ライフサイエンスコーパス: proteobacteria

1 ability is probably widespread among aquatic proteobacteria.

2 tivity over the ATPase turnover in the alpha-proteobacteria.

3 ed Bacteroidetes and Firmicutes with reduced Proteobacteria.

4 ly related to the genera Paracoccus of alpha-Proteobacteria.

5 is widespread and conserved among the gamma-proteobacteria.

6 on of TH17-related genes was associated with Proteobacteria.

7 bserved between biopsy eosinophil values and Proteobacteria.

8 ription factor CuxR in plant symbiotic alpha-proteobacteria.

9 from cyanobacteria, mitochondria arose from proteobacteria.

10 DNA binding protein conserved in most gamma-proteobacteria.

11 evolved more recently as a direct target in Proteobacteria.

12 Bacilli (Firmicutes), and in alpha and beta Proteobacteria.

13 erial community dominated by beta- and gamma-Proteobacteria.

14 mechanism of F1F0-ATPase regulation in alpha-proteobacteria.

15 his has not been demonstrated in other alpha-proteobacteria.

16 d in bacteria as phylogenetically distant as proteobacteria.

17 n and growth rate among 13 strains of marine Proteobacteria.

18 ccinyl-CoA in non-plant eukaryotes and alpha-proteobacteria.

19 nstructed SahR regulons in the genomes of 62 Proteobacteria.

20 portance to the specific lifestyles of alpha-proteobacteria.

21 ctinobacteria, Bacteroidetes, Firmicutes and Proteobacteria.

22 n mice primarily by decreasing the levels of Proteobacteria.

23 ly similar to that of chloroplasts and other proteobacteria.

24 acterium belonging to sulfur-degrading alpha-proteobacteria.

25 re found in other Actinobacteria, as well as Proteobacteria.

26 which are also conserved among diverse alpha-Proteobacteria.

27 ust was low, but dominated by Firmicutes and Proteobacteria.

28 istinct genes in a set of 22 alpha and gamma proteobacteria.

29 pecies and in many polarly flagellated gamma proteobacteria.

30 RYGB; 37% of increased bacteria belonged to Proteobacteria.

31 ms using KCl as a main osmoprotectant to the Proteobacteria.

32 in relative abundances of Actinobacteria and Proteobacteria.

33 ded Enterococcus, Streptococcus, and various Proteobacteria.

34 of the phyla Firmicutes, Bacteroidetes, and Proteobacteria.

35 characterized by a relative expansion of the Proteobacteria.

36 pical of the enzymes from actinobacteria and proteobacteria.

37 teria, Chloroflexi, Deinococcus-Thermus, and Proteobacteria.

38 acteriodetes and a corresponding increase in Proteobacteria.

39 ion pathways and transcriptional regulons in Proteobacteria.

40 samples were Actinobacteria, Firmicutes, and Proteobacteria.

41 throughout the Firmicutes, Fusobacteria and Proteobacteria.

42 alN catabolism and its regulation in diverse Proteobacteria.

43 acteroidetes, Firmicutes, Actinobacteria and Proteobacteria.

44 ous pathway that arose specifically in alpha-proteobacteria.

45 unctions is widely distributed in pathogenic Proteobacteria.

46 g results from bacteriophage infecting gamma-Proteobacteria.

47 ent growth inhibition (CDI) systems of gamma-proteobacteria.

48 of the phyla Firmicutes, Bacteroidetes, and Proteobacteria.

49 d consensus-degenerate primers targeting the Proteobacteria.

50 characterized by a preponderance (c. 90%) of Proteobacteria.

51 a(13)C taxa, with methane-metabolizing gamma-proteobacteria.

52 present in beta-, gamma-, delta- and epsilon-proteobacteria.

53 ately drawn from the phyla Bacteroidetes and Proteobacteria.

54 Fusobacteria, Firmicutes, Actinobacteria and Proteobacteria.

55 red community dominated by Acidobacteria and Proteobacteria.

