ライフサイエンスコーパス: CFU

1 CFU counts in lungs by 28% (P < .05), 34%, and 2.0 log10

2 CFUs were summarised as median and interquartile range (

3 ited microbial growth (from 1.4 x 10(7) to 0 CFU/mL) and hindered biodegradation.

4 hower aerosols ranged from ~10(-2) to ~10(0) CFU per L and ~10(1) to ~10(3) CFU per L for infection a

5 ity with a limit of detection (LOD) of 10(0) CFU/mL (1-9 CFU/mL), real-time target specificity.

6 The LAMP-STR quantitated sea in 10-1,000 CFU (7.2-720 copies).

7 n respond to bacterial challenge with 25,000 CFU Pseudomonas aeruginosa embedded into agarose beads t

8 K. oxytoca, or Proteus mirabilis at >=50,000 CFU/mL, (2) identification of an ESBL gene by uropathoge

9 ubjects without a face mask (difference 1.07 CFUs; P = .001), subjects with a loose face mask (differ

10 nge from 5 to 100 CFU/mL with a LOD of 0.093 CFU/mL.

11 ple and specific assay to detect as low as 1 CFU mL(-1) of E. coli in water within 6 hours by targeti

12 entrations, and microorganisms in blood at 1 CFU mL(-1) (colony forming unit per milliliter) threefol

13 ineered bacteriophages accurately detected 1 CFU in either 25 g of ground turkey with a 7 h enrichmen

14 1 mL (CFU mL(-1)) by the naked eye and 10(1) CFU mL(-1) using ImageJ software.

15 across a range of cell cultures - from 10(1) CFU/ml to 10(9) CFU/ml.

16 with a low limit of detection of 1.5 * 10(1) CFU/mL.

17 ere 5 genome equivalents per reaction and 10 CFU/ml blood for both the B. anthracis Sterne and V1B st

18 d detected 10(4) CFU/g in ground pork and 10 CFU/mL in milk in 5-7 days, LAMP-AuNP could detect down

19 entification with a limit-of-detection at 10 CFU/muL for 5% diluted whole blood samples.

20 es with a lower concentration of E. coli (10 CFU/mL; colony-forming unit per mL) as well as maintain

21 Furthermore, approximately <10 CFU per mL L. pneumophila may be appropriate for healthc

22 W to the same target of Escherichia coli <10 CFU/100 mL and used to irrigate lettuce plants (Lactuca

23 mit of the device has been shown to reach 10 CFU/mL for Pseudomonas aeruginosa and Staphylococcus aur

24 5-7 days, LAMP-AuNP could detect down to 10 CFU/g for both samples in 27 minutes.

25 say LOD was 8.5 CFU/ml for F. tularensis, 10 CFU/ml for B. anthracis, and 4.5 CFU/ml for Y. pestis Th

26 f detection for this bacterial sensor was 10 CFU/ml and ability of this FRET immunosensor for Campylo

27 stically significant impedance change was 10 CFU/mL.

28 tracheal instillation of E. coli (1.5-2 x 10 CFU/kg).

29 ere inoculated with H. pylori (10(8-) 10(10) CFU/mL; 1 mL/rat.) for 3 consecutive days; and (3) HP +

30 G was reduced by 0.39, 0.96 and 0.73 log(10) CFU following subcutaneous (s.c.) BCG, intranasal (i.n.)

31 ne), whereas CHX reduced 1.4 and 1.2 log(10) CFU mL(-1) .

32 givalis viability, with 2.78 and 1.7 log(10) CFU mL(-1) of reduction in both single and multi-species

33 P. aeruginosa and OPP-C mean log(10) CFU/cm(2) counts were higher in p-trap and tail pipe bio

34 lactic acid bacteria increased by 2 Log(10) CFU/mL (LU), whereas mold decreased by 1 LU, E. coli and

35 nt on solid culture by 0.84 +/- 0.02 log(10) CFU/ml at 23 degrees C (P < 0.001) and 0.85 +/- 0.01 log

36 rees C (P < 0.001) and 0.85 +/- 0.01 log(10) CFU/ml at 30 degrees C (P < 0.001), respectively.

