ライフサイエンスコーパス: Ross River virus

1 ant viruses, including chikungunya virus and Ross River virus.

2 used by other arthritogenic viruses, such as Ross River virus.

3 the E2 ectodomain in both Sindbis virus and Ross River virus.

4 itogenic alphaviruses, chikungunya virus and Ross River virus.

5 the distantly related dual-host alphavirus, Ross River virus.

6 assembled core particles of both Sindbis and Ross River viruses.

7 rions and compare their structure to that of Ross River virus, a togavirus belonging the genus Alphav

8 n this study, we show that two alphaviruses, Ross River virus and Chikungunya virus, lack the conserv

9 id protein gene from a different alphavirus, Ross River virus, and the second was to make deletions i

10 cluding Sindbis virus, Semliki Forest virus, Ross River virus, and Venezuelan equine encephalitis vir

11 Sindbis virus and Ross River virus are alphaviruses whose nonstructural pr

12 us, harboring the nsP4 of chikungunya virus, Ross River virus, BFV, or SINV were viable.

13 ted with a related arthritogenic alphavirus, Ross River virus, but not in mice infected with West Nil

14 espite their similarities, Sindbis virus and Ross River virus capsid proteins do not form mixed core-

15 e encephalitis virus, chikungunya virus, and Ross River virus challenges.

16 anged the length and/or charge of the NTD of Ross River virus CP and found that changing the charge o

17 One change in Ross River virus E1 (Gln-411-->Leu) and one change in Si

18 ave isolated in both Sindbis virus E2 and in Ross River virus E1 a series of suppressing mutations th

19 uring passage of a chimeric virus containing Ross River virus E1 and Sindbis virus E2, the E2 change

20 Interestingly, all sequenced Ross River viruses encode either a tyrosine or a histidi

21 of Sindbis virus are replaced with those of Ross River virus grow very poorly, but upon passage, ada

22 Among tropical pathogens, malaria and Ross River virus had lower thermal optima (25-26oC) whil

23 e nucleocapsid proteins of Sindbis virus and Ross River virus have been produced in a T7-based Escher

24 this modification expands the host range of Ross River virus in cultured cells to cells of avian ori

25 spects have diverged from the Semliki Forest/Ross River virus lineage.

26 s using mammalian- and mosquito cell-derived Ross River virus (mam-RRV and mos-RRV, respectively) ind

27 with previous results, mosquito-cell-derived Ross River virus (mos-RRV) and Venezuelan equine encepha

28 Replication in both BHK and avian cells of Ross River virus mutants N218K and N218R was inhibited b

29 Ross River virus mutants that had increased replication

30 and polyprotein cleavage between Sindbis and Ross River virus mutants, despite the mutations being ma

31 iruses, including the Sindbis-group viruses, Ross River virus, O'nyong-nyong virus, and Chikungunya v

32 ed with reconstructions of Sindbis virus and Ross River virus particles.

33 the 6K gene had been replaced with that from Ross River virus (RR) produced wild-type levels of nucle

34 tions in E2 of Sindbis virus (SIN) and E1 of Ross River virus (RR) that allow these two glycoproteins

35 Arthritogenic alphaviruses such as Ross River virus (RRV) and chikungunya virus (CHIKV) cau

36 Arthritogenic alphaviruses, including Ross River virus (RRV) and chikungunya virus, are mosqui

37 Ross River virus (RRV) and Semliki Forest virus (SFV) ar

38 orporate the glycoproteins of the alphavirus Ross River virus (RRV) and utilize them for entry into c

39 Chikungunya virus (CHIKV) and Ross River virus (RRV) cause a debilitating, and often c

40 studied, and the most severe of 24 cases of Ross River virus (RRV) disease studied.

41 Utilizing a mouse model of Ross River virus (RRV) disease, we found that the primar

42 The CPs of SINV and Ross River virus (RRV) do not form phenotypically mixed

43 ther the vesicular stomatitis virus (VSV) or Ross River virus (RRV) envelope surface glycoproteins.

44 This study investigated potential Ross River virus (RRV) exposure sites in Greater Brisban

45 Ross River virus (RRV) is a mosquito-borne alphavirus th

46 Ross River virus (RRV) is one of a group of mosquito-tra

47 that contain the structural protein genes of Ross River virus (RRV) to investigate the location of th

48 explored vertebrate diversity and potential Ross River virus (RRV) transmission pathways by analysin

49 alphaviruses, chikungunya virus (CHIKV) and Ross River virus (RRV), and assessed the early antiviral

50 RTANCE Arthritogenic alphaviruses, including Ross River virus (RRV), are human pathogens that cause d

51 Ross River virus (RRV), Barmah Forest virus (BFV), and d

52 Ross River virus (RRV), chikungunya virus, and related a

53 ramework to a medically important arbovirus, Ross River virus (RRV), in Brisbane, Australia.

54 Arthritogenic alphaviruses, including Ross River virus (RRV), infect humans and cause debilita

55 ses, including chikungunya virus (CHIKV) and Ross River virus (RRV), pose significant public health t

56 Arthritogenic alphaviruses including Ross River virus (RRV), Sindbis virus, and chikungunya v

57 ctor pseudotyped with the glycoproteins from Ross River Virus (RRV).

58 f the PE2 coding region of the T48 strain of Ross River virus (RRV-T48) with that from the attenuated

59 kes and is detectably different from that of Ross River virus spikes.

60 Passage of Ross River virus strain NB5092 in avian cells has been p

61 ing Sindbis virus nonstructural proteins and Ross River virus structural proteins growing considerabl

62 rity between these Sindbis virus mutants and Ross River virus suggests that E3 may also be present in

63 l form a heterodimer with glycoprotein E1 of Ross River virus that is cleaved to an E2/E1 heterodimer

64 imensions similar to that of the icosahedral Ross River virus, the present results indicate that rube

65 Cell surface binding of another alphavirus, Ross River virus, was found to be independent of heparan