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1 each aphids) and Bemisia tabaci (silver leaf whitefly).
2 resulting in elevated cAMP levels within the whitefly.
3 ons in CMD-infected cassava and viruliferous whiteflies.
4 ent acquired and subsequently transmitted by whiteflies.
5 )' for this new endosymbiont associated with whiteflies.
6 y exacerbate MYMIV impact by attracting more whiteflies.
7 y susceptible tomato and by local and exotic whiteflies.
8 storical tritrophic relationships in Bemisia whiteflies.
9 GS-2 episomes were also found in virions and whiteflies.
10 nto virions and transmitted as an episome by whiteflies.
11 ed structural constituent of cuticle in male whiteflies.
12 primary endoparasitoids of scale insects and whiteflies.
13 ptera, such as scale insects, mealybugs, and whiteflies.
14 plant resistance against begomoviruses, high whitefly abundance, and whitefly's ability to develop in
15                                              Whiteflies acquired virus by feeding on singly infected
16 robust subculturing and produces hundreds of whitefly adults per month.
17                                       Axenic whitefly adults were able to acquire and transmit a bego
18 phidomorpha), scale insects (Coccidomorpha), whiteflies (Aleyrodomorpha) and psyllids (Psylloidea).
19 arental cassava varieties, ECU72 tolerant to whiteflies and COL2246 a susceptible line, have been use
20              Recent reports of resistance in whiteflies and mosquitoes demonstrate the need to identi
21 ew infraorder, are revealed to be related to whiteflies and psyllids.
22  Hemiptera), including aphids, planthoppers, whiteflies and stink bugs, present one of the greatest c
23 r respective probabilities of acquisition by whiteflies and to the titers of each segment acquired an
24 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
25 s are that cassava genotypes possessing both whitefly and disease resistances are needed urgently.
26 emonstrates how begomovirus retention within whitefly and its transmission can be modulated by alteri
27                 Hemipterans (such as aphids, whiteflies, and leafhoppers) are some of the most devast
28 ther species, females are endoparasitoids of whiteflies, and males are primary endoparasitoids of egg
29 emipteran insects such as aphids, mealybugs, whiteflies, and psyllids.
30                                    Psyllids, whiteflies, aphids, and mealybugs are members of the sub
31                                              Whiteflies are small sap-sucking insects including B. ta
32 d performance and sex-ratio bias of infected whiteflies are sufficient to explain the spread of Ricke
33 )-specific phosphodiesterase-4 (PDE4) of the whitefly as an interacting partner with capsid proteins
34 nts corroborated the role of beta-myrcene in whitefly attraction.
35                                          The whitefly Bemisia tabaci (Genn.) is a pest and vector of
36 a PGRP gene, BtPGRP, encodes a PGRP from the whitefly Bemisia tabaci (MEAM1) that binds and kills bac
37                                          The whitefly Bemisia tabaci is a cosmopolitan, highly polyph
38 dy, the gender difference in the sweetpotato whitefly Bemisia tabaci was investigated using Illumina-
39 unique process of nitrogen metabolism in the whitefly Bemisia tabaci, a global pest.
40 um of whiteflies, including the sweet potato whitefly Bemisia tabaci, and provides essential nutrient
41 tivated during feeding by a pest insect, the whitefly Bemisia tabaci, and the resulting hydrogen cyan
42 pathogen of tomato crops, is vectored by the whitefly Bemisia tabaci, yet the mechanisms underlying T
43 ssociated with insecticide resistance in the whitefly Bemisia tabaci.
44                                              Whiteflies (Bemisia tabaci) and the diseases they transm
45 that influence the defense mechanism against whitefly (Bemisia tabaci Asia II 7) and leafminer (Phtho
46 egomoviruses, transmitted by the sweetpotato whitefly (Bemisia tabaci Gennadius), are the causal agen
47 sypii Glover) and the non-vector, silverleaf whitefly (Bemisia tabaci Gennadius).
48 development of the phloem-feeding silverleaf whitefly (Bemisia tabaci type B; SLWF) on Arabidopsis (A
49                                              Whitefly (Bemisia tabaci) and aphid (Myzus persicae) pop
50 roxyfen in 84 populations of the sweetpotato whitefly (Bemisia tabaci) from cotton fields in central
51          High populations of African cassava whitefly (Bemisia tabaci) have been associated with epid
52                                              Whitefly (Bemisia tabaci) is a pest in this region that
53 s (Macrosiphum euphorbiae), and sweet potato whitefly (Bemisia tabaci).
54 ly driven by two so-called supervectors: the whitefly, Bemisia tabaci, and the Western flower thrips,
55  transmitted specifically by the sweetpotato whitefly, Bemisia tabaci, in a semipersistent manner.
56 invasive agricultural pest, the sweet potato whitefly, Bemisia tabaci, in just 6 years.
57                                          The whitefly, Bemisia tabaci, is an important agricultural p
58  further show that ToMoLCV is transmitted by whiteflies, but not mechanically.
