ライフサイエンスコーパス: Prevotella

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

2 igher levels of Porphyromonas (p < 0.05) and Prevotella.

3 uch as Peptostreptococcus, Porphyromonas and Prevotella.

4 Leptotrichia, Neisseria, Porphyromonas, and Prevotella.

5 domonas and Lactobacillus and a reduction in Prevotella.

6 trol group had a gut microbiota dominated by Prevotella.

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

8 electively reduced the relative abundance of Prevotella.

9 ished primarily by levels of Bacteroides and Prevotella.

10 nd relative abundances of Bifidobacteria and Prevotella.

11 that Lak phages infect bacteria of the genus Prevotella.

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

13 and 94 genera were represented primarily by Prevotella (17.9%) and Bacteroidaceae G-1 (14.3%).

14 nimals (46.7%) while Bacteroides (11.6%) and Prevotella (18.9%) were the most abundant in captive ani

15 .95x10(-5), 4.39x10(-4), and 1.51x10(-4) for Prevotella 2, Prevotella 7, Tyzzerella, and Tyzzerella 4

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

17 39x10(-4), and 1.51x10(-4) for Prevotella 2, Prevotella 7, Tyzzerella, and Tyzzerella 4, respectively

18 luded Actinomyces (10.5%), Olsenella (9.4%), Prevotella (8.8%), Propionibacterium (7.2%), Streptococc

19 nd low rates of gastrointestinal carriage of Prevotella, a commensal bacterial genus that produces sh

20 Increases in Prevotella abundance correlated with a reduction in Bact

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

22 its (OTUs) falling within the Streptococcus, Prevotella, Acinetobacter, Treponema, and Lactobacillus

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

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

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

26 ignificantly associated with the presence of Prevotella amnii (risk ratio [RR], 2.21; 95% confidence

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

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

29 Bifidobacterium and Prevotella amounts were significantly increased by RW an

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

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

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

33 ion of SCFA-producing bacteria of the genera Prevotella and Bifidobacterium, which increased fecal an

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

35 Similarly, Prevotella and Campylobacter (P < 0.05) decreased in str

36 show that coupling CRISPR-Cpf1 (CRISPR from Prevotella and Francisella 1) to a CRISPR RNA (crRNA) ar

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

38 Prevotella and Leptotrichia species were the only charac

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

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

41 phaga, Porphyromonas, and Pseudomonas, while Prevotella and Selenomonas are increased in RA and Selen

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

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

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

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

46 ed children had lower relative abundances of Prevotella and Veillonella.

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

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

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

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

51 roles, including Turicibacter, Akkermansia, Prevotella, and Clostridium Using a correlation network

52 nsistent underrepresentation of Bacteroides, Prevotella, and Coprococcus in allergic compared to nona

53 Porphyromonas, Lachnospiraceae unclassified, Prevotella, and Phascolarctobacterium were also selected

54 ty, elevated relative abundance of the genus Prevotella, and reduced levels of the genus Bacteroides

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

56 Three genera, Bacteroides, Prevotella, and Ruminococcus, were the most common dysbi

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

58 BDL included the enrichment of Akkermansia, Prevotella, Bacteroides and unclassified Ruminococcaceae

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

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

61 virulent strains of G. vaginalis, as well as Prevotella bivia and Atopobium vaginae.

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

63 Prevotella bivia and Prevotella corporis had a loss of v

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

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

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

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

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

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

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

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

72 1.14 A), and the CBM from its homolog in the Prevotella bryantii B14 Xyn10C (1.68 A) reveal an unanti

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

74 f pigs fed with 12% CP were less enriched in Prevotella, but had higher relative abundance of Christe

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

76 0.002), Actinomyces sp. HOT 448 (p = 0.003), Prevotella cluster IV (p = 0.021), and Streptococcus sp.

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

78 Gut-dwelling Prevotella copri (P. copri), the most prevalent Prevotel

79 ed 20 circular genomes, including genomes of Prevotella copri and a candidate Cibiobacter sp.

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

81 in fecal samples shows maternal carriage of Prevotella copri during pregnancy strongly predicts the

82 Prevotella copri is a common human gut microbe that has

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

84 vanced fibrosis in the validation cohort and Prevotella copri remained the strongest predictive micro

85 High abundance of Prevotella copri was associated with more severe fibrosi

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

87 erm-free mice before Listeria infection with Prevotella copri, an abundant gut-commensal bacteria, bu

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

89 Prevotella copri, which was enriched in patients with ad

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

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

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

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

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

95 nd bacteria were Fusobacterium nucleatum and Prevotella denticola.

