ライフサイエンスコーパス: mosquito

1 the new coronavirus could be transmitted by mosquitoes".

2 gametocytes is essential for transmission to mosquitos.

3 so provide favorable breeding conditions for mosquitos.

4 ng flavivirus transmitted to humans by Aedes mosquitos.

5 aren't detected in Microsporidia MB infected mosquitoes.

6 onpregnant macaques and to be transmitted by mosquitoes.

7 uction and distribution of high-quality male mosquitoes.

8 nditions on anesthetized Anopheles stephensi mosquitoes.

9 s much faster acting against fruit flies and mosquitoes.

10 by reconfiguring phospholipids in humans and mosquitoes.

11 S411A Kunjin increases viral pathogenesis in mosquitoes.

12 efficacy in controlling pyrethroid resistant mosquitoes.

13 nd the occurrence of Haemagogus and Sabethes mosquitoes.

14 ith pyrethroid susceptible Anopheles farauti mosquitoes.

15 rminant of the vectorial capacity of malaria mosquitoes.

16 due to parasite inoculations from different mosquitoes.

17 d pathogens through direct interactions with mosquitoes.

18 lacebo three hr before CHMI with Pf-infected mosquitoes.

19 anti-phase between day- versus night-biting mosquitoes.

20 not detect the presence of strictly sylvatic mosquitoes.

21 equines following transmission from infected mosquitoes.

22 cells and in wild-type mice, but not in live mosquitoes.

23 f SARS-CoV-2 to infect and be transmitted by mosquitoes.

24 used by viruses transmitted by Aedes aegypti mosquitoes.

25 such as Elizabethkingia in the midgut of the mosquitoes.

26 R = 2.04: P = 0.01) and homozygote resistant mosquitoes.

27 oid, by more than 10 times against Anopheles mosquitoes.

28 ding to Pf/Pv coinfection in 21% of infected mosquitoes.

29 nd enhancing vectorial capacity in Anopheles mosquitoes.

30 k species and clone-specific transmission to mosquitoes.

31 control may involve targeting sugar-feeding mosquitoes.

32 near complete prevention of transmission to mosquitoes.

33 uses (arboviruses) transmitted by Aedes spp. mosquitoes(1,2).

34 at it might also be applicable to monitoring mosquito activity.

35 n and by knocking out the forked gene in the mosquito (Ae-Forked; a known actin-bundling protein) by

36 ORco ex vivo and repelled adult Asian tiger mosquitoes (Ae. albopictus).

37 The range of the mosquito Aedes aegypti continues to expand, putting more

38 geosmin on the behavior of the yellow fever mosquito Aedes aegypti.

39 fungus (Zancudomyces culisetae) in a larval mosquito (Aedes aegypti) digestive tract affected microb

40 ishes the male sex (M/m) in the yellow fever mosquito, Aedes aegypti Nix, a gene in the M-locus, was

41 Three widely distributed species of mosquito; Aedes aegypti, Ae. albopictus and Culex quinqu

42 ctive mosquitoes) that emphasized changes in mosquito age.

43 Calcium imaging experiments in the mosquito AL revealed that nonanal and lilac aldehyde eac

44 cant bottlenecks as they transit through the mosquito and are transmitted to their mammalian host.

45 Mosquitoes and breeding water were sampled from the farm

46 o better understand parasite transmission to mosquitoes and develop models for early-clinical evaluat

47 ggest that sleep-like states likely occur in mosquitoes and discuss the potential role of sleep in re

48 adaptability of the virus to replication in mosquitoes and mammalian hosts is still elusive.

49 s no evidence of direct interactions between mosquitoes and marine mammals in nature, and it remains

50 tools, the Photonic Fence detects and tracks mosquitoes and other flying insects and can apply lethal

51 ween species of Diptera, such as Drosophila, mosquitoes and sand flies.

