ライフサイエンスコーパス: Aedes

1 e of infected female mosquitoes of the genus Aedes.

2 ransmitted mainly by mosquitoes of the genus Aedes.

3 Aedes (Ae.) aegypti is the primary vector for dengue vir

4 ity inhibitor of Anopheles (An.) gambiae and Aedes (Ae.) aegypti Kir1 channels that incapacitates adu

5 Here, we reported a newly cloned mosquito Aedes (Ae.) aegypti salivary allergen.

6 uence of the yellow fever and Dengue vector, Aedes aegypti (Aa), has enabled a comparative phylogenom

7 thione S-transferase (GST) from the mosquito Aedes aegypti (aagste2), selected in the field as a majo

8 omain D7 proteins from Anopheles gambiae and Aedes aegypti (AeD7), respectively, were shown to bind b

9 loned from the renal (Malpighian) tubules of Aedes aegypti (AeKir1).

10 In females of the mosquito vector Aedes aegypti (L.), aedeskinins are known to stimulate f

11 We show that Aedes aegypti Aag2 cells - an immune responsive cell lin

12 tein-coding genes is 22% larger than that of Aedes aegypti and 52% larger than that of Anopheles gamb

13 d-borne viruses, is transmitted to humans by Aedes aegypti and A. albopictus mosquitoes in tropical a

14 ype 1 [DENV-1] to DENV-4) are transmitted by Aedes aegypti and A. albopictus mosquitoes, causing up t

15 -emerging arbovirus transmitted to humans by Aedes aegypti and Ae. albopictus mosquitoes, causes debi

16 gaviridae, which is transmitted to humans by Aedes aegypti and Ae. albopictus.

17 nya virus (CHIKV) is primarily spread by the Aedes aegypti and Aedes albopictus mosquito vectors.

18 Chikungunya virus (CHIKV) is transmitted by Aedes aegypti and Aedes albopictus mosquitoes and causes

19 virus (DENV1-DENV4) are spread primarily by Aedes aegypti and Aedes albopictus mosquitoes, whose geo

20 IKV) is a reemerging pathogen transmitted by Aedes aegypti and Aedes albopictus mosquitoes.

21 porary distribution of their shared vectors, Aedes aegypti and Aedes albopictus remains incomplete an

22 ly includes two key mosquito vector species: Aedes aegypti and Aedes albopictus The model was paramet

23 , we highlight biological characteristics of Aedes aegypti and Aedes albopictus, 2 invasive mosquito

24 s, include the release of Wolbachia-infected Aedes aegypti and Aedes albopictus, for either its virus

25 A unique feature of the R7 photoreceptors in Aedes aegypti and Anopheles gambiae is the extreme apica

26 For example, ITmD37E sequences from Aedes aegypti and Anopheles gambiae, which have an estim

27 tive detector of human skin odorants in both Aedes aegypti and Anopheles gambiae.

28 mmune gene repertoire compared with those of Aedes aegypti and Anopheles gambiae.

29 re insecticidal to larvae of the mosquitoes, Aedes aegypti and Anopheles gambiae.

30 ediculus humanus humanus, Anopheles gambiae, Aedes Aegypti and Culex pipiens quinquefasciatus is nota

31 s ancient within mosquitoes, being shared by Aedes aegypti and Culex pipiens.

32 mosquitoes (three Anopheles gambiae genomes, Aedes aegypti and Culex quinquefasciatus), tick (Ixodes

33 , in two closely related species of insects: Aedes aegypti and Culex quinquefasciatus.

34 We use Aedes aegypti and dengue virus (DENV) for illustrative p

35 o maintaining homeostasis in the gut of both Aedes aegypti and Drosophila melanogaster.

