ライフサイエンスコーパス: microbial composition

1 egration of only two datasets (phenotype and microbial composition).

2 abundance collectively accounted for 53% of microbial composition.

3 th developmental transitions and diet on gut microbial composition.

4 iotic therapy leading toward a gram-negative microbial composition.

5 has been associated with a distinct colonic microbial composition.

6 tion seen in the interindividual distance of microbial composition.

7 al relationships between metabolites and gut microbial composition.

8 aches on datasets with previously identified microbial composition.

9 ) influences cumulative charge, current, and microbial composition.

10 ations associated with alteration in mucosal microbial composition.

11 ting health using an individual's unique gut microbial composition.

12 a, while outer sabkha samples show different microbial composition.

13 t plus kanamycin (KAN) to quantify shifts in microbial composition.

14 controls with corresponding effects on fecal microbial composition.

15 hether they provide information about airway microbial composition.

16 e mediated by age and sex differences in gut microbial composition.

17 ith cardiometabolic health vary depending on microbial composition.

18 Host phylogeny is a major determinant of gut microbial composition.

19 elial lymphocytes and changed the intestinal microbial composition.

20 ociated with gastric H. pylori load and lung microbial composition.

21 itions, correspond to alterations to the gut microbial composition.

22 as conducted as a readout for changes in gut microbial composition.

23 geny was a strong driver of species-specific microbial composition.

24 ems and alters gastrointestinal function and microbial composition.

25 tion within the social network predicted gut microbial composition.

26 ing-based analysis to determine the baseline microbial composition.

27 veal its potential role in shaping human gut microbial composition.

28 althy controls exhibited similar subgingival microbial compositions.

29 andom errors well even without including gut microbial compositions.

30 C-reactive protein, fecal calprotectin, and microbial composition (16S-ribosomal RNA sequencing) wer

31 V infection of the GIT leads to dysregulated microbial composition, a cascade of metabolic alteration

32 s struggled to explain the high variation in microbial composition across individuals.

33 es to reveal patterns driving differences in microbial composition across phenotypes.

34 Micro-DeMix facilitates the comparison of microbial compositions across different GI regions withi

35 as the most influential factor of intestinal microbial composition acutely following VSG.

36 S disaccharides had a profound impact on gut microbial composition, affecting the abundance of 13.6%

37 hydrological shifts correlated to changes in microbial composition, alpha, beta and phylogenetic dive

38 strating the shared impact of factors on gut microbial composition also showed notable topological si

39 ad a significant long-term effect on patient microbial compositions, although this was primarily driv

40 vealed important quantitative differences in microbial composition among BXD strains.

41 and consistently demonstrated differences in microbial composition among the three sets of samples.

42 Infant gut microbial composition among vaginally born babies became

43 The UniFrac distances and microbial composition analysis showed significant differ

44 tagenomic sequencing was used to measure the microbial composition and abundance at the phylum, class

45 in soil carbon was driven by changes in soil microbial composition and activity.

46 gnaling and that the brain can in turn alter microbial composition and behavior via the autonomic ner

47 Overall, seawater microbial composition and biogeochemistry were influence

48 unity to gain unprecedented insight into the microbial composition and biomolecular activity of true

49 o explore the relationship between shifts in microbial composition and changes in periodontal health

50 microbiology, it is possible to dissect the microbial composition and complex interactions in suppre

51 dy demonstrates that SMEAR robustly predicts microbial composition and diversity from digital images

52 practice with soybeans was found to increase microbial composition and diversity in carrot plantation

53 We show that prolonged shifts in gut microbial composition and diversity induced by long-term

54 analysis was conducted to determine the soil microbial composition and diversity of the soils used in

55 of recovery for baseline assessments of gut microbial composition and diversity using 16S-based meta

56 Our results showed that gut microbial composition and diversity varied by season.

57 were marked health-associated alterations in microbial composition and diversity, including different

58 diseases have expanded our insight into how microbial composition and function affect the human host

59 Accordingly, the evaluation of a patient's microbial composition and function and its subsequent ta

60 proteomics, and metabonomics, differences in microbial composition and function are being linked to h

61 types, we tested how spatial variability in microbial composition and function changed in response t

62 Similarly, microbial composition and function exhibit circadian rhy

63 and gnotobiotic colonizations to define the microbial composition and function in fecal samples obta

64 Altered microbial composition and function in inflammatory bowel

65 Here, we characterized microbial composition and function, and gut-brain metabo

66 ng of predator-prey interactions, changes in microbial composition and function, and subsequent reper

67 rients, depleted prebiotics, additives), gut microbial composition and function, host metabolic expen

68 fluence of biogeography and individuality on microbial composition and function.

