ライフサイエンスコーパス: mosquito vector

1 d why DENV reconfigures phospholipids in the mosquito vector.

2 ical role of the selective advantages in the mosquito vector.

3 formation and sporogonic development in the mosquito vector.

4 the microfilaria reservoir available to the mosquito vector.

5 n in humans and pathogen transmission to the mosquito vector.

6 cle of Plasmodium in the vertebrate host and mosquito vector.

7 the male gamete in the midgut of the female mosquito vector.

8 a persistent, nonpathogenic infection in the mosquito vector.

9 but essential for male gametogenesis in the mosquito vector.

10 , nor for gametogenesis and sporogony in the mosquito vector.

11 sion of parasites from the human host to the mosquito vector.

12 that are responsible for transmission to the mosquito vector.

13 ria parasite and occurs in the midgut of the mosquito vector.

14 cal interactions with the blood meal and the mosquito vector.

15 e population losses as it passes through its mosquito vector.

16 the difficulty of sustainable control of the mosquito vector.

17 parasites undergo a sporogonic cycle in the mosquito vector.

18 ametocytes, the only stages infective to the mosquito vector.

19 lead to infection even in the absence of the mosquito vector.

20 ncreasing due to geographic expansion of the mosquito vector.

21 y wide feeding host-range for the Haemagogus mosquito vector.

22 stages of parasite transmission through the mosquito vector.

23 hosts: a vertebrate and the female Anopheles mosquito vector.

24 e a platform to further study this important mosquito vector.

25 eld strain (FS) of Aedes aegypti, the dengue mosquito vector.

26 brate host and persistent replication in the mosquito vector.

27 icative sexual stage necessary to infect the mosquito vector.

28 completion of Plasmodium development in the mosquito vector.

29 tes and the ookinetes and sporozoites of the mosquito vector.

30 erythrocytes and hepatocytes, as well as the mosquito vector.

31 s a complex life cycle in a human host and a mosquito vector.

32 ission while minimizing fitness costs to its mosquito vector.

33 dition, was essential for development in the mosquito vector.

34 es, called gametocytes, are infective to the mosquito vector.

35 , oocyst and sporozoite formation inside the mosquito vector.

36 ular invasive stages that develop within the mosquito vector.

37 gional differences in the human host and the mosquito vector.

38 ol is reliant on insecticides to control the mosquito vector.

39 s with changing climatic suitability for the mosquito vector.

40 ed by insecticide resistance in some malaria mosquito vectors.

41 fitness, and likely would not be purified by mosquito vectors.

42 so block Plasmodium parasite transmission to mosquito vectors.

43 s essential for efficient virus infection of mosquito vectors.

44 s on the attractiveness of infected hosts to mosquito vectors.

45 must reduce malaria transmission through the mosquito vectors.

46 cytes of Anopheles gambiae and Aedes aegypti mosquito vectors.

47 smodium falciparum sexual stage parasites to mosquito vectors.

48 n feeding behavior and climate adaptation of mosquito vectors.

49 resistant strains might be more infective to mosquito vectors.

50 rotropic flavivirus transmitted to humans by mosquito vectors.

51 develop a persistent, life-long infection in mosquito vectors.

52 he coevolution between malaria parasites and mosquito vectors.

53 plification hosts for efficient infection of mosquito vectors.

54 remia that results in efficient infection of mosquito vectors.

55 fication of the Anopheles gambiae complex of mosquito vectors.

56 ndscape and abundance of medically important mosquito vectors.

57 bout how Plasmodium parasites adapt to their mosquito vectors.

58 ilability of high-quality genomes of several mosquito vectors.

59 tat conditions on the shape of the virome in mosquito vectors.

60 the way towards using CI to control malaria mosquito vectors.

61 lating chemosensory function and controlling mosquito vectors.

62 smissible stage than the average lifespan of mosquito vectors.

63 more rapidly than behavioural shifts within mosquito vectors.

64 y inadvertently promote the proliferation of mosquito vectors.

65 ce, and lack of transmissibility in the main mosquito vectors.

66 o block Plasmodium transmission to Anopheles mosquito vectors.

67 ed livestock products or multiple species of mosquito vectors.

68 n for up to 3 months without the presence of mosquito vectors.

69 ed vertically and sexually in addition to by mosquito vectors.

70 rtially restore pyrethroid susceptibility in mosquito vectors.

71 al network connecting flaviviruses and their mosquito vectors.

