ライフサイエンスコーパス: microbiota composition

1 oth the intestine and plasma via altered gut microbiota composition.

2 Many (58%) did not report an analysis of microbiota composition.

3 also birth order had a strong effect on the microbiota composition.

4 ade inflammation and specific changes in gut microbiota composition.

5 rRNA pyrosequencing was used to investigate microbiota composition.

6 il proportion was the strongest predictor of microbiota composition.

7 es within the gut, profoundly influences gut microbiota composition.

8 highly variable and are associated with gut microbiota composition.

9 bacterial growth, which ultimately dictates microbiota composition.

10 duce gastric acid secretion and modulate gut microbiota composition.

11 owth of different bacteria, drive changes in microbiota composition.

12 ortant drivers of the early-life respiratory microbiota composition.

13 d, furthermore, altered the larva-associated microbiota composition.

14 ute to variation in marine mammal distal gut microbiota composition.

15 time antibiotic use after weaning, and fecal microbiota composition.

16 ions between H. pylori strain properties and microbiota composition.

17 y mass index is associated with neonatal gut microbiota composition.

18 ic population or carriage of the cagPAI with microbiota composition.

19 nses after oral immunization and affects the microbiota composition.

20 etary response was determined in part by gut microbiota composition.

21 ixed model, we estimated the heritability of microbiota composition.

22 pcidin induction is influenced by intestinal microbiota composition.

23 ut humoral response and to maintain a normal microbiota composition.

24 ediates intestinal homeostasis and regulates microbiota composition.

25 tes susceptibility to disease by controlling microbiota composition.

26 us, ultrafine particles ingestion alters gut microbiota composition, accompanied by increased atherog

27 Our findings suggest that microbiota composition affects disease outcome and may e

28 Mounting evidence indicates that gut microbiota composition affects obesity and diabetes, as

29 The microbiota composition analysis revealed higher abundanc

30 Fecal microbiota composition analysis was performed in a subco

31 In the subcohort of 42 children with fecal microbiota composition analysis, the children with short

32 hanges in gut permeability are linked to gut-microbiota composition and activity in alcohol-dependent

33 s with COPD and how they are associated with microbiota composition and airway neutrophil function.

34 e, a recently described regulator of colonic microbiota composition and biogeographical distribution,

35 of pathogen resistance, in turn, affect the microbiota composition and create an environment that ex

36 We hypothesized that the respiratory microbiota composition and development in infancy is aff

37 isease outcome and may explain links between microbiota composition and disease susceptibility.

38 results provide insights into the human lung microbiota composition and function and their link to hu

39 nce that diet exerts on microbes, changes in microbiota composition and function can alter host funct

40 lts indicate that the human gastrointestinal microbiota composition and function vary throughout the

41 studies to characterize natural variation in microbiota composition and function, identify important

42 We assessed the effects of FMT on microbiota composition and function, mucosal immune resp

43 s with metabolic syndrome on the recipients' microbiota composition and glucose metabolism.

44 enetically distinct strain influence the gut microbiota composition and immune key markers in mice.

45 udies have established a primary role of the microbiota composition and intestinal permeability in su

46 ttle is known about the consequences for gut microbiota composition and metabolic activity and for la

47 lammation, which correlates with altered gut microbiota composition and metabolic syndrome, both pres

48 wel disease (IBD) is associated with altered microbiota composition and metabolism, but it is unclear

49 We further investigate the gut microbiota composition and microbiota-metabolite relatio

50 een associated with long-term changes in gut microbiota composition and more recently also with chang

51 ce of environmental and lifestyle factors on microbiota composition and pancreatic autoimmunity.

52 ota interactions, we mapped loci controlling microbiota composition and prioritized candidate genes.

53 ith a broad spectrum antibiotic modifies gut microbiota composition and promotes anti-inflammatory re

54 rentiation of T(reg) cells affects commensal microbiota composition and serves a distinct, essential

55 ant starch type 4 (RS4) enriched diet on gut microbiota composition and short-chain fatty acid (SCFA)

56 sm, and we examined correlations between gut microbiota composition and signaling pathways.

57 splaying despair behavior, we found that the microbiota composition and the metabolic signature drama

58 targets for CH4 mitigation at the levels of microbiota composition and transcriptional regulation.