56 bacteria, NBs are found exclusively in gamma-proteobacteria.

57 -oxidizing genes under sulfide stress in the Proteobacteria.

58 rides reduced the prevalence of inflammatory Proteobacteria.

59 LB), is a non culturable member of the alpha-proteobacteria.

60 h the phyla Anaerolinea, Ignavibacteria, and Proteobacteria.

61 teins from beta-, gamma-, delta- and epsilon-proteobacteria.

62 nolytic gene clusters from Bacteroidetes and Proteobacteria.

63 free-living and obligate intracellular alpha-proteobacteria.

64 ed with the Alphaproteobacteria class of the Proteobacteria.

65 system which is highly conserved among gamma-proteobacteria.

66 f Paracoccus denitrificans and related alpha-proteobacteria.

67 H was primarily represented by heterotrophic Proteobacteria.

68 th the medicated pigs showing an increase in Proteobacteria (1-11%) compared with nonmedicated pigs a

69 S sequences, followed by Firmicutes (12.0%), Proteobacteria (10.4%), Verrucomicrobia (1.2%) and Syner

70 lostridia (48.5%), Bacilli (27.9%), and beta-Proteobacteria (13.4%).

71 ominated by three phyla: Firmicutes (62.9%), Proteobacteria (29.9%) and Fusobacteria (9.6%).

72 he microbiota (90%), whereas in digesta both Proteobacteria (47%) and Firmicutes (38%) showed high ab

73 e the office environment was predominated by Proteobacteria (55.2%).

74 rity), primarily from Firmicutes (92.6%) and Proteobacteria (6.9%), via 16S rRNA gene amplicon sequen

75 e chicken blood microbiota were dominated by Proteobacteria (60.58% +/- 0.65) followed by Bactroidete

76 ovel lineages of podoviruses infecting alpha-proteobacteria, a bacterial class critical to oceanic ca

77 ase subgroup 1beta in tested alpha- and beta-proteobacteria, a branched-chain aminotransferase in tes

78 la related to Firmicutes, Bacteroidetes, and Proteobacteria accelerated manure biodegradation likely

79 Porphyromonas gingivalis or ligature, gamma-proteobacteria accumulate and stimulate host immune resp

80 ial sequences were related to Cyanobacteria, Proteobacteria, Actinobacteria and Bacteriodetes previou

81 "and "F-type" which were highly abundant in Proteobacteria, Actinobacteria and Firmicutes, respectiv

82 The microbiome was dominated by Proteobacteria, Actinobacteria, Bacteroidetes, Chlorofle

83 The metagenomic analysis showed that Proteobacteria, Actinobacteria, Bacteroidetes, Cyanobact

84 Firmicutes increased sharply, whereas Proteobacteria, Actinobacteria, Cyanobacteria and Acidob

85 They commonly occurred in the phyla of Proteobacteria, Actinobacteria, Firmicutes, and Cyanobac

86 ntained 5 major bacterial phyla: Firmicutes, Proteobacteria, Actinobacteria, Fusobacterium, and Bacte

87 In delta-proteobacteria, an additional cysteine tRNA with an 8/4

88 Chloroflexi and Crenarchaeota, but lower for Proteobacteria and Actinobacteria in highly contaminated

89 oportion of oxygen-tolerant organisms of the Proteobacteria and Actinobacteria phyla associated with

90 ated by specific groups/species belonging to Proteobacteria and Actinobacteria phyla; however, simila

91 Heterotrophic Proteobacteria and Actinobacteria were isolated from Lak

92 sity between mothers, an overall increase in Proteobacteria and Actinobacteria, and reduced richness.

93 ession of these genes have been predicted in proteobacteria and actinobacteria.

94 bited low diversity communities dominated by Proteobacteria and Actinobacteria.

