FeLV-induced feline leukemia as a natural model for leukemia pathophysiology study (review)
https://doi.org/10.29326/2304-196X-2023-12-1-29-37
Abstract
Leukemia is alarge group of diseases different in etiopathogenetic mechanisms and common in almost all mammalian species. There view focuses on feline leukemia, a common disease of domestic and wild felids (Carnivora, Felidae), being one of the main causes of their deaths. Feline leukemia pathogenesis and etiology are described; possible methods for the infection treatment and prevention, as well as possibility of using cats as a model for feline leukemia study areassessed. Feline leukemia etiological agent is a feline leukemia virus (FeLV), having single-stranded RNA genomesurrounded with icosahedral capsidformedbyp27 capsid protein monomers. Leukemia clinical man ifestations in felids depend on high virulence of the virus and the disease is characterized with pronounced clinical picture and multipleorgan dysfunction. Treatment of leukemia in cats is ineffective and is mainly aimedat maintaining the functions of the body organs and systems. Immunomodulators and chemotherapy are alsoused. Vaccination isusedas apreventive measure, but commercially available adjuvanted and non-adjuvanted vaccinesdo not confer effective protection from the infection. The leukemia virus is reportedin wildfelids includingrare and endangeredfeline species that is undoubtedly affects their population sizes. Despite veryfew data on leukemia, the reported cases show that leukemia in large cats is also severe and fatal. Feline leukemia, despite the accumulated of data, remainsan on going serious and unresolved problem not only for veterinarians, but also for ecologists, zoologists and virologists involvedin the research related to the feline family, study of retroviruses and biodiversity conservation on the planet. Furthe rapplied and fund a mental research and verification there of in the field of feline leukemia virus study, leukemia treatment and prevention are required.
About the Authors
T. V. TabakaevaRussian Federation
Tatyana V. Tabakaeva, Researcher, Laboratory of Ectoparasitology
Vladivostok
A. V. Tsybulsky
Russian Federation
Alexander V. Tsybulsky, Candidate of Science (Medicine), Associate Professor, Department of Biochemistry, Microbiology and Biotechnology
Vladivostok
K. A. Baranchugova
Russian Federation
Ksenya A. Baranchugova, Post-Graduate Student, Veterinarian
Vladivostok
I. V. Galkina
Russian Federation
Irina V. Galkina, Candidate of Science (Medicine), Leading Researcher, Laboratory for Microorganism Ecology
Vladivostok
M. Yu. Shchelkanov
Russian Federation
Mikhail Yu. Shchelkanov, Doctor of Science (Biology), Director, Somov Institute of Epidemiology and Microbiology
Vladivostok
References
1. Hotta T. Clonality in hematopoietic disorders. Int. J. Hematol. 1997; 66 (4): 403–412. DOI: 10.1016/s0925-5710(97)00092-3.
2. Smirnova S. Yu., Sidorova Yu. V., Ryzhikova N. V., Sychevskaya K. A., Parovichnikova E. N., Sudarikov A. B. Evolution of tumor clones in adult acute lymphoblastic leukemia. Acta Naturae. 2016; 8 (4): 100–109. DOI: 10.32607/20758251-2016-8-4-100-109.
3. Roug I. K., McCartney L. B. Metastatic non-Hodgkin lymphoma presenting as low back pain and radiculopathy: a case report. J. Chiropr. Med. 2012; 11 (3): 202–206. DOI: 10.1016/j.jcm.2012.05.008.
4. Moskvina T. V., Shchelkanov M. Yu., Tsybulski A. V. FeLV-infection: problems and prospects of vaccine prevention and interferon-therapy of feline leukemia. Russian Journal of Infection and Immunity. 2021; 11 (4): 624–634. DOI: 10.15789/2220-7619-FPA-882. (in Russ.)
5. Guidance on Virology. Human and Animal Viruses and Viral Infections. Ed. by D. K. Lvov. Moscow: Meditsinskoe informatsionnoe agentstvo; 2013; 1200 p. (in Russ.)
