ライフサイエンスコーパス: Culex

1 though similar advances have been lagging in Culex.

2 er mosquitoes, advances have been lacking in Culex.

3 ansmitting mosquito vector species Aedes and Culex.

4 S functions as a suitable larval habitat for Culex, Ae. aegypti and Ae. albopictus in southern Califo

5 In culicine (Culex, Aedes) and anopheline mosquitoes (Anopheles), emb

6 ed, predominantly belonging to three genera: Culex, Aedes, and Anopheles, with significant difference

7 ene drives have been demonstrated to include Culex alongside Anopheles and Aedes, and pave the way fo

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

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

10 ultiple species within the Aedes, Anopheles, Culex, and Psorophora genera.

11 avior of a Culex subgenus Micraedes species, Culex antillummagnorum (Dyar), and provide the first evi

12 The Culex AO sequence contains a molybdopterin cofactor bind

13 itoes of three genera, Aedes, Anopheles, and Culex are able to locate and land on surface-active mana

14 he evolution and drivers of such an atypical Culex behavior and indicate that our understanding of Cu

15 A reduction of over 35% of adult Culex biting densities was recorded.

16 Conversely, in Culex cells and mosquitoes, we saw a minimal impact of s

17 ith host preference were identified on all 3 Culex chromosomes, and these genomic regions contained c

18 Species from the Culex coronator complex are Neotropical species and pote

19 Species from the Culex coronator complex were first detected in the Unite

20 Culex coronator was first described in Trinidad and Toba

21 avior and indicate that our understanding of Culex ecology and behavior remains incomplete.

22 anko iflavirus-1 was especially prevalent in Culex eknomios (88.4%) and Ochlerotatus serratus (88.0%)

23 lacement of species for Aedes, Anopheles and Culex genera clustering in single clades as expected.

24 hould be utilized in habitats containing non-Culex genera while a mix of AIs should be utilized where

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

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

27 , distance to rubber plantations (100 m) and Culex larval presence were identified as risk factors fo

28 health belonging to the genera Ochlerotatus, Culex, Limatus, Mansonia, Psorophora, and Sabethes, with

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

30 assays identified VEEV complex RNA in three Culex (Melanoconion) vomerifer pools, leading to VEEV is

31 , including Culex pipiens, Aedes albopictus, Culex modestus, Anopheles maculipennis sensu lato and Oc

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

33 ant mortality rates in Aedes, Anopheles, and Culex mosquito larvae and adults.

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

35 ated to each other and to those from a local Culex mosquito pool and an Alphamesonivirus-1 previously

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

37 he expanding distribution of its vector, the Culex mosquito, and climatic changes causing heavy monso

38 asmic incompatibility in some strains of the Culex mosquito.

39 ort future technology development to control Culex mosquitoes and provide valuable insight for improv

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

41 Culex mosquitoes are a global vector for multiple human

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

43 ngoing transmission after MDA in areas where Culex mosquitoes are the main transmission vector, sugge

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

45 Culex mosquitoes frequently feed on birds during spring

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

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

48 Culex mosquitoes introduce the pathogens responsible for

49 d that the survival of Aedes, Anopheles, and Culex mosquitoes is negatively impacted by consumptive e

50 Culex mosquitoes particularly Culex quinquefasciatus are

51 Culex mosquitoes pose a significant public health threat

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

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

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

55 ide resistance has threatened the control of Culex mosquitoes, advances in CRISPR genome-editing tool

56 (RVF) is a zoonosis transmitted by Aedes and Culex mosquitoes, and is considered a priority pathogen

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

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

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

60 iously shown to strongly repel Anopheles and Culex mosquitoes, we examined the bioactivities of the i

61 development of these technologies to control Culex mosquitoes.

62 ly related to virus sequences found in local Culex mosquitoes.

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

64 cessary for DEET reception and repellency in Culex mosquitoes.

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

66 ed to vertebrate hosts primarily by infected Culex mosquitoes.

67 Here, we establish the mosquito-infecting Culex narnavirus 1 (CxNV1) as a model to investigate the

68 or the ambigrammatic genome configuration in Culex narnavirus 1, which suggests a model for how trans

69 sociated with one specific mosquito species (Culex nebulosus), which increased in relative abundance

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

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

72 Culex nigripalpus nucleopolyhedrovirus (CuniNPV) was the

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

74 osition attractant pheromone of the mosquito Culex pipens.