96 nity composition, and revealed a Bacteroides/Prevotella dichotomy aligned with inflammation and dieta

97 encoded by Prevotella ihumii (PiCas12a) and Prevotella disiens (PdCas12a) shared over 95% amino-acid

98 ransitions between Bacteroides-dominated and Prevotella-dominated communities were rare, suggesting t

99 eking to transition between Bacteroides- and Prevotella-dominated communities will need to identify p

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

101 onism least frequent in individuals with the Prevotella-enriched enterotype.

102 stinct microbiota signature characterized by Prevotella enrichment and increased alpha diversity, whi

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

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

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

106 ndance of Parabacteroides, Adlercreutzia and Prevotella genera.

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

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

109 ated metabolic and phylogenetic diversity of Prevotella genus.

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

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

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

113 including Bacteroides, Parabacteroides, and Prevotella gut species, as well as pathogenic Prevotella

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

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

116 particular, two Cas12a nucleases encoded by Prevotella ihumii (PiCas12a) and Prevotella disiens (PdC

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

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

119 sed in RA and Selenomonas, Leptotrichia, and Prevotella in SLE.

120 ia and increase of the relative abundance of Prevotella in the gut, thereby preventing the destructio

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

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

123 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

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

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

126 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

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

128 hyromonas gingivalis (P.g.), 5.3 x 10(3) for Prevotella intermedia (P.i.), and 5.8 x 10(4) for Aggreg

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

130 tans (Aa), Fusobacterium nucleatum (Fn), and Prevotella intermedia (Pi) was done by quantitative poly

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

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

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

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

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

136 Prevotella intermedia and Porphyromonas gingivalis incre

137 Prevotella intermedia and Treponema denticola (Td) level

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

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

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

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

142 Prevotella intermedia is an oral bacterium implicated in

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

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

145 onema denticola, Fusobacterium nucleatum and Prevotella intermedia) in saliva samples.

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

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

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

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

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

151 Porphyromonas gingivalis, Prevotella intermedia, and Fusobacterium nucleatum activ

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

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

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

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

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

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

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

159 We found that Prevotella intermedia, Campylobacter Rectus, Factor 2 (P

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

161 t a higher abundance of Treponema denticola, Prevotella intermedia, Fretibacterium sp. HOT360 and low

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

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

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

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

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

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

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

169 coccus-like species and lower proportions of Prevotella intermedia, Peptostreptococcus micros, Fusoba

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

171 valuated the levels of periodontal pathogens Prevotella intermedia, Porphyromonas gingivalis, Trepone

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

173 phyromonas gingivalis, Tannerella forsythia, Prevotella intermedia, Prevotella nigrescens, and Trepon

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

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

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

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

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

179 nomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia, Tannerella forsythia, Fusobacteri

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

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

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

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

184 ptococcus mutans, Actinomyces naeslundii and Prevotella intermedia.

185 etemcomitans), Porphyromonas gingivalis, and Prevotella intermedia.

186 s the growth of Porphyromonas gingivalis and Prevotella intermedia.

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

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

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

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

191 Prevotella may have role in COVID-2019 outbreak and shou

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

193 Prevotella melaninogenica was not recovered after 24 or

194 o Campylobacter rectus, Veillonella parvula, Prevotella melaninogenica were consistently associated w

195 r Rectus, Factor 2 (Pi/Prevotella nigrescens/Prevotella melaninogenica), and the Orange-Red cluster i

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

197 served after exposure to commensal bacterium Prevotella melaninogenica.

198 era (false discovery rate < 0.05), including Prevotella, Mitsuokella, Fusobacterium, Desulfovibrio, a

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

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

201 anulicatella elegans, Porphyromonas pasteri, Prevotella nanceiensis and Streptococcus oralis decrease

202 such as Neisseria lactamica, Streptococcus, Prevotella nanceiensis, Fusobacterium, and Janthinobacte

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

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

205 For example, the bacterium Prevotella nigrescens contains a distinctive bifunctiona

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

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

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

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

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

211 Tannerella forsythia, Prevotella intermedia, Prevotella nigrescens, and Treponema denticola) and the

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

213 termedia, Campylobacter Rectus, Factor 2 (Pi/Prevotella nigrescens/Prevotella melaninogenica), and th

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

215 was to evaluate species-specific effects of Prevotella on the human endometrial epithelium.

