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1 ransmitted mainly by mosquitoes of the genus Aedes.
2 ity inhibitor of Anopheles (An.) gambiae and Aedes (Ae.) aegypti Kir1 channels that incapacitates adu
4 e a comprehensive picture of the lipidome of Aedes aegypti (Aag2) cells infected with Wolbachia only,
7 ition to its important role in protection of Aedes aegypti against heme exposure, also acts as a dige
8 -activator odorants identified originally in Aedes aegypti also showed varying ability to reduce the
9 d-borne viruses, is transmitted to humans by Aedes aegypti and A. albopictus mosquitoes in tropical a
10 ype 1 [DENV-1] to DENV-4) are transmitted by Aedes aegypti and A. albopictus mosquitoes, causing up t
11 -emerging arbovirus transmitted to humans by Aedes aegypti and Ae. albopictus mosquitoes, causes debi
13 nya virus (CHIKV) is primarily spread by the Aedes aegypti and Aedes albopictus mosquito vectors.
14 Chikungunya virus (CHIKV) is transmitted by Aedes aegypti and Aedes albopictus mosquitoes and causes
16 porary distribution of their shared vectors, Aedes aegypti and Aedes albopictus remains incomplete an
17 ly includes two key mosquito vector species: Aedes aegypti and Aedes albopictus The model was paramet
18 , we highlight biological characteristics of Aedes aegypti and Aedes albopictus, 2 invasive mosquito
19 s, include the release of Wolbachia-infected Aedes aegypti and Aedes albopictus, for either its virus
20 l DENV transmission by the mosquito vectors, Aedes aegypti and Aedes albopictus, using the Wolbachia
29 unya viruses are transmitted by the mosquito Aedes aegypti and pose a substantial threat to global pu
30 tionally, recombinant ZIKV is infectious for Aedes aegypti and thus provides a means to examine virus
33 idemic spread widely to many countries where Aedes Aegypti as the main transmitting vector is endemic
34 age-specific and density dependent change in Aedes aegypti behaviour towards host cues when exposed t
36 nificantly shortens the EIP of ZIKV-infected Aedes aegypti by enhancing virus dissemination from the
38 quito larvae and pupae, including from field Aedes aegypti can acquire ZIKV from contaminated aquatic
39 fitness of two clades of DENV serotype 2 in Aedes aegypti cells and mosquitoes collected from the re
41 RNAi suppressor B2 from Flock House virus or Aedes aegypti dicer-2 (Aedicer-2) using a constitutive h
42 ntal data on the effects of transfluthrin on Aedes aegypti explores how SR effects interact to impact
46 te the impacts of Brugia malayi infection on Aedes aegypti flight parameters: distance, average speed
50 eloped for the major mosquito disease vector Aedes aegypti Here, we describe the generation of multip
51 S1 was successfully detected in spiked adult Aedes aegypti homogenate over a broad dynamic range with
52 quitoes Anopheles gambiae, An. coluzzii, and Aedes aegypti in which we determine that ~90% of all pro
63 ction with different membranes, including in Aedes aegypti larval brush border membrane vesicles, sma
65 This study sought to gain insights into how Aedes aegypti midgut microbes and life history traits ar
67 owed by exposure to feeding by an uninfected Aedes aegypti mosquito at day 42 to assess subsequent ri
74 V) is primarily transmitted to humans by the Aedes aegypti mosquito, human-to-human transmission has
75 us-Zika virus-spread by the same vector, the Aedes aegypti mosquito, that also carries dengue, yellow
76 ging flavivirus primarily transmitted by the Aedes aegypti mosquito, we screened for antigenic SG pro
77 orne flavivirus predominantly transmitted by Aedes aegypti mosquitoes and poses a global human health
81 previously observed that orco mutant female Aedes aegypti mosquitoes are strongly attracted to human
84 nitiated infection and transmission rates in Aedes aegypti mosquitoes comparable to those of the prim
85 fevers, a strain of transgenically modified Aedes aegypti mosquitoes containing a dominant lethal ge
