Confusions in orbivirus protein classification

Meik Dilcher; Manfred Weidmann

doi:10.1186/1743-422X-9-166

. 2012 Aug 21;9:166. doi: 10.1186/1743-422X-9-166

Confusions in orbivirus protein classification

Meik Dilcher ^1,^✉, Manfred Weidmann ¹

PMCID: PMC3494582 PMID: 22909086

Abstract

An extensive comparative analysis of orbivirus genomes revealed four cases of unclear numeration and protein designation, due to confused reference to protein size or segment size by which they are encoded. A concise nomenclature based on type species, sequence homology and functional characteristics independent of segment or protein size is suggested.

Keywords: Reoviridae, Orbivirus, Protein classification

Background

The genus Orbivirus is one of 15 in the family of Reoviridae containing 22 serogroups (species) and at least 160 different serotypes (strains) [1]. Orbiviruses are transmitted by insects (midges, flies, mosquitoes) or by ticks. Their double-stranded RNA (dsRNA) genomes consist of 10 segments coding for seven structural and at least three non-structural proteins. Orbiviruses have no envelope but a double-shelled icosahedral capsid [2] and include pathogenic agents of wild animals (Epizootic hemorrhagic disease virus (EHDV)), domestic animals (Bluetongue virus (BTV) and African horse sickness virus (AHSV)), and of man (Kemerovo virus (KEMV)) [3]. Type species of the genus is the Culicoides midge transmitted BTV. Insect-borne orbiviruses are much better characterized than tick-transmitted orbiviruses for which few sequences have been described: Broadhaven virus (BRDV, partial) [4], Sandy Bay virus (SBaV, partial (formerly Nugget virus)) [5-8], St Croix River virus (SCRV, complete genome) [9], Great Island virus (GIV, complete genome) [7].

Recently we determined the complete genomes of Tribeč virus (TRBV) and KEMV in a pyrosequencing approach [10] complementing available partial information on segments 1, 2 and 6 of these viruses and of Lipovnik virus (LIPV) [7].

During our extensive comparative analysis of orbivirus genomes we noticed four cases of unclear numeration and protein designation (see Tables 1 and 2). Some laboratories classify orbivirus proteins according to the size of the proteins whereas others use the size of genome segments from which they are encoded.

Table 1.

Comparison of the genome segments and encoded proteins of BTV, YUOV, TRBV, KEMV and GIV

BTV (insect-transmitted)				YUOV (insect-transmitted)				TRBV (tick-transmitted)				KEMV (tick-transmitted)				GIV (tick-transmitted)
Segment 1	VP1 (Pol)	150 kDa	RNA-dep.-RNA- Polymerase	Segment 1	VP1 (Pol)	151 kDa	RNA-dep.-RNA- Polymerase	Segment 1	VP1 (Pol)	146 kDa	RNA-dep.-RNA- Polymerase	Segment 1	VP1 (Pol)	146 kDa	RNA-dep.-RNA- Polymerase	Segment 1	VP1 (Pol)	147 kDa	RNA-dep.-RNA- Polymerase
3944 bp	ACR58458	1302 AA		3393 bp	YP_443925	1315 AA		3892 bp	HQ266581	1284 AA		3896 bp	HQ266591	1285 AA		3897 bp	ADM88592	1285 AA

Segment 2	VP2	111 kDa	Outer shell	Segment 2	VP2 (T2)	107 kDa	Inner shell	Segment 2	VP3 (T2)	102 kDa	Inner shell	Segment 2	VP3 (T2)	103 kDa	Inner shell	Segment 2	VP2 (T2)	103 kDa	Inner shell
2953 bp	ACR58459	956 AA		2900 bp	YP_443926	940 AA		2793 bp	HQ266582	908 AA		2792 bp	HQ266592	908 AA		2794 bp	ADM88593	908 AA

Segment 3	VP3 (T2)	103 kDa	Inner shell	Segment 3	VP3	100 kDa	Outer shell	Segment 3	VP4 (CaP)	72 kDa	Capping Enzyme	Segment 3	VP4 (CaP)	72 kDa	Capping Enzyme	Segment 3	VP3 (CaP)	73 kDa	Capping Enzyme
2772 bp	ACR58460	901 AA	Inner shell	2688 bp	YP_443927	873 AA	Outer shell	1935 bp	HQ266583	628 AA	Capping Enzyme	1934 bp	HQ266593	632 AA	Capping Enzyme	1936 bp	ADM88594	635 AA	Capping Enzyme

