ライフサイエンスコーパス: feces

1 ine (below the cut-off value of 10 mug Hb/ g feces).

2 erocytes, cause diarrhea, and be shed in the feces.

3 e evaluated on four different pools of human feces.

4 fects on the microbiota composition of human feces.

5 egg density plateau of about 1000 eggs/g of feces.

6 t correlate with a higher fungal load in the feces.

7 obotic platform for direct analysis of human feces.

8 nation of virus shedding in oropharynges and feces.

9 cteroidetes, and increased Firmicutes in the feces.

10 reater in secondary environments compared to feces.

11 g rates of pathogens originating from animal feces.

12 rstanding the molecular composition of human feces.

13 host-associated bacteria in animal or human feces.

14 ed in seawater and in gull, cat, and raccoon feces.

15 secretions, oviposition materials, and even feces.

16 HDM extracts, as well as purified bodies and feces.

17 Pseudomonadaceae and Shewanellaceae in their feces.

18 e of viable E. coli populations in livestock feces.

19 groups 1, 6, 18, and 23 well represented in feces.

20 subsequently deposited on the host with the feces.

21 discovered shared by chicken, pig and human feces.

22 significant ARG enrichment in adult chicken feces.

23 the animals but are mostly released with the feces.

24 n facility that adequately retains or treats feces.

25 IgEs to allergens present in mite bodies and feces.

26 d, as assessed by detection of SIVcpz RNA in feces.

27 spp. and Clostridiaceae in high weight hard feces.

28 d animal (avian, cattle, poultry, and swine) feces.

29 approach to extract metabolic information in feces.

30 , and Akkermansia spp. were enriched in soft feces.

31 ermine the overall metabolite composition of feces.

32 igh RNA copy numbers detectable in serum and feces.

33 ion, were measured in intestinal tissues and feces.

34 genomic and metatranscriptomic sequencing of feces.

35 ios at which nutrients are deposited through feces.

36 transfer of cholesterol from macrophages to feces.

37 for screening the metabolite composition in feces.

38 e nitrogen-to-phosphorus ratios of herbivore feces.

39 Infected badgers shed M. bovis in their feces.

40 he abundance of distinct microbial genera in feces.

41 or, subsequent to, FIT >15 mug hemoglobin/g feces.

42 versity of antimicrobial resistance genes in feces.

43 hemical signatures from animal carcasses and feces.

44 t; 39.8 +/- 51.2 g) than loggerhead turtles (feces; 1.6 +/- 3.7 g, gut; 9.7 +/- 15.0 g).

45 positivity thresholds <=10 mug hemoglobin/g feces, 10 to <=20 mug/g, 20 to <=30 mug/g, and >30 mug/g

46 y attributed to bacterial cells in the donor feces (~1011 per gram of human wet stool).

47 443-535 mg/kg feces) compared with 698 mg/kg feces (1438-244 mg/kg feces), P = 0.03].

48 10), and green turtles ingested more debris (feces; 15.8 +/- 33.4 g, gut; 39.8 +/- 51.2 g) than logge

49 each participant, duplicate meals (0-96 h), feces (24-120 h), and indoor/outdoor dust (<250 mum) wer

50 children who died [median (IQR): 1360 mg/kg feces (2443-535 mg/kg feces) compared with 698 mg/kg fec

51 cial debris appeared in all green turtles in feces (25/25) and gut contents (10/10), and green turtle

52 erovirus RNA was more commonly identified in feces (42 of 44 [95%]), rectal swabs (35 of 37 [95%]), a

53 s, viral RNA was detected more frequently in feces (80%) and particularly in blood (85%), and antivir

54 Omadacycline is excreted unchanged in feces (81.1%) and urine (14.4%), with low potential for

55 sferred with Blastocystis sp. negative donor feces (93%, 76/82).

56 sferred with Blastocystis sp.-negative donor feces (93%, 76/82).

57 oth enamel and, together with vegetation and feces, analyzed for delta(26)Mg, delta(13)C, Sr/Ca, and

58 D. farinae extracts, manufactured from both feces and bodies.

59 re of transmission vehicles, including human feces and breast milk.

