ライフサイエンスコーパス: Photorhabdus

1 s immune response is induced specifically by Photorhabdus.

2 serves to highlight the similarities between Photorhabdus, a genus of bacteria that infects invertebr

3 e time as being pathogenic to insect larvae, Photorhabdus also have a mutualistic relationship with e

4 e against diverse strains of Xenorhabdus and Photorhabdus and was not correlated with phylogenetic di

5 Photorhabdus and Xenorhabdus appear very similar at the

6 s controlling pathogenicity and mutualism in Photorhabdus and Xenorhabdus are very different.

7 Photorhabdus and Xenorhabdus bacteria colonize the intes

8 Photorhabdus and Xenorhabdus bacteria therefore engage i

9 Bacteria belonging to the genera Photorhabdus and Xenorhabdus participate in a trilateral

10 edge of the molecular mechanisms utilized by Photorhabdus and Xenorhabdus to control their host-depen

11 69 strains of the entomopathogenic bacteria Photorhabdus and Xenorhabdus were analyzed by MALDI-MS(2

12 as within Citrobacter, Erwinia, Escherichia, Photorhabdus, and Yersinia species.

13 Photorhabdus are bacteria found colonizing the gut of a

14 re, recently identified clinical isolates of Photorhabdus are helping us to understand how human path

15 suggesting that aspects of iron metaboism in Photorhabdus are important during the symbiosis with the

16 The dual nature of Photorhabdus as a pathogen and mutualist makes it a supe

17 oU homologs from Pseudomonas fluorescens and Photorhabdus asymbiotica also localized to the plasma me

18 we apply RVA to the emerging human pathogen Photorhabdus asymbiotica using "gain of toxicity" assays

19 tion system in the insect and human pathogen Photorhabdus asymbiotica.

20 lated organisms Photorhabdus luminescens and Photorhabdus asymbiotica.

21 Photorhabdus bacteria have recently been established as

22 Photorhabdus bacteria live in a 'symbiosis of pathogens'

23 The nature of the insecticidal activity of Photorhabdus bacteria was investigated for its potential

24 duce in the insect cadaver by feeding on the Photorhabdus biomass.

25 Photorhabdus can be isolated in two phenotypically disti

26 Adherent Photorhabdus cells in maternal nematode intestines had t

27 Photorhabdus colonization of Heterorhabditis bacteriopho

28 The toxin complex (tc) genes of Photorhabdus encode insecticidal, high molecular weight

29 icant overlap in the genetic requirements of Photorhabdus for these contrasting interactions.

30 Members of the gammaproteobacterial Photorhabdus genus share mutualistic relationships with

31 As Photorhabdus has never been found outside a host animal,

32 iles (IJs) of Heterorhabditis, which contain Photorhabdus in their gut, can infect and kill Drosophil

33 etion of the plasmid-encoded homologs of the Photorhabdus insect-related (Pir) toxins PirA and PirB.

34 Once inside the insect the IJ release Photorhabdus into the haemolymph where the bacteria rapi

35 Photorhabdus is a genus of entomopathogenic Gram-negativ

36 Photorhabdus is a genus of insect-pathogenic bacteria th

37 Photorhabdus is a member of the family Enterobacteriacea

38 Photorhabdus is a potent insect pathogenic bacterium tha

39 ase TccC3 from the insect bacterial pathogen Photorhabdus luminescence modifies actin to force its ag

40 for transport of TccC3 toxin and established Photorhabdus luminescence TccC3 as a toxin suitable for

41 Both the bacterium Photorhabdus luminescens alone and its symbiotic Photorh

42 ir response against two pathogenic bacteria (Photorhabdus luminescens and Enterococcus faecalis) and

43 as well as in the closely related organisms Photorhabdus luminescens and Photorhabdus asymbiotica.

44 al alternative toxin genes from the bacteria Photorhabdus luminescens and Xenorhabdus nematophilus.

45 Photorhabdus luminescens bacteria have a variable life h

46 nematodes that have evolved a mutualism with Photorhabdus luminescens bacteria to function as highly

47 The tcdA gene of Photorhabdus luminescens encodes a 283-kDa protein, toxi

48 The entomopathogenic bacterium Photorhabdus luminescens exhibits phase variation when c

49 The lux operon derived from Photorhabdus luminescens incorporated into bacterial gen

50 ade by insertion of the luxCDABE operon from Photorhabdus luminescens into the P. syringae chromosome

