» Articles » PMID: 36463252

Natural Reservoir Rousettus Aegyptiacus Bat Host Model of Orthonairovirus Infection Identifies Potential Zoonotic Spillover Mechanisms

Overview
Journal Sci Rep
Specialty Science
Date 2022 Dec 3
PMID 36463252
Authors
Affiliations
Soon will be listed here.
Abstract

The human-pathogenic Kasokero virus (KASV; genus Orthonairovirus) has been isolated from the sera of Egyptian rousette bats (ERBs; Rousettus aegyptiacus) captured in Uganda and unengorged Ornithodoros (Reticulinasus) faini ticks collected from the rock crevices of ERB colonies in South Africa and Uganda. Although evidence suggests that KASV is maintained in an enzootic transmission cycle between O. (R.) faini ticks and ERBs with potential for incidental virus spillover to humans through the bite of an infected tick, the vertebrate reservoir status of ERBs for KASV has never been experimentally evaluated. Furthermore, the potential for bat-to-bat and bat-to-human transmission of KASV is unknown. Herein, we inoculate two groups of ERBs with KASV; one group of bats is serially sampled to assess viremia, oral, fecal, and urinary shedding and the second group of bats is serially euthanized to assess virus-tissue tropism. Throughout the study, none of the bats exhibit overt signs of clinical disease. Following the detection of high KASV loads of long duration in blood, oral, fecal, and urine specimens collected from ERBs in the serial sampling group, all bats seroconvert to KASV. ERBs from the serial euthanasia group exhibit high KASV loads indicative of virus replication in the skin at the inoculation site, spleen, and inguinal lymph node tissue, and histopathology and in situ hybridization reveal virus replication in the liver and self-limiting, KASV-induced lymphohistiocytic hepatitis. The results of this study suggest that ERBs are competent, natural vertebrate reservoir hosts for KASV that can sustain viremias of appropriate magnitude and duration to support virus maintenance through bat-tick-bat transmission cycles. Viral shedding data suggests that KASV might also be transmitted bat-to-bat and highlights the potential for KASV spillover to humans through contact with infectious oral secretions, feces, or urine.

Citing Articles

Evidence-Based Guidance for One Health Preparedness, Prevention, and Response Strategies to Marburg Virus Disease Outbreaks.

Muvunyi C, Ngabonziza J, Bigirimana N, Ndembi N, Siddig E, Kaseya J Diseases. 2024; 12(12.

PMID: 39727639 PMC: 11727285. DOI: 10.3390/diseases12120309.


Fruit Bats Do Not Support Productive Replication of Cedar Virus upon Experimental Challenge.

Mohl B, Diederich S, Fischer K, Balkema-Buschmann A Viruses. 2024; 16(9).

PMID: 39339836 PMC: 11435843. DOI: 10.3390/v16091359.


Disease tolerance as immune defense strategy in bats: One size fits all?.

Pei G, Balkema-Buschmann A, Dorhoi A PLoS Pathog. 2024; 20(9):e1012471.

PMID: 39236038 PMC: 11376593. DOI: 10.1371/journal.ppat.1012471.


Tick-borne viruses and their risk to public health in the Caribbean: Spotlight on bats as reservoirs in Cuba.

Antunez M, Marin Montesinos J, Corduneanu A, Obregon D, Moutailler S, Cabezas-Cruz A Heliyon. 2024; 10(4):e26118.

PMID: 38375245 PMC: 10875593. DOI: 10.1016/j.heliyon.2024.e26118.


Tick salivary gland components dampen Kasokero virus infection and shedding in its vertebrate reservoir, the Egyptian rousette bat (Rousettus aegyptiacus).

Schuh A, Amman B, Guito J, Graziano J, Sealy T, Towner J Parasit Vectors. 2023; 16(1):249.

PMID: 37488618 PMC: 10367358. DOI: 10.1186/s13071-023-05853-7.


References
1.
Ge X, Li J, Yang X, Chmura A, Zhu G, Epstein J . Isolation and characterization of a bat SARS-like coronavirus that uses the ACE2 receptor. Nature. 2013; 503(7477):535-8. PMC: 5389864. DOI: 10.1038/nature12711. View

2.
Memish Z, Mishra N, Olival K, Fagbo S, Kapoor V, Epstein J . Middle East respiratory syndrome coronavirus in bats, Saudi Arabia. Emerg Infect Dis. 2013; 19(11):1819-23. PMC: 3837665. DOI: 10.3201/eid1911.131172. View

3.
Swanepoel R, Smit S, Rollin P, Formenty P, Leman P, Kemp A . Studies of reservoir hosts for Marburg virus. Emerg Infect Dis. 2008; 13(12):1847-51. PMC: 2876776. DOI: 10.3201/eid1312.071115. View

4.
Towner J, Amman B, Sealy T, Carroll S, Comer J, Kemp A . Isolation of genetically diverse Marburg viruses from Egyptian fruit bats. PLoS Pathog. 2009; 5(7):e1000536. PMC: 2713404. DOI: 10.1371/journal.ppat.1000536. View

5.
Amman B, Carroll S, Reed Z, Sealy T, Balinandi S, Swanepoel R . Seasonal pulses of Marburg virus circulation in juvenile Rousettus aegyptiacus bats coincide with periods of increased risk of human infection. PLoS Pathog. 2012; 8(10):e1002877. PMC: 3464226. DOI: 10.1371/journal.ppat.1002877. View