Analyze Diet
Virology journal2014; 11; 151; doi: 10.1186/1743-422X-11-151

Antiviral potency and functional analysis of tetherin orthologues encoded by horse and donkey.

Abstract: Tetherin is an interferon-inducible host cell factor that blocks the viral particle release of the enveloped viruses. Most knowledge regarding the interaction between tetherin and viruses has been obtained using the primate lentiviral system. However, much less is known about the functional roles of tetherin on other lentiviruses. Equine infectious anemia virus (EIAV) is an important macrophage-tropic lentivirus that has been widely used as a practical model for investigating the evolution of the host-virus relationship. The host range of EIAV is reported to include all members of the Equidae family. However, EIAV has different clinical responses in horse and donkey. It's intriguing to investigate the similarities and differences between the tetherin orthologues encoded by horse and donkey. Results: We report here that there are two equine tetherin orthologues. Compared to horse tetherin, there are three valine amino acid deletions within the transmembrane domain and three distinct mutations within the ectodomain of donkey tetherin. However, the antiviral activity of donkey tetherin was not affected by amino acid deletion or substitution. In addition, both tetherin orthologues encoded by horse and donkey are similarly sensitive to EIAV Env protein, and equally activate NF-κB signaling. Conclusions: Our data suggest that both tetherin orthologues encoded by horse and donkey showed similar antiviral activities and abilities to induce NF-κB signaling. In addition, the phenomenon about the differential responses of horses and donkeys to infection with EIAV was not related with the differences in the structure of the corresponding tetherin orthologues.
Publication Date: 2014-08-27 PubMed ID: 25158826PubMed Central: PMC4152588DOI: 10.1186/1743-422X-11-151Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research investigated differences in a specific antiviral protein, tetherin, found in horses and donkeys, and how these differences might influence susceptibility to a particular virus, EIAV. Despite structural differences, both horse and donkey versions of tetherin were found to be similarly effective at suppressing the virus and inducing a particular immune response.

Objectives and Background

  • The overall objective of this research was to comprehend the functional roles and viral interaction of tetherin. Tetherin plays a crucial role in blocking the release of enveloped viruses. However, most of the available knowledge is based on primate lentiviral systems, and less is known about its effect on lentiviruses like EIAV.
  • EIAV, a lentivirus that infects macrophages, is known to affect all members of the Equidae family, which includes horses and donkeys. But it was observed that EIAV has different clinical responses in both these animals. The research thus targeted to explore the role of tetherin in these distinct responses.

Methods and Findings

  • Your researchers identified two types of tetherin in equids (horses and donkeys). The donkey’s version of the protein had three redundant valine amino acids in its transmembrane domain and three distinct mutations in its ectodomain compared to the horse’s version.
  • Despite these differences, the donkey’s version of tetherin was found to be as effective as the horse’s at blocking the virus. This effectiveness was not affected by the amino acid deletions or substitutions in the donkey’s tetherin.
  • Both versions of tetherin were equally sensitive to the EIAV Env protein and had similar capabilities to activate NF-κB signaling, an immune response.

Conclusions

  • The research concluded that both horse and donkey tetherin, despite their structural differences, showed similar antiviral activities and abilities to induce NF-κB signaling.
  • The differences in the clinical responses of horses and donkeys to EIAV was determined as not related to the differences between their corresponding tetherin proteins.

Cite This Article

APA
Yin X, Guo M, Gu Q, Wu X, Wei P, Wang X. (2014). Antiviral potency and functional analysis of tetherin orthologues encoded by horse and donkey. Virol J, 11, 151. https://doi.org/10.1186/1743-422X-11-151

Publication

ISSN: 1743-422X
NlmUniqueID: 101231645
Country: England
Language: English
Volume: 11
Pages: 151
PII: 151

Researcher Affiliations

Yin, Xin
    Guo, Miaomiao
      Gu, Qinyong
        Wu, Xingliang
          Wei, Ping
          • College of Veterinary Medicine, Northeast Agricultural University, Harbin, China. weiiping@163.com.
          Wang, Xiaojun