69 e, partially mediated through changes in gut microbial composition and function.

70 pe-specific and symptom-related variation in microbial composition and function.

71 on of metagenome sequencing to elucidate the microbial composition and functional capacity present in

72 16S rRNA gene was sequenced to determine gut microbial composition and functionality.

73 ree fatty acids, could further influence the microbial composition and immune responses.

74 may also have favorable effects on the fecal microbial composition and incidence of diarrhea in infan

75 olitis can promote tumorigenesis by altering microbial composition and inducing the expansion of micr

76 hat effectively reinstated the dysbiotic-gut microbial composition and intestinal microenvironment in

77 erely report associations between intestinal microbial composition and metabolic disorders such as ob

78 ects of gastrointestinal UFP exposure on gut microbial composition and metabolic function using an in

79 However, how plants determine the microbial composition and network interactions is still

80 d large variations in colony development and microbial composition and no observable negative impact

81 However, little is known about the microbial composition and pathways that mediate these ac

82 Microbial composition and PC function were examined in m

83 ed significant beta-diversity differences in microbial composition and predicted genetic functional p

84 Changes in microbial composition and predicted metagenomic function

85 in clinically, they have been noted to alter microbial composition and promote bacterial translocatio

86 such as antibiotic administration, can alter microbial composition and result in the loss of coloniza

87 Breastfeeding affected gut microbial composition and seemed to protect from sensiti

88 Furthermore, IC enhanced the active microbial composition and strong positive correlations w

89 and site were significantly associated with microbial composition and that maternal factors determin

90 d then compare the association between fecal microbial composition and the adiposity phenotypes in a

91 nity level reveal a tri-stability pattern in microbial composition and the emergence of three distinc

92 Microbial composition and the mechanisms of interaction

93 uantify the association between longitudinal microbial composition and time-to-event outcomes.

94 Data were processed to identify the microbial composition and to assess alpha and beta diver

95 e impact of human behaviors on diets and gut microbial composition and, backwards, through a control

96 associated with alterations in specific gut microbial compositions and subclinical levels of gut inf

97 g and metagenomic sequencing to examine oral microbial compositions and their functional variations i

98 s fragilis corrects gut permeability, alters microbial composition, and ameliorates defects in commun

99 enzyme immunoassay), lipopolysaccharide, gut microbial composition, and food frequency questionnaire

100 Dietary factors, microbial composition, and metabolism are intimately int

101 assessing the host response (transcriptome), microbial composition, and microbial function (metatrans

102 The effects of chewing on in vivo biofilm, microbial composition, and spatial arrangement were exam

103 a, tree-guided empirical Bayes estimation of microbial compositions, and tree-based multiscale regres

104 Notably, microbial composition appeared to converge in the active

105 Changes in microbial composition are implicated in the increasing p

106 These differences in gut microbial composition are influenced by host-genetics, w

107 ncreases risk for asthma, and distinct nasal microbial compositions are associated with asthma.

108 We tested whether microbial composition at 1 year of age is associated wit

109 omposition at a given time point affects the microbial composition at a later time point.

110 Beta diversity result showed similar kind of microbial composition between inner and edge sabkha, whi

111 There were no observed differences in gut microbial composition between INR and IR.

112 bsence of Bifidobacterium and differences in microbial composition between the sexes that probably re

113 evidenced by a profound difference in rumen microbial composition between the two age groups.

114 ultidomain approach revealed stable distinct microbial compositions between thermal phenotypes.

115 hat both host genotype and environment shape microbial composition, but the relative importance of ge

116 onship between drug exposures and changes in microbial composition by developing and applying a new c

117 mal MER levels and characterised their rumen microbial composition by performing shotgun metagenomics

118 Additionally, we show that the gut microbial composition can be utilized to predict serum u

119 The impact of BTPs on colon microbial composition can now be assessed by microbiomic

120 ering patients into subgroups based on their microbial compositions can greatly enhance our understan

121 addition, we discovered an alteration of gut microbial composition change because of combinatorial tr

122 ing of the associations between longitudinal microbial composition changes and disease outcomes.

