Abstract

Boid Inclusion Body Disease (BIBD) is a potentially fatal disease reported in captive boid snakes worldwide that is caused by reptarenavirus infection. Although the detection of intracytoplasmic inclusion bodies (IB) in blood cells serves as the gold standard for the ante mortem diagnosis of BIBD, the mechanisms underlying IB formation and the pathogenesis of BIBD are unknown. Knowledge on the reptile immune system is sparse compared to the mammalian counterpart, and in particular the response towards reptarenavirus infection is practically unknown. Herein, we investigated a breeding collection of 70 Boa constrictor snakes for BIBD, reptarenavirus viraemia, anti-reptarenavirus IgM and IgY antibodies, and population parameters. Using NGS and RT-PCR on pooled blood samples of snakes with and without BIBD, we could identify three different reptarenavirus S segments in the collection. The examination of individual samples by RT-PCR indicated that the presence of University of Giessen virus (UGV)-like S segment strongly correlates with IB formation. We could also demonstrate a negative correlation between BIBD and the presence of anti-UGV NP IgY antibodies. Further evidence of an association between antibody response and BIBD is the finding that the level of anti-reptarenavirus antibodies measured by ELISA was lower in snakes with BIBD. Furthermore, female snakes had a significantly lower body weight when they had BIBD. Taken together our findings suggest that the detection of the UGV-/S6-like S segment and the presence of anti-reptarenavirus IgY antibodies might serve as a prognostic tool for predicting the development of BIBD.

Highlights

  • Boid inclusion body disease (BIBD) is a widespread disease of captive boid snakes known since the 1970s [1,2,3]

  • We confirmed the association of the inclusion bodies (IB) with reptarenavirus infection by Reverse transcriptase-polymerase chain reaction (RT-PCR), considering this as further proof of the disease and evidence that affected animals will eventually develop clinical signs [13]

  • We investigated the association between BIBD, pathogen detection, population parameters and serological findings in a cohort of snakes from one breeding colony

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Summary

Objectives

As we aimed to study the immune response using NP as the antigen, we used the S segment primers of our previous study [1] in RT-PCRs to screen the pools, and identified two additional S segments (S5-like and TSMV-2) within the pools

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Results
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