75 We then performed competition assays between Culex pipiens and Aedes albopictus in low nutrient envir

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

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

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

79 For both Culex pipiens and Culex vansomereni, adults emerging fro

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

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

82 While Culex torrentium, Culex pipiens biotype pipiens, Aedes aegypti, and Aedes

83 opictus and a representative native mosquito Culex pipiens by three native and widespread cyclopoid c

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

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

86 ruses, including WNV, Culex tarsalis and the Culex pipiens complex, increased 17-21-fold with irrigat

87 Assessing Culex pipiens dissemination efficiency and calculating t

88 nst the third instar larvae of the mosquito, Culex pipiens even at concentration of 2 ppm.

89 vector competence of the temperate mosquito Culex pipiens f.

90 a widely cited example of urban adaptation, Culex pipiens form molestus, also known as the London Un

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

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

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

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

95 Culex pipiens is a major carrier of the West Nile Virus,

96 Culex pipiens is the mosquito that vectors West Nile Vir

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

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

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

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

101 om individual ovary metagenomes of four wild Culex pipiens mosquitoes captured in France.

102 nyavirus close to Umbre virus, were found in Culex pipiens mosquitoes captured in the south of France

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

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

105 We monitored the survival of Culex pipiens mosquitoes throughout the development of t

106 lly tested using larval Aedes albopictus and Culex pipiens mosquitoes to assess mortality and percent

107 We validate its presence in additional Culex pipiens mosquitoes using PCR, long-read sequencing

108 ith the multiple duplicated alleles found in Culex pipiens mosquitoes).

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

110 cifically on West Nile virus transmission by Culex pipiens mosquitoes.

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

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

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

114 Two vectors of West Nile virus, Culex pipiens pipiens and Cx. p.

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

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

117 Donor, Culex pipiens quinquefasciatus mosquitoes infected with

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

119 tected USUV RNA in host-seeking adult female Culex pipiens s.l. as well as in adults reared from fiel

120 nce at the index site identified USUV RNA in Culex pipiens s.l. following the outbreak.

121 The northern house mosquito Culex pipiens sensu stricto is one of the most important

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

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

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

125 The Northern house mosquito (Culex pipiens) and the tiger mosquito (Aedes albopictus)

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

127 thern (Culex quinquefasciatus) and northern (Culex pipiens) house mosquito.

128 ceptibility to S-methoprene was evaluated in Culex pipiens, a globally important vector species.

129 h detected high species diversity, including Culex pipiens, Aedes albopictus, Culex modestus, Anophel

130 n of 10 vector-pathogen pairs of mosquitoes (Culex pipiens, Cx. quinquefascsiatus, Cx. tarsalis, and

131 o a heat spike in the larvae of the mosquito Culex pipiens.

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

133 ference in the polymorphic mosquito species, Culex pipiens.

134 female A. albopictus, Anopheles sinensis and Culex pipiens.

135 n into cycle in the Northern house mosquito, Culex pipiens.

136 ring adult ileum development in the mosquito Culex pipiens.

137 The expansion of insecticide resistance in Culex populations could affect the effectiveness of curr

138 In this study, female Aedes aegypti and Culex quinquefasciastus were exposed to sub-lethal doses

139 he predominant species (54.82%), followed by Culex quinquefasciatus (6.92%).

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

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

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

143 Culex quinquefasciatus (the southern house mosquito) is

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

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

146 indings reveal the extensive distribution of Culex quinquefasciatus and Aedes albopictus, with Aedes

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

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

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

150 ants improve transgenesis efficiency in both Culex quinquefasciatus and Drosophila melanogaster and b

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

152 together act as a toxin toward the mosquito Culex quinquefasciatus and have potential use in biocont

153 Culex mosquitoes particularly Culex quinquefasciatus are important arboviral and filar

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

155 ased transgenesis to generate and validate a Culex quinquefasciatus Cas9-expressing line.

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

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

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

159 al and fungal microbiota from two laboratory Culex quinquefasciatus isolines (wild type and tetracycl

160 at gravid Aedes aegypti, Ae. albopictus, and Culex quinquefasciatus laid significantly more eggs in c

161 arvicidal activity against Aedes aegypti and Culex quinquefasciatus larvae.

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

163 gical relevance of two D7 long proteins from Culex quinquefasciatus mosquito, the vector of filaria p

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

165 ion rates in surviving S411A Kunjin-infected Culex quinquefasciatus mosquitoes were observed, but S41

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

167 onality may influence reproductive traits of Culex quinquefasciatus mosquitoes.

