Screening competition and cross-feeding interactions during utilization of human milk oligosaccharides by gut microbes

Romina Díaz , Daniel Garrido

Microbiome Research Reports ›› 2024, Vol. 3 ›› Issue (1) : 12

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Microbiome Research Reports ›› 2024, Vol. 3 ›› Issue (1) :12 DOI: 10.20517/mrr.2023.61
Original Article

Screening competition and cross-feeding interactions during utilization of human milk oligosaccharides by gut microbes

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Abstract

Background: The infant gut microbiome is a complex community that influences short- and long-term health. Its assembly and composition are governed by variables such as the feeding type. Breast milk provides infants an important supply of human milk oligosaccharides (HMO), a broad family of carbohydrates comprising neutral, fucosylated, and sialylated molecules. There is a positive association between HMOs and the overrepresentation of Bifidobacterium species in the infant gut, which is sustained by multiple molecular determinants present in the genomes of these species. Infant-gut-associated Bifidobacterium species usually share a similar niche and display similar HMO inclinations, suggesting they compete for these resources. There is also strong evidence of cross-feeding interactions between HMO-derived molecules and bifidobacteria.

Methods: In this study, we screened for unidirectional and bidirectional interactions between Bifidobacterium and other species using individual HMO. Bifidobacterium bifidum and Bacteroides thetaiotaomicron increased the growth of several other species when their supernatants were used, probably mediated by the partial degradation of HMO. In contrast, Bifidobacterium longum subsp. infantis. supernatants did not exhibit positive growth.

Results:Bifidobacterium species compete for lacto-N-tetraose, which is associated with reduced bidirectional growth. The outcome of these interactions was HMO-dependent, in which the two species could compete for one substrate but cross-feed on another. 2’-fucosyllactose and lacto-N-neotetraose are associated with several positive interactions that generally originate from the partial degradation of these HMOs.

Conclusion: This study presents evidence for complex interactions during HMO utilization, which can be cooperative or competitive, depending on the nature of the HMO. This information could be useful for understanding how breast milk supports the growth of some Bifidobacterium species, shaping the ecology of this important microbial community.

Keywords

Bifidobacterium / cross-feeding interactions / HMO / infant gut microbiome

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Romina Díaz, Daniel Garrido. Screening competition and cross-feeding interactions during utilization of human milk oligosaccharides by gut microbes. Microbiome Research Reports, 2024, 3(1): 12 DOI:10.20517/mrr.2023.61

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References

[1]

La Rosa PS,Zhou Y.Patterned progression of bacterial populations in the premature infant gut.Proc Natl Acad Sci U S A2014;111:12522-7 PMCID:PMC4151715

[2]

Dominguez-Bello MG,Shen N.Partial restoration of the microbiota of cesarean-born infants via vaginal microbial transfer.Nat Med2016;22:250-3 PMCID:PMC5062956

[3]

Iizumi T,Ruiz V.Gut microbiome and antibiotics.Arch Med Res2017;48:727-34

[4]

Bäckhed F,Peng Y.Dynamics and stabilization of the human gut microbiome during the first year of life.Cell Host Microbe2015;17:690-703

[5]

Tanaka M.Development of the gut microbiota in infancy and its impact on health in later life.Allergol Int2017;66:515-22

[6]

Heintz C.You are what you host: microbiome modulation of the aging process.Cell2014;156:408-11 PMCID:PMC3956044

[7]

Henrick BM,Lakshmikanth T.Bifidobacteria-mediated immune system imprinting early in life.Cell2021;184:3884-98.e11

[8]

Thomson P.Chapter 5 - human milk oligosaccharides and health promotion through the gut microbiome. In: Watson RR, Collier RJ, Preedy VR, editors. Dairy in human health and disease across the lifespan. Elsevier; 2017. pp. 73-86.