95 f GapR, which are ubiquitous among the alpha-proteobacteria and are encoded on multiple bacteriophage

96 Proteobacteria and Bacteroidetes persisted in WD-fed FXR

97 Proteobacteria and Bacteroidetes rhodopsins were the mos

98 The soybean rhizosphere was enriched in Proteobacteria and Bacteroidetes, and had relatively low

99 ory system is conserved throughout the gamma-proteobacteria and controls key pathways in central carb

100 raries from the four mats were similar, with Proteobacteria and Cyanobacteria being the most abundant

101 on is typified by both expansions in aerobic Proteobacteria and decreases in anaerobic Firmicutes and

102 g the 15 phyla identified, the abundances of Proteobacteria and Deferribacteres were changed in infec

103 ortunistic pathogens belonging to the phylum Proteobacteria and Enterococcus genus have also been lin

104 cription factor, YjiE, which is conserved in proteobacteria and eukaryotes.

105 and phylogenetic diversity, was dominated by Proteobacteria and Euryarchaeota and was significantly e

106 al changes following ZVI exposure, with more Proteobacteria and fewer Bacteroidetes in the ZVI-amende

107 Proteobacteria and Firmicutes penetrated small intestina

108 unities are dominated by the bacterial phyla Proteobacteria and Firmicutes.

109 in both bloom and control samples with Alpha-proteobacteria and Gamma-proteobacteria being the predom

110 Data showed that the dominant alpha-proteobacteria and gamma-proteobacteria communities in b

111 a proportional increase in the gram negative Proteobacteria and gram positive Actinobacteria phyla; t

112 omoserine lactones is the paradigm for QS in Proteobacteria and is particularly well understood in th

113 ride, a cell wall component of Gram-negative Proteobacteria and known inducer of lupus in mice, into

114 ersity and an altered composition, with more Proteobacteria and less Bacteroidetes compared with heal

115 corticosteroids alone led to enrichment for Proteobacteria and members of other phyla.

116 gues are present in alpha-, beta-, and gamma-proteobacteria and multiple eukaryotes, including humans

117 nd identified a protein termed BioR in alpha-proteobacteria and predicted that BioR would have the bi

118 ned on a normal diet (including increases in Proteobacteria and striking decreases in Bacterioidetes)

119 ugh MapZ orthologs/homologs is widespread in proteobacteria and that the use of allosterically regula

120 e different symbiont phylotypes (one epsilon-proteobacteria and two gamma-proteobacteria) that formed

121 by a reduction in the relative abundance of Proteobacteria and Verrucomicrobia (specifically Akkerma

122 bligate methanotrophs belonging to the Phyla Proteobacteria and Verrucomicrobia require oxygen for re

123 real growth phenotype datasets for E. coli, proteobacteria and yeast.

124 ce of Bacteroidetes, followed by Firmicutes, Proteobacteria, and Actinobacteria phyla.

125 otypes across the Bacteroidetes, Firmicutes, Proteobacteria, and Actinobacteria, the four most common

126 nes serve as quorum-sensing signals for many Proteobacteria, and acyl-homoserine lactone signaling is

127 obiota devoid of opportunistic pathogens and Proteobacteria, and conventional SPF mice that harbor a

128 s of other P. putida strains, in other gamma-Proteobacteria, and in beta- and alpha-Proteobacteria, f

129 ded in a wide range of host-associated alpha-proteobacteria, and it is likely that the VtlR genetic s

130 found that CrsR is conserved in many aquatic proteobacteria, and most of the time it is associated wi

131 terized by increased numbers of Akkermansia, Proteobacteria, and TM7 in the GF diet group.

132 tified a core earthworm community comprising Proteobacteria ( approximately 50%) and Actinobacteria (

133 Many Proteobacteria are capable of quorum sensing using N-acy

134 Several species of delta proteobacteria are capable of reducing insoluble metal o

135 Members of the phylum Proteobacteria are most prominent among bacteria causing

136 spectroscopic properties Nap from different Proteobacteria are phylogenetically distinct.

137 gamma-Proteobacteria are produced in the majority of mixed fun

138 N2 fixation rates indicates that these gamma-proteobacteria are unlikely to be responsible for previo

139 n oral, nasal, stool, skin, and vagina, with Proteobacteria as the dominant phylum (60 %).

