ライフサイエンスコーパス: arterivirus

1 a new virus family which includes the genus arterivirus.

2 aused not by SHFV but by two novel divergent arteriviruses.

3 ree open reading frames not present in other arteriviruses.

4 sitive-sense, single-stranded RNA [ssRNA(+)] arteriviruses.

5 es, and compared it to those of LV and other arteriviruses.

6 are related to ORFs 2 through 4 of the other arteriviruses.

7 three more ORFs on its genome than the other arteriviruses.

8 ree additional ORFs as compared to the other arteriviruses.

9 ns of evolution differ markedly among simian arteriviruses and among host species.

10 logenetic and geographic range of the simian arteriviruses and define baboons as a natural host for t

11 ng improved live attenuated vaccines against arteriviruses and other viruses encoding similar dual-sp

12 th each other as well as with those of other arteriviruses, and the predicted catalytic residues were

13 Simian arteriviruses are a diverse clade of viruses infecting c

14 Simian arteriviruses are a diverse group of related viruses tha

15 tive macaque colonies by showing that simian arteriviruses are actively circulating in captive baboon

16 Arteriviruses are economically important positive-strand

17 dition to SIV, simian pegiviruses and simian arteriviruses are widespread and prevalent among many Af

18 lends credibility to the hypothesis that an arterivirus can manipulate cellular miRNAs to enhance vi

19 ults indicate that multiple divergent simian arteriviruses can cause SHF.

20 ur data suggest a need to modify the current arterivirus classification.

21 ants provide potential antiviral targets for arterivirus disease control and prevention.

22 Similar to other arteriviruses, EAV primarily targets cells of the monocy

23 Other arteriviruses encode one or two active PLP1s.

24 ehydrogenase-elevating virus, a benign mouse arterivirus, exacerbates the pathogenicity of IgM anti-p

25 s (family Flaviviridae) and two novel simian arteriviruses (family Arteriviridae) in wild African gre

26 s and add another layer to the complexity of arterivirus genome expression.

27 netic and geographic diversity of the simian arteriviruses, identify baboons as a natural host of the

28 SHFV is unique among arteriviruses in having three N-terminal papain-like pro

29 capsid-forming domain of a distantly related arterivirus indicates a conserved mechanism of nucleocap

30 However, arterivirus infection in wild nonhuman primates had not

31 e is known about deubiquitylation in pig and arterivirus infection.

32 g body of evidence that suggests that simian arterivirus infections are common in Old World monkeys o

33 The 3'(-)NCR RNA of another arterivirus, lactate dehydrogenase-elevating virus C (LD

34 ther, these features suggest that the simian arteriviruses may be "preemergent" zoonotic pathogens.

35 ts that one of these virus types, the simian arteriviruses, may have the potential to jump between di

36 we report the first dimeric structure of the arterivirus nsp11 from PRRSV at 2.75-A resolution.

37 we report the first crystal structure of the arterivirus nsp11 protein from PRRSV, which exhibits a u

38 Other arterivirus PLP1s cleave only in cis at a single downstr

39 FV PLP1alpha catalytic Cys63 is unique among arterivirus PLP1s in being adjacent to an Ala instead of

40 stead of the canonical Tyr observed in other arterivirus PLP1s.

41 Like other arteriviruses, porcine reproductive and respiratory synd

42 Unusually, this arterivirus PRF signal lacks an obvious stimulatory RNA

43 During replication, arteriviruses produce a 3' coterminal, nested set of sub

44 rt, we demonstrate that the N protein of the arterivirus PRRSV participates in viral RNA replication

45 The arteriviruses recently identified in wild monkeys have h

46 cation of two novel, highly divergent simian arteriviruses related to SHFV, Mikumi yellow baboon viru

47 may help elucidate the mechanism underlying arterivirus replication and may represent great potentia

48 This enzyme is essential for arterivirus replication by cleaving a site within the vi

49 nsp11 endoribonuclease plays a vital role in arterivirus replication, but its precise roles and mecha

50 ndoU superfamily and plays a crucial role in arterivirus replication.

51 ndrome virus (PRRSV) is a recently described arterivirus responsible for disease in swine worldwide.

52 f the cellular proteins are conserved in all arterivirus RNAs and that these cell proteins may be uti

53 he negative-strand RNA [3'(-)NCR RNA] of the arterivirus simian hemorrhagic fever virus (SHFV) is 209

54 Nine TRSs were previously reported for the arterivirus Simian hemorrhagic fever virus (SHFV).

55 Simian hemorrhagic fever virus (SHFV) is an arterivirus that causes severe disease in captive macaqu

56 ed RNA viruses, comprising coronaviruses and arteriviruses, that employ a unique strategy of disconti

57 ome virus (PRRSV), and apparently most other arteriviruses, use an additional PRF mechanism to access

58 s known of the association of PRRSV or other arteriviruses with gonadal tissues.