Abstract

BackgroundNutritional interventions often fail to prevent growth failure in childhood and adolescent malnutrition and the mechanisms remain unclear. Recent studies revealed altered microbiota in malnourished children and anorexia nervosa. To facilitate mechanistic studies under physiologically relevant conditions, we established a mouse model of growth failure following chronic dietary restriction and examined microbiota in relation to age, diet, body weight, and anabolic treatment.MethodsFour-week-old female BALB/c mice (n = 12/group) were fed ad libitum (AL) or offered limited food to abolish weight gain (LF). A subset of restricted mice was treated with an insulin-like growth factor 1 (IGF1) analog. Food access was restored in a subset of untreated LF (LF-RF) and IGF1-treated LF mice (TLF-RF) on day 97. Gut microbiota were determined on days 69, 96–99 and 120 by next generation sequencing of the V3–5 region of the 16S rRNA gene. Microbiota–host factor associations were analyzed by distance-based PERMANOVA and quantified by the coefficient of determination R2 for age, diet, and normalized body weight change (Δbwt). Microbial taxa on day 120 were compared following fitting with an overdispersed Poisson regression model. The machine learning algorithm Random Forests was used to predict age based on the microbiota.ResultsOn day 120, Δbwt in AL, LF, LF-RF, and TLF-RF mice was 52 ± 3, –6 ± 1*, 40 ± 3*, and 46 ± 2 % (*, P < 0.05 versus AL). Age and diet, but not Δbwt, were associated with gut microbiota composition. Age explained a larger proportion of the microbiota variability than diet or Δbwt. Random Forests predicted chronological age based on the microbiota and indicated microbiota immaturity in the LF mice before, but not after, refeeding. However, on day 120, the microbiota community structure of LF-RF mice was significantly different from that of both AL and LF mice. IGF1 mitigated the difference from the AL group. Refed groups had a higher abundance of Bacteroidetes and Proteobacteria and a lower abundance of Firmicutes than AL mice.ConclusionsPersistent growth failure can be induced by 97-day dietary restriction in young female mice and is associated with microbiota changes seen in lean mice and individuals and anorexia nervosa. IGF1 facilitates recovery of body weights and microbiota.Electronic supplementary materialThe online version of this article (doi:10.1186/s13073-016-0357-1) contains supplementary material, which is available to authorized users.

Highlights

  • Nutritional interventions often fail to prevent growth failure in childhood and adolescent malnutrition and the mechanisms remain unclear

  • Upon restoration of ad libitum feeding on day 97, Normalized body weight change from day 0 (Δbwt) of Limited-fed-refed group (LF-RF) mice increased rapidly for 12 days before assuming a time-course paralleling AL values approximately 12 % below normalized AL weights, a significant difference maintained to the end of the study

  • The body weight differentials observed at the end of the study occurred in the absence of significant differences in average food intake among AL, LF-RF, and Treated limited-fed-refed group (TLF-RF) mice calculated from the intake measured on days 117 and 123 (Fig. 1e)

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Summary

Introduction

Nutritional interventions often fail to prevent growth failure in childhood and adolescent malnutrition and the mechanisms remain unclear. Recent studies revealed altered microbiota in malnourished children and anorexia nervosa. To facilitate mechanistic studies under physiologically relevant conditions, we established a mouse model of growth failure following chronic dietary restriction and examined microbiota in relation to age, diet, body weight, and anabolic treatment. Therapeutic food interventions have reduced mortality in childhood malnutrition [5] and, together with behavioral, family-based, and pharmacological treatments, can achieve weight gain in patients with anorexia nervosa [2, 6]. Intestinal microbiota altered by diet and other disease-related conditions may limit nutritional rehabilitation in patients with malnutrition and wasting of various etiologies

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