60 rformed RNA-Seq on exfoliated cells found in feces and compared these data to RNA-Seq from both the s

61 Antibiotics reduced bacterial load in feces and could promote the formation of renal calcium c

62 Feces and diet were assayed for Mn, fat, and gross energ

63 (ADE) was calculated from ADDM and the GE of feces and diet; apparent digestibility of fat (ADfat) wa

64 on biopsies and exfoliated colonocyte RNA in feces and fecal microbial community composition, and to

65 Since top 7 serogroup-positive cattle feces and ground beef can also contain nonadulterant E.

66 loggerhead and green turtles in addition to feces and gut contents analyses from 2007 to 2015.

67 uency of occurrences of artificial debris in feces and gut contents collected from loggerhead turtles

68 metabolic fingerprinting workflow for human feces and in vitro digestive fluids.

69 es, Deferribacteres, and Spirochaetes in the feces and increased abundance of Pasteurella in the orop

70 hly 90% to zero by day 30, and is highest in feces and lower respiratory tract samples.

71 Transplanting mice with human feces and O. formigenes introduced new microbial populat

72 These changes in bacterial abundance in the feces and oropharynx correlated with lower asthmatic res

73 between congener-specific concentrations in feces and serum were found for all BDEs except BDE-197 a

74 ed the concentration of nitroso compounds in feces and small intestinal content.

75 ples and recovery of viable virus from mouse feces and small intestine suggest that these pests may p

76 os of both species were retrieved from fresh feces and survived beyond hatching.

77 The bacterial profiles of feces and the mucosa of sigmoid colon, but not duodenum,

78 MF(lim) by controlling the Z-values of their feces and the volume reduction of the food in the gastro

79 lyzed to assess topographical homogeneity of feces and to evaluate storage duration-, temperature-, a

80 the excretion and treatment of human waste (feces and urine) in low and middle income countries (LMI

81 nsecutive weeks and sampled cutaneous mucus, feces and water at 0, 7 &14 days.

82 Symptoms involve diarrhea with watery feces and weight loss that have their functional correla

83 detection method for S. typhimurium in bird feces and whole milk.

84 Samples of feces and/or colon contents were collected and volatile

85 l cultures (e.g., intestinal contents, human feces) and reduce TMAO levels in mice fed a high-choline

86 ive result from an FIT (>15 mug hemoglobin/g feces) and subsequent colonoscopy (reference standard) w

87 feces), at a uniform threshold (15 mug Hb/g feces), and at adjusted thresholds yielding defined leve

88 ence of heavy infections (>=400 eggs/gram of feces), and total prevalence being particularly importan

89 containing vertebrate resources: 23% DNA, 5% feces, and 14% contained both.

90 e orally dosed compound is eliminated in the feces, and a major fraction of the absorbed compound is

91 At baseline and every 4 wk, blood, urine, feces, and anthropometric and body composition measures

92 entified on an assembled scaffold of chicken feces, and are carried by human pathogens.

93 ls from pure cultures, culture-spiked cattle feces, and culture-spiked ground beef.

94 L did not develop infection or shed virus in feces, and IgG anti-HEV antibody levels were unchanged (

95 its reduced levels of IgA in the serum, gut, feces, and lactating mammary gland.

96 affected pigs, environmental samples, mouse feces, and mouse small intestine.

97 Bacterial composition of feces, and mucosa of the duodenum and sigmoid colon was

98 thyl hydroxychromanol (alpha-CEHC) in urine, feces, and plasma that were catabolized from administere

99 ces were 3.8%, 1.6%, and 0.02% in the urine, feces, and reference cohorts, respectively.

100 testinal [GI]) colonization, shedding within feces, and transmission of K. pneumoniae through the fec

101 measurements of calories of nutrient intake, feces, and urine by bomb calorimetry.

102 lth risks associated with exposure to animal feces; and factors influencing concentrations and sheddi

103 ors related to points of contact with animal feces; animal fecal contamination of food; cultural beha

104 In feces, antibiotics drastically decreased trisulfides but

105 mination is likely to be minimal unless bird feces are deposited close to the land-sea interface.