[9]

Horta BL,Victora CG.Long-term consequences of breastfeeding on cholesterol, obesity, systolic blood pressure and type 2 diabetes: a systematic review and meta-analysis.Acta Paediatr2015;104:30-7

[10]

Moubareck CA.Human milk microbiota and oligosaccharides: a glimpse into benefits, diversity, and correlations.Nutrients2021;13:1123 PMCID:PMC8067037

[11]

Samuel TM,Lebumfacil JD.Dynamics of human milk oligosaccharides in early lactation and relation with growth and appetitive traits of Filipino breastfed infants.Sci Rep2022;12:17304 PMCID:PMC9569346

[12]

Lawson MAE,Kujawska M.Breast milk-derived human milk oligosaccharides promote Bifidobacterium interactions within a single ecosystem.ISME J2020;14:635-48 PMCID:PMC6976680

[13]

Turroni F,Duranti S,van Sinderen D.Glycan utilization and cross-feeding activities by bifidobacteria.Trends Microbiol2018;26:339-50

[14]

Ferretti P,Tett A.Mother-to-infant microbial transmission from different body sites shapes the developing infant gut microbiome.Cell Host Microbe2018;24:133-45.e5 PMCID:PMC6716579

[15]

James K,Bottacini F.Bifidobacterium breve UCC2003 metabolises the human milk oligosaccharides lacto-N-tetraose and lacto-N-neo-tetraose through overlapping, yet distinct pathways.Sci Rep2016;6:38560 PMCID:PMC5144078

[16]

Sela DA,Adeuya A.The genome sequence of Bifidobacterium longum subsp. infantis reveals adaptations for milk utilization within the infant microbiome.Proc Natl Acad Sci U S A2008;105:18964-9 PMCID:PMC2596198

[17]

Yassour M,Hogstrom LJ.Strain-level analysis of mother-to-child bacterial transmission during the first few months of life.Cell Host Microbe2018;24:146-54.e4 PMCID:PMC6091882

[18]

Thomson P,Garrido D.Human milk oligosaccharides and infant gut bifidobacteria: molecular strategies for their utilization.Food Microbiol2018;75:37-46

[19]

Faust K.Microbial interactions: from networks to models.Nat Rev Microbiol2012;10:538-50

[20]

Belzer C,Aalvink S.Microbial metabolic networks at the mucus layer lead to diet-independent butyrate and vitamin B12 production by intestinal symbionts.mBio2017;8:e00770-17 PMCID:PMC5605934

[21]

Falony G,Leroy F.Coculture fermentations of Bifidobacterium species and Bacteroides thetaiotaomicron reveal a mechanistic insight into the prebiotic effect of inulin-type fructans.Appl Environ Microbiol2009;75:2312-9 PMCID:PMC2675216

[22]

Shetty SA,Atashgahi S,Smidt H.Inter-species metabolic interactions in an in-vitro minimal human gut microbiome of core bacteria.NPJ Biofilms Microbiomes2022;8:21 PMCID:PMC8993927

[23]

Egan M.Chapter 8 - carbohydrate metabolism in bifidobacteria. In: Mattarelli P, Biavati B, Holzapfel WH, Wood BJB, editors. The bifidobacteria and related organisms. Elsevier; 2018. pp. 145-64.

[24]

Gotoh A,Sakanaka M.Sharing of human milk oligosaccharides degradants within bifidobacterial communities in faecal cultures supplemented with Bifidobacterium bifidum.Sci Rep2018;8:13958 PMCID:PMC6143587

[25]

Walsh C,van Sinderen D.Human milk oligosaccharide-sharing by a consortium of infant derived Bifidobacterium species.Sci Rep2022;12:4143 PMCID:PMC8907170

[26]

Nishiyama K,Uribayashi K,Mukai T.Two extracellular sialidases from Bifidobacterium bifidum promote the degradation of sialyl-oligosaccharides and support the growth of Bifidobacterium breve.Anaerobe2018;52:22-8

[27]

Ojima MN,Arzamasov AA.Priority effects shape the structure of infant-type Bifidobacterium communities on human milk oligosaccharides.ISME J2022;16:2265-79 PMCID:PMC9381805

[28]

Flint HJ,Scott KP.Interactions and competition within the microbial community of the human colon: links between diet and health.Environ Microbiol2007;9:1101-11

[29]

Medina DA,Ovalle A,Garrido D.Prebiotics mediate microbial interactions in a consortium of the infant gut microbiome.Int J Mol Sci2017;18:2095 PMCID:PMC5666777

[30]

de Vos MGJ, Zagorski M, McNally A, Bollenbach T. Interaction networks, ecological stability, and collective antibiotic tolerance in polymicrobial infections.Proc Natl Acad Sci U S A2017;114:10666-71 PMCID:PMC5635929

[31]

Tuomivaara ST,O’Neill MA.Generation and structural validation of a library of diverse xyloglucan-derived oligosaccharides, including an update on xyloglucan nomenclature.Carbohydr Res2015;402:56-66

[32]

