Fig. 1: Positivity rates of respiratory pathogens in ambient air in nursery locations (red) compared to clinical samples from a local hospital (black/grey). | Nature Communications

Fig. 1: Positivity rates of respiratory pathogens in ambient air in nursery locations (red) compared to clinical samples from a local hospital (black/grey).

From: Indoor air surveillance and factors associated with respiratory pathogen detection in community settings in Belgium

Fig. 1

Each panel represents qPCR test results of one of the 29 targeted pathogens, plotted by sampling date. Each pathogen which was positive in at least one air sample is shown. For SARS-CoV-2, the TaqPath results are shown. The individual red datapoints represent the positive and negative ambient air samples taken in a nursery (0 = negative, 1 = positive). This was the most stable age group regarding sampling frequency, occupancy and the continued presence of the same group of individuals (Supplementary Fig. 1). Red lines and shaded areas show a corresponding LOcally weEighted Scatterplot Smoothing (LOESS) regression of the positivity rate for each pathogen with 95% confidence intervals. We included 121 air samples. For comparison, we retrieved the 206 results of the same 29 pathogen multiplex qPCR respiratory panel, performed in 0–3 year old children with respiratory infections at University Hospitals Leuven between October 2021 and May 2022. This hospital is adjacent to the nursery. Individual black datapoints represent the respiratory samples (0 = negative, 1 = positive). Black lines and shaded areas show a corresponding LOESS regression of the positivity rate for each pathogen with 95% confidence intervals. An association between results from both sample types can be observed for SARS-CoV-2 (N positive air samples = 46) and, with much less positive samples, for enterovirus D68 and influenza A virus (N positive air samples = 4 for each). Supplementary Fig. 2 shows the corresponding results for all sites.

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