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1 ant receptors in Drosophila melanogaster and Aedes albopictus.
2 t females and males of the arbovirus vector, Aedes albopictus.
3 y the global spread of the invasive mosquito Aedes albopictus.
4 tly introduced in central Africa, along with Aedes albopictus.
5 untry, probably facilitated by the spread of Aedes albopictus.
6 bution of two key vectors: Aedes aegypti and Aedes albopictus.
7  the world's most invasive mosquito species, Aedes albopictus.
8 of Sindbis virus in cells of the insect host Aedes albopictus.
9 ted by the encounter of a different species, Aedes albopictus.
10 om cells derived from both Aedes aegypti and Aedes albopictus.
11 rse dipteran species, including the mosquito Aedes albopictus.
12 logical characteristics of Aedes aegypti and Aedes albopictus, 2 invasive mosquito species and primar
13 ica and Asia, the adaptation of the virus to Aedes albopictus, a mosquito species with an almost worl
14 ecause of genetic adaptation of the virus to Aedes albopictus, a species that thrives in temperate re
15  wMel strain of Drosophila melanogaster into Aedes albopictus, a vector of dengue and other arbovirus
16                          The distribution of Aedes albopictus across west Africa is well documented.
17                                     Multiple Aedes albopictus-adaptive fitness peaks became available
18 arcelona, Spain, as an example, and focus on Aedes albopictus, an invasive vector species of concern
19 rds the highly invasive Asian tiger mosquito Aedes albopictus and a representative native mosquito Cu
20 20E) in CW assessment and pupation timing in Aedes albopictus and Ae. aegypti, vectors of arboviruses
21             In south Florida, the mosquitoes Aedes albopictus and Aedes aegypti often co-occur in wat
22 ofile RNA viromes of individual co-occurring Aedes albopictus and Aedes vexans mosquitoes across a 2,
23 ainers were periodically tested using larval Aedes albopictus and Culex pipiens mosquitoes to assess
24 hropod cell lines (derived from An. gambiae, Aedes albopictus and Drosophila melanogaster) and six mo
25 utogenous strain in the Asian tiger mosquito Aedes albopictus and examined an F(1) intercross populat
26 d a Wolbachia superinfection in the mosquito Aedes albopictus and found the infection to be associate
27 ecay during a viral infection in both C6/36 (Aedes albopictus) and baby hamster kidney cells.
28  infected mosquito cell cultures (C6/36 from Aedes albopictus) and embryos (Aedes triseriatus).
29 48Aa1 susceptibility of Anopheles stephensi, Aedes albopictus, and Culex tarsalis larvae-substantiall
30 ured model for the invasive mosquito vector, Aedes albopictus, and dengue, the second most prevalent
31 ting, and feeding dynamics of Aedes aegypti, Aedes albopictus, Anopheles stephensi, and Anopheles col
32                                              Aedes albopictus, another highly invasive arbovirus vect
33 ns by the mosquito vectors Aedes aegypti and Aedes albopictus are hypothesized to have evolved from s
34          Among mosquitoes, Aedes aegypti and Aedes albopictus are two invasive mosquito species in th
35 al control strategies are failing to contain Aedes albopictus as an emerging major vector for dengue.
36 e, and the range of invasive species such as Aedes albopictus (Asian Tiger Mosquito) is expanding.
37 hat occurs in many insect species, including Aedes albopictus (Asian tiger mosquito).
38  to control populations of the dengue vector Aedes albopictus, but CI-inducing strains are not known
39                                       In the Aedes albopictus C/wStr1 mosquito cell line, wStr mainta
40  the expression plasmids and introduced into Aedes albopictus C6/36 cells by electroporation or into
41 were detected by culturing mosquito pools on Aedes albopictus (C6/36) cell cultures.
42 nt viruses were generated and used to infect Aedes albopictus (C6/36) mosquito cells, which were chal
43 dbis produced from three different mosquito (Aedes albopictus) cell lines; one other insect cell line
44 licate in mammalian BHK-21 cells or mosquito Aedes albopictus cells and rapidly reverted catalyticall
45                                           In Aedes albopictus cells at 34.5 degrees C, neither nsP1 s
46 arison of density-arrested and cycling C6/36 Aedes albopictus cells infected with a low-passage DEN2
47 e protein interactome of dengue virus NS1 in Aedes albopictus cells was investigated using a proximit
48 roteins were targeted to the Golgi region of Aedes albopictus cells, both in the presence and absence
49                After transfection into C6/36 Aedes albopictus cells, constructs generated comparable
50 N-2; Jamaica) genome was expressed in C6/36 (Aedes albopictus) cells in either the sense or the antis
51                                       C6/36 (Aedes albopictus) cells were stably transformed with a p
52                                              Aedes albopictus collected in 2001 and 2011 from LA Coun
53                                 The invasive Aedes albopictus, commonly known as the Asian tiger mosq
54  by cross-species matings, could explain how Aedes albopictus competitively displaces Aedes aegypti p
55  species diversity, including Culex pipiens, Aedes albopictus, Culex modestus, Anopheles maculipennis
56 s (Anopheles sinensis, Armigeres subalbatus, Aedes albopictus, Culex quinquefasciatus and Cu. tritaen
57 field-based studies of the invasive mosquito Aedes albopictus demonstrate its competency to transmit
58  and Aedes japonicus showed no transmission, Aedes albopictus demonstrated low transmission at higher
59 uito (Culex pipiens) and the tiger mosquito (Aedes albopictus) enter an overwintering dormancy known
60 engue virus and chikungunya virus as well as Aedes albopictus for ZIKV, suggesting that this phenomen
61 ease of Wolbachia-infected Aedes aegypti and Aedes albopictus, for either its virus-blocking capabili
62 irus (CHIKV) to infect and be transmitted by Aedes albopictus has increased the geographical range at
63 nt from the mosquito and yellow fever vector Aedes albopictus, has been characterized.
