ライフサイエンスコーパス: Aeromonas

1 ., compared to 3.0 x 10(5) for the wild-type Aeromonas.

2 ctomycetales, Acinetobacter, Pseudomonas and Aeromonas.

3 ary was used to help speciate 52 isolates of Aeromonas.

4 of TagA characterization from any species of Aeromonas.

5 f the PCR-Luminex assay were 89% and 94% for Aeromonas, 89% and 93% for Campylobacter, 96% and 95% fo

6 Aeromonas, a ubiquitous waterborne bacterium, has been p

7 ique V6 sequences represented Acinetobacter, Aeromonas and Trichococcus, which collectively account f

8 MS correctly discriminated between all Aeromonas and V. cholerae isolates.

9 these four species when members of the genus Aeromonas are isolated from human clinical sources.

10 presentative of the 17 recognized species of Aeromonas, as well as 3 reference strains from genus Vib

11 the T3SS are crucial in the pathogenesis of Aeromonas-associated infections.

12 developing isogenic mutants of the wild-type Aeromonas by using a suicide vector.

13 tly in fecal specimens, including pathogenic Aeromonas, Campylobacter jejuni, Campylobacter coli, Sal

14 We sought Aeromonas, Campylobacter, Escherichia coli O157:H7, Plei

15 Of the bacterial pathogens (Aeromonas, Campylobacter, Salmonella, and Vibrio species

16 py, whereas culture filtrates from wild-type Aeromonas caused complete destruction of the microvilli.

17 Aeromonas caviae is a Gram-negative, motile and rod-shap

18 Aeromonas caviae is a model organism for this process as

19 Aeromonas caviae Sch3N possesses a small genomic island

20 lococcus chromogenes, Staphylococcus hyicus, Aeromonas caviae, Pseudomonas aeruginosa, Stenotrophomon

21 richia coli, a finding which implies that in Aeromonas, cell division may be linked to quorum sensing

22 utagenesis were used to evaluate the role of Aeromonas cytotoxic enterotoxin (Act) in the pathogenesi

23 ly from potential surface colonizers such as Aeromonas, Enterobacter, Pseudomonas, and Thauera.

24 psC to -N, which are similar to GSP genes of Aeromonas, Erwinia, Klebsiella, Pseudomonas, and Xanthom

25 tal of 193 strains representing 14 different Aeromonas genomospecies were evaluated for 63 phenotypic

26 iated populations including Trichococcus and Aeromonas had temporal patterns similar to either Acinet

27 Human diseases caused by species of Aeromonas have been classified into two major groups: se

28 hydrophila together with either EpsE or its Aeromonas homologue, ExeE, to complement the secretion d

29 pestris (xps), Pseudomonas aeruginosa (xcp), Aeromonas hydrophila (exe), and Vibrio cholerae (eps).

30 ompetent individual with multiple strains of Aeromonas hydrophila (NF1-NF4), the latter three constit

31 e (PilA), Pseudomonas aeruginosa (PilA), and Aeromonas hydrophila (TapA).

32 Here, we demonstrate that one such, Aeromonas hydrophila AhQnr, is soluble, stable, and reli

33 Spent culture supernatants from both Aeromonas hydrophila and Aeromonas salmonicida activate

34 s a toxin secreted by the bacterial pathogen Aeromonas hydrophila and is capable of killing target ce

35 duced by Vibrio cholerae, Vibrio vulnificus, Aeromonas hydrophila and other Gram-negative bacteria.

36 in the virulence of diarrheal isolate SSU of Aeromonas hydrophila and showed that VasH, a sigma(54) a

37 five septic groups receiving an infusion of Aeromonas hydrophila at 0.2 mL/kg/hr, gradually increasi

38 The complete genome of Aeromonas hydrophila ATCC 7966(T) was sequenced.

39 ressed enolase from diarrheal isolate SSU of Aeromonas hydrophila bound to human plasminogen and faci

40 Members of the Aeromonas hydrophila complex (A. hydrophila, HG2, and A.

41 tx) of an environmental isolate ATCC 7966 of Aeromonas hydrophila consists of six genes (rtxACHBDE) o

42 Three enterotoxins from the Aeromonas hydrophila diarrheal isolate SSU have been mol

43 product displayed 87% sequence similarity to Aeromonas hydrophila ExeE, a member of the PulE (GspE) f

44 site infection with ciprofloxacin-resistant Aeromonas hydrophila following leech therapy.

45 ody group (n = 5), which received continuous Aeromonas hydrophila infusion plus antiprostacyclin anti

46 otoxin Act from a diarrheal isolate, SSU, of Aeromonas hydrophila is aerolysin related and crucial to

47 Aeromonas hydrophila is both a human and animal pathogen

48 iron transport in the fresh water bacterium Aeromonas hydrophila is found to occur by means of an in

49 a isolates, 1 Serratia marcescens isolate, 1 Aeromonas hydrophila isolate, 1 Aeromonas veronii isolat

50 Aeromonas hydrophila leads to both intestinal and extrai

51 irus or M. rosenbergii nodovirus), bacteria (Aeromonas hydrophila or Vibrio harveyi) or heavy metals

52 onicida phages (44RR2.8t, 25 and 31) and one Aeromonas hydrophila phage (Aeh1).