123 This study measures microbial composition changes during biofilm overgrowth

124 quantitative and qualitative changes in gut microbial composition, changes in microbial functionalit

125 FP diets markedly altered microbial composition, characterized by increases in Mur

126 Our data reveal marked changes in microbial composition co-occurring with changes in hydro

127 eatic secretion showed only minor changes in microbial composition, comparable to the ones seen in pr

128 gh these mechanisms, OMZ expansion may alter microbial composition, competition, diversity and functi

129 ever, responses of plants to the turnover in microbial composition depended on the identity of the se

130 The microbial composition, determined by 16S rRNA gene seque

131 Sample clustering derived from ulcer microbial composition did not show geographical patterns

132 Microbial composition did not significantly change over

133 at patients with Crohn's disease (CD) have a microbial composition different from healthy individuals

134 Dysbiosis, an imbalance in gut microbial composition, disrupts immune regulation, metab

135 ciality) are associated with patterns of gut microbial composition (diversity and similarity) between

136 ecomposer communities, within a litter type, microbial composition drives variation in the quantity o

137 ment through converging modifications to gut microbial composition during pregnancy and transmission

138 to prevent or reduce pain, yet its impact on microbial composition during sampling remains unclear.

139 Deviations from healthy microbial compositions (dysbiosis) have been linked with

140 ight alleviate diseases arising from altered microbial composition ('dysbiosis').

141 strong responders, based on differential gut microbial composition (e.g., Lactobacillus, Bacteroides,

142 promoted colitis, indicating that changes in microbial composition enhanced chronic colitis in those

143 inistration of HD5 effectively altered cecal microbial composition, especially increased Akkermansia

144 on as a factor significantly influencing gut microbial composition following colorectal surgery, whil

145 This study aimed to determine the salivary microbial composition for 10 HIV-seropositive subjects,

146 alling for a systematic consideration of gut microbial composition for personalized diet recommendati

147 yer perceptron) was able to discriminate gut microbial composition from CFS versus HCs with excellent

148 by providing a comprehensive analysis of the microbial composition from various bacterial communities

149 Here, we uncover a gradient of intestinal microbial compositions from rural through urban Tanzania

150 Altered gut microbial composition has been widely acknowledged as a

151 tary interventions based on individuals' gut microbial compositions holds great promise for precision

152 e, improves survival, and does not alter gut microbial composition; however, by allowing dose intensi

153 Although chitin influences gut microbial composition, ILC2-mediated tissue adaptation a

154 d to differ in relation to pregnancy status, microbial composition, immune activation, and pregnancy

155 To this end, we tested predictors of gut microbial composition in a well-studied population of wi

156 as well as a significant change in the oral microbial composition in both TLR2 and TLR4 KO mice demo

157 ificant between-group differences in the gut microbial composition in CFS compared to HCs were noted.

158 ness of therapies aimed at modifying the gut microbial composition in CFS patients.

159 cing revealed that inflammation modifies gut microbial composition in colitis-susceptible interleukin

160 Recent studies suggest that microbial composition in crustal habitats is variable in

161 edict environmental characteristics based on microbial composition in datasets where beta-diversity m

162 n lead to caries development by altering the microbial composition in dental plaque, but little is kn

163 e course-specific, supporting a role for gut microbial composition in EAE pathogenesis.

164 d that only a minority of taxa depend on the microbial composition in earlier times.

165 Our results suggest that upper airway microbial composition in infancy contributes to the deve

166 enomic sequencing to investigate the role of microbial composition in mediating anxiety- and depressi

167 Changes in the microbial composition in mice after BDL included the enr

168 act as a bioactive compound and modulate gut microbial composition in mice.

169 hnology has been widely used to quantify the microbial composition in order to understand its impacts

170 FMT) represents a feasible way to manipulate microbial composition in patients, with a potential bene

171 There were significant shifts in microbial composition in pigs maintained on a diet conta

172 larly, we demonstrate that the effect of the microbial composition in previous time points on the abu

173 Finally, we profiled the microbial composition in The Cancer Genome Atlas gastric

174 In addition, the gut microbial composition in the CFS patients contained a mu

175 ither directly or through alterations of the microbial composition in the gut.