140 is CbiX can generally be identified in alpha-proteobacteria as the terminal enzyme of siroheme biosyn

141 tial, including members of Bacteroidetes and Proteobacteria, as well as several poorly characterized

142 on in the gut--Bacteroidetes, Firmicutes and Proteobacteria--as well as one aerobic pathogen (Staphyl

143 1 month (P = .02 and P = .01) and the phylum Proteobacteria at 12 months of age (P = .02).

144 al classes that are active in the gut (gamma-Proteobacteria, Bacilli and Actinobacteria), all of whic

145 ne phyla, among which the most abundant were Proteobacteria, Bacteroidetes and Chloroflexi.

146 otic microbial assemblages were dominated by Proteobacteria, Bacteroidetes, and Actinobacteria.

147 bacteria in C. elegans habitats, with phyla Proteobacteria, Bacteroidetes, Firmicutes, and Actinobac

148 The proteobacteria Bdellovibrio bacteriovorus and Micavibrio

149 eobacteria dominated in Stage 1, but epsilon-Proteobacteria became more important in Stages 2 and 3,

150 omposition of the ileal bacterial community (Proteobacteria became the most abundant species).

151 samples with Alpha-proteobacteria and Gamma-proteobacteria being the predominant classes detected.

152 attern emerged with Bacteria from the phylum Proteobacteria being the prominent taxon among the fores

153 largely conserved at the phylum level, with Proteobacteria (beta-proteobateria), Bacteroidetes, and

154 species richness, and relative abundance of Proteobacteria, but was negatively correlated with relat

155 plants include nitrogen-fixing Gram-negative proteobacteria called rhizobia that are able to interact

156 ow here that the evolution of gene blocks in proteobacteria can be described by a small set of events

157 d with low-grade inflammation, and harboring proteobacteria can drive and/or instigate chronic coliti

158 in the sediments were facultative anaerobic Proteobacteria capable of coping with OAI-associated red

159 d in three main groups: select heterotrophic Proteobacteria, chemoautotrophic Thaumarchaeota, and pho

160 e bacteria in the clouds belong to the gamma-Proteobacteria class, among which the Pseudomonas genus

161 Perturbations eliciting an expansion of Proteobacteria coincided with ectopic lesions and tissue

162 obacteria, but depleted in Bacteroidetes and Proteobacteria common to mammalians, is compositionally

163 the dominant alpha-proteobacteria and gamma-proteobacteria communities in bulk soil and root endosph

164 months, when the microbiota had stabilized, Proteobacteria, comprising gram-negative organisms, were

165 In gamma-proteobacteria, CsrA activity is competitively antagoniz

166 in all steps while the relative abundance of Proteobacteria decreased as processing progressed.

167 y increased abundance of the bacterial phyla Proteobacteria, Deferribacteres, and TM7, among which th

168 Firmicutes (appearance of Erysipelotrichi), Proteobacteria (Desulfovibrionales) and Verrucomicrobia,

169 mation, and had already evolved before alpha-proteobacteria developed into mitochondria.

170 sputum total leukocyte values (predominantly Proteobacteria) differed markedly from those associated

171 Mic60 homologues from alpha-proteobacteria display the same membrane deforming activ

172 irmicutes-dominant, whereas WT TPN mice were Proteobacteria-domiant.