Segment 4	VP4 (CaP)	75 kDa	Capping Enzyme	Segment 4	VP4 (CaP)	74 kDa	Capping Enzyme	Segment 4	NS1 (TuP)	62 kDa	Formes Tubules	Segment 4	VP2	63 kDa	Outer shell	Segment 4	NS1 (TuP)	60 kDa	Formes Tubules
1980 bp	ACR58461	644 AA	Capping Enzyme	1993 bp	YP_443928	645 AA	Capping Enzyme	1734 bp	HQ266584	529 AA	Formes Tubules	1730 bp	HQ266594	554 AA	Outer shell	1731 bp	ADM88595	531 AA	Formes Tubules

Segment 5	NS1 (TuP)	64 kDa	Forms Tubules	Segment 5	NS1 (TuP)	67 kDa	Forms Tubules	Segment 5	VP2	62 kDa	Outer shell	Segment 5	NS1 (TuP)	60 kDa	Formes Tubules	Segment 5	VP4	62 kDa	Outer shell
1769 bp	ACR58463	552 AA	Forms Tubules	1957 bp	YP_443929	574 AA	Forms Tubules	1730 bp	HQ266585	554 AA	Outer shell	1719 bp	HQ266595	529 AA	Formes Tubules	1722 bp	ADM88596	551 AA	Outer shell

Segment 6	VP5	59 kDa	Outer shell	Segment 6	VP5	59 kDa	Outer shell	Segment 6	VP5	59 kDa	Outer shell	Segment 6	VP5	59 kDa	Outer shell	Segment 6	VP5	60 kDa	Outer shell
1638 bp	ACR58462	526 AA		1683 bp	YP_443930	535 AA		1668 bp	HQ266586	537 AA		1668 bp	HQ266596	537 AA		1666 bp	ADM88597	537 AA

Segment 7	VP7 (T13)	39 kDa	Inner shell	Segment 7	NS2 (ViP)	48 kDa	Viral inclusion body matrix protein	Segment 7	NS2 (ViP)	41 kDa	Viral inclusion body matrix protein	Segment 7	NS2 (ViP)	41 kDa	Viral inclusion body matrix protein	Segment 7	VP7 (T13)	40 kDa	Inner shell
1156 bp	ACR58464	349 AA	Inner shell	1504 bp	YP_443931	435 AA	Viral inclusion body matrix protein	1196 bp	HQ266587	368 AA	Viral inclusion body matrix protein	1197 bp	HQ266597	368 AA	Viral inclusion body matrix protein	1181 bp	ADM88598	357 AA	Inner shell

Segment 8	NS2 (ViP)	41 kDa	Viral inclusion body matrix protein	Segment 8	VP7 (T13)	40 kDa	Inner shell	Segment 8	VP7 (T13)	40 kDa	Inner shell	Segment 8	VP7 (T13)	40 kDa	Inner shell	Segment 8	NS2 (ViP)	39 kDa	Viral inclusion body matrix protein
1125 bp	ACR58465	354 AA	Viral inclusion body matrix protein	1191 bp	YP_443932	355 AA	Inner shell	1184 bp	HQ266588	357 AA	Inner shell	1183 bp	HQ266598	357 AA	Inner shell	1172 bp	ADM88599	359 AA	Viral inclusion body matrix protein

Segment 9	VP6 (Hel)	36 kDa	ssRNA and dsRNA binding helicase	Segment 9	VP6 (Hel)	37 kDa	ssRNA and dsRNA binding helicase	Segment 9	VP6 (Hel)	33 kDa	ssRNA and dsRNA binding helicase	Segment 9	VP6 (Hel)	34 kDa	ssRNA and dsRNA binding helicase	Segment 9	VP6 (Hel)	34 kDa	ssRNA and dsRNA binding helicase
1049 bp	ACR58466	329 AA	ssRNA and dsRNA binding helicase	1082 bp	YP_443933	338 AA	ssRNA and dsRNA binding helicase	1034 bp	HQ266589	312 AA	ssRNA and dsRNA binding helicase	1049 bp	HQ266599	317 AA	ssRNA and dsRNA binding helicase	1056 bp	AMD88600	321 AA	ssRNA and dsRNA binding helicase