176 Patients with mild asthma have an altered microbial composition in the respiratory tract that is s

177 between dietary patterns and measures of gut microbial composition in this sample of community-dwelli

178 dance can be predicted based on the previous microbial composition) in longitudinal studies, which ca

179 les of dietary components that alter the gut microbial composition include prebiotics and resistant s

180 Many factors are known to influence gut microbial composition, including diet.

181 effects of salinity, via alterations in soil microbial composition, increased invasive performance wh

182 rmore, the ALINCH-Q microspheres altered the microbial compositions, increased the relative abundance

183 functional profiles, but less variable than microbial composition, indicative of subject-specific wh

184 g filters, gel lubrication did not alter the microbial composition, individual taxa abundance or alph

185 Metagenomics/metabolomics indicate microbial composition is associated with functional shif

186 rement error; if the underlying variation in microbial composition is large among samples, rarefactio

187 Considering that the gut microbial composition is modulated by diet, we tested th

188 Although salt amendment strongly impacted microbial composition, it did not increase the predictab

189 -control study to investigate differences in microbial composition, it is fundamental to assess the s

190 nitine supplementation in mice altered cecal microbial composition, markedly enhanced synthesis of TM

191 r and a cost-effective method to profile the microbial compositions, marker-gene sequencing cannot pr

192 o environmental changes, which influence the microbial composition, matrix formation and expression o

193 ross IgAN cohorts, functional alterations in microbial composition may contribute to disease pathogen

194 ollectively, our data suggest that shifts in microbial composition may play a role in the pathogenesi

195 As such, gut microbial composition may provide valuable information o

196 C) and nitrogen (N) which can influence soil microbial composition (MCC) and enzyme activities, and h

197 Fecal microbial composition, metabolites, and pH of infants re

198 ur findings indicate that despite changes in microbial composition, microbial functional pathways wer

199 Additionally, we observed that microbial composition modulated the protective associati

200 Treatment operations drove the microbial composition more strongly than sampling time.

201 e and pregnancy, while daily fluctuations in microbial composition observed through culture-independe

202 ith streptomycin, substantial changes in the microbial composition occurred, with a marked loss of po

203 Little is known about how the microbial composition of a community and the potential f

204 Learning associations of traits with the microbial composition of a set of samples is a fundament

205 how these phytochemicals could modulate the microbial composition of a soil in the absence of the pl

206 nfected mosquito survival, and perturbed the microbial composition of adult mosquito midguts.

207 ferent strategies were explored to shift the microbial composition of AGS from methanogenic to exoele

208 a cost effective method for quantifying the microbial composition of an environment, such as the hum

209 To investigate the microbial composition of atherosclerotic plaques and tes

210 Our results revealed that microbial composition of bacteria, archaea and fungi in

211 re-independent technology to investigate the microbial composition of biofilms inside showerheads as

212 ata to investigate their reliability for the microbial composition of both liquid and solid forms of

213 We explore the microbial composition of challenging, heterogeneous clin

214 The microbial composition of dental plaque from 42 severe EC

215 encing to characterize the global pattern of microbial composition of fecal samples from 196 hospital

216 ies in people and are in consonance with the microbial composition of feline subgingival sites.

217 Microbial composition of house dust may influence allerg

218 The microbial composition of induced sputum specimens collec

219 assess the effects of dental flossing on the microbial composition of interproximal plaque samples in

220 In this study, the rumen microbial composition of late lactation dairy cows grazi

221 Characterizing the microbial composition of metagenomic samples is crucial

222 technique toward the characterization of the microbial composition of microbiota as it is nondestruct

223 Microbial composition of nasopharyngeal swab samples sub

224 ur studies provide further evidence that the microbial composition of our gut has an important role i

225 PDT promotes changes in the microbial composition of periodontitis patients' subging

226 continue to be valuable for determining the microbial composition of samples.

227 In replicate soil columns, the efficacy and microbial composition of soil bioaugmented with the ureo

228 is article we summarize our knowledge on the microbial composition of the 5 best-characterized body s

229 In addition, we compared the microbial composition of the experimental inocula with t

230 the ability of the probiotic to modulate the microbial composition of the gastrointestinal tract.

231 Microbial composition of the gut may be an important fac

232 After four generations, the microbial composition of the insect gut was evaluated to

233 In swine, studies that have investigated the microbial composition of the oral cavity of pigs are sca

234 usal relationships between the chemistry and microbial composition of the rhizosphere.

235 The microbial composition of the samples was determined usin

236 as performed to investigate the influence of microbial composition of the transplanted material on th

237 ation sequencing to evaluate the subgingival microbial composition of young patients with severe peri

238 ctonic setting influence the geochemical and microbial compositions of these hydrothermal ecosystems.