173 Proteobacteria dominated in immature stages while Firmic

174 Based on pyrosequencing analyses, beta-Proteobacteria dominated in Stage 1, but epsilon-Proteob

175 In mucosa, Proteobacteria dominated the microbiota (90%), whereas i

176 63; 95% CI, 1.22-5.32; P = 0.015), and gamma-proteobacteria domination of fecal microbiota (HR, 2.64;

177 5% CI, 1.42-31.80; P = 0.016), whereas gamma-proteobacteria domination predicted PCs postengraftment

178 Postengraftment PCs and gamma-proteobacteria domination were predictive of mortality.

179 The mechanisms enabling the outgrowth of Proteobacteria during inflammation are incompletely unde

180 hat in contrast to other characterised Gamma-proteobacteria, E. coli Sxy is positively autoregulated

181 A few species in the class of gamma-proteobacteria encode a cytoplasmic N-glycosylation syst

182 However, the observation that proteobacteria encode a large number of GGDEF proteins,

183 representation in any of the disease groups, Proteobacteria, Enterobacteriaceae, and Escherichia were

184 ctinobacteria, Bacteroidetes, Firmicutes and Proteobacteria (especially Roseobacter of its alpha line

185 Transient high levels of proteobacteria, especially enterobacteria species includ

186 icantly decreased, while those of the phylum Proteobacteria, especially the family Enterobacteriaceae

187 typing of IgA-coated cecal microbiota showed Proteobacteria evading antibody coating in the TLR5(-/-)

188 specificity are widespread in all classes of Proteobacteria, except Deltaproteobacteria, and in flowe

189 ocathode bacterial community was enriched in Proteobacteria, exoelectrogens, and putative producers o

190 Antibiotic treatment, leading to Proteobacteria expansion, further enhanced gluten-induce

191 microbial diversity reduction occurred with Proteobacteria expansion.

192 o the previously characterized fusobacteria, proteobacteria, firmicutes, and bacteroidetes.

193 dicate that multi-domain proteins evolved in Proteobacteria for specific functions in maintaining cel

194 gamma-Proteobacteria, and in beta- and alpha-Proteobacteria, for example, in genomes of Enterobacteri

195 rom OP11, Actinobacteria, Bacteroidetes, and Proteobacteria found in high relative abundance across a

196 ti MCE domain-containing proteins evolved in Proteobacteria from single-domain proteins.

197 The relative abundance of Proteobacteria, Gammaproteobacteria, Enterobacteriales,

198 eterocystous cyanobacteria and heterotrophic proteobacteria had the genetic potential for N2 fixation

199 xamined osmoprotection in the photosynthetic Proteobacteria Halorhodospira halophila and Halorhodospi

200 In particular, outgrowth of gamma-proteobacteria has been linked to the etiology of inflam

201 lation in Caulobacter, indicating that alpha-proteobacteria have retained HvyA activity.

202 nt homology to Francisella tularensis (gamma-proteobacteria) have been characterized in several tick

203 e found in the genomes of other marine alpha-proteobacteria, implying lipid renovation is a common st

204 detected in association with an expansion of Proteobacteria in both UC and CD, while expression of li

205 well as a dramatic increase of Gram-negative Proteobacteria in HFD+BDL versus CTRL+BDL mice.

206 revealed unique, competition-based roles for Proteobacteria in multiple distinct habitats.

207 the proportion of the phylum Firmicutes and Proteobacteria in stool was significantly decreased and

208 observed a significantly higher abundance of Proteobacteria in the anterior nares in non-SSTI partici

209 c bypass is the comparative overabundance of Proteobacteria in the distal gut microbiome, which is di

210 revealed decreased Firmicutes and increased Proteobacteria in ulcerated sites, as compared with heal

211 tinobacteria (including M. tuberculosis) and Proteobacteria (including Escherichia coli).

212 acteria, Actinobacteria, Verrucomicrobia and Proteobacteria (including SAR11).

213 0 orthologues are found in a subset of alpha-proteobacteria, including Agrobacterium tumefaciens Usin

214 is an important nutrient for several alpha-2 Proteobacteria, including N2-fixing plant endosymbionts

215 site, and was dominated by alpha- and beta- proteobacteria, including Rhodobacter, Methylibium, Rhod

216 Other highly labeled species were primarily Proteobacteria, including: Mesorhizobium sp., Variovorax

217 Sequences of gram-negative Proteobacteria increased from 1% to 46% with monensin, b

218 genetic level, Bacteroidetes decreased while Proteobacteria increased in the CRS group at the phylum

219 receptors were found in different classes of proteobacteria, indicating that this mode of response to

220 ites, but CsrA in bacteria outside the gamma-proteobacteria is antagonized by a protein called FliW.