            MeSH Terms

            • Amino Acid Sequence
            • Animals
            • Antigens, CD / genetics
            • Antigens, CD / metabolism
            • Antigens, CD / pharmacology
            • Antiviral Agents / pharmacology
            • Cells, Cultured
            • Cloning, Molecular
            • Equidae / genetics
            • Equidae / metabolism
            • Gene Expression Regulation
            • Humans
            • Infectious Anemia Virus, Equine / drug effects
            • Macrophages / metabolism
            • Membrane Glycoproteins / genetics
            • Membrane Glycoproteins / metabolism
            • Membrane Glycoproteins / pharmacology
            • Molecular Sequence Data
            • Mutation
            • NF-kappa B / genetics
            • NF-kappa B / metabolism
            • Protein Isoforms
            • Signal Transduction
            • T-Lymphocytes / metabolism

            References

            This article includes 31 references
            1. Neil SJ. The antiviral activities of tetherin.. Curr Top Microbiol Immunol 2013;371:67-104.
              pubmed: 23686232doi: 10.1007/978-3-642-37765-5_3google scholar: lookup
            2. Pan XB, Qu XW, Jiang D, Zhao XL, Han JC, Wei L. BST2/Tetherin inhibits hepatitis C virus production in human hepatoma cells.. Antiviral Res 2013 Apr;98(1):54-60.
            3. Weissenhorn W, Miguet N, Aschman N, Renesto P, Usami Y, Gottlinger HG. Structural basis of tetherin function.. Curr HIV Res 2012 Jun;10(4):298-306.
              doi: 10.2174/157016212800792487pubmed: 22524178google scholar: lookup
            4. Tokarev A, Suarez M, Kwan W, Fitzpatrick K, Singh R, Guatelli J. Stimulation of NF-κB activity by the HIV restriction factor BST2.. J Virol 2013 Feb;87(4):2046-57.
              doi: 10.1128/JVI.02272-12pmc: PMC3571454pubmed: 23221546google scholar: lookup
            5. Galão RP, Le Tortorec A, Pickering S, Kueck T, Neil SJ. Innate sensing of HIV-1 assembly by Tetherin induces NFκB-dependent proinflammatory responses.. Cell Host Microbe 2012 Nov 15;12(5):633-44.
              doi: 10.1016/j.chom.2012.10.007pmc: PMC3556742pubmed: 23159053google scholar: lookup
            6. Mangeat B, Cavagliotti L, Lehmann M, Gers-Huber G, Kaur I, Thomas Y, Kaiser L, Piguet V. Influenza virus partially counteracts restriction imposed by tetherin/BST-2.. J Biol Chem 2012 Jun 22;287(26):22015-29.
              doi: 10.1074/jbc.M111.319996pmc: PMC3381161pubmed: 22493439google scholar: lookup
            7. Yin X, Hu Z, Gu Q, Wu X, Zheng YH, Wei P, Wang X. Equine tetherin blocks retrovirus release and its activity is antagonized by equine infectious anemia virus envelope protein.. J Virol 2014 Jan;88(2):1259-70.
              doi: 10.1128/JVI.03148-13pmc: PMC3911658pubmed: 24227834google scholar: lookup
            8. Morrison JH, Guevara RB, Marcano AC, Saenz DT, Fadel HJ, Rogstad DK, Poeschla EM. Feline immunodeficiency virus envelope glycoproteins antagonize tetherin through a distinctive mechanism that requires virion incorporation.. J Virol 2014 Mar;88(6):3255-72.
              doi: 10.1128/JVI.03814-13pmc: PMC3957917pubmed: 24390322google scholar: lookup
            9. Jones PH, Maric M, Madison MN, Maury W, Roller RJ, Okeoma CM. BST-2/tetherin-mediated restriction of chikungunya (CHIKV) VLP budding is counteracted by CHIKV non-structural protein 1 (nsP1).. Virology 2013 Mar 30;438(1):37-49.
