ライフサイエンスコーパス: insect vector

1 ounters during residence in the sandfly, its insect vector.

2 transmission through its mammalian host and insect vector.

3 enome organization, sequence similarity, and insect vector.

4 ria parasite and both its mammalian host and insect vector.

5 omastigotes, the parasite forms found in the insect vector.

6 rtant for cell survival in the midgut of its insect vector.

7 rectly alters host selection behavior by its insect vector.

8 s to reduce pathogen transmission through an insect vector.

9 inside the alimentary tract of the sand fly insect vector.

10 ature conditions encountered in the host and insect vector.

11 the genomes of the malaria parasite and its insect vector.

12 site viability in the mammalian host and the insect vector.

13 motif responsible for interactions with the insect vector.

14 survival in both the mammalian host and the insect vector.

15 and to prevent onward spread of the virus by insect vectors.

16 s and viruses with zoonotic cycles involving insect vectors.

17 and increased susceptibility to phytoplasma insect vectors.

18 l strategies for circulative movement in all insect vectors.

19 Many plant and animal viruses are spread by insect vectors.

20 k competing microbes, and perhaps to attract insect vectors.

21 m of several plant viruses that propagate in insect vectors.

22 c development of Plasmodium parasites within insect vectors.

23 ing of the interaction between pathogens and insect vectors.

24 ic diseases are transmitted by blood-feeding insect vectors.

25 city, or are splash dispersed, soilborne, or insect vectored.

26 ved mechanism for increasing transmission by insect vectors across generations.

27 of the genus, behavioural differences among insect vectors allows for broader hypotheses that relate

28 a very rare co-occurrence of pollen with its insect vector and provides substantiating evidence that

29 ght play in the physiology of this important insect vector and suggests targets for intervention.

30 s new approaches to control infection in the insect vector and the mammalian host.

31 has a digenetic life cycle that involves the insect vector and the mammalian host.

32 ncluding histidine for stages present in the insect vectors and fatty acids by intracellular amastigo

33 naling Factor (DSF), is required to colonize insect vectors and to suppress virulence to grape.

34 e environmental changes, alternating between insect vectors and vertebrate hosts.

35 tants are able to colonize the mouthparts of insect vectors and wild-type strains but are not transmi

36 habdoviruses are persistently transmitted by insect vectors, and a few putative plant rhabdoviruses a

37 IKV replication in both vertebrate hosts and insect vectors, and for virulence in mice.

38 laria parasite Plasmodium falciparum and the insect vector Anopheles gambiae paves the way for scient

39 rasite sexual stages that persist within the insect vector, anopheline mosquitoes, or target mosquito

40 leading to acquisition of infectivity in the insect vector are now accessible to laboratory investiga

41 Insect vectors are required for the transmission of many

42 llow for crop protection, virus receptors in insect vectors are unknown.

43 se include exploitation of the same group of insect vectors (blackflies of the Simulium damnosum comp

44 sa population, introduced into grapevines by insect vectors, can multiply and spread throughout the v

45 r of the circular form is much higher in the insect vector compared with the plant, and expression le

46 t genome sequence of a bona fide Pantoea sp. insect-vectored cotton pathogen.

47 duction of host pathogens for the control of insect vectored diseases such as bovine tuberculosis or

48 ntial tool for the control or eradication of insect-vectored diseases.

49 that the pathogens are orally acquired by an insect vector during the taking of a blood meal, which d

50 The insect vector-dwelling epimastigote form of the organism

51 at LmPOT1 was expressed predominantly in the insect vector form of L. major, and immunofluorescence d

52 nditionally lethal mutations that render the insect vector form of the parasite auxotrophic for polya

53 ta adometdc null mutants were created in the insect vector form of the parasite by double targeted ge

54 mines, required spermidine for growth in its insect vector form, and was adversely impacted in its ab

55 the 1980s due to the spread of the important insect vector Frankliniella occidentalis and the discove

56 These plant viruses move through the insect vector, from the gut lumen into the hemolymph or

57 ve facilitated the agnostic interrogation of insect vector genomes, giving medical entomologists acce

58 importance worldwide as the pathogen and its insect vectors have been disseminated.