221 achnospiraceae/Clostridiales), the second by Proteobacteria (Klebsiella/Enterobacter), the third by B

222 al mucosal tissue, and fusobacteria and beta-Proteobacteria levels increased with advancing cancer st

223 o-Bacteroidetes ratios and endotoxin-bearing Proteobacteria levels-but also maintains intestinal barr

224 ifferently than what was described for other proteobacteria like Escherichia coli We argue that this

225 In several Proteobacteria, LuxI-type enzymes catalyze the biosynthe

226 obacteriaceae family of human gut-associated Proteobacteria maintain a GUS operon under the transcrip

227 clear that T2S is largely restricted to the Proteobacteria, occurring in many, but not all, genera i

228 a similar Hg(II) uptake mechanism within the proteobacteria of accidental Hg(II) transport through he

229 roteins encoded in the genomes of other beta-proteobacteria of the Azoarcus/Thauera group further sug

230 Proteobacteria often co-ordinate responses to carbon sou

231 f the variation in the relative abundance of Proteobacteria on the skin of healthy individuals, suppo

232 or bacteria, likely reflecting the ancestral proteobacteria origin of mitochondria.

233 was the dominant phylum in MF pups, whereas Proteobacteria (P < 0.001) and Bacteroidetes (P < 0.05)

234 Fusobacteria (p < 0.007) and epsilon- Proteobacteria (p < 0.01) were enriched on tumour when c

235 utes (P </=0.001), fusobacteria (P = 0.003), proteobacteria (P </=0.001), synergistetes (P = 0.04), a

236 tinobacteria, Bacteroidetes, Firmicutes, and Proteobacteria phyla, we found that potent Nod-like rece

237 profoundly significant increase in taxa from Proteobacteria phylum in comparison to healthy subjects.

238 d after supplementation with a member of the Proteobacteria phylum, an enteroadherent Escherichia col

239 reased at exacerbation were primarily of the Proteobacteria phylum, including nontypical COPD pathoge

240 of some functional microorganisms, including Proteobacteria, Planctomycetales, Acinetobacter, Pseudom

241 However, many proteobacteria possess LuxR receptors, yet lack any LuxI

242 ellicle biofilms formed by Bacteroidetes and Proteobacteria (predominantly of the alpha and gamma cla

243 n isolate of the SAR11 clade of marine alpha-proteobacteria, produces methane from MPn, stoichiometri

244 cterization revealed a high Bacteroidetes to Proteobacteria ratio in healthy animals.

245 tures in many lower organisms, in particular proteobacteria, remains poorly understood and incomplete

246 r enrichment or reductions of Firmicutes and Proteobacteria, respectively, at a false discovery rate

247 tingly, alignments of FlgG from most epsilon proteobacteria reveal a conserved site of modification.

248 ding Actinobacteria, alpha-,beta-, and gamma-proteobacteria, revealing a common role of this Amadori

249 apples and reconstructed microbiomes: alpha-Proteobacteria-rich communities promote proliferation, w

250 ection of the phosphate-sensing machinery in proteobacteria shows that adaptive, not neutral, mutatio

251 In the gamma-proteobacteria, small non-coding RNAs (sRNAs) use molecu

252 idium clusters IV and XIVa and a decrease in Proteobacteria species.

253 among soil bacteria with Actinobacteria and Proteobacteria, specifically Betaproteobacteria and Gamm

254 In alpha-proteobacteria, strict regulation of cell cycle progress

255 bic bacteria and an expansion of facultative Proteobacteria such as commensal E. coli.

256 oidaceae was reduced, whereas Firmicutes and Proteobacteria, such as Ruminococcaceae, Lachnospiraceae

257 logs of FlgJ produced by the beta- and gamma-proteobacteria, such as Salmonella enterica, Vibrio spp.

