ライフサイエンスコーパス: Prevotella

1 imal fat (Bacteroides) versus carbohydrates (Prevotella).

2 electively reduced the relative abundance of Prevotella.

3 ished primarily by levels of Bacteroides and Prevotella.

4 sobacterium, bacteroides, porphyromonas, and prevotella.

5 uch as Peptostreptococcus, Porphyromonas and Prevotella.

6 Leptotrichia, Neisseria, Porphyromonas, and Prevotella.

7 domonas and Lactobacillus and a reduction in Prevotella.

8 trol group had a gut microbiota dominated by Prevotella.

9 o) mice was characterized by an outgrowth of Prevotella.

10 Streptococcus (39%), Prevotella (17%), and Veilonella (14%) were most prevale

11 .95x10(-5), 4.39x10(-4), and 1.51x10(-4) for Prevotella 2, Prevotella 7, Tyzzerella, and Tyzzerella 4

12 val bleeding were associated with the genera Prevotella (22.25% x 20%), Streptococcus (19.83% x 17.61

13 39x10(-4), and 1.51x10(-4) for Prevotella 2, Prevotella 7, Tyzzerella, and Tyzzerella 4, respectively

14 Increases in Prevotella abundance correlated with a reduction in Bact

15 ncreased in NASH and F>/=2 patients, whereas Prevotella abundance was decreased.

16 h caries activity were also characterized by Prevotella, Actinomyces, and Capnocytophaga species and

17 onizers, including species of Streptococcus, Prevotella, Actinomyces, and Veillonella.

18 versity, with an increased representation of Prevotella, Akkermansia, and Lachnospiraceae Taken toget

19 ssociated bacterium 1 [BVAB1], BVAB2, BVAB3, Prevotella amnii, Prevotella pallens, Parvimonas micra,

20 of operational taxonomic unit 1341 (OTU1341; Prevotella) among individuals with fibroblasts responsiv

21 Bifidobacterium and Prevotella amounts were significantly increased by RW an

22 RW consumption increases Bifidobacterium and Prevotella amounts, which may have beneficial effects by

23 Cells of the genera Prevotella and Actinomyces showed the most interspecies

24 c of pus, the culture of which grew E. coli, Prevotella and Bacteroides fragilis.

25 ir native microbes and become colonized with Prevotella and Bacteroides, the dominant genera in the m

26 lyphenols, particularly against Bacteroides, Prevotella and Blautia coccoides-Eubacterium rectale.

27 The most commonly encountered anaerobes were Prevotella and Fusobacterium species.

28 Prevotella and Leptotrichia species were the only charac

29 Two gram-negative anaerobic rod taxa, Prevotella and Porphyromonas, predominated, contrasting

30 cispirillum, as well as members of the genus Prevotella and segmented filamentous bacteria, was trans

31 ibrosis pathogens and in other bacteria (eg, Prevotella and Streptococcus spp) detected in the airway

32 and Pseudomonas) and low stimulatory (e.g., Prevotella and Streptococcus) bacteria, "inflammatory" a

33 fying treatment show increased abundances of Prevotella and Sutterella, and decreased Sarcina, compar

34 HIV BAL contained an increased abundance of Prevotella and Veillonella, bacteria previously associat

35 to CpG-ODN responsive fibroblasts, OTU1341 (Prevotella), and Shannon index of microbial diversity in

36 eta and with the proportions of Selenomonas, Prevotella, and 5 species-level phylotypes.

37 in diverse anaerobes such as Peptoniphilus, Prevotella, and Anaerococcus species.

38 cally colonized by Actinomyces, Selenomonas, Prevotella, and Capnocytophaga.

39 Bacteroides, Lactobacillus, Collinsella and Prevotella, and reduction of Escherichia and Enterococcu

40 those of the genera Lactobacillus, Pantoea, Prevotella, and Selenomonas.

41 cantly increased the number of Enterococcus, Prevotella, Bacteroides, Bifidobacterium, Bacteroides un

42 degrading bacterial genera like Fibrobacter, Prevotella, Bacteroides, Clostridium and Ruminococcus in

43 Six strains of Prevotella bivia and 4 of Gardnerella vaginalis were exa

44 crease in the frequency and concentration of Prevotella bivia and black-pigmented Prevotella species.