Segment 10	NS3	26 kDa	Glycoprotein	Segment 10	NS3	28 kDa	Glycoprotein	Segment 10	NS3	23 kDa	Glycoprotein	Segment 10	NS3	23 kDA	Glycoprotein	Segment 10	NS3	19 kDa	Glycoprotein
822 bp	ACR58467	229 AA		825 bp	YP_443934	253 AA		705 bp	HQ266590	214 AA		707 bp	HQ266600	214AA		703 bp	ADM88602	171 AA

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Outer and inner shell proteins are labeled in bold. GenBank and SwissProt accession numbers are indicated.

Table 2.

Comparison of the genome segments and encoded proteins of SCRV, PHSV, BRDV and LIPV

SCRV (tick-transmitted)				PHSV (isolates only known from horses)				BRDV (tick-transmitted)				LIPV (tick-transmitted)
Segment 1	VP1 (Pol)	151 kDa	RNA-dep.-RNA-Polymerase	Segment 1	VP1 (Pol)	151 kDa	RNA-dep.-RNA-Polymerase	Segment 1				Segment 1	VP1 (Pol)	146 kDa	RNA-dep.-RNA-Polymerase
4089 bp	YP_052942	1345 AA	RNA-dep.-RNA-Polymerase	3987 bp	YP_460038	1311 AA	RNA-dep.-RNA-Polymerase	Segment 1				3892 bp	ADM88603	1284 AA	RNA-dep.-RNA-Polymerase

Segment 2	VP2 (T2)	98 kDa	Inner shell	Segment 2	VP3 (T2)	105 kDa	Inner shell	Segment 2	VP2 (T2)	103 kDa	Inner shell	Segment 2	VP2 (T2)	103 kDa	Inner shell
2747 bp	YP_052943	890 AA		2856 bp	YP_460039	925 AA			P35934	908 AA		2793 bp	ADM88604	908 AA

Segment 3	VP3	74 kDa	Outer shell	Segment 3	VP2	104 kDa	Outer shell	Segment 3				Segment 3
2024 bp	YP_052944	654 AA		2747 bp	YP_460040	881 AA

Segment 4	VP4 (CaP)	74 kDa	Capping Enzyme	Segment 4	VP4 (CaP)	74 kDa	Capping Enzyme	Segment 4	VP4 †	63 kDa †	Outer shell	Segment 4
2017 bp	YP_052945	643 AA	Capping Enzyme	1996 bp	YP_460041	646 AA	Capping Enzyme	Segment 4	VP4 †	63 kDa †	Outer shell	Segment 4

Segment 5	VP5	57 kDa	Outer shell	Segment 5	NS1 (TuP)	64 kDa	Forms Tubules	Segment 5	VP5	53 kDa	Outer shell	Segment 5
1664 bp	YP_052946	517 AA		1784 bp	YP_460045	554 AA		1658 bp	P21230	480 AA

Segment 6	NS1 (TuP)	58 kDa	Forms Tubules	Segment 6	VP5	59 kDa	Outer shell	Segment 6	NS1 (TuP)	60 kDa	Formes Tubules	Segment 6	VP5	502 AA ††	Outer shell
1657 bp	YP_052947	517 AA		1695 bp	YP_460042	529 AA		1714 bp	2115436A	537 AA		1509 bp ††	ADM88605

Segment 7	NS2 (ViP)	51 kDa	Viral inclusion body matrix protein	Segment 7	NS2 (ViP)	48 kDa	Viral inclusion body matrix protein	Segment 7	VP7 (T13)	40 kDa	Inner shell	Segment 7
1463 bp	YP_052948	462 AA	Viral inclusion body matrix protein	1613 bp	YP_460046	435 AA	Viral inclusion body matrix protein		P35935	356 AA	Inner shell	Segment 7