36 Discovery of the Muta1 element from Aedes aegypti and its successful transposition in yeast

37 p and physiology of aaNATs from the mosquito Aedes aegypti and serve as a reference for studying the

38 AT transposons, AeBuster1, from the mosquito Aedes aegypti and TcBuster from the red flour beetle Tri

39 tionally, recombinant ZIKV is infectious for Aedes aegypti and thus provides a means to examine virus

40 Aedes albopictus is secondary to Aedes aegypti as a vector of dengue viruses (DENVs) in s

41 idemic spread widely to many countries where Aedes Aegypti as the main transmitting vector is endemic

42 age-specific and density dependent change in Aedes aegypti behaviour towards host cues when exposed t

43 otein inhibits RNA silencing in the mosquito Aedes aegypti by interfering with Dicer.

44 We now show that an Aedes aegypti C-type lectin, mosGCTL-1, is induced by WN

45 A recent Aedes aegypti case study demonstrates the viability of o

46 fitness of two clades of DENV serotype 2 in Aedes aegypti cells and mosquitoes collected from the re

47 Overexpressing wild-type AeSCP-2 in the Aedes aegypti cultured Aag-2 cells resulted in an increa

48 imensional solution structures of SCP-2 from Aedes aegypti determined by NMR spectroscopy in its liga

49 occurred in 95-100% of the larval cohorts of Aedes aegypti developing at those sites.

50 Aedes aegypti egg survival was unaffected by exposure to

51 The mosquito Aedes aegypti expresses the long-wavelength rhodopsin Aa

52 In this study behavioral assays identified Aedes aegypti females that were insensitive to DEET, and

53 In Aedes aegypti females, the ammonia released during blood

54 The yellow fever mosquito Aedes aegypti forms aerial swarms that serve as mating a

55 h DENV serotype 2 strain 1232 at sites where Aedes aegypti had or had not probed immediately prior.

56 le as the primary vector for dengue viruses, Aedes aegypti has a long history as a genetic model orga

57 The yellow fever mosquito Aedes aegypti has been the subject of extensive genetic

58 A 'domestic' form of the mosquito Aedes aegypti has evolved to specialize in biting humans

59 omorphic sex chromosomes, while the mosquito Aedes aegypti has homomorphic sex chromosomes.

60 The mosquito Aedes aegypti has ten PPO genes in the genome, four of w

61 Anopheles gambiae and Aedes aegypti have evolved a strong preference for human

62 eloped for the major mosquito disease vector Aedes aegypti Here, we describe the generation of multip

63 S1 was successfully detected in spiked adult Aedes aegypti homogenate over a broad dynamic range with

64 s in JH responsive Aag-2 cells revealed that Aedes aegypti homologues of both Met and SRC are require

65 ciphered how Wolbachia infection affects the Aedes aegypti host in inducing resistance to DENV.

66 nt populations of the yellow fever mosquito, Aedes aegypti in the southeastern United States and in B

67 pression of a sodium channel, AaNav1-1, from Aedes aegypti in Xenopus oocytes, and the functional exa

68 terfering RNAs (viRNAs), 21 nt in length, in Aedes aegypti infected with the mosquito-borne virus, Si

69 The gene Aedes aegypti intestinal mucin 1 (AeIMUC1) encodes a put

70 gal-specific immune response in the mosquito Aedes aegypti involves the Toll immune pathway transduce

71 The mosquito Aedes aegypti is a major vector of numerous viral diseas

72 Sex determination in the mosquito Aedes aegypti is governed by a dominant male-determining

73 The mosquito Aedes aegypti is more widely dispersed now than at any t

74 The mosquito Aedes aegypti is one of the most important disease vecto

75 The mosquito Aedes aegypti is the major vector of arboviral diseases,

76 The mosquito Aedes aegypti is the principal vector for the yellow fev

77 The mosquito Aedes aegypti is the principal vector of dengue and yell

78 Aedes aegypti kynurenine aminotransferase (AeKAT) is a m

79 rculates in the hemolymph of pupal and adult Aedes aegypti males and females.

80 Aedes aegypti manipulated genetically to express gene-sp

81 irus (SINV) strain MRE16 efficiently infects Aedes aegypti midgut epithelial cells (MEC), but laborat

82 Aedes aegypti mosGCTLs facilitate colonization by multip

83 uantification of the effects of Wolbachia in Aedes aegypti mosquito cells and midgut.