37 P. aeruginosa and OPP-C mean log(10) CFU/ml counts were also higher (p < 0.05) in HCP compare

38 50] in the sertraline group vs 0.47 -log(10) CFU/mL per day [0.40-0.54] in the placebo group; p=0.59)

39 id was similar between groups (0.43 -log(10) CFU/mL per day [95% CI 0.37-0.50] in the sertraline grou

40 The results showed that up to 3.51 log(10)CFU/g B. cereus spore inactivation was achieved with 8 k

41 Gy of gamma radiation, and up to 1.69 log(10)CFU/g reductions could be achieved after 28s of catalyti

42 riophages had a limit of detection of 10-100 CFU per mL in culture without enrichment.

43 th an ULD or a conventional Mtb dose (50-100 CFU) that correlated with lung bacterial burdens and pre

44 ity (300 fg/well, corresponding to about 100 CFU per reaction mixture volume).

45 wed detection limits as low as 7, 40 and 100 CFU/mL for S. aureus in pure broth culture, and inoculat

46 The pLFS could detect as low as 100 CFU/ml of E. coli O157:H7 in buffer and 600 CFU/ml E. co

47 a range below the food safety control (<100 CFU/g).

48 steria detection with high sensitivity (<100 CFU/mL in 2 h) that can be paired with many antibody or

49 f the MRSA aptasensor swab was less than 100 CFU/ml and theoretically using a standard curve, was 2 C

50 inically relevant linear range from 5 to 100 CFU/mL with a LOD of 0.093 CFU/mL.

51 olony-forming units (CFU) in vitro and <1000 CFU in the lungs of mice.

52 limit: 391 CFU/mL, sensitivity: 0.6 nm/1000 CFU mL(-1); 1646 nm/RIU).

53 t (94 CFU/mL), high sensitivity (2.9 nm/1000 CFU mL(-1); 3135 nm/RIU) and profound specificity as com

54 current guidance documents of less than 1000 CFU per L, while DALY-based guidance suggests lower crit

55 nt colony forming units (CFUs) at 1 per 1000 CFUs in as little as 48 hrs.

56 forming units [CFU] and group 2: 0.5-1 x 103 CFU).

57 onstrating an attack rate of 80% with 10(11) CFU of H10407 ETEC.

58 (PBS) alone and then challenged with 10(11) CFU of H10407.

59 allenged orogastrically with 10(9) to 10(11) CFU of the human pathogenic CFA/I(+) ETEC strain H10407

60 ight face mask without tape (difference 1.13 CFUs; P < .001).

61 es, the limits of detection were 178 and 133 CFU g(-1) or mL(-1), respectively.

62 or achieved a limit of detection (LOD) of 14 CFU/mL, the lowest reported to-date using EIS-phage sens

63 nd a 95% confidence interval from 122 to 140 CFU mL(-1).

64 The limits of detection (LODs) were 150 CFU/ml or 3 fg/mul of DNA for B. pertussis and 1,500 CFU

65 Genius PCR assay limit of detection was 0.16 CFU/PCR test or 4.16 genome copies (GCs)/test.

66 QR:15-82), 2.5% PI had a median growth of 18 CFUs (IQR:10-32) and 5% PI had a median growth of 2 CFUs

67 te an extrapolated limit of detection of 2.2 CFU/ml from experimental data in buffer solution with no

68 sfully detected concentrations as low as 9.2 CFU/mL in laboratory samples and 920 CFU/mL in apple jui

69 itive, exhibiting a limit of detection of ~2 CFU mL(-1).

70 esulting in a limit of detection (LoD) of ~2 CFU/mL.

71 theoretically using a standard curve, was 2 CFU/ml.