6. Tsybulsky A., Tabakaeva T., Klimovich A., Shchelkanov M., Kostetsky E., Aliev M., Degtyarenko A. Interferon status and expression of p53 and gadd45g genes in leukaemogenic FeLV infection in domestic cats. Adv. Anim. Vet. Sci. 2022; 10 (3): 565–572. DOI: 10.17582/journal.aavs/2022/10.3.565.572.
7. Shchelkanov M. Yu., Yarygina M. V., Galkina I. V., Kiku P. F. The dialectic approach to biomedical ethics as a foundation of its implementation in actual social cultural traditions. Problems of Social Hygiene, Public Health and History of Medicine. 2019; 27 (4): 414–417. DOI: 10.32687/0869-866X2019-27-4-414-417. (in Russ.)
8. Shchelkanov M. Yu., Galkina I. V., Aramilev S. A., Surovyi A. L., Fomenko P. V., Zhuravlev Yu. N. Far Eastern bank of biological materials from big cats (Pantherinae) as an improvement tool of the practice of enforcement of Articles 226.1 and 258.1 of the Criminal Code of the Russian Federation. Russian Journal of Criminology. 2017; 11 (1): 146–153. DOI: 10.17150/2500- 4255.2017.11(1).146-153. (in Russ.)
9. Szilasi A., Dénes L., Balka G. Feline leukemia virus (FeLV): literature review. Magyar Állatorvosok Lapja. 2018; 140 (8): 457–472. (in Hungarian)
10. Weiss A. T., Klopfleisch R., Gruber A. D. Prevalence of feline leukaemia provirus DNA in feline lymphomas. J. Feline Med. Surg. 2010; 12 (12): 929–935. DOI: 10.1016/j.jfms.2010.07.006.
11. Brown M. A., Cunningham M. W., Roca A. L., Troyer J. L., Johnson W. E., O’Brien S. J. Genetic characterization of feline leukemia virus from Florida panthers. Emerg. Infect. Dis. 2008; 14 (2): 252–259. DOI: 10.3201/ eid1402.070981.
12. Filoni C., Helfer-Hungerbuehler A. K., Catão-Dias J. L., Marques M. C., Torres L. N., Reinacher M., Hofmann-Lehmann R. Putative progressive and abortive feline leukemia virus infection outcomes in captive jaguarundis (Puma yagouaroundi). Virol. J. 2017; 14 (1):226. DOI: 10.1186/s12985-017- 0889-z.
13. Shchelkanov M. Yu., Soinov L. A., Zalunin V. V., Gumennyi D. A., Yudin A. N., Natan A. A., et al. One-parameter discrete model of the genetic diversity. J. Biomol. Struct. Dyn. 1998; 15 (5): 887–894. DOI: 10.1080/07391 102.1998.10508210.
14. Shchelkanov M. Yu., Yudin A. N., Antonov A. V., Soinov L. A., Zalunin V. V., Vedenov A. A., Karamov E. V. Variability analysis of HIV-1 gp120 V3 region: II. Hierarchy of taxons. J. Biomol. Struct. Dyn. 1997; 15 (2): 231–241. DOI: 10.1080/07391102.1997.10508188.
15. Harrison T. M., McKnight C. A., Sikarskie J. G., Kitchell B. E., Garner M. M., Raymond J. T., et al. Malignant lymphoma in African lions (Panthera leo). Vet. Pathol. 2010; 47 (5): 952–957. DOI: 10.1177/0300985810375054.
16. Shchelkanov M. Yu., Soinov L. A., Yudin A. N., Denisov M. V., Slavsky A. A., Petrenko M. S., Vedenov A. A. Stochastic properties of oneparameter discrete model of genetic diversity in the unique random parameter case. J. Biomol. Struct. Dyn. 1999; 17 (3): 597–605. DOI: 10.1080/07 391102.1999.10508389.
17. Bolin L. L., Levy L. S. Viral determinants of FeLV infection and pathogenesis: lessons learned from analysis of a natural cohort. Viruses. 2011; 3 (9): 1681–1698. DOI: 10.3390/v3091681.