84 We show here that the Aedes aegypti mosquito possesses two distinct light-driv

85 in displays sequence identities of 70% to an Aedes aegypti mosquito TA receptor, followed by 60% to a

86 The Aedes aegypti mosquito transmits arboviruses, including

87 The Zika outbreak, spread by the Aedes aegypti mosquito, highlights the need to create hi

88 V) is primarily transmitted to humans by the Aedes aegypti mosquito, human-to-human transmission has

89 us-Zika virus-spread by the same vector, the Aedes aegypti mosquito, that also carries dengue, yellow

90 Dengue virus infection in Aedes aegypti mosquitoes activates the JAK-STAT immune s

91 Aedes aegypti mosquitoes are important vectors of viral

92 Aedes aegypti mosquitoes are responsible for transmittin

93 n in mosquitoes, we manipulated apoptosis in Aedes aegypti mosquitoes by silencing the expression of

94 Aedes aegypti mosquitoes carrying a conditionally lethal

95 nitiated infection and transmission rates in Aedes aegypti mosquitoes comparable to those of the prim

96 n from symptomatic dengue cases (n = 208) to Aedes aegypti mosquitoes during 407 independent exposure

97 f the endosymbiotic bacterium Wolbachia into Aedes aegypti mosquitoes has the potential to greatly re

98 Chikungunya virus is mainly transmitted by Aedes aegypti mosquitoes in tropical and subtropical reg

99 WsnRNAs were detected in Aedes aegypti mosquitoes infected with the wMelPop-CLA s

100 Here, we show that in female Aedes aegypti mosquitoes JH III control of gene expressi

101 Xanthine dehydrogenase-1 silencing in Aedes aegypti mosquitoes promotes a blood feeding-induce

102 tive disposal of nitrogen waste in blood-fed Aedes aegypti mosquitoes requires alanine aminotransfera

103 ), Cecropin A, and Defensin A, in transgenic Aedes aegypti mosquitoes results in the cooperative anti

104 nate metabolic pathway for urea synthesis in Aedes aegypti mosquitoes that converts uric acid to urea

105 f Wolbachia can reduce the permissiveness of Aedes aegypti mosquitoes to disseminated arboviral infec

106 Female Aedes aegypti mosquitoes typically mate only once with o

107 Aedes aegypti mosquitoes vector several arboviruses of g

108 Field-collected and laboratory-colonized Aedes aegypti mosquitoes were fed on blood containing ea

109 ENV), deep sequencing data of virus-infected Aedes aegypti mosquitoes were used.

110 osis during arbovirus infection by infecting Aedes aegypti mosquitoes with a Sindbis virus (SINV) clo

111 achia spreads rapidly through populations of Aedes aegypti mosquitoes, and strongly inhibits infectio

112 ication of dengue virus when introduced into Aedes aegypti mosquitoes, as well as to stimulate chroni

113 ilar rates of infection and dissemination in Aedes aegypti mosquitoes, suggesting differing roles for

114 and DENV together in the saliva of infected Aedes aegypti mosquitoes, these findings suggest a mecha

115 However, in 2007, vectored by Aedes aegypti mosquitoes, ZIKV caused the first notewort

116 3 and -4, which are transmitted to people by Aedes aegypti mosquitoes.

117 f the intracellular bacterium Wolbachia into Aedes aegypti mosquitoes.

118 a subunit of the heteromeric CO2 receptor in Aedes aegypti mosquitoes.

119 cells, and for productive DENV infection of Aedes aegypti mosquitoes.

120 s carbon routes during ammonia metabolism of Aedes aegypti mosquitoes.

121 cing ZIKV genomes from infected patients and Aedes aegypti mosquitoes.

122 is required for DENV-2 replication in adult Aedes aegypti mosquitos implying that the requirement fo

123 opical disease that is transmitted by female Aedes Aegypti mosquitos.