72 is H37Rv in all spiked animal samples were 2 CFU/ml compared to 15.6 CFU/ml for humans, while the LOD

73 QR:10-32) and 5% PI had a median growth of 2 CFUs (IQR:0-5).

74 tion of S. typhimurium was found to be 10(2) CFU mL(-1) in culturing solution without any pre-enrichm

75 mL in these aqueous samples in 3 h and 10(2) CFU/mL after 7 h.

76 e limit of detection was approximately 10(2) CFU/mL and the total bacterial aerosol concentration was

77 5) CFU/ml in either women or men (or >=10(2) CFU/ml of a single bacterial species from a single cathe

78 ntration, with a limit-of-detection at 10(2) CFU/muL for buffer samples, and binary target or no-targ

79 (n = 87), and 50% for those with EFA < 0.20 CFU/mL/day (n = 187).

80 For sonication culture, >=20 CFU of bacteria per 10 ml of sonicate fluid was consider

81 re 1,800 CFU.ml(-1) for B. pertussis and 213 CFU.ml(-1) for B. parapertussis The assay detected 16/18

82 us detection at concentrations as low as 224 CFU/ml can be achieved within a short time span of 30 mi

83 A limit of detection (LoD) up to 240 CFU/mL, comensurate with cut-off for UTIs (10(3)-10(5) C

84 Control plates had a median growth of 25 CFUs (interquartile range [IQR]:15-40), 1% PI plates had

85 within 45 min at the detection limit of 0.3 CFU per 25 g of raw seafood.

86 target) would result in an estimate of 12.3 CFU per L (arithmetic mean of samples across multiple fi

87 0)]) and intranasal challenge with 5 x 10(3) CFU (50 LD(50)) of virulent Y. pestis This protection wa

88 tion of Salmonella at levels as low as 10(3) CFU mL(-1).

89 h conventional fixture would be 1.06 x 10(3) CFU per L (faucets), 8.84 x 10(3) CFU per L (toilets), a

90 06 x 10(3) CFU per L (faucets), 8.84 x 10(3) CFU per L (toilets), and 14.4 CFU per L (showers).

91 1.02 x 10(5), 8.59 x 10(5), and 1.40 x 10(3) CFU per L for faucets, toilets, and showers, respectivel

92 -2) to ~10(0) CFU per L and ~10(1) to ~10(3) CFU per L for infection and CSI dose response models, re

93 ection risk target would give a 1.20 x 10(3) CFU per L mean for multiple fixtures and single sample c

94 antibiotic with low bacterial counts (10(3) CFU) in 20 min; thus, redox properties of CDs has the po

95 y of NTHi from 6 x 10(5) CFU/ml to 9 x 10(3) CFU/ml (P = 0.0004).

96 AST on E. coli with a concentration of 10(3) CFU/mL is presented.

97 mits of detection at 1 x 10(3) to 10 x 10(3) CFU/ml or as few as 50 CFU per assay.

98 concentration of the MF-SERS system is 10(3) CFU/mL, which is 4 orders of magnitude lower than that u

99 6) CFU/ml and a detection limit of 3 x 10(3) CFU/ml.

100 le detection limit of the biosensor is 10(3) CFU/mL.

101 ntrations of Escherichia coli reaching 10(3) CFU/ml.

102 sible to detect bacteria in milk at 1 x 10(3)CFU.ml(-1), which corresponds to the limit set in Europe

103 ns, while the LOD for M. bovis SB0121 was 30 CFU/ml compared to 143.4 CFU/ml for M. bovis BCG in huma

104 -40), 1% PI plates had a median growth of 30 CFUs (IQR:15-82), 2.5% PI had a median growth of 18 CFUs

105 fiber optic SPR sensor (detection limit: 391 CFU/mL, sensitivity: 0.6 nm/1000 CFU mL(-1); 1646 nm/RIU

106 with a limit of detection (LOD) of 131 +/- 4 CFU mL(-1) and a 95% confidence interval from 122 to 140

107 , 8.84 x 10(3) CFU per L (toilets), and 14.4 CFU per L (showers).

108 bovis SB0121 was 30 CFU/ml compared to 143.4 CFU/ml for M. bovis BCG in humans.

