ライフサイエンスコーパス: CFU

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

2 lture and expressed as colony-forming units (CFU).

3 little as one bacterial colony forming unit (cfu).

4 teria with a detection limit of >/= 5 x 10(5)CFU.

5 time frame that correlated with reduced lung CFU.

6 a seeded concentration of approximately 150 CFU.

7 silosis for at least 28 days, as measured by CFU.

8 = 50) vaccination and inoculated with 80,000 CFU/100 mul of Streptococcus pneumoniae (6B) per naris.

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

10 contamination below a detection limit of 10 CFU/25 cm(2) (0.4 CFU/cm(2)).

11 ring 20 years were 507 colony forming units (CFU)/5 plate every year.

12 ed kitchen floors (Beta: -0.65 log10 E. coli CFU/900 cm(2); 95% CI: -1.15, -0.16).

13 n and dirt floors (Beta: -1.18 log10 E. coli CFU/900 cm(2); 95% confidence interval [CI]: -1.77, -0.6

14 e veterinary practice was able to reduce the CFU and biofilm biomass of all three Gram-negative speci

15 onan production (mucoid colonies 200 mug per CFU and no detectable capsule production in the non-muco

16 tently high correlation coefficients between CFU and relative bioluminescence; P. aeruginosa ATCC9027

17 The relationship between culturable counts (CFU) and quantitative PCR (qPCR) cell equivalent counts

18 es higher fibroblastic colony-forming units (CFUs) and mesensphere capacity, criteria for assessing s

19 orally to serotype Kentucky received 10 exp9 CFU, and hens injected with serotype Enteritidis receive

20 solates were observed to have a reduction in CFU, and minimal effects were observed for P. aeruginosa

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

22 However, the CFU assay is difficult to standardize and requires 2 wee

23 ion functional in vitro colony-forming unit (CFU) assay for single cells that differentiates down bot

24 (+) (LSK) cells, and by colony forming unit (CFU) assay.

25 neumococci developed significantly more lung CFUs at 48 h.

26 rming units [CFUs]) increased from 4% of all CFUs at week 4 to 16% at week 12, indicating transductio

27 dard incubator at 37 degrees C, with TTD and CFU being monitored for up to 72 h.

28 gle specimen spiked with approximately 1,500 CFU bla(KPC) Klebsiella pneumoniae; however, the detecti

29 Apc(Min/+) mice were infected with CR (10(8) CFU); BLT1(-/-)Apc(Min/+) mice, azoxymethane (AOM)/dextr

30 g agents (EDTA formulations) reduced E. coli CFU but were ineffective at disrupting preformed biofilm

31 pores and led to a 26-fold reduction in lung CFU by 6 d postinfection versus nondepleted mice.

32 d the biofilm bacterial burden of S. aureus (CFU cm(-2)) by three logs with no statistically signific

33 s contaminated ( approximately 1.34 +/- 6.88 CFU/cm(2) C. difficile spores).

34 ow a detection limit of 10 CFU/25 cm(2) (0.4 CFU/cm(2)).

35 (lake) and 1.7 x 10(4) (sedimentation pond) cfu (colony forming units)/100 mL.

36 CI, 0.22-0.28), was strongly correlated with CFU content as well as ALDH(br) content of the CBU.

37 he correlations among ALDH(br), CD34(+), and CFU content of 3908 segments over a 5-year period.

38 lular M. tuberculosis growth (as measured by CFU count).

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

40 Second, stable necrotic granulomas with low CFU counts and limited inflammation are characterized by

41 ably, comparative evaluation showed that MTB CFU counts in BBD-treated mice were lower than those in

42 B-infected mice could significantly decrease CFU counts in the lung and spleen.

43 ells), proliferation by colony forming unit (CFU) counts, and differentiation by staining for the pre

44 e specificity was lowered to 89.5% with a 12-CFU cutoff.

45 by reduced abscess severities and decreased CFU densities compared to those in naive controls.

46 ositivity rates of 0%, 0%, 30%, and 100% and CFU detection of blood culture at 0%, 0%, 0%, and 10% po

47 For detecting hVISA/VISA on BHI-V3, a 2-CFU/droplet cutoff provided 98.5% sensitivity and 93.8%

48 These results suggest that 2-CFU/droplet cutoffs on BHI-V4 and BHI-V3 best approximat

49 For VISA screening on BHI-V4, a cutoff of 2 CFU/droplet provided 100% sensitivity and 97.7% specific

50 and enhances the formation of Epo-sensitive CFU-E progenitors.

