ライフサイエンスコーパス: TSWV

1 TSWV acquisition inhibition assays revealed that thrips

2 TSWV and the thrips Frankliniella fusca and Frankliniell

3 TSWV is transmitted to plants via thrips (Thysanoptera:

4 P21 compromised Tsw-mediated defence against TSWV.

5 resistance in tomato for protection against TSWV.

6 es were higher for sympatric than allopatric TSWV isolate-T. tabaci isoline pairings, virus titers in

7 leiotropic effects of mutations have allowed TSWV to rapidly adapt to new hosts and expand its host r

8 ferences in virus titers in the vector among TSWV isolate-T. tabaci isoline pairings in relation to d

9 , WFT egg-laying (oviposition) decreased and TSWV inoculation was suppressed.

10 he small RNA expression profiles of IYSV and TSWV in single- and dually-infected datura plants showed

11 s this goal, we examined WFT oviposition and TSWV inoculation behavior on tomato lines bred to exude

12 to mediate resistance to WFT oviposition and TSWV inoculation on tomato leaves.

13 dicate that the interaction of T. tabaci and TSWV isolate genetic determinants underlie successful tr

14 daptation is occurring between T. tabaci and TSWV isolates.

15 fit management of WFT as direct pests and as TSWV vectors.

16 -S binds to larval thrips guts and decreases TSWV acquisition provide evidence that G(N) may serve as

17 eir midguts compared to thrips that were fed TSWV only.

18 on for TYLCSV and >85% only after 8 days for TSWV, demonstrating its suitability for early detection

19 (Datura stramonium) is a permissive host for TSWV, while it restricts the movement of IYSV to inocula

20 The current disease management for TSWV is based mainly on breeding tomato cultivars contai

21 at the glycoproteins may not be required for TSWV infection of plant hosts but are required for trans

22 A functional cell is requisite for TSWV infection and cell-to-cell movement; thus, this beh

23 To understand how TSWV adapts to different hosts, we experimentally passag

24 plants infected with both viruses, however, TSWV facilitated the selective movement of the viral gen

25 The goals of this project were to identify TSWV-interacting proteins (TIPs) that interact directly

26 est the hypothesis that G(N) plays a role in TSWV acquisition by thrips, we expressed and purified a

27 ested for their ability to transmit multiple TSWV isolates collected at the same and different locati

28 No TSWV NSs-specific siRNAs were detected either in the ino

29 cant increase in the normalized abundance of TSWV nucleocapsid RNA from 2 to 21 h after a 3-h acquisi

30 viral ligand that mediates the attachment of TSWV to receptors displayed on the epithelial cells of t

31 on in determining transmission efficiency of TSWV by T. tabaci.

32 roteins play important roles in the entry of TSWV into the insect midgut, the first site of infection

33 ability of T. tabaci to transmit isolates of TSWV, and to examine the possibility that genetic intera

34 ts ability to transmit different isolates of TSWV.

35 dually-infected plants had reduced levels of TSWV N gene-specific small interfering RNAs (siRNAs).

36 us conferring resistance to a broad range of TSWV strains.

37 Despite the extensive replication of TSWV in midgut and salivary glands, there is little to n

38 ssibility by thrips to the medium (M) RNA of TSWV.

39 several Sw-5 resistance-breaking strains of TSWV have been identified.

40 to quantify variation in transmissibility of TSWV isolates by T. tabaci, in the ability of T. tabaci

41 rminants underlie successful transmission of TSWV by T. tabaci.

42 alized nature of this species as a vector of TSWV.

43 ed importance of this species as a vector of TSWV.

44 s is one of nine competent thrips vectors of TSWV transmission to plant hosts.

45 suggests that G(N) is organized as dimers on TSWV's outer shell.

46 viruses as compared to the presence of only TSWV NSs.

47 oded by tomato spotted wilt orthotospovirus (TSWV), contains an unusually large leucine-rich repeat (

48 thrips that were concomitantly fed purified TSWV and G(N)-S had reduced amounts of virus in their mi

49 Similarly, TSWV isolates are transmitted at different efficiencies

50 isolates (SLIs) were generated from a single TSWV isolate that was inefficiently transmitted by thrip

51 rips vector, we identified and validated six TSWV-interacting proteins from Frankliniella occidentali

52 Results further demonstrate that TSWV titers in the vector were unrelated to virus titers

53 The TSWV G(N)-interacting proteins provide new targets for d

54 The TSWV nucleocapsid protein and human cytomegalovirus glyc

55 Although the structure of the TSWV G(N) is different from other bunyavirus G(N) protei

56 lin, were able to interact directly with the TSWV attachment protein, G(N), in insect cells.

57 NA generated from F. occidentalis exposed to TSWV.

58 that L1 thrips display a complex reaction to TSWV infection and provide new insights toward unravelin

59 al as they have some levels of resistance to TSWV.

60 possible involvement in peanut resistance to TSWV.

61 (L1) of F. occidentalis mounts a response to TSWV that protects it from pathogenic effects caused by

62 ns were significantly altered in response to TSWV.

63 Tomato spotted wilt tospovirus (TSWV), one of the most important plant viruses, causes y

64 robability of an isofemale line transmitting TSWV varied among virus isolates, and the probability of

65 -pathogenic virus tomato spotted wilt virus (TSWV) encodes a structural glycoprotein (G(N)) that, lik

66 , which transmits Tomato spotted wilt virus (TSWV) in a persistent and propagative manner, varies gre

67 ibed not only for Tomato spotted wilt virus (TSWV) in pepper and tomato but also for other vegetable

68 primary vector of Tomato spotted wilt virus (TSWV) in some areas of the world, it is not an important

69 Tomato spotted wilt virus (TSWV) is a devastating disease to peanut growers in the

70 Tomato spotted wilt virus (TSWV) is a generalist pathogen with one of the broadest

71 y thrips-vectored tomato spotted wilt virus (TSWV) is a very serious problem in peanut (Arachis hypog

72 ed wilt caused by tomato spotted wilt virus (TSWV) is one of the major peanut (Arachis hypogaea L.) d

73 Tomato spotted wilt virus (TSWV) is transmitted by Frankliniella occidentalis in a

74 Tomato spotted wilt virus (TSWV) is transmitted exclusively by thrips in nature.

75 opulations of the tomato spotted wilt virus (TSWV) using microscopy and tomography.

76 Tomato spotted wilt virus (TSWV), a member of the Tospovirus genus within the Bunya

77 N (G(N)) from the tomato spotted wilt virus (TSWV), a representative member of the Tospoviridae famil

78 plant bunyavirus tomato spotted wilt virus (TSWV), and the most efficient thrips vector, we identifi

79 at infection with Tomato spotted wilt virus (TSWV), type member of the only plant-infecting genus in

80 virus (IYSV) and Tomato spotted wilt virus (TSWV), were investigated for inter-virus interactions at

81 irus (TYLCSV) and Tomato spotted wilt virus (TSWV).

82 gande), vector of tomato spotted wilt virus (TSWV).

83 eocapsid (N) protein of tomato spotted wilt (TSWV) tospovirus.

84 refore, this bin-map and QTL associated with TSWV resistance made it possible for functional gene map

85 proteins (TIPs) that interact directly with TSWV G(N) and to localize the expression of these protei

86 Male thrips infected with TSWV fed more than uninfected males, with the frequency