53 lysin-related cytotoxic enterotoxin (Act) of Aeromonas hydrophila possesses multiple biological activ

54 A cytotoxic enterotoxin (Act) of Aeromonas hydrophila possesses several biological activi

55 A cytotoxic enterotoxin (Act) of Aeromonas hydrophila possesses several biological activi

56 hC is a cytotoxic, actin-targeting mART from Aeromonas hydrophila PPD134/91.

57 ng multiple pathogens, including a strain of Aeromonas hydrophila resistant to amikacin, tobramycin,

58 Aeromonas hydrophila secretes several extracellular prot

59 Polar and lateral flagellin proteins from Aeromonas hydrophila strain AH-3 (serotype O34) were fou

60 a 5.4-kb pil gene cluster that resembles the Aeromonas hydrophila tap gene cluster and other type IV-

61 ated strains of a diarrheal isolate, SSU, of Aeromonas hydrophila that exhibited a 50 to 53% reductio

62 ated with the cytotoxic enterotoxin (Act) of Aeromonas hydrophila to examine global cellular transcri

63 mposed of EpsL and its homologue, ExeL, from Aeromonas hydrophila together with either EpsE or its Ae

64 ed with Dam was essential for attenuation of Aeromonas hydrophila virulence.

65 An Aeromonas hydrophila VolA homolog complements a V. chole

66 ncoding the cytotoxic enterotoxin (Act) from Aeromonas hydrophila was hyperexpressed with the pET, pT

67 ptic control group (n = 6), in which 1010/mL Aeromonas hydrophila was infused intravenously at 0.2 mL

68 bacterial viability of Escherichia coli and Aeromonas hydrophila were compared to spherical nanostru

69 ng the various virulence factors produced by Aeromonas hydrophila, a type II secretion system (T2SS)-

70 bp), isolated in 1971 from the fish pathogen Aeromonas hydrophila, and of the cryptic IncA/C plasmid

71 ne expression from Photorhabdus luminescens, Aeromonas hydrophila, and Vibrio parahaemolyticus are al

72 during transit through turtles colonized by Aeromonas hydrophila, leading to the hypothesis that Sdi

73 In Aeromonas hydrophila, the ahyI gene encodes a protein re

74 antagonism against Edwardsiella ictaluri and Aeromonas hydrophila, the causative agents of enteric se

75 . of Vibrio cholerae, Vibrio vulnificus, and Aeromonas hydrophila.

76 holerae and by the closely related bacterium Aeromonas hydrophila.

77 hromosomal DNA of a diarrheal isolate SSU of Aeromonas hydrophila.

78 d gene (vacB) from a clinical isolate SSU of Aeromonas hydrophila.

79 , or TagA, from a diarrheal isolate, SSU, of Aeromonas hydrophila.

80 t of a Type IIH R-M system from the pathogen Aeromonas hydrophila.

81 mal operon from the diarrheal isolate SSU of Aeromonas hydrophila.

82 onal responses to a cytotoxic enterotoxin of Aeromonas hydrophila.

83 ch by verifying a predicted effector TseC in Aeromonas hydrophila.

84 ite dynamics of apo CphA beta-lactamase from Aeromonas hydropila and its complex with a beta-lactam a

85 Two unusual cases of Aeromonas infection are described, one associated with b

86 Amikacin is a first-line treatment for Aeromonas infection due to high efficacy.

87 n related and crucial to the pathogenesis of Aeromonas infections.

88 The genus Aeromonas is one of several medically significant genera

89 We characterized a collection of 268 Aeromonas isolates from diverse sources (clinical, anima

90 cells of both reference strains and unknown Aeromonas isolates obtained from water distribution syst

91 caused by aerolysin, a pore-forming toxin of Aeromonas; it involved primarily the endoplasmic reticul

92 Aeromonas jandaei AER 14 (formerly Aeromonas sobria AER

93 number of isolates of each were as follows: Aeromonas jandaei, 17; A. schubertii, 12; A. trota, 15;

94 and accurately classify species of the genus Aeromonas, making it a powerful tool especially suited f

95 lished a role for Act in the pathogenesis of Aeromonas-mediated infections.

96 injected with a sublethal dose of wild-type Aeromonas or the revertant, but not the isogenic mutant,

97 We deleted the gene encoding Aeromonas outer membrane protein B (AopB), which is pred

98 s in the presence of the aminopeptidase from Aeromonas proteolytica (AAP) containing either Zn(II) or

99 The aminopeptidase from Aeromonas proteolytica (AAP) is uncompetitively inhibite

100 butanoy]-leucine) to the aminopeptidase from Aeromonas proteolytica (AAP) was examined by both spectr

101 d (LPA) with the leucine aminopeptidase from Aeromonas proteolytica (AAP) was investigated.