59 The associations between gut microbiota composition and WAT gene expression increased

60 re also believed to act as modulators of the microbiota composition and, consequently, as agents that

61 e were variable shifts in faecal and mucosal microbiota composition and, in some patients, changes in

62 try, and biochemical assays to determine the microbiota compositions and the physiological and metabo

63 Plasma corticosterone, microbiota composition, and cecal short-chain fatty acid

64 nent alterations in anti-commensal immunity, microbiota composition, and chronic inflammation, which

65 ions and serum vitamin K concentrations, gut microbiota composition, and inflammation.Fecal and serum

66 t the hypothesis that a distortion in normal microbiota composition, and not an enrichment of potenti

67 and serum menaquinone concentrations, fecal microbiota composition, and plasma and fecal cytokine co

68 ation between feeding strategies, intestinal microbiota composition, and the development of NEC.We pe

69 In three subjects, the Malassezia microbiota composition appeared relatively stable over t

70 Alterations in microbiota composition are associated with susceptibilit

71 Shifts in commensal microbiota composition are emerging as a hallmark of gas

72 ce indicate that MHC-mediated differences in microbiota composition are sufficient to explain suscept

73 ary antibiotic therapy, but their effects on microbiota composition are undetermined.

74 ularly important for predicting steady-state microbiota composition as it imposes significant restric

75 ome was within-patient change in respiratory microbiota composition (assessed by Bray-Curtis index) b

76 he quantity and source of dietary protein on microbiota composition, bacterial metabolite production,

77 The change in microbiota composition between baseline and week 48 was

78 terial strains and incorporates variation in microbiota composition between people, while also allowi

79 tly different microbiota, and segregation of microbiota composition between periodontitis and health

80 he use of microarrays.HPDs did not alter the microbiota composition, but induced a shift in bacterial

81 nificant alpha-defensin-dependent changes in microbiota composition, but not in total bacterial numbe

82 Secondary end points were safety and microbiota composition by phylogenetic microarray in fec

83 microbiota and revealed that differences in microbiota composition can be associated with inflammato

84 lain how antibiotic-mediated switches in the microbiota composition can result from simple social int

85 We discuss how shifts in the microbiota composition change host susceptibility to inf

86 We also found that CB0313.1 modulated gut microbiota composition, characterized by a decreased rat

87 gnizes flagellin, have an altered intestinal microbiota composition compared with wild-type mice; the

88 Ten years ago, we discovered that microbiota composition controls intestinal T cell homeos

89 Here, we show that commensal microbiota composition critically regulates the generati

90 i et al. (2017) show that RegIIIbeta impacts microbiota composition, decreasing vitamin B6 production

91 Here we show that gut microbiota composition depends on interactions between h

92 Using gnotobiotic mice we show that microbiota composition determines the magnitude and patt

93 many factors that determine the human colon microbiota composition, diet is an important one because

94 therapy had independent and rapid effects on microbiota composition distinct from other stressor-indu

95 of exacerbations, suggesting that changes in microbiota composition do not account for exacerbations.

96 yet the role of the immune system in shaping microbiota composition during an organism's life span ha

97 We explored variation in Tibetan macaque gut microbiota composition during winter and spring seasons.

98 Microbiota composition (dysbiosis) was evaluated by Pyro

99 s can be used to obtain predicted changes in microbiota composition for improved health.

100 Larval survival, growth, microbiota composition, gene expression profiles and dis

101 ons between breastfeeding and nasopharyngeal microbiota composition had disappeared.

102 es are not clear; modification of intestinal microbiota composition has been reported to reflect anim

103 Perturbations in intestinal microbiota composition have been associated with a varie

104 Microbiota compositions have great implications in human

105 Host diet is known to alter microbiota composition, implying that dietary treatments

106 Here we examined factors that affect microbiota composition in a large (n = 645) mouse advanc

107 omponent, abolished rhythmicity in the fecal microbiota composition in both genders.

108 n gut microbiota, we compared the intestinal microbiota composition in children with at least two dia

109 e reasons underlying striking differences in microbiota composition in independently evolved, yet fun

110 phimurium infection is strongly modulated by microbiota composition in individual lines.

