Persistent G. lamblia impairs growth in a murine malnutrition model

J Clin Invest. 2013 Jun;123(6):2672-84. doi: 10.1172/JCI67294.


Giardia lamblia infections are nearly universal among children in low-income countries and are syndemic with the triumvirate of malnutrition, diarrhea, and developmental growth delays. Amidst the morass of early childhood enteropathogen exposures in these populations, G. lamblia–specific associations with persistent diarrhea, cognitive deficits, stunting, and nutrient deficiencies have demonstrated conflicting results, placing endemic pediatric giardiasis in a state of equipoise. Many infections in endemic settings appear to be asymptomatic/ subclinical, further contributing to uncertainty regarding a causal link between G. lamblia infection and developmental delay. We used G. lamblia H3 cyst infection in a weaned mouse model of malnutrition to demonstrate that persistent giardiasis leads to epithelial cell apoptosis and crypt hyperplasia. Infection was associated with a Th2-biased inflammatory response and impaired growth. Malnutrition accentuated the severity of these growth decrements. Faltering malnourished mice exhibited impaired compensatory responses following infection and demonstrated an absence of crypt hyperplasia and subsequently blunted villus architecture. Concomitantly, severe malnutrition prevented increases in B220+ cells in the lamina propria as well as mucosal Il4 and Il5 mRNA in response to infection. These findings add insight into the potential role of G. lamblia as a "stunting" pathogen and suggest that, similarly, malnourished children may be at increased risk of G. lamblia– potentiated growth decrements.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Disease Models, Animal
  • Duodenum / immunology
  • Duodenum / metabolism
  • Duodenum / parasitology
  • Eosinophils / immunology
  • Eosinophils / parasitology
  • Gene Expression
  • Giardia lamblia / immunology*
  • Giardiasis / complications*
  • Giardiasis / immunology
  • Giardiasis / parasitology
  • Growth Disorders / immunology
  • Growth Disorders / parasitology*
  • Host-Parasite Interactions
  • Humans
  • Ileum / immunology
  • Ileum / parasitology
  • Ileum / pathology
  • Interleukin-4 / genetics
  • Interleukin-4 / metabolism
  • Interleukin-5 / genetics
  • Interleukin-5 / metabolism
  • Intestinal Mucosa / parasitology
  • Intestinal Mucosa / pathology
  • Lymphocyte Count
  • Male
  • Malnutrition / complications*
  • Malnutrition / immunology
  • Malnutrition / parasitology
  • Mice
  • Mice, Inbred C57BL
  • Parasite Load


  • Interleukin-5
  • Interleukin-4