End-to-end plaque counting and virus titration from laboratory plate images with deep learning

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Abstract

Plaque assays are the gold standard for quantifying infectious virus, yet plaque enumeration is still routinely performed manually, making virus titration labor-intensive, subjective, and difficult to standardize across analysts and laboratories. Existing automated methods primarily address individual tasks, such as plaque segmentation or counting, but do not provide an integrated workflow from plate images to biological quantification. In this paper we present Titra, an end-to-end workflow for automated cytopathic effect (CPE)-based virus titration from standard photographs of plaque assay plates. The workflow combines automatic well detection, plaque segmentation, post-processing for instance separation, plaque counting, and plaque-forming units per millilitre (PFU/mL) estimation within a single web-based platform that also enables experiment management and expert review. The approach was evaluated using images from three viral species (Mayaro virus, Coxsackievirus B3, and vaccinia virus), two plate formats (6- and 12-well), and heterogeneous image acquisition conditions, including both a newly curated dataset and the public VACVPlaque dataset. Automated plaque counts showed strong agreement with manual annotations (Pearson correlation coefficients of 0.98 for MAYV/CVB3 and 0.88 for VACV), while PFU/mL estimates closely matched manual calculations for the MAYV/CVB3 dataset (Pearson r=0.975). Comparative experiments against U-Net, StarDist, HSD-WBR, and PyPlaque demonstrated competitive segmentation and counting performance, with the proposed approach achieving the highest Dice and mAP on the public VACVPlaque dataset.

Author summary

Plaque assays are widely used to measure infectious virus, but manually counting plaques is labor-intensive and can vary between researchers. We developed Titra, an automated workflow that analyzes photographs of plaque assay plates, detects assay wells, counts viral plaques, and calculates virus concentration in plaque-forming units per milliliter (PFU/mL). The workflow also provides a web-based interface that allows researchers to review and correct automated results when needed. We evaluated the approach using images of Mayaro virus, Coxsackievirus B3, and vaccinia virus acquired from different plate formats and imaging conditions. Automated plaque counts showed strong agreement with manual annotations and with counts from four independent experts. Although performance decreased in wells containing highly confluent plaques, these cases were also the most challenging for manual annotation. Our findings demonstrate that automated plaque assay analysis can substantially reduce routine manual effort while preserving expert review and providing reliable virus titration.

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