258 in various archaea, cyanobacteria, and some proteobacteria, such as the enterobacterium, Serratia sp

259 Three phyla, Proteobacteria, Tenericutes and TM7, and 11 genera, incl

260 ed in a genome from a different subphylum of Proteobacteria than that in which the molecule had first

261 Rok, an analog of H-NS from gamma-proteobacteria that affects chromosome architecture and

262 Micavibrio aeruginosavorus are Gram-negative proteobacteria that are obligate predators of other Gram

263 ecies of non-pathogenic and pathogenic gamma-proteobacteria that infect different hosts, including hu

264 minase in fluorescent pseudomonads and other proteobacteria that we termed PtaA for "periplasmic tran

265 es (one epsilon-proteobacteria and two gamma-proteobacteria) that formed specific associations with o

266 was found to be distinct from those found in proteobacteria, the degradosomes of which are assembled

267 hia coli and the majority of beta- and gamma-proteobacteria, the fourth step of lipid A biosynthesis,

268 In Escherichia coli and other gamma-proteobacteria, the PhoQ-PhoP two-component signaling sy

269 In Escherichia coli and other gamma-proteobacteria, the transcription factor Crl stimulates

270 hundreds of BGCs distributed throughout the Proteobacteria; their products are aryl polyenes, lipids

271 samples had a greater than 10% abundance of Proteobacteria, there were only 19/196 (10%) positive cu

272 nsduction system utilized by a wide range of proteobacteria to sense environmental changes in oxygen

273 widespread molecular weapon deployed by many Proteobacteria to target effectors/toxins into both euka

274 rce generation are highly conserved from the Proteobacteria to the Firmicutes.

275 Widely found in animal and plant-associated proteobacteria, type VI secretion systems (T6SSs) are po

276 under purifying selection but have, in alpha-proteobacteria, undergone a burst of diversification fol

277 alpha-Proteobacteria uniquely integrate features of two-compon

278 Many Proteobacteria use acyl-homoserine lactone-mediated quor

279 Many Proteobacteria use N-acyl-homoserine lactone (acyl-HSL)

280 In the IBD group, Firmicutes, Proteobacteria, Verrucomicrobia, and Fusobacteria were s

281 this response has been well characterized in proteobacteria, very little is known about the effectors

282 In these patients, the increase in Proteobacteria was due to a single operational taxonomic

283 An increase in the relative abundance of Proteobacteria was observed in the posttransplantation s

284 dazole administration, whereas domination by Proteobacteria was reduced 10-fold by fluoroquinolone ad

285 Proteobacteria was the most dominant phylum in all sampl

286 The abundances of Fusobacteria and Proteobacteria were also remarkably increased in asympto

287 Fifteen strains within the Proteobacteria were isolated using a systematic enrichme

288 Microbiota disruption and elevated Proteobacteria were not significantly correlated to pati

289 Proteobacteria were present in higher proportions in ast

290 In mice lacking RELMbeta, Proteobacteria were present in the inner mucus layer and

291 ominant phyla (Bacteroidetes, Firmicutes and Proteobacteria) were similar.

292 acteria, and Deinococcus-Thermus, but not in Proteobacteria, where (p)ppGpp regulates RNA polymerase

293 he role of TolC has largely been explored in proteobacteria, where it functions as a metabolite and p

294 KO also had reduced Firmicutes and increased Proteobacteria, which could be reversed by Abx.

295 RCDI patients were dominated by Proteobacteria with Escherichia coli and Klebsiella most

296 ngly conserved in more closely related alpha-proteobacteria with similar ecological niches as S. meli

297 s alone primarily decreased the abundance of Proteobacteria, with the prolonged suppression of some m

298 is associated with significant expansion of Proteobacteria within the intestinal microbiota and incr

299 As can directly modulate mRNA degradation in Proteobacteria without interfering with translation.

300 TLR1 promotes acute enteric infection by the proteobacteria Yersinia enterocolitica.