Institute of Veterinary Pathology, Leipzig University, Leipzig, Germany.
Institute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany.
Sci Rep. 2024 Apr 16;14(1):8766. doi: 10.1038/s41598-024-59239-5.
As immunohistochemistry is valuable for determining tissue and cell tropism of avian influenza viruses (AIV), but time-consuming, an artificial intelligence-based workflow was developed to automate the AIV antigen quantification. Organ samples from experimental AIV infections including brain, heart, lung and spleen on one slide, and liver and kidney on another slide were stained for influenza A-matrixprotein and analyzed with QuPath: Random trees algorithms were trained to identify the organs on each slide, followed by threshold-based quantification of the immunoreactive area. The algorithms were trained and tested on two different slide sets, then retrained on both and validated on a third set. Except for the kidney, the best algorithms for organ selection correctly identified the largest proportion of the organ area. For most organs, the immunoreactive area assessed following organ selection was significantly and positively correlated to a manually assessed semiquantitative score. In the validation set, intravenously infected chickens showed a generally higher percentage of immunoreactive area than chickens infected oculonasally. Variability between the slide sets and a similar tissue texture of some organs limited the ability of the algorithms to select certain organs. Generally, suitable correlations of the immunoreactivity data results were achieved, facilitating high-throughput analysis of AIV tissue tropism.
由于免疫组织化学对于确定禽流感病毒(AIV)的组织和细胞趋向性很有价值,但耗时较长,因此开发了一种基于人工智能的工作流程来自动进行 AIV 抗原定量。在一张载玻片上包括脑、心、肺和脾,在另一张载玻片上包括肝和肾,对实验性 AIV 感染的器官样本进行流感 A-基质蛋白染色,并使用 QuPath 进行分析:随机树算法被训练来识别每张载玻片上的器官,然后基于阈值对免疫反应区域进行定量。这些算法在两个不同的载玻片集上进行了训练和测试,然后在两个集上重新进行了训练,并在第三个集上进行了验证。除了肾脏,用于器官选择的最佳算法正确地识别了最大比例的器官区域。对于大多数器官,在进行器官选择后评估的免疫反应区域与手动评估的半定量评分呈显著正相关。在验证集中,静脉感染的鸡比经眼鼻感染的鸡显示出更高比例的免疫反应区域。载玻片集之间的差异以及某些器官的相似组织纹理限制了算法选择某些器官的能力。总的来说,实现了免疫反应数据结果的适当相关性,从而促进了 AIV 组织趋向性的高通量分析。