2020
Lugli, G A; Duranti, S; Milani, C; Mancabelli, L; Turroni, F; Alessandri, G; Longhi, G; Anzalone, R; Viappinai, A; Tarrachini, C; Bernasconi, S; Yonemitsu, C; Bode, L; Goran, M I; Ossiprandi, M C; van Sinderen, D; Ventura, M
Investigating bifidobacteria and human milk oligosaccharide composition of lactating mothers Journal Article
In: FEMS Microbiol. Ecol., vol. 96, no. 5, 2020.
Abstract | Links | BibTeX | Tags: bifidobacteria
@article{pmid32188978,
title = {Investigating bifidobacteria and human milk oligosaccharide composition of lactating mothers},
author = {G A Lugli and S Duranti and C Milani and L Mancabelli and F Turroni and G Alessandri and G Longhi and R Anzalone and A Viappinai and C Tarrachini and S Bernasconi and C Yonemitsu and L Bode and M I Goran and M C Ossiprandi and D van Sinderen and M Ventura},
url = {https://pubmed.ncbi.nlm.nih.gov/32188978/},
doi = {10.1093/femsec/fiaa049},
year = {2020},
date = {2020-03-19},
urldate = {2020-03-01},
journal = {FEMS Microbiol. Ecol.},
volume = {96},
number = {5},
abstract = {Human milk is known to carry its own microbiota, of which the precise origin remains obscure. Breast-feeding allows mother-to-baby transmission of microorganisms as well as transfer of many other milk components, such as human milk oligosaccharides (HMOs), which act as metabolizable substrates for particular bacteria, such as bifidobacteria, residing in infant intestinal tract. In the current study, we report HMO composition of 249 human milk samples, in 163 of which we quantified the abundance of members of the Bifidobacterium genus using a combination of metagenomic and flow cytometric approaches. Metagenomic data allowed us to identify four clusters dominated by Bifidobacterium adolescentis and Bifidobacterium pseudolongum, Bifidobacterium crudilactis, or Bifidobacterium dentium, as well as a cluster represented by a heterogeneous mix of bifidobacterial species such as Bifidobacterium breve and Bifidobacterium longum. Furthermore, in vitro growth assays on HMOs coupled with in silico glycobiome analyses allowed us to elucidate that members of the Bifidobacterium bifidum and B. breve species exhibit the highest ability to degrade and grow on HMOs. Altogether these findings indicate that the bifidobacterial component of the human milk microbiota is not strictly correlated to their ability to metabolize HMOs.},
keywords = {bifidobacteria},
pubstate = {published},
tppubtype = {article}
}
Human milk is known to carry its own microbiota, of which the precise origin remains obscure. Breast-feeding allows mother-to-baby transmission of microorganisms as well as transfer of many other milk components, such as human milk oligosaccharides (HMOs), which act as metabolizable substrates for particular bacteria, such as bifidobacteria, residing in infant intestinal tract. In the current study, we report HMO composition of 249 human milk samples, in 163 of which we quantified the abundance of members of the Bifidobacterium genus using a combination of metagenomic and flow cytometric approaches. Metagenomic data allowed us to identify four clusters dominated by Bifidobacterium adolescentis and Bifidobacterium pseudolongum, Bifidobacterium crudilactis, or Bifidobacterium dentium, as well as a cluster represented by a heterogeneous mix of bifidobacterial species such as Bifidobacterium breve and Bifidobacterium longum. Furthermore, in vitro growth assays on HMOs coupled with in silico glycobiome analyses allowed us to elucidate that members of the Bifidobacterium bifidum and B. breve species exhibit the highest ability to degrade and grow on HMOs. Altogether these findings indicate that the bifidobacterial component of the human milk microbiota is not strictly correlated to their ability to metabolize HMOs.