Segment 8	VP7 (T13)	41 kDa	Inner shell	Segment 8	VP7 (T13)	40 kDa	Inner shell	Segment 8				Segment 8
1256 bp	YP_052949	379 AA		1180 bp	YP_460044	353 AA

Segment 9	VP6 (Hel)	26 kDa	ssRNA and dsRNA binding helicase	Segment 9	VP6 (Hel)	37 kDa	ssRNA and dsRNA binding helicase	Segment 9				Segment 9
764 bp	YP_052950	232 AA		1071 bp	YP_460043	334 AA

Segment 10	NS3	24 kDa	Glycoprotein	Segment 10	NS3	28 kDa	Glycoprotein	Segment 10	NS3	22 kDa	Glycoprotein	Segment 10
764 bp	YP_052951	224 AA		819 bp	YP_460047	255 AA			P32555	205 AA

Open in a new tab

Outer and inner shell proteins are labeled in bold. GenBank and SwissProt accession numbers are indicated.

†: [12,13], GenBank entry missing.

††: partial sequence.

(i) The inner shell protein T2 for example can be encoded by segment 2 (tick- and mosquito-borne orbiviruses) or segment 3 (Culicoides-borne orbiviruses). This leads to some laboratories labeling this protein VP2(T2) (e.g. GIV), while others designate it VP3(T2) as in the type species BTV. For Peruvian horse sickness virus (PHSV) however, the segment 2 encoded protein is designated VP3(T2) although it is larger (925 amino acids) than the segment 3 encoded VP2 protein (881 amino acids) [11]. To avoid confusion with the outer shell protein VP2 we suggest to exclusively use VP3(T2) for all T2 proteins.

(ii) VP2 and VP2 homologous proteins can be encoded by segments 2, 3, 4 and 5 and are designated VP2, VP3 (YUOV, SCRV) or VP4 (BRDV segment 4 ( [12,13], sequence entry to GenBank missing)), GIV segment 5). Because of the location on the outer capsid and the described sequence similarity with other VP2 proteins, we suggest that the VP4 proteins (BRDV, GIV) as well as the VP3 proteins (YUOV, SCRV) should be uniformly termed VP2, even though tick-borne VP2 proteins have only half the size of insect-borne VP2 proteins [13].

(iii) The capping enzyme VP4(CaP) can be encoded by segment 4 (BTV, YUOV, SCRV etc.) or segment 3 (TRBV, KEMV). In GIV this protein is designated VP3(CaP) [7] and should be renamed VP4(CaP) to avoid confusions with VP3(T2).

(iv) In most cases VP5 is encoded by segment 6 and comprises a component of the outer shell that might be involved in membrane fusion and penetration [14]. TRBV and KEMV also encode VP5 on segment 6. The highest similarity of TRBV VP5 is to LIPV VP5 (95.6%), again encoded by segment 6 [7]. However, VP5 of BRDV is described as encoded by segment 5 [15]. Since in the classification of the viral genome segments bigger segments have smaller segment numbers, and the size of BRDV segment 6 (1714 bp) encoding the NS1(TuP) [16] is larger than the size of BRDV segment 5 (1658 bp) encoding VP5, a reassignment of BRDV segment 5 and 6 (a vice versa switch) seems necessary.

To summarize, it would be much more helpful if the nomenclature of the viral proteins in orbiviruses would reflect the sequence homology and functional relationship rather than protein size or encoding segment size, since the sizes of the orbivirus genome segments sometimes only differ slightly, which leads to even closely related viruses such as TRBV and KEMV encoding VP2 and NS1(TuP) on different genome segments. We therefore suggest the following concise nomenclature based on the type species BTV and on sequence homology and functional characteristics independent of segment or protein size: VP1(Pol), VP2, VP3(T2), VP4(CaP), VP5, VP6(Hel), VP7(T13), NS1(TuP), NS2(ViP), NS3.

Competing interests

The authors declare that they have no competing interests.

Author’s contributions

MD and MW wrote the paper. Both authors read and approved the final manuscript.

Contributor Information

Meik Dilcher, Email: meik.dilcher@medizin.uni-goettingen.de.

Manfred Weidmann, Email: mweidma@gwdg.de.

