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The New Members of Filoviridae Family: Distribution, Natural Reservoirs, Potential Epidemic Danger

https://doi.org/10.35825/2587-5728-2019-3-4-329-336

EDN: tunwgf

Abstract

The purpose of the work is to analyze the distribution, natural reservoirs and potential epidemic hazard of new members of the Filoviridae family – Bombali viruses (genus Ebolavirus), Lloviu (genus Cuevavirus), Mengla (genus Dianlovirus), Xylang (genus Striavirus), and Hungjiao (genus Thamnovirus). New filoviruses were detected in Africa (Bombali virus), Europe (Llovi virus) and in Southeast Asia (Mengla, Xylang and Hungjiao viruses). Bats are a natural reservoir for all known filoviruses. This fact is confirmed by the information about the detection of genomic RNA and virus-specific antibodies in them. The isolation of the genomic RNA of filoviruses from bats with the subsequent sequencing and phylogenetic analysis made it possible to identify the Bombali, Lloviu, Mengla, Xylang and Hungjiao viruses as new representatives of the Filoviridae family and to establish their position on the phylogenetic tree of the Filoviridae family. Despite the current lack of information about the isolation of biologically active virus from bats, as well as in spite of lack of established connection between new filoviruses and human diseases, the information that newly identified filoviruses use the same receptors (Neumann-Peak protein) to enter sensitive cells, as the Ebola and Marburg viruses, that are pathogenic for humans, the possible pathogenetic potential of new filoviruses poses a great threat to people living in the territories, inhabited by bats. The possibility of the emergence of new emergent filovirus infections on the territory of Russia necessitates an in-depth study of bats as a natural reservoir of filoviruses in nature.

About the Authors

T. E. Sizikova
Federal State Budgetary Establishment «48 Central Scientific Research Institute» of the Ministry of the Defence of the Russian Federation
Russian Federation

Tatyana Eugenievna Sizikova. Researcher. Candidate of Biological Sciences

Oktyabrskiy Street 11, Sergiev Posad 141306



N. V. Boyarskaya
Federal State Budgetary Establishment «48 Central Scientific Research Institute» of the Ministry of the Defence of the Russian Federation
Russian Federation

Natalya Vasilyevna Boyarskaya. Researcher

Oktyabrskiy Street 11, Sergiev Posad 141306



A. V. Kovalchuk
Federal State Budgetary Establishment «48 Central Scientific Research Institute» of the Ministry of the Defence of the Russian Federation
Russian Federation

Alexey Valerievich Kovalchuk. Head of the Scientific Research Department, Candidate of Medical Sciences

Oktyabrskiy Street 11, Sergiev Posad 141306



V. N. Lebedev
Federal State Budgetary Establishment «48 Central Scientific Research Institute» of the Ministry of the Defence of the Russian Federation
Russian Federation

Vitaly Nikolayevich Lebedev. Leading Researcher. Doctor of Biological Sciences, Professor

Oktyabrskiy Street 11, Sergiev Posad 141306



S. V. Borisevich
Federal State Budgetary Establishment «48 Central Scientific Research Institute» of the Ministry of the Defence of the Russian Federation
Russian Federation

Sergey Vladimirovich Borisevich. Head of the FSBE «48 Central Scientific Research Institute». Doctor of Biological Sciences, Corresponding Member of RAS 

Oktyabrskiy Street 11, Sergiev Posad 141306



References

1. Radoshitzky S.R., Bavari S., Jahrling P.B., Cuhn J.H. Filoviruses // In: Medical aspects of biological warfare / Ed. Carr J.H. Border Institute, Fort Sam Houston, 2018. P. 569–614.

2. Sanchez A., Geisbert T.W., Feldmann H. Filoviridae: Marburg and Ebola viruses // In: Fields Virology. 5th ed. / Eds. Knipe D.M., Howley P.M. Philadelphia: Lippincott William & Wilkins, a Wolters Kluwer Business. 2007. P. 1409–1448.