102 The aminopeptidase from Aeromonas proteolytica (AAP) was titrated with copper, w

103 tuted derivatives of the aminopeptidase from Aeromonas proteolytica (AAP) were probed by EPR spectros

104 inding properties to the aminopeptidase from Aeromonas proteolytica (AAP), and the observed divalent

105 inding inhibitors of the aminopeptidase from Aeromonas proteolytica (AAP).

106 trate selectivity of the aminopeptidase from Aeromonas proteolytica (AAP).

107 ed by the co-catalytic metallohydrolase from Aeromonas proteolytica (AAP).

108 e sites of peptidase T, carboxypeptidase G2, Aeromonas proteolytica aminopeptidase, carboxypeptidase

109 The aminopeptidase from Aeromonas proteolytica serves as a paradigm for the stud

110 inus, a substrate for an aminopeptidase from Aeromonas proteolytica.

111 solates were unrelated and provided data for Aeromonas reference genomes.

112 ernatants from both Aeromonas hydrophila and Aeromonas salmonicida activate a range of biosensors res

113 of this species, the Gram negative bacterium Aeromonas salmonicida and the virus VHSV, using microarr

114 ter membrane protein OmpA were identified in Aeromonas salmonicida by sodium dodecyl sulfate-polyacry

115 hree coliphages (RB43, RB49 and RB69), three Aeromonas salmonicida phages (44RR2.8t, 25 and 31) and o

116 In two T4 relatives that grow in Aeromonas salmonicida phages 44RR and 25, gene 43 is fra

117 proposed for Escherichia coli ATCC 25922 and Aeromonas salmonicida subsp. salmonicida ATCC 33658 at 2

118 nd Blastococcus, and by the Cys codon UGU in Aeromonas salmonicida was confirmed by metabolic labelin

119 d by IS1358 from Vibrio cholerae, ISAS1 from Aeromonas salmonicida, and H-rpt in Escherichia coli K-1

120 h the fish pathogens, Streptococcus iniae or Aeromonas salmonicida.

121 e described, one associated with bacteremia (Aeromonas schubertii) and another in which the organism

122 Aeromonas jandaei AER 14 (formerly Aeromonas sobria AER 14) expresses three inducible beta-

123 the exception of several pathogens, notably Aeromonas sp. (23.8%) by FilmArray and Yersinia enteroco

124 ate that they were potential human pathogens Aeromonas sp., Stenotrophomonas sp. and an unculturable

125 acterial pore-forming toxins (aerolysin from Aeromonas species and alpha-toxin from Staphylococcus au

126 d a response regulator were cloned from each Aeromonas species and termed ahyRI and asaRI, respective

127 reening tests and familiarity with the newer Aeromonas species could prevent initial misidentificatio

128 was linked to raffinose fermentation in all Aeromonas species except A. jandaei.

129 rveillance cultures and a stool culture grew Aeromonas species from three patients over a 6-week peri

130 he most frequent pathogen), Giardia lamblia, Aeromonas species, Campylobacter species, and rotavirus

131 rom ahyI and asaI, respectively, and in both Aeromonas species, the genes downstream have been identi

132 Fifty-six isolates of four Aeromonas species, which have been documented as causati

133 mpylobacter jejuni, Salmonella enterica, and Aeromonas spp.

134 s known about the colonization mechanisms of Aeromonas spp.

135 are few reports of aminoglycoside-resistant Aeromonas spp.

136 allenge strains: Acinetobacter spp. (n = 9), Aeromonas spp. (n = 8), Chryseobacterium spp. (n = 28),

137 A survey of different Aeromonas spp. by PCR revealed that possession of two ta

138 ) of 23 rDNA-positive patients, grouped with Aeromonas spp. in phylogenetic studies.

139 ding some identified in clinical isolates of Aeromonas spp. or Vibrio spp., may confer upon this orga

140 lysin is a channel-forming toxin secreted by Aeromonas spp. that binds to glycosyl phosphatidylinosit

141 lysin, a channel-forming protein secreted by Aeromonas spp., which is structurally and functionally r

142 he crop, comprising the genetically amenable Aeromonas veronii and a Rikenella-like bacterium.

143 was recovered from an infected gall bladder (Aeromonas veronii biotype veronii).

144 To define the role of Bfp in Aeromonas veronii bv. Sobria adherence, a 22-kb locus en

145 stigate the metal-binding sites of ImiS from Aeromonas veronii bv. sobria in catalytically active (1-

146 s isolate, 1 Aeromonas hydrophila isolate, 1 Aeromonas veronii isolate, 2 Chryseobacterium meningosep

147 s at 1 dpf with individual bacterial species Aeromonas veronii or Vibrio cholerae was sufficient to b

148 ation with the resident intestinal bacterium Aeromonas veronii results in elevated epithelial cell pr

149 Aeromonas veronii, one of the leech symbionts, can be ge

150 hogens were important in selected sites (eg, Aeromonas, Vibrio cholerae O1, Campylobacter jejuni).

151 unusual or aberrant properties for the genus Aeromonas were also detected in the collection of 428 st

152 uced virulence in mice compared to wild-type Aeromonas when injected intraperitoneally (i.p.).