109 ith a sensitivity of approximately 3 x 10(4) CFU from the kidneys.

110 coli cell detection and from 1 to 4 x 10(4) CFU mL(-1) E. coli quantification.

111 ckness burn wounds inoculated with 1 x 10(4) CFU of P. aeruginosa.

112 ocus-forming units of rotavirus, <1 x 10(-4) CFU of Vibrio cholerae, and <9 x 10(-6) Cryptosporidium

113 While the culture method detected 10(4) CFU/g in ground pork and 10 CFU/mL in milk in 5-7 days,

114 e detected with a linear range between 10(4) CFU/ml and 5 x 10(6) CFU/ml and a detection limit of 3 x

115 Any urine specimen with >=10(4) CFU/ml group B Streptococcus is significant for asymptom

116 In simulated infections, if >=10(4) CFU/ml of N. gonorrhoeae was present, sequencing of the

117 aureus with starting concentration of 10(4) CFU/mL were removed from 5 mL blood in a few hours.

118 f Streptococcus pneumonia from 50 to 5x10(4) CFU/mL were successfully performed in 25% human serum.

119 arensis, 10 CFU/ml for B. anthracis, and 4.5 CFU/ml for Y. pestis The sensitivity was 100% at the LOD

120 The assay LOD was 8.5 CFU/ml for F. tularensis, 10 CFU/ml for B. anthracis, an

121 gainst subcutaneous challenge with 8 x 10(5) CFU (80,000 50% lethal dose [LD(50)]) and intranasal cha

122 teria concentrations ranging from 10 - 10(5) CFU mL(-1).

123 ing underneath them two catheters with 10(5) CFU of P. aeruginosa before the surgical wounds were her

124 ghest for both Escherichia coli (4.2 x 10(5) CFU/mg) and Staphylococcus aureus (6.1 x 10(5) CFU/mg) v

125 U/mg) and Staphylococcus aureus (6.1 x 10(5) CFU/mg) via growth inhibition and cytoplasmic membrane d

126 and egg samples with 10(3), 10(4) and 10(5) CFU/mL E. coli O157:H7 were 106.98, 96.52 and 102.65 (in

127 he sensing system falls between 10 and 10(5) CFU/mL in a buffer solution by cyclic voltammetry (CV) m

128 er, all bacterial targets reported as >10(5) CFU/ml in culture were reported as >=10(5) genomic copie

129 isolated in a quantitative count of >=10(5) CFU/ml in either women or men (or >=10(2) CFU/ml of a si

130 ies isolated in a quantitative count >=10(5) CFU/ml in men; and a single catheterized urine specimen

131 at the concentration of approximately 10(5) CFU/mL in these aqueous samples in 3 h and 10(2) CFU/mL

132 , isolated in quantitative counts of >=10(5) CFU/ml in women, including pregnant women; a single void

133 colonization density of NTHi from 6 x 10(5) CFU/ml to 9 x 10(3) CFU/ml (P = 0.0004).

134 he LFIA's limit of detection was 3.0 x 10(5) CFU/mL with B. pertussis cells in buffer, 6.2 x 10(5) CF

135 th B. pertussis cells in buffer, 6.2 x 10(5) CFU/mL with nasopharyngeal washes from a non-human prima

136 sitivity (Limit of detection-LoD, 6.54*10(5) CFU/ml) of the Lamb wave traveling on the polymeric devi

137 linear range of quantitation was 10(2)-10(5) CFU/ml.

138 mensurate with cut-off for UTIs (10(3)-10(5) CFUs/mL) was achieved.

139 x 10(3) to 10 x 10(3) CFU/ml or as few as 50 CFU per assay.

140 reshold (n = 43) or count differences of >50 CFU (n = 11).

141 n samples with a lower detection limit of 50 CFU/mL.