              doi: 10.1016/j.virol.2013.01.010pmc: PMC4086190pubmed: 23411007google scholar: lookup
            10. Blondeau C, Pelchen-Matthews A, Mlcochova P, Marsh M, Milne RS, Towers GJ. Tetherin restricts herpes simplex virus 1 and is antagonized by glycoprotein M.. J Virol 2013 Dec;87(24):13124-33.
              doi: 10.1128/JVI.02250-13pmc: PMC3838283pubmed: 24067975google scholar: lookup
            11. Celestino M, Calistri A, Del Vecchio C, Salata C, Chiuppesi F, Pistello M, Borsetti A, Palù G, Parolin C. Feline tetherin is characterized by a short N-terminal region and is counteracted by the feline immunodeficiency virus envelope glycoprotein.. J Virol 2012 Jun;86(12):6688-700.
              doi: 10.1128/JVI.07037-11pmc: PMC3393548pubmed: 22514338google scholar: lookup
            12. Zhang F, Wilson SJ, Landford WC, Virgen B, Gregory D, Johnson MC, Munch J, Kirchhoff F, Bieniasz PD, Hatziioannou T. Nef proteins from simian immunodeficiency viruses are tetherin antagonists.. Cell Host Microbe 2009 Jul 23;6(1):54-67.
              doi: 10.1016/j.chom.2009.05.008pmc: PMC2852097pubmed: 19501037google scholar: lookup
            13. Kaletsky RL, Francica JR, Agrawal-Gamse C, Bates P. Tetherin-mediated restriction of filovirus budding is antagonized by the Ebola glycoprotein.. Proc Natl Acad Sci U S A 2009 Feb 24;106(8):2886-91.
              doi: 10.1073/pnas.0811014106pmc: PMC2650360pubmed: 19179289google scholar: lookup
            14. Jia B, Serra-Moreno R, Neidermyer W, Rahmberg A, Mackey J, Fofana IB, Johnson WE, Westmoreland S, Evans DT. Species-specific activity of SIV Nef and HIV-1 Vpu in overcoming restriction by tetherin/BST2.. PLoS Pathog 2009 May;5(5):e1000429.
            15. Gupta RK, Mlcochova P, Pelchen-Matthews A, Petit SJ, Mattiuzzo G, Pillay D, Takeuchi Y, Marsh M, Towers GJ. Simian immunodeficiency virus envelope glycoprotein counteracts tetherin/BST-2/CD317 by intracellular sequestration.. Proc Natl Acad Sci U S A 2009 Dec 8;106(49):20889-94.
              doi: 10.1073/pnas.0907075106pmc: PMC2791628pubmed: 19864625google scholar: lookup
            16. Neil SJ, Zang T, Bieniasz PD. Tetherin inhibits retrovirus release and is antagonized by HIV-1 Vpu.. Nature 2008 Jan 24;451(7177):425-30.
              doi: 10.1038/nature06553pubmed: 18200009google scholar: lookup
            17. Zenner HL, Mauricio R, Banting G, Crump CM. Herpes simplex virus 1 counteracts tetherin restriction via its virion host shutoff activity.. J Virol 2013 Dec;87(24):13115-23.
              doi: 10.1128/JVI.02167-13pmc: PMC3838292pubmed: 24067977google scholar: lookup
            18. Cook RF, Leroux C, Issel CJ. Equine infectious anemia and equine infectious anemia virus in 2013: a review.. Vet Microbiol 2013 Nov 29;167(1-2):181-204.
              doi: 10.1016/j.vetmic.2013.09.031pubmed: 24183747google scholar: lookup
            19. Dong JB, Zhu W, Cook FR, Goto Y, Horii Y, Haga T. Identification of a novel equine infectious anemia virus field strain isolated from feral horses in southern Japan.. J Gen Virol 2013 Feb;94(Pt 2):360-365.
              doi: 10.1099/vir.0.047498-0pubmed: 23100364google scholar: lookup
            20. Cook SJ, Cook RF, Montelaro RC, Issel CJ. Differential responses of Equus caballus and Equus asinus to infection with two pathogenic strains of equine infectious anemia virus.. Vet Microbiol 2001 Mar 20;79(2):93-109.
