TY - JOUR
T1 - Composition and stability of the vervet monkey milk microbiome
AU - Petrullo, Lauren
AU - Jorgensen, Matthew J.
AU - Snyder-Mackler, Noah
AU - Lu, Amy
N1 - Funding Information: This work was supported by the National Institutes of Health CTSA pilot grant [UL1-TR001420, Donald Mcclain PI], a P40 grant [OD010965, Matthew Jorgensen PI], Stony Brook University, the University of Washington, and the Turner Fellowship program at Stony Brook University (to L.P.). The authors would like to thank the veterinary and technical staff of the Vervet Research Colony, especially Edison Floyd and Chrissy Long for their role in sample collections, and Katie Hinde for providing expertise and protocol guidance for milk sample collection. We would also like to thank Sierra Sams at the University of Washington for assistance with extractions and sequencing, and two anonymous reviewers for their helpful input on earlier versions of this manuscript. Publisher Copyright: © 2019 Wiley Periodicals, Inc.
PY - 2019/10/1
Y1 - 2019/10/1
N2 - The human milk microbiome is vertically transmitted to offspring during the postnatal period and has emerged as a critical driver of infant immune and metabolic development. Despite this importance in humans, the milk microbiome of nonhuman primates remains largely unexplored. This dearth of comparative work precludes our ability to understand how species-specific differences in the milk microbiome may differentially drive maternal effects and limits how translational models can be used to understand the role of vertically transmitted milk microbes in human development. Here, we present the first culture-independent data on the milk microbiome of a nonhuman primate. We collected milk and matched fecal microbiome samples at early and late lactation from a cohort of captive lactating vervet monkeys (N = 15). We found that, similar to humans, the vervet monkey milk microbiome comprises a shared community of taxa that are universally present across individuals. However, unlike in humans, this shared community is dominated by the genera Lactobacillus, Bacteroides, and Prevotella. We also found that, in contrast to previous culture-dependent studies in humans, the vervet milk microbiome exhibits greater alpha-diversity than the gut microbiome across lactation. Finally, we did not find support for the translocation of microbes from the gut to the mammary gland within females (i.e., “entero-mammary pathway”). Taken together, our results show that the vervet monkey milk microbiome is taxonomically diverse, distinct from the gut microbiome, and largely stable. These findings demonstrate that the milk microbiome is a unique substrate that may selectively favor the establishment and persistence of particular microbes across lactation and highlights the need for future experimental studies on the origin of microbes in milk.
AB - The human milk microbiome is vertically transmitted to offspring during the postnatal period and has emerged as a critical driver of infant immune and metabolic development. Despite this importance in humans, the milk microbiome of nonhuman primates remains largely unexplored. This dearth of comparative work precludes our ability to understand how species-specific differences in the milk microbiome may differentially drive maternal effects and limits how translational models can be used to understand the role of vertically transmitted milk microbes in human development. Here, we present the first culture-independent data on the milk microbiome of a nonhuman primate. We collected milk and matched fecal microbiome samples at early and late lactation from a cohort of captive lactating vervet monkeys (N = 15). We found that, similar to humans, the vervet monkey milk microbiome comprises a shared community of taxa that are universally present across individuals. However, unlike in humans, this shared community is dominated by the genera Lactobacillus, Bacteroides, and Prevotella. We also found that, in contrast to previous culture-dependent studies in humans, the vervet milk microbiome exhibits greater alpha-diversity than the gut microbiome across lactation. Finally, we did not find support for the translocation of microbes from the gut to the mammary gland within females (i.e., “entero-mammary pathway”). Taken together, our results show that the vervet monkey milk microbiome is taxonomically diverse, distinct from the gut microbiome, and largely stable. These findings demonstrate that the milk microbiome is a unique substrate that may selectively favor the establishment and persistence of particular microbes across lactation and highlights the need for future experimental studies on the origin of microbes in milk.
KW - gut
KW - microbiome
KW - milk
KW - vervet monkey
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U2 - 10.1002/ajp.22982
DO - 10.1002/ajp.22982
M3 - Article
C2 - 31106877
SN - 0275-2565
VL - 81
JO - American Journal of Primatology
JF - American Journal of Primatology
IS - 10-11
M1 - e22982
ER -