106 the polysaccharide compositions of food and feces are determined, further illustrating the utility o

107 liver, whereas stable naked virions shed in feces are optimized for environmental transmission.

108 study investigated the feasibility of using feces as a noninvasive matrix to estimate serum concentr

109 ehold, and b) the use of human and/or animal feces as fertilizer.

110 The hepatitis E virus (HEV) sheds into feces as nonenveloped virions but circulates in the bloo

111 differential bacterial communities in their feces as well as serum metabolomics profile.

112 es, revealing coprostanol, a proxy for human feces, as the most abundant sterol (seawater: 45.1-20.3

113 rus was stable in the absence of bacteria or feces at most temperatures, M132V virus was stabilized b

114 tyrate and propionate (>=95th percentile) in feces at the age of one year had significantly less atop

115 temperatures, M132V virus was stabilized by feces at very high temperatures.

116 t most temperatures but can be stabilized by feces at very high temperatures.

117 turers' thresholds (range, 2.0-17.0 mug Hb/g feces), at a uniform threshold (15 mug Hb/g feces), and

118 tor 8a (IR8a) is essential for acid-mediated feces avoidance in ovipositing hawkmoths.

119 (oculomotor) avoidance of disgusting images (feces) before and after an "exposure" intervention (mone

120 Extracts prepared only from Adj-Vac group feces blocked O157 adherence to epithelial cells.

121 Plants, feces, bulk milk and cheese samples were collected on tw

122 wn as nutrient sources through deposition of feces, but also may deposit large quantities of energy i

123 the abundance of Bifidobacterium species in feces by 5-fold (P = .009; q = 0.144).

124 odology for extraction and analysis of fresh feces by NMR-based metabolomics.

125 externalities; for example, safe disposal of feces by one household prevents disease transmission to

126 creased levels of 2 miRNAs and hemoglobin in feces can identify patients with AAs or CRC more accurat

127 shedding SVA in oral and nasal secretions or feces can serve as sources of infection to other suscept

128 Feces collected from adult recipients allo-HSCT at engra

129 the bacterial load of EHEC O157:H7 strain in feces, colon and caecum tissues after murine infection.

130 dian (IQR): 1360 mg/kg feces (2443-535 mg/kg feces) compared with 698 mg/kg feces (1438-244 mg/kg fec

131 serum concentrations of tetra-decaBDEs from feces concentrations and enable a noninvasive sampling m

132 er for heavy-feces-containing than for light-feces-containing liquid-suspended specimens.

133 T) values for bla(KPC) were higher for heavy-feces-containing than for light-feces-containing liquid-

134 Animal feces contribute to fecal contamination, and fecal indic

135 e identify routes of contamination by animal feces, control measures to reduce human exposure, and pr

136 Here we describe fossilized feces (coprolites) that demonstrate recurring consumptio

137 As fossilized feces, coprolites represent direct evidence of animal be

138 Contamination by young children's feces could be identified and distinguished separately f

139 6, -207, -208, and -209 were detected in the feces creating a matched data set (feces-serum, n = 21).

140 ta diversity of the microbiome measured from feces demonstrated significant differences between The J

141 ility), did not affect the overall amount of feces deposited but led to changes in the average body s

142 Feces deposited in areas of higher rainfall and reduced

143 sferred with Blastocystis sp. positive donor feces did not report any significant difference in bowel

144 sferred with Blastocystis sp.-positive donor feces did not report any significant differences in bowe

145 n the GI tract and levels of shedding in the feces differed among the clinical isolates tested.

146 tal colons were removed, and colon contents (feces, distal colon, and tumor) were collected.

147 of P. aeruginosa from the bloodstream to the feces during bacteremia, a process that promotes transmi

148 ant and that this deterrence is based on the feces-emitted carboxylic acids 3-methylpentanoic acid an

149 those associated with human, dog, and mouse feces, exhibit AQI-dependent incidence dynamics.

