# Immunohistochemical investigation of canine lymph nodes collected during a rabies outbreak in South Africa

**Authors:** Redwan Rahmat, Matthijs F. Ravensberg, Debby Schipper, Keshia Kroh, Edwin J.B. Veldhuis Kroeze, Thijs Kuiken, Claude Sabeta, Corine H. GeurtsvanKessel, Carmen W.E. Embregts

PMC · DOI: 10.1099/jgv.0.002166 · The Journal of General Virology · 2025-11-06

## TL;DR

This study examines immune changes in dogs during a rabies outbreak in South Africa using lymph node samples and histological analysis.

## Contribution

A reproducible framework for quantifying immune cell organization in field-collected tissues during natural rabies virus exposure.

## Key findings

- Rabies virus RNA was detected in 27 out of 36 rabies-suspect dogs.
- Germinal-center density and marker-based metrics did not differ between RABV+ and RABV− dogs.
- Outbreak dogs showed generally lower values compared to healthy reference dogs.

## Abstract

Rabies is a fatal zoonosis that impairs host immune function, yet effects on peripheral lymphoid architecture are poorly defined. During a 2021–2022 rabies virus (RABV) outbreak in South Africa, we collected cervical lymph nodes from 36 rabies-suspect dogs; RABV RNA was detected in 27. Canine distemper virus RNA was detected in a subset across both RABV-positive (RABV+) and RABV-negative (RABV−) groups and was not associated with clinical-sign count. We set up a computer-assisted histological analysis tool to quantify germinal-centre (GC) nucleus density and immunohistochemistry for CD20, PNA and IBA1 to profile B cells, GC activity and macrophages. Within the outbreak cohort, GC density and marker-based metrics did not differ between RABV+ and RABV− dogs. Two healthy dogs were included as reference tissues; values in outbreak dogs were generally lower, but these contrasts are contextual given the limited, non-matched controls. This study provides a reproducible framework for quantifying immune cell organization in field-collected tissues during natural RABV exposure and highlights the need for larger, geographically matched control groups and complementary functional immune measurements.

## Linked entities

- **Proteins:** MS4A1 (membrane spanning 4-domains A1), LOC112777417 (galactose-binding lectin), AIF1 (allograft inflammatory factor 1)
- **Diseases:** rabies (MONDO:0019173), canine distemper (MONDO:0025397)
- **Species:** Canis lupus familiaris (taxon 9615)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12591502/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12591502/full.md

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Source: https://tomesphere.com/paper/PMC12591502