142 The detection limit was 50 CFU/mL.

143 r 3 fg/mul of DNA for B. pertussis and 1,500 CFU/ml or 10 fg/mul of DNA for B. parapertussis A total

144 in the real chicken sample at less than 500 CFU mL(-1), the minimum infectious dose for C. jejuni wh

145 CFU/mL, and its lower detection limit was 58 CFU/mL.

146 nimal samples were 2 CFU/ml compared to 15.6 CFU/ml for humans, while the LOD for M. bovis SB0121 was

147 e dose of 1 x 10(4), 1 x 10(5), or 1 x 10(6) CFU of B. abortus S19 or the vaccine candidate B. abortu

148 ear range between 10(4) CFU/ml and 5 x 10(6) CFU/ml and a detection limit of 3 x 10(3) CFU/ml.

149 d concentration range from 10(2) up to 10(6) CFU/mL in both buffer fluids and relevant food samples (

150 on AlN on silicon substrate (LoD, 1.04*10(6) CFU/ml).

151 rium ranging from 1.4 x 10(2) to 1.4 x 10(6) CFU/mL, and its lower detection limit was 58 CFU/mL.

152 iles and total fungi counts were below 10(6) CFU/mL, showing good microbiological stability.

153 CFU/ml of E. coli O157:H7 in buffer and 600 CFU/ml E. coli O157:H7 in liquid food systems.

154 ects with a loose face mask (difference 0.67 CFUs; P = .034), and subjects with a tight face mask wit

155 mean CFUs per milliliter (90 596 and 114 683 CFU/mL for serogroup B and C strains, respectively; P <

156 with an intranasal inoculation of 5 x 10(7) CFU M. muris 24 h before coinfection.

157 lowed by intranasal challenge with 5 x 10(7) CFU of NTHi R2866 Spec(r) Mice were pretreated or not wi

158 B/c mice, even at an infective dose of 10(7) CFU.mL(-1).

159 ureus with a starting concentration of 10(7) CFU/mL and 95.4 +/- 1.0% of Methicillin-resistant Staphy

160 in the concentration range from 50 to 10(7) CFU/mL within 100 min was achieved.

161 presence of higher bacterial inoculum (10(7) CFU/mL) or by lowering the pH in standard media to simul

162 acterial concentrations as high as 8 x 10(7) CFU/mL.

163 l response curves performed with 10(0)-10(7) CFUs/mL of E. coli K12 in synthetic urine yielded recove

164 ures with populations ranging from 1 to 10(7)CFU/10mL were detected in a single step without any prep

165 ration was carried out using 10(7) and 10(8) CFU mL(-1) Pseudomonas fluorescens to study the effects

166 ight times on days 1-4 and 8-11 at 5 x 10(8) CFU/dose, followed by a 2-week asthma induction protocol

167 neumococcal inoculum (1 x 10(6) to 1 x 10(8) CFU/mouse) and postinfection lung bacterial burden did n

168 constitute an obstacle to L. casei 01 (>10(8)CFU/g) during storage.

169 The limits of detection (LoDs) were 1,800 CFU.ml(-1) for B. pertussis and 213 CFU.ml(-1) for B. pa

170 The method has a limit of detection of 845 CFU/mL and excellent discrimination against high concent

171 d in a limit of detection (LoD) as low as 86 CFU/mL and 94 CFU/mL for S. typhimurium and S. enteritid

172 imit of detection (LOD) of 10(0) CFU/mL (1-9 CFU/mL), real-time target specificity.

173 f cell cultures - from 10(1) CFU/ml to 10(9) CFU/ml.

174 as 9.2 CFU/mL in laboratory samples and 920 CFU/mL in apple juice samples in ~90 min.

175 the same mask without tape (difference 0.93 CFUs [95% confidence interval 0.32-1.55]; P = .003).

176 f detection (LoD) as low as 86 CFU/mL and 94 CFU/mL for S. typhimurium and S. enteritidis, respective

177 bits better performance, detection limit (94 CFU/mL), high sensitivity (2.9 nm/1000 CFU mL(-1); 3135

178 ty and stress resistance, employing qPCR and CFU counts to measure abundance of core microbiota taxa

179 ed to be the difference between MPN(rpf) and CFU.