59 acts of the transmission of plant viruses by insect vectors have been studied for more than a century

60 mRNA is constitutively expressed by both the insect vector (i.e. promastigote) and mammalian (i.e. am

61 type T. cruzi across humans, reservoirs, and insect vectors in 2 acute outbreaks of presumptive oral

62 Malaria infection is initiated when the insect vector injects Plasmodium sporozoites into a susc

63 The virus route within the insect vector is amply documented in many cases, but the

64 site interacts with the immune system of the insect vector is unknown.

65 ers the course of Y. pestis infection in its insect vector, leading to a change in blood-feeding beha

66 bloodstream (mammalian host) and procyclic (insect vector) life cycle stages, and KHARON is thus cri

67 number of plant viruses are transmitted via insect vectors, little is known at the molecular level a

68 As there is no cure for HLB, insect vector management is considered one strategy to h

69 d be relevant to parasite development in the insect vector, modulates the sensitivity of trypanosomes

70 ed to human hosts by the bite of an obligate insect vector, mosquito species in the genus Anopheles,

71 tory fruit flies and wild populations of two insect vectors: mosquitoes and sandflies.

72 Here, working with Rhodnius prolixus, the insect vector of Chagas disease, we show that an ovary d

73 NAi response mainly resembling that of other insect vectors of arboviruses.

74 invertebrates at pandemic levels, including insect vectors of devastating infectious diseases.

75 s of biological properties characteristic of insect vectors of disease, such as hematophagy and compe

76 nia is attractive to many insects, including insect vectors of disease.

77 maniasis, confer polyamine auxotrophy to the insect vector or promastigote form of the parasite.

78 species through direct physical contact, via insect vectors or parasitism, are thought to underlie th

79 amended life-cycle in which wind-dispersed, insect-vectored or water-spread conidia infect ash and m

80 y in the glucose-depleted environment of the insect vector primarily on the mitochondrial oxidative p

81 clearly distinct develomental stages: in the insect vector (procyclic stage) the cells generate the b

82 f a plant virus and its interacting host and insect vector proteins determine whether a virus will be

83 ent and/or replication of the viruses in the insect vectors require specific interactions between vir

84 ted to survive in the mammalian host and the insect vector, respectively.

85 It is hypothesized that a component of insect vector saliva, rather than the parasite itself ma

86 By blocking parasite development within the insect vector, TBVs effectively disrupt transmission and

87 ider host range is likely to increase as the insects vectoring the "Ca.

88 evelopment of the Plasmodium parasite in its insect vector, the Anopheles mosquito.

89 engages in a symbiotic partnership with its insect vector, the Monochamus beetle, as well as associa

90 rth larval stage (LIV) upon encountering its insect vector, the Monochamus pine sawyer beetle, inside

91 In the insect vector, the parasite relies on amino acid catabol

92 the procyclic form (PCF) in the bloodsucking insect vector, the tsetse fly.

93 heme supplied by its vertebrate host or its insect vector, the tsetse fly.

94 ergences of the co-distributed hematophagous insect vectors, the sand fly Lutzomyia longipalpis s.l.,

95 al transfer of viruses, for example, through insect vectors; third, parallel origin from related gene

96 rasites colonize numerous metazoan hosts and insect vectors through their life cycles, with the need

97 Many pathogens that either rely on an insect vector to complete their life cycle (e.g., Trypan

98 ellular parasite transmitted from a reduviid insect vector to humans by exposure of mucosal surfaces

99 s and insects just like arboviruses that use insect vectors to infect plants.

100 es, which results in increased attraction of insect vectors to the plant, and, hence, to increased pa

101 ogical factors and transmission processes of insect-vectored viruses on the effectiveness of insectic

102 namics of disease epidemics and evolution of insect-vectored viruses.

103 Although several plant viruses infect their insect vectors, we have shown that vector infection by a

104 c stage develops in the midgut of the tsetse insect vector, where they rely on proline as carbon sour

105 in metacyclic promastigotes (the form in the insect vector which is infective to mammalian macrophage