150 uivalent counts of Escherichia coli in dairy feces exposed to different environmental conditions and

151 anaviruses and their detection in organs and feces followed over time by PCR, immunohistochemistry an

152 shed one strain >10(1) log10 CFU/g in their feces for 16.4 days, which persisted in the environment

153 was defined as at least 400 eggs per gram of feces for S. mansoni infection or as more than 50 eggs p

154 This mutant virus does not require feces for stability at most temperatures but can be stab

155 nce of tests in detecting M. bovis in badger feces for the Department for Environment, Food, and Rura

156 Finally, feces from 10 healthy individuals and 13 patients diagno

157 ate such effects of RT storage, we collected feces from 29 healthy infants (0-3 months) and partition

158 he presence of the gene for intimin (eae) in feces from 42% of kittens.

159 rom catch basins, a constructed wetland, and feces from a beef cattle feedlot were compared over a tw

160 Feces from axenic cockroaches (no microorganisms in the

161 Here, we show that feces from conspecific caterpillars are sufficient to de

162 1 copy of human REG3A transgene but were fed feces from control mice (not expressing hREG3A) as newbo

163 m REG3A-TG mice had lower levels of ROS than feces from control mice during DSS administration.

164 S-induced colitis after cohousing or feeding feces from control mice.

165 , compared with their counterparts receiving feces from healthy controls.

166 e assigned to groups that underwent FMT with feces from healthy donors or were given autologous fecal

167 We analyzed blood and feces from healthy donors, patients with selective IgA d

168 in humans, we colonized germ-free mice with feces from healthy or cow's milk allergic (CMA) infants(

169 In feces from healthy participants, the main groups detecte

170 For humanization, we transplanted pooled feces from healthy, noncolonized human donors supplement

171 associated with lower levels of SCFAs in the feces from infected rats.

172 Feces from mice were analyzed by 16s ribosomal RNA seque

173 Compared with feces from wild-type mice, feces from mice with defects in TGFB signaling had incre

174 equencing of prokaryotic 16S rRNA present in feces from naive mice and those exhibiting CP-EAE or RR-

175 exhibited unacceptable cross-reactions with feces from other hosts.

176 Cohoused and germ-free mice fed feces from REG3A-TG mice and given DSS developed less-se

177 ed survival times compared with mice not fed feces from REG3A-TG mice.

178 FAs in various biological samples, including feces from stressed rats, sera of patients with kidney d

179 e number of matching short sequence reads in feces from the 92 animals in the two clinical and the he

180 Sanitation interventions that isolate human feces from the environment may reduce transmission but h

181 d shotgun metagenomic sequencing analyses of feces from wild-type mice and mice with defects in TGFB

182 Compared with feces from wild-type mice, feces from mice with defects

183 l samples from Hol(Tg/Tg) mice compared with feces from wild-type mice; fecal microbiomes of mice giv

184 result was increased from 15 to 47 mug Hb/g feces halfway through 2014.

185 Here, we unexpectedly found that transfer of feces harvested at peak disease from the experimental au

186 Exposure to animal feces has been associated with diarrhea, soil-transmitte

187 Nutrients released through herbivore feces have the potential to influence plant-available nu

188 ermine clinical status, serologies and serum/feces HEV RNA every 4 months.

189 16S-rDNA-encoding sequence analysis in feces identified a significant reduction in the short-ch

190 Extensive anaerobic subculturing of human feces identified no single commensal capable of l-carnit

191 ated from serum, urine, salivary glands, and feces in a murine model.

192 of a parent in childhood, exposure to animal feces in infancy, birth in the dry season, or duration o

193 atter, other components in unprocessed human feces include colonocytes (~107 per gram of wet stool),

194 Differences in Pb species between diet and feces indicated that transformation of Pb species can oc

195 Gs (7762 x/Gb) was detected in adult chicken feces, indicating higher ARG contamination level than ot

196 ile acid pool (~3 g in human) is excreted in feces, indicating the large recycling capacity and high

197 Sepsis was induced by cultivated autologous feces inoculation in anesthetized, mechanically ventilat

198 Ranavirus-exposed smooth newts shed virus in feces intermittently and infection was seen in the absen

199 Microscopic examination of feces is a standard laboratory method for diagnosing gas

200 EPE in urine or feces is a substantial risk factor for subsequent EPE-BS

201 sistance disseminating from animal and human feces is an urgent public issue.