64 e Culex pipiens Complex, and, most recently, Aedes albopictus have been facilitated by worldwide ship
65 competition assays between Culex pipiens and Aedes albopictus in low nutrient environments using mult
66  detect stable and persistent populations of Aedes albopictus in three Iowa counties.
67                                              Aedes albopictus is a competent vector of several arbovi
68                     The Asian tiger mosquito Aedes albopictus is globally expanding and has become th
69                                              Aedes albopictus is secondary to Aedes aegypti as a vect
70                    The Asian tiger mosquito, Aedes albopictus, is an anthropophilic aggressive daytim
71 ficiency in a historically secondary vector, Aedes albopictus, leading to speculation that this was a
72                                   Control of Aedes albopictus, major dengue and chikungunya vector, i
73                    Strikingly, we found that Aedes albopictus males bypass female control when attemp
74  (Dirofilaria immitis) between eight natural Aedes albopictus mosquito populations representing areas
75 ive CHIKV strains to an atypical vector, the Aedes albopictus mosquito that is ubiquitously distribut
76 is primarily spread by the Aedes aegypti and Aedes albopictus mosquito vectors.
77                                        Three Aedes albopictus (mosquito) cell lines persistently infe
78  (CHIKV) is transmitted by Aedes aegypti and Aedes albopictus mosquitoes and causes febrile illness w
79 on ex vivo and inducing anosmic behaviors to Aedes albopictus mosquitoes in vivo.
80 identified a bacterium from the gut of field Aedes albopictus mosquitoes named Rosenbergiella sp. YN4
81                            Aedes aegypti and Aedes albopictus mosquitoes spread major vector-borne vi
82  in larger populations of juvenile and adult Aedes albopictus mosquitoes surviving the winter without
83 rent Wolbachia strains: wAlbB (isolated from Aedes albopictus mosquitoes) and wStri (isolated from th
84 (2 isolates), wMau (11-fold enrichment), and Aedes albopictus mosquitoes, wAlbB (200-fold enrichment)
85 4) are spread primarily by Aedes aegypti and Aedes albopictus mosquitoes, whose geographic range cont
86 ed to humans by the bite of Aedes aegypti or Aedes albopictus mosquitoes, with millions of infections
87  we examine how taste stimuli are encoded by Aedes albopictus mosquitoes-a highly invasive disease ve
88 ng pathogen transmitted by Aedes aegypti and Aedes albopictus mosquitoes.
89 n mosquito cells, mammalian cells, mice, and Aedes albopictus mosquitoes.
90 he virus is transmitted by Aedes aegypti and Aedes albopictus mosquitoes.
91 ithin 100 m, p = 0.028); and total burden of Aedes albopictus (number of female and male larvae and a
92 ned diapause timing of an invasive mosquito, Aedes albopictus, on two continents.
93 volume ovitraps to control Aedes aegypti and Aedes albopictus populations has shown promise across mu
94 y, the highly invasive Asian tiger mosquito, Aedes albopictus, rapidly displaced resident populations
95 n of their shared vectors, Aedes aegypti and Aedes albopictus remains incomplete and is complicated b
96           Comparative analysis revealed that Aedes albopictus, separated from Aedes aegypti by ~35 mi
97                                     Finally, Aedes albopictus serves as a case study for how to apply
98 ngly non-linear in Aedes aegypti (Linnaeus), Aedes albopictus (Skuse), and Aedes triseriatus (Say) mo
99                    The Asian tiger mosquito, Aedes albopictus (Skuse), is an invasive species with su
100 near the homes of coinfected patients, and 1 Aedes albopictus specimen was found to be positive for b
101 y mosquito vector species: Aedes aegypti and Aedes albopictus The model was parameterized and calibra
102 of respondents where it repels the mosquito, Aedes albopictus Thus, self-anointing behavior helps to
103 so analyzed mosquito population dynamics for Aedes albopictus under ambient and microclimatic conditi
104 n by the mosquito vectors, Aedes aegypti and Aedes albopictus, using the Wolbachia symbiont.
105 s in mosquito and mammalian cells, mice, and Aedes albopictus vector mosquitoes.
106 n on the number of life-cycle completions of Aedes albopictus via its impact on local microclimates.
107 owed CHIKV to exploit a new epidemic vector, Aedes albopictus, via an A226V substitution in the E1 en
108                                              Aedes albopictus was not affected by competition in eith
109  2011, a population of Asian tiger mosquito (Aedes albopictus) was discovered in Los Angeles (LA) Cou
110  from Spodoptera exigua, Helicoverpa zea and Aedes albopictus, whereas cells from Drosophila melanoga
111 of Ae. aegypti carrying Wolbachia wAlbB from Aedes albopictus with a local strain, we generated a wAl
112 e distribution of Culex quinquefasciatus and Aedes albopictus, with Aedes aegypti concentrated in hig

 
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