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Gut Microbes and Milk Compounds Tackle Childhood Malnutrition

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Two women in laboratory look at glass lab slide.
Food scientist Daniela Barile and graduate student Tian Tian study milk sugar compounds as part of a study showing the role these compounds play in nourishing health-promoting gut microbes in infants. (Gregory Urquiaga/ϲϿ Davis)

Quick Summary

  • Gut microbes can help prevent stunted growth
  • Milk sugars nourish health-promoting gut microbes
  • Cow's milk and human milk provide these sugars

The “forests” of microbes that naturally grow in babies’ guts are increasingly recognized as key players in childhood health and nutrition.

In two newly published studies, research teams led by Washington University, St. Louis, in collaboration with ϲϿ Davis scientists, demonstrate that gut microbes can contribute to or prevent impaired growth and that specific sugar compounds found in milk can help promote growth by nourishing gut microbes.

One study suggests that there may be opportunity for the dairy industry to play an important role in helping to develop novel foods and therapies.

Results from the two studies offer hope for reducing malnutrition, which each year kills 3.1 million children globally, accounts for 45 percent of deaths among children under age 5, and robs millions of the surviving children of their physical and intellectual potential.

Now appearing in Science and Cell

In one of the new studies, scientists found evidence that impaired “maturation” of babies’ gut microbe communities can directly contribute to poor growth.  Their findings will be reported Feb. 19 in the journal .

In the other study, researchers demonstrated that certain complex sugar compounds found in human milk, and to a lesser extent in cow’s milk, nourish health-promoting gut microbes and may be important ingredients for future therapies.  The findings of that study will appear Feb. 19 in the journal .

Both studies were led by acclaimed gut-microbiome researcher Jeffrey I. Gordon of the University of Washington School of Medicine in St. Louis. The studies involved germ-free mice and/or piglets as research models.

“This research provides a microbial view of human development and suggests potential new therapies for malnutrition that target gut microbes in order to promote healthy growth,” said Gordon, the Dr. Robert J. Glaser Distinguished University Professor and director of Washington University’s Center for Genome Sciences and Systems Biology.

“Current ‘ready-to-use’ therapeutic foods have reduced mortality from malnutrition, but these children continue to show lingering long-term effects, including stunted growth, impaired neurodevelopment and dysfunctional immune systems,” Gordon said.

Maturity of infant gut microbe communities

The study published in built upon earlier findings, which showed that undernourished children have immature, underdeveloped microbiota, or communities of microbes, in their guts.

To examine the relationship between underdeveloped microbiota and growth, the researchers transferred microbes from either healthy or undernourished 6- and 18-month-old children into “germ-free” mice, which had been specially raised to have no pre-existing gut microbes of their own. The mice were then fed diets that mirrored the diets of either the healthy or undernourished children.

The researchers found that mice receiving microbes from undernourished children developed impaired growth patterns, similar to those seen in the undernourished children, even though there was no significant difference in food consumption between the groups.

Furthermore, researchers found that when mice from both groups were housed together and had the opportunity to pick up microbes from each other, they soon developed similar collections of microbes in their guts. The researchers found that the microbes that originated in healthy children seemed to correct abnormal growth patterns in mice that had first received microbes from undernourished children.

The researchers also found that the collection of microbes derived from 6-month-old children had a greater impact on growth than did microbes from 18-month-old children.

“The findings clearly indicate that the proper development of the gut microbiota is important for normal growth,” said study co-author Kathryn Dewey, ϲϿ Davis distinguished professor of nutrition. Dewey coordinates an international research consortium focused on improving maternal and infant nutrition in Africa.

A solution to stunting found in cow’s milk?

In the study reported in the journal , the researchers explored the connection between infant undernutrition and certain oligosaccharides, which are sugar compounds found in human breast milk and at much lower levels in cow’s milk.

They found that a specific type of these compounds called sialylated milk sugars are present at lower levels in the breast milk of mothers of undernourished, stunted children than in the breast milk of mothers of healthy children.

To explore that correlation, the researchers transferred gut microbes from a stunted and underweight infant into germ-free mice and also into germ-free piglets. Then they fed a diet that was supplemented with oligosaccharides derived from cow’s milk to the germ-free mice and germ-free piglets.

The results demonstrated that the sugar from cow’s milk improved growth and healthy metabolic processes in the mice and pigs that had received the malnourished infant’s gut microbes.

“In short, the study demonstrated that these specific complex milk sugars nourish the infant gut microbes introduced to the mouse and pig models, leading to improvements in a number of factors associated with growth and health,” said the study’s co-author David Mills, a professor of food science and technology at ϲϿ Davis.

Partnering with cheese maker

Oligosaccharides derived from cow’s milk for this study were provided by Hilmar Cheese Company.  Hilmar’s cheese-processing facility in Merced County, California, has the technical capacity and expertise to separate the oligosaccharides from whey, a valuable byproduct of the cheese-making process.

“This is a wonderful example of the dairy industry serving as a hands-on partner with ϲϿ Davis researchers to make these high-end milk byproducts available for research,” said Mills.

“The particular excitement about this approach is the rapid nature by which this technology can be translated into novel foods and therapies, given the potentially massive oligosaccharide streams available for capture from the dairy industry worldwide,” he said.

Tedd Struckmeyer, a study co-author and Hilmar Cheese Company’s vice president of engineering, noted that the study results are intriguing.

“We are delighted to contribute our expertise in milk fractionation. Our innovation focus is on making more from milk and looking for unique milk properties that can be used to improve human nutrition,” Struckmeyer said. “We hope these studies stimulate further research funding to advance the understanding and availability of beneficial products.”

Collaborators

In addition to Washington University, ϲϿ Davis, and Hilmar Cheese Company, collaborating institutions included the University of Malawi, the University of Tampere in Finland, Duke University, Centre National de la Recherche Scientifique and Aix-Marseille Université in France, King Abdulaziz University in Saudi Arabia, the Russian Academy of Sciences in Moscow, and the Sanford Burnham Prebys Medical Discovery Institute in La Jolla, California.

ϲϿ Davis collaborators included Dewey and Joshua M. Jorgenson on the study published in Science. Mills, Dewey, Jorgenson, Daniela Barile, Carlito Lebrilla, Jasmine C.C. Davis and Sarah Totten (now at Stanford University) are the ϲϿ Davis co-authors on the study published in Cell.

Funding sources

Funding for both studies was provided by the Bill & Melinda Gates Foundation, the National Institutes of Health and the U.S. Agency for International Development.  In addition, the Academy of Finland provided support for the study published in Science.

Media Resources

David Mills, Food Science and Technology, (530) 754-7821, damills@ucdavis.edu

Kathryn Dewey, Nutrition, 530-752-0851, kgdewey@ucdavis.edu

Pat Bailey, News and Media Relations, ϲϿ Davis, 530-219-9640, pjbailey@ucdavis.edu

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