Abstract

BackgroundAcute diarrhea is a leading cause of morbidity and mortality in children, particularly in those under the age of 5 years. Rotavirus is recognized as the leading cause of acute diarrhea in children, however, the contribution of bacterial pathogens as causative agents varies throughout the world. Here we report a hospital-based prospective study to analyze the characteristics of bacterial pathogens associated with acute diarrhea in children under 5 years of age.MethodsStool samples were collected from 508 patients with acute diarrhea under 5 years of age who presented at our hospital. Nine pathogens were isolated and identified by culturing, serology or PCR, these included Salmonella spp., Shigella spp., Vibrio cholerae, diarrheagenic Escherichia coli (DEC), Aeromonas spp., Plesiomonas spp., Vibrio parahaemolyticus, Campylobacter spp. and Yersinia enterocolitica. Antimicrobial sensitivity tests of these pathogens were conducted. The most commonly detected pathogen, Salmonella spp., was further investigated by PCR and sequencing of antibiotic resistance-related genes.ResultsPathogens were identified in 20.1 % of the 508 samples. The most commonly detected pathogens were Salmonella spp. (8.5 %), followed by DEC (4.7 %), Campylobacter jejuni (3.0 %) and Aeromonas spp. (2.0 %). The resistance rates to ampicillin and tetracycline in Salmonella spp. were >60 %, but were <30 % to cephalosporins and quinolones. More than 50 % of DEC strains displayed resistance to ampicillin, cefotaxime and tetracycline, and 60 % of C. jejuni strains were resistant to ciprofloxacin but highly sensitive to the other antibiotics. Among 12 cephalosporin-resistant Salmonella isolates, TEM-1 and CTX-M-14 determinants were present in two (16.7 %) isolates. PCR screening for plasmid-mediated quinolone resistance genes revealed gyrA mutations in one of three highly quinolone resistant isolates.ConclusionsSalmonella spp., DEC, Campylobacter spp. and Aeromonas spp. were the most commonly detected bacterial pathogens in children under the age of 5 years with acute diarrhea. Our findings indicate that ampicillin and tetracycline are not suitable as first line therapeutic drugs against Salmonella spp. Resistance to third generation cephalosporins and quinolones was also detected. TEM-1 and CTX-M-14 genetic determinants, and gyrA mutations, were the major mechanisms associated with high levels of cephalosporin and quinolone resistance, respectively, in Salmonella isolates.

Highlights

  • Acute diarrhea is a leading cause of morbidity and mortality in children, in those under the age of 5 years

  • A report from Spain indicated that Campylobacter spp. and Salmonella spp. were the primary bacterial pathogens, accounting for 22.2 % and 16.4 % of cases of acute diarrhea in children, respectively [11]

  • There was a significant difference in the duration of diarrhea across the three age groups in the all studied pathogens, whereas no significant difference was observed in the duration of diarrhea and symptoms across the three age groups with Salmonella infection

Read more

Summary

Introduction

Acute diarrhea is a leading cause of morbidity and mortality in children, in those under the age of 5 years. We report a hospital-based prospective study to analyze the characteristics of bacterial pathogens associated with acute diarrhea in children under 5 years of age. Diarrhea is one of the leading causes of morbidity and mortality in children under the age of 5 years worldwide, especially in developing countries such as sub-Saharan Africa and south Asia according to the report of the Global Enteric Multicenter Study (GEMS) [1]. A report from Spain indicated that Campylobacter spp. and Salmonella spp. were the primary bacterial pathogens, accounting for 22.2 % and 16.4 % of cases of acute diarrhea in children, respectively [11]. Whereas in Turkey, Salmonella spp. (25.6 %) and C. jejuni (18.3 %) were the main causes of acute gastroenteritis in children [12]

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call