ライフサイエンスコーパス: Culex

1 er of RVFV into other anthrophillic vectors (Culex and Anopheles sp. mosquitoes), and, importantly, c

2 thologs are present in the genomes of Aedes, Culex, and Anopheles mosquito species.

3 The Culex AO sequence contains a molybdopterin cofactor bind

4 r abundances than those of mosquitoes of the Culex genus, within which the viral abundance reached 16

5 A concurrent increase in detections of Culex larvae in aquatic habitats associated with stream

6 exclusively in the Spissipes section of the Culex (Melanoconion) subgenus.

7 lified esterase genes in a highly dispersive Culex mosquito have suggested that insecticide resistanc

8 PBOH and PBCHO, both of which are toxic to Culex mosquito larvae, can be further metabolized by CYP

9 s that were up-regulated in highly resistant Culex mosquito strains, HAmCq(G8) and MAmCq(G6), respect

10 asmic incompatibility in some strains of the Culex mosquito.

11 through matching of flight-tone harmonics in Culex mosquitoes and suggest that difference tones are u

12 Aedes and Culex mosquitoes are the main culprits, spreading infect

13 conducted a whole transcriptome analysis of Culex mosquitoes following permethrin selection.

14 nome level between resistant and susceptible Culex mosquitoes identified one and three GPCR-related g

15 , leading to significantly higher catches of Culex mosquitoes in traps baited with binary than in tho

16 Culex mosquitoes introduce the pathogens responsible for

17 ffective inhibitors of the CO(2) response in Culex mosquitoes that transmit West Nile fever and filar

18 egulated expression in insecticide resistant Culex mosquitoes through transcriptional profiling compa

19 West Nile virus, which is transmitted by Culex mosquitoes while feeding on birds and humans, has

20 enylacteate, which was demonstrated to repel Culex mosquitoes, and secondarily to citronellal, a know

21 were effective against strains of Aedes and Culex mosquitoes, demonstrating that electrostatic netti

22 tions in other field and permethrin selected Culex mosquitoes, finding that the co-existence of all 9

23 cessary for DEET reception and repellency in Culex mosquitoes.

24 srupts CO(2)-mediated hut entry behaviour of Culex mosquitoes.

25 y up-regulated but also induced in resistant Culex mosquitoes.

26 ed to vertebrate hosts primarily by infected Culex mosquitoes.

27 irions (ODVs) of the nucleopolyhedrovirus of Culex nigripalpus (CuniNPV) were purified by Ludox densi

28 s that infects larval stages of the mosquito Culex nigripalpus (CuniNPV).

29 Culex nigripalpus nucleopolyhedrovirus (CuniNPV) was the

30 Here we show that the Culex orthologue of Vago (CxVago) is up-regulated in res

31 osition attractant pheromone of the mosquito Culex pipens.

32 le virus (WNV), previously was isolated from Culex pipiens and Aedes rossicus mosquitoes in the Czech

33 was isolated from two species of mosquitoes, Culex pipiens and Aedes vexans, and from brain tissues o

34 after blood feeding in two other mosquitoes (Culex pipiens and Anopheles gambiae) and the bed bug, Ci

35 ctipennis, and Anopheles punctulatus groups; Culex pipiens and the Culex subgenus Melanoconion; and t

36 fied between surface-dwelling populations of Culex pipiens and the so-called molestus form found in t

37 In the Old World, some mosquitoes in the Culex pipiens complex are excellent enzootic vectors of

38 of the vector mosquitoes Aedes aegypti, the Culex pipiens Complex, and, most recently, Aedes albopic

39 was vertically transmitted to 2 F(1) female Culex pipiens from a naturally infected female collected

40 cDNA from a WN virus isolate recovered from Culex pipiens in Connecticut was expressed in Escherichi

41 ticide resistance gene Ester in the mosquito Culex pipiens in the Montpellier area, southern France.

42 rmone signaling direct entry of the mosquito Culex pipiens into its overwintering adult diapause, and

43 Culex pipiens is the mosquito that vectors West Nile Vir

44 intering dormancy (diapause) in the mosquito Culex pipiens is the switch in females from blood feedin

45 In the Culex pipiens mosquito group (including the filariasis v

46 this hypothesis using different incompatible Culex pipiens mosquito strains and show that CI persists

47 he function of sfRNA during WNV infection of Culex pipiens mosquitoes and evaluated its role in deter

48 l-sib design was set up in which families of Culex pipiens mosquitoes collected from the field were r

49 HCR), a phenotype first described in 1999 in Culex pipiens mosquitoes surviving chlorpyrifos doses 1

50 WN virus was recovered from Culex pipiens mosquitoes, the most likely vector, and an

51 and transmission rates of West Nile virus in Culex pipiens mosquitoes.

52 sly associated with pyrethroid resistance in Culex pipiens pallens was also over-transcribed in VK.

53 of mosGCTL in another major mosquito vector (Culex pipiens pallens) also impairs the survival of gut

54 y receptor neurons (ORNs) on the antennae of Culex pipiens quinquefasciatus (Cx. quinquefasciatus).

55 umanus, Anopheles gambiae, Aedes Aegypti and Culex pipiens quinquefasciatus is notable.

56 Donor, Culex pipiens quinquefasciatus mosquitoes infected with

57 LPs to address biological questions in vivo, Culex pipiens quinquefasciatus mosquitoes were orally an

58 . quinquefasciatus is one species within the Culex pipiens species complex and can be found throughou

59 bachia strains circulating in the California Culex pipiens species complex, (2) investigate Wolbachia

60 lengths of late summer program the mosquito Culex pipiens to enter a reproductive diapause character

61 The populations of an aquatic invertebrate (Culex pipiens) exposed over several generations to repea

62 ring adult ileum development in the mosquito Culex pipiens.

