| |
Genus: Teschovirus
Species: Porcine teschovirus
Serotype: Porcine teschovirus 1 (PTV-1)
(formerly porcine enterovirus 1) |
|
| 5' UTR |
L |
VP4 |
VP2 |
VP3 |
VP1 |
2A |
2B |
2C |
3A |
3B |
3C |
3D |
3' UTR |
|
Serotype: Porcine teschovirus 2 (PTV-2)
(formerly porcine enterovirus
2) |
|
| 5' UTR |
L |
VP4 |
VP2 |
VP3 |
VP1 |
2A |
2B |
2C |
3A |
3B |
3C |
3D |
3' UTR |
|
Serotype: Porcine teschovirus 3 (PTV-3)
(formerly porcine enterovirus
3) |
|
| 5' UTR |
L |
VP4 |
VP2 |
VP3 |
VP1 |
2A |
2B |
2C |
3A |
3B |
3C |
3D |
3' UTR |
|
Serotype: Porcine teschovirus 4 (PTV-4)
(formerly porcine enterovirus
4) |
|
| 5' UTR |
L |
VP4 |
VP2 |
VP3 |
VP1 |
2A |
2B |
2C |
3A |
3B |
3C |
3D |
3' UTR |
|
Serotype: Porcine teschovirus 5 (PTV-5)
(formerly porcine enterovirus 5) |
|
| 5' UTR |
L |
VP4 |
VP2 |
VP3 |
VP1 |
2A |
2B |
2C |
3A |
3B |
3C |
3D |
3' UTR |
|
Serotype: Porcine teschovirus 6 (PTV-6)
(formerly porcine enterovirus
6) |
|
| 5' UTR |
L |
VP4 |
VP2 |
VP3 |
VP1 |
2A |
2B |
2C |
3A |
3B |
3C |
3D |
3' UTR |
|
Serotype: Porcine teschovirus 7 (PTV-7)
(formerly porcine enterovirus
7) |
|
| 5' UTR |
L |
VP4 |
VP2 |
VP3 |
VP1 |
2A |
2B |
2C |
3A |
3B |
3C |
3D |
3' UTR |
|
Serotype: Porcine teschovirus 8 (PTV-8)
(formerly porcine enterovirus
11) |
|
| 5' UTR |
L |
VP4 |
VP2 |
VP3 |
VP1 |
2A |
2B |
2C |
3A |
3B |
3C |
3D |
3' UTR |
|
Serotype: Porcine teschovirus 9 (PTV-9)
(formerly porcine enterovirus
12) |
|
| 5' UTR |
L |
VP4 |
VP2 |
VP3 |
VP1 |
2A |
2B |
2C |
3A |
3B |
3C |
3D |
3' UTR |
|
Serotype: Porcine teschovirus 10 (PTV-10)
(formerly porcine enterovirus
13) |
|
| 5' UTR |
L |
VP4 |
VP2 |
VP3 |
VP1 |
2A |
2B |
2C |
3A |
3B |
3C |
3D |
3' UTR |
|
|
Serotype: Porcine teschovirus 11 (PTV-11) |
|
| 5' UTR |
L |
VP4 |
VP2 |
VP3 |
VP1 |
2A |
2B |
2C |
3A |
3B |
3C |
3D |
3' UTR |
|
| |
|
|
(White areas indicate genes which haven't yet been
sequenced completely;
grey areas are where only partial sequences exist)
| Virus |
Strain |
Region |
Length |
Accession No. |
Reference |
Comments |
|
|
| PTV-1 |
F65 |
CG* |
7110 |
AJ011380 |
Doherty et al., 1999 |
|
| PTV-1 |
Talfan§ |
3D |
1593 |
AB021646 |
Kaku et al., 1999 |
|
|
CG* |
7108 |
AF231769 |
Zell et al., 2001 |
|
|
CG* |
7088 |
AB038528 |
Kaku et al., 2001 |
|
|
PTV-1 |
Teschen-Konratice |
CG* |
7013 |
AF231768 |
Zell et al., 2001 |
|
|
PTV-1 |
Teschen-Bozen 654 |
CG* |
7109 |
AF231767 |
Zell et al., 2001 |
|
|
PTV-1 |