180 nto individual PCR mixtures and B. anthracis CFU into human blood.

181 , allowing detection of as low as 1 C. auris CFU per reaction within 3 h.

182 etection (LOD) of the assay was one C. auris CFU/PCR.

183 is sensitive enough to detect ~100 bacterial CFU/mL but has the potential to estimate even lower conc

184 pe (M+V+) exhibited higher average bacterial CFU per IJ than did high-Lrp (M+V-) or no-Lrp (M-V-) str

185 ing the surface application, total bacterial CFU at Hospitals A and B declined by 64% and 75%, respec

186 the surface application, the total bacterial CFUs at Hospitals A and B declined by 79% and 75%, respe

187 units [CFUs]) + inulin (1 g), LS (1 billion CFU) or placebo.

188 donors, with telomere length in CH vs non-CH CFUs showing varying patterns.

189 Number of microbial colonies (CFU) was recorded.

190 After adjusting for other confounders, CFU and age remained significantly associated with MG dr

191 56 days, lack of quantitative sputum culture CFU count data, and no examination of the correlation of

192 at day 16, there was significantly decreased CFU (Analysis of variance, p = 0.001) in the photobiomod

193 5med immature colony-forming unit-erythroid (CFU-E) population.

194 eMegEs), and colony-forming units-erythroid (CFU-Es), as well as myeloid and erythroid blood cells.

195 (10), 1.3 log(10), and 2.4 log(10) estimated CFU/ml for 16S rRNA, tmRNA, pre-16S rRNA, and rpoB, resp

196 ting surgical mask with tape developed fewer CFUs compared with subjects wearing the same mask withou

197 gical mask with tape had significantly fewer CFUs compared with subjects without a face mask (differe

198 Clonogenic assay for CFU- granulocyte-monocyte suggested that HMGB1 may be re

199 ole combination significantly reduced fungal CFU burdens in infected nematodes by ~75-96%.

200 a cell line CEM and the normal hematopoietic CFU-GM.

201 Older homes were found to have higher CFU compared to newer homes.

202 Individuals with higher CFU counts in the home had more severe MG dropout, after

203 This finding suggests that home CFU exposure may impact MG dropout, one of the DE measur

204 and inhibited the expansion of the immature CFU-E subset.

205 shed platelets and saw a similar decrease in CFU.

206 DS gave significantly better improvements in CFU, wound area, and wound strength compared to photobio

207 tions as evident by significant reduction in CFU (>90%) at 5-10 times lower concentrations than that

208 ll density, indicating that the reduction in CFU number is explained by cells entering into a Viable

209 rain LH128-GFP showed about 99% reduction in CFU while microscopic counts of GFP-expressing cells wer

210 ibition) and 97.60% (dispersal) reduction in CFU with exposure to 40 mM amino acids.

211 lung lesion burden and a 0.7 log decrease in CFUs.

212 osfomycin separately significantly increased CFUs, by approximately 3 logs and 1 log, respectively, c

213 Instrumented CFU significantly associated with 2 DE measures: corneal

214 ophilic and psychrotrophic bacteria (1-2 log CFU/g) were obtained with 5% PT treatment compared to th

215 7:H7 for 30 min to achieve a 3.2 +/- 0.2 log CFU/mL reduction.

216 ecific fish spoilers were reduced by 2-4 log CFU/g in wrapped sample during the chilled storage perio

217 gar manufacturers was reduced by up to 4 log CFU/ml, and phenotypic differences in colony size and co

218 microbial load of the settled must was 4-log CFU/mL for both yeast and moulds, and slightly lower for

219 l viable counts increased slowly up to 6 log CFU g(-1) at the end of storage, coliform bacteria disap

220 L. fermentum strains had counts of >6 log CFU/g on day 60 and/or 90 of refrigeration storage.

221 esulted in higher probiotic survival (>6 log CFU/mL in product and simulated gastrointestinal conditi

222 to mandarin juice, resulting in up to 6 log CFU/mL microbial count reduction.