Díaz R,Orellana G.Comparative genomic analysis of novel Bifidobacterium longum subsp. longum strains reveals functional divergence in the human gut microbiota.Microorganisms2021;9:1906 PMCID:PMC8470182

[33]

Marcobal A,Sonnenburg ED.Bacteroides in the infant gut consume milk oligosaccharides via mucus-utilization pathways.Cell Host Microbe2011;10:507-14 PMCID:PMC3227561

[34]

Arboleya S,Ryan CA,Ross PR.Bosom buddies: the symbiotic relationship between infants and Bifidobacterium longum ssp. longum and ssp. infantis. genetic and probiotic features.Annu Rev Food Sci Technol2016;7:1-21

[35]

LoCascio RG,Sela DA,Mills DA.Broad conservation of milk utilization genes in Bifidobacterium longum subsp. infantis as revealed by comparative genomic hybridization.Appl Environ Microbiol2010;76:7373-81 PMCID:PMC2976205

[36]

Garrido D,Mills DA.Consumption of human milk glycoconjugates by infant-associated bifidobacteria: mechanisms and implications.Microbiology2013;159:649-64 PMCID:PMC4083661

[37]

Hidalgo-Cantabrana C,Ruiz L,Sánchez B.Bifidobacteria and their health-promoting effects.Microbiol Spectr2017;5:73-98

[38]

Kitaoka M.Bifidobacterial enzymes involved in the metabolism of human milk oligosaccharides.Adv Nutr2012;3:422S-9S PMCID:PMC3649479

[39]

Chia LW,Blijenberg B.Bacteroides thetaiotaomicron fosters the growth of butyrate-producing Anaerostipes caccae in the presence of lactose and total human milk carbohydrates.Microorganisms2020;8:1513 PMCID:PMC7601031

[40]

Banerjee S,van der Heijden MGA.Keystone taxa as drivers of microbiome structure and functioning.Nat Rev Microbiol2018;16:567-76

[41]

Marriage BJ,Goehring KC,Williams JA.Infants fed a lower calorie formula with 2’FL show growth and 2’FL uptake like breast-fed infants.J Pediatr Gastroenterol Nutr2015;61:649-58 PMCID:PMC4645963

[42]

Katoh T,Sakanaka M,Gotoh A.Enzymatic adaptation of Bifidobacterium bifidum to host glycans, viewed from glycoside hydrolyases and carbohydrate-binding modules.Microorganisms2020;8:481 PMCID:PMC7232152

[43]

Ojima MN,Sakanaka M,Odamaki T.Ecological and molecular perspectives on responders and non-responders to probiotics and prebiotics.Curr Opin Biotechnol2022;73:108-20

[44]

McGuire MK,McGuire MA.What’s normal? Oligosaccharide concentrations and profiles in milk produced by healthy women vary geographically.Am J Clin Nutr2017;105:1086-100 PMCID:PMC5402033

[45]

Garrido D,Lemay DG,German JB.Erratum: comparative transcriptomics reveals key differences in the response to milk oligosaccharides of infant gut-associated bifidobacteria.Sci Rep2015;5:15311 PMCID:PMC4629190

[46]

Turroni F,Pass DA.Diversity of bifidobacteria within the infant gut microbiota.PLoS One2012;7:e36957 PMCID:PMC3350489

[47]

Horigome A,Odamaki T,Xiao JZ.Colonization of supplemented Bifidobacterium breve M-16V in low birth weight infants and its effects on their gut microbiota weeks post-administration.Front Microbiol2021;12:610080 PMCID:PMC8058467

[48]

Pichler MJ,Shuoker B.Butyrate producing colonic Clostridiales metabolise human milk oligosaccharides and cross feed on mucin via conserved pathways.Nat Commun2020;11:3285 PMCID:PMC7335108

[49]

Gutiérrez N.Species deletions from microbiome consortia reveal key metabolic interactions between gut microbes.mSystems2019;4:e00185-19 PMCID:PMC6635622

[50]

Angelakis E,Raoult D.Related actions of probiotics and antibiotics on gut microbiota and weight modification.Lancet Infect Dis2013;13:889-99

[51]

Castanys-Muñoz E,Vazquez E.Building a beneficial microbiome from birth.Adv Nutr2016;7:323-30 PMCID:PMC4785476

[52]

Liu H,Qi Q.Production of lactate in Escherichia coli by redox regulation genetically and physiologically.Appl Biochem Biotechnol2011;164:162-9

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