# Attenuation of canine distemper virus leads to a potent antiviral innate immune response with restricted infection of alveolar macrophages

## TL;DR

This study compares how two strains of canine distemper virus affect alveolar macrophages, revealing differences in immune response and virus spread.

## Contribution

The first transcriptomic analysis of primary alveolar macrophages during early morbillivirus infection.

## Key findings

- CDV R252 causes higher infection and virus production in alveolar macrophages compared to the attenuated Ond strain.
- CDV Ond triggers stronger pro-inflammatory and cell death pathways, including increased apoptosis and interferon signaling.
- Transcriptome changes suggest CDV infection disrupts normal alveolar macrophage functions and homeostasis.

## Abstract

Canine distemper virus (CDV, species Morbillivirus canis) is a highly contagious pathogen with a broad host range among carnivores. In common with measles virus, alveolar macrophages (AMs) are among the first target cells of infection in the respiratory tract. Therefore, in vitro infections of primary canine AMs were performed with the attenuated Onderstepoort (Ond) and field R252 strain of CDV over a period of 6 days. This showed that AMs are permissive to CDV infection and that such infections are productive with respect to the release of new virus particles. Phenotypic differences were observed over the entire course of the experiment, as higher levels of infection and virus production were observed in CDV R252-infected AMs, while infection with CDV Ond resulted in more prominent cytopathic effects, including syncytium formation. Transcriptome analyses of samples from 1 day post-infection via total RNA sequencing demonstrated further marked differences with respect to the pro-inflammatory response and cell death pathways. CDV Ond-infected AMs exhibited robust induction of pro-inflammatory mediators including type I interferon-related signaling pathways, whereas CDV R252-infected cells showed much weaker expression of these pathways. These transcriptomic differences were further highlighted by the detection of the highest rates of cell apoptosis and lactate dehydrogenase activity in the supernatants of CDV Ond-infected AM cultures over the entire course of the experiment. In addition, transcriptome differences indicate disturbances of homeostatic AM functions associated with CDV infection. These results provide insights into early events in the pathogenesis of CDV infection and mechanisms underlying vaccine strain attenuation.

Morbilliviruses, including canine distemper virus (CDV) and human measles virus, cause severe systemic disease with respiratory distress, immunosuppression, and neurologic signs. While natural infection in dogs has become rare due to efficient vaccination, outbreaks in wildlife populations can be devastating, and concerns about zoonotic potential of CDV have been raised. The impact of CDV infection on the transcriptome of alveolar macrophages has not been elucidated thus far. Knowledge about early events in CDV pathogenesis and phenotypic consequences of vaccine attenuation is therefore necessary to protect endangered wildlife populations and might furthermore serve as a model for human measles. This study presents the first transcriptomic analyses of primary AMs during the initial phase of morbillivirus infection. These results provide insights into early events in the pathogenesis of CDV infection and mechanisms serving to restrict the spread of an attenuated virus strain.