grant

Milk Analytics Core

Organization UNIVERSITY OF CALIFORNIA, SAN DIEGOLocation LA JOLLA, UNITED STATESPosted 10 Sept 2021Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY202527E10 Antigen4-O-beta-D-galactopyranosyl-D-glucoseAliquotAnalytic ChemistryAnalytical ChemistryAntibiotic AgentsAntibiotic DrugsAntibiotic TherapyAntibiotic TreatmentAntibioticsAssayBioassayBiologicalBiological AssayBiomedical ResearchBreast FeedingBreast MilkBreast fedBreast fed infantBreastfedBreastfed infantBreastfeedingBreastmilkCalcium-Binding Myeloid Protein P8,14CalgranulinCaliforniaCalprotectinCell BodyCellsChildhoodClinicalClinical SciencesCollaborationsCollectionCommunitiesComplexCoupledDNA mutationDataData ScienceDetectionDiseaseDisorderEndocrine Gland SecretionEsteroproteasesFluorescenceGLP-1Genetic ChangeGenetic defectGenetic mutationGestationGlp-1GoalsGrowth AgentsGrowth FactorGrowth SubstancesHPLCHigh Performance Liquid ChromatographyHigh Pressure Liquid ChromatographyHigh Speed Liquid ChromatographyHormonesHuman CharacteristicsHuman MilkHuman Mother's MilkHuman NatureImmunoassayInfantInfant DevelopmentInfant HealthInfant MortalityInfant Mortality TotalInvestigatorsKnowledgeL1 AntigenLactationLactoseLeukocyte L1 Antigen ComplexLeukocyte L1 ProteinLipidsMacronutrientsMacronutrients NutritionMammary Gland MilkMaternal and Child HealthMeasurementMeasuresMiceMice MammalsMicrobeMicronutrientsMigratory Inhibitory Factor-Related Protein MRPMilkMiscellaneous AntibioticMother's MilkMothersMurineMusMutationMyelomonocytic Antigen L1NIR SpectroscopyNear-Infrared SpectrometryNear-Infrared SpectroscopyOligosaccharidesOutcomeParticipantPeptidasesPeptide HydrolasesPeptidesPerformancePregnancyProtease GeneProteasesProteinasesProteinsProteins Growth FactorsProteolytic EnzymesProtocolProtocols documentationR-Series Research ProjectsR01 MechanismR01 ProgramResearchResearch GrantsResearch PersonnelResearch Project GrantsResearch ProjectsResearch ResourcesResearchersResourcesRisk ReductionRoleSafetySamplingServicesTechnologyTherapeuticTherapeutic AgentsTherapeutic HormoneUniversitiesValidationWomananalytical toolanalyze microbiomeassay developmentbacterial disease treatmentbacterial infectious disease treatmentbiologicbiological heterogeneitybreast feeding infantbreastfeeding infantcytokinedeath among infantsdeath in first year of lifedeath in infancydeath in infantsdesigndesigningexperiencefeedinggenome mutationghrelinglucagon-like peptide 1human milk oligosaccharidesimprovedinfant deathinfant demiseinfant morbidity/mortalityinfantile deathlactatinglactationallipidomicsmacromoleculematernal milkmetabolism measurementmetabolomicsmetabonomicsmicrobiomemicrobiome analysismilk fat globulemilk microbiomemilkfat globulemortality in infantsoperationoperationspediatricpharmacometricsprogramsreduce riskreduce risksreduce that riskreduce the riskreduce these risksreduces riskreduces the riskreducing riskreducing the riskresponserisk-reducingsample collectionsialylationskillssocial rolespecimen collectiontechnology implementationtechnology validationvalidations
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Full Description

ABSTRACT
The University of California San Diego (UC San Diego) MPRINT Center of Excellence in Therapeutics (CET)

involves a human milk (HM)-centered approach to investigate the role of maternal and pediatric therapeutics at

intersections of the mother-milk-infant ‘triad’. Key among the overall goals of the MPRINT CET are to assess

how maternal antibiotics impact HM composition and how HM components alter safety and efficacy of these

important pediatric therapeutic agents. HM composition analysis, however, is not trivial. HM composition is highly

dynamic and changes throughout lactation, indeed even throughout the course of a single feeding. HM is a

complex matrix that includes cells and microbes as well as large molecule aggregates like the milk fat globule.

HM also contains a unique set of molecules, the human milk oligosaccharides (HMOs), which represent the third

most abundant component of HM after lactose and lipids. Thus, the dynamic, complex, and unique nature of HM

requires specific collection protocols, assay development, and assay validation. With over 20 years of experience

in HM research, the Milk Analytics Core (MAC) will provide overall guidance and advice to MPRINT CET

investigators and staff. MAC will provide HM collection protocols and ready-to-ship sample collection kits to the

Clinical and Data Science Projects (Aim 1a) and receive HM samples for composition analysis (Aim 1b).

Depending on project needs, MAC offers macronutrient, oligosaccharide, and bioactive measurements as well

as milk microbiome analysis, the latter in collaboration with the UC San Diego Microbiome Core, which operates

independently of, but frequently in partnership with, our team. MAC will also provide mouse milk oligosaccharide

and microbiome analyses to the Research Project team (Aim 1c), applying our detailed prior knowledge of how

the St3gal4 mutation under study markedly depletes sialylated milk oligosaccharide content. Data generated

from our analyses will be returned to the respective project teams for integration. Separate HM aliquots from the

same samples will be passed directly on to the Pharmacometrics and Analytical Chemistry Core for antibiotic

drug quantification, and that data will likewise be directly returned to the respective project teams. In addition to

already established services, MAC will develop and validate new HM-specific assays by expanding the analyte

portfolio of the existing multiplex immunoassay platform (Aim 2a) and by engaging and activating other UC San

Diego researchers to apply and validate their unique technologies to HM research (Aim 2b). We envision MAC

to become a comprehensive milk analytics core with knowledge, skills, and technology, serving as a resource to

this and other MPRINT CETs and the biomedical research community at large. Together, we will be able to

generate a better understanding how antibiotic treatment during pregnancy and lactation impacts the mother-

milk-infant ‘triad’, inform and adjust precision in therapeutics, and ultimately improve maternal-child health.

Grant Number: 5P50HD106463-05
NIH Institute/Center: NIH

Principal Investigator: Lars Bode

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