51 and erythroid colony-forming unit (BFU-E and CFU-E) colonies, the clonogenic assays that quantify ear

52 From the CFU-E/proerythroblast (CD71(+) Ter119(-) cells) stage on

53 yte/macrophage, burst-forming unit-erythroid/CFU-erythroid, and CFU-granulocyte/erythroid/macrophage/

54 e colony-forming unit erythroid progenitors (CFU-Es) that respond to Epo are either too few in number

55 mean residual lung fungal burdens of <1,000 CFU from an otherwise lethal C. posadasii intranasal inf

56 ith starting concentrations as low as 10(0) CFU, from 100 or 250 mL of culture broth within similar

57 to generate colony-forming unit-fibroblasts (CFU-Fs) on plastic and the large cell numbers required f

58 sor cells that give rise to plastic-adherent CFU-Fs.

59 nd whole milk with detection limits of 10(5) CFU g(-1) and 10(3) CFU mL(-1), respectively, and this i

60 ated lactobacilli also remained high (>7 log cfu g(-1)) for 2months at 4 degrees C.

61 more bacteria than the estimated ID50 (2.83 CFU g(-1)), consistent with a soil-borne reservoir emerg

62 her than 6.5 and 7 log colony-forming units (CFU) g(-1) of cheese at the 1st and 28th days of storage

63 ining a total of 10(7) colony-forming units (CFU)/g of Bifidobacterium bifidum, Bifidobacterium breve

64 e therapy killed 7 log colony-forming units (CFUs)/g of fibrin clots in 6 hours.

65 n promoted an increase of approximately 3log CFU/g cycles of the microorganisms and the storage proce

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

67 llin provided significant reduction (1.73log CFU/g) in yeast-mold growth.

68 ins (Lactobacillus + Lactococcus (6 x 10(10) CFU/g), Bifidobacterium (1 x 10(10)/g), Propionibacteriu

69 counts to the limit of detection (2.0 log10 CFU/g), whereas metronidazole was associated with mean C

70 Above densities of 4.2 x 10(10) cfu/g, QS Salmonella had similar expression levels to co

71 rvival, with presented values of about 9 log CFU/g, ranging from 7.11 to 9.21 log CFU/g, respectively

72 t 9 log CFU/g, ranging from 7.11 to 9.21 log CFU/g, respectively.

73 obacillus rhamnosus GG were higher than 10(6)cfu/g.

74 Recovered S. aureus was calculated as cfu/g.

75 vo, single-dose phage therapy killed 2.5 log CFUs/g of vegetations in 6 hours (P < .001 vs untreated

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

77 st-forming unit-erythroid/CFU-erythroid, and CFU-granulocyte/erythroid/macrophage/MK) irrespective of

78 (colony-forming unit-megakaryocyte [CFU-MK], CFU-granulocyte/macrophage, burst-forming unit-erythroid

79 achieved following challenge with 1-5 x 103 CFU (group 1), which resulted in an attack rate of 12 of

80 Colony-forming units (CFUs) have been previously shown to predict CBU potency,

81 nd blood, respectively, corresponding to 2-7 CFUs immobilized on the detecting electrode.

82 -1) are capable of detecting approximately 5 CFU in 7 hours.

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

84 d by increases in bioluminescence, S. aureus CFU in tissue, and death within the first 7 days.

85 c detection of S. aureus cells as low as 682 CFU in whole blood.

86 ed were unaffected except for an increase in CFUs in the colon.

87 0 is approximately 100 colony-forming units (CFU) in vitro and <1000 CFU in the lungs of mice.

88 wed by intratracheal Escherichia coli (10(6) CFU) in wild-type mice or those lacking hepatocyte STAT3

89 e progenitor colonies (colony-forming units [CFUs]) increased from 4% of all CFUs at week 4 to 16% at

90 CFU inferred from qPCR analysis were positively correlat

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

92 d with serotype Enteritidis received 10 exp7 CFU intramuscularly.

93 imalis VKB) at a dose of 50 mg/kg (5 x 10(9) CFU/kg) (g) (intragastrically).

94 (6)/g)) at a dose of 140 mg/kg (1.4 x 10(10) CFU/kg).

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

96 ve detection of Shigella on the single-digit CFU level suggests the feasibility of the direct detecti

97 stool and blood matrixes at the single-digit CFU level.