124 Florida, the mosquitoes Aedes albopictus and Aedes aegypti often co-occur in water-filled containers

125 NV) are transmitted to humans by the bite of Aedes aegypti or Aedes albopictus mosquitoes, with milli

126 t hairpin RNAs (shRNAs) corresponding to the Aedes aegypti orthologs of fasciculation and elongation

127 el driven by meteorological data to simulate Aedes aegypti populations and dengue cases in 23 locatio

128 Serine protease activity in Aedes aegypti saliva augmented virus infectivity in vitr

129 The mosquito Aedes aegypti shows a robust response, losing nearly all

130 N(1575)Y + L(1014)F were introduced into an Aedes aegypti sodium channel, AaNav1-1, and the mutants

131 ction and assignment results for the protein Aedes aegypti sterol carrier protein 2.

132 tion; particularly, for the 1.3 GB genome of Aedes aegypti the mean value of prediction Sensitivity a

133 Here we elucidate the basic rules of Aedes aegypti thermotaxis and test the function of candi

134 COPI functions in the Yellow Fever mosquito Aedes aegypti to interfere with blood meal digestion.

135 Blood feeding by the vector mosquito Aedes aegypti triggers the release of two neurohormones,

136 imfast (Slif) from the yellow-fever mosquito Aedes aegypti using codon-optimized heterologous express

137 ful completion of the infection cycle in the Aedes aegypti vector, which is initiated in the midgut t

138 Aedes aegypti was negatively affected by interspecific c

139 sed of large bacterial-type proteins that in Aedes aegypti were implicated as receptors for Plasmodiu

140 ciatus, and Cx. pipiens) and bridge vectors (Aedes aegypti) have differential impacts on viral mutati

141 rs of human pathogens (Anopheles gambiae and Aedes aegypti) imbibing multiple bloodmeals during a gon

142 Mosquitoes (Aedes aegypti) were genetically modified to exhibit impa

143 ea squirt (Ciona savignyi) and the mosquito (Aedes aegypti).

144 antennal lobe of the yellow fever mosquito, Aedes aegypti, a major vector of arboviral diseases.

145 ms such as Bombyx mori, Tribolium casteneum, Aedes aegypti, and Anopheles stephensi.

146 quences are available for Anopheles gambiae, Aedes aegypti, and Culex quinquefasciatus.

147 nt region has expanded in Anopheles gambiae, Aedes aegypti, and Tribolium castaneum, while the PF rep

148 nome information for three mosquito species: Aedes aegypti, Anopheles gambiae and Culex quinquefascia

149 e sequence data are available for 3 species, Aedes aegypti, Anopheles gambiae, and Culex quinquefasci

150 Aegyptin, a secreted salivary protein from Aedes aegypti, binds collagen and inhibits platelet aggr

151 In the yellow fever and dengue vector Aedes aegypti, both sexes interact acoustically by shift

152 uced local populations of the dengue vector, Aedes aegypti, but challenges remain in scale and in sep

153 including DENV and Zika virus transmitted by Aedes aegypti, continue to be a threat to global health

154 ted that several mosquito species, including Aedes aegypti, do not develop beyond the first instar wh

155 host and, when introduced into the mosquito Aedes aegypti, halves its life span.

156 ards the vertebrate host and, in the case of Aedes aegypti, increased sensitivity to skin odours.

157 rior studies with the yellow fever mosquito, Aedes aegypti, indicated blood feeding stimulates egg pr

158 quitoes of the major vector of Dengue fever, Aedes aegypti, is cyclic because of its dependence on bl

159 of movement of the primary mosquito vector, Aedes aegypti, local human movements may be an important

160 on hosts and peridomestic mosquitoes, mainly Aedes aegypti, mediate human-to-human transmission.

