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Published on: April 27, 2011
Retrospective analysis of possible associations between Pneumocystis spp. and five immunosuppressive viral pathogens
Branislav Kureljušić1, Vesna Milićević1, Dimitrije Glišić1
1Institute of Veterinary Medicine of Serbia, Janisa Janulisa 14, 11000, Belgrade, Serbia.
Abstract:
Pneumocystis spp. proliferate under immunosuppressive conditions in mammalian lungs, and several pathogens have been discussed as potential contributors to fungal proliferation. This study aimed to investigate the possible associations between Pneumocystis spp. and immunosuppressive viruses in Serbian wild mammals. A total of 108 wild carnivores - including golden jackals (Canis aureus), Eurasian badgers (Meles meles), and red foxes (Vulpes vulpes) - were collected from Veliko Gradište, Stara Pazova, and Ugrinovci during the 2022/2023 hunting season. The presence of Pneumocystis spp., canine parvovirus 2 (CPV-2), pseudorabies virus (PRV), canine distemper virus, canine coronavirus, and canine herpesvirus was assessed using conventional PCR and real-time PCR. Pneumocystis spp. were detected in 40.7% of all sampled animals (20/60 golden jackals, 4/9 Eurasian badgers, and 20/39 red foxes). CPV-2 was detected in three golden jackals (5.0% of tested golden jackals, 2.8% of all sampled animals), while PRV was found in two golden jackals (3.3% of tested golden jackals) and three red foxes (7.7% of tested red foxes; overall 4.6%). Co-infections of Pneumocystis spp. and PRV were identified in one golden jackal and two red foxes, while Pneumocystis spp. were absent in CPV-2-positive animals. All samples tested negative for other viral pathogens. No significant differences in the pathogens' presence were observed between age groups, sexes, or sampling locations. The mean threshold cycle (Ct) values were 33.6 for Pneumocystis spp., 24.0 for CPV-2, and 31.3 for PRV. While the CPV-2 and PRV viral loads were high in co-infected samples, Pneumocystis spp. loads were associated only with subclinical infections. These findings suggest that the examined viral pathogens were unlikely to play a significant role in the development of clinically apparent Pneumocystis pneumonia, despite their potential to modulate or impair immune function. However, given the low viral prevalence and the lack of histopathological evaluation, a potential contribution of viral immunomodulation cannot be completely excluded.
Insights
This study found Pneumocystis spp. in 40.7% of Serbian wild carnivores, but co-infections with canine parvovirus 2 (CPV-2) or pseudorabies virus (PRV) were rare and did not correlate with severe Pneumocystis pneumonia.
Area of Science:
- Veterinary Medicine
- Wildlife Ecology
- Mycology
- Virology
Background:
- Pneumocystis spp. are opportunistic fungi causing pneumonia in immunosuppressed mammals.
- Several viral pathogens are suspected of contributing to Pneumocystis proliferation.
- The role of viruses in Pneumocystis pneumonia in wild carnivores remains unclear.
Purpose of the Study:
- To investigate associations between Pneumocystis spp. and common immunosuppressive viruses in Serbian wild carnivores.
- To determine the prevalence of Pneumocystis spp., canine parvovirus 2 (CPV-2), and pseudorabies virus (PRV) in golden jackals, Eurasian badgers, and red foxes.
- To assess potential co-infections and their impact on Pneumocystis spp. loads.
Main Methods:
- Collected 108 wild carnivores (golden jackals, Eurasian badgers, red foxes) from Serbia.
- Utilized conventional and real-time PCR to detect Pneumocystis spp., CPV-2, PRV, canine distemper virus, canine coronavirus, and canine herpesvirus.
- Analyzed pathogen prevalence, co-infections, and pathogen loads (Ct values) across different animal groups and locations.
Main Results:
- Pneumocystis spp. detected in 40.7% of animals; CPV-2 in 2.8%; PRV in 4.6%.
- Co-infections observed: Pneumocystis spp. and PRV in three animals; Pneumocystis spp. absent in CPV-2 positive animals.
- Pneumocystis spp. loads were associated with subclinical infections, while CPV-2 and PRV loads were high in co-infected samples.
Conclusions:
- The studied viruses (CPV-2, PRV) are unlikely to be major drivers of clinically apparent Pneumocystis pneumonia in these wild carnivores.
- Viral immunomodulation's role in Pneumocystis pneumonia cannot be entirely excluded due to low viral prevalence and lack of histopathology.
- Further research is needed to fully understand virus-fungus interactions in wildlife immunology.
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