86 f the endosymbiotic bacterium Wolbachia into Aedes aegypti mosquitoes has the potential to greatly re
87 Chikungunya virus is mainly transmitted by Aedes aegypti mosquitoes in tropical and subtropical reg
91 tive disposal of nitrogen waste in blood-fed Aedes aegypti mosquitoes requires alanine aminotransfera
92 a virus is predominantly mosquito-borne, and Aedes aegypti mosquitoes serve as a key vector for Zika
93 ere evaluated as mosquito repellents against Aedes aegypti mosquitoes that transmit the Zika and Deng
94 s experimental study we film the landings of Aedes aegypti mosquitoes to characterize landing behavio
95 f Wolbachia can reduce the permissiveness of Aedes aegypti mosquitoes to disseminated arboviral infec
98 and dissemination rates were not different, Aedes aegypti mosquitoes transmitted ZIKV I1404 more poo
104 osis during arbovirus infection by infecting Aedes aegypti mosquitoes with a Sindbis virus (SINV) clo
105 achia spreads rapidly through populations of Aedes aegypti mosquitoes, and strongly inhibits infectio
106 with a closely related partitivirus found in Aedes aegypti mosquitoes, is transmitted from infected f
107 between outbreaks of viruses transmitted by Aedes aegypti mosquitoes, such as chikungunya, dengue, a
108 ilar rates of infection and dissemination in Aedes aegypti mosquitoes, suggesting differing roles for
109 previously reported the generation of axenic Aedes aegypti mosquitoes, the primary vector of several
110 and DENV together in the saliva of infected Aedes aegypti mosquitoes, these findings suggest a mecha
120 is required for DENV-2 replication in adult Aedes aegypti mosquitos implying that the requirement fo
123 male sex (M/m) in the yellow fever mosquito, Aedes aegypti Nix, a gene in the M-locus, was shown to b
124 usly, the functional ablation of a family of Aedes aegypti olfactory receptors, the odorant receptors
125 t hairpin RNAs (shRNAs) corresponding to the Aedes aegypti orthologs of fasciculation and elongation
126 el driven by meteorological data to simulate Aedes aegypti populations and dengue cases in 23 locatio
127 show that a satellite repeat in the mosquito Aedes aegypti promotes sequence-specific gene silencing
129 N(1575)Y + L(1014)F were introduced into an Aedes aegypti sodium channel, AaNav1-1, and the mutants
134 imfast (Slif) from the yellow-fever mosquito Aedes aegypti using codon-optimized heterologous express
135 ful completion of the infection cycle in the Aedes aegypti vector, which is initiated in the midgut t
136 e find that a saliva-specific protein, named Aedes aegypti venom allergen-1 (AaVA-1), promotes dengue
139 ancudomyces culisetae) in a larval mosquito (Aedes aegypti) digestive tract affected microbiomes in l
140 ciatus, and Cx. pipiens) and bridge vectors (Aedes aegypti) have differential impacts on viral mutati
141 hree widely distributed species of mosquito; Aedes aegypti, Ae. albopictus and Culex quinquefasciatus
143 otion, pose, biting, and feeding dynamics of Aedes aegypti, Aedes albopictus, Anopheles stephensi, an
145 mechanistic phenology model and apply it to Aedes aegypti, an invasive mosquito vector for arbovirus
146 e show that Aedes spp. mosquitoes, including Aedes aegypti, are effective pollinators of the Platanth
147 ize that mosquito vector species, especially Aedes aegypti, are locally concentrated primarily in tho
148 Aegyptin, a secreted salivary protein from Aedes aegypti, binds collagen and inhibits platelet aggr
149 uced local populations of the dengue vector, Aedes aegypti, but challenges remain in scale and in sep
150 including DENV and Zika virus transmitted by Aedes aegypti, continue to be a threat to global health
151 ted that several mosquito species, including Aedes aegypti, do not develop beyond the first instar wh
152 ing ZIKV is expressed and fully processed in Aedes aegypti, ensuring the formation of mature syntheti
153 on hosts and peridomestic mosquitoes, mainly Aedes aegypti, mediate human-to-human transmission.
