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1 ature conditions encountered in the host and insect vector.
2  the genomes of the malaria parasite and its insect vector.
3  motif responsible for interactions with the insect vector.
4  survival in both the mammalian host and the insect vector.
5 ounters during residence in the sandfly, its insect vector.
6 e arbovirus preservation within its whitefly insect vector.
7  in the procyclic developmental stage in the insect vector.
8 itating viral transmission by attracting the insect vector.
9 osine monophosphate (cAMP) expression of its insect vector.
10 smitted from plant to plant by thrips as the insect vector.
11  inside the alimentary tract of the sand fly insect vector.
12 site viability in the mammalian host and the insect vector.
13  transmission through its mammalian host and insect vector.
14 enome organization, sequence similarity, and insect vector.
15 ria parasite and both its mammalian host and insect vector.
16 omastigotes, the parasite forms found in the insect vector.
17 rtant for cell survival in the midgut of its insect vector.
18 rectly alters host selection behavior by its insect vector.
19 s to reduce pathogen transmission through an insect vector.
20 c development of Plasmodium parasites within insect vectors.
21 ing of the interaction between pathogens and insect vectors.
22 ic diseases are transmitted by blood-feeding insect vectors.
23  global agriculture by rapidly spreading via insect vectors.
24 istance, and on host plant interactions with insect vectors.
25        Many plant viruses are transmitted by insect vectors.
26 n food security and are often transmitted by insect vectors.
27 tor activity and population proliferation of insect vectors.
28 netic relationships among Wolbachia of other insect vectors.
29 ess and viral transmission capacity of their insect vectors.
30 and to prevent onward spread of the virus by insect vectors.
31 must import it from their mammalian hosts or insect vectors.
32 s and viruses with zoonotic cycles involving insect vectors.
33  and increased susceptibility to phytoplasma insect vectors.
34 l strategies for circulative movement in all insect vectors.
35  Many plant and animal viruses are spread by insect vectors.
36 k competing microbes, and perhaps to attract insect vectors.
37 e spatiotemporal dynamics of phytoplasmas in insect vectors.
38 m of several plant viruses that propagate in insect vectors.
39 city, or are splash dispersed, soilborne, or insect vectored.
40 ved mechanism for increasing transmission by insect vectors across generations.
41  of the genus, behavioural differences among insect vectors allows for broader hypotheses that relate
42                                              Insect vectors also bite nonhuman hosts, linking them in
43 e tool that can rapidly detect INSV from its insect vector and from plants.
44 ever, the impact(s) of DcFLV presence on the insect vector and its interaction with the CLas phytopat
45 a very rare co-occurrence of pollen with its insect vector and provides substantiating evidence that
46 ght play in the physiology of this important insect vector and suggests targets for intervention.
47 te Trypanosoma brucei alternates between the insect vector and the mammalian host and proliferates th
48 has a digenetic life cycle that involves the insect vector and the mammalian host.
49 s new approaches to control infection in the insect vector and the mammalian host.
50                          Human movement into insect vector and wildlife reservoir habitats determines
51 ncluding histidine for stages present in the insect vectors and fatty acids by intracellular amastigo
52  intensified interactions between pathogens, insect vectors and people around habitat edges.
53 strategies to interact with their hemipteran insect vectors and plant hosts.
54  provide novel opportunities for controlling insect vectors and plant viruses, which can be used in t
55 iruses can modulate the interactions between insect vectors and plants via the jasmonate, salicylic a
56 naling Factor (DSF), is required to colonize insect vectors and to suppress virulence to grape.
57 e environmental changes, alternating between insect vectors and vertebrate hosts.
58 tants are able to colonize the mouthparts of insect vectors and wild-type strains but are not transmi
59 nnected network model that incorporates both insect-vectored and sexual transmission of this pathogen
60 habdoviruses are persistently transmitted by insect vectors, and a few putative plant rhabdoviruses a
61 tobacco and periwinkle, CLas-bearing psyllid insect vectors, and CLas cocultured with other bacteria
62 IKV replication in both vertebrate hosts and insect vectors, and for virulence in mice.
63        The interactions among plant viruses, insect vectors, and host plants have been well studied;
64 ticidal techniques that reduce the number of insect vectors, and population modification (replacement
65  viral modulation of plant interactions with insect vectors, and suggest future directions of researc
66 laria parasite Plasmodium falciparum and the insect vector Anopheles gambiae paves the way for scient
67 rasite sexual stages that persist within the insect vector, anopheline mosquitoes, or target mosquito
68 leading to acquisition of infectivity in the insect vector are now accessible to laboratory investiga
69 inable and effective means to control flying insect vectors are critically needed, especially with wi
70                                              Insect vectors are required for the transmission of many
71                                              Insect vectors are responsible for spreading many infect
72 llow for crop protection, virus receptors in insect vectors are unknown.
