Objective
Diarrheal diseases are a leading cause of morbidity and mortality worldwide, but the etiology of diarrhea and its relationship to nutritional outcomes in resource-limited settings is poorly defined. We sought to determine the etiology of community-acquired diarrhea in Tanzanian infants, and to assess the association with anthropometrics and novel intestinal biomarkers.
Methods
A convenience sample of infants in a trial of zinc and/or multivitamin supplementation in Tanzania was selected. Subjects were enrolled at age 6 weeks and followed for 18 months. Stool samples were obtained from children with acute diarrhea. A novel, PCR-based TaqMan array was used to screen stool for 15 enteropathogens. A subset of subjects had serum gastrointestinal biomarkers measured.
Results
123 subjects with diarrhea were enrolled. The mean ± SD age at stool sample collection was 12.4 ± 3.9 months. Thirty-five enteropathogens were identified in 34 (27.6%) subjects: 11 rotavirus, 9 Cryptosporidium spp, 7 Shigella spp, 3 Campylobacter jejuni / coli, 3 ST-enterotoxigenic E. coli and 2 enteropathogenic E. coli. Subjects with any identified enteropathogen had significantly lower weight-for-length z scores (−0.55 ± 1.10 vs. 0.03 ± 1.30, p=0.03) at the final clinic visit, compared to those without an identified pathogen. Fifty of the 123 subjects (40.7%) had serum analyzed for antibodies to LPS and flagellin. Subjects with any identified enteropathogen had lower IgA antibodies to LPS (0.75 ± 0.27 vs. 1.13 ± 0.77, p=0.01) and flagellin (0.52 ± 0.16 vs. 0.73 ± 0.47, p=0.02), compared to those without an identified pathogen.
Conclusion
This quantitative PCR method may allow identification of enteropathogens that place children at higher risk for suboptimal growth. IgA anti-LPS and flagellin antibodies hold promise as emerging intestinal biomarkers.