59 the management of begomoviruses by targeting whitefly cAMP using chemicals, botanicals, or RNAi-based
60 n dynamics and genetic patterns by comparing whiteflies collected on cassava in 1997, during the firs
61  7, a putative species of the Bemisia tabaci whitefly complex (Hemiptera: Aleyrodidae), and occasiona
62                          The Bemisia cassava whitefly complex includes species that cause severe crop
63                              Currently, this whitefly complex is divided into species and subgroups (
64 , it is a relatively unexplored strategy for whitefly control.
65  of individual fields with varying levels of whitefly density crops under low and high disease pressu
66 formation indicating an involvement of SA in whitefly-derived plant defence against Agrobacterium.
67 NAs that silence BtPMaT1, thus impairing the whiteflies' detoxification ability.
68 urce plant and the ratios transmitted by the whitefly did not differ from one - the ratio at which th
69 both viruses, DNA-A:DNA-B ratios acquired by whiteflies differed from those in the source plant and t
70 a mosaic begomovirus (CMB) in Bemisia tabaci whitefly, diminished the perceived importance of whitefl
71  12 d, but the proportion of RT-PCR positive whiteflies dropped to 55% by 3 d.
72 mutant CPm genotypes were not transmitted by whiteflies, even though virion concentrations were above
73                           Mortality of adult whiteflies exposed to dsRNA by feeding on N. tabacum pla
74  SLW3) induced systemically after silverleaf whitefly feeding were identified.
75 ns or recombinant virus capsid components to whiteflies, followed by feeding them antibodies to the v
76 ing RNA interference (RNAi) to down regulate whitefly genes by expressing their homologous double str
77         Results indicated that knock down of whitefly genes involved in neuronal transmission and tra
78                             Groups of thirty whiteflies given a 24 h of inoculation access period (IA
79 RiTBi may be a relatively recent intruder in whiteflies given its low abundance in the field and rela
80                                   Greenhouse whitefly (GWF) Trialeurodes vaporariorum and Western flo
81 resistance and the transmission of SEGS-2 by whiteflies has major implications for the long-term dura
82 eptional horizontal gene transfer event, the whitefly has acquired the plant-derived phenolic glucosi
83 ttsia distributes throughout the body of its whitefly host.
84 y immunity and provides insight into how the whitefly immunity acts in complex mechanisms of Begomovi
85 ork addresses a visible gap in understanding whitefly immunity and provides insight into how the whit
86                             The tolerance to whiteflies in the F2 population was further enhanced.
87 efly, diminished the perceived importance of whitefly in CMB epidemics.
88  obligate primary endosymbiotic bacterium of whiteflies, including the sweet potato whitefly Bemisia
89   As a result, apoptosis is activated in the whitefly increasing viral load.
90 358 genome-wide SNPs from 62 Bemisia cassava whitefly individuals belonging to sub-Saharan African sp
91  CCYV, and the proportion of RT-PCR positive whitefly individuals reached to 100% at 48 h of AAP.
92       Other proteins, such as the Silverleaf Whitefly-Induced Protein1, Mitogen Activated Protein Kin
93  evaluated, both in planta and in vitro, how whitefly infestation affects crown gall disease.
94       These results suggest that aboveground whitefly infestation elicits systemic defence responses
95 ana leaves were exposed to a sucking insect (whitefly) infestation and benzothiadiazole (BTH) for 7 d
96                                              Whitefly-infested plants exhibited at least a two-fold r
97       Endogenous SA content was augmented in whitefly-infested plants upon Agrobacterium inoculation.
98 acterium-mediated transformation of roots of whitefly-infested plants was clearly inhibited when comp
99 was three times higher in root exudates from whitefly-infested plants.
100 facilitate arbovirus preservation within its whitefly insect vector.
101 , Hemiptera (cicadas, aphids, scale insects, whiteflies, leafhoppers, and bugs), Coleoptera (beetles)
102 Hemipteroid assemblage that includes aphids, whiteflies, leafhoppers, planthoppers, and thrips.
103 ing of virus transmission by aphids, thrips, whiteflies, leafhoppers, planthoppers, treehoppers, mite
104    Disruption of genes/pathways critical for whitefly-mediated transmission can be effective for the
105   The results of this study demonstrate that whitefly-mediated transmission of begomoviruses is regul
106 and even more strongly upregulated following whitefly-mediated TYLCV inoculation.
107 pull-down assay and co-immunolocalization in whitefly midgut.
108 by real time quantitative PCR indicated that whitefly mortality was attributable to the down-regulati
109 , synergism, or antagonism in terms of total whitefly mortality.
110  of B. tabaci, resulted in significant adult whitefly mortality.
111 rstand interactions between three organisms: whitefly, N. benthamiana and Agrobacterium.
112 fly vector biotype but not within those of a whitefly nonvector biotype.
113 as with warm climates and are transmitted by whiteflies of the Bemisia tabaci complex.
114         We also identified BtMEDOR6 as a key whitefly olfactory receptor of beta-myrcene involved in
115 e is the establishment of a colony of axenic whiteflies on tissue-cultured plants.