154 epidemics presumably involve transmission by Aedes aegypti, no direct evidence of vector involvement
157 ive organs of the arboviral vector mosquito, Aedes aegypti, prompting us to explore the role of AMTs
158 erkingdom cue for the yellow fever mosquito, Aedes aegypti, seeking blood-meals as well as ovipositio
159 s gambiae and Anopheles coluzzii, as well as Aedes aegypti, the cosmopolitan vector of dengue, chikun
160 opheles gambiae, Culex quinquefasciatus, and Aedes aegypti, the latter an important Zika and Dengue v
161 flavivirus that is primarily transmitted by Aedes aegypti, the mosquito vector also important in tra
163 -mediated cassette exchange (RMCE) system to Aedes aegypti, the vector of dengue, chikungunya, and Zi
164 and the globally important mosquito species, Aedes aegypti, through a combination of live mosquito ex
166 tissue from larvae of the non-target insect Aedes aegypti, we isolated a number of phage for further
167 he first time to study sperm of the mosquito Aedes aegypti, we reveal that sperm shed their entire ou
168 ransferred from Drosophila into the mosquito Aedes aegypti, where it can block the transmission of de
169 ines ZIKV infectivity in its mosquito vector Aedes aegypti, which acquires ZIKV via a blood meal.
171 hroids are the main adulticides used against Aedes aegypti, which vectors pathogens such as Zika viru
192 rium Wolbachia, deliberately introduced into Aedes aegyptimosquitoes, have been shown to be able to s
193 e, and the range of invasive species such as Aedes albopictus (Asian Tiger Mosquito) is expanding.
195 rds the highly invasive Asian tiger mosquito Aedes albopictus and a representative native mosquito Cu
196 hropod cell lines (derived from An. gambiae, Aedes albopictus and Drosophila melanogaster) and six mo
197 al control strategies are failing to contain Aedes albopictus as an emerging major vector for dengue.
198 licate in mammalian BHK-21 cells or mosquito Aedes albopictus cells and rapidly reverted catalyticall
199 engue virus and chikungunya virus as well as Aedes albopictus for ZIKV, suggesting that this phenomen
202 (Dirofilaria immitis) between eight natural Aedes albopictus mosquito populations representing areas
204 (CHIKV) is transmitted by Aedes aegypti and Aedes albopictus mosquitoes and causes febrile illness w
205 rent Wolbachia strains: wAlbB (isolated from Aedes albopictus mosquitoes) and wStri (isolated from th
206 (2 isolates), wMau (11-fold enrichment), and Aedes albopictus mosquitoes, wAlbB (200-fold enrichment)
208 n of their shared vectors, Aedes aegypti and Aedes albopictus remains incomplete and is complicated b
209 y mosquito vector species: Aedes aegypti and Aedes albopictus The model was parameterized and calibra
210 logical characteristics of Aedes aegypti and Aedes albopictus, 2 invasive mosquito species and primar
211 ica and Asia, the adaptation of the virus to Aedes albopictus, a mosquito species with an almost worl
212 ecause of genetic adaptation of the virus to Aedes albopictus, a species that thrives in temperate re
213 ting, and feeding dynamics of Aedes aegypti, Aedes albopictus, Anopheles stephensi, and Anopheles col
215 s (Anopheles sinensis, Armigeres subalbatus, Aedes albopictus, Culex quinquefasciatus and Cu. tritaen
216 ease of Wolbachia-infected Aedes aegypti and Aedes albopictus, for either its virus-blocking capabili
217 ficiency in a historically secondary vector, Aedes albopictus, leading to speculation that this was a
225 de classes were effective against strains of Aedes and Culex mosquitoes, demonstrating that electrost
228 The cDNA library was transfected into C6/36 (Aedes) and Vero (primate) cells, with subsequent deep se