202 Although feces is often abundant and can be collected noninvasive

203 gallbladder can then seed the intestines and feces, leading to transmission to uninfected cage-mate m

204 To track young children's feces (<3 years old) separately from other human-associa

205 on interventions that directly address child feces management.

206 Unsafe disposal of children's feces may contribute to this continued exposure, but its

207 to -0.09, P = 0.02), and time to passage of feces (mean difference -0.90 days, 95% CI -1.48 to -0.32

208 to -0.32, P < 0.0001) and time to passage of feces (mean difference -1.09 days, 95% CI -2.03 to -0.15

209 Escherichia coli, was retrieved from chicken feces metagenomes and was determined to carry diverse AR

210 ere followed from their first EPE finding in feces (n = 5513) or urine (n = 17189).

211 Bacterial communities were determined from feces obtained from domestic pigs (Sus scrofa) raised un

212 Although the SARS-CoV-2 RNA was found in the feces of 3 patients and in the duodenal wall of the pati

213 Feces of 43 children were collected prior, during and af

214 lone-resistant Escherichia coli are found in feces of 8.8% of healthy women, with most bacteria belon

215 ng of a metagenomic library derived from the feces of an AB donor enabled discovery of a significantl

216 Genotyping of cagA from feces of both infected and uninfected participants revea

217 of colonic GMB communities derived from the feces of captive specimens, leaving our understanding of

218 af-associated microbes were reflected in the feces of caterpillars consuming the same plants.

219 saguini was isolated from the intestines and feces of cotton-top tamarins (CTTs) with chronic colitis

220 es and more IgA-coated commensal bacteria in feces of DeltaDC mice.

221 a miRNA-microbiome axis and suggest that the feces of diseased subjects might be enriched with miRNAs

222 significant expansion of the pathogen in the feces of I-Ab(DeltaIEC) mice compared with I-Ab(WT) mice

223 nly mature S. mansoni eggs are shed into the feces of mice and humans.

224 Transplantation of microbiota from feces of mice fed the wheat- or ATI-containing diets to

225 mily Erysipelotrichaceae was enriched in the feces of mice on the AhR ligand-free diet but returned t

226 lly, we show that miR-30d is enriched in the feces of peak EAE and untreated MS patients.

227 The feces of pigs fed with 12% CP were less enriched in Prev

228 ow protein expression of E. coli LdcC in the feces of stage 1 breast cancer patients.

229 Serum and feces of subjects with MS exhibited significantly reduce

230 ermore, O157-specific IgA levels detected in feces of the Adj-Vac group were significantly lower in N

231 lum, Elusimicrobia were more abundant in the feces of treated cattle, however, there were no differen

232 he small intestine and were shed less in the feces of wild-type mice, and such defects were rescued i

233 umption of food contaminated with triatomine feces or didelphid secretions.

234 Helicobacter sp. was detected in 69% of feces or intestinal samples from 116 CTTs.

235 Incomplete removal of child and animal feces or the compound (versus community-wide) scale of i

236 hs strongly preferred the extract of control feces over the fecal extract of axenic cockroaches.

237 ompared with 698 mg/kg feces (1438-244 mg/kg feces), P = 0.03].

238 osed to pathogens from poorly managed animal feces, particularly in communities where animals live in

239 The chemical composition of feces plays an important role in human metabolism.

240 ecal microbiota transplantation (FMT), using feces provided by healthy donors.

241 rve as novel biomarkers of impaired liver-to-feces RCT in vivo.

242 mparison with low-fat diet, whereas liver-to-feces RCT was preserved after MUFA-HFD.

243 Macrophage-to-feces RCT, HDL efflux capacity, and HDL proteomic profil

244 SFA-HFD impaired liver-to-feces RCT, increased hepatic inflammation, and reduced A

245 rnover. Incubation of RV with SFB-containing feces reduced infectivity in vitro, suggesting direct ne

246 reduced food and water intake, combined with feces replete with lipid and bile acid, indicated a phen

247 h A. muciniphila after FMT with nonresponder feces restored the efficacy of PD-1 blockade in an inter

248 onic enemas with ion compositions similar to feces resulted in high local tissue levels with minimal

249 d, analysis of 24 h collections of urine and feces revealed recovery of less than 4% of the administe

250 We used the first feces sample of each patient (meconium), as well as the

251 ch patient (meconium), as well as the last 2 feces samples prior to development of NEC.