216 microbiome clusters, dominated by the genus Prevotella or Bacteroides.

217 ed with AL in C-seal patients, in particular Prevotella oralis (P = 0.007).

218 Prevotella oralis and S. oralis levels were significantl

219 associated with decreases in anaerobes (ie, Prevotella organisms; P < .001).

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

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

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

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

224 changes in bacterial abundance, Barnesiella, Prevotella, Paraprevotella, Hallela, Anaerovorax, Succin

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

226 It was found that overexpressed Prevotella proteins can promote viral infection.

227 lysis between SARS-CoV-2 and overrepresented Prevotella proteins with human proteome.

228 As per the results, Prevotella proteins, but not viral proteins, are involve

229 la, Neisseria, Fusobacterium, Streptococcus, Prevotella, Pseudomonas, and Actinomyces) were almost ab

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

231 abundance of 30 taxa, such as an increase in Prevotella (q < .0001) and a decrease of Bacteroides (q

232 .48; P 0.03) and anaerobic bacteria, such as Prevotella (RES, 0.25; P < 0.001) and Veillonella (RES,

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

234 The Prevotella-rich cluster was largely composed of men who

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

236 er use of protease inhibitors, compared with Prevotella-rich MSM.

237 The Prevotella ruminicola 23 genome encodes three different

238 Prevotella ruminicola 23 is an obligate anaerobic bacter

239 lla species, Megasphaera micronuciformis and Prevotella saliva increased.

240 e in the abundance in Streptococcus spp. and Prevotella salivae was associated with 48% (95% CI: 9%,

241 e in the abundance in Streptococcus spp. and Prevotella salivae was associated with 48% (95% credible

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

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

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

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

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

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

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

249 tically inactive Type VI-B Cas13 enzyme from Prevotella sp. P5-125 (dPspCas13b) to m6A demethylase Al

250 imalis) or mestizos (Mobiluncus mulieris and Prevotella sp.).

251 risk of CLD than those with Streptococcus or Prevotella (SP)-dominated microbiota (RR = 1.48, p = 0.0

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

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

254 of BVAB1, Sneathia amnii, TM7-H1, a group of Prevotella species and nine additional taxa.

255 Prevotella species are commonly isolated from the reprod

256 Collectively, findings indicate that Prevotella species are metabolically diverse and overall

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

258 votella copri (P. copri), the most prevalent Prevotella species in the human gut, have been associate

259 cus, Haemophilus, Neisseria, Veillonella and Prevotella species predominated to biofilms comprising a

260 Prevotella species were prevalent in all specimens and r

261 despread in gut communities that contain the Prevotella species, and conclude that megaphages, with f

262 Infections with Prevotella species, including P. bivia, did not result i

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

264 d enterotypes enriched with Clostridiales or Prevotella species.

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

266 revotella gut species, as well as pathogenic Prevotella species.

267 ollowed by later enrichment of Neisseria and Prevotella spp.

268 analysis to systemically characterize murine Prevotella spp.

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

270 Prevotella spp. are the most predominant bacteria detect

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

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

273 n infected patients revealed overrepresented Prevotella spp. producing certain proteins in abundance.

274 abundance in Streptococcus vestibularis and Prevotella spp. was associated with 63% (95% CI: 17%, 83

275 abundance in Streptococcus vestibularis and Prevotella spp. was associated with 63% (95% CrI, 17-83%

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

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

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

279 associated with good dental health, whereas Prevotella spp., Streptococcus mutans, and Human herpesv

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

281 We identify Prevotella strains that are more abundant at 1 month in

282 Thirteen Prevotella strains, originally isolated from the human o

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

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

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

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

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

288 ecific anaerobic taxa including Megasphaera, Prevotella timonensis and Gardnerella vaginalis are asso

289 dy of the Latino population shows increasing Prevotella to Bacteroides ratio with greater obesity.

290 o the USA at an early age have reductions in Prevotella to Bacteroides ratios that persist across the

291 high bacterial and fungal diversity and high Prevotella to Bacteroides ratios, compared to USA-born a

292 he hypothesis that interaction between diet, Prevotella-to-Bacteriodes ratio (P/B ratio), and AMY1 CN

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

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

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

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

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

298 t the relative abundances of Bacteroides and Prevotella were significantly correlated with certain se

299 , which belong to the genera Bacteroides and Prevotella, were identified to promote fibrotic pathogen

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