63 osquitoes, being shared by Aedes aegypti and Culex pipiens.

64 allography and NMR 3D structures of OBP1 for Culex quinquefasciatus (CquiOBP1) bound to an ovipositio

65 ecies, Aedes aegypti, Anopheles gambiae, and Culex quinquefasciatus (Diptera: Culicidae), representin

66 was obtained from the common house mosquito Culex quinquefasciatus (Say) through cloning and sequenc

67 Culex quinquefasciatus (the southern house mosquito) is

68 d replication in C7/10 mosquito cells and in Culex quinquefasciatus after intrathoracic inoculation.

69 -transmitting mosquitoes: Anopheles gambiae, Culex quinquefasciatus and A. aegypti.

70 ons in the entire mosquito sodium channel of Culex quinquefasciatus and analyzing their evolutionary

71 sis, Armigeres subalbatus, Aedes albopictus, Culex quinquefasciatus and Cu. tritaeniorhynchus) collec

72 in the continental United States, including Culex quinquefasciatus and Cx. pipiens.

73 rimiphos methyl CS was highly active against Culex quinquefasciatus and gave control for 10 months in

74 n where the mosquitoes Anopheles gambiae and Culex quinquefasciatus are resistant to pyrethroids but

75 ng speculation that other mosquitoes such as Culex quinquefasciatus could be involved.

76 We show that field-collected Ugandan Culex quinquefasciatus display CNV for the voltage-gated

77 hole-body microbiome of the mosquito species Culex quinquefasciatus in various larval stadia and foll

78 Aa1/Cry49Aa1 proteins (LC50 for third instar Culex quinquefasciatus larvae: 15.9 ng/ml and 6.3 ng/ml

79 Finally, we used an in vivo fitness assay in Culex quinquefasciatus mosquitoes and chickens to determ

80 ession profiles of resistant and susceptible Culex quinquefasciatus mosquitoes, using a combination o

81 The mosquito Culex quinquefasciatus poses a substantial threat to hum

82 In the eastern United States, Culex quinquefasciatus response to projected climate cha

83 artment visits for asthma and skin rash, and Culex quinquefasciatus species-specific vector index (an

84 hole-genome sequencing data for the mosquito Culex quinquefasciatus strain JHB.

85 Anopheles gambiae genomes, Aedes aegypti and Culex quinquefasciatus), tick (Ixodes scapularis), body

86 pecies: Aedes aegypti, Anopheles gambiae and Culex quinquefasciatus, a body louse Pediculus humanus a

87 A similar phenomenon was also observed in Culex quinquefasciatus, a natural vector of WNV, further

88 vector species including Anopheles gambiae, Culex quinquefasciatus, and Aedes aegypti, the latter an

89 are favorable for the sole mosquito vector, Culex quinquefasciatus, and extrinsic sporogonic develop

90 king females of the southern house mosquito, Culex quinquefasciatus, and the yellow fever mosquito, A

91 ed toxicity against larvae of the mosquitoes Culex quinquefasciatus, Anopheles gambiae, and Ochlerota

92 to CryIV proteins in larvae of the mosquito, Culex quinquefasciatus, can be suppressed or reduced mar

93 f the mosquito disease vectors Aeaegypti and Culex quinquefasciatus, each consisting of three scaffol

94 The southern house mosquito, Culex quinquefasciatus, has one of the most acute and ec

95 ons in the entire mosquito sodium channel of Culex quinquefasciatus, the prevalence of which were str

96 ment of insecticide resistance in mosquitoes Culex quinquefasciatus, we conducted a whole transcripto

97 Here we show frequency matching in Culex quinquefasciatus, where the wing-beat frequencies

98 elated species of insects: Aedes aegypti and Culex quinquefasciatus.

99 or CquiOR136 of the southern house mosquito, Culex quinquefasciatus.

100 nes in insecticide resistance of mosquitoes, Culex quinquefasciatus.

101 -reared pyrethroid susceptible and resistant Culex quinquefasciatus.

102 le for Anopheles gambiae, Aedes aegypti, and Culex quinquefasciatus.

103 virus diversity than sampling location, with Culex species harboring more viruses at higher abundance

104 he viromes were very similar among the three Culex species studied, suggesting that the host taxon pl

105 Culicine mosquitoes such as Aedes spp. and Culex spp. are important vectors of other human pathogen

106 Here we show variation between incompatible Culex strains in two Wolbachia ankyrin repeat-encoding g

107 These differences from the Culex study may stem both from differences in the popula

108 es punctulatus groups; Culex pipiens and the Culex subgenus Melanoconion; and the tribe Sabethini.

109 ed AO activity by a range of insecticides in Culex, suggest that this AO may play a role in insectici

110 th WNV through the bite of a single infected Culex tarsalis mosquito exhibited 5- to 10-fold-higher v

111 We previously showed that Culex tarsalis mosquito saliva and salivary gland extrac

112 We have shown that Culex tarsalis mosquito saliva and SGE enhance the repli

113 . stephensi, Ae. albopictus, Ae. aegypti and Culex tarsalis).

114 Here, we determine whether WNV enzootic (Culex tarsalis, Cx. quinquefasciatus, and Cx. pipiens) a

115 isolated from mosquitoes, designated Guaico Culex virus (GCXV).