52 characterize the vertical stratification of mosquitoes and their associations with microclimate and

53 -CoV-2 virus is unable to replicate in these mosquitoes and therefore cannot be transmitted to people

54 nvironmental suitability for the presence of mosquitoes and viruses becomes one of the most important

55 us (TCRV) has been isolated from fruit bats, mosquitoes, and ticks, whereas all other known New World

56 competitive, sterile male Wolbachia-infected mosquitoes, and use of these males in a large-scale supp

57 ite effector molecules to the malaria vector mosquito, Anopheles gambiae The drive system targets the

58 While Aedes species of mosquito are the primary vector for ZIKV, sexual transmi

59 Mosquitoes are considered to be the deadliest animals on

60 Male mosquitoes are exclusively dependent on plant nectar or

61 Specifically, sleep studies in mosquitoes are lacking despite considerable focus on how

62 Anopheles gambiae mosquitoes are the most important vectors of human malar

63 Anthropophilic female mosquitoes are well known for their strong attraction to

64 While mosquitos are the primary vector for the spread of the v

65 malaria parasite transmission from humans to mosquitoes, are key targets for malaria elimination.

66 Mathematical models of mosquito-barrier interactions identified alternative bar

67 % blood-feeding inhibition of An. gambiae sl mosquitoes before and after 20 standardised washes and s

68 This highlights the importance of mosquito behavioural adaptations to vector control, and

69 lts demonstrate the ecological importance of mosquitoes beyond operating as disease vectors and open

70 s the potential role of sleep in relation to mosquito biology and their ability to function as diseas

71 ns induced by IBSM (n = 66), sporozoites via mosquito bite (n = 336), or injection (n = 51).

72 n PfCSP mAbs at mediating protection against mosquito bite challenge in mice.

73 ecticide were highly effective in preventing mosquito bites and reducing transmission, and essential

74 ease in the number of potentially infectious mosquito bites, increased partial blood-feeding and redu

75 ived primaquine, chloroquine, and uninfected mosquito bites.

76 The biteOscope provides a new perspective on mosquito blood feeding, enabling the high-throughput qua

77 st 1 female and 1 male gametocyte per 2.5 uL mosquito bloodmeal.

78 Mosquito borne viral diseases are an emerging threat as

79 tin) in reducing virus infection for several mosquito borne viruses including flaviviruses (dengue vi

80 ents and models suggest that climate affects mosquito-borne disease transmission.

81 x. abundance, which could reduce the risk of mosquito-borne disease while helping urban utilities mai

82 Japanese encephalitis (JE) is a mosquito-borne disease, known for its high mortality and

83 o salivary proteins protects animals against mosquito-borne disease.

84 Although crucial for the spread of mosquito-borne diseases, blood feeding remains poorly un

85 r control is the primary approach to prevent mosquito-borne diseases.

86 Because ZIKV is a mosquito-borne flavivirus with a high degree of sequence

87 replication of dengue virus (DENV) and other mosquito-borne flaviviruses.

88 Mosquito-borne helminth infections are responsible for a

89 Zika virus (ZIKV) is a mosquito-borne human pathogen that causes congenital Zik

90 nhanced personal protection against multiple mosquito-borne infectious diseases.

91 Zika virus (ZIKV) is a mosquito-borne member of the Flaviviridae family that ha

92 Zika virus (ZIKV) is a mosquito-borne pathogen with increasing public health si

93 tured surveillance and response programs for mosquito-borne virus control.

94 Dengue virus (DENV) is a mosquito-borne virus that infects upward of 300 million

95 ogy to support the prevention and control of mosquito-borne virus threats.

96 promise and may be particularly relevant for mosquito-borne viruses.

97 iruses, the most common of which include the mosquito-borne West Nile virus, St.

98 t flaviviruses distinct from the established mosquito-borne, tick-borne, insect-only, and unknown-vec

99 idual-based simulation models called MBITES (Mosquito Bout-based and Individual-based Transmission Ec

100 this sensory information is processed in the mosquito brain.

101 model for a process-based representation of mosquito breeding habitat availability.

102 icals to insecticide resistance in Anopheles mosquitoes breeding on vegetable farms in southern Benin

103 is not known; however, an arbovirus-infected mosquito can inoculate extravascular host tissues with v

104 Whether mosquitoes can successfully take a blood meal is not kno

105 Field releases of mosquitoes carrying bacterial symbionts that reduce vect

106 icient population modification with >=95% of mosquitoes carrying the drive within 5-11 generations ov

107 actors (namely, the (sibling) species of the mosquito caught) (respective Akaike information criterio

108 the 3'UTR that enhances viral replication in mosquito cells led to an overall increase in the amount

109 ion of specific sfRNAs in both mammalian and mosquito cells.