72 ion is the effective management of Anopheles mosquito vectors.

73 n monitoring and modeling arboviruses within mosquito vectors.

74 al prevalence of dengue virus (DENV) and its mosquito vectors.

75 tial to discover novel feeding deterrents of mosquito vectors.

76 , their management relies on controlling the mosquito vectors.

77 iology, evolution, and dispersal of the main mosquito vectors.

78 ad by the Aedes aegypti and Aedes albopictus mosquito vectors.

79 and use them to infect native and non-native mosquito vectors.

80 e first in the United States to characterize mosquito vector abundance and diversity on commercial sw

81 In females of the mosquito vector Aedes aegypti (L.), aedeskinins are know

82 incompatible insect technique (IIT) with the mosquito vector Aedes aegypti in northern Australia in a

83 igenaemia determines ZIKV infectivity in its mosquito vector Aedes aegypti, which acquires ZIKV via a

84 viruses (VEEV) readily infect the epizootic mosquito vector Aedes taeniorhynchus.

85 EN) that are transmitted among humans by the mosquito vectors Aedes aegypti and Aedes albopictus are

86 Dengue virus (DENV) and its primary mosquito vectors Aedes spp. have spread to every contine

87 restricted range of movement of the primary mosquito vector, Aedes aegypti, local human movements ma

88 for its efficient maintenance in the dengue mosquito vector, Aedes aegypti.

89 otypically structured model for the invasive mosquito vector, Aedes albopictus, and dengue, the secon

90 approach to control DENV transmission by the mosquito vectors, Aedes aegypti and Aedes albopictus, us

91 ns worldwide, and the expanding range of the mosquito vector, affected in part by climate change, inc

92 n and genotype-phenotype associations in the mosquito vector, along with sexual reproduction, have hi

93 primarily transmitted by Aedes aegypti, the mosquito vector also important in transmission of the fl

94 Here, we use a single pairing of the Asian mosquito vector, An. stephensi and the human malaria par

95 ct of a complex developmental process in the mosquito vector and are destined to infect the mammalian

96 nthase completely blocks transmission to the mosquito vector and could potentially be targeted for di

97 equisite for transmission from humans to the mosquito vector and has emerged as a target for interven

98 at body of knowledge about the parasite, its mosquito vector and human host.

99 e key ecological links between the Aedes sp. mosquito vector and humans.

100 opmental stages of the parasite, both in the mosquito vector and in the human host.

101 ell invasion and replication within both the mosquito vector and mammalian host.

102 its effects on the population growth of the mosquito vector and on pathogen development within the v

103 e host, through the different tissues of its mosquito vector and onwards to infect a new vertebrate h

104 Interactions between the Anopheles mosquito vector and Plasmodium parasites shape how malar

105 for malaria control in the mammalian and the mosquito vector and provide a molecular basis for the st

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

107 l factors, including increased spread of the mosquito vector and rapid urbanization.

108 , successively invade salivary glands in the mosquito vector and the liver in the mammalian host.

109 oites must infect the salivary glands of the mosquito vector and the liver of the mammalian host; bot

110 site that invades the salivary glands of the mosquito vector and the liver of the vertebrate host, ex

111 During their passage within the mosquito vector and the vertebrate host, sporozoites dis

112 amics in that it is concurrently spread by a mosquito vector and through sexual contact.

113 geneity, attributable to the dynamics of the mosquito vector and to the characteristics and mobility

114 ity for surveillance of WN virus activity in mosquito vectors and avian hosts, and, in addition, it i

115 malaria transmitted by pyrethroid-resistant mosquito vectors and could thus be a crucial addition to

116 d that WNV is well adapted to the ecology of mosquito vectors and diverse avian hosts in the United S

117 al heterogeneity on the contact rate between mosquito vectors and hosts.

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

119 The ecology of mosquito vectors and malaria parasites affect the incide

120 e result of parasite adaptation to sympatric mosquito vectors and may be an important factor driving

121 our understanding of viral diversity within mosquito vectors and provides information that opens the

122 cific region where the presence of competent mosquito vectors and suitable climatic conditions could

123 insecticide resistance that has developed in mosquito vectors and the drug resistance of pathogens.

124 ave facilitated the spread of both efficient mosquito vectors and the four dengue virus serotypes bet

125 e these viruses incapable of transmission by mosquito vectors and to differentially regulate expressi

126 The spread of both mosquito vectors and viruses has led to the resurgence o

127 cell invasion and block transmission to the mosquito vector, and to vaccines to other extracellular

128 piled infection data from sentinel chickens, mosquito vectors, and human cases in Iowa over a 15 year

129 ria and the greatest diversity of parasites, mosquito vectors, and human victims.