111 A comparison of root and gut microbiota composition in multiple host species belongin

112 These QTL affect microbiota composition in three ways; some loci control

113 also been implicated as determinants of the microbiota composition, including exclusion of pathogens

114 lulose-based diet had similar changes in gut microbiota composition, indicating that diet can modify

115 We investigated whether specific microbiota compositions influence immune responses to gl

116 Host immunity shapes intestinal microbiota composition, influencing health and disease.

117 tasis by controlling host defense responses, microbiota composition, intestinal inflammation and tiss

118 Gut microbiota composition is a contributing factor to the s

119 iabetic effect of bariatric surgery, and gut microbiota composition may alter intestinal nutrient-sen

120 Patterns of spatial variation in microbiota composition may help explain Staphylococcus a

121 A human study suggested that luminal microbiota composition may influence the host's intestin

122 al consortia to individuals with compromised microbiota composition may reduce inter-patient transmis

123 Diet-induced alterations in microbiota composition might influence fat absorption, p

124 Differences in microbiota composition might influence the response to a

125 Changes in gastric microbiota composition might promote GIN in achlorhydric

126 In this study, we examined the microbiota composition of allo-HSCT recipients to identi

127 Data on perinatal pet ownership, WB, and the microbiota composition of faecal samples of the infants

128 Microbiota composition of specific pathogen-free (SPF) I

129 Although imbalances in gut microbiota composition, or "dysbiosis," are associated w

130 tion without affecting disease severity, gut microbiota composition, or gut permeability.

131 dataset, individuality was a major driver of microbiota composition (P = 0.002) and was more pronounc

132 erythromycin caused a significant change in microbiota composition (p=0.03 [by analysis of similarit

133 estinal tract is regulated by the intestinal microbiota composition, particularly the presence of seg

134 Our findings suggest that microbiota composition, perhaps Clostridium spp., contri

135 nd adipose tissue insulin sensitivity, fecal microbiota composition, plasma and fecal SCFA, energy ex

136 e previously showed differences in mucus gut microbiota composition preceded colitis-induced inflamma

137 In addition, alterations in microbiota composition preceded the onset of diarrhea, s

138 ranscript levels, metabolite levels, and gut microbiota composition, provide a framework for understa

139 We report that altering the microbiota composition reduces CRC in APC(Min/+)MSH2(-/-

140 t cold exposure leads to marked shift of the microbiota composition, referred to as cold microbiota.

141 Further, the changes in intestinal microbiota composition related to the improvement of thi

142 Restoration and maintenance of a healthy gut microbiota composition requires effective therapies to r

143 The analysis of the microbiota composition revealed a decrease of the relati

144 onas aeruginosa, erythromycin did not change microbiota composition significantly.

145 l physics, we calculate the duration of each microbiota composition state.

146 (median age, 35 d) were divisible into three microbiota composition states (NGM1-3).

147 atory machinery of the host and the resident microbiota composition, such that disturbances in one tr

148 neficial" influence of older siblings on the microbiota composition suggests that this microbiota may

149 ach geographic locale displayed a unique gut-microbiota composition that could not be fully explained

150 Perturbations in the gastrointestinal (GI) microbiota composition that occur as a result of antibio

151 In addition to alterations in gut microbiota composition, the metabolic potential of gut m

152 acteristics at sites of infection will shape microbiota composition through exerting selective pressu

153 Identifying differences in microbiota composition through the use of 16S rRNA gene

154 Strategies to use changes in microbiota composition to effect health improvements req

155 use of nutritional strategies to program the microbiota composition to favor a more beneficial bacter

156 Microbiota composition was analysed by a combination of

157 Fecal and rectal biopsy-associated microbiota composition was analyzed by 16S ribosomal DNA

158 Microbiota composition was characterized using 16S ribos

159 Microbiota composition was determined by 16S rRNA gene s

160 Microbiota composition was determined in 167 participant

161 Microbiota composition was determined using 16S ribosoma

162 Microbiota composition was heterogeneous, but there was

163 The gastric microbiota composition was highly variable between indiv

164 ere examined for basal phenotypes, including microbiota composition; we also analyzed responses to pa

165 etabolic disease and inflammation, and fecal microbiota composition were assessed.

166 Dietary habits affect gut microbiota composition, whereas endotoxins produced by G

167 Analysis revealed significant segregation of microbiota compositions which was validated by Beta dive

168 ciated with significantly altered intestinal microbiota composition, which was linked to an impaired

169 tribution, HF diet also drastically affected microbiota composition with a profile characterized by t

170 ection accelerated the rate of change in gut microbiota composition within individuals for periods of

171 Diet impacts microbiota composition, yet mechanisms that link dietary