ライフサイエンスコーパス: Mycobacterium marinum

1 ram-positive bacterium Bacillus subtilis, or Mycobacterium marinum.

2 ents of lipooligosaccharide IV (LOS-IV) from Mycobacterium marinum.

3 r for the analysis of culture filtrates from Mycobacterium marinum.

4 m tuberculosis, Mycobacterium bovis BCG, and Mycobacterium marinum.

5 complexity, the secreted protein fraction of Mycobacterium marinum.

6 istinct patterns of innate susceptibility to Mycobacterium marinum.

7 nd mel2, that affect macrophage infection by Mycobacterium marinum.

8 urally susceptible to tuberculosis caused by Mycobacterium marinum.

9 acterium tuberculosis, and 85.9% homology to Mycobacterium marinum.

10 urA-katG loci in the nontuberculous pathogen Mycobacterium marinum.

11 alyse the initial response of neutrophils to Mycobacterium marinum, a close genetic relative of M. tu

12 generated a mutation in the erp homologue of Mycobacterium marinum, a close genetic relative of M. tu

13 urally susceptible to tuberculosis caused by Mycobacterium marinum, a close genetic relative of the c

14 ographic structure determination of NAT from Mycobacterium marinum, a close relative of the pathogeni

15 Finally, we show that Mycobacterium marinum, a model organism for M. tuberculo

16 r and its consequences during infection with Mycobacterium marinum, a natural fish pathogen.

17 Mycobacterium marinum, a natural pathogen of fish and fr

18 Here we show that Mycobacterium marinum, a natural pathogen of fish and fr

19 Mycobacterium marinum, a relatively rapid-growing fish a

20 Mycobacterium marinum, a well-recognized cutaneous patho

21 In Mycobacterium marinum, an established model for ESX-1 se

22 Here we inactivated the oxyR gene in Mycobacterium marinum, an organism used to model M. tube

23 collaborated to characterize an outbreak of Mycobacterium marinum and other nontuberculous mycobacte

24 ycolyl-diarabino-glycerol, was purified from Mycobacterium marinum and subsequently identified as a 5

25 sterase) in the opportunistic human pathogen Mycobacterium marinum and the characterization of this m

26 or studying mycobacterial pathogenesis using Mycobacterium marinum and the goldfish, Carassius auratu

27 andii, is closely related to M. ulcerans and Mycobacterium marinum, and as further evidence is gather

28 Mycobacterium ulcerans and Mycobacterium marinum are closely related pathogens whic

29 Mycobacterium tuberculosis and Mycobacterium marinum are thought to exert virulence, in

30 re challenged with Salmonella typhimurium or Mycobacterium marinum at earlier stages of development,

31 teins and a complex protein mixture from the Mycobacterium marinum bacterial secretome.

32 is essential for ESX-5-mediated secretion in Mycobacterium marinum, but for which the role in secreti

33 duction was isolated from the photochromogen Mycobacterium marinum by heterologous complementation of

34 network that results in iniBAC induction in Mycobacterium marinum By transposon mutagenesis, we iden

35 In zebrafish, we find that susceptibility to Mycobacterium marinum can result from either inadequate

36 Mycobacterium marinum causes long-term subclinical granu

37 Mycobacterium marinum causes tuberculosis-like disease i

38 We describe a case of Mycobacterium marinum demonstrating robust cord formatio

39 Mycobacterium marinum, found commonly in salt water and

40 Mycobacterium marinum grows at an optimal temperature of

41 Mycobacterium marinum has recently been used as a model

42 screen for determinants of susceptibility to Mycobacterium marinum identified a hypersusceptible muta

43 However, analysis of Mycobacterium marinum in zebrafish has shown that the ea

44 Mycobacterium marinum-infected zebrafish are used to stu

45 Here, we deploy Mycobacterium marinum-infected zebrafish larvae for in v

46 We monitored transparent Mycobacterium marinum-infected zebrafish live to conduct

47 We report a case of cutaneous Mycobacterium marinum infection in a renal transplant re

48 we examine the pathogenesis associated with Mycobacterium marinum infection in the fly.

49 es host immune responses in vivo, we studied Mycobacterium marinum infection in two different hosts:

50 f the tuberculous granuloma in the zebrafish-Mycobacterium marinum infection model, which is characte

51 restricting mycobacteria growth, we examined Mycobacterium marinum infection of Drosophila S2 cells.

52 et al., (2016) using the zebrafish model of Mycobacterium marinum infection provides new insights in

53 Mycobacterium marinum is a pathogenic mycobacterial spec

54 Mycobacterium marinum is a waterborne pathogen responsib

55 Mycobacterium marinum is an established model for discov

56 Mycobacterium marinum is closely related to Mycobacteriu

57 ation to conclude that the MMAR_0039 gene in Mycobacterium marinum is required to promote Esx-1 expor

58 Mycobacterium marinum, like Mycobacterium tuberculosis,

59 We have found a Mycobacterium marinum locus of two genes that is require

60 We recently constructed a Mycobacterium marinum mel2 locus mutant, which is known

61 antimicrobial activity was assessed against Mycobacterium marinum (Mm) (a model for Mtb), Pseudomona

62 tion using the esxA/esxB knockout strains of Mycobacterium marinum (Mm) and Mtb.

63 uberculosis, and the second vector tested in Mycobacterium marinum (Mm).

64 Here, using the zebrafish-Mycobacterium marinum model, we found that mycobacterial

65 Within 1 day of injection of Mycobacterium marinum, MsNramp expression was highly ind

66 Mycobacterium marinum mutants with transposon insertions

67 In Drosophila infected with Mycobacterium marinum, mycobacterium-induced STAT activi

68 We characterized the Mycobacterium marinum phagosome by using a variety of en

69 erculosis, and its close pathogenic relative Mycobacterium marinum, preferentially recruit and infect

70 We conducted a genetic screen to identify Mycobacterium marinum strains which failed to lyse amoeb

71 Drosophila melanogaster infected with Mycobacterium marinum suffer metabolic wasting similar t

72 However, work in zebrafish infected with Mycobacterium marinum suggests that granulomas contribut

73 We analyzed the gene expression profile of Mycobacterium marinum, the cause of fish and amphibian t

74 several genes preferentially expressed when Mycobacterium marinum, the cause of fish and amphibian t

75 cobacterium liflandii, and the fish pathogen Mycobacterium marinum; the structural diversity in the m

76 cobacterium bovis Bacille Calmette-Guerin or Mycobacterium marinum to thiacetazone, a second line ant

77 We show here that superinfecting Mycobacterium marinum traffic rapidly into preexisting g

78 ecent studies have shown that superinfecting Mycobacterium marinum traffic rapidly to established fis

79 A screen of Mycobacterium marinum transposon mutant library led to i

80 e secretion of PE_PGRS proteins by screening Mycobacterium marinum transposon mutants for secretion d

81 Finally, we show that flies infected with Mycobacterium marinum undergo a process like wasting: Th

82 A carboxylic acid reductase (CAR) from Mycobacterium marinum was found to convert a wide range

83 a transposon insertion mutant (cpsA::Tn) of Mycobacterium marinum was studied.

84 we determined for the intracellular pathogen Mycobacterium marinum whether it uses conserved strategi

85 regulating the levels of ESX-1 substrates in Mycobacterium marinum WhiB6 is a transcription factor th

86 gravis developed a cutaneous infection with Mycobacterium marinum, which apparently resolved followi

87 Using Mycobacterium marinum-zebrafish and the surrogate MsmRv3

88 Using the Mycobacterium marinum-zebrafish model, Cronan et al. (20