110 during infection by using isotope tracing in mosquito cells.

111 nts underwent Plasmodium falciparum-infected mosquito challenge (controlled human malaria infection)

112 funestus accounted for over 80% of Anopheles mosquitoes collected by light trap and PSC in all sites.

113 onsistently associated with vector-dominated mosquito communities for a wide range of human and lives

114 g mechanisms underlying vector prevalence in mosquito communities, and opens up new opportunities for

115 annual site-level collections and metrics of mosquito community composition with generalized linear/a

116 Unlike host-related behaviors of mosquitoes, comparatively less is understood about the m

117 Adult male and female mosquitoes consume sugar as floral and extrafloral necta

118 Spatial repellents (SRs) reduce human-mosquito contact by preventing mosquito entrance into hu

119 y and results from this study can be used by mosquito control agencies to identify habitats that shou

120 ste might be exploited in new strategies for mosquito control, which may be urgently needed as the ge

121 insects, improved understanding of taste in mosquitoes could provide new mechanistic insight into ma

122 fos and to a heat spike in the larvae of the mosquito Culex pipiens.

123 transmission of 10 vector-pathogen pairs of mosquitoes (Culex pipiens, Cx. quinquefascsiatus, Cx. ta

124 and bites from 12-15 P. falciparum-infected mosquitoes (CVac-chloroquine arm) at 3 monthly iteration

125 acts the fecundity as homozygote susceptible mosquitoes (CYP6P9a-SS) lay more eggs than heterozygote

126 Both reduction in temperature and mosquito-derived XA or elevated pH are required for trig

127 combined with extended periods suitable for mosquito development is simulated to accelerate the vect

128 ctions of colonized and wild-derived African mosquitoes do not prevent cleavage in vitro by the Cas9/

129 Unlike Dipteran relatives, mosquitoes do not visibly prepare for landing with leg a

130 s may not necessarily spread efficiently via mosquitoes during epidemics.IMPORTANCE Although Zika vir

131 or-borne illnesses, the determination of the mosquitoes' ecological role, and the design of efficient

132 By pairing observations of mosquito ecology with environmental monitoring, we quant

133 s related Platanthera species-not visited by mosquitoes-emit scents dominated by lilac aldehyde.

134 reduce human-mosquito contact by preventing mosquito entrance into human-occupied spaces and interfe

135 this approach in public health and nuisance-mosquito eradication programs.

136 were more infectious to Anopheles stephensi mosquitoes, essentially doubling prevalence of infected

137 ly taking place in Africa will drive further mosquito evolution, causing a shift toward human-biting

138 Nocturnal mosquitoes exhibit a behavioral response to divert away

139 Aedes aegypti and Anopheles coluzzii mosquitoes exhibit diurnal and nocturnal behaviors, resp

140 ds we explored the effect of household-level mosquito exposure and individual insecticide-treated net

141 however, ITN use did moderate the effect of mosquito exposure on morbidity.

142 istently low and insensitive to variation in mosquito exposure.

143 (AP) of complement by saliva from Anopheles mosquitoes facilitates feeding by blocking production of

144 to people even in the unlikely event that a mosquito fed upon a viremic host.

145 se in glycogen and lipid levels over time in mosquitoes fed on erythritol.

146 etween mosquito vectors and human hosts when mosquitoes feed during the night.

147 not complete the two-injection regimen with mosquito feeding at day 42, but were included in the saf

148 mediated knockdown of AeOBP22 led to reduced mosquito feeding behaviors.

149 was a significant increase in competence for mosquitoes feeding in the evening (18:00), and a signifi

150 sion via bridge vectors, which are competent mosquitoes feeding on both humans and wild animals.

151 nbound momentum by more than half before the mosquito firmly attaches to a surface.