3. Kuhn J.H., Becker S., Ebihara H. et al. Proposal for a revised taxonomy of the family Filoviridae: classification, names of taxa and viruses, and virus abbreviations // Arch Virol. 2010. V. 155. № 12. P. 2083–2103. https://doi.org/10.1007/s00705-010-0814-x

4. Towner J.S., Sealy T.K., Khristova M.L. et al. Newly Discovered Ebola Virus Associated with Hemorrhagic Fever Outbreak in Uganda // PLoS Pathog. 2008. V. 4. № 11. P. 1–6. https://doi.org/10.1371/journal.ppat1000212

5. Nikegasong J.N., Onyebujoh P. Response to the Ebola virus disease outbreak in DRC // Lancet. 2018. V. 391. P. 2395– 2398. https://doi.org/10.1016/S0140-6736(18)31326-6

6. Olival K.J., Islam A., Yu M., Anthony S.J. et al. Ebola virus antibodies in fruit bats, Bangladesh // Emerg Infect Dis. 2013. V. 19. P. 270–273. https://doi.org/10.3201/eid1902.120524

7. Piot P., Muyembe J.J., Edmunds W.J. Ebola in west Africa: from disease outbreak to humanitarian crisis // Lancet Infect. Dis. 2014. V. 14. № 11. P. 1034–1035. https://doi.org/10.1016/S1473-3099(14)70956-9

8. Kuzmin I.V., Niezgoda M., Franka R. et al. Marburg virus in fruit bat, Kenya // Emerg Infect Dis. 2010. V. 16. № 2. P. 352–354. https://doi.org/10.3201/eid1602.091269

9. Leroy E.M., Kumulungui B., Pourrut X., Rouquet P. et al. Fruit bats as reservoirs of Ebola virus // Nature. 2005. V. 438. № 7068. P. 575–576. https://doi.org/10.1038/438575a

10. Olival K.J., Hayman D.T.S. Filoviruses in Bats: current knowledge and future directions // Viruses. 2014. V. 6. P. 1759–1788. https://doi.org/10.3390/v6041759

11. Swanepoel R., Smit S.B., Rollin P.E. et al. Studies of reservoir hosts for Marburg virus // Emerg Infect Dis. 2007. V. 13. № 12. Р. 1847–1851. https://doi.org/10.3201/eid1312.071115

12. Taniguchi S., Watanabe S., Masangkay J.S. et al. Reston Ebolavirus antibodies in bats, the Philippines // Emerg Infect Dis. 2011. V. 17. № 8. Р. 1559–1560. https://doi.org/10.3201/eid1708.101693

13. Towner J.S., Pourrut X., Albariño C.G. et al. Marburg virus infection detected in a common African bat // PLoS One. 2007. V. 2. № 8. P. 1–5. https://doi.org/10.1371/journal.pone.0000764

14. He B., Feng Y., Zhang H. et al. Filovirus RNA in fruit bats, China // Emerg. Infect. Dis. 2015. V. 21. P. 1675–1677. https://doi.org/10.3201/eid2109.150260

15. Jayme S.I., Field H.E., de Jong C. et al. Molecular evidence of Ebola Reston virus infection in Philippine bats // J. Virol. 2015. V. 12. № 107. P. 1–8. https://doi.org/10.1186/s12985-015-0331-3

16. Negredo A., Palacios G., Vazquez-Moron S. et al. Discovery of an Ebola-like filovirus in Europe // PLoS Pathog. 2011. V. 7. № 10. Р. 1–8. https://doi.org/10.1371/journal.ppat.1002304

17. Towner J.S., Amman B.R., Sealy T.K. et al. Isolation of genetically diverse Marburg viruses from Egyptian fruit bats // PLoS Pathog. 2009. V. 5. № 7. P. 1–9. https://doi.org/10.1371/journal.ppat.1000536

18. Goldstein T., Anthony S.J., Gbakima A. et al. The discovery of Bombali virus adds further support for bats as hosts of ebolaviruses // Nat. Microbiol. 2018. V. 3. P. 1084–1089. https://doi.org/10.1038/s41564-018-0227-2

19. Amman B.R., Carroll S.A., Reed Z.D. et al. Seasonal pulses of Marburg virus circulation in juvenile Rousettus aegyptiacus bats coincide with periods of increased risk of human infection // PLoS Pathog. 2012. V. 8. № 10. P. 1–11. https://doi.org/10.1371/journal.ppat.1002877

