Abstract

Despite the impact of childhood diarrhea on morbidity and mortality, our understanding of its sequelae has been significantly hampered by the lack of studies that examine samples across the entire intestinal tract. Infant rhesus macaques are naturally susceptible to human enteric pathogens and recapitulate the hallmarks of diarrheal disease such as intestinal inflammation and growth faltering. Here, we examined intestinal biopsies, lamina propria leukocytes, luminal contents, and fecal samples from healthy infants and those experiencing growth faltering with distant acute or chronic active diarrhea. We show that growth faltering in the presence or absence of active diarrhea is associated with a heightened systemic and mucosal pro-inflammatory state centered in the colon. Moreover, polyclonal stimulation of colonic lamina propria leukocytes resulted in a dampened cytokine response, indicative of immune exhaustion. We also detected a functional and taxonomic shift in the luminal microbiome across multiple gut sites including the migration of Streptococcus and Prevotella species between the small and large intestine, suggesting a decompartmentalization of gut microbial communities. Our studies provide valuable insight into the outcomes of diarrheal diseases and growth faltering not attainable in humans and lays the groundwork to test interventions in a controlled and reproducible setting.

Highlights

  • Despite significant improvements in healthcare delivery and sanitation, over 500,000 children under the age of 5 die of diarrheal disease every year[1]

  • Cohort description and systemic markers of growth faltering and diarrhea In this study, a total of 17 6–12-month old infant macaques were classified into three groups; Healthy growth (HG), Growth Faltering with acute distance or no history of diarrhea (GF), and Growth Faltering with active chronic diarrhea (GF-DX) based on growth rate and clinical status at the time of necropsy

  • We further explored the impact of growth faltering/diarrhea on colonic lamina propria leukocytes (LPL) response to PMAi using RNA-seq

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Summary

Introduction

Despite significant improvements in healthcare delivery and sanitation, over 500,000 children under the age of 5 die of diarrheal disease every year[1]. Diarrhea results in a dangerous feedback loop of malnutrition[3,4,5,6] and intestinal damage[3,7,8], which leads to growth faltering, poor responses to oral vaccination[9,10,11,12], and diminished resilience to subsequent enteric infections[13]. This cycle can occur even in the absence of overt diarrhea[14,15]. These subclinical infections are believed to perpetuate intestinal damage and restrict healthy growth[18]

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