51 Photorhabdus luminescens is a pathogen of insects that s

52 The bacterium Photorhabdus luminescens is a symbiont of the entomopath

53 Photorhabdus luminescens is carried in the gut of the in

54 Photorhabdus luminescens is known for its symbiosis with

55 Photorhabdus luminescens is released into the insect blo

56 Although Photorhabdus luminescens is symbiotic with nematodes tha

57 re transformed with plasmid DNA containing a Photorhabdus luminescens lux operon (luxABCDE) that was

58 ndom fusions of E. coli chromosomal DNA to a Photorhabdus luminescens luxCDABE reporter allowed preci

59 random fusions of Escherichia coli DNA to a Photorhabdus luminescens luxCDABE reporter was used as a

60 d fusions of random E. coli DNA fragments to Photorhabdus luminescens luxCDABE were screened for biol

61 enterica subsp. enterica serovar Typhi CT18, Photorhabdus luminescens subsp. laumondii TT01, Chromoba

62 The Gram-negative entomopathogenic bacterium Photorhabdus luminescens symbiotically lives in insect-i

63 identified an orphan protein (Plu2236) from Photorhabdus luminescens that catalyzes stilbene epoxida

64 B (TcdB2) and class C (TccC3) proteins from Photorhabdus luminescens to the Xenorhabdus XptA2 protei

65 Differential metabolomic profiling in Photorhabdus luminescens TT01 and Xenorhabdus nematophil

66 -type strain killed the potential competitor Photorhabdus luminescens TT01.

67 synthase hybrid biosynthetic gene cluster in Photorhabdus luminescens using genome synteny analysis.

68 f the fatty acid (FA) reductase complex from Photorhabdus luminescens was coupled with aldehyde decar

69 the activators of T3SS gene expression from Photorhabdus luminescens, Aeromonas hydrophila, and Vibr

70 resistance gene, a modified lux operon from Photorhabdus luminescens, and approximately 650 bp of ho

71 hi genomes, and in the database sequences of Photorhabdus luminescens, and Chromobacterium violaceum.

72 bditis bacteriophora, its bacterial symbiont Photorhabdus luminescens, and the fruit fly Drosophila m

73 The bacterium, Photorhabdus luminescens, is an insect pathogen that als

74 nsect pathogens, Xenorhabdus nematophila and Photorhabdus luminescens, produce rhabduscin, an amidogl

75 ed a toxin secreted by a different bacterium Photorhabdus luminescens, which lives in the gut of ento

76 ith the TcdA1 component of the Tc toxin from Photorhabdus luminescens, which preferentially kills ins

77 f the different life stages of the bacterium Photorhabdus luminescens, which resulted in the isolatio

78 al data for the LuxAB and Fre reactions from Photorhabdus luminescens-the source of modern Lux report

79 ional gene in the entomopathogenic bacterium Photorhabdus luminescens.

80 toxin encoding genes of the insect pathogen Photorhabdus luminescens.

81 group, as is a defective prophage element in Photorhabdus luminescens.

82 pilloides and the entomopathogenic bacteria, Photorhabdus luminescens.

83 e excreted by the entomopathogenic bacterium Photorhabdus luminescens.

84 During the course of infection, Photorhabdus multiplies rapidly within the insect, produ

85 Screening 8000 Photorhabdus mutants for defects in IJ colonization reve

86 orhabdus luminescens alone and its symbiotic Photorhabdus-nematode complex are known to be highly pat

87 ive toxins from V. vulnificus, Yersinia sp., Photorhabdus sp., and Xenorhabdus sp.; and a filamentous

88 Xenorhabdus and Photorhabdus species dedicate a large amount of resource

89 y could lead to an understanding of how some Photorhabdus species have made the leap to becoming huma

90 Photorhabdus species produce a family of stilbenes, with

91 Xenorhabdus and Photorhabdus spp. are gram negative gamma proteobacteria

92 Toxin complexes from Xenorhabdus and Photorhabdus spp. bacteria represent novel insecticidal

93 logical studies suggest that Xenorhabdus and Photorhabdus spp. may serve as valuable model systems fo

94 ver, we have analyzed more than 90 different Photorhabdus strains by HPLC/MS and showed that these DA

95 Maternal nematodes acquire Photorhabdus symbionts as a persistent intestinal biofil

96 In this study we use Photorhabdus temperata K122 to show that genes involved

97 In this study, we use Photorhabdus temperata strain K122 to show that these pr

98 Here, we describe novel genomic islands from Photorhabdus that are involved in symbiosis and pathogen

99 aratuses, such as type VI secretion systems, Photorhabdus virulence cassettes, and R-type tailocins.

100 native root positions; the nematode symbiont Photorhabdus was identified as a disruptor whose omissio

101 rm burrows into insect prey and regurgitates Photorhabdus, which goes on to kill the insect.