73 plant viruses manipulating behavior of their insect vectors as a strategy to maximize infection of pl
74 s retained for a far shorter duration in its insect vector (Bemisia tabaci whitefly) than had previou
75 se include exploitation of the same group of insect vectors (blackflies of the Simulium damnosum comp
76 nt in the insect pest control and preventing insect vector-borne human diseases.
77 cell abscission of the procyclic form in the insect vector, but is necessary for the initiation of ce
78 been observed on the outer midgut surface of insect vectors, but not in planta.
79 lar mechanism to increase transmission to an insect vector by exploitation of a mammalian complement
80 sa population, introduced into grapevines by insect vectors, can multiply and spread throughout the v
81  lectin targeting a2,6-linked sialic acid in insect vector cells.
82 tin targeting alpha2,6-linked sialic acid in insect vector cells.
83 excellent adaptive advantages for CLs during insect vector colonization helping with host retention,
84 r of the circular form is much higher in the insect vector compared with the plant, and expression le
85 s (subjected to standard Ministry of Health, Insect Vector Control efforts).
86 t genome sequence of a bona fide Pantoea sp. insect-vectored cotton pathogen.
87 ily rhythms in the blood-feeding activity of insect vectors determine the time of day that parasites
88 duction of host pathogens for the control of insect vectored diseases such as bovine tuberculosis or
89 ntial tool for the control or eradication of insect-vectored diseases.
90 that the pathogens are orally acquired by an insect vector during the taking of a blood meal, which d
91                                          The insect vector-dwelling epimastigote form of the organism
92 mammalian-infective bloodstream form and the insect vector-dwelling procyclic form.
93 natural antibody to facilitate mating in the insect vector establishes a new paradigm of parasite-hos
94                        Plant viruses rely on insect vectors for transmission among plant hosts, but m
95 at LmPOT1 was expressed predominantly in the insect vector form of L. major, and immunofluorescence d
96 nditionally lethal mutations that render the insect vector form of the parasite auxotrophic for polya
97 ta adometdc null mutants were created in the insect vector form of the parasite by double targeted ge
98 mines, required spermidine for growth in its insect vector form, and was adversely impacted in its ab
99 the 1980s due to the spread of the important insect vector Frankliniella occidentalis and the discove
100         These plant viruses move through the insect vector, from the gut lumen into the hemolymph or
101 ve facilitated the agnostic interrogation of insect vector genomes, giving medical entomologists acce
102 importance worldwide as the pathogen and its insect vectors have been disseminated.
103 acts of the transmission of plant viruses by insect vectors have been studied for more than a century
104               Often, plant viruses and their insect vectors have multiple potential host plant specie
105 mRNA is constitutively expressed by both the insect vector (i.e. promastigote) and mammalian (i.e. am
106 ce the duration a pathogen is retained in an insect vector (i.e., retention period) is of particular
107 type T. cruzi across humans, reservoirs, and insect vectors in 2 acute outbreaks of presumptive oral
108              Phytoplasmas are transmitted by insect vectors in a persistent propagative manner; howev
109 for the fundamental life-cycle components of insect vectors in the laboratory.
110    Utilizing a representative mammalian host-insect vector infection and transmission model, we provi
111      Malaria infection is initiated when the insect vector injects Plasmodium sporozoites into a susc
112                   The virus route within the insect vector is amply documented in many cases, but the
113 site interacts with the immune system of the insect vector is unknown.
114                              The presence of insect vectors is a key prerequisite for transmission of
115 ers the course of Y. pestis infection in its insect vector, leading to a change in blood-feeding beha
116  bloodstream (mammalian host) and procyclic (insect vector) life cycle stages, and KHARON is thus cri
117  number of plant viruses are transmitted via insect vectors, little is known at the molecular level a
118                 As there is no cure for HLB, insect vector management is considered one strategy to h
119                                    Moreover, insect vectors may not prefer plant species to which pla
120                                              Insect vector microbiomes are essential for insect funct
121 d be relevant to parasite development in the insect vector, modulates the sensitivity of trypanosomes
122 ed to human hosts by the bite of an obligate insect vector, mosquito species in the genus Anopheles,
123 tory fruit flies and wild populations of two insect vectors: mosquitoes and sandflies.
124    Here, working with Rhodnius prolixus, the insect vector of Chagas disease, we show that an ovary d
125 NAi response mainly resembling that of other insect vectors of arboviruses.
126  invertebrates at pandemic levels, including insect vectors of devastating infectious diseases.
127 solution for long-lasting protection against insect vectors of disease could be attained by manipulat
128 s of biological properties characteristic of insect vectors of disease, such as hematophagy and compe
129 nia is attractive to many insects, including insect vectors of disease.
130 , and fungal pathogens, parasitic weeds, and insect vectors of plant pathogens.
131 er molecular testing of either tree hosts or insect vectors offer feasible alternatives.
132 maniasis, confer polyamine auxotrophy to the insect vector or promastigote form of the parasite.