223 S and 1% Quillaja saponin resulted in >6 log CFU/ml reduction in Salmonella population.

224 L. fermentum strains had counts of >9 log CFU/g and contents of QUE and RES of >200 ug/mg in formu

225 cum, ileum and jejunum, by more than one log CFU/g when compared to the no-probiotic control group.

226 ions were highly synergistic, killing >6 log CFUs/g of vegetations in 6 hours and successfully treati

227 he method covers the range of 0.65-7.87 Log (CFU/cm(2)) and produces results in 1-8 hrs.

228 n lungs by 28% (P < .05), 34%, and 2.0 log10 CFU units (P < .05) compared with BCG-WT, respectively.

229 the 3-step technique vs median RF 1.04 log10 CFU [interquartile range 0.49-1.52] for the 6-step techn

230 ontrol was -0.11 (95% CI, -.29 to .07) log10 CFU/mL/day faster with single dose (n = 16); -0.05 (95%

231 = 18); and -0.13 (95% CI, -.35 to .09) log10 CFU/mL/day faster with 3 doses (n = 18).

232 curve and gulls shed one strain >10(1) log10 CFU/g in their feces for 16.4 days, which persisted in t

233 (n = 16); -0.05 (95% CI, -.20 to .10) log10 CFU/mL/day faster with 2 doses (n = 18); and -0.13 (95%

234 An EFA threshold of > = 0.20 log10 CFU/mL/day was associated with similar 18-week mortality

235 EFA for daily L-AmB was -0.41 log10 CFU/mL/day (standard deviation, 0.11; n = 17).

236 with vancomycin yielded medians of 0.1 log10 CFUs per K-wire, respectively.

237 MRSA from bones (0.10, 3.02, and 0.10 log10 CFUs/g, respectively) than did no treatment (4.36 log10

238 pectively) than did no treatment (4.36 log10 CFUs/g) or vancomycin alone (4.64 log10 CFUs/g) (both P

239 og10 CFUs/g) or vancomycin alone (4.64 log10 CFUs/g) (both P <= .02).

240 apy recovered medians of 1.76 and 2.91 log10 CFUs/g per K-wire, respectively.

241 rming units (CFUs) per gram of bone or log10 CFUs per K-wire, respectively.

242 However, quarters of MSC cows had lower CFU log/mL in milk compared to quarters of NEG cows.

243 re was a >22-fold increase in geometric mean CFUs per milliliter (90 596 and 114 683 CFU/mL for serog

244 patients with low IL-10 (35.5 vs 0.5 median CFU/mL; P = .044).

245 ction of 10(2) colony forming unit per 1 mL (CFU mL(-1)) by the naked eye and 10(1) CFU mL(-1) using

246 c. + mucosal boost) log(10) reduction in MTB CFU was found.

247 TCH, a further 0.58 log(10) reduction in MTB CFU was revealed in the i.n. group.

248 as associated with a 3% increase in nutrient CFU (95% confidence interval [CI] = 0.01 to 0.04; P < .0

249 When comparing the amount of CFU isolated from carious biopsies from different colour

250 tectable bacillary load (estimated number of CFU [eCFU] per milliliter) by 0.66 +/- 0.21 log(10) at 2

251 al culture optical density and the number of CFU.

252 in three ways: by determining the numbers of CFU recovered from the lysates of the infected monolayer

253 ood samples spiked with different numbers of CFU were used to measure the analytical limit of detecti

254 F. tularensis DNA in buffer or CFU of F. tularensis was spiked into human or macaque bl

255 P3 presented significantly different reduced CFU/mL reduction in comparison to the negative control (

256 with the number at stasis, and only reduced CFUs by approximately 1 log and 2 logs, respectively, co

257 Nylon brush were most effective in reducing CFU counts (P < 0.01 versus control), whereas Chlorhexid

258 icillin-treated mice colonized with a single CFU, VRE rapidly diversified and expanded into distinct

259 SEM, Raman), and microbiological techniques (CFU, OD(600), ATP-levels).

260 The CFU/mL for subgingival yeasts were higher in group A tha

261 The CFU/mL for subgingival yeasts were higher in group B tha

262 r 1 week postinfection) as measured by total CFU.