161 epidemics presumably involve transmission by Aedes aegypti, no direct evidence of vector involvement

162 The yellow fever mosquito, Aedes aegypti, particularly in Neotropical regions, is t

163 erkingdom cue for the yellow fever mosquito, Aedes aegypti, seeking blood-meals as well as ovipositio

164 s gambiae and Anopheles coluzzii, as well as Aedes aegypti, the cosmopolitan vector of dengue, chikun

165 In the mosquito Aedes aegypti, the expression of two fat body genes invo

166 The yellow fever mosquito, Aedes aegypti, the global vector of dengue and yellow fe

167 opheles gambiae, Culex quinquefasciatus, and Aedes aegypti, the latter an important Zika and Dengue v

168 flavivirus that is primarily transmitted by Aedes aegypti, the mosquito vector also important in tra

169 We present a draft sequence of the genome of Aedes aegypti, the primary vector for yellow fever and d

170 Aedes aegypti, the primary vector of dengue virus, is we

171 In the mosquito Aedes aegypti, the sex-determining chromosomes are homom

172 -mediated cassette exchange (RMCE) system to Aedes aegypti, the vector of dengue, chikungunya, and Zi

173 We found that in the mosquito Aedes aegypti, there are two distinct melanization activ

174 thologous gene of the yellow fever mosquito, Aedes aegypti, to control sex- and tissue-specific expre

175 ignated OX3604C, of the major dengue vector, Aedes aegypti, was engineered to have a repressible fema

176 By using the yellow fever mosquito, Aedes aegypti, we demonstrate that this boost in tempera

177 Using the mosquito Aedes aegypti, we determined that mutations in the FokI

178 tissue from larvae of the non-target insect Aedes aegypti, we isolated a number of phage for further

179 ransferred from Drosophila into the mosquito Aedes aegypti, where it can block the transmission of de

180 ines ZIKV infectivity in its mosquito vector Aedes aegypti, which acquires ZIKV via a blood meal.

181 the family of 30-kDa salivary allergens from Aedes aegypti, whose function remained elusive thus far.

182 viduals may become infected by more than one Aedes aegypti-borne virus at a time.

183 Sequencing of small RNAs from KC and Aedes aegypti-derived Aag2 cells infected with BTV or th

184 e transmitted by the disease vector mosquito Aedes aegypti.

185 alanine aminotransferase (ALAT) in blood-fed Aedes aegypti.

186 eles stephensi and the yellow fever mosquito Aedes aegypti.

187 he male and female germline, in the mosquito Aedes aegypti.

188 of spermatozoa in the yellow fever mosquito, Aedes aegypti.

189 t maintenance in the dengue mosquito vector, Aedes aegypti.

190 n (PE) development in the fat body of female Aedes aegypti.

191 feeding and egg development in the mosquito Aedes aegypti.

192 f fruit flies and the yellow fever mosquito, Aedes aegypti.

193 cally relevant range for humans and infected Aedes aegypti.

194 pora allata-corpora cardiaca of the mosquito Aedes aegypti.

195 ivergent relative, the yellow fever mosquito Aedes aegypti.

196 2 cDNA clone from the yellow fever mosquito, Aedes aegypti.

197 e to the biology and behavior of its vector, Aedes aegypti.

198 quefasciatus, and the yellow fever mosquito, Aedes aegypti.

199 E-binding proteins from the mosquito species Aedes aegypti.

200 y arthropods, generally, using the mosquito, Aedes aegypti.

201 homeostasis and dengue virus replication in Aedes aegypti.

202 es from the mosquitoes Anopheles gambiae and Aedes aegypti.

203 rium Wolbachia, deliberately introduced into Aedes aegyptimosquitoes, have been shown to be able to s

204 e, and the range of invasive species such as Aedes albopictus (Asian Tiger Mosquito) is expanding.

205 were detected by culturing mosquito pools on Aedes albopictus (C6/36) cell cultures.

206 The Asian tiger mosquito, Aedes albopictus (Skuse), is an invasive species with su

207 In south Florida, the mosquitoes Aedes albopictus and Aedes aegypti often co-occur in wat

208 hropod cell lines (derived from An. gambiae, Aedes albopictus and Drosophila melanogaster) and six mo

209 utogenous strain in the Asian tiger mosquito Aedes albopictus and examined an F(1) intercross populat

210 In the Aedes albopictus C/wStr1 mosquito cell line, wStr mainta

211 licate in mammalian BHK-21 cells or mosquito Aedes albopictus cells and rapidly reverted catalyticall

212 Aedes albopictus collected in 2001 and 2011 from LA Coun

213 irus (CHIKV) to infect and be transmitted by Aedes albopictus has increased the geographical range at

214 Aedes albopictus is secondary to Aedes aegypti as a vect

215 ive CHIKV strains to an atypical vector, the Aedes albopictus mosquito that is ubiquitously distribut

216 is primarily spread by the Aedes aegypti and Aedes albopictus mosquito vectors.