152 e transmitted to mosquitoes, with individual mosquitoes frequently carrying multiple transmitted clon

153 predictive maps of resistance phenotypes in mosquitoes from the Anopheles gambiae complex across Afr

154 compared the whole genomes of 40 individual mosquitoes from two locations in Eurasia and two in Nort

155 t the abundance of conserved target sites in mosquito genomes and the inherent flexibility in CGD des

156 Like most higher organisms, mosquitoes harbor a highly diverse and dynamic microbial

157 ce that the average trap night collection of mosquitoes has increased by ~ 60% and statewide species

158 Mosquitoes have daily rhythms in behaviors and show a wi

159 ambda-cyhalothrin-free breeding sites, where mosquitoes have developed resistance to lambda-cyhalothr

160 of cooling, suggesting that during evolution mosquito heat seeking relied on cooling-mediated repulsi

161 l strategies are found to depend strongly on mosquito hopping rates, levels of door-to-door complianc

162 ignificant enthusiasm for genetic control of mosquitoes; however, no such system has been developed i

163 the primary ZIKV transmission cycle is human-mosquito-human, mutations in one host must be retained i

164 farmers, and Anopheles coluzzii was the main mosquito identified.

165 is to detect anatomical components within a mosquito image.

166 , we test our architecture trained only with mosquito images on bumblebee images.

167 The landing force of the average mosquito in our study is approximately 40 [Formula: see

168 t simulate the behavior and ecology of adult mosquitoes in exquisite detail on complex resource lands

169 ecticidal effect against Anopheles stephensi mosquitoes in laboratory conditions was not noticed, in

170 manatee, a federally threatened species, and mosquitoes in nature.

171 lts show that wAlbB Wolbachia can persist in mosquitoes in urban settings and decrease dengue inciden

172 While mosquito infection and pathogen development are one poss

173 In membrane feeding mosquito infection experiments, we found that gametocyte

174 Direct feeding assays resulted in mosquito infections from 9/12 participants following IBS

175 tween urban landscape, thermal features, and mosquito infestations.

176 ore day- versus night-biting female and male mosquitoes' innate temporal attraction/avoidance behavio

177 Mosquito inoculation of humans with arthritogenic alphav

178 The rebound response of a landing mosquito is well-characterized by a passive mass-spring-

179 nt spread of malaria from infected humans to mosquitoes is a major challenge for malaria elimination

180 show that 20E-triggered oviposition in these mosquitoes is regulated by the stress- and immune-respon

181 rentiation to gametes (gametogenesis) within mosquitos is essential for malaria parasite transmission

182 mmunity, reducing the burden of infection in mosquitoes, is a well-acknowledged but poorly quantified

183 e likelihood or intensity of transmission to mosquitoes, is more speculative in nature but is convinc

184 hrough the bite of infected female Anopheles mosquitos, is one of the main causes of mortality in man

185 minate the aquatic environments inhabited by mosquito juveniles.

186 sleeping under the LLINs (bite reduction and mosquitoes killed).

187 Acoustic larviciding (AL) occurs by exposing mosquito larvae to acoustic energy that ruptures their d

188 ction that may be enhanced by experience, as mosquitoes learn to recognize available sugar rewards.

189 was shown that Dengue virus infection of the mosquito led to an in increased expression of the odoran

190 t agricultural pests at large scale, but not mosquitoes, mainly because of challenges with consistent

191 an primates (NHP) and forest canopy-dwelling mosquitoes, mainly Haemagogus-spp and Sabethes-spp.

192 ntify habitats that should be prioritized in mosquito management and control actions, as well as to g

193 However, their role in shaping the mosquito microbiota is not well understood.

194 we review the structure and function of the mosquito microbiota, including bacteria, fungi, and viru

195 of An. arabiensis in Kenya, localized to the mosquito midgut and ovaries, and is not associated with

196 The roles of mosquito midgut proteins and parasite interaction during

197 This study aims to identify mosquito midgut proteins that interact with and affect P

198 ent activation and ookinete elimination upon mosquito midgut traversal.

199 ti by enhancing virus dissemination from the mosquito midgut.

200 ormation in Bti to dissolution in the larval mosquito midgut.

201 Plasmodium invasion of mosquito midguts is a mandatory step for malaria transmi

202 oor toward understanding the neural basis of mosquito nectar-seeking behaviors.

