ライフサイエンスコーパス: Spodoptera

1 ptera insects, especially genes of the genus Spodoptera.

2 rotein, an event that initiates apoptosis in Spodoptera and Drosophila.

3 ns and key conserved motifs of OBPs in genus Spodoptera are identified by MEME, and their putative ro

4 AP, Op-IAP3 failed to bind or inhibit native Spodoptera caspases.

5 ORF1 protein expressed in either E. coli or Spodoptera cells forms high molecular weight structures

6 e lefs prevented AcMNPV-induced apoptosis of Spodoptera cells, whereas silencing the nonreplicative l

7 isolated in Peru from the Southern armyworm (Spodoptera eridania).

8 isolated in Peru from the Southern armyworm, Spodoptera eridania.

9 Spodoptera exempta larvae infected with WT SpexNPV were

10 ht genetically distinguishable variants from Spodoptera exempta nucleopolyhedrovirus (SpexNPV) isolat

11 xia in caterpillars of the African armyworm (Spodoptera exempta) by asking how individuals change the

12 ions of a major crop pest, African armyworm (Spodoptera exempta), which show that the prevalence and

13 SpexNPV) isolated from the African armyworm, Spodoptera exempta.

14 olenoyl-l-Gln) present in the regurgitant of Spodoptera exigua (beet armyworm caterpillars) activates

15 cies indicates that saliva from the noctuids Spodoptera exigua and Heliothis virescens also induced P

16 Caterpillar larvae of the beet armyworm Spodoptera exigua Hubner show a clear feeding preference

17 cae) and one generalist caterpillar species (Spodoptera exigua Hubner).

18 eins from Lymantria dispar MNPV (LdMNPV) and Spodoptera exigua MNPV (SeMNPV) mediate membrane fusion

19 35)) and a cosmid representing a fragment of Spodoptera exigua nucleopolyhedrovirus (SeMNPV), a viral

20 PROPEP3 precursor gene is rapidly induced by Spodoptera exigua oral secretions.

21 Caterpillars of the generalist herbivore Spodoptera exigua reared on transgenic plants gained mor

22 optera (S. litura, Spodoptera littoralis and Spodoptera exigua) had a relatively close evolutionary r

23 seedlings attacked by beet armyworm larvae (Spodoptera exigua) produce a mixture of terpenoid and in

24 worm (Spodoptera frugiperda), beet armyworm (Spodoptera exigua), tobacco budworm (Heliothis virescens

25 lworm Helicoverpa zea, and the beet armyworm Spodoptera exigua, 100% mortality was observed against a

26 ible to infection by PaV included those from Spodoptera exigua, Helicoverpa zea and Aedes albopictus,

27 Beet armyworm, Spodoptera exigua, is a major pest of cotton around the

28 3h (HvAV-3h) has been recently isolated from Spodoptera exigua, without parasitoid vector identified

29 olecular mechanisms of the pupal melanism in Spodoptera exigua.

30 syringae pv tomato (Pst) and the insect pest Spodoptera exigua.

31 psis thaliana) with the generalist herbivore Spodoptera exigua.

32 e to larval herbivory by the beet army worm, Spodoptera exigua.

33 es against the chewing insect beet armyworm (Spodoptera exigua; BAW).

34 Spodoptera frugiperda (J.

35 Hence, we extended our previous studies on Spodoptera frugiperda (Sf) FDL to include GNT-I and -II.

36 We report that transfection of Spodoptera frugiperda (SF-21) cells with ie2 was suffici

37 encoding the predicted full-length leptin in Spodoptera frugiperda (Sf-9) cells by infection with the

38 used an immunocytochemical staining assay of Spodoptera frugiperda (Sf-9) cells which were infected w

39 vitro viability of the insect cell line from Spodoptera frugiperda (SF-9) was observed in the presenc

40 tamin D-24-hydroxylase has been expressed in Spodoptera frugiperda (Sf21) insect cells using the prev

41 the presence and absence of phospholamban in Spodoptera frugiperda (Sf21) insect cells.

42 ailanthus moth), and an ovarian cell line of Spodoptera frugiperda (Sf9) (fall armyworm).

43 lines of H. zea and the ovarian cell line of Spodoptera frugiperda (Sf9) and a loss of function analy

44 kinase present in the nucleus of both insect Spodoptera frugiperda (Sf9) and human Jurkat cells.

