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1 ) assay that can detect INSV from individual thrips.
2 nificantly improved survivorship of infected thrips.
3 d at the same and different locations as the thrips.
4 , whiteflies, leafhoppers, planthoppers, and thrips.
5 e closing of conduits for global movement of thrips.
6 plotype that is inefficiently transmitted by thrips.
7 solate that was inefficiently transmitted by thrips.
8 minant associated with virus transmission by thrips.
9 sts but are required for transmissibility by thrips.
10 oth herbivores, and B96 is also resistant to thrips.
11                               Western flower thrips also responded to FA profiles that included iC4,
12     Three of the 30 SLIs were transmitted by thrips, and 27 were not.
13 ts (all ants and termites; some bees, wasps, thrips, and beetles), snapping shrimp, and naked mole ra
14 ressed the growth of B. bassiana in infected thrips, and significantly improved survivorship of infec
15 ave also evolved in less-studied groups like thrips, aphids and polyembryonic wasps.
16                                              Thrips are among the stealthiest of insect invaders due
17                                Many invasive thrips are notorious for causing extensive crop damage,
18 volatile emissions increase dramatically and thrips are repelled.
19                                  For cycads, thrips are specialized pollinators.
20 ruses are transmitted from plant to plant by thrips as the insect vector.
21 rtion of females among progeny from infected thrips at 12 degrees C was higher than at 24 degrees C.
22 diversity were maintained in both plants and thrips between transmission events.
23 0 species, the Acercaria (lice, plant lices, thrips, bugs) including number of economically important
24  and G(C), are critical for the infection of thrips, but they are not required for the initial infect
25                  Small arthropod pests, like thrips, can cause crop damage through virus transfer, wh
26 ptor, mediating the virus acquisition by the thrips carrier.
27 ct microbiomes that had different effects on thrips, chlorogenic acid concentrations in leaves and pl
28  to provide evidence of a locally persistent thrips core virome that characterizes each population.
29  we examine factors facilitating invasion by thrips, damage caused by these insects, pre- and post-in
30  Our findings support the hypothesis that L1 thrips display a complex reaction to TSWV infection and
31            In the Australian Outback, Acacia thrips Dunatothrips aneurae (Thysanoptera) glue Acacia p
32 monstrated rates of genomic evolution within thrips, extensive sampling is needed to fully understand
33                                 TSWV and the thrips Frankliniella fusca and Frankliniella occidentali
34  consistently induced resistance against the thrips Frankliniella occidentalis, but not against the m
35 to attack by spider mites and western flower thrips (Frankliniella occidentalis), another cell-conten
36  in which it also replicates, western flower thrips (Frankliniella occidentalis).
37       INSV is vectored by the western flower thrips, Frankliniella occidentalis, a small insect pest
38 efly, Bemisia tabaci, and the Western flower thrips, Frankliniella occidentalis.
39  be effective at immobilizing a target pest, thrips, Frankliniella occidentalis.
40     Our findings that G(N)-S binds to larval thrips guts and decreases TSWV acquisition provide evide
41 rips midguts when purified G(N)-S was fed to thrips in an in vivo binding assay.
42 rin are commonly used insecticides to manage thrips in China, and laboratory bioassays demonstrated t
43 t virus (TSWV) is transmitted exclusively by thrips in nature.
44 esides understanding the role of jassids and thrips in particular, in producing the best cup characte
45   Derived features of mitochondrial tRNAs in thrips include gene duplications, anticodon mutations, l
46                                         Male thrips infected with TSWV fed more than uninfected males
47  first report on gene expression dynamics in thrips infested Darjeeling tea leaves can be extrapolate
48 n the assay was used on field populations of thrips, INSV was successfully identified and quantified
49                                 Pollen-laden thrips leave male cycad cones en masse during the daily
50 died the mating behaviour of the bean flower thrips Megalurothrips sjostedti (Trybom) (Thysanoptera:
51 o thrips midguts, indicating that the G(N)-S-thrips midgut interaction is specific.
52 ors displayed on the epithelial cells of the thrips midgut.
53              We detected specific binding to thrips midguts when purified G(N)-S was fed to thrips in
54 tomegalovirus glycoprotein B did not bind to thrips midguts, indicating that the G(N)-S-thrips midgut
55                                              Thrips mitochondrial genomes are marked by high rates of
56                     Phylogenetic analysis of thrips mitochondrial sequence data supports the monophyl
57 y established for four groups: Thysanoptera (thrips), Neuroptera (lacewings), Diptera (flies), and no
58                  In this study, we collected thrips of these species from 12 field populations in var
59 lower thrips [WFT]) and Thrips tabaci (onion thrips [OT]) are insect species that greatly impact hort
60 e and female individuals) and its specialist thrips pollinator, Cycadothrips chadwicki.