263 antral glands in addition to measuring total CFU.

264 fection (1 or 3 months postinfection), total CFU were highly variable but similar for wild-type and s

265 The log-transformed CFU ratio at T=0 was predictive for ESBL-E carriage at T

266 ed by conventional agar colony forming unit (CFU) and most probable number (MPN) with Rpf supplementa

267 ein (CRP) and bacterial colony forming unit (CFU) confirmed improved bacterial clearance.

268 organ colony-forming unit (CFU) counts.

269 (n = 25) or 30 billion colony-forming unit (CFU) of a mixture of six viable strains including 107 mg

270 otic used per bacterial colony forming unit (CFU), not by the absolute antibiotic concentration, as s

271 on range of 10(4)-10(8) colony forming unit (CFU)/ml.

272 lity was quantified by colony forming units (CFU mL(-1) ), and biofilm images were acquired by confoc

273 to identify bacterial colony forming units (CFU) and percent of sites positive for select clinically

274 tween bioluminescence, colony-forming units (CFU) count and fluorescence were obtained for BKC concen

275 We assessed colony forming units (CFU) counts, biofilm removal, surface changes via scanni

276 these provided log(10) colony forming units (CFU) data from caries biopsies following colour and hard

277 0 is approximately 100 colony-forming units (CFU) in vitro and <1000 CFU in the lungs of mice.

278 than 0 and 10 or more colony-forming units (CFU) of aerobic bacterial growth on either sampling loca

279 ntaining <1000 E. coli colony-forming units (CFU) per 100 mL removes E. coli from hands with>99.9% pr

280 a dramatic decrease in Colony Forming Units (CFU) upon soil inoculation but this behavior is not well

281 c cell count (SCC) and colony forming units (CFU).

282 it of detection of 300 colony forming units (CFU)/mL for C. trachomatis and 1500CFU/mL for N. gonorrh

283 and control <0.2 log10 colony-forming units (CFU)/mL/day.

284 detection of only 100 colony-forming units (CFU)/reaction was obtained, and all necessary microfluid

285 Counting of viable colony forming units (CFU/mL) and confocal laser scanning microscopy were perf

286 res were the number of colony-forming units (CFUs) and microbial species.

287 to identify bacterial colony forming units (CFUs) and the percent of sites positive for select, clin

288 ence of drug resistant colony forming units (CFUs) at 1 per 1000 CFUs in as little as 48 hrs.

289 were reported as log10 colony-forming units (CFUs) per gram of bone or log10 CFUs per K-wire, respect

290 The log10-transformed colony-forming units (CFUs) per mL CSF were analyzed by general linear regress

291 in B and T cells; (2) colony-forming units (CFUs) revealed clonal evolution or multiple independent

292 72 h and the number of Colony Forming Units (CFUs) was determined.

293 uced the P. aeruginosa colony-forming units (CFUs), by approximately 2 and 5 logs, compared with stas

294 , corresponding to 121 colony-forming units (CFUs)/mL of MTB strain H37Rv.

295 (median RF 0.97 log10 colony-forming units [CFU] [interquartile range 0.39-1.59] for the 3-step tech

296 ls (group 1: 1-5 x 103 colony-forming units [CFU] and group 2: 0.5-1 x 103 CFU).

297 ontained LS (1 billion colony forming units [CFUs]) + inulin (1 g), LS (1 billion CFU) or placebo.

298 ological examination (colony forming units, [CFU]), wound area measurement, wound closure rate, wound

299 r signal was determined and then TVC values (CFU/cm(2)) were calculated using the calibration equatio

300 easures did not significantly associate with CFU.

301 am-negative bacteria aerosols in vitro, with CFU reductions observed as early as within 5 min, and in