45 cellular sugar nucleotide levels of cultured Spodoptera frugiperda (Sf9) and Trichoplusia ni (High Fi

46 Therefore, Spodoptera frugiperda (Sf9) cells and baculovirus have b

47 Using fusion proteins in Spodoptera frugiperda (Sf9) cells and independently expr

48 duced at 5% of the total protein of infected Spodoptera frugiperda (Sf9) cells and were purified to >

49 Spodoptera frugiperda (Sf9) cells have proved a suitable

50 ) was purified to homogeneity (60-fold) from Spodoptera frugiperda (Sf9) cells infected with baculovi

51 th cytochrome P450 reductase (CPR) in insect Spodoptera frugiperda (Sf9) cells using a baculovirus-me

52 ine erythropoietin receptor was expressed in Spodoptera frugiperda (Sf9) cells using a recombinant ba

53 Norwalk virus open reading frame 3 (ORF3) in Spodoptera frugiperda (Sf9) cells yields two major forms

54 to label recombinant proteins with biotin in Spodoptera frugiperda (Sf9) cells, and we describe a col

55 roxytryptamine1A receptor, when expressed in Spodoptera frugiperda (Sf9) cells, facilitates the bindi

56 eered into baculovirus DNA for expression in Spodoptera frugiperda (Sf9) cells.

57 tailing the use of proteins overexpressed in Spodoptera frugiperda (Sf9) cells.

58 ntified using recombinant cPLA2 expressed in Spodoptera frugiperda (Sf9) cells.

59 A baculovirus/Spodoptera frugiperda (Sf9) expression system was harnes

60 Spodoptera frugiperda (Sf9) importin-alpha-16 is a trans

61 ks in the sialic acid synthesis pathway in a Spodoptera frugiperda (Sf9) insect cell line and devised

62 ngle capsid protein of Norwalk virus (NV) in Spodoptera frugiperda (Sf9) insect cells infected with r

63 Spodoptera frugiperda (Sf9) insect cells secreted a clas

64 hCtf4 plus the hCMG complex), coinfection of Spodoptera frugiperda (Sf9) insect cells with viruses ex

65 ntracellular and extracellular expression in Spodoptera frugiperda (Sf9) insect cells, respectively.

66 4-kinases, AtPI4Kalpha1 and AtPI4Kbeta1, in Spodoptera frugiperda (Sf9) insect cells.

67 ncated forms, have been expressed in insect (Spodoptera frugiperda (Sf9)) cells using recombinant bac

68 An insect ovarian cell, Spodoptera frugiperda (Sf9), has been widely used to exp

69 to express functional myosin 15-S1 using the Spodoptera frugiperda (Sf9)-baculovirus system, we disco

70 The receptors were then expressed in Spodoptera frugiperda 9 (Sf9) cells using the baculoviru

71 ied to homogeneity from baculovirus-infected Spodoptera frugiperda 9 insect cells.

72 ted and undifferentiated Caco-2) and insect (Spodoptera frugiperda 9) ovary.

73 a frugiperda infected with the type species, Spodoptera frugiperda ascovirus 1a (SfAV-1a), sampling t

74 we sequenced the genome of the type species Spodoptera frugiperda ascovirus 1a (SfAV-1a).

75 fied 21 structural proteins in the virion of Spodoptera frugiperda ascovirus 1a (SfAV1a), a virus wit

76 analysis of genome expression in vivo by the Spodoptera frugiperda ascovirus shows that inhibitors of

77 The Spodoptera frugiperda ascovirus, a DNA virus that attack

78 sion is observed in a cell line derived from Spodoptera frugiperda but not in a cell line derived fro

79 Spodoptera frugiperda caterpillars were infected with a

80 ed as active Fab molecules by coinfection of Spodoptera frugiperda cell lines with recombinant baculo

81 pressed this protein in Escherichia coli and Spodoptera frugiperda cells and have shown that it binds

82 Membranes from Spodoptera frugiperda cells expressing CB(1) and CB(2) r

83 The Spodoptera frugiperda cells expressing each recombinant

84 Using Spodoptera frugiperda cells expression system, we compar

85 viral RNA polymerase, has been expressed in Spodoptera frugiperda cells infected with recombinant ba

86 ents with recombinant InsP(3)R1 expressed in Spodoptera frugiperda cells we discovered that E2100D an

87 nt caused widespread apoptosis in permissive Spodoptera frugiperda cells, ablation of IE1 and IE0 pre

88 while they did not bind either Mus dunni or Spodoptera frugiperda cells, cells which are resistant t

89 a new member of the CKII family derived from Spodoptera frugiperda cells.

