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The Smallest Capsid Protein Mediates Binding of the Essential Tegument Protein pp150 to Stabilize DNA-Containing Capsids in Human Cytomegalovirus


Human cytomegalovirus (HCMV) is a ubiquitous herpesvirus that causes birth defects in newborns and life-threatening complications in immunocompromised individuals. Among all human herpesviruses, HCMV contains a much larger dsDNA genome within a similarly-sized capsid compared to the others, and it was proposed to require pp150, a tegument protein only found in cytomegaloviruses, to stabilize its genome-containing capsid. However, little is known about how pp150 interacts with the underlying capsid. Moreover, the smallest capsid protein (SCP), while dispensable in herpes simplex virus type 1, was shown to play essential, yet undefined, role in HCMV infection. Here, by cryo electron microscopy (cryoEM), we determine three-dimensional structures of HCMV capsid (no pp150) and virion (with pp150) at sub-nanometer resolution. Comparison of these two structures reveals that each pp150 tegument density is composed of two helix bundles connected by a long central helix. Correlation between the resolved helices and sequence-based secondary structure prediction maps the tegument density to the N-terminal half of pp150. The structures also show that SCP mediates interactions between the capsid and pp150 at the upper helix bundle of pp150. Consistent with this structural observation, ribozyme inhibition of SCP expression in HCMV-infected cells impairs the formation of DNA-containing viral particles and reduces viral yield by 10,000 fold. By cryoEM reconstruction of the resulting “SCP-deficient” viral particles, we further demonstrate that SCP is required for pp150 functionally binding to the capsid. Together, our structural and biochemical results point to a mechanism whereby SCP recruits pp150 to stabilize genome-containing capsid for the production of infectious HCMV virion.


Vyšlo v časopise: The Smallest Capsid Protein Mediates Binding of the Essential Tegument Protein pp150 to Stabilize DNA-Containing Capsids in Human Cytomegalovirus. PLoS Pathog 9(8): e32767. doi:10.1371/journal.ppat.1003525
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1003525

Souhrn

Human cytomegalovirus (HCMV) is a ubiquitous herpesvirus that causes birth defects in newborns and life-threatening complications in immunocompromised individuals. Among all human herpesviruses, HCMV contains a much larger dsDNA genome within a similarly-sized capsid compared to the others, and it was proposed to require pp150, a tegument protein only found in cytomegaloviruses, to stabilize its genome-containing capsid. However, little is known about how pp150 interacts with the underlying capsid. Moreover, the smallest capsid protein (SCP), while dispensable in herpes simplex virus type 1, was shown to play essential, yet undefined, role in HCMV infection. Here, by cryo electron microscopy (cryoEM), we determine three-dimensional structures of HCMV capsid (no pp150) and virion (with pp150) at sub-nanometer resolution. Comparison of these two structures reveals that each pp150 tegument density is composed of two helix bundles connected by a long central helix. Correlation between the resolved helices and sequence-based secondary structure prediction maps the tegument density to the N-terminal half of pp150. The structures also show that SCP mediates interactions between the capsid and pp150 at the upper helix bundle of pp150. Consistent with this structural observation, ribozyme inhibition of SCP expression in HCMV-infected cells impairs the formation of DNA-containing viral particles and reduces viral yield by 10,000 fold. By cryoEM reconstruction of the resulting “SCP-deficient” viral particles, we further demonstrate that SCP is required for pp150 functionally binding to the capsid. Together, our structural and biochemical results point to a mechanism whereby SCP recruits pp150 to stabilize genome-containing capsid for the production of infectious HCMV virion.


Zdroje

1. Mocarski ES, Shenk T, Pass RF (2007) Cytomegalovirus. In: Knipe DM, Howley PM, Griffin DE, Martin MA, Lamb RA et al.., editors. Fields Virology. Philadelphia, PA: Lippincott/Williams & Wilkins. pp. 2701–2771.

2. BrittWJ, BoppanaS (2004) Human cytomegalovirus virion proteins. Hum Immunol 65: 395–402.

3. CheeM, RudolphSA, PlachterB, BarrellB, JahnG (1989) Identification of the major capsid protein gene of human cytomegalovirus. J Virol 63: 1345–1353.