217 (CHIKV) is transmitted by Aedes aegypti and Aedes albopictus mosquitoes and causes febrile illness w

218 rent Wolbachia strains: wAlbB (isolated from Aedes albopictus mosquitoes) and wStri (isolated from th

219 4) are spread primarily by Aedes aegypti and Aedes albopictus mosquitoes, whose geographic range cont

220 ed to humans by the bite of Aedes aegypti or Aedes albopictus mosquitoes, with millions of infections

221 n mosquito cells, mammalian cells, mice, and Aedes albopictus mosquitoes.

222 ng pathogen transmitted by Aedes aegypti and Aedes albopictus mosquitoes.

223 n of their shared vectors, Aedes aegypti and Aedes albopictus remains incomplete and is complicated b

224 near the homes of coinfected patients, and 1 Aedes albopictus specimen was found to be positive for b

225 y mosquito vector species: Aedes aegypti and Aedes albopictus The model was parameterized and calibra

226 s in mosquito and mammalian cells, mice, and Aedes albopictus vector mosquitoes.

227 Aedes albopictus was not affected by competition in eith

228 ecay during a viral infection in both C6/36 (Aedes albopictus) and baby hamster kidney cells.

229 dbis produced from three different mosquito (Aedes albopictus) cell lines; one other insect cell line

230 2011, a population of Asian tiger mosquito (Aedes albopictus) was discovered in Los Angeles (LA) Cou

231 logical characteristics of Aedes aegypti and Aedes albopictus, 2 invasive mosquito species and primar

232 ica and Asia, the adaptation of the virus to Aedes albopictus, a mosquito species with an almost worl

233 ecause of genetic adaptation of the virus to Aedes albopictus, a species that thrives in temperate re

234 wMel strain of Drosophila melanogaster into Aedes albopictus, a vector of dengue and other arbovirus

235 Aedes albopictus, another highly invasive arbovirus vect

236 s (Anopheles sinensis, Armigeres subalbatus, Aedes albopictus, Culex quinquefasciatus and Cu. tritaen

237 ease of Wolbachia-infected Aedes aegypti and Aedes albopictus, for either its virus-blocking capabili

238 nt from the mosquito and yellow fever vector Aedes albopictus, has been characterized.

239 The Asian tiger mosquito, Aedes albopictus, is an anthropophilic aggressive daytim

240 ficiency in a historically secondary vector, Aedes albopictus, leading to speculation that this was a

241 Control of Aedes albopictus, major dengue and chikungunya vector, i

242 y, the highly invasive Asian tiger mosquito, Aedes albopictus, rapidly displaced resident populations

243 owed CHIKV to exploit a new epidemic vector, Aedes albopictus, via an A226V substitution in the E1 en

244 Multiple Aedes albopictus-adaptive fitness peaks became available

245 y the global spread of the invasive mosquito Aedes albopictus.

246 tly introduced in central Africa, along with Aedes albopictus.

247 untry, probably facilitated by the spread of Aedes albopictus.

248 cts, including Drosophila and the mosquitoes Aedes and Anopheles.

249 Aedes and Culex mosquitoes are the main culprits, spread

250 de classes were effective against strains of Aedes and Culex mosquitoes, demonstrating that electrost

251 In this study, we implicate HP-I, an Aedes- and male-specific peptide transferred to females

252 the virus genome showed that EPEV roots the Aedes-associated mosquito-borne flaviviruses, including

253 Yokose virus, and Sokoluk virus and also the Aedes-associated mosquito-borne flaviviruses, which incl

254 enyan populations of the yellow fever vector Aedes bromeliae and its relative Aedes metallicus, and i

255 mic incompatibility, or both; the release of Aedes carrying dominant lethal genes, such as the OX513A

256 and orthologs are present in the genomes of Aedes, Culex, and Anopheles mosquito species.

