542
ISSN
  • 1613-4125 (ISSN-L)
  • 1613-4133
OpenAlex
W2002073455
Cited by
13
References
28
Citations by year
2026: 1 · 2024: 1 · 2023: 1 · 2022: 1 · 2020: 1 · 2019: 2 · 2015: 1 · 2013: 2 · 2012: 1
FWCI
2.34
Type
journal article
Language
en
Open access
closed
Locations
  • Molecular Nutrition & Food Research (publishedVersion)
  • PubMed (publishedVersion)
  • OpenAgrar (submittedVersion)
Topics
  • Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
  • Life Sciences › Immunology and Microbiology › Microbiology › Antimicrobial Peptides and Activities
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
Keywords
human beta-defensin 2, Lactobacillus fermentum, probiotic bacteria, Caco-2 cells, suppression subtractive hybridization, glycosyltransferases, MreC, intestinal barrier, innate immunity, gut microbiota
MeSH terms
Bacterial Proteins, Base Sequence, Carbohydrate Epimerases, Carrier Proteins, Gene Expression Regulation, Glycosylation, Humans, Molecular Sequence Data, Species Specificity, Genome, Bacterial, In Situ Hybridization, Caco-2 Cells, Enterocytes, beta-Defensins, Pennisetum, Limosilactobacillus fermentum

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