              doi: 10.1016/S0378-1135(00)00348-5pubmed: 11230932google scholar: lookup
            21. Dietrich I, McMonagle EL, Petit SJ, Vijayakrishnan S, Logan N, Chan CN, Towers GJ, Hosie MJ, Willett BJ. Feline tetherin efficiently restricts release of feline immunodeficiency virus but not spreading of infection.. J Virol 2011 Jun;85(12):5840-52.
              doi: 10.1128/JVI.00071-11pmc: PMC3126296pubmed: 21490095google scholar: lookup
            22. Takeda E, Nakagawa S, Nakaya Y, Tanaka A, Miyazawa T, Yasuda J. Identification and functional analysis of three isoforms of bovine BST-2.. PLoS One 2012;7(7):e41483.
            23. Hanson MA, Roth CB, Jo E, Griffith MT, Scott FL, Reinhart G, Desale H, Clemons B, Cahalan SM, Schuerer SC, Sanna MG, Han GW, Kuhn P, Rosen H, Stevens RC. Crystal structure of a lipid G protein-coupled receptor.. Science 2012 Feb 17;335(6070):851-5.
              doi: 10.1126/science.1215904pmc: PMC3338336pubmed: 22344443google scholar: lookup
            24. Lippold S, Knapp M, Kuznetsova T, Leonard JA, Benecke N, Ludwig A, Rasmussen M, Cooper A, Weinstock J, Willerslev E, Shapiro B, Hofreiter M. Discovery of lost diversity of paternal horse lineages using ancient DNA.. Nat Commun 2011 Aug 23;2:450.
              doi: 10.1038/ncomms1447pubmed: 21863017google scholar: lookup
            25. Andrew AJ, Miyagi E, Kao S, Strebel K. The formation of cysteine-linked dimers of BST-2/tetherin is important for inhibition of HIV-1 virus release but not for sensitivity to Vpu.. Retrovirology 2009 Sep 8;6:80.
              doi: 10.1186/1742-4690-6-80pmc: PMC2754425pubmed: 19737401google scholar: lookup
            26. Fukuma A, Abe M, Morikawa Y, Miyazawa T, Yasuda J. Cloning and characterization of the antiviral activity of feline Tetherin/BST-2.. PLoS One 2011 Mar 29;6(3):e18247.
            27. Coleman CM, Spearman P, Wu L. Tetherin does not significantly restrict dendritic cell-mediated HIV-1 transmission and its expression is upregulated by newly synthesized HIV-1 Nef.. Retrovirology 2011 Apr 19;8:26.
              doi: 10.1186/1742-4690-8-26pmc: PMC3108291pubmed: 21504576google scholar: lookup
            28. Perez-Caballero D, Zang T, Ebrahimi A, McNatt MW, Gregory DA, Johnson MC, Bieniasz PD. Tetherin inhibits HIV-1 release by directly tethering virions to cells.. Cell 2009 Oct 30;139(3):499-511.
              doi: 10.1016/j.cell.2009.08.039pmc: PMC2844890pubmed: 19879838google scholar: lookup
            29. Zhang J, Liang C. BST-2 diminishes HIV-1 infectivity.. J Virol 2010 Dec;84(23):12336-43.
              doi: 10.1128/JVI.01228-10pmc: PMC2976413pubmed: 20861258google scholar: lookup
            30. Cocka LJ, Bates P. Identification of alternatively translated Tetherin isoforms with differing antiviral and signaling activities.. PLoS Pathog 2012 Sep;8(9):e1002931.
            31. Weinelt J, Neil SJ. Differential sensitivities of tetherin isoforms to counteraction by primate lentiviruses.. J Virol 2014 May;88(10):5845-58.
              doi: 10.1128/JVI.03818-13pmc: PMC4019096pubmed: 24623426google scholar: lookup

            Citations

            This article has been cited 1 times.
            1. Lee W, Park KD, Taye M, Lee C, Kim H, Lee HK, Shin D. Analysis of cross-population differentiation between Thoroughbred and Jeju horses.. Asian-Australas J Anim Sci 2018 Aug;31(8):1110-1118.
              doi: 10.5713/ajas.17.0460pubmed: 29268585google scholar: lookup