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1  in the presence, but not in the absence, of Arcobacter.
2 s expression of known 'virulence' factors by Arcobacter.
3  colonized by relatives of animal-associated Arcobacter.
4 , and Halomonas, and autotrophs belonging to Arcobacter.
5 an also support mutualism, as shown here for Arcobacter and Breviatea.
6 cteria from polar sediments, and two genera, Arcobacter and Herminiimonas, are isolated for the first
7 ial OTUs were affiliated with Sulfuricurvum, Arcobacter and Sulfurospirillum spp. detected in other o
8 ized strains of Campylobacter, Helicobacter, Arcobacter, and Wolinella succinogenes and 13 Campylobac
9 ucture of a voltage-gated Na(+) channel from Arcobacter butzleri (NavAb) captured in a closed-pore co
10                                              Arcobacter butzleri and ETBF were detected in 8% and 7%
11 iglets each were infected per os with either Arcobacter butzleri ATCC 49616, Arcobacter cryaerophilus
12 pshots of the wild-type Na(V)Ab channel from Arcobacter butzleri captured in two potentially inactiva
13 rvices to annotate a newly sequenced genome--Arcobacter butzleri ED-1.
14                                              Arcobacter butzleri is an emerging pathogen that has bee
15 ructure of a prokaryotic sodium channel from Arcobacter butzleri is characterised.
16                                              Arcobacter butzleri is considered to be an emerging huma
17 ng Escherichia coli, Listeria monocytogenes, Arcobacter butzleri, Helicobacter pylori, Cryptosporidiu
18 ructure of a prokaryotic sodium channel from Arcobacter butzleri, we are able to determine the steps
19  with either Arcobacter butzleri ATCC 49616, Arcobacter cryaerophilus 1B ATCC 43159, Arcobacter skirr
20              In order to further investigate Arcobacter diversity, 792 faecal samples were collected
21 domonas, Psychromonas (Gammaproteobacteria), Arcobacter (Epsilonproteobacteria) and Herminiimonas (Be
22 e and activity of related hydrogen-consuming Arcobacter, indicating that mutualistic interaction betw
23  show that the association of L. limosa with Arcobacter is driven by the transfer of hydrogen and is
24 al Microbiome Database revealed that Vibrio, Arcobacter, Rhizobiaceae and Rhodobacteraceae sequences
25 616, Arcobacter cryaerophilus 1B ATCC 43159, Arcobacter skirrowii CCUG 10374, or the three field stra
26                    Only one of the bacteria, Arcobacter sp. (JF831360) increased substantially in rel
27 tudy examined established enteric pathogens, Arcobacter species and enterotoxigenic Bacteroides fragi
28 edding and colonization of tissues, of three Arcobacter species in 1-day-old cesarean-derived colostr
29  strains of Campylobacter, Helicobacter, and Arcobacter spp. and 59 Penner serotype reference strains
30                                              Arcobacter spp. were cultured from rectal swab samples o
31                                  At necropsy Arcobacter spp. were cultured from the liver, kidney, il
32                                              Arcobacter spp. were detected at least once in rectal sw
33                      These data suggest that Arcobacter spp., especially A. butzleri, can colonize ne
34  Thiomicrospira denitrificans and Candidatus Arcobacter sulfidicus, two chemolithoautotrophic sulfur
35  in members of the related genera Wolinella, Arcobacter, Sulfurospirillum, and Campylobacter.
36                                              Arcobacter was isolated from 42.5% of the samples and th
37                                              Arcobacters were detected in the rectal swab sample of t