4. GibsonW, BaxterMK, ClopperKS (1996) Cytomegalovirus “missing” capsid protein identified as heat-aggregable product of human cytomegalovirus UL46. J Virol 70: 7454–7461.

5. GibsonW, ClopperKS, BrittWJ, BaxterMK (1996) Human cytomegalovirus (HCMV) smallest capsid protein identified as product of short open reading frame located between HCMV UL48 and UL49. J Virol 70: 5680–5683.

6. BaldickCJJr, ShenkT (1996) Proteins associated with purified human cytomegalovirus particles. J Virol 70: 6097–6105.

7. ButcherSJ, AitkenJ, MitchellJ, GowenB, DarganDJ (1998) Structure of the human cytomegalovirus B capsid by electron cryomicroscopy and image reconstruction. J Struct Biol 124: 70–76.

8. TrusBL, GibsonW, ChengN, StevenAC (1999) Capsid structure of simian cytomegalovirus from cryoelectron microscopy: evidence for tegument attachment sites. J Virol 73: 2181–2192.

9. ZhouZH, DoughertyM, JakanaJ, HeJ, RixonFJ, et al. (2000) Seeing the herpesvirus capsid at 8.5 A. Science 288: 877–880.

10. YuX, ShahS, AtanasovI, LoP, LiuF, et al. (2005) Three-dimensional localization of the smallest capsid protein in the human cytomegalovirus capsid. J Virol 79: 1327–1332.

11. TrusBL, HeymannJB, NealonK, ChengN, NewcombWW, et al. (2001) Capsid structure of Kaposi's sarcoma-associated herpesvirus, a gammaherpesvirus, compared to those of an alphaherpesvirus, herpes simplex virus type 1, and a betaherpesvirus, cytomegalovirus. J Virol 75: 2879–2890.

12. BorstEM, MathysS, WagnerM, MuranyiW, MesserleM (2001) Genetic evidence of an essential role for cytomegalovirus small capsid protein in viral growth. J Virol 75: 1450–1458.

13. ChenDH, JiangH, LeeM, LiuF, ZhouZH (1999) Three-dimensional visualization of tegument/capsid interactions in the intact human cytomegalovirus. Virology 260: 10–16.

14. ZhouZH, ChenDH, JakanaJ, RixonFJ, ChiuW (1999) Visualization of tegument-capsid interactions and DNA in intact herpes simplex virus type 1 virions. J Virol 73: 3210–3218.

15. ChenDH, JakanaJ, McNabD, MitchellJ, ZhouZH, et al. (2001) The pattern of tegument-capsid interaction in the herpes simplex virus type 1 virion is not influenced by the small hexon-associated protein VP26. J Virol 75: 11863–11867.

16. TrusBL, NewcombWW, ChengN, CardoneG, MarekovL, et al. (2007) Allosteric signaling and a nuclear exit strategy: binding of UL25/UL17 heterodimers to DNA-Filled HSV-1 capsids. Mol Cell 26: 479–489.

17. MeyerHH, RipaltiA, LandiniMP, RadsakK, KernHF, et al. (1997) Human cytomegalovirus late-phase maturation is blocked by stably expressed UL32 antisense mRNA in astrocytoma cells. J Gen Virol 78 (Pt 10) 2621–2631.

18. YuX, ShahS, LeeM, DaiW, LoP, et al. (2011) Biochemical and structural characterization of the capsid-bound tegument proteins of human cytomegalovirus. J Struct Biol 174: 451–460.

19. YuX, TrangP, ShahS, AtanasovI, KimYH, et al. (2005) Dissecting human cytomegalovirus gene function and capsid maturation by ribozyme targeting and electron cryomicroscopy. Proc Natl Acad Sci U S A 102: 7103–7108.

20. BowmanBR, BakerML, RixonFJ, ChiuW, QuiochoFA (2003) Structure of the herpesvirus major capsid protein. EMBO J 22: 757–765.

21. ZhouZH, PrasadBV, JakanaJ, RixonFJ, ChiuW (1994) Protein subunit structures in the herpes simplex virus A-capsid determined from 400 kV spot-scan electron cryomicroscopy. J Mol Biol 242: 456–469.

