ライフサイエンスコーパス: whitefly

1 each aphids) and Bemisia tabaci (silver leaf whitefly).

2 nto virions and transmitted as an episome by whiteflies.

3 storical tritrophic relationships in Bemisia whiteflies.

4 ed structural constituent of cuticle in male whiteflies.

5 GS-2 episomes were also found in virions and whiteflies.

6 primary endoparasitoids of scale insects and whiteflies.

7 ptera, such as scale insects, mealybugs, and whiteflies.

8 Recent reports of resistance in whiteflies and mosquitoes demonstrate the need to identi

9 Hemiptera), including aphids, planthoppers, whiteflies and stink bugs, present one of the greatest c

10 t population values of 26.3 and 39.2 mug per whitefly and 23.1 and 35.2 mug per aphid for BGL-1 and u

11 ther species, females are endoparasitoids of whiteflies, and males are primary endoparasitoids of egg

12 Psyllids, whiteflies, aphids, and mealybugs are members of the sub

13 Whiteflies are small sap-sucking insects including B. ta

14 d performance and sex-ratio bias of infected whiteflies are sufficient to explain the spread of Ricke

15 The whitefly Bemisia tabaci (Genn.) is a pest and vector of

16 a PGRP gene, BtPGRP, encodes a PGRP from the whitefly Bemisia tabaci (MEAM1) that binds and kills bac

17 dy, the gender difference in the sweetpotato whitefly Bemisia tabaci was investigated using Illumina-

18 um of whiteflies, including the sweet potato whitefly Bemisia tabaci, and provides essential nutrient

19 development of the phloem-feeding silverleaf whitefly (Bemisia tabaci type B; SLWF) on Arabidopsis (A

20 Whitefly (Bemisia tabaci) and aphid (Myzus persicae) pop

21 roxyfen in 84 populations of the sweetpotato whitefly (Bemisia tabaci) from cotton fields in central

22 s (Macrosiphum euphorbiae), and sweet potato whitefly (Bemisia tabaci).

23 ly driven by two so-called supervectors: the whitefly, Bemisia tabaci, and the Western flower thrips,

24 transmitted specifically by the sweetpotato whitefly, Bemisia tabaci, in a semipersistent manner.

25 invasive agricultural pest, the sweet potato whitefly, Bemisia tabaci, in just 6 years.

26 The whitefly, Bemisia tabaci, is an important agricultural p

27 formation indicating an involvement of SA in whitefly-derived plant defence against Agrobacterium.

28 12 d, but the proportion of RT-PCR positive whiteflies dropped to 55% by 3 d.

29 mutant CPm genotypes were not transmitted by whiteflies, even though virion concentrations were above

30 Mortality of adult whiteflies exposed to dsRNA by feeding on N. tabacum pla

31 SLW3) induced systemically after silverleaf whitefly feeding were identified.

32 ns or recombinant virus capsid components to whiteflies, followed by feeding them antibodies to the v

33 ing RNA interference (RNAi) to down regulate whitefly genes by expressing their homologous double str

34 Results indicated that knock down of whitefly genes involved in neuronal transmission and tra

35 Groups of thirty whiteflies given a 24 h of inoculation access period (IA

36 resistance and the transmission of SEGS-2 by whiteflies has major implications for the long-term dura

37 y immunity and provides insight into how the whitefly immunity acts in complex mechanisms of Begomovi

38 ork addresses a visible gap in understanding whitefly immunity and provides insight into how the whit

39 obligate primary endosymbiotic bacterium of whiteflies, including the sweet potato whitefly Bemisia

40 CCYV, and the proportion of RT-PCR positive whitefly individuals reached to 100% at 48 h of AAP.

41 Other proteins, such as the Silverleaf Whitefly-Induced Protein1, Mitogen Activated Protein Kin

42 evaluated, both in planta and in vitro, how whitefly infestation affects crown gall disease.

43 These results suggest that aboveground whitefly infestation elicits systemic defence responses

44 ana leaves were exposed to a sucking insect (whitefly) infestation and benzothiadiazole (BTH) for 7 d

45 Whitefly-infested plants exhibited at least a two-fold r

46 Endogenous SA content was augmented in whitefly-infested plants upon Agrobacterium inoculation.

47 acterium-mediated transformation of roots of whitefly-infested plants was clearly inhibited when comp

48 was three times higher in root exudates from whitefly-infested plants.

49 Hemipteroid assemblage that includes aphids, whiteflies, leafhoppers, planthoppers, and thrips.

50 ing of virus transmission by aphids, thrips, whiteflies, leafhoppers, planthoppers, treehoppers, mite

51 and even more strongly upregulated following whitefly-mediated TYLCV inoculation.

52 by real time quantitative PCR indicated that whitefly mortality was attributable to the down-regulati

53 of B. tabaci, resulted in significant adult whitefly mortality.

54 rstand interactions between three organisms: whitefly, N. benthamiana and Agrobacterium.

55 fly vector biotype but not within those of a whitefly nonvector biotype.

56 as with warm climates and are transmitted by whiteflies of the Bemisia tabaci complex.

57 used worldwide for the biological control of whiteflies on vegetables and ornamental plants grown in

58 immature E. formosa, population dynamics of whitefly-parasitoid interactions, and commercial use in

59 tative releases into greenhouses to suppress whitefly population growth.

60 , has potential as a bio-pesticide to reduce whitefly population size and thereby decrease virus spre

61 h uninfected whiteflies, Rickettsia-infected whiteflies produced more offspring, had higher survival

62 Whiteflies required >/=1 h of acquisition access period

63 fed to whitefly vectors, significantly more whiteflies retained the recombinant minor coat protein (

64 Compared with uninfected whiteflies, Rickettsia-infected whiteflies produced more

65 The silverleaf whitefly (SLWF; Bemisia tabaci type B) is a good model f

66 plants has great potential for management of whiteflies to reduce plant virus disease spread.

67 We investigated whitefly transmission of Lettuce infectious yellows viru

68 systemic plant movement but is required for whitefly transmission.

69 able of both systemic movement in plants and whitefly transmission.

70 All characterized whitefly-transmitted geminiviruses (begomoviruses) with

71 Most whitefly-transmitted geminiviruses possess bipartite DNA

72 at controlling pests such as the greenhouse whitefly Trialeurodes vaporariorum (Westwood) which are

73 zed in the anterior foregut or cibarium of a whitefly vector biotype but not within those of a whitef

74 ese locations strongly corresponded with the whitefly vector transmission of LIYV.

75 ases as well as their associated viruses and whitefly vector.

76 strated previously and in the present study, whitefly vectors failed to transmit virions preincubated

77 g host range, semipersistent transmission by whitefly vectors, and impact on diverse cropping systems

78 V capsid components were individually fed to whitefly vectors, significantly more whiteflies retained

79 anism in the anterior foregut or cibarium of whitefly vectors.

80 e closely related silverleaf and sweetpotato whiteflies were observed.

81 it on samples from fission yeast, mouse and whitefly, whose reference genome is not yet available.