230 A, indicate that mosquitoes of three genera, Aedes, Anopheles, and Culex are able to locate and land
232 the virus genome showed that EPEV roots the Aedes-associated mosquito-borne flaviviruses, including
233 Yokose virus, and Sokoluk virus and also the Aedes-associated mosquito-borne flaviviruses, which incl
235 has the potential to more effectively impact Aedes-borne diseases, but its implementation requires ca
237 ited States of America, the vast majority of Aedes-borne infections are imported from endemic regions
238 mic incompatibility, or both; the release of Aedes carrying dominant lethal genes, such as the OX513A
242 be a molecular barrier effect that prevents Aedes from detecting skin-associated molecular attractan
243 to genera, with viromes of mosquitoes of the Aedes genus exhibiting substantially less diversity and
246 rrelation between imported cases, density of Aedes larvae, climate variables and dengue fever occurre
249 ased biomarkers of exposure to Anopheles and Aedes mosquito bites could be helpful tools for evaluati
251 pipientis wMel is a novel strategy to reduce Aedes mosquito competency for flavivirus infection.
253 study is the first to consider the spread of Aedes mosquito vectors to project dengue suitability.
254 ic expansion is attributed to the success of Aedes mosquito vectors, but local epidemiological driver
255 ika Forest and in crushed suspensions of the Aedes mosquito, which is one of the vectors for Zika vir
256 ng infectious disease that is transmitted by Aedes mosquitoes and causes severe health and economic b
259 In contrast, RNA polymerase I promoters from Aedes mosquitoes exhibited strong species specificity.
262 one of the most used insecticides to control Aedes mosquitoes, despite the development of pyrethroid
263 CHIKV) and transmitted to humans by infected Aedes mosquitoes, has posed a global threat in several c
264 transmitted from human to human by bites of Aedes mosquitoes, recent evidence indicates that ZIKV ca
266 against Drosophila as well as Anopheles and Aedes mosquitoes, the former identified as disease vecto
267 ered in Uganda in 1947 and is transmitted by Aedes mosquitoes, which also act as vectors for dengue a
268 Although ZIKV is primarily transmitted by Aedes mosquitoes, ZIKV RNA is detectable in blood and se
273 thropod-borne virus transmitted primarily by Aedes mosquitos and is major cause of disease in tropica
275 ]-borne diseases' environmental suitability (AeDES) of transmission in the conterminous United States
277 d in a mixture of bovine red blood cells and Aedes physiological saline, with ATP as a phagostimulant
278 s of mosquitoes to eliminate or modify local Aedes populations are being developed, with several curr
279 les is known to be principally nocturnal and Aedes principally diurnal, details of mosquito activity
280 o both gSG6-P1 (Anopheles) and Nterm-34-kDa (Aedes) salivary peptides as validated biomarkers of resp
283 that is primarily transmitted and spread by Aedes species mosquitoes but is also sexually transmissi
288 V) is a re-emerged flavivirus transmitted by Aedes spp mosquitoes that has caused outbreaks of fever
289 irus (DENV) and its primary mosquito vectors Aedes spp. have spread to every continent except Antarct
293 ead of other arboviruses carried by invasive Aedes spp., such as Chikungunya and Zika, seem to be fol
295 vities of the identified antagonists against Aedes, the third major genus of the Culicidae family.
298 man mobility in the epidemiology of emerging Aedes-transmitted viral diseases is recognized but not f
299 t settings, the primary intervention against Aedes-transmitted viruses is vector control, such as ind
300 r analyzing the seasonal predictive skill of AeDES, we briefly consider the recent Zika epidemic, and