133 species through direct physical contact, via insect vectors or parasitism, are thought to underlie th
134  amended life-cycle in which wind-dispersed, insect-vectored or water-spread conidia infect ash and m
135 sizes and genes with longer exons; moreover, insect-vectored pathogens possess fewer genes compared t
136  estimates for many diseases, especially for insect-vectored pathogens, such as Flavescence doree (FD
137 ) is widely applicable and relevant to other insect-vectored plant pathogen systems involving multipl
138 demonstrate how SAP05 protein effectors from insect-vectored plant pathogenic phytoplasmas take contr
139 n the plant but serve as attractants for the insect vector, presumably promoting pathogen spread in a
140 ough these viruses do not replicate in their insect vectors, previous studies have demonstrated virul
141 y in the glucose-depleted environment of the insect vector primarily on the mitochondrial oxidative p
142 clearly distinct develomental stages: in the insect vector (procyclic stage) the cells generate the b
143 f a plant virus and its interacting host and insect vector proteins determine whether a virus will be
144 interactions between pathogens/parasites and insect vectors remain poorly understood.
145 ent and/or replication of the viruses in the insect vectors require specific interactions between vir
146 ted to survive in the mammalian host and the insect vector, respectively.
147 ed among eukaryotes, but SAP05 does not bind insect vector RPN10.
148       It is hypothesized that a component of insect vector saliva, rather than the parasite itself ma
149 borne viruses, infect vertebrate species and insect vectors separated by hundreds of millions of year
150 n of other eukaryotic pathogens inside their insect vectors, such as Plasmodium spp, Trypanosoma bruc
151 uired to complete the parasitic cycle in the insect vector, suggesting that FRDg may play a role in t
152  By blocking parasite development within the insect vector, TBVs effectively disrupt transmission and
153 ematodes and arthropods worldwide, including insect vectors that transmit dengue, West Nile, and Zika
154 onmental drivers influence life processes of insect vectors that transmit human disease.
155 gellated parasitic protozoan, and within the insect vector the parasite transitions from the trypomas
156 ider host range is likely to increase as the insects vectoring the "Ca.
157 evelopment of the Plasmodium parasite in its insect vector, the Anopheles mosquito.
158 us") on physiochemical conditions within its insect vector, the Asian citrus psyllid (ACP), and wheth
159  engages in a symbiotic partnership with its insect vector, the Monochamus beetle, as well as associa
160 rth larval stage (LIV) upon encountering its insect vector, the Monochamus pine sawyer beetle, inside
161                                       In the insect vector, the parasite relies on amino acid catabol
162  heme supplied by its vertebrate host or its insect vector, the tsetse fly.
163 the procyclic form (PCF) in the bloodsucking insect vector, the tsetse fly.
164 ergences of the co-distributed hematophagous insect vectors, the sand fly Lutzomyia longipalpis s.l.,
165 al transfer of viruses, for example, through insect vectors; third, parallel origin from related gene
166 rasites colonize numerous metazoan hosts and insect vectors through their life cycles, with the need
167        Many pathogens that either rely on an insect vector to complete their life cycle (e.g., Trypan
168 ellular parasite transmitted from a reduviid insect vector to humans by exposure of mucosal surfaces
169 e SRBSDV proliferation; this also repels the insect vector to reduce infestation.
170 rdable methods of detecting pathogens inside insect vectors to facilitate surveillance.
171 s and insects just like arboviruses that use insect vectors to infect plants.
172 ch cases, can plant viruses manipulate their insect vectors to preferentially feed and oviposit on pl
173 es, which results in increased attraction of insect vectors to the plant, and, hence, to increased pa
174 pathogenic insect viruses (baculoviruses) or insect-vectored viruses (e.g., flaviviruses, alphaviruse
175                                        Thus, insect-vectored viruses appear to traffic in opposite di
176                                 In addition, insect-vectored viruses must also navigate through the p
177           Both insect pathogenic viruses and insect-vectored viruses must navigate through the polari
178 ogical factors and transmission processes of insect-vectored viruses on the effectiveness of insectic
179                                          For insect-vectored viruses, an oppositely oriented process
180 namics of disease epidemics and evolution of insect-vectored viruses.
181  Although several plant viruses infect their insect vectors, we have shown that vector infection by a
182 c stage develops in the midgut of the tsetse insect vector, where they rely on proline as carbon sour
183 nd precise compositional microanalysis of an insect vector which can contribute to the early detectio
184 in metacyclic promastigotes (the form in the insect vector which is infective to mammalian macrophage
185 nteraction may alter the physiology of their insect vector, which may also promote the growth and tra
186 ilitate understanding of its role within the insect vector, which may assist in developing tools for
187 d interactions of host plant, phloem-feeding insect vector with endosymbionts and persistently transm
188                  The recent outbreaks of the insect-vectored Zika virus have demonstrated its potenti

 
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