61 r virus characterization in a subset of four thrips populations maintained in the laboratory allowed
62 us studies suggest that genetic variation of thrips populations, virus isolates, or both are importan
63                              Fungal-infected thrips preferentially moved to cooler areas (~12 degrees
64 interactors with G(N) These newly discovered thrips protein-G(N) interactions are important for a bet
65        The goal of this work was to identify thrips proteins that bind directly to the viral attachme
66                                   Two of the thrips proteins, endocuticle structural glycoprotein and
67                Using these sequences, the L1 thrips proteome that resolved on a two-dimensional gel w
68 ard library of B157 (tea clone infested with thrips), providing us transcripts related to aroma and f
69 e population, which are not transmissible by thrips, rather than with the presence of a dominant hapl
70 ufficient to explain the observed sequential thrips' repellence (push) and attraction (pull).
71 etaceous amber of Spain, wherein four female thrips representing a genus and two species in the famil
72 olatile emissions diminish and cones attract thrips, resulting in pollination of female cones.
73 Behavioral and electrophysiological tests on thrips reveal that variations in b-myrcene and ocimene e
74 e PCR (RT-PCR) analysis of virus titer in L1 thrips revealed a significant increase in the normalized
75 n we assigned putative viral contigs to each thrips sample by real-time reverse transcription-quantit
76 o cooler areas (~12 degrees C) while healthy thrips sought out warmer temperatures (~24 degrees C).
77 just eight gene blocks conserved between any thrips species and the ancestral insect mitochondrial ge
78                                          The thrips species Frankliniella occidentalis and Thrips tab
79              Tospoviruses and their vectors, thrips species in the order Thysanoptera, represent a ma
80  shows broad similarities with that of other thrips species that form aggregations, but also shows so
81 the mitochondrial genomes of four additional thrips species, adding three extra families and an addit
82 wo model systems for tospovirus-transmitting thrips species, of utmost importance for the direct and
83  surface when attempting to manage incursive thrips species.
84 ation of Neohydatothrips variabilis (soybean thrips [ST]) from the United States.
85 cidentalis (western flower thrips [WFT]) and Thrips tabaci (onion thrips [OT]) are insect species tha
86 hrips species Frankliniella occidentalis and Thrips tabaci are highly invasive and damaging agricultu
87                           Isofemale lines of Thrips tabaci from multiple locations were tested for th
88                                              Thrips tabaci, which transmits Tomato spotted wilt virus
89  acquisition inhibition assays revealed that thrips that were concomitantly fed purified TSWV and G(N
90 mounts of virus in their midguts compared to thrips that were fed TSWV only.
91                              Many species of thrips (Thysanoptera) in the family Thripidae form matin
92            TSWV is transmitted to plants via thrips (Thysanoptera: Thripidae), which transmit the vir
93 on of these proteins in relation to virus in thrips tissues of principal importance along the route o
94 c system was used to map transmissibility by thrips to the medium (M) RNA of TSWV.
95   The complex and specific interplay between thrips, tospoviruses, and their shared plant hosts leads
96                                    A partial thrips transcriptome was generated using 454-Titanium se
97 lved protein spots were identified using the thrips transcriptome.
98              Sequence analysis of the M RNA, thrips transmissibility assays, G(C) protein analysis, a
99 (C) ORF of the M RNA resulted in the loss of thrips transmissibility without inhibition of virion ass
100                    To locate determinants of thrips transmission in the M RNA, 30 single-lesion isola
101                                              Thrips-transmitted Iris yellow spot virus is an economic
102 nt and virus resistance in plants.IMPORTANCE Thrips-transmitted viruses cause devastating losses to n
103 insect infestation, particularly jassids and thrips triggers the aroma and flavour formation in Darje
104  G(N), during infection and dissemination in thrips vector tissues are unknown.
105 tabaci isoline pairings, virus titers in the thrips vector were significantly lower in the sympatric
106 aviridae, alters the feeding behavior of its thrips vector, Frankliniella occidentalis (Pergande).
107 ed wilt virus (TSWV), and the most efficient thrips vector, we identified and validated six TSWV-inte
108 isition-efficient developmental stage of the thrips vector.
109                Tomato spotted wilt caused by thrips-vectored tomato spotted wilt virus (TSWV) is a ve
110 niella occidentalis is one of nine competent thrips vectors of TSWV transmission to plant hosts.
111         Owing to the difficulty in combating thrips vectors with insecticides, the best way to limit/
112 ew tools that could rapidly detect INSV from thrips vectors would enhance our ability to predict wher
113 on and transmission of Tospoviruses by their thrips vectors.
114                                          The thrips virome characterized includes several novel virus
115 hat G(N) plays a role in TSWV acquisition by thrips, we expressed and purified a soluble, recombinant
116 Trialeurodes vaporariorum and Western flower thrips (WFT) Frankliniella occidentalis, are major horti
117  virus vectors, including the western flower thrips (WFT), Frankliniella occidentalis (Pergande), vec
118   Frankliniella occidentalis (western flower thrips [WFT]) and Thrips tabaci (onion thrips [OT]) are
119 derstanding of virus transmission by aphids, thrips, whiteflies, leafhoppers, planthoppers, treehoppe

 
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