203 Female mosquitoes need a blood meal to reproduce, and in obtain

204 Day- versus night-biting mosquitoes occupy distinct time-of-day niches [2, 3].

205 When sugar sources are scarce, female mosquitoes of some species can compensate by taking larg

206 s National Park, Florida, USA, indicate that mosquitoes of three genera, Aedes, Anopheles, and Culex

207 Although understanding of mosquito olfaction has progressed dramatically in recent

208 The mosquito P47Rec has two natterin-like domains and binds

209 These data add to our understanding of mosquito-parasite interactions and identify PIMMS43 as a

210 Among 12 persons who infected mosquitoes, polymerase chain reaction and amplicon deep

211 Three mosquito pools were positive for YFV, 2 Haemagogus leuco

212 Marked mosquito pools with stable isotopes were used to estimat

213 and the negative effect this may have on the mosquito population could elicit substantial impact in t

214 s across Kenya and determined the changes in mosquito population genetic diversity after 20 years of

215 luable component of a field-ready strain for mosquito population modification to control malaria tran

216 Earlier work demonstrated that mosquito populations and their vector potential are depe

217 An ability to characterize the age of mosquito populations could provide cost-effective and co

218 predicted to have a quicker impact on female mosquito populations than previously developed gene driv

219 asting insecticidal nets (LLINs) has created mosquito populations that are largely pyrethroid-resista

220 present in the standing genetic variation of mosquito populations will be detrimental to the deployme

221 to search can have profound consequences for mosquito populations' capacity to transmit pathogens.

222 f reproduction has been proposed to suppress mosquito populations, elucidation of biological processe

223 pe males never display, suggesting that male mosquitoes possess the central or peripheral neural circ

224 Mosquitoes preferred sucrose when a choice was given but

225 itten by the virus-infected AaVA-1-deficient mosquitoes present a lower viremia and prolonged surviva

226 Two features inspired by the mosquito proboscis were adopted for MPI insertion in pro

227 The reproductive success of these mosquitoes relies on a single copulation event after whi

228 Instead mosquitoes rely on damping by deforming two forelimbs an

229 d infections are more readily transmitted to mosquitoes remains unknown.

230 Our results also suggest that the enhanced mosquito repellency by antagonist mixtures is due to add

231 tive to N,N-diethyl-meta-toluamide (DEET), a mosquito repellent.

232 blood-feeding is essential for anautogenous mosquito reproduction, the transcriptional response to b

233 ociated with exposure to sporozoite-infected mosquitoes (RR, 1.24; 95% CI, 1.11-1.38).

234 he microbiome has a much lower effect on the mosquito's gene expression than previously thought with

235 hogen development are one possible part of a mosquito's state, that is not our main focus.

236 rant binding protein 22 (AeOBP22) within the mosquito salivary gland and that siRNA mediated knockdow

237 s essential for sporozoite gliding motility, mosquito salivary gland invasion and mouse infection.

238 In animal models, immunity to mosquito salivary proteins protects animals against mosq

239 At peak mosquito season, the number of female mosquitoes was 95.

240 discuss targets of monoclonal antibodies in mosquito sexual stages of Plasmodium.

241 The Aedesaegypti mosquito shows extreme sexual dimorphism in feeding.

242 This work demonstrates the high efficacy of mosquito SIT in an area ninefold larger than in previous

243 ally significant driver of pathogen-carrying mosquito species (disease vectors) that pose a health ri

244 Males of both diurnal and nocturnal mosquito species show reduced UV light avoidance in anti

245 Most Anopheles mosquito species that are of major importance as human m

246 consisted of 1500 smartphone images of nine mosquito species trapped in Florida.

247 on ITS2 and COX1 genes revealed 21 Anopheles mosquito species, including two previously unreported no

248 Viruses transmitted by Aedes mosquitoes, such as dengue, Zika, and chikungunya, have

249 e on the Miami-Dade County, Florida immature mosquito surveillance system based on requested by citiz

250 investing in integrated climate, health and mosquito surveillance systems, building regional and loc

251 seven candidate genes significantly changed mosquitoes' susceptibility to P. falciparum.

252 has progressed dramatically in recent years, mosquito taste remains greatly understudied.

253 yzed P. vivax DMFA (PvDMFA) data from 22,236 mosquitoes tested from 96 independent assays.

