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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

30 The TSWV nucleocapsid protein and human cytomegalovirus glyc

31 NA generated from F. occidentalis exposed to TSWV.

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

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

34 ns were significantly altered in response to TSWV.

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

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

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

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

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

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

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

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

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

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

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

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