Acknowledgments

This work was supported by the Federal Ministry of Education and Research (BMBF), grant number 01KI0710, “Research on Zoonotic Infectious Diseases” program, “Emerging arthropode-borne viral infections in Germany: Pathogenesis, diagnostics and surveillance” and the BMBF funded research program “Potential release-oriented biothreat emergency diagnostics (P.R.O.B.E)” for civil security of the German Federal Government as part of the high-tech strategy for Germany.

References

Attoui H, Mertens PPC, Becnel J, Belaganahalli S, Bergoin M, Brussaard CP, Chappell JD, Ciarlet M, del Vas M, Dermody TS, In: Virus taxonomy ninth report of the international committee on taxonomy of viruses. King AMQ, Adams MJ, Carstens EB, Lefkowitz EJ, editor. Elsevier: Adacemic Press; 2011. Orbiviruses, Reoviridae; pp. 592–603. [Google Scholar]
Attoui H, Jaafar FM, Belhouchet M, Aldrovandi N, Tao SJ, Chen BQ, Liang GD, Tesh RB, de Micco P, de Lamballerie X. Yunnan orbivirus, a new orbivirus species isolated from Culex tritaeniorhynchus mosquitoes in China. J Gen Virol. 2005;86:3409–3417. doi: 10.1099/vir.0.81258-0. [DOI] [PubMed] [Google Scholar]
Gorman BM. Variation in orbiviruses. J Gen Virol. 1979;44:1–15. doi: 10.1099/0022-1317-44-1-1. [DOI] [PubMed] [Google Scholar]
Moss SR, Jones LD, Nuttall PA. Comparison of the major structural core proteins of tick-borne and culicoides-borne orbiviruses. J Gen Virol. 1992;73:2585–2590. doi: 10.1099/0022-1317-73-10-2585. [DOI] [PubMed] [Google Scholar]
Doherty RL, Carley JG, Murray MD, Main AJ, Kay BH, Domrow R. Isolation of arboviruses (Kemerovo-Group, Sakhalin-Group) from ixodes-uriae collected at Macquarie Island, Southern Ocean. Am J Trop Med Hyg. 1975;24:521–526. doi: 10.4269/ajtmh.1975.24.521. [DOI] [PubMed] [Google Scholar]
Gorman BM, Taylor J, Morton HC, Melzer AJ, Young PR. Characterization of nugget virus, a serotype of the kemerovo group of orbiviruses. Aust J Exp Biol Med Sci. 1984;62:101–115. doi: 10.1038/icb.1984.10. [DOI] [PubMed] [Google Scholar]
Belhouchet M, Jaafar FM, Tesh RB, Grimes J, Maan S, Mertens P, Attoui H. Complete sequence of the Great Island virus and comparison with the T2 and outer-capsid proteins of Kemerovo, Lipovnik and Tribec viruses (genus Orbivirus, family Reoviridae) J Gen Virol. 2010;91:2985–2993. doi: 10.1099/vir.0.024760-0. [DOI] [PubMed] [Google Scholar]
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Attoui H, Stirling JM, Munderloh UG, Billoir F, Brookes SM, Burroughs JN, de Micco P, Mertens PPC, de Lamballerie X. Complete sequence characterization of the genome of the St Croix River virus, a new orbivirus isolated from cells of Ixodes scapularis. J Gen Virol. 2001;82:795–804. doi: 10.1099/0022-1317-82-4-795. [DOI] [PubMed] [Google Scholar]
Dilcher M, Hasib L, Lechner M, Wieseke N, Middendorf M, Marz M, Koch A, Spiegel M, Dobler G, Hufert FT, Weidmann M. Genetic characterization of Tribeč virus and Kemerovo virus, two tick-transmitted human-pathogenic Orbiviruses. Virology. 2012;423:68–76. doi: 10.1016/j.virol.2011.11.020. [DOI] [PubMed] [Google Scholar]
Attoui H, Mendez-Lopez MR, Rao SJ, Hurtado-Alendes A, Lizaraso-Caparo F, Jaafar FM, Samuel AR, Belhouchet M, Pritchard LI, Melville L. et al. Peruvian horse sickness virus and Yunnan orbivirus, isolated from vertebrates and mosquitoes in Peru and Australia. Virology. 2009;394:298–310. doi: 10.1016/j.virol.2009.08.032. [DOI] [PubMed] [Google Scholar]
Moss SR, Nuttall PA. Subcore-like and core-like particles of Broadhaven Virus (Brdv), a tick-borne orbivirus, synthesized from baculovirus-expressed Vp2 and Vp7, the major core proteins of Brdv. Virus Res. 1994;32:401–407. doi: 10.1016/0168-1702(94)90088-4. [DOI] [PubMed] [Google Scholar]
Schoehn G, Moss SR, Nuttall PA, Hewat EA. Structure of Broadhaven virus by cryoelectron microscopy: Correlation of structural and antigenic properties of Broadhaven virus and bluetongue virus outer capsid proteins. Virology. 1997;235:191–200. doi: 10.1006/viro.1997.8685. [DOI] [PubMed] [Google Scholar]
Zhang X, Boyce M, Bhattacharya B, Zhang XK, Schein S, Roy P, Zhou ZH. Bluetongue virus coat protein VP2 contains sialic acid-binding domains, and VP5 resembles enveloped virus fusion proteins. Proc Natl Acad Sci U S A. 2010;107:6292–6297. doi: 10.1073/pnas.0913403107. [DOI] [PMC free article] [PubMed] [Google Scholar]
Moss SR, Fukusho A, Nuttall PA. Rna segment 5 of Broadhaven virus, a tick-borne orbivirus, shows sequence homology with segment-5 of bluetongue virus. Virology. 1990;179:482–484. doi: 10.1016/0042-6822(90)90320-Q. [DOI] [PubMed] [Google Scholar]
Moss SR, Nuttall PA. Comparison of the nonstructural protein, Ns1, of tick-borne and insect-borne orbiviruses. Virus Res. 1995;36:287–292. doi: 10.1016/0168-1702(95)00004-A. [DOI] [PubMed] [Google Scholar]

