ライフサイエンスコーパス: pea aphid

1 as a major effect on feeding behavior in the pea aphid.

2 luded potential apparent competition with AR pea aphids.

3 tic basis of a male wing polymorphism in the pea aphid Acyrthosiphon pisum (Hemiptera: Aphididae).

4 not negatively affect the performance of the pea aphid Acyrthosiphon pisum Harris, a sap-feeding inse

5 Genetic diversity in the pea aphid Acyrthosiphon pisum was investigated by a rest

6 in two highly specialized host races of the pea aphid (Acyrthosiphon pisum pisum; Hemiptera : Aphidi

7 f a mutually obligate symbiosis, between the pea aphid (Acyrthosiphon pisum) and its maternally trans

8 lf-matings between two parental genotypes of pea aphid (Acyrthosiphon pisum) differing in virulence o

9 protein is important in the survival of the pea aphid (Acyrthosiphon pisum) on fava bean, a host pla

10 We use the pea aphid (Acyrthosiphon pisum) to address this problem.

11 ants are also compromised in immunity to the pea aphid (Acyrthosiphon pisum), for which Arabidopsis i

12 e three most common facultative symbionts of pea aphid (Acyrthosiphon pisum), the bacterium Regiella

13 nsa, increase the fitness of their host, the pea aphid (Acyrthosiphon pisum), under natural condition

14 l for the study of incipient speciation, the pea aphid (Acyrthosiphon pisum).

15 esistance has been previously documented for pea aphids (Acyrthosiphon pisum) attacked by the parasit

16 Experiments on pea aphids (Acyrthosiphon pisum) have demonstrated that

17 of settling and survival on dodder vines by pea aphids (Acyrthosiphon pisum) were reduced significan

18 oth ecological and evolutionary responses of pea aphids (Acyrthosiphon pisum), a common agricultural

19 In pea aphids (Acyrthosiphon pisum), several inherited endo

20 hanced binding and toxicity against both the pea aphid, Acyrthosiphon pisum, and the green peach aphi

21 The pea aphid, Acyrthosiphon pisum, maintains extreme variat

22 s (PEMV) coat protein (CP) in the gut of the pea aphid, Acyrthosiphon pisum, using a far-Western blot

23 Armet, namely as an effector protein in the pea aphid, Acyrthosiphon pisum.

24 ivery of fused proteins into the hemocoel of pea aphids, Acyrthosiphon pisum, without virion assembly

25 an) in red and green colour morphs of clonal pea aphids, Acyrthosiphon pisum.

26 ions of secondary symbionts carried by 1,104 pea aphids, Acyrthosiphon pisum.

27 CR pea aphids always had fitness losses when on broad bean

28 nomes were consistently abundant in infected pea aphids, and related phages were found in all tested

29 Pea aphids are typically unwinged but produce winged off

30 Inoculation of pea aphid Armet protein into tobacco leaves induced a tr

31 Pea aphid Armet's physical and chemical properties and i

32 ) were found to differ in ability to protect pea aphids attacked by the parasitoid Aphidius ervi.

33 atiles that attract parasitic wasps, and the pea aphid can carry facultative endosymbiotic bacteria t

34 We confirm that three types of pea aphid clones coexist in natural populations, those p

35 predation in complex agricultural mosaic on pea aphid clover and alfalfa races.

36 Host-associated races of pea aphid discriminate between plant species in race-spe

37 Pea aphids display a red-green color polymorphism, which

38 tative symbioses in Acyrthosiphon pisum (the pea aphid) for vulnerability of the aphid host to a hyme

39 We compared pea aphid gene expression between bacteriocytes and othe

40 pped reads from the re-sequencing data of 33 pea aphid genomes from individuals specialized on differ

41 lycosylated receptor aminopeptidase N in the pea aphid gut and is transcytosed across the gut epithel

42 Insertion of a 12-aa pea aphid gut-binding peptide by adding to or replacing

43 Pea aphids have an obligate nutritional symbiosis with t

44 as dramatic effects on the heat tolerance of pea aphid hosts (Acyrthosiphon pisum).

45 ng seven strains of Buchnera aphidicola from pea aphid hosts.

46 rial symbionts, which occur in a majority of pea aphids in field populations.

47 The wing polyphenism of pea aphids is a compelling laboratory model with which t

48 lysis reveals that male wing polymorphism in pea aphids is determined by a single locus, two alleles

49 potential source of physiological stress in pea aphids is infection by other microorganisms, includi

50 Our results suggest that feeding behavior in pea aphids is neither simple nor highly polygenic.

51 We placed experimental populations of two pea aphid lines, each with and without symbionts, in fiv

52 olyphenism is transgenerational, in that the pea aphid mother experiences the environmental signals,

53 rotein C002 is crucial in the feeding of the pea aphid on fava bean.

54 ss on clover race (CR) and alfalfa race (AR) pea aphids on broad bean, red clover and alfalfa alone.

55 Plants fed upon by pea aphids release volatiles that attract parasitic wasp

56 a bellii (a tick-associated bacterium) and a pea-aphid Rickettsia.

57 In the pea aphid, some of the seven known species of facultativ

58 ed proteins have extensive homology with the pea aphid SymL and Escherichia coli GroEL chaperonin.

59 Pea aphids thus obtain protection from natural enemies t

60 lant virus pea enation mosaic virus into the pea aphid vector.

61 By amplifying DNA from hemolymph of infected pea aphids, we obtained a set of genomic sequences of H.

62 he genetic basis of wing polymorphism in the pea aphid, which can produce either winged or wingless m