254 ) is a neurotropic alphavirus transmitted by mosquitoes that causes encephalitis and death in humans(

255 Mosquitoes that survived exposure to the net were kept i

256 sporozoite rate (the proportion of infective mosquitoes) that emphasized changes in mosquito age.

257 orted the generation of axenic Aedes aegypti mosquitoes, the primary vector of several human pathogen

258 biology and vectorial capacity of Anopheles mosquitoes, the vectors of malaria parasites.

259 host environments, both within blood-feeding mosquitoes, their definitive hosts, and in vertebrates,

260 separately extract anatomical components of mosquitoes-thorax, wings, abdomen and legs from images.

261 vioral states and state transitions of adult mosquitoes through a sequence of activity bouts.

262 esent the biteOscope, a device that attracts mosquitoes to a host mimic which they bite to obtain an

263 study we film the landings of Aedes aegypti mosquitoes to characterize landing behaviors and kinetic

264 ole-genome sequence data from 375 individual mosquitoes to identify a single underlying ancestry comp

265 However, chemical cues possibly luring mosquitoes to swarms have not been adequately investigat

266 Hemocytes limit the capacity of mosquitoes to transmit human pathogens.

267 d represents an important source of human-to-mosquito transmission of Plasmodium falciparum.

268 to how flaviviruses control pathogenesis and mosquito transmission through the nonstructural protein

269 itosis in the gametogony and is required for mosquito transmission.

270 Mosquitoes transmit pathogens that kill >700,000 people

271 Many mosquito transmitted viruses of the genera Alphavirus an

272 velopment of climate services to help manage mosquito-transmitted disease epidemics.

273 Zika virus (ZIKV), a mosquito-transmitted flavivirus, is linked to microcepha

274 Alphaviruses are emerging, mosquito-transmitted RNA viruses with poorly understood

275 Yellow fever (YF) is a mosquito-transmitted viral disease that causes tens of t

276 late the capacity of insect disease vectors (mosquitoes, tsetse flies, sandflies) to transmit parasit

277 to reduce malaria parasite infection in the mosquito vector and provide new insight into the mechani

278 l and apply it to Aedes aegypti, an invasive mosquito vector for arboviruses (e.g. dengue, zika and y

279 Aedes aegypti is the principal mosquito vector for many arboviruses that increasingly i

280 due to the co-prevalence of the transmitting mosquito vector species Aedes and Culex.

281 possible for marine mammals to be exposed to mosquito-vectored pathogens through direct interactions

282 ns unknown how wild cetaceans are exposed to mosquito-vectored pathogens.

283 ria transmission by limiting contact between mosquito vectors and human hosts when mosquitoes feed du

284 Besides its strong insecticidal effect on mosquito vectors of the disease, ivermectin inhibits Pla

285 hat is spread by travelers and adapts to new mosquito vectors that live in temperate climates.

286 ly capture the biology and behaviour of many mosquito vectors that refeed frequently (every 2-3 d)(4)

287 rtially restore pyrethroid susceptibility in mosquito vectors.

288 t peak mosquito season, the number of female mosquitoes was 95.5% lower (95% CI, 93.6-96.9) in releas

289 ered in a laboratory colony of Aedes aegypti mosquitoes was similarly efficient.

290 shown to strongly repel Anopheles and Culex mosquitoes, we examined the bioactivities of the identif

291 nderstand the influence of the microbiome on mosquitoes, we examined the transcriptomes of axenic and

292 calcium imaging from transgenic PUb-GCaMP6s mosquitoes, we show that Ae. aegypti code geosmin in a q

293 Blood fed Anopheles mosquitoes were collected from a malaria endemic village

294 However, when mosquitoes were maintained under more realistic fluctuat

295 S411A Kunjin-infected Culex quinquefasciatus mosquitoes were observed, but S411A Kunjin infection res

296 P2 silencing fully restores mortality of the mosquitoes, whereas SAP2 overexpression results in incre

297 standardised washes and sterilised blood-fed mosquitoes which remained alive after exposure to the ne

298 sitivity for shrimp, crab, ticks, moths, and mosquitoes, while ImmunoCAP((R)) tests were negative for

299 difference was observed in the life span of mosquitoes with different genotypes (chi(2) = 1.6; P = 0

300 arasite clones in humans were transmitted to mosquitoes, with individual mosquitoes frequently carryi