45 Prevotella bivia and Prevotella corporis had a loss of v

46 requent isolate in bite wounds and resembles Prevotella bivia in colony morphology and saccharolytic

47 Peptostreptococcus asaccharolyticus and Prevotella bivia stimulated HIV expression in monocytoid

48 c bacterial phyla (Gardnerella vaginalis and Prevotella bivia) were strongly associated with cervicov

49 h bacterial vaginosis (Atopobium vaginae and Prevotella bivia).

50 -associated bacteria, Gardnerella vaginalis, Prevotella bivia, and Peptostreptococcus anaerobius, aci

51 ardnerella vaginalis, Atopobium vaginae, and Prevotella bivia, at the incident visit and when concent

52 h as Atopobium vaginae, Mobiluncus mulieris, Prevotella bivia, Fusobacterium nucleatum, and Peptoniph

53 er loss of viability for Mycoplasma hominis, Prevotella bivia, Prevotella corporis, and Peptoniphilus

54 philus asaccharolyticus, Mycoplasma hominis, Prevotella bivia, Prevotella corporis, Porphyromonas asa

55 Prevotella bryantii B(1)4 is a member of the phylum Bact

56 Prevotella bryantii B(1)4 is a rumen bacterium that effi

57 1.14 A), and the CBM from its homolog in the Prevotella bryantii B14 Xyn10C (1.68 A) reveal an unanti

58 l5A), from the symbiotic rumen Bacteroidetes Prevotella bryantii B14.

59 prevalences of Fusobacterium, Campylobacter, Prevotella, Capnocytophaga, Selenomonas, Actinomyces, Gr

60 0.002), Actinomyces sp. HOT 448 (p = 0.003), Prevotella cluster IV (p = 0.021), and Streptococcus sp.

61 for >/=2 years had levels of Bacteroides and Prevotella compared to those of the control group.

62 We identified the presence of Prevotella copri as strongly correlated with disease in

63 a high parasite burden and expansion of the Prevotella copri level was associated with diarrhea.

64 ubspecies (e.g., for Eubacterium rectale and Prevotella copri) or continuous microbial genetic variat

65 the abundance of Prevotella melaninogenica, Prevotella copri, and Prevotella sp. C561 and decreases

66 Prevotella bivia and Prevotella corporis had a loss of viability in both tran

67 ty for Mycoplasma hominis, Prevotella bivia, Prevotella corporis, and Peptoniphilus asaccharolyticus

68 ticus, Mycoplasma hominis, Prevotella bivia, Prevotella corporis, Porphyromonas asaccharolytica, Mobi

69 ens were identified and include the anaerobe Prevotella denticola, a Lysobacter sp., and members of t

70 terium saphenum, Porphyromonas endodontalis, Prevotella denticola, and Cryptobacterium curtum.

71 nd bacteria were Fusobacterium nucleatum and Prevotella denticola.

72 a identified in this study suggest that taxa Prevotella, Dorea, and Phascolarctobacterium may be taxa

73 In a microbiome of the Prevotella enterotype, fructooligosaccharides, and sorgh

74 ression, Porphyromonas (FDR p-value = 0.02), Prevotella (FDR p-value = 0.03), Anaerococcus (FDR p-val

75 the isolates represented 19 novel species of Prevotella, Fusobacterium, Streptococcus, Actinomyces, C

76 ndance of Parabacteroides, Adlercreutzia and Prevotella genera.

77 We also identified unique Prevotella genes that correlated with disease.

78 tis is enriched in microbes belonging to the Prevotella genus.

79 ghly abundant in situ such as members of the Prevotella genus.

80 ed as the ratio of Bacteroides-Porphyromonas-Prevotella group (BPP) to Bifidobacterium species.

81 her 2-4-log(10) CFU reduction of Bacteroides/Prevotella group organisms, which persisted to day 28 of

82 Prevotella heparinolytica was also frequently isolated f

83 r from two cat bites and Bacteroides tectum, Prevotella heparinolytica, and several porphyromonas spe

84 bacteria, including Fusobacterium nucleatum, Prevotella heparinolytica, Prevotella spp., Peptostrepto

85 measure total bacterial counts, Bacteroides/Prevotella (herein referred to as Bacteroidetes), Clostr

86 damentally different, with a predominance of Prevotella in native Africans (enterotype 2) and of Bact

87 f several gut bacteria taxa, Bacteroides and Prevotella in particular, differed between these groups,

88 lated with increased oral anaerobes, such as Prevotella in the lung, and with M. tuberculosis antigen

89 l cavity (eg, Veillonella, Leptotrichia, and Prevotella) increased significantly.