130 glaciation, increased anthropophilia of the mosquito vectors, and the spread of agriculture.

131 the same natural macaque hosts and Anopheles mosquito vectors, and therefore have a similar epidemiol

132 smodium parasite transmission by the African mosquito vector Anopheles gambiae depends on finely tune

133 asite-resistance island (PRI) of the African mosquito vector, Anopheles gambiae, was mapped to five g

134 implications of a range expansion of dengue mosquito vectors are severe.

135 an/reptilian Plasmodium parasites, spread by mosquito vectors, are ancestral sister taxa, from which

136 rong surveillance system for malaria and its mosquito vector as an essential pillar of the malaria el

137 species, and could be transferred into other mosquito vectors as part of control programs.

138 sistance to pathogens, or even eliminate the mosquito vectors, as a means of control.

139 rrent malaria-control methods, several novel mosquito vector-based control strategies have been propo

140 he parasite stages transmitted to and by the mosquito vector because they may represent more vulnerab

141 acilitated virus acquisition by their native mosquito vectors because the protein enabled the virus t

142 Blocking these pathogens in the mosquito vector before they are transmitted to humans is

143 Given that malaria mosquito vectors belong to a species complex comprising

144 d animal pathogens, which are transmitted by mosquito vectors between vertebrate hosts.

145 on the regulatory elements is available for mosquito vectors but is scant for other vectors.

146 ansion is attributed to the success of Aedes mosquito vectors, but local epidemiological drivers are

147 laria is transmitted from vertebrate host to mosquito vector by mature sexual blood-living stages cal

148 Dengue Virus (DENV), a flavivirus spread by mosquito vectors, can cause vascular leakage and hemorrh

149 ite's interplay with both the human host and mosquito vector cannot be underestimated.

150 nding of the roles of mosquito phagocytes in mosquito vector competence and demonstrates the utility

151 ssible biological significance and effect on mosquito vector competence for arboviruses.

152 les of apoptosis and caspases in determining mosquito vector competence for arboviruses.

153 veral insect pest species, but its effect on mosquito vector control has been limited.

154 rea-wide application of combined IIT-SIT for mosquito vector control.

155 the orthologues of mosGCTL in another major mosquito vector (Culex pipiens pallens) also impairs the

156 ture and moisture are favorable for the sole mosquito vector, Culex quinquefasciatus, and extrinsic s

157 that the viruses initially delivered by the mosquito vector differ from those generated in subsequen

158 the successful reduction of infection in the mosquito vector, direct evidence that there is an onward

159 novel approaches to combating the spread of mosquito-vectored diseases.

160 in parts of Africa where climate drives both mosquito vector dynamics and parasite development rates.

161 ite drug resistance and host susceptibility, mosquito vector ecology and transmission seasonality.

162 ansition through multiple mammalian host and mosquito vector environments.

163 ent and more recent human interactions shape mosquito vector evolution.

164 risk of dengue transmission should competent mosquito vectors expand their range.

165 ia parasites occurs when nocturnal Anopheles mosquito vectors feed on human blood.

166 The wide endemic range of mosquito-vectored flaviviruses-such as Zika virus and de

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

168 Aedes aegypti (Linnaeus, 1762), the primary mosquito vector for dengue and other arboviral pathogens

169 Here, we show that the major mosquito vector for dengue virus uses the JAK-STAT pathw

170 site Brugia malayi that requires a competent mosquito vector for its development and transmission.

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

172 m parasites must complete development in the mosquito vector for transmission to occur.

173 The mosquito vectors for this virus are globally distributed

174 Mosquitoes vector harmful pathogens that infect millions

175 ia ookinetes to cross the midgut wall of the mosquito vector has been (and continues to be) controver

176 Surveillance of avian hosts and mosquito vectors has been insufficient to elucidate the

177 tomics and the complete genome sequencing of mosquito vectors have increased our knowledge of the SG

178 erefore, we hypothesized that changes in the mosquito vector host range might have contributed to the

179 e part to its replication in and spread by a mosquito vector host.

180 the infective stage injected by bite of the mosquito vector, however, whole parasite vaccines presen

181 inea, where the level of transmission by the mosquito vector, human infection rates and clinical morb

182 In addition to spreading via mosquito vectors, human WEEV infections can potentially

183 evented parasites from developing within the mosquito vector in standard membrane feeding assays.