90 hesis and late gene expression in permissive Spodoptera frugiperda cells.

91 a recombinant enzyme in Escherichia coli and Spodoptera frugiperda cells.

92 dy transcription in vivo in third instars of Spodoptera frugiperda infected with the type species, Sp

93 A baculovirus/Spodoptera frugiperda insect cell system was used to exp

94 opyridine-sensitive calcium (Ca) channels in Spodoptera frugiperda insect cells (Sf9 cells) by infect

95 mutants known to affect viral infectivity in Spodoptera frugiperda insect cells and Nicotiana tabacum

96 e cardiac Ca-ATPase expressed in Sf21 cells (Spodoptera frugiperda insect cells) have been carried ou

97 The noctuid moth Spodoptera frugiperda ranks as one of the world's worst

98 Spodoptera frugiperda retinol dehydratase catalyzes the

99 apoptosis protein (IAP) homolog, SfIAP, from Spodoptera frugiperda Sf-21 cells, a host of insect bacu

100 pase-1 and caspase-3, to induce apoptosis in Spodoptera frugiperda Sf-21 insect cells.

101 that virus-like particles (VLPs) produced in Spodoptera frugiperda Sf-9 cells from recombinant baculo

102 Drosophila S2 cells or the Sf-IAP protein in Spodoptera frugiperda Sf21 cells by RNA interference (RN

103 totic suppressor gene p35 cause apoptosis in Spodoptera frugiperda SF21 cells.

104 The Spodoptera frugiperda Sf9 cell line is used as a cell su

105 tylhexosaminidase from the culture medium of Spodoptera frugiperda Sf9 cells (Sfhex).

106 timulated Raf kinase in baculovirus-infected Spodoptera frugiperda Sf9 cells and was able to directly

107 and MsRel2 in Drosophila melanogaster S2 and Spodoptera frugiperda Sf9 cells can activate AMP gene pr

108 (v) Lysates of Spodoptera frugiperda Sf9 cells doubly infected with bac

109 eoclasts, has been functionally expressed in Spodoptera frugiperda Sf9 cells using the Autographa cal

110 hydrolase has been functionally expressed in Spodoptera frugiperda Sf9 cells using the Autographa cal

111 ts were viable in Trichoplusia ni High 5 and Spodoptera frugiperda Sf9 cells.

112 nant maspin produced in baculovirus-infected Spodoptera frugiperda Sf9 insect cells [rMaspin(i)] bind

113 at the N-terminal leader of two insect IAPs, Spodoptera frugiperda SfIAP and Drosophila melanogaster

114 h2, we have identified and cloned the insect Spodoptera frugiperda target of the baculovirus antiapop

115 24, Snf7, Vps46, and Vps60) were cloned from Spodoptera frugiperda Using a viral complementation syst

116 for AcMNPV replication, we cloned a cDNA of Spodoptera frugiperda VPS4, a key regulator for disassem

117 ereas cells from Drosophila melanogaster and Spodoptera frugiperda were refractory to infection.

118 he crop-defoliating pest, the fall armyworm (Spodoptera frugiperda) and its species-specific baculovi

119 se (TPH) has been expressed in insect cells (Spodoptera frugiperda) as a histidine-tagged enzyme.

120 Sf9 (Spodoptera frugiperda) cells overexpressing recombinant

121 nts for the transport activity by using Sf9 (Spodoptera frugiperda) cells, characterized the subcellu

122 ied several maize proteins in fall armyworm (Spodoptera frugiperda) frass that potentially play a rol

123 n cowpea (Vigna unguiculata), fall armyworm (Spodoptera frugiperda) herbivory and oral secretions (OS

124 igna unguiculata) responds to Fall armyworm (Spodoptera frugiperda) herbivory through the detection o

125 The fall armyworm (Spodoptera frugiperda) is a devastating pest of corn in

126 guiculata) plants attacked by fall armyworm (Spodoptera frugiperda) larvae.

