Abstract

Background: Respiratory Syncytial Virus (RSV) is the major cause of severe acute respiratory tract illness in young children worldwide and a main pathogen for the elderly and immune-compromised people. In the absence of vaccines or effective treatments, a better characterization of the pathogenesis of RSV infection is required. To date, the pathophysiology of the disease and its diagnosis has mostly relied on chest X-ray and genome detection in nasopharyngeal swabs. The development of new imaging approaches is instrumental to further the description of RSV spread, virus–host interactions and related acute respiratory disease, at the level of the entire lung. Methods: By combining tissue clearing, 3D microscopy and image processing, we developed a novel visualization tool of RSV infection in undissected mouse lungs. Results: Whole tissue analysis allowed the identification of infected cell subtypes, based on both morphological traits and position within the cellular network. Furthermore, 3D imaging was also valuable to detect the cytoplasmic viral factories, also called inclusion bodies, a hallmark of RSV infection. Conclusions: Whole lung clearing and 3D deep imaging represents an unprecedented visualization method of infected lungs to allow insight into RSV pathophysiology and improve the 2D histology analyses.

Highlights

  • The respiratory syncytial virus (RSV) belongs to the Mononegavirales order and the Pneumoviridae family [1]

  • We recently explored the distribution of Respiratory Syncytial Virus (RSV) infection cells in the nasal cavity of infected mouse, through development of tissue clearing and 3D light sheet imaging [19]

  • Our results describe novel visualization tools opening the way to the study of pathogen co-infections, comparison of RSV tropism in different physiological conditions or host pathogen interaction

Read more

Summary

Introduction

The respiratory syncytial virus (RSV) belongs to the Mononegavirales order and the Pneumoviridae family [1] It is the most common cause of severe respiratory tract disease in young children worldwide and is responsible for millions of hospitalizations and thousands of deaths per year [2,3]. Recent evidence demonstrated the capacity of RSV to replicate in neurons both in vitro in N2a neuronal cells [17,18] and in vivo in the olfactory neurons of the olfactory mucosa [19]. In these cases, infected cells have been identified by immunostaining of RSV antigens. Conclusions: Whole lung clearing and 3D deep imaging represents an unprecedented visualization method of infected lungs to allow insight into RSV pathophysiology and improve the 2D histology analyses

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call