22. BaxterMK, GibsonW (2001) Cytomegalovirus basic phosphoprotein (pUL32) binds to capsids in vitro through its amino one-third. J Virol 75: 6865–6873.

23. KilaniAF, TrangP, JoS, HsuA, KimJ, et al. (2000) RNase P ribozymes selected in vitro to cleave a viral mRNA effectively inhibit its expression in cell culture. J Biol Chem 275: 10611–10622.

24. TrangP, LeeM, NepomucenoE, KimJ, ZhuH, et al. (2000) Effective inhibition of human cytomegalovirus gene expression and replication by a ribozyme derived from the catalytic RNA subunit of RNase P from Escherichia coli. Proc Natl Acad Sci U S A 97: 5812–5817.

25. BooyFP, NewcombWW, TrusBL, BrownJC, BakerTS, et al. (1991) Liquid-crystalline, phage-like packing of encapsidated DNA in herpes simplex virus. Cell 64: 1007–1015.

26. BhellaD, RixonFJ, DarganDJ (2000) Cryomicroscopy of human cytomegalovirus virions reveals more densely packed genomic DNA than in herpes simplex virus type 1. J Mol Biol 295: 155–161.

27. YuXK, O'ConnorCM, AtanasovI, DamaniaB, KedesDH, et al. (2003) Three-dimensional structures of the A, B, and C capsids of rhesus monkey rhadinovirus: insights into gammaherpesvirus capsid assembly, maturation, and DNA packaging. J Virol 77: 13182–13193.

28. DesaiP, DeLucaNA, PersonS (1998) Herpes simplex virus type 1 VP26 is not essential for replication in cell culture but influences production of infectious virus in the nervous system of infected mice. Virology 247: 115–124.

29. PerkinsEM, AnackerD, DavisA, SankarV, AmbinderRF, et al. (2008) Small capsid protein pORF65 is essential for assembly of Kaposi's sarcoma-associated herpesvirus capsids. J Virol 82: 7201–7211.

30. SathishN, YuanY (2010) Functional characterization of Kaposi's sarcoma-associated herpesvirus small capsid protein by bacterial artificial chromosome-based mutagenesis. Virology 407: 306–318.

31. KilaniAF, TrangP, JoS, HsuA, KimJ, et al. (2000) RNase P ribozymes selected in vitro to cleave a viral mRNA effectively inhibit its expressionin cell culture. J Biol Chem 275: 10611–10622.

32. MillerAD, RosmanGJ (1989) Improved retroviral vectors for gene transfer and expression. Biotechniques 7: 980–982, 984–986, 989–990.

33. ToA, BaiY, ShenA, GongH, UmamotoS, et al. (2011) Yeast two hybrid analyses reveal novel binary interactions between human cytomegalovirus-encoded virion proteins. PLoS One 6: e17796.

34. MindellJA, GrigorieffN (2003) Accurate determination of local defocus and specimen tilt in electron microscopy. J Struct Biol 142: 334–347.

35. LiangY, KeEY, ZhouZH (2002) IMIRS: a high-resolution 3D reconstruction package integrated with a relational image database. J Struct Biol 137: 292–304.

36. LiuH, ChengL, ZengS, CaiC, ZhouZH, et al. (2008) Symmetry-adapted spherical harmonics method for high-resolution 3D single-particle reconstructions. J Struct Biol 161: 64–73.

37. PettersenEF, GoddardTD, HuangCC, CouchGS, GreenblattDM, et al. (2004) UCSF Chimera–a visualization system for exploratory research and analysis. J Comput Chem 25: 1605–1612.

38. JonesDT (1999) Protein secondary structure prediction based on position-specific scoring matrices. J Mol Biol 292: 195–202.

39. StevenAC, RobertsCR, HayJ, BisherME, PunT, et al. (1986) Hexavalent capsomers of herpes simplex virus type 2: symmetry, shape, dimensions, and oligomeric status. J Virol 57: 578–584.

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Hygiena a epidemiológia Infekčné lekárstvo Laboratórium

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PLOS Pathogens


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