18. Anderson M. M., Lauring A. S., Robertson S., Dirks C., Overbaugh J. Feline Pit2 functions as a receptor for subgroup B feline leukemia viruses. J. Virol. 2001; 75 (22): 10563–10572. DOI: 10.1128/JVI.75.22.10563- 10572.2001.
19. Mendoza R., Anderson M. M., Overbaugh J. A putative thiamine transport protein is a receptor for feline leukemia virus subgroup A. J. Virol. 2006; 80 (7): 3378–3385. DOI: 10.1128/JVI.80.7.3378-3385.2006.
20. Phipps A. J., Chen H., Hayes K. A., Roy-Burman P., Mathes L. E. Differential pathogenicity of two feline leukemia virus subgroup A molecular clones, pFRA and pF6A. J. Virol. 2000; 74 (13): 5796–5801. DOI: 10.1128/ jvi.74.13.5796-5801.2000.
21. Vobis M., D’Haese J., Mehlhorn H., Mencke N. Evidence of horizontal transmission of feline leukemia virus by the cat flea (Ctenocephalides felis). Parasitol. Res. 2003; 91 (6): 467–470. DOI: 10.1007/s00436-003-0949-8.
22. Cunningham M. W., Brown M. A., Shindle D. B., Terrell S. P., Hayes K. A., Ferree B. C., et al. Epizootiology and management of feline leukemia virus in the Florida puma. J. Wildl. Dis. 2008; 44 (3): 537–552. DOI: 10.7589/0090- 3558-44.3.537.
23. Guimaraes A. M., Brandão P. E., de Moraes W., Cubas Z. S., Santos L. C., Villarreal L. Y., et al. Survey of feline leukemia virus and feline coronaviruses in captive neotropical wild felids from Southern Brazil. J. Zoo Wildl. Med. 2009; 40 (2): 360–364. DOI: 10.1638/2008-0067.1.
24. Sleeman J. M., Keane J. M., Johnson J. S., Brown R. J., Woude S. V. Feline leukemia virus in a captive bobcat. J. Wildl. Dis. 2001; 37 (1): 194–200. DOI: 10.7589/0090-3558-37.1.194.
25. Leutenegger C. M., Hofmann-Lehmann R., Riols C., Liberek M., Worel G., Lups P., et al. Viral infections in free-living populations of the European wildcat. J. Wildl. Dis. 1999; 35 (4): 678–686. DOI: 10.7589/0090- 3558-35.4.678.
26. Tangsudjai S., Malidang S., Phonarknguen R., Boonyarittichaikit R., Pattanarangsan R., Buddhirongawatr R., Chaichoun K. Feline leukemia virus (FeLV) in captive wild felids in Thailand during 2004–2005. J. Appl. Anim. Sci. 2010; 3 (1–3): 25–31.
27. Moskvina T., Klimovich A., Stenkova A., Tsybulsky A., Tabakaev A., Shchelkanov M. The prevalence of FeLV and FIV infection in cats and hematological changes and clinical signs in FeLV/FIV infected cats from Vladivostok, Russia. Adv. Anim. Vet. Sci. 2019: 7 (7): 570–573. DOI: 10.17582/journal. aavs/2019/7.7.570.573.
28. Weiss R. A. The discovery of endogenous retroviruses. Retrovirology. 2006; 3:67. DOI: 10.1186/1742-4690-3-67.
29. Levy J. K., Burling A. Feline leukemia virus and related diseases in cats – overview. Generalized Conditions. MSD Veterinary Manual. 2018; 9 р.
30. Hisasue M., Nagashima N., Nishigaki K., Fukuzawa I., Ura S., Katae H., et al. Myelodysplastic syndromes and acute myeloid leukemia in cats infected with feline leukemia virus clone33 containing a unique long terminal repeat. Int. J. Cancer. 2009; 124 (5): 1133–1141. DOI: 10.1002/ ijc.24050.
31. Marker L., Munson L., Basson P. A., Quackenbush S. Multicentric T-cell lymphoma associated with feline leukemia virus infection in a captive Namibian cheetah (Acinonyx jubatus). J. Wildl. Dis. 2003; 39 (3): 690–695. DOI: 10.7589/0090-3558-39.3.690.
