Multiple recombination events between endogenous retroviral elements and feline leukemia virus

Author:

Ngo Minh Ha1,AbuEed Loai1,Kawasaki Junna2ORCID,Oishi Naoki3,Pramono Didik1,Kimura Tohru4,Sakurai Masashi5,Watanabe Kenji6,Mizukami Yoichi6,Ochi Haruyo1,Anai Yukari1,Odahara Yuka1,Umehara Daigo1,Kawamura Maki7,Watanabe Shinya1,Miyake Ariko1,Nishigaki Kazuo1ORCID

Affiliation:

1. Laboratory of Molecular Immunology and Infectious Disease, Joint Graduate School of Veterinary Medicine, Yamaguchi University, Yoshida, Yamaguchi, Japan

2. Faculty of Science and Engineering, Waseda University, Okubo, Shinjuku-ku, Tokyo, Japan

3. Oishi Animal Clinic, Oshu-shi, Iwate, Japan

4. Joint Graduate School of Veterinary Medicine, Yamaguchi University, Yoshida, Yamaguchi, Japan

5. Laboratory of Veterinary Pathology, Joint Faculty of Veterinary Medicine, Yamaguchi University, Yoshida, Yamaguchi, Japan

6. Institute of Gene Research, Science Research Center, Yamaguchi University, Minami-kogushi, Ube, Japan

7. Life Science Division, Advanced Technology Institute, Yamaguchi University, Yoshida, Yamaguchi, Japan

Abstract

ABSTRACT Feline leukemia virus (FeLV) is an exogenous retrovirus that causes malignant hematopoietic disorders in domestic cats, and its virulence may be closely associated with viral sequences. FeLV is classified into several subgroups, including A, B, C, D, E, and T, based on viral receptor interference properties or receptor usage. However, the transmission manner and disease specificity of the recombinant viruses FeLV-D and FeLV-B remain unclear. The aim of this study was to understand recombination events between exogenous and endogenous retroviruses within a host and elucidate the emergence and transmission of recombinant viruses. We observed multiple recombination events involving endogenous retroviruses (ERVs) in FeLV from a family of domestic cats kept in one house; two of these cats (ON-T and ON-C) presented with lymphoma and leukemia, respectively. Clonal integration of FeLV-D was observed in the ON-T case, suggesting an association with FeLV-D pathogenesis. Notably, the receptor usage of FeLV-B observed in ON-T was mediated by feline Pit1 and feline Pit2, whereas only feline Pit1 was used in ON-C. Furthermore, XR-FeLV, a recombinant FeLV containing an unrelated sequence referred to the X-region, which is homologous to a portion of the 5′-leader sequence of Felis catus endogenous gammaretrovirus 4 (FcERV-gamma4), was isolated. Genetic analysis suggested that most recombinant viruses occurred de novo ; however, the possibility of FeLV-B transmission was also recognized in the family. This study demonstrated the occurrence of multiple recombination events between exogenous and endogenous retroviruses in domestic cats, highlighting the contribution of ERVs to pathogenic recombinant viruses. IMPORTANCE Feline leukemia virus subgroup A (FeLV-A) is primarily transmitted among cats. During viral transmission, genetic changes in the viral genome lead to the emergence of novel FeLV subgroups or variants with altered virulence. We isolated three FeLV subgroups (A, B, and D) and XR-FeLV from two cats and identified multiple recombination events in feline endogenous retroviruses (ERVs), such as enFeLV, ERV-DC, and FcERV-gamma4, which are present in the cat genome. This study highlights the pathogenic contribution of ERVs in the emergence of FeLV-B, FeLV-D, and XR-FeLV in a feline population.

Funder

MEXT | Japan Society for the Promotion of Science

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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