ライフサイエンスコーパス: bacterial symbiont

1 eals an unexpected toxin-producing defensive bacterial symbiont.

2 an extreme sex-ratio distortion caused by a bacterial symbiont.

3 unction in interactions with insect hosts or bacterial symbionts.

4 algarvensis, a gutless marine worm, and its bacterial symbionts.

5 cascades to tissues housing light-producing bacterial symbionts.

6 and share the products with sulfate-reducing bacterial symbionts.

7 xonomic groups harbor maternally transmitted bacterial symbionts.

8 gellates are typically colonized by specific bacterial symbionts.

9 logical functions of colonization factors in bacterial symbionts.

10 ized with a consortium of 15 sequenced human bacterial symbionts, 13 of which harbored one or more pr

11 Wolbachia is a common maternally inherited bacterial symbiont able to induce crossing sterilities k

12 Bacterial symbionts and fungal and bacterial pathogens i

13 These bacterial symbionts and pathogens each contain a homolog

14 rrently known about the interactions between bacterial symbionts and their hosts.

15 transmitted micro-organisms, but while their bacterial symbionts are well-studied, little is known ab

16 udy we investigate a mutation in an obligate bacterial symbiont (Buchnera), which has dramatic effect

17 stratified water and can harbor diazotrophic bacterial symbionts, but does not support eutrophication

18 control groups, the predominant families of bacterial symbionts change with each larval instar despi

19 ri (Hemiptera: Pseudococcidae) contains dual bacterial symbionts existing with an unprecedented organ

20 s at deep-sea hydrothermal vents depend upon bacterial symbionts for nutrition, and thus the mechanis

21 are cooperatively constructed to deliver the bacterial symbiont from the root surface to cells in the

22 Most insect groups harbor obligate bacterial symbionts from the alpha-proteobacterial genus

23 a horizontal gene transfer is targeted to a bacterial symbiont, further blurring the distinction bet

24 The role of symbiosis in bacterial symbiont genome evolution is well understood,

25 Upon colonizing juvenile squids, bacterial symbionts grow on host-supplied nutrients, whi

26 e to A. ervi is infection by the facultative bacterial symbiont Hamiltonella defensa.

27 between angiosperms and nitrogen-fixing (N2) bacterial symbionts housed in nodules.

28 ng the association between mealybugs and two bacterial symbionts, Husnik et al. (2013) demonstrated t

29 New research suggests that secondary bacterial symbionts in insects act as a mechanism for ho

30 Animals house a community of bacterial symbionts in their digestive tracts that contr

31 These clams host chemoautotrophic bacterial symbionts in their gills that synthesize organ

32 complex symbioses with at least two obligate bacterial symbionts, inhabiting specialized host cells (

33 cated that the LPS behaves similar to intact bacterial symbionts, interacting with host cells in the

34 Before maternally inherited bacterial symbionts like Wolbachia, which cause cytoplas

35 Animals are typically colonized by diverse bacterial symbionts, many of which are commensal and, in

36 Nevertheless, bacterial symbionts may play an important role in determ

37 ourced from two known mechanisms: protective bacterial symbionts, most commonly Hamiltonella defensa,

38 Sinorhizobium meliloti is a nitrogen-fixing bacterial symbiont of alfalfa and related legumes.

39 o select for strains of Wolbachia wMelPop (a bacterial symbiont of fruit flies) that differed in copy

40 (QS) in Sinorhizobium meliloti, the N-fixing bacterial symbiont of Medicago host plants, involves at

41 ago sativa and Arabidopsis thaliana) and the bacterial symbiont of one of these species (Sinorhizobiu

42 ecies Sin-1, a nitrogen-fixing Gram-negative bacterial symbiont of Sesbania, was determined by compos

43 le bacterium Vibrio fischeri is the specific bacterial symbiont of the Hawaiian squid Euprymna scolop

44 The bacterial symbiont of the hydrothermal vent tubeworm fix

45 We investigated bacterial symbionts of Adelges tsugae, a pest of hemlock

46 Maternally inherited bacterial symbionts of arthropods are common, yet symbio

47 t is hosted by a ciliated protist, Euplotes; bacterial symbionts of ciliates are still poorly known b

48 Bacterial symbionts of fungus-growing ants occupy a high

49 y genomes have been discovered from numerous bacterial symbionts of insect hosts.

50 ve been described from nutrient-provisioning bacterial symbionts of several insect lineages [1-5].

51 Exceptions to this rule are found among the bacterial symbionts of surgeonfish; Epulopiscium spp. ar

52 n marine invertebrates and their cooperative bacterial symbionts offer access to an understanding of

53 nematode Heterorhabditis bacteriophora, its bacterial symbiont Photorhabdus luminescens, and the fru

54 s (including some thyasirid species) without bacterial symbionts show no comparable foot extension be

55 RaxP and RaxQ are similar to the bacterial symbiont Sinorhizobium meliloti host specifici

56 plants to nodulation factors produced by the bacterial symbiont Sinorhizobium meliloti using a dual-d

57 ion, the absence of a known obligate partner bacterial symbiont suggests that Uzinura alone can suppl

58 ave formed stable associations with pairs of bacterial symbionts that live in specialized cells and p

59 Many animals show intimate interactions with bacterial symbionts that provision hosts with limiting n

60 rein we highlight metabolic contributions of bacterial symbionts that reside within tsetse flies, bed

61 one strategy used by maternally transmitted bacterial symbionts to boost transmission and spread in

62 mes that form indeterminate nodules in which bacterial symbionts undergo terminal differentiation.

63 ly stages of the squid-vibrio symbiosis, the bacterial symbiont Vibrio fischeri encounters host-deriv

64 In aphids, facultative bacterial symbionts, which benefit hosts by conferring r

65 other microorganisms, including facultative bacterial symbionts, which occur in a majority of pea ap

66 The obligate bacterial symbiont Wigglesworthia glossinidia is critica

67 We found that introducing a bacterial symbiont with a protective (but not a non-prot

68 oskeleton through the activity of an ancient bacterial symbiont with a tiny genome that serves as a f

69 at these mobile genetic elements can endow a bacterial symbiont with benefits that extend to the anim

70 Vibrio fischeri is the bacterial symbiont within the light-emitting organ of th

71 The bacterial symbiont Wolbachia can cause cytoplasmic incom

72 rnative to traditional control measures, the bacterial symbiont Wolbachia has been transferred from D

73 any maternally inherited factor such as the bacterial symbiont Wolbachia.