98 ishes or on collagen membrane and assayed by CFU, live-dead staining using confocal microscopy, trans

99 lotype, were infected with a lower dose of 3 CFU M. tuberculosis All animals mounted similar T-cell r

100 cells at weeks 1 and 3 after high-dose (500 CFU) M. tuberculosis infection exhibited significantly l

101 committed Mk and E progenitors identified as CFU-Mk and burst forming unit-E.

102 ferentiates down both the Mk and E lineages (CFU-Mk/E), which allowed development and validation of a

103 ble HPCs (colony-forming unit-megakaryocyte [CFU-MK], CFU-granulocyte/macrophage, burst-forming unit-

104 entration ranges of 0.99 x 10(4)3.98 x 10(9) cfu mL(-1) and 103.97 x 10(7) cfu mL(-1) which resulted

105 resulted in detection limits of 1.99 x 10(4) cfu mL(-1) and 50 cfu mL(-1), respectively.

106 with a limit of quantification (LOQ) of 100 CFU mL(-1) and a limit of detection (LOD) of 3 CFU mL(-1

107 a limit of quantification (LOQ) of 1 x 10(1) CFU mL(-1) and a limit of detection (LOD) of 6 CFU mL(-1

108 This assay had a detection limit of 10(2) CFU mL(-1) for S. typhimurium, providing an instrument-f

109 , could be detected with LODs of approx. 2-4 CFU mL(-1) in an assay time of approx. 140 min.

110 of 10 CFU mL(-1) in standard buffer and 100 CFU mL(-1) in bottled water and milk.

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

112 performance with a limit of detection of 10 CFU mL(-1) in standard buffer and 100 CFU mL(-1) in bott

113 bacterial concentration from 3 x 10(8) to 38 cfu mL(-1) in the solution with C70-TiO2 thin film in th

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

115 A detection limit (DL) of 2 CFU mL(-1) was reached after 120 min of solar exposure f

116 4)3.98 x 10(9) cfu mL(-1) and 103.97 x 10(7) cfu mL(-1) which resulted in detection limits of 1.99 x

117 urium in the concentration range 10(2)-10(8) CFU mL(-1) with high selectivity over other model pathog

118 n spiked (1 x 10(2), 1 x 10(4) and 1 x 10(6) CFU mL(-1)) apple juice samples.

119 and high detection sensitivity (as low as 10 CFU mL(-1)).

120 in 20min) even at a low concentration of 50 CFU mL(-1), rapid antibacterial rate (100% killing in 30

121 etection limits of 10(5) CFU g(-1) and 10(3) CFU mL(-1), respectively, and this is the first publishe

122 ion limits of 1.99 x 10(4) cfu mL(-1) and 50 cfu mL(-1), respectively.

123 he concentration range 1 x 10(1) to 1 x 10(8)CFU mL(-1), with a limit of quantification (LOQ) of 1 x

124 U mL(-1) and a limit of detection (LOD) of 3 CFU mL(-1).

125 U mL(-1) and a limit of detection (LOD) of 6 CFU mL(-1).

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

127 ns starting from 10(1) colony forming units (CFU)mL(-1) in KCl and from 10(2) CFUmL(-1) in artificial

128 detection (LOD) of 150 colony forming unit (CFU)mL(-1) of C. jejuni in solution.

129 n initial count of >/=1 colony-forming unit (cfu)/mL after an 8-h infection.

130 concentration of 10(2) colony forming units (CFU)/mL and -88.1+/-6.3mV/pH over a pH range of 1-13) an

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

132 of genomic DNA and 10 colony-forming units (CFU)/ml of bacterial cells with dynamic ranges of 0-100n

133 the LPG-ISAM to 10(2) colony forming units (CFU)/ml of MR S. aureus (MRSA) for 50 min., light transm

134 g 1000 E. coli O157:H7 colony-forming units (cfu)/mL, or approximately 500 E. coli O157:H7 and approx

135 m with the limit of detection (LOD) of 10(4) CFU.mL(-1) and the analysis time of 10 min.

136 pyranoside (IPTG), we were able to detect 10 CFU.mL(-1) in drinking water after 6 h of pre-enrichment

137 The optimized method provided LOD of 100 CFU.mL(-1) with linear range up to 10(6) CFU.mL(-1).

138 100 CFU.mL(-1) with linear range up to 10(6) CFU.mL(-1).

139 an initial bacterial concentration of 10(2) CFU.mL(-1).

140 08 CFU/mL yielded greater IL-10 than did 103 CFU/mL (4.