ライフサイエンスコーパス: thrips

1 d at the same and different locations as the thrips.

2 , whiteflies, leafhoppers, planthoppers, and thrips.

3 e closing of conduits for global movement of thrips.

4 plotype that is inefficiently transmitted by thrips.

5 solate that was inefficiently transmitted by thrips.

6 minant associated with virus transmission by thrips.

7 sts but are required for transmissibility by thrips.

8 Three of the 30 SLIs were transmitted by thrips, and 27 were not.

9 ts (all ants and termites; some bees, wasps, thrips, and beetles), snapping shrimp, and naked mole ra

10 ave also evolved in less-studied groups like thrips, aphids and polyembryonic wasps.

11 Thrips are among the stealthiest of insect invaders due

12 Many invasive thrips are notorious for causing extensive crop damage,

13 volatile emissions increase dramatically and thrips are repelled.

14 For cycads, thrips are specialized pollinators.

15 0 species, the Acercaria (lice, plant lices, thrips, bugs) including number of economically important

16 and G(C), are critical for the infection of thrips, but they are not required for the initial infect

17 we examine factors facilitating invasion by thrips, damage caused by these insects, pre- and post-in

18 Our findings support the hypothesis that L1 thrips display a complex reaction to TSWV infection and

19 TSWV and the thrips Frankliniella fusca and Frankliniella occidentali

20 to attack by spider mites and western flower thrips (Frankliniella occidentalis), another cell-conten

21 efly, Bemisia tabaci, and the Western flower thrips, Frankliniella occidentalis.

22 Our findings that G(N)-S binds to larval thrips guts and decreases TSWV acquisition provide evide

23 rips midguts when purified G(N)-S was fed to thrips in an in vivo binding assay.

24 rin are commonly used insecticides to manage thrips in China, and laboratory bioassays demonstrated t

25 t virus (TSWV) is transmitted exclusively by thrips in nature.

26 esides understanding the role of jassids and thrips in particular, in producing the best cup characte

27 Male thrips infected with TSWV fed more than uninfected males

28 first report on gene expression dynamics in thrips infested Darjeeling tea leaves can be extrapolate

29 Pollen-laden thrips leave male cycad cones en masse during the daily

30 o thrips midguts, indicating that the G(N)-S-thrips midgut interaction is specific.

31 ors displayed on the epithelial cells of the thrips midgut.

32 We detected specific binding to thrips midguts when purified G(N)-S was fed to thrips in

33 tomegalovirus glycoprotein B did not bind to thrips midguts, indicating that the G(N)-S-thrips midgut

34 y established for four groups: Thysanoptera (thrips), Neuroptera (lacewings), Diptera (flies), and no

35 e and female individuals) and its specialist thrips pollinator, Cycadothrips chadwicki.

36 us studies suggest that genetic variation of thrips populations, virus isolates, or both are importan

37 Using these sequences, the L1 thrips proteome that resolved on a two-dimensional gel w

38 ard library of B157 (tea clone infested with thrips), providing us transcripts related to aroma and f

39 e population, which are not transmissible by thrips, rather than with the presence of a dominant hapl

40 ufficient to explain the observed sequential thrips' repellence (push) and attraction (pull).

41 etaceous amber of Spain, wherein four female thrips representing a genus and two species in the famil

42 olatile emissions diminish and cones attract thrips, resulting in pollination of female cones.

43 Behavioral and electrophysiological tests on thrips reveal that variations in b-myrcene and ocimene e

44 e PCR (RT-PCR) analysis of virus titer in L1 thrips revealed a significant increase in the normalized

45 The thrips species Frankliniella occidentalis and Thrips tab

46 Tospoviruses and their vectors, thrips species in the order Thysanoptera, represent a ma

47 surface when attempting to manage incursive thrips species.

48 hrips species Frankliniella occidentalis and Thrips tabaci are highly invasive and damaging agricultu

49 Isofemale lines of Thrips tabaci from multiple locations were tested for th

50 acquisition inhibition assays revealed that thrips that were concomitantly fed purified TSWV and G(N

51 mounts of virus in their midguts compared to thrips that were fed TSWV only.

52 TSWV is transmitted to plants via thrips (Thysanoptera: Thripidae), which transmit the vir

53 c system was used to map transmissibility by thrips to the medium (M) RNA of TSWV.

54 The complex and specific interplay between thrips, tospoviruses, and their shared plant hosts leads

55 A partial thrips transcriptome was generated using 454-Titanium se

56 lved protein spots were identified using the thrips transcriptome.

57 Sequence analysis of the M RNA, thrips transmissibility assays, G(C) protein analysis, a

58 (C) ORF of the M RNA resulted in the loss of thrips transmissibility without inhibition of virion ass

59 To locate determinants of thrips transmission in the M RNA, 30 single-lesion isola

60 Thrips-transmitted Iris yellow spot virus is an economic

61 insect infestation, particularly jassids and thrips triggers the aroma and flavour formation in Darje

62 aviridae, alters the feeding behavior of its thrips vector, Frankliniella occidentalis (Pergande).

63 Tomato spotted wilt caused by thrips-vectored tomato spotted wilt virus (TSWV) is a ve

64 Owing to the difficulty in combating thrips vectors with insecticides, the best way to limit/

65 on and transmission of Tospoviruses by their thrips vectors.

66 hat G(N) plays a role in TSWV acquisition by thrips, we expressed and purified a soluble, recombinant

67 derstanding of virus transmission by aphids, thrips, whiteflies, leafhoppers, planthoppers, treehoppe