Koala retrovirus (KoRV) subtypes and their impact on captive koala (Phascolarctos cinereus) health
Autor: | Abul Hashem, Hiroko Sakurai, Kyoko Tsukiyama-Kohara, Shinsaku Ochiai, Kyoya Mochizuki, Fumie Maetani, Taiki Eiei, Nanao Ito, Mohammad Enamul Hoque Kayesh, Ayaka Ito, Takayuki Asai |
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Rok vydání: | 2021 |
Předmět: |
0303 health sciences
education.field_of_study biology 030306 microbiology Population RNA General Medicine medicine.disease biology.organism_classification Virology Peripheral blood mononuclear cell 03 medical and health sciences Phascolarctos cinereus biology.animal Coinfection medicine Koala retrovirus education Viral load Gene 030304 developmental biology |
Zdroj: | Archives of Virology. 166:1893-1901 |
ISSN: | 1432-8798 0304-8608 |
Popis: | Koala retrovirus (KoRV), a major pathogen of koalas, exists in both endogenous (KoRV-A) and exogenous forms (KoRV-B to J). However, the impact of infection with multiple subtypes is not well understood. Accordingly, in this study, we surveyed a representative sample from a Japanese zoo population to determine the infection status for three KoRV subtypes (KoRV-A, B, and C) and to investigate the proviral and RNA load profiles in animals with single- and multiple-subtype infections, using peripheral blood mononuclear cells (PBMCs) and plasma. Six koalas were evaluated in the study; all were infected with KoRV-A, and two koalas were coinfected with non-A subtypes (KoRV-B and/or KoRV-C). The highest KoRV total RNA and viral loads in PBMCs and plasma were found in a koala infected with multiple subtypes (KoRV-A, -B and -C). The other koala infected with multiple subtypes (KoRV-A and B) showed the highest proviral PBMC load but the lowest RNA copy number in PBMC and plasma. PBMCs from this animal were cultured for further investigation, and KoRV RNA was detected in the cells and culture supernatant after 7 and/or 14 days. The koalas harboring multiple subtypes had a higher white blood cell count than those harboring only KoRV-A and were judged to be leukemic, and they subsequently died due to lymphoma. Accordingly, we conclude that coinfection with multiple KoRV subtypes may be linked to more-severe disease. In a sequence alignment, the detected KoRV-A env gene showed 100% sequence identity to the reference gene, whereas the KoRV-B and -C env genes varied from their reference sequences. |
Databáze: | OpenAIRE |
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