127 ied two plant chitinases from fall armyworm (Spodoptera frugiperda) larval frass that suppress herbiv

128 alytically active form in insect cells (Sf9, Spodoptera frugiperda) transfected with BDH-cDNA in bacu

129 ck cutworm (Agrotis ipsilon), fall armyworm (Spodoptera frugiperda), beet armyworm (Spodoptera exigua

130 optosis in cultured SF21 cells from the moth Spodoptera frugiperda, a model insect system.

131 Rice plants fed on by fall armyworm (Spodoptera frugiperda, FAW) caterpillars emit a blend of

132 the principal effector caspase of the insect Spodoptera frugiperda, is presented here.

133 The Sf9 cell line, derived from Spodoptera frugiperda, is used as a cell substrate for b

134 he model insects Drosophila melanogaster and Spodoptera frugiperda, respectively, are rapidly deplete

135 Spodoptera frugiperda, S. exigua and Manduca sexta larva

136 only high-mannose glycans; (b) insect cells (Spodoptera frugiperda, Sf9), which confer mainly paucima

137 ne Sf9, derived from the lepidopteran insect Spodoptera frugiperda, stimulated a DNA damage response,

138 In the larvae of Spodoptera frugiperda, the organism from which Sf-9 cell

139 f Bt crops, resistance of the fall armyworm, Spodoptera frugiperda, to Cry1F maize has occurred in Pu

140 g is only observed when Mant-GDP is bound to Spodoptera frugiperda-expressed Cdc42Hs and is not detec

141 n assays in the SF-21 cell line derived from Spodoptera frugiperda.

142 which converts retinol to anhydroretinol in Spodoptera frugiperda.

143 , a cell line derived from the fall armyworm Spodoptera frugiperda.

144 , the native, short-lived IAP of host insect Spodoptera frugiperda.

145 lls derived from the permissive AcMNPV host, Spodoptera frugiperda.

146 e Innexin2 orthologue of an ichnovirus host, Spodoptera frugiperda.

147 ncipal cellular IAP of the lepidopteran host Spodoptera frugiperda.

148 rincipal effector caspase of the host insect Spodoptera frugiperda.

149 ding this enzyme in the lepidopteran insect, Spodoptera frugiperda.

150 lines; one other insect cell line, Sf21 from Spodoptera frugiperda; and BHK (mammalian) cells were me

151 ruses were used to produce active enzymes in Spodoptera frugiperta (SF9) cells.

152 t were heterologously expressed by using the Spodoptera fugiperda-baculovirus-based system and were s

153 hormone (FSH) mutant protein was produced in Spodoptera furgiperda (Sf)-9 insect cells to serve as a

154 H2Av, AcMNPV blocked phosphorylation of the Spodoptera H2AX homolog (SfH2AX).

155 this survey focused on insect larva feeding (Spodoptera littoralis and Manduca sexta) that triggers d

156 genes from the genus Spodoptera (S. litura, Spodoptera littoralis and Spodoptera exigua) had a relat

157 nces of maize (Zea mays) leaf infestation by Spodoptera littoralis caterpillars for the root-feeding

158 resistance against the generalist herbivore Spodoptera littoralis that was attenuated in JA biosynth

159 prothoracic glands of last instar larvae of Spodoptera littoralis was detected and analysed by HPLC-

160 ing of an immune gene in a lepidopteran host Spodoptera littoralis, leaving the midgut microbiota una

161 liana) and the generalist herbivorous insect Spodoptera littoralis, little is known about early event

162 sing larvae of the Egyptian cotton leafworm, Spodoptera littoralis, we found that despite its apparen

163 vae of the generalist lepidopteran herbivore Spodoptera littoralis.

164 mely susceptible to the generalist herbivore Spodoptera littoralis.

165 ental viruses but also a nonpermissive host (Spodoptera litura).

166 challenged a 'donor' plant with caterpillar Spodoptera litura, and investigated defence responses an

167 BP genes from the antennal transcriptomes of Spodoptera litura.

168 monstrated that the OBP genes from the genus Spodoptera (S. litura, Spodoptera littoralis and Spodopt

169 y effectively induced cell death in cultured Spodoptera Sf-9 cells, and this death was antagonized by

170 otton for enhanced control of Heliothine and Spodoptera species, our model suggests the possibility o