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Diversity and temporal dynamics of primate milk microbiomes.
Muletz-Wolz, Carly R; Kurata, Naoko P; Himschoot, Elizabeth A; Wenker, Elizabeth S; Quinn, Elizabeth A; Hinde, Katie; Power, Michael L; Fleischer, Robert C.
Afiliação
  • Muletz-Wolz CR; Center for Conservation Genomics, Smithsonian Conservation Biology Institute, National Zoological Park, Washington, District of Columbia.
  • Kurata NP; Center for Conservation Genomics, Smithsonian Conservation Biology Institute, National Zoological Park, Washington, District of Columbia.
  • Himschoot EA; The Graduate Center, The City University of New York, New York, New York.
  • Wenker ES; Department of Ichthyology, American Museum of Natural History, New York, New York.
  • Quinn EA; Nutrition Laboratory and Conservation Ecology Center, Smithsonian Conservation Biology Institute, National Zoological Park, Washington, District of Columbia.
  • Hinde K; Nutrition Laboratory and Conservation Ecology Center, Smithsonian Conservation Biology Institute, National Zoological Park, Washington, District of Columbia.
  • Power ML; Department of Anthropology, Washington University in St. Louis, St. Louis, Missouri.
  • Fleischer RC; School of Human Evolution and Social Change, Arizona State University, Tempe, Arizona.
Am J Primatol ; 81(10-11): e22994, 2019 10.
Article em En | MEDLINE | ID: mdl-31219214
ABSTRACT
Milk is inhabited by a community of bacteria and is one of the first postnatal sources of microbial exposure for mammalian young. Bacteria in breast milk may enhance immune development, improve intestinal health, and stimulate the gut-brain axis for infants. Variation in milk microbiome structure (e.g., operational taxonomic unit [OTU] diversity, community composition) may lead to different infant developmental outcomes. Milk microbiome structure may depend on evolutionary processes acting at the host species level and ecological processes occurring over lactation time, among others. We quantified milk microbiomes using 16S rRNA high-throughput sequencing for nine primate species and for six primate mothers sampled over lactation. Our data set included humans (Homo sapiens, Philippines and USA) and eight nonhuman primate species living in captivity (bonobo [Pan paniscus], chimpanzee [Pan troglodytes], western lowland gorilla [Gorilla gorilla gorilla], Bornean orangutan [Pongo pygmaeus], Sumatran orangutan [Pongo abelii], rhesus macaque [Macaca mulatta], owl monkey [Aotus nancymaae]) and in the wild (mantled howler monkey [Alouatta palliata]). For a subset of the data, we paired microbiome data with nutrient and hormone assay results to quantify the effect of milk chemistry on milk microbiomes. We detected a core primate milk microbiome of seven bacterial OTUs indicating a robust relationship between these bacteria and primate species. Milk microbiomes differed among primate species with rhesus macaques, humans and mantled howler monkeys having notably distinct milk microbiomes. Gross energy in milk from protein and fat explained some of the variations in microbiome composition among species. Microbiome composition changed in a predictable manner for three primate mothers over lactation time, suggesting that different bacterial communities may be selected for as the infant ages. Our results contribute to understanding ecological and evolutionary relationships between bacteria and primate hosts, which can have applied benefits for humans and endangered primates in our care.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Primatas / Leite / Microbiota / Leite Humano Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans Idioma: En Revista: Am J Primatol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Primatas / Leite / Microbiota / Leite Humano Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans Idioma: En Revista: Am J Primatol Ano de publicação: 2019 Tipo de documento: Article