90 5) cells versus 3.8 x 10(5) cells; P <0.05), Prevotella intermedia (25.7 x 10(5) cells versus 9.8 x 1

91 s Streptococcus sanguis (59.5%), followed by Prevotella intermedia (43.4%), Tannerella forsythensis (

92 us (90%/76%), Eubacterium nodatum (64%/30%), Prevotella intermedia (58%/54%), and Eikenella corrodens

93 cetemcomitans, Porphyromonas gingivalis, and Prevotella intermedia (including Prevotella nigrescens)

94 The periodontal species were: Prevotella intermedia (n = 4), Prevotella nigrescens (n

95 a (odds ratio [OR]=1.7; 95% CI, 1.2 to 2.3), Prevotella intermedia (OR=1.5; 95% CI, 1.1 to 2.0), Capn

96 Treponema denticola and Prevotella intermedia (P = 0.01 and P = 0.02, respective

97 l pathogens Porphyromonas gingivalis (P.g.), Prevotella intermedia (P.i.), Campylobacter recta (C.r.)

98 On the contrary, Prevotella intermedia (Pi) and Bacteroides forsythus (Bf

99 ans (Aa), Porphyromonas gingivalis (Pg), and Prevotella intermedia (Pi) in periodontal pockets follow

100 phyromonas gingivalis, Tannerella forsythia, Prevotella intermedia (Pi), and Treponema denticola sign

101 orsythensis (Tf), Campylobacter rectus (Cr), Prevotella intermedia (Pi), Capnocytophaga species (Cs),

102 l presence of Porphyromonas gingivalis (Pg), Prevotella intermedia (Pi), Tannerella forsythia (Tf), a

103 erial DNA for Porphyromonas gingivalis (Pg), Prevotella intermedia (Pi), Treponema denticola (Td), an

104 and some evidence supporting association of Prevotella intermedia and Campylobacter rectus with the

105 Prevotella intermedia and Porphyromonas gingivalis incre

106 Prevotella intermedia and Treponema denticola (Td) level

107 ent of Fusobacterium nucleatum ATCC25586 and Prevotella intermedia ATCC25611 on keratinocytes preincu

108 The oral bacterium Prevotella intermedia attaches to and invades gingival e

109 helpers such as Propionibacterium acnes and Prevotella intermedia for stimulation, with best growth

110 that Eubacterium minutum was correlated with Prevotella intermedia in peri-implantitis sites, which s

111 Prevotella intermedia is an oral bacterium implicated in

112 were positively associated with SUP, whereas Prevotella intermedia presented a negative association w

113 nnerella forsythia, Treponema denticola, and Prevotella intermedia was evaluated qualitatively by con

114 forsythensis, Porphyromonas gingivalis, and Prevotella intermedia) members of the Cytophaga-Flavobac

115 inomycetemcomitans, Tannerella forsythia, or Prevotella intermedia) versus those with only one (P <0.

116 rpose of this study was to determine whether Prevotella intermedia, a putative periodontal pathogen,

117 ella forsythia (previously T. forsythensis), Prevotella intermedia, Aggregatibacter actinomycetemcomi

118 iodontal pathogens (Fusobacterium nucleatum, Prevotella intermedia, and Campylobacter rectus), two re

119 nnerella forsythia, Fusobacterium nucleatum, Prevotella intermedia, and Campylobacter rectus.

120 Porphyromonas gingivalis, Prevotella intermedia, and Fusobacterium nucleatum activ

121 ral species, e.g., Porphyromonas gingivalis, Prevotella intermedia, and Fusobacterium nucleatum, have

122 luding Actinobacillus actinomycetemcomitans, Prevotella intermedia, and Porphyromonas gingivalis.