Teschen-Tirol |
L(p)-P1-2ABC(p) |
3395 |
AF296097 |
Zell et al., 2001 |
|
|
PTV-1 |
Teschen-199 |
L(p)-P1-2AB(p) |
3035 |
AF296098 |
Zell et al., 2001 |
|
|
PTV-1 |
PS34 |
L(p)-P1-2ABC(p) |
3440 |
AF296105 |
Zell et al., 2001 |
|
|
PTV-1 |
Vir 1626/89 |
CG* |
7112 |
AF296103 |
Zell et al., 2001 |
|
|
PTV-1 |
Vir 1627/89 |
CG* |
7112 |
AF296104 |
Zell et al., 2001 |
|
|
PTV-1 |
DS562/91 |
CG* |
7008 |
AF296100 |
Zell et al., 2001 |
|
|
PTV-1 |
Sek 549/98 |
L(p)-P1-2ABC(p) |
3434 |
AF296101 |
Zell et al., 2001 |
|
|
PTV-1 |
Vir 2236/99 |
CG* |
7009 |
AF296102 |
Zell et al., 2001 |
|
|
PTV-1 |
IBRSV-VII |
L(p)-P1-2ABC(p) |
3433 |
AF296099 |
Zell et al., 2001 |
|
|
PTV-1 |
5-D-VIII |
L(p)-P1-2AB(p) |
3040 |
AF296106 |
Zell et al., 2001 |
|
|
PTV-1 |
SF12 (J1) |
VP2(p) |
150 |
AB049553 |
Kaku et al., 2001 |
|
|
3D(p) |
844 |
AB049536 |
Kaku et al., 2001 |
|
|
|
|
PTV-2 |
T80§ |
CG* |
7017 |
AF296087 |
Zell et al., 2001 |
|
|
VP2(p) |
150 |
AB049546 |
Kaku et al., 2001 |
|
|
3D(p) |
844 |
AB049529 |
Kaku et al., 2001 |
|
|
PTV-2 |
Vir 6711-12/83 |
CG* |
7017 |
AF296107 |
Zell et al., 2001 |
|
|
PTV-2 |
Vir 6793/83 |
CG* |
7017 |
AF296108 |
Zell et al., 2001 |
|
|
PTV-2 |
Vir 480/87 |
CG* |
7019 |
AF296109 |
Zell et al., 2001 |
|
|
PTV-2 |
Sek 49/99 |
L(p)-P1-2ABC(p) |
3479 |
AF296110 |
Zell et al., 2001 |
|
|
PTV-2 |
SFK10 (J2) |
VP2(p) |
150 |
AB049554 |
Kaku et al., 2001 |
|
|
3D(p) |
844 |
AB049537 |
Kaku et al., 2001 |
|
|
|
|
PTV-3 |
O2b§ |
CG* |
7012 |
AF296088 |
Zell et al., 2001 |
|
|
VP2(p) |
150 |
AB049547 |
Kaku et al., 2001 |
|
|
3D(p) |
844 |
AB049530 |
Kaku et al., 2001 |
|
|
PTV-3 |
SFK30 (J7) |
VP2(p) |
150 |
AB049557 |
Kaku et al., 2001 |
|
|
3D(p) |
844 |
AB049540 |
Kaku et al., 2001 |
|
|
|
|
PTV-4 |
PS36§ |
CG* |
7014 |
AF296089 |
Zell et al., 2001 |
|
|
VP2(p) |
150 |
AB049548 |
Kaku et al., 2001 |
|
|
3D(p) |
844 |
AB049531 |
Kaku et al., 2001 |
|
|
PEV-4 |
Vir 918-19/85 |
CG* |
7015 |
AF296111 |
Zell et al., 2001 |
|
|
PTV-4 |
Vir 3764/86 |
CG* |
7015 |
AF296112 |
Zell et al., 2001 |
|
|
PTV-4 |
Vir 2500/99 |
CG* |
7015 |
AF296113 |
Zell et al., 2001 |
|
|
|
|
PTV-5 |
F26§ |
CG* |
7008 |
AF296090 |
Zell et al., 2001 |
|
|
VP2(p) |
150 |
AB049549 |
Kaku et al., 2001 |
|
|
3D(p) |
844 |
AB049532 |
Kaku et al., 2001 |
|
|
PTV-5 |
Vir 1806/89 |
L(p)-P1-2AB(p) |
3254 |
AF296114 |
Zell et al., 2001 |
|
|
PTV-5 |
SF1 ( J3) |
VP2(p) |
150 |
AB049555 |
Kaku et al., 2001 |
