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Yale Researchers Use Single-Cell Analysis and Machine Learning to Identify Major COVID-19 Target

By HospiMedica International staff writers
Posted on 30 May 2020
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Image: The Respiratory Epithelium (Photo courtesy of Wikimedia Commons)
Image: The Respiratory Epithelium (Photo courtesy of Wikimedia Commons)
Scientists at the Yale School of Medicine (New Haven, CT, USA) are using single-cell RNA sequencing of infected human bronchial epithelial cells (HBECs) to learn how SARS-CoV-2 infects and alters healthy cells.

In the study, the scientists identified ciliated cells as the major target of SARS-CoV-2 infection. The bronchial epithelium acts as a protective barrier against allergens and pathogens. Cilia removes mucus and other particles from the respiratory tract. Their findings offer insight into how the virus causes disease. The scientists infected HBECs in an air-liquid interface with SARS-CoV-2. Over a period of three days, they used single-cell RNA sequencing to identify signatures of infection dynamics such as the number of infected cells across cell types, and whether SARS-CoV-2 activated an immune response in infected cells.

The scientists utilized advanced algorithms to develop working hypotheses and used electron microscopy to learn about the structural basis of the virus and target cells. These observations provide insights about host-virus interaction to measure SARS-CoV-2 cell tropism, or the ability of the virus to infect different cell types, as identified by the algorithms. After three days, thousands of cultured cells became infected. The scientists analyzed data from the infected cells along with neighboring bystander cells. They observed ciliated cells were 83% of the infected cells. These cells were the first and primary source of infection throughout the study. The virus also targeted other epithelial cell types including basal and club cells. The goblet, neuroendocrine, tuft cells, and ionocytes were less likely to become infected.

The gene signatures revealed an innate immune response associated with a protein called Interleukin 6 (IL-6). The analysis also showed a shift in the polyadenylated viral transcripts. Lastly, the (uninfected) bystander cells also showed an immune response, likely due to signals from the infected cells. Pulling from tens of thousands of genes, the algorithms locate the genetic differences between infected and non-infected cells. In the next phase of this study, the scientists will examine the severity of SARS-CoV-2 compared to other types of coronaviruses, and conduct tests in animal models.

“Machine learning allows us to generate hypotheses. It’s a different way of doing science. We go in with as few hypotheses as possible. Measure everything we can measure, and the algorithms present the hypothesis to us,” said senior author David van Dijk, PhD, an assistant professor of medicine in the Section of Cardiovascular Medicine and Computer Science.

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Yale School of Medicine


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