257 We identified Aedes CYC as a MET-interacting protein using yeast two-h

258 We show Aedes distributions to be the widest ever recorded; now

259 nd activation of programmed autophagy in the Aedes fat body at the end of vitellogenesis.

260 to genera, with viromes of mosquitoes of the Aedes genus exhibiting substantially less diversity and

261 virus (ZIKV) is an emerging mosquito-borne (Aedes genus) arbovirus of the Flaviviridae family.

262 Aedes hensilli was the predominant mosquito species iden

263 erence (RNAi) approach, we demonstrated that Aedes HR3 plays a critical role in a timely termination

264 Aedes japonicus japonicus (Theobald) (Diptera: Culicidae

265 ence containing an E-box-like motif from the Aedes Kr-h1 gene promoter specifically interacted with a

266 ancient origin of the sex chromosomes in the Aedes lineage.

267 ever vector Aedes bromeliae and its relative Aedes metallicus, and in Mansonia uniformis and Mansonia

268 pipientis wMel is a novel strategy to reduce Aedes mosquito competency for flavivirus infection.

269 to a broad host and vector range, including Aedes mosquito species.

270 ic expansion is attributed to the success of Aedes mosquito vectors, but local epidemiological driver

271 ika Forest and in crushed suspensions of the Aedes mosquito, which is one of the vectors for Zika vir

272 ng infectious disease that is transmitted by Aedes mosquitoes and causes severe health and economic b

273 cycle between nonhuman primates and arboreal Aedes mosquitoes in Southeast Asia and West Africa.

274 nown arbovirus, o'nyong-nyong virus, whereas Aedes mosquitoes transmit many.

275 between miRNA gene clusters in Anopheles and Aedes mosquitoes, and in D. melanogaster suggest the los

276 al signaling activity is likely conserved in Aedes mosquitoes, because genetic or pharmacologic manip

277 one of the most used insecticides to control Aedes mosquitoes, despite the development of pyrethroid

278 ation as well as source-finding behaviour in Aedes mosquitoes, even after the odour is no longer pres

279 transmitted from human to human by bites of Aedes mosquitoes, recent evidence indicates that ZIKV ca

280 ered in Uganda in 1947 and is transmitted by Aedes mosquitoes, which also act as vectors for dengue a

281 e alphavirus and is transmitted to humans by Aedes mosquitoes.

282 Alphavirus that is transmitted to humans by Aedes mosquitoes.

283 o-borne flaviviruses transmitted by infected Aedes mosquitoes.

284 iral infection transmitted between humans by Aedes mosquitoes.

285 viruses at higher abundance than those from Aedes mosquitoes.

286 thropod-borne virus transmitted primarily by Aedes mosquitos and is major cause of disease in tropica

287 d in a mixture of bovine red blood cells and Aedes physiological saline, with ATP as a phagostimulant

288 s of mosquitoes to eliminate or modify local Aedes populations are being developed, with several curr

289 thought to be due to failure to control the Aedes populations, uncontrolled urbanization, population

290 eviously was isolated from Culex pipiens and Aedes rossicus mosquitoes in the Czech Republic, and phy

291 ock provide key ecological links between the Aedes sp. mosquito vector and humans.

292 recognized as an arthropod-borne virus with Aedes species mosquitoes as the primary vector.

293 Transmitted through the bite of Aedes species mosquitoes, CHIKV is responsible for an ac

294 CHIKV is transmitted by Aedes species of mosquitoes and is capable of an epidemi

295 Culicine mosquitoes such as Aedes spp. and Culex spp. are important vectors of other

296 irus (DENV) and its primary mosquito vectors Aedes spp. have spread to every continent except Antarct

297 ead of other arboviruses carried by invasive Aedes spp., such as Chikungunya and Zika, seem to be fol

298 consider the potential role of the mosquito Aedes taeniorhynchus in maintaining the flavivirus West

299 trengthen programmes and enhance research in aedes-transmitted diseases.

300 Aedes triseriatus mosquitoes transovarially transmit (TO