20. Hayman D.T.S., Emmerich P., Yu M. et al. LongTerm survival of an urban fruit bat seropositive for Ebola and Lagos bat viruses // PLoS One. 2010. V. 5. № 8. P. 1–3. https://doi.org/10.1371/journal.pone.0011978

21. Hayman D.T.S., McCrea R., Restif O. et al. Demography of straw-colored fruit bats in Ghana // J. Mammal. 2012. V. 93. P. 1393–1404. https://doi.org/10.1644/11-mamm-a-270.1

22. Mutere F.A. Breeding cycles in tropical bats in Uganda // J. Ecology. 1968. V. 56. № 2. Р. 8–9.

23. Thomas D.W. Annual migration of three species of West African fruit bats (Chiroptera: Pteropodidae) // Can. J. Zool. 1983. V. 61. № 10. P. 2266–2272. https://doi.org/10.1139/z83-299

24. Anderson R.M., May R.M. Population biology of infectious diseases: Part I // Nature. 1979. V. 280. № 5721. P. 361–367. https://doi.org/10.1038/280361a0

25. Crameri G., Todd S., Grimley S. et al. Establishment, immortalisation and characterisation of pteropid bat cell lines // PLoS One. 2009. V. 4. № 12. Р. 1–9. https://doi.org/10.1371/journal.pone.0008266

26. Jordan I., Munster V.J., Sandig V. Authentication of the R06E fruit bat cell line // Viruses. 2012. V. 4. № 5. P. 889– 900. https://doi.org/10.3390/v4050889

27. Paweska J.T., Jansen van Vuren P., Masumu J. et al. Virological and serological findings in Rousettus aegyptiacus experimentally inoculated with Vero cells-adapted hogan strain of Marburg virus // PLoS One. 2012. V. 7. № 9. P. 1–11. https://doi.org/10.1371/journal.pone.0045479

28. Swanepoel R., Leman P.A., Burt F.J. et al. Experimental inoculation of plants and animals with Ebola virus // Emerg. Infect. Dis. 1996. V. 2. № 4. Р. 321–325. https://doi.org/10.3201/eid0204.960407

29. Yuan J., Zhang Y., Li J. et al. Serological evidence of ebolavirus infection in bats, China // J. Virol. 2012. V. 9. P. 236. https://doi.org/10.1186/1743-422X-9-236

30. Wang L., Shi Z., Yang X.L, Kuhn J.H. One new genus including one new species in the mononegaviral family Filoviridae // ICTV. 2019. № 2019.011 M. https://doi. org/10.13140/RG.2.2.17179.11045

31. Yang X.L., Tan C.W., Anderson D.E. et al. Characterization of filovirus (Mengla virus) from Rousettus bats in China // Nat. Microbiol. 2019. V. 4. № 3. P. 390–395. https://doi.org/10.1038/s41564-018-0328-y

32. Yang X.L., Zhang Y.Z., Jiang R.D. et al. Genetically Diverse Filoviruses in Rousettus and Eonycteris spp. Bats, China, 2009 and 2015 // Emerg. Infect. Dis. 2017. V. 23. № 3. P. 482–486. https://doi.org/10.3201/eid2303.161119

33. Hofmann-Winkler H., Kaup F., Pohlman S. Host cell factors in filovirus entry; novel players, new insights // Viruses. 2012. V. 4. № 12. P. 3336–3362. https://doi.org/10.3390/v4123336

34. Miller E.H., Obernosterer G., Raaben M. et al. Ebola virus entry requires the host-programmed recognition of an intracellular recognition of an intracellular receptor // EMBO J. 2012. V. 31. № 8. P. 1947–1960. https://doi.org/10.1038/emboj.2012.53


Review

For citations:


Sizikova T.E., Boyarskaya N.V., Kovalchuk A.V., Lebedev V.N., Borisevich S.V. The New Members of Filoviridae Family: Distribution, Natural Reservoirs, Potential Epidemic Danger. Journal of NBC Protection Corps. 2019;3(4):329-336. (In Russ.) https://doi.org/10.35825/2587-5728-2019-3-4-329-336. EDN: tunwgf

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