168 requencies between and within individuals of Culex quinquefasciatus over time.

169 Culex quinquefasciatus plays an important role in transm

170 All Culex quinquefasciatus populations except one displayed

171 The mosquito Culex quinquefasciatus poses a substantial threat to hum

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

173 Culex quinquefasciatus Say is a mosquito distributed in

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

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

176 evaluate the susceptibility of the mosquito Culex quinquefasciatus to bacterial agents, a population

177 Aedes aegypti and Culex quinquefasciatus were found year-round throughout

178 of two common disease vectors, the southern (Culex quinquefasciatus) and northern (Culex pipiens) hou

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

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

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

182 tentially virus transmitting insect species (Culex quinquefasciatus, Aedes aegypti) as well as scient

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

184 Diptera (Stomoxys calcitrans, Aedes aegypti, Culex quinquefasciatus, and Culicoides nubeculosus) from

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

186 we test a CRISPR-based homing gene drive for Culex quinquefasciatus, and show that the inheritance of

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

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

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

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

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

192 mosquito; Aedes aegypti, Ae. albopictus and Culex quinquefasciatus, representing the two most signif

193 ed four model vector species (Aedes aegypti, Culex quinquefasciatus, Stomoxys calcitrans, and Culicoi

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

195 The southern house mosquito, Culex quinquefasciatus, utilizes two odorant receptors,

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

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

198 cies-Aedes aegypti, Anopheles stephensi, and Culex quinquefasciatus-and all four gonotrophic stages o

199 hich is transmitted by the invasive mosquito Culex quinquefasciatus.

200 sis of resistance mechanisms in the mosquito Culex quinquefasciatus.

201 icide resistance in a mosquito population of Culex quinquefasciatus.

202 urban environments such as Aedes aegypti and Culex quinquefasciatus.

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

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

205 nes in insecticide resistance of mosquitoes, Culex quinquefasciatus.

206 -reared pyrethroid susceptible and resistant Culex quinquefasciatus.

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

208 t important regional West Nile virus vector, Culex quinquefasciatus.

209 e the first evidence, to our knowledge, of a Culex species aerially and skip-ovipositing, rather than

210 ow little regarding the reproduction of many Culex species and subgenera.

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

212 us (WNV), a neurotropic flavivirus spread by Culex species mosquitoes, is the leading cause of mosqui

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

214 invertebrate cells, American robins, and two Culex species with WNV and/or SLEV.

215 Transmitted primarily by Culex species, WNV transmission requires the complex int

216 Here, we develop a Culex-specific Cas9/gRNA expression toolkit and use site

217 cionia frustrana) and disease vectors (e.g., Culex spp).

218 sphaericus is an effective AI for control of Culex spp.

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

220 Field results demonstrated elimination of Culex spp. from treated containers while container breed

221 he continental United States, is vectored by Culex spp. mosquitoes.

222 on a measure of infection prevalence in the Culex spp. mosquitos, its primary vectors, known as the

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

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

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

226 s, we document the oviposition behavior of a Culex subgenus Micraedes species, Culex antillummagnorum

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

228 Culex tarsalis also transmitted EILV via saliva, suggest

229 ctors of several arboviruses, including WNV, Culex tarsalis and the Culex pipiens complex, increased

230 a tool to target pathogenic viruses that use Culex tarsalis as a vector.

231 erences data, we provide strong support that Culex tarsalis is the most important vector of human WNV

232 f Anopheles stephensi, Aedes albopictus, and Culex tarsalis larvae-substantially increasing the poten

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

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

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

236 We examine if populations of the Culex tarsalis mosquito, a West Nile virus (WNV) vector,

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

238 ism in five mosquito species: Aedes aegypti, Culex tarsalis, Anopheles gambiae, Anopheles stephensi,

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

240 We find that Culex tarsalis-a vector of harmful human pathogens, incl

241 While Culex torrentium, Culex pipiens biotype pipiens, Aedes a

242 For Culex-transmission settings with a low (5%) baseline mf

243 For both Culex pipiens and Culex vansomereni, adults emerging from Prosopis and Par

244 In addition, Culex vectors demonstrated predator avoidance behavior d

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

246 Mosquitoes in the genus Culex, which contains over 800 species across 28 subgene

247 In nature, both are transmitted by Culex, with wild birds, including jays, sparrows, and ro