32. Neil J. C., Fulton R., Rigby M., Stewart M. Feline leukaemia virus: generation of pathogenic and oncogenic variants. Curr. Top. Microbiol. Immunol. 1991; 171: 67–93. DOI: 10.1007/978-3-642-76524-7_4.
33. Jarrett O. Pathogenicity of feline leukemia virus is commonly associated with variant viruses. Leukemia. 1992; 6 (Suppl 3): 153S–154S. PMID: 1318467.
34. Rojko J. L., Kociba G. J. Pathogenesis of infection by the feline leukemia virus. J. Am. Vet. Med. Assoc. 1991; 199 (10): 1305–1310. PMID: 1666072.
35. Hartmann K. Efficacy of antiviral chemotherapy for retrovirus-infected cats: What does the current literature tell us? J. Feline. Med. Surg. 2015; 17 (11): 925–939. DOI: 10.1177/1098612X15610676.
36. Patel M., Carritt K., Lane J., Jayappa H., Stahl M., Bourgeois M. Comparative efficacy of feline leukemia virus (FeLV) inactivated whole-virus vaccine and canarypox virus-vectored vaccine during virulent FeLV challenge and immunosuppression. Clin. Vaccine Immunol. 2015; 22 (7): 798–805. DOI: 10.1128/CVI.00034-15.
37. Wardley R. C., Berlinski P. J., Thomsen D. R., Meyer A. L., Post L. E. The use of feline herpesvirus and baculovirus as vaccine vectors for the gag and env genes of feline leukaemia virus. J. Gen. Virol. 1992; 73 (7): 1811–1818. DOI: 10.1099/0022-1317-73-7-1811.
38. Pikunov D. G., Miquelle D. G., Abramov V. K., Nikolaev I. G., Seredkin I. V., Murzin A. A., Korkishko V. G. A survey of Far Eastern leopard (Panthera pardus orientalis) and Amur tiger (Panthera tigris altaica) populations in southwest Primorski Krai, Russian Far East (February 2003). Vladivostok; 2003. 66 р. Available at: https://www.save-leopard.ru/_ld/0/61_7-download.pdf. (in Russ.)
39. Seryodkin I. V., Goodrich D. M., Lewis D., Miquelle D. G., Esaulova N. V., Konyaev S. V., et al. Infectious and endoparasitic diseases of the Amur tiger. Bulletin of KrasGAU. 2015; 12: 185–191. eLIBRARY ID: 25054295. (in Russ.)
40. Gilbert M., Miquelle D. G., Goodrich J. M., Reeve R., Cleaveland S., Matthews L., Joly D. O. Estimating the potential impact of canine distemper virus on the Amur tiger population (Panthera tigris altaica) in Russia. PLoS One. 2014; 9 (10):e110811. DOI: 10.1371/journal.pone.0110811.
41. Lyubchenko E. N., Korotkova I. P., Ivanchuk G. B., Kukharenko N. C. Pathomorphological changes in organs under alimentary dystrophy of wild feline of the Far East. Far Eastern Agrarian Bulletin. 2019; 1 (49): 66–72. DOI: 10.24411/1999-6837-2019-11010. (in Russ.)
42. Jung I., Kim Y. S., Jee H., Sohn S. Y., Yoo H. S., Kim D. Y., et al. Feline panleukopenia virus infection in a Siberian tiger (Panthera tigris altaica). J. Vet. Clin. 2009; 26 (5): 504–507.
43. Lewis J., Tomlinson A., Gilbert M., Alshinetski M., Arzhanova T., Goncharuk M., et al. Assessing the health risks of reintroduction: The example of the Amur leopard, Panthera pardus orientalis. Transbound. Emerg. Dis. 2020; 67 (3): 1177–1188. DOI: 10.1111/tbed.13449.
44. Moskvina T. V., Schelkanov M. Yu., Begun M. A. Endoparasites of the Siberian tiger (Panthera tigris altaica). Integrative Zoology. 2018; 13 (5): 507–516. DOI: 10.1111/1749-4877.12342.