[B1] Attoui H, Mertens PPC, Becnel J, Belaganahalli S, Bergoin M, Brussaard CP, Chappell JD, Ciarlet M, del Vas M, Dermody TS, In: Virus taxonomy ninth report of the international committee on taxonomy of viruses. King AMQ, Adams MJ, Carstens EB, Lefkowitz EJ, editor. Elsevier: Adacemic Press; 2011. Orbiviruses, Reoviridae; pp. 592–603. [Google Scholar]

[B2] Attoui H, Jaafar FM, Belhouchet M, Aldrovandi N, Tao SJ, Chen BQ, Liang GD, Tesh RB, de Micco P, de Lamballerie X. Yunnan orbivirus, a new orbivirus species isolated from Culex tritaeniorhynchus mosquitoes in China. J Gen Virol. 2005;86:3409–3417. doi: 10.1099/vir.0.81258-0. [DOI] [PubMed] [Google Scholar]

[B3] Gorman BM. Variation in orbiviruses. J Gen Virol. 1979;44:1–15. doi: 10.1099/0022-1317-44-1-1. [DOI] [PubMed] [Google Scholar]

[B4] Moss SR, Jones LD, Nuttall PA. Comparison of the major structural core proteins of tick-borne and culicoides-borne orbiviruses. J Gen Virol. 1992;73:2585–2590. doi: 10.1099/0022-1317-73-10-2585. [DOI] [PubMed] [Google Scholar]

[B5] Doherty RL, Carley JG, Murray MD, Main AJ, Kay BH, Domrow R. Isolation of arboviruses (Kemerovo-Group, Sakhalin-Group) from ixodes-uriae collected at Macquarie Island, Southern Ocean. Am J Trop Med Hyg. 1975;24:521–526. doi: 10.4269/ajtmh.1975.24.521. [DOI] [PubMed] [Google Scholar]

[B6] Gorman BM, Taylor J, Morton HC, Melzer AJ, Young PR. Characterization of nugget virus, a serotype of the kemerovo group of orbiviruses. Aust J Exp Biol Med Sci. 1984;62:101–115. doi: 10.1038/icb.1984.10. [DOI] [PubMed] [Google Scholar]