123 vels of P. gingivalis, Tannerella forsythia, Prevotella intermedia, and Prevotella nigrescens were st

124 teroides fragilis, Streptococcus pneumoniae, Prevotella intermedia, and Staphylococcus intermedius we

125 Porphyromonas gingivalis, Prevotella intermedia, and T. forsythia were significant

126 nnerella forsythia, Fusobacterium nucleatum, Prevotella intermedia, and total bacteria.

127 y against Bacteroides vulgatus, B. fragilis, Prevotella intermedia, and, to a lesser extent, against

128 Prevotella intermedia, Bacteroides forsythus, and Capnoc

129 ella forsythia (previously T. forsythensis), Prevotella intermedia, Campylobacter rectus, and Fusobac

130 alis, Aggregatibacter actinomycetemcomitans, Prevotella intermedia, Eikenella corrodens, and Fusobact

131 ed bacteria Bacteroides thetaiotaomicron and Prevotella intermedia, function as immunological adjuvan

132 iodontal pathogens Porphyromonas gingivalis, Prevotella intermedia, Fusobacterium nucleatum, and Aggr

133 organisms such as Porphyromonas gingivalis, Prevotella intermedia, Fusobacterium nucleatum, and Tann

134 nomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia, Fusobacterium nucleatum, Campylob

135 tectable levels of Porphyromonas gingivalis, Prevotella intermedia, Fusobacterium nucleatum, Campylob

136 e of four common pulpal pathogens, including Prevotella intermedia, Fusobacterium nucleatum, Peptostr

137 erial challenge, an infection protocol using Prevotella intermedia, Fusobacterium nucleatum, Peptostr

138 with a mixture of four anaerobic pathogens, Prevotella intermedia, Fusobacterium nucleatum, Streptoc

139 hniques to identify Fusobacterium nucleatum, Prevotella intermedia, oral Campylobacter species, Eiken

140 myces viscosus, Campylobacter rectus/showae, Prevotella intermedia, Parvimonas micra, Eubacterium nod

141 ously Actinobacillus actinomycetemcomitans), Prevotella intermedia, Porphyromonas gingivalis, Tannere

142 dontal species, P. gingivalis, B. forsythus, Prevotella intermedia, Prevotella nigrescens, and Campyl

143 ikenella corrodens, Tannerella forsythensis, Prevotella intermedia, Prevotella nigrescens, and Trepon

144 hyromonas gingivalis, Bacteroides forsythus, Prevotella intermedia, Prevotella nigrescens, and Trepon

145 ence and levels of Porphyromonas gingivalis, Prevotella intermedia, Prevotella nigrescense, and Epste

146 proteinase of another periodontal pathogen, Prevotella intermedia, resulted in a strong synergistic

147 Putative periodontopathogens such as Prevotella intermedia, Selenomonas noxia, Fusobacterium

148 eases in levels of Prevotella nigrescens and Prevotella intermedia, serum IL-6sr, and GCF IL-1beta.

149 Here we report that a clinical isolate of Prevotella intermedia, strain 17, was found to invade a

150 xture of four anaerobic pathogens, including Prevotella intermedia, Streptococcus intermedius, Fusoba

151 cterium nucleatum, Porphyromonas gingivalis, Prevotella intermedia, Tannerella forsythia (previously

152 ously Actinobacillus actinomycetemcomitans], Prevotella intermedia, Tannerella forsythia [previously

153 phyromonas gingivalis, Tannerella forsythia, Prevotella intermedia, Treponema denticola, and Aggregat

154 ptococcus intermedius, Parvimonas micra, and Prevotella intermedia, was inoculated into subcutaneousl

155 omonas gingivalis, Tannerella forsythia, and Prevotella intermedia, were clustered into modules in th

156 ium nucleatum, Porphyromonas gingivalis, and Prevotella intermedia, were examined for their ability t

157 ytophaga sputigena, Eikenella corrodens, and Prevotella intermedia-like species than group EP.

158 lla corrodens, Porphyromonas gingivalis, and Prevotella intermedia-to invade human coronary artery en

159 ptococcus mutans, Actinomyces naeslundii and Prevotella intermedia.

160 etemcomitans), Porphyromonas gingivalis, and Prevotella intermedia.

161 des forsythus, Porphyromonas gingivalis, and Prevotella intermedia.