184 e and therefore drive the persistence of the mosquito vector in the context of ZIKV infection.

185 e a measurable effect on transmission by the mosquito vector in vivo.

186 data relating to monkey hosts and Anopheles mosquito vectors in Indonesian Borneo.

187 diagnosis but also virologic surveillance of mosquito vectors in the field.

188 h it is transmitted, and the role of various mosquito vectors in the recent outbreaks.

189 sage has resulted in increased resistance in mosquito vectors, including C. quinquefasciatus.

190 ributions, and are strongly predicted by the mosquito vector index.

191 ria, undergo crucial developments within the mosquito vector, initiated by the formation of male and

192 e Plasmodium falciparum within a susceptible mosquito vector is a prerequisite for the transmission o

193 he life cycle of the malaria parasite in its mosquito vector is essential for developing new strategi

194 This mosquito vector is highly domesticated, living in close

195 we consider important because combating the mosquito vector is the only way to contain dengue transm

196 virus infection in southeast Asia, where the mosquito vector is widespread and other arboviruses circ

197 comprehensive understanding of the virome in mosquito vectors is crucial for assessing the potential

198 , close surveillance in animals, humans, and mosquito vectors is necessary to detect the presence of

199 As pyrethroid resistance evolves in mosquito vectors, it will be useful to understand how th

200 It circulates through mosquito vectors mainly of the Aedes family and a mammal

201 lection for efficient infection of epizootic mosquito vectors may mediate VEE emergence.

202 n, the virus quickly adapted to infect local mosquito vectors more efficiently than the originally in

203 ons do not naturally occur in some important mosquito vectors, notably Aedes aegypti.

204 Saliva from the mosquito vector of flaviviruses is capable of changing t

205 s of Anopheles stephensi, a major anopheline mosquito vector of human malaria in Asia.

206 d humidity adaptation of A. gambiae, a major mosquito vector of human malaria in sub-Saharan Africa.

207 e, and Anopheles gambiae, the most important mosquito vector of malaria in sub-Saharan Africa.

208 Anopheles gambiae, which has been the major mosquito vector of the malaria parasite Plasmodium falci

209 We find a major mosquito vector of these viruses-Aedes aegypti-can carry

210 the southern house mosquito) is an important mosquito vector of viruses such as West Nile virus and S

211 cits a response from many insects, including mosquito vectors of diseases such as malaria and yellow

212 ic modification of the vectorial capacity of mosquito vectors of human disease requires promoters cap

213 standing regulation of gene transcription in mosquito vectors of human diseases.

214 s gambiae species complex, the major African mosquito vectors of human malaria.

215 ration of synthetic repellents against major mosquito vectors of infectious diseases.

216 During the long Sahelian dry season, mosquito vectors of malaria are expected to perish when

217 Mosquito vectors of malaria in Southeast Asia readily fe

218 e plantations provide ideal habitats for the mosquito vectors of malaria, dengue, and chikungunya.

219 , are capable of generating large numbers of mosquito vectors of malaria, which causes more than 400,

220 gies of major agricultural pests but also on mosquito vectors of serious human diseases such as Dengu

221 ntribute to our understanding of ISVs within mosquito vectors of the Culicidae family in the Eastern

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

223 aised concerns that climate change may cause mosquito vectors of these diseases to expand into more t

224 hird, highly focused feeding patterns of the mosquito vectors of WNV result in unexpected host specie

225 est connectivity, factors that may favor the mosquito vectors of yellow fever.

226 against Zika virus and to identify possible mosquito vectors of Zika virus.

227 architecture of osmoregulation in Anopheles mosquitoes, vectors of human malaria.

228 hinery in cells of both mammalian (host) and mosquito (vector) origin.

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

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

231 This model interconnects a homogeneous mosquito vector population with a heterogeneous human ho

232 deforestation and agriculture, can influence mosquito vector populations and malaria transmission.

233 The use of pesticides to reduce mosquito vector populations is a cornerstone of global m

234 rile insect technique does not only suppress mosquito vector populations through the induction of ste

235 ggests adaptation to different human host or mosquito vector populations.

236 luding increased air travel and uncontrolled mosquito vector populations.

237 tion of whether malaria parasites kill their mosquito vectors remains open.

