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DOI 10.1016/j.micpath.2017.08.014

Медицинская библиотека · Microbial pathogenesis · 2017

Bifidobacterium obtained from mother's milk and their infant stool; A comparative genotyping and antibacterial analysis.

Eshaghi Morteza, Bibalan Meysam Hasannejad, Rohani Mahdi, Esghaei Maryam, Douraghi Masoumeh, Talebi Malihe, Pourshafie Mohammad Reza

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Аннотация

Antibacterial activity of Bifidobacterium species has been considered as an important probiotic property for development of human gut immunity. This study was conducted to assess the genotypes and antibacterial activities of the native Bifidobacterium isolates obtained from the human's breast milk and the feces of their paired infants. Fifty-six samples from twenty-eight mothers' milk and paired infants feces were collected and cultured. Suspicious colonies were picked up and confirmed by phenotypic and molecular identifications. Randomly amplified polymorphic DNA (RAPD-PCR) and antibacterial activity were carried out. Amongst 56 samples, 41 different Bifidobacterium species including 12 B. breve, 14 B. longum, and 15 B. bifidum were isolated. Out of which, 12 isolates including B. longum (6), B. breve (4) and B. bifidum (2) were shared between six mother-infant pairs. Only three strains of B. longum showed 100% similarity in their RAPD-PCR. No significant difference was observed in the antibacterial activity of the Bifidobacterium isolates, with the same or different RAPD-PCR profile, against the enteric bacteria. Overall, 29% of the Bifidobacteria species isolated from the mothers milk and their paired infants feces were shared. All species of Bifidobacteria showed the universal role of antipathogens activities irrespective of the host and the isolation site.

Для цитирования: Eshaghi Morteza, Bibalan Meysam Hasannejad, Rohani Mahdi, Esghaei Maryam, Douraghi Masoumeh, Talebi Malihe, Pourshafie Mohammad Reza. Bifidobacterium obtained from mother's milk and their infant stool; A comparative genotyping and antibacterial analysis.. Microbial pathogenesis. 2017. DOI: 10.1016/j.micpath.2017.08.014.

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