Phenotypic and Transcriptional Changes of Pulmonary Immune Responses in Dogs Following Canine Distemper Virus Infection.
Elisa ChludzinskiJohanna KlemensMałgorzata CiurkiewiczRobert GeffersPauline PöpperlMelanie StoffDai-Lun ShinGeorg HerrlerAndreas BeinekePublished in: International journal of molecular sciences (2022)
Canine distemper virus (CDV), a morbillivirus within the family Paramyxoviridae , is a highly contagious infectious agent causing a multisystemic, devastating disease in a broad range of host species, characterized by severe immunosuppression, encephalitis and pneumonia. The present study aimed at investigating pulmonary immune responses of CDV-infected dogs in situ using immunohistochemistry and whole transcriptome analyses by bulk RNA sequencing. Spatiotemporal analysis of phenotypic changes revealed pulmonary immune responses primarily driven by MHC-II + , Iba-1 + and CD204 + innate immune cells during acute and subacute infection phases, which paralleled pathologic lesion development and coincided with high viral loads in CDV-infected lungs. CD20 + B cell numbers initially declined, followed by lymphoid repopulation in the advanced disease phase. Transcriptome analysis demonstrated an increased expression of transcripts related to innate immunity, antiviral defense mechanisms, type I interferon responses and regulation of cell death in the lung of CDV-infected dogs. Molecular analyses also revealed disturbed cytokine responses with a pro-inflammatory M1 macrophage polarization and impaired mucociliary defense in CDV-infected lungs. The exploratory study provides detailed data on CDV-related pulmonary immune responses, expanding the list of immunologic parameters potentially leading to viral elimination and virus-induced pulmonary immunopathology in canine distemper.
Keyphrases
- immune response
- pulmonary hypertension
- dendritic cells
- single cell
- cell death
- toll like receptor
- gene expression
- sars cov
- poor prognosis
- liver failure
- dna methylation
- early onset
- neoadjuvant chemotherapy
- respiratory failure
- rna seq
- radiation therapy
- intensive care unit
- artificial intelligence
- genome wide
- nk cells
- aortic dissection