238 Transmission from the vertebrate host to the mosquito vector represents a major population bottleneck

239 red blood cells, while transmission to their mosquito vector requires asexual blood-stage parasites t

240 rasites (Plasmodium spp.) from humans to the mosquito vector requires differentiation from asexual st

241 aria parasite from the mammalian host to the mosquito vector requires the formation of adequately ada

242 Anopheles gambiae is a major mosquito vector responsible for malaria transmission, wh

243 ed cells of Anopheles gambiae, the principle mosquito vector responsible for the transmission of over

244 Anopheles gambiae is the mosquito vector responsible for transmitting Plasmodium

245 e emergence of insecticide resistance within mosquito vectors risks jeopardizing the future efficacy

246 ssee, with special emphasis on the potential mosquito vector(s).

247 ific interactions of the sporozoite with the mosquito vector salivary glands or the mammalian host he

248 ites' transmission stage that resides in the mosquito vector salivary glands, can transform into earl

249 Aedes aegypti mosquitoes vector several arboviruses of global health s

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

251 nization often result in increased levels of mosquito vector species and vector-borne pathogen transm

252 Determining how mosquito vector species composition and abundance depend

253 However, longitudinal shifts in mosquito vector species composition were evident within

254 We hypothesize that mosquito vector species, especially Aedes aegypti, are l

255 and stable transformation of this important mosquito vector species.

256 irus (ZIKV) that explicitly includes two key mosquito vector species: Aedes aegypti and Aedes albopic

257 iency of malaria parasite development within mosquito vectors (sporogony) is a critical determinant o

258 gly significant public health problem as its mosquito vectors spread over greater areas; no vaccines

259 Given the wide distribution of CHIKV mosquito vectors, studies to determine the geographic ex

260 aging tool, is promising in transforming the mosquito vector surveillance programs by reducing the bu

261 ckage in terms of the fitness imposed to the mosquito vector that expresses either molecule.

262 The mosquito vector that transmits this virus is widespread

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

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

265 ients for use in novel biopesticides against mosquito vectors that transmit malaria.

266 trol malaria is by controlling the Anopheles mosquito vectors that transmit the parasites.

267 Along with its mosquito vector, the Alphavirus chikungunya virus (CHIKV

268 EV strains are opportunistic in their use of mosquito vectors, the most widespread outbreaks appear t

269 velopment of malarial parasites within their mosquito vector, thereby abrogating the cascade of secon

270 n an effort to limit ZIKV replication in the mosquito vector, thereby interrupting the transmission a

271 rapidly lose the capacity to develop in the mosquito vector through a defect in exsheathment and ina

272 ch causes febrile illness, is transmitted by mosquito vectors throughout tropical and subtropical reg

273 Plasmodium, must survive and develop in the mosquito vector to be successfully transmitted to a new

274 uality that the parasite must sustain in the mosquito vector to complete its life cycle.

275 e pathogens successfully transition from the mosquito vector to the vertebrate host is an important a

276 volving human amplification and peridomestic mosquito vectors to cause major epidemics.

277 ncidence because of the sensitivity of their mosquito vectors to climate.

278 timately require the genetic manipulation of mosquito vectors to disrupt virus transmission to human

279 ing the feasibility of genetically modifying mosquito vectors to impair their ability to transmit the

280 have been suggested to alter the behavior of mosquito vectors to increase the likelihood of transmiss

281 mic regions, where water availability limits mosquito vectors to only part of the year.

282 is the first to consider the spread of Aedes mosquito vectors to project dengue suitability.

283 ing the temperature from that present in its mosquito vectors to that of its human host.

284 outbreaks have been contained by controlling mosquito vectors using insecticide-based approaches.

285 rus genus of the family Togaviridae contains mosquito-vectored viruses that primarily cause either ar

286 on due to its profound effect on ectothermic mosquito vectors, viruses, and their interaction.

287 d in widespread development of resistance in mosquito vectors, warranting continuous monitoring and i

288 gunya virus (CHIKV) to study adaptation to a mosquito vector, we evaluated mutations associated with

289 Malaria mosquito vectors were captured 3 months before, during,

290 ation between Plasmodium parasites and their mosquito vectors, which shapes parasite virulence both i

291 clear picture into the role of small RNAs in mosquito vectors will pave the way to the utilization of

292 cal model for the population dynamics of the mosquito vector with the temperature time series and the

293 omplex interplay between bird reservoirs and mosquito vectors, with human cases the result of epizoot

294 P. falciparum to a new human host requires a mosquito vector within which sexual replication occurs.