Public health laboratory capacity

A resilient health system is able to generate a robust increase in essential services. When a pandemic, epidemic or other infectious disease occurs, identifying, containing and controlling it requires the scale up of laboratory services. This was evident during the COVID-19 pandemic, with diagnostic testing and genomic sequencing services under stress at the beginning of the pandemic. Genomic surveillance of SARS-CoV-2 (the virus that causes COVID-19) allows detection, monitoring and assessment of new virus variants (ECDC, 2021[1]). When it replicates, SARS-CoV-2 can manifest changes in its genome. Scaled up capacity is especially important when mutations are associated with changes in transmissibility or the effectiveness of countermeasures such as vaccines. The cost of sequencing has fallen over time but still requires substantial investment in staff, equipment and bioinformatics infrastructure.

A review of capacity for SARS-CoV-2 in EU countries identified most did not have the capacity to sequence the 5-10% of positive specimens suggested by the EC in January 2021 (ECDC, 2021[2]). Nineteen (of 27 EU/EEA countries) were sequencing less than 1% of positive specimens at the beginning of 2021. During 2021, there was a rapid expansion in sequencing: 1.8 million SARS-CoV-2 samples were sequenced in the 27 EU countries, Norway and Iceland. This was a 15-fold increase over 2020 and the percentage of positive tests sequenced increased from less than 1% in 2020 to an average of 7% across countries (4.3% weighted) in 2021 (Figure 8.5). There was, however, wide variation between countries. Six EU countries sequenced 10% or more of new cases and two EU countries sequenced less than 1%.

Sequencing an appropriate proportion of new cases over time also matters. The ECDC issued guidance for representative SARS-CoV-2 monitoring using genomic surveillance (ECDC, 2021[1]). Three countries met this guidance over 2021 for all weeks (Denmark, the Netherlands and Spain), while eight countries met this guidance for less than 10 weeks over 2021 (Figure 8.6). More countries were able to meet the thresholds in the later months of 2021 than earlier, demonstrating an increase in sequencing capacity.

Despite a rapid expansion in sequencing capacity in 2021, further improvements are crucial to ensure better and more timely evidence for decision-making in health systems and beyond. The ability to rapidly undertake sequencing and share the results is important to effective global responses.

References

[2] ECDC (2021), Detection and characterisation capability and capacity for SARS-CoV-2 variants within the EU/EEA, https://www.ecdc.europa.eu/en/publications-data/detection-and-characterisation-capability-and-capacity-sars-cov-2-variants.

[1] ECDC (2021), Guidance for representative and targeted genomic SARS-CoV-2 monitoring, https://www.ecdc.europa.eu/en/publications-data/guidance-representative-and-targeted-genomic-sars-cov-2-monitoring.

Metadata, Legal and Rights

This document, as well as any data and map included herein, are without prejudice to the status of or sovereignty over any territory, to the delimitation of international frontiers and boundaries and to the name of any territory, city or area. Extracts from publications may be subject to additional disclaimers, which are set out in the complete version of the publication, available at the link provided.

© OECD/European Union 2022

The use of this work, whether digital or print, is governed by the Terms and Conditions to be found at https://www.oecd.org/termsandconditions.