162 us anaerobius, Porphyromonas gingivalis, and Prevotella intermedia.

163 bacteria (BPB) Porphyromonas gingivalis and Prevotella intermedia.

164 species, including Porphyromonas gingivalis, Prevotella intermedia/nigrescens, Bacteroides forsythus,

165 One or more test species, most often Prevotella intermedia/nigrescens, Streptococcus constell

166 nt in isolating Porphyromonas gingivalis and Prevotella intermedia/nigrescens.

167 of prevalence, Fusobacterium, enteric rods, Prevotella intermedia/Prevotella nigrescens, Capnocytoph

168 Porphyromonas gingivalis and especially Prevotella intermedius/nigrescens were often identified

169 The role of A geminatus and Prevotella/Leptotrichia species in this process merits f

170 companied by marked reductions in intestinal Prevotella levels and significantly reduced pro-IL-1beta

171 Common taxa in BV(+) women were Prevotella, Megasphaera, Gardnerella, Coriobacterineae,

172 Prevotella melaninogenica was not recovered after 24 or

173 Hemolytic strain 361B of Prevotella melaninogenica, a putative etiologic agent of

174 s demonstrated increases in the abundance of Prevotella melaninogenica, Prevotella copri, and Prevote

175 served after exposure to commensal bacterium Prevotella melaninogenica.

176 m with P. bivia, Prevotella oralis group, or Prevotella melaninogenica.

177 mples was associated with >30 Gardnerella or Prevotella morphotypes per high-power field, as detected

178 patients), Haemophilus influenzae (n = 12), Prevotella (n = 18), and Veillonella (n = 13).

179 species were: Prevotella intermedia (n = 4), Prevotella nigrescens (n = 4), and Porphyromonas gingiva

180 ociated with CHD among ever smokers, whereas Prevotella nigrescens (OR=1.7; 95% CI, 1.1 to 2.6), Acti

181 ores) and significant decreases in levels of Prevotella nigrescens and Prevotella intermedia, serum I

182 ontal pathogens Porphyromonas gingivalis and Prevotella nigrescens induced periodontitis in mice, as

183 ster pneumosintes, Tannerella forsythia, and Prevotella nigrescens than SUP sites from patients with

184 Prevotella nigrescens was the only species (p < 0.05) si

185 erella forsythia, Prevotella intermedia, and Prevotella nigrescens were statistically significantly h

186 ivalis, and Prevotella intermedia (including Prevotella nigrescens) was investigated.

187 nted anaerobes (Porphyromonas gingivalis and Prevotella nigrescens) were significantly reduced (P </=

188 ivalis, B. forsythus, Prevotella intermedia, Prevotella nigrescens, and Campylobacter rectus were det

189 nerella forsythensis, Prevotella intermedia, Prevotella nigrescens, and Treponema denticola before an

190 acteroides forsythus, Prevotella intermedia, Prevotella nigrescens, and Treponema denticola.

191 cterium, enteric rods, Prevotella intermedia/Prevotella nigrescens, Capnocytophaga, Propionibacterium

192 e, C. gingivalis, E. corrodens, C. concisus, Prevotella nigrescens, T. forsythia, and Dialister pneum

193 hyromonas gingivalis, Prevotella intermedia, Prevotella nigrescense, and Epstein-Barr virus (EBV).

194 Prevotella oralis and S. oralis levels were significantl

195 ious kits associate B. tectum with P. bivia, Prevotella oralis group, or Prevotella melaninogenica.

196 in endodontic samples included P. tannerae, Prevotella oris, and A. baumannii.

197 on the Actinobacillus actinomycetemcomitans, Prevotella oris, Staphylococcus aureus, and Propionibact

198 binoxylans significantly promoted one single Prevotella OTU with equally high production of total SCF

199 s." Several microbial members (Ruminococcus, Prevotella, Oxalobacter and Coprococcus) were detected a

200 m 1 [BVAB1], BVAB2, BVAB3, Prevotella amnii, Prevotella pallens, Parvimonas micra, Megasphaera, Gardn

201 Gemella, Mogibacterium, Peptostreptococcus, Prevotella, Propionibacterium, Selenomonas, Solobacteriu

202 Instead, Bifidobacterium, Gardnerella, Prevotella, Pseudomonas, or Streptococcus predominated.

203 .48; P 0.03) and anaerobic bacteria, such as Prevotella (RES, 0.25; P < 0.001) and Veillonella (RES,