[B7] Belhouchet M, Jaafar FM, Tesh RB, Grimes J, Maan S, Mertens P, Attoui H. Complete sequence of the Great Island virus and comparison with the T2 and outer-capsid proteins of Kemerovo, Lipovnik and Tribec viruses (genus Orbivirus, family Reoviridae) J Gen Virol. 2010;91:2985–2993. doi: 10.1099/vir.0.024760-0. [DOI] [PubMed] [Google Scholar]

[B8] Major L, Linn ML, Slade RW, Schroder WA, Hyatt AD. et al. Ticks associated with Macquarie Island penguins carry arboviruses from four genera. PLoS One. 2009;4:e4375. doi: 10.1371/journal.pone.0004375. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B9] Attoui H, Stirling JM, Munderloh UG, Billoir F, Brookes SM, Burroughs JN, de Micco P, Mertens PPC, de Lamballerie X. Complete sequence characterization of the genome of the St Croix River virus, a new orbivirus isolated from cells of Ixodes scapularis. J Gen Virol. 2001;82:795–804. doi: 10.1099/0022-1317-82-4-795. [DOI] [PubMed] [Google Scholar]

[B10] Dilcher M, Hasib L, Lechner M, Wieseke N, Middendorf M, Marz M, Koch A, Spiegel M, Dobler G, Hufert FT, Weidmann M. Genetic characterization of Tribeč virus and Kemerovo virus, two tick-transmitted human-pathogenic Orbiviruses. Virology. 2012;423:68–76. doi: 10.1016/j.virol.2011.11.020. [DOI] [PubMed] [Google Scholar]

[B11] Attoui H, Mendez-Lopez MR, Rao SJ, Hurtado-Alendes A, Lizaraso-Caparo F, Jaafar FM, Samuel AR, Belhouchet M, Pritchard LI, Melville L. et al. Peruvian horse sickness virus and Yunnan orbivirus, isolated from vertebrates and mosquitoes in Peru and Australia. Virology. 2009;394:298–310. doi: 10.1016/j.virol.2009.08.032. [DOI] [PubMed] [Google Scholar]

[B12] Moss SR, Nuttall PA. Subcore-like and core-like particles of Broadhaven Virus (Brdv), a tick-borne orbivirus, synthesized from baculovirus-expressed Vp2 and Vp7, the major core proteins of Brdv. Virus Res. 1994;32:401–407. doi: 10.1016/0168-1702(94)90088-4. [DOI] [PubMed] [Google Scholar]

[B13] Schoehn G, Moss SR, Nuttall PA, Hewat EA. Structure of Broadhaven virus by cryoelectron microscopy: Correlation of structural and antigenic properties of Broadhaven virus and bluetongue virus outer capsid proteins. Virology. 1997;235:191–200. doi: 10.1006/viro.1997.8685. [DOI] [PubMed] [Google Scholar]

[B14] Zhang X, Boyce M, Bhattacharya B, Zhang XK, Schein S, Roy P, Zhou ZH. Bluetongue virus coat protein VP2 contains sialic acid-binding domains, and VP5 resembles enveloped virus fusion proteins. Proc Natl Acad Sci U S A. 2010;107:6292–6297. doi: 10.1073/pnas.0913403107. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B15] Moss SR, Fukusho A, Nuttall PA. Rna segment 5 of Broadhaven virus, a tick-borne orbivirus, shows sequence homology with segment-5 of bluetongue virus. Virology. 1990;179:482–484. doi: 10.1016/0042-6822(90)90320-Q. [DOI] [PubMed] [Google Scholar]

[B16] Moss SR, Nuttall PA. Comparison of the nonstructural protein, Ns1, of tick-borne and insect-borne orbiviruses. Virus Res. 1995;36:287–292. doi: 10.1016/0168-1702(95)00004-A. [DOI] [PubMed] [Google Scholar]

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Confusions in orbivirus protein classification

Meik Dilcher

Manfred Weidmann

Abstract

Background

Table 1.

Table 2.

Competing interests

Author’s contributions

Contributor Information

Acknowledgments

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PERMALINK

Confusions in orbivirus protein classification

Meik Dilcher

Manfred Weidmann

Abstract

Background

Table 1.

Table 2.

Competing interests

Author’s contributions

Contributor Information

Acknowledgments

References

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