bioRxiv Science⌕ Search

bioRxiv · 10.1101/2023.05.04.539354

EXTRANEURAL RABIES VIRUS INFECTION LEADS TO TISSUE DAMAGE AND CELL DEATH IN MICE

Abstract

Rabies, a fatal neurological disease caused by Lyssavirus rabies (RABV), poses a significant threat to public health globally. Despite extensive studies on RABV-induced neuropathology, the involvement of extraneural organs during rabies pathogenesis and the tropisms of wild-type strains to different organs remain largely unknown. Here, we investigated the tropism of a dog and bat RABV variant to three different extraneural tissues (kidneys, lungs and liver) and characterized cellular and tissue damage associated with infection in mice over 30 days. Our results reveal that RABV may have a tropism for the kidneys and cause tissue-specific cellular damage. Furthermore, we propose that RABV spreads to extraneural tissues simultaneously with central nervous system (CNS) infection. Understanding the involvement of extraneural organs in rabies pathogenesis may contribute to the development of effective treatment strategies of this fatal disease. AUTHOR SUMMARYRabies is a lethal viral infection that targets the nervous system and generally can be transmitted to humans by bites of infected animals. While there has been significant research focused on how the virus damages the brain, little is known about how the infection affects other organs in the periphery. To address this knowledge gap, we conducted an experimental study to investigate the effects of two distinct wild strains of the virus, one isolated from dogs and the other from bats, on the lungs, liver, and kidneys in mice model of infection. Our findings suggest that the rabies virus infection leads to cell death and produces specific lesions in each of these organs, and we hypothesize that rabies virus may spread to these tissues at the same time as the brain, which possible contributes to the disease outcome. These findings enhance our understanding on how rabies virus targets organs outside the nervous system and its pathology in these different systems.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Leal Rodrigues, E. D., Pacheco da Silva, V., Bastos Chaves, V. G., de Sousa Moraes, C. N., de Souza Pereira, S., Nogueira Lima, A. L., Fernandes Barbosa Coelho, T., da Costa Vasconcelos, P. F., Ribeiro Cruz, A. C., Medeiros Neves Casseb, L.. 2023-05-04. EXTRANEURAL RABIES VIRUS INFECTION LEADS TO TISSUE DAMAGE AND CELL DEATH IN MICE. https://doi.org/10.1101/2023.05.04.539354

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Common viral infections seed regionally distinct resident memory T cells in the human CNS

T cells persist in the central nervous system (CNS) and can drive both protection and neurological disease. How these cells are organized in humans and what they recognize is largely unknown. Here, we profiled CD8 T cells across anatomically distinct CNS regions, obtained through on-site autopsies and temporal lobe resection surgeries, using single-cell RNA sequencing, paired T cell receptor sequencing, and DNA-barcoded tetramers. Resident memory T cells (TRM) specific for Epstein-Barr virus, cytomegalovirus, influenza A, and SARS-CoV-2 were identified across CNS compartments. Anatomical location was the strongest correlate of TRM cell state, with leptomeningeal cells adopting a cytokine-poised TRM program, whereas brain TRM cells were transcriptionally restrained. Cells of the same clonotype spanned tissues yet adopted local transcriptional states. Viral specificity added another layer of TRM heterogeneity with GZMK/GZMA-expressing EBV-specific populations and interferon-stimulated gene signatures in SARS-CoV-2 and Influenza A-specific cells. The human CNS thus harbors regionally distinct CD8+ TRM shaped by common viral exposures.

immunology↗

A regulatory T cell signature provides a shared molecular basis for the therapeutic window of opportunity in rheumatic disease

Rheumatic diseases, including rheumatoid arthritis (RA), spondyloarthritis (SpA) and osteoarthritis (OA), show distinct phenotypes yet respond to overlapping therapies, implicating shared immune mechanisms. In the Transimmunom cohort, we profiled peripheral blood from 240 individuals (47 healthy, 44 OA, 91 RA, 58 SpA) across deep immunophenotyping, immunoproteomics and Treg-Teff transcriptomics. Single-layer analyses revealed broader Treg than Teff remodeling, along with a shared pattern of reduced activated Tregs and expanded Helios+ Tregs across all diseases, alongside a decrease in functional Treg subpopulations, including CTLA4+ and CD45RA- Tregs. In RA specifically, LAG3+ Tregs were also expanded. Combining omics layers outperformed single-layer approaches for disease classification. Among individual layers, Treg transcriptomes were most discriminative, and integration uncovered disease-specific programs. Unsupervised clustering identified a cross-disease cluster independent of activity, treatment and age, mapping to early disease (<= years) and dominated by a Treg dysfunction-associated program. These results provide a biological rationale for the therapeutic "window of opportunity" concept and duration-stratified Treg-directed trials.

immunology↗

Inhibitory Fc Receptor sets a time limit on macrophage response to IgG

Antibodies engage both activating Fc Receptors and the inhibitory receptor Fc{gamma}RIIB. Why macrophages need a dedicated inhibitory receptor rather than simply tuning activating receptor signaling is unclear. Using DNA-based chimeric receptors and in silico modeling, we independently controlled activating and inhibitory Fc Receptors. We found that Fc{gamma}RIIB imposed a time limit on macrophage phagocytosis and ERK signaling. The time limit is due to activating Fc Receptors converting PI(4,5)P2 to PI(3,4,5)P3, which is subsequently converted to PI(3,4)P2 by Fc{gamma}RIIB. This leads to a pulse of active signaling, which is sufficient for phagocytosis of small bacteria-sized targets but not phagocytosis of large targets and TNF secretion. Unlike engaging Fc{gamma}RIIB, reducing activating Fc Receptor signaling decreased initiation of phagocytosis, the speed of PI(3,4,5)P3 generation, and the amplitude of ERK signaling. Our results demonstrate that Fc{gamma}RIIB controls the duration of IgG signaling, while the activating Fc Receptors control sensitivity.

immunology↗