204 of the Bacteroidetes genera Bacteroides and Prevotella, respectively, in seropositive subjects with

205 ndividuals in the U.S. was most similar to a Prevotella-rich community composition typically observed

206 The Prevotella ruminicola 23 genome encodes three different

207 Prevotella ruminicola 23 is an obligate anaerobic bacter

208 ies and those free of caries by Actinomyces, Prevotella, Selenomonas, Streptococcus, and Mycoplasma.

209 than those from children without halitosis; Prevotella shahii had higher relative abundance and prev

210 mation, including those reported previously (Prevotella, Sneathia, Aerococcus, Fusobacterium, and Gem

211 ked with reduced (L. crispatus) or elevated (Prevotella, Sneathia, and other anaerobes) inflammation

212 homology with epitopes from proteins of the Prevotella sp. and Butyricimonas sp., another gut commen

213 with epitopes from sulfatase proteins of the Prevotella sp. and Parabacteroides sp., whereas the HLA-

214 otella melaninogenica, Prevotella copri, and Prevotella sp. C561 and decreases in Bacteroides spp.

215 The predominant isolates were Prevotella sp., Porphyromonas sp., Fusobacterium nucleat

216 anaerobes were gram-positive cocci (45.2%), Prevotella species (13.6%), Porphyromonas species (11.3%

217 Streptococcus parasanguinis (p = 0.013), and Prevotella species (p < 0.02).

218 bpopulations of P. bivia and black-pigmented Prevotella species emerged 7 to 12 days after therapy ev

219 Prevotella species were prevalent in all specimens and r

220 ecies, six pigmenting and five nonpigmenting Prevotella species, Bacteroides forsythus, three Capnocy

221 iome-including Bacteroides, Selenomonas, and Prevotella species-is maintained in distal metastases, d

222 d enterotypes enriched with Clostridiales or Prevotella species.

223 tion of Prevotella bivia and black-pigmented Prevotella species.

224 ollowed by later enrichment of Neisseria and Prevotella spp.

225 tes), Peptostreptococcus spp. (72 isolates), Prevotella spp. (71 isolates), Fusobacterium spp. (21 is

226 tions in the numbers of both the Bacteroides-Prevotella spp. and the Clostridium-histolyticum groups,

227 Prevotella spp. are the most predominant bacteria detect

228 At the genus level, Prevotella spp. decreased in the CRS group, while Staphy

229 , and might be linked to previously reported Prevotella spp. population imbalances relative to other

230 (that included Porphyromonas gingivalis and Prevotella spp.) was positively associated (odds ratio [

231 Actinomyces naeslundii, Prevotella spp., and Porphyromonas gingivalis increased

232 terium nucleatum, Prevotella heparinolytica, Prevotella spp., Peptostreptococcus micros, Streptococcu

233 onas endodontalis, Porphyromonas gingivalis, Prevotella spp., Tannerella forsythia, Dialister spp., S

234 cesarean delivered infants had enrichment of Prevotella, Streptococcus and Trabulsiella.

235 in samples from asthmatic patients, whereas Prevotella, Streptococcus, and Veillonella species were

236 cal members of the healthy steady state (eg, Prevotella, Streptococcus, and Veillonella).

237 In contrast, other taxa including Prevotella, Streptococcus, Rothia and Veillonella were a

238 both amplified and nonamplified samples were Prevotella tannerae and Acinetobacter baumannii at frequ

239 Furthermore, enrichment in Prevotella, Treponema and unclassified Bacteroidetes, as

240 Here, we show that the dominance of Prevotella versus Bacteroides in fecal innocula, identif

241 tribute to health, however, an overgrowth of Prevotella was observed due to exposure to M. aeruginosa

242 ides, Parabacteroides, Faecalibacterium, and Prevotella was reduced compared to controls.

243 nus in the infant gut overall, Dialister and Prevotella were negatively correlated with morbidity, an

244 In spring, the abundance of the genus Prevotella, which is associated with digestion of carboh

245 Prevotella zoogleoformans, occasionally isolated from do