Abstract

Infectious diseases remain a serious public health concern globally, while the need for reliable and representative surveillance systems remains as acute as ever. The public health surveillance of infectious diseases uses reported positive results from sentinel clinical laboratories or laboratory networks, to survey the presence of specific microbial agents known to constitute a threat to public health in a given population. This monitoring activity is commonly based on a representative fraction of the microbiology laboratories nationally reporting to a single central reference point. However, in recent years a number of clinical microbiology laboratories (CML) have undergone a process of consolidation involving a shift toward laboratory amalgamation and closer real-time informational linkage. This report aims to investigate whether such merging activities might have a potential impact on infectious diseases surveillance. Influenza data was used from Belgian public health surveillance 2014–2017, to evaluate whether national infection trends could be estimated equally as effectively from only just one centralized CML serving the wider Brussels area (LHUB-ULB). The overall comparison reveals that there is a close correlation and representativeness of the LHUB-ULB data to the national and international data for the same time periods, both on epidemiological and molecular grounds. Notably, the effectiveness of the LHUB-ULB surveillance remains partially subject to local regional variations. A subset of the Influenza samples had their whole genome sequenced so that the observed epidemiological trends could be correlated to molecular observations from the same period, as an added-value proposition. These results illustrate that the real-time integration of high-throughput whole genome sequencing platforms available in consolidated CMLs into the public health surveillance system is not only credible but also advantageous to use for future surveillance and prediction purposes. This can be most effective when implemented for automatic detection systems that might include multiple layers of information and timely implementation of control strategies.

Highlights

  • Infectious diseases remain a serious public health concern in industrialized and low- and middle-income countries

  • In our routine surveillance perspective, all patients diagnosed with flu infection by either ImmunoChromatographic Test (ICT), Lateral Flow Chromatography (LFC), molecular diagnostic tests or by cell culture methods are considered as notifiable cases of flu infection

  • To better assess the input of the LHUB-ULB as early warning lab for molecular surveillance, the genomes of 39 randomly selected Influenza A(H1N1)pdm09 isolates obtained from patients attending the emergency room of Saint-Pierre University Hospital, located in Brussels (01/02/2016 to 15/03/2016), were whole genome sequenced and compared to equivalent Influenza A(H1N1)pdm09 sequences deposited at the Epiflu database for the same location and period and against France, Germany, Netherland and UK-derived sequences from the same time period (Table of all isolate IDs used in this study are included in the Supplemental Digital Content 1)

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Summary

Introduction

Infectious diseases remain a serious public health concern in industrialized and low- and middle-income countries. Due to their considerable effect on global human demographics [1, 2] and the economy [3, 4], the public health community has developed many surveillance strategies and systems to improve infectious disease surveillance around the world. Even if diagnostic and computer resources have expanded considerably, infectious disease surveillance remains challenging. One of the more established surveillance strategies, known as traditional public health surveillance of infectious diseases, is the use of reported positive results from sentinel clinical laboratories or laboratory networks to survey the presence of specific microbial agents known to constitute a threat to public health in a given population [7]

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