116 used worldwide for the biological control of whiteflies on vegetables and ornamental plants grown in
117  immature E. formosa, population dynamics of whitefly-parasitoid interactions, and commercial use in
118 enables a wide range of hypotheses regarding whitefly phytopathology without the expense, facilities,
119  and R3 alfalfa could substantially suppress whitefly population expansion in the field.
120 tative releases into greenhouses to suppress whitefly population growth.
121 , has potential as a bio-pesticide to reduce whitefly population size and thereby decrease virus spre
122 rtite begomoviruses was facilitated by local whitefly populations and the highly susceptible tomato h
123 era: Aleyrodidae), and occasionally in field whitefly populations.
124 cies is shown as well as in vitro testing of whitefly preference for different plants.
125  susceptible-resistant mixtures whatever the whitefly pressure.
126 b-Saharan Africa under different disease and whitefly pressure.
127 h uninfected whiteflies, Rickettsia-infected whiteflies produced more offspring, had higher survival
128                                              Whitefly proliferation on more than two dozen plant spec
129                                              Whiteflies required >/=1 h of acquisition access period
130            Although not consistent among all whitefly resistance sub-groups, targeted LC-MS analysis
131 spectrum in these populations indicated that whitefly resistance to MEAM1 is multigenic.
132      The F1 generation has been screened for whitefly resistance, and progeny identified displaying e
133 ures generated clustering of accessions into whitefly resistant and susceptible groups, and different
134  fed to whitefly vectors, significantly more whiteflies retained the recombinant minor coat protein (
135                     Compared with uninfected whiteflies, Rickettsia-infected whiteflies produced more
136  begomoviruses, high whitefly abundance, and whitefly's ability to develop insecticide resistance rap
137                               The silverleaf whitefly (SLWF; Bemisia tabaci type B) is a good model f
138                                          The whitefly species composition changed: in 1997, SSA1, SSA
139 uses in cassava linked to high abundances of whitefly species within the Bemisia tabaci complex.
140 ED and NW1) were assessed on the four lines, whitefly species-specific responses to R1, R2 and R3 pla
141 merged well before the introduction of MEAM1 whiteflies, suggesting that the evolution of NW monopart
142 rgeted metabolomics was used to characterise whitefly susceptible and tolerant sub-groups.
143 uration in its insect vector (Bemisia tabaci whitefly) than had previously been assumed.
144  to Rickettsia_bellii_MEAM1 found earlier in whiteflies, the new Rickettsia species has more gene fam
145                     The transfer of emerging whiteflies through coupled tissue culture vessels to new
146 the hijacking of microbial genes has allowed whiteflies to develop a highly economic and stable nitro
147                            This gene enables whiteflies to neutralize phenolic glucosides.
148 plants has great potential for management of whiteflies to reduce plant virus disease spread.
149 olamine-binding protein (PEBP) in its vector whitefly to downregulate MAPK signaling cascade.
150 e generation of a bi-parental population for whitefly tolerance/susceptibility enabled the identifica
151                              We investigated whitefly transmission of Lettuce infectious yellows viru
152  on the biology of the virus (host range and whitefly transmission) will be useful in developing and
153  systemic plant movement but is required for whitefly transmission.
154 able of both systemic movement in plants and whitefly transmission.
155 ava mosaic disease is caused by a complex of whitefly-transmitted begomoviruses, which often occur in
156 ANCE Worldwide, diseases of tomato caused by whitefly-transmitted geminiviruses (begomoviruses) cause
157                            All characterized whitefly-transmitted geminiviruses (begomoviruses) with
158                                         Most whitefly-transmitted geminiviruses possess bipartite DNA
159                            Begomoviruses are whitefly-transmitted ss-DNA viruses that infect dicotyle
160  at controlling pests such as the greenhouse whitefly Trialeurodes vaporariorum (Westwood) which are
161                                   Greenhouse whitefly (Trialeurodes vaporariorum) is a major global p
162 llected on cassava in 1997, during the first whitefly upsurges in Uganda, with collections made in 20
163 y: Geminiviridae, Genus: Begomovirus) by the whitefly vector Bemisia tabaci MEAM1 (Gennadius) in toma
164 zed in the anterior foregut or cibarium of a whitefly vector biotype but not within those of a whitef
165 ese locations strongly corresponded with the whitefly vector transmission of LIYV.
166 ases as well as their associated viruses and whitefly vector.
167       Individual viruses exist in plants and whitefly vectors as populations comprising both genome s
168 strated previously and in the present study, whitefly vectors failed to transmit virions preincubated
169 g host range, semipersistent transmission by whitefly vectors, and impact on diverse cropping systems
170 V capsid components were individually fed to whitefly vectors, significantly more whiteflies retained
171 anism in the anterior foregut or cibarium of whitefly vectors.
172 e closely related silverleaf and sweetpotato whiteflies were observed.
173  it on samples from fission yeast, mouse and whitefly, whose reference genome is not yet available.
174 t multigenic and multi-faceted resistance to whiteflies with each B. tabaci species displaying distin

 
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