ライフサイエンスコーパス: Aeromonas

1 ctomycetales, Acinetobacter, Pseudomonas and Aeromonas.

2 ., compared to 3.0 x 10(5) for the wild-type 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 Patescibacteria, and Myxococcota) and genus (Aeromonas and NS11.12_marine_group) levels that effectiv

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

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

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

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

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

13 s a beta-pore-forming toxin produced by most Aeromonas bacteria, which has attracted large attention

14 obiome-depleted fish with sorbitol-degrading Aeromonas bacterial strains rescued the steatotic liver

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

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

17 were tested for 9 bacterial enteropathogens: Aeromonas, Campylobacter, Escherichia coli O157, other S

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

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

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

21 le CMP-Pse5Ac7Ac synthetase enzyme PseF from Aeromonas caviae and utilise it in combination with the

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

23 Aeromonas caviae is a model organism for this process as

24 Aeromonas caviae Sch3N possesses a small genomic island

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

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

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

28 Two isolates (A and B) from fatal cases of Aeromonas dhakensis bacteremia were characterized using

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

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

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

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

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

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

35 pathogenic Gram negative bacteria, including Aeromonas hydrophila (AhlABC).

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

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

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

39 lytic bacteriophage infecting hypervirulent Aeromonas hydrophila (vAh) was isolated and characterize

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

41 e A. dhakensis SSU and environmental isolate Aeromonas hydrophila American Type Culture Collection_79

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

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

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

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

46 n of three pathogens, Aeromonas salmonicida, Aeromonas hydrophila and Vibrio harveyi, to Atlantic sal

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

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

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

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

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

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

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

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

55 le for survive of the Mugil cephalus against Aeromonas hydrophila infection.

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

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

58 Aeromonas hydrophila is both a human and animal pathogen

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

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

61 Aeromonas hydrophila leads to both intestinal and extrai

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

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

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

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

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

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

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

69 Aeromonas hydrophila secretes several extracellular prot

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

71 ciitis (NF) caused by mixed infection with 4 Aeromonas hydrophila strains (NF1-NF4).

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

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

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

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

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

77 An Aeromonas hydrophila VolA homolog complements a V. chole

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

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

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

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

82 nological increase in Mugil cephalus against Aeromonas hydrophila, according to the current research.

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

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

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

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

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

88 holerae and by the closely related bacterium Aeromonas hydrophila.

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

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

91 due to motile Aeromonas septicemia caused by Aeromonas hydrophila.

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

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

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

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

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

97 onal responses to a cytotoxic enterotoxin of Aeromonas hydrophila.

98 monella enterica, Staphylococcus aureus, and Aeromonas hydrophilia were observed across sample types.

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

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

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

102 One hundred five patients with Aeromonas infections and 112 isolates were identified, t

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

104 The genus Aeromonas is one of several medically significant genera

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

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

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

108 Aeromonas jandaei AER 14 (formerly Aeromonas sobria AER

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

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

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

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

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

114 LuxR(ARM81ld) detects host Aeromonas-produced C4-HSL, and in response, activates th

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

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

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

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

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

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

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

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

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

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

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

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

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

128 acterial strains from four genera, including Aeromonas, Pseudomonas, Shewanella, and Sphingopyxis.

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

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

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

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

133 , we monitored the real-time evolution of an Aeromonas salmonicida clone in response to successive an

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

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

136 W) or particulated bacterin from an atypical Aeromonas salmonicida strain.

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

138 ative bacteria, namely Lactococcus garvieae, Aeromonas salmonicida subsp. salmonicida, and Yersinia r

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

140 n challenged with bacterial (formalin-killed Aeromonas salmonicida) or viral-like (polyriboinosinic p

141 we investigated adhesion of three pathogens, Aeromonas salmonicida, Aeromonas hydrophila and Vibrio h

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

143 ring controlled challenges with the pathogen Aeromonas salmonicida.

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

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

146 economic losses in aquaculture due to motile Aeromonas septicemia caused by Aeromonas hydrophila.

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

148 ddition, the optimal recognition sequence of Aeromonas sobria proline aminopeptidase was determined b

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

150 Coculture of V. fischeri with the Aeromonas sp. ARM81 lysogen suppresses phage ARM81ld vir

151 M81ld is a prophage of the aquatic bacterium Aeromonas sp. ARM81, and it encodes a homolog of a bacte

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

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

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

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

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

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

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

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

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

161 E coli, Shigella spp (non-dysentery cases), Aeromonas spp, Cryptosporidium spp, and Entamoeba histol

162 mpylobacter jejuni, Salmonella enterica, and Aeromonas spp.

163 s known about the colonization mechanisms of Aeromonas spp.

164 are few reports of aminoglycoside-resistant Aeromonas spp.

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

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

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

168 ostic methods may aid in identifying correct Aeromonas spp. of significant clinical importance.

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

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

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

172 e, we describe a mucin-sensing pathway in an Aeromonas symbiont of zebrafish, Aer01.

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

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

175 e repeating unit of the exopolysaccharide of Aeromonas veronii bv.

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

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

178 By tracking the experimental evolution of Aeromonas veronii in gnotobiotic zebrafish, we identify

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

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

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

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

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

184 Aeromonas virulence may not be entirely dependent on the

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

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