252 quantify Z-values by equilibrating food and feces samples, which have been homogenized and spiked wi

253 habitation with animals, provision of animal feces scoops, controlling animal movement, creating safe

254 The feces-serum associations found can be used to estimate s

255 ed in the feces creating a matched data set (feces-serum, n = 21).

256 as-associated quinolones and rhamnolipids in feces, setting the stage for metabolome-microbiome-wide

257 Hence, rectal swabs without visible feces should not be routinely rejected from testing.

258 esolution LC-MS analysis of bile, urine, and feces showed metabolic products derived from 4-PCB 11 su

259 f the copper pheophytins are excreted in the feces showing almost no absorption of copper-chlorophyll

260 filled intestines, abdominal pain, excessive feces, steatorrhea, and malnutrition.

261 and laundry) and blackwater (i.e., urine and feces) streams in terms of their loadings of ambient spe

262 ing ceftriaxone from the wetland compared to feces, suggesting resistance to this antibiotic may not

263 nstructed and serially filled with simulated feces tagged with four different iodine concentrations (

264 miRNAs were also found to be deregulated in feces (technical validation).

265 of several bacterial taxa in both blood and feces that correlate with the presence of LF, thus defin

266 where domestic animals are exposed to human feces that have been disposed in pits and open drains.

267 ion patterns) were monitored following human feces transfer.

268 impacts of exposure to poorly managed animal feces transmitted via water, sanitation, and hygiene (WA

269 ed bioreactors inoculated with healthy human feces, treated with clindamycin and infected with C diff

270 pounds in urine (UHPLC-MS/MS), bile acids in feces (UHPLC-QTOF), gastrointestinal conditions (ingesti

271 ed virus in nasal washes, saliva, urine, and feces up to 8 days post-infection.

272 DL-derived (3)H-cholesterol excretion in the feces was 107% higher (P < 0.001).

273 ian total daily excretion of menaquinones in feces was 850 nmol/d but was highly variable (range: 64-

274 Generic extraction of freeze-dried feces was achieved by solid-liquid extraction using meth

275 ribution of different Pb species in diet and feces was also affected by dietary P level.

276 each rejected in pseudofeces and egested in feces was determined.

277 mong environmental samples, young children's feces were almost always identified as the dominant sour

278 Markers for young children's feces were also detected in standing water and streams,

279 Feces were collected and analyzed by 16S ribosomal RNA g

280 Feces were collected and analyzed by 16S ribosomal RNA g

281 Feces were collected and assessed for consistency and oc

282 Feces were collected and microbiota were analyzed by 16S

283 Feces were collected and proportions of microbiota were

284 tivity, and psychological data and blood and feces were collected at baseline and at 8 weeks and 3 mo

285 Feces were collected at different time points after infe

286 Feces were collected before and after treatment initiati

287 Prior to harvest, composited feces were collected for characterization of the microbi

288 Additionally, feces were collected for seven days post-inoculation to

289 Feces were collected from mice and the composition of th

290 Feces were collected from mice on wheat-containing, ATI-

291 Herring gull regurgitates and feces were collected from several colonies with TBBPA-BD

292 bsequently, serum samples, tonsil swabs, and feces were collected from sows (n = 22) and their piglet

293 Feces were collected twice a week.

294 ands, surfaces) whereas older children/adult feces were often identified as the dominant source outsi

295 Feces were the major route of excretion; cumulatively ac

296 ult (hemoglobin concentration of 10 mug Hb/g feces) were invited for consultation and scheduled for c

297 al RNA amplicon sequencing were performed on feces, whereas urine and fecal metabolites were analyzed

298 role in the flow of macrophage-derived UC to feces, while the plasma increase of APOB-containing lipo

299 tinguished separately from older child/adult feces with high sensitivity and specificity in water and

300 (gt3) infections were cleared from liver and feces within 8 pegIFNalpha doses in all mice and relapse