45. Voronova A. N., Vainutis K. S., Tabakaeva T. V., Sapotsky M. V., Kakareka N. N., Volkov Y. G., et al. Molecular identification of the trematode P. ichunensis stat. n. from lungs of siberian tigers justified reappraisal of Paragonimus westermani species complex. J. Parasit. Dis. 2022; 46 (3): 744–753. DOI: 10.1007/s12639-022-01481-7.
46. Lyubchenko E. N., Korotkova I. P., Fomenko P. V. Lymphoma of the Amur tigris. Aktual’nye voprosy i innovatsionnye tekhnologii v veterinarnoi meditsine, zhivotnovodstve i prirodookhrannom komplekse: materialy Mezhdunarodnoi nauchno-prakticheskoi konferentsii, posvyashchennoi 40-letnemu yubileyu so dnya obrazovaniya veterinarnogo fakul’teta (6–8 noyabrya 2019 g.). Ch. 1 = Current aspects and innovative technologies in veterinary field, animal farming industry and environmental field. Proceedings of the International Scientific and Practical Conference devoted to the 40th Anniversary of the Veterinary Faculty establishment (November 6–8, 2019). Part 1. Ussuriysk: FSBEI HE Primorskaya SAA; 2019; 177–180. eLIBRARY ID: 42374757. (in Russ.)
47. Reyes M. F., Barrios E. R., Favila M. J. B., Moralde K. I. A., Flores M. L. S. Prevalence of feline immunodeficiency virus, feline leukemia virus and Toxoplasma gondii in captive tigers (Panthera tigris) in a wildlife facility in the Philippines. Philipp. J. Vet. Anim. Sci. 2017; 43 (1): 38–43.
48. Huang S., Li X., Guo L., You D., Xie W., Xu H., et al. Prevalence of four viruses in captive Siberian tigers from Northeastern China. Transbound. Emerg. Dis. 2022; 69 (5): e1434–e1444. DOI: 10.1111/tbed.14475.
49. Liu E., Ma L., Huang S., You D., Guo L., Li X., et al. The first feline immunodeficiency virus from Siberian tigers (Panthera tigris altaica) in Northeastern China. Arch. Virol. 2022; 167 (2): 545–551. DOI: 10.1007/ s00705-022-05370-5.
50. De la Cruz-Hernández N. I., Merino-Charres J. O., Salinas-Navarrete E. M., Monreal Garcia A. E., Martinez Burnes J., Rangel Lucio J. A. R., Vene gas-Barrera C. Amyloidosis associated with feline leukemia virus in a white bengal tiger (Panthera tigris tigris). Thai. J. Vet. Med. 2016; 46 (4): 679–683.
51. Rolim V. M., Casagrande R. A., Wouters A. T., Driemeier D., Pavarini S. P. Myocarditis caused by feline immunodeficiency virus in five cats with hypertrophic cardiomyopathy. J. Comp. Pathol. 2016; 154 (1): 3–8. DOI: 10.1016/j.jcpa.2015.10.180.
52. Keller D. L., Steinberg H., Sladky K. K. Disseminated histoplasmosis in a Bengal tiger (Panthera tigris). J. Zoo. Wildl. Med. 2011; 42 (4): 727–731. DOI: 10.1638/2010-0206.1.
53. Tabakaeva T. V., Klimovich A. A., Tsybulsky A. V., Tabakaev A. V., Shchelkanov M. Yu. Retroviral infections of cats in Vladivostok, Russia. The 2nd International Conference on Northeast Asia Biodiversity (August 27–31, 2019): Abstract Gather. Baishan, China; 2019; 30. Available at: https://www. biosoil.ru/files/publications/00018494.pdf
Review
For citations:
Tabakaeva T.V., Tsybulsky A.V., Baranchugova K.A., Galkina I.V., Shchelkanov M.Yu. FeLV-induced feline leukemia as a natural model for leukemia pathophysiology study (review). Veterinary Science Today. 2023;12(1):29-37. https://doi.org/10.29326/2304-196X-2023-12-1-29-37