Abstract

Acute gastrointestinal infection (AGI) represents a significant public health concern. To control and treat AGI, it is critical to quickly and accurately identify its causes. The use of novel multiplex molecular assays for pathogen detection and identification provides a unique opportunity to improve pathogen detection, and better understand risk factors and burden associated with AGI in the community. In this study, de-identified results from BioFire® FilmArray® Gastrointestinal (GI) Panel were obtained from January 01, 2016 to October 31, 2018 through BioFire® Syndromic Trends (Trend), a cloud database. Data was analyzed to describe the occurrence of pathogens causing AGI across United States sites and the relative rankings of pathogens monitored by FoodNet, a CDC surveillance system were compared. During the period of the study, the number of tests performed increased 10-fold and overall, 42.6% were positive for one or more pathogens. Seventy percent of the detections were bacteria, 25% viruses, and 4% parasites. Clostridium difficile, enteropathogenic Escherichia coli (EPEC) and norovirus were the most frequently detected pathogens. Seasonality was observed for several pathogens including astrovirus, rotavirus, and norovirus, EPEC, and Campylobacter. The co-detection rate was 10.2%. Enterotoxigenic E. coli (ETEC), Plesiomonas shigelloides, enteroaggregative E. coli (EAEC), and Entamoeba histolytica were detected with another pathogen over 60% of the time, while less than 30% of C. difficile and Cyclospora cayetanensis were detected with another pathogen. Positive correlations among co-detections were found between Shigella/Enteroinvasive E. coli with E. histolytica, and ETEC with EAEC. Overall, the relative ranking of detections for the eight GI pathogens monitored by FoodNet and BioFire Trend were similar for five of them. AGI data from BioFire Trend is available in near real-time and represents a rich data source for the study of disease burden and GI pathogen circulation in the community, especially for those pathogens not often targeted by surveillance.

Highlights

  • Every year around the world, 1.5 to 2.5 million children under the age of five die from diarrhea, one of the main symptoms of acute gastrointestinal infections (AGI) [1]

  • Enterotoxigenic E. coli (ETEC), Plesiomonas shigelloides, enteroaggregative E. coli (EAEC), and Entamoeba histolytica were detected with another pathogen over 60% of the time, while less than 30% of C. difficile and Cyclospora cayetanensis were detected with another pathogen

  • Clostridium difficile (30.4%; 15,257/50,192), Enteropathogenic Escherichia coli (EPEC) (15.6%; 7,848/50,192), and norovirus (11.1%; 5,567/50,192;), represented over half (57.1%) of the pathogens detected during the 34 months of the study (Fig 2)

Read more

Summary

Introduction

Every year around the world, 1.5 to 2.5 million children under the age of five die from diarrhea, one of the main symptoms of acute gastrointestinal infections (AGI) [1]. In the United States, AGI accounts for 178.8 million cases a year [2], representing a significant burden to public health. To effectively control and reduce the disease burden associated with AGI, it is critical to understand which agent is causing the disease, how frequently and when infection occurs in the population, and the potential sources of exposure. Surveillance systems often rely on cases that are reported to public health authorities to compile and analyze this information and monitor the occurrence of illnesses in a population. Among the critical events that must occur for a disease to be reported to authorities is the identification of the AGI agent(s) by clinical laboratories [3]. The quick and accurate identification of the cause of illness is essential for the effective treatment of AGI patients, which can result in shorter hospital stays, appropriate use of antimicrobials, avoidance of unnecessary isolation of patients, and cost savings [4, 5]

Methods
Results
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