239 16 S rRNA gene sequencing showed the microbial compositions of wastewaters to be widely varia

240 h has highlighted significant effects of gut microbial composition on obesity.

241 Small intestinal microbial composition, on the other hand, is significant

242 While E2 exposure did not alter microbial composition or putative function, colonized E2

243 le is known about the factors that alter the microbial composition or their contribution to liver dis

244 children were found in bacterial diversity, microbial composition, or single-genus abundances.

245 eous and dynamic with substantial changes in microbial composition over time and only few taxa persis

246 th remodeled the gut microbiota with similar microbial composition, Parabacteroides distasonis was mo

247 Gut microbial composition pre and post-transplant was altere

248 ckens to CTB or LTB causes shifts in the gut microbial composition, providing evidence for new toxin

249 asurements demonstrated correlations between microbial composition, puff volume, and metabolic disrup

250 However, existing studies focus on microbial composition rather than transcriptional activi

251 nd columns allowed the identification of the microbial composition regardless if the well contains si

252 ality resistance was regulated by changes in microbial composition (relative abundance of phylotypes)

253 Correlation of microbial composition represents integration of only two

254 ework may offer predictions not only for how microbial composition responds to changing environmental

255 used 16S rRNA gene amplicons to evaluate how microbial compositions shift in response to exposure of

256 As a direct consequence, microbial composition shifts dramatically, and spontaneo

257 unity participants and provide insights into microbial composition shifts in response to physiologica

258 Microbial composition showed high variability across coh

259 oth mitigated oral dysbiosis and altered gut microbial composition, signifying potential broader impl

260 on and integration of subject-level factors, microbial composition, systemic immune response, and gin

261 Microbial composition tended to differ between children

262 plots explained two times more variation in microbial composition than native plants.

263 including shifts in BA signaling and altered microbial composition that confer a transmissible phenot

264 Identifying breast and gut microbial compositions that respond positively to certai

265 able therapeutic strategies for shifting the microbial composition to a healthy configuration.

266 (> 15%), illustrating the importance of gut microbial composition to animal behaviour.

267 rom breast milk shape neonate and infant gut microbial composition to be protective against environme

268 file corrector (METRIC), which leverages gut microbial compositions to correct random errors in self-

269 study, we analyzed a coastal sabkha for its microbial composition using 16S rDNA and whole metagenom

270 l three critical window periods and analysed microbial composition using 16S rRNA gene sequencing.

271 estradiol levels correlate with subgingival microbial composition using checkerboard DNA-DNA hybridi

272 The microbial composition varied among the individuals, but

273 The fecal microbial composition was analyzed by Genetic Analysis G

274 Microbial composition was assessed by Genetic Analysis G

275 weekly over a period of 13 weeks, and stool microbial composition was assessed using 16S rRNA gene s

276 In asthmatic patients airway microbial composition was associated with airway eosinop

277 Microbial composition was compared between those with/wi

278 ds were measured by colorimetric assays, and microbial composition was determined by 16S pyrosequenci

279 Microbial composition was evaluated by the core microbio

280 Gut microbial composition was explored using 16S ribosomal r

281 and Main Results: An increased similarity of microbial composition was found between MWF samples and

282 Microbial composition was fundamentally different, with

283 Recovery of the gut microbial composition was incomplete two months after TP

284 Microbial composition was not affected by intensified me

285 Our ability to predict soil microbial composition was not improved by incorporating

286 Microbial composition was not related to inflammatory su

287 annon diversity indices; however, a distinct microbial composition was observed in COVID-19 patients

288 Differences in microbial composition were also observed in dust samples

289 diversity of the microbiome, and changes in microbial composition were observed until the 12th month

290 ase, and yet significant changes in the oral microbial composition were observed.

291 Three strata with different microbial composition were obtained in the samples at ba

292 /-) mice exhibit profound alterations in gut microbial composition, which contributes to inflammation

293 s that utilize NGS data as input to decipher microbial composition, which output can predict function

294 Disinfection had the greatest impact on microbial composition, which was further refined by filt

295 variations led to robust adjustments in the microbial composition while still maintaining the ontoge

296 intake, had strong directional influences on microbial composition, while salivary factors like flow

297 This change in microbial composition with age occurs in parallel with a

298 Successional control over microbial composition with forest recovery suggests stro

299 diet, was strongly associated with a defined microbial composition, with an increased abundance of fi

300 Here, we evaluated site-specific microbial composition within the vaginal ecosystem and e