|
|
3D(p) |
844 |
AB049538 |
Kaku et al., 2001 |
|
|
|
|
PTV-6 |
PS37§ |
CG* |
7018 |
AF296091 |
Zell et al., 2001 |
|
|
VP2(p) |
150 |
AB049550 |
Kaku et al., 2001 |
|
|
3D(p) |
844 |
AB049533 |
Kaku et al., 2001 |
|
|
PTV-6 |
Vir 3634/85 |
CG* |
7017 |
AF296115 |
Zell et al., 2001 |
|
|
PTV-6 |
21-SZ |
CG* |
7018 |
AF296117 |
Zell et al., 2001 |
|
|
PTV-6 |
Vir 289/89 |
L(p)-P1-2ABC(p) |
3784 |
AF296116 |
Zell et al., 2001 |
|
|
PTV-6 |
SFG12 ( J5) |
VP2(p) |
150 |
AB049556 |
Kaku et al., 2001 |
|
|
3D(p) |
844 |
AB049539 |
Kaku et al., 2001 |
|
|
PTV-6 |
50L4 (J9) |
VP2(p) |
150 |
AB049558 |
Kaku et al., 2001 |
|
|
3D(p) |
844 |
AB049541 |
Kaku et al., 2001 |
|
|
|
|
PTV-7 |
F43§ |
CG* |
7014 |
AF296092 |
Zell et al., 2001 |
|
|
VP2(p) |
150 |
AB049551 |
Kaku et al., 2001 |
|
|
3D(p) |
844 |
AB049534 |
Kaku et al., 2001 |
|
|
|
|
PTV-8 |
UKG/173/74§ |
CG* |
7017 |
AF296093 |
Zell et al., 2001 |
|
|
VP2(p) |
150 |
AB049552 |
Kaku et al., 2001 |
|
|
3D(p) |
844 |
AB049535 |
Kaku et al., 2001 |
|
|
PTV-8 |
25-T-VII |
CG* |
7018 |
AF296118 |
Zell et al., 2001 |
|
|
|
|
PTV-9 |
Vir-2899/84§ |
CG* |
7006 |
AF296094 |
Zell et al., 2001 |
|
|
|
|
PTV-10 |
Vir 461/88§ |
CG* |
7018 |
AF296119 |
Zell et al., 2001 |
|
|
PTV-10 |
Vir 460/88 |
CG* |
7009 |
AF296095 |
Zell et al., 2001 |
|
|
|
|
PTV-11 |
Dresden§ |
CG* |
7111 |
AF296096 |
Zell et al., 2001 |
|
|
PTV-11 |
UKG 53/81 |
L(p)-P1-2AB(p) |
3045 |
AF296120 |
Zell et al., 2001 |
|
|
PTV-11 |
DS 1696/91 |
L(p)-P1-2A |
2982 |
AF296121 |
Zell et al., 2001 |
|
CG = complete genome; (p) = partial gene sequence;
§ prototype strain
*5' end of the genome missing |
Doherty, M., Todd, D., McFerran, N. and Hoey, E.M..(1999). Sequence analysis of a
porcine enterovirus serotype 1 isolate: relationships with other picornaviruses. J Gen
Virol. 80:1929-1941.
Kaku, Y., Yamada, S., Murakami, Y. (1999). Sequence determination and phylogenetic
analysis of RNA-dependent RNA polymerase (RdRp) of the porcine enterovirus 1 (PEV-1)
Talfan strain. Arch. Virol. 144: 1845-1852.
Kaku, Y., Sarai, A. and Murakami, Y. (2001). Genetic reclassification of porcine
enteroviruses. J. Gen. Virol. 82: 417-424.
Zell, R., Dauber, M., Krumbholz, A.,
Henke, A., Birch-Hirschfeld, E., Stelzner, A., Prager, D. and Wurm, R.
(2001). Porcine teschoviruses comprise at least eleven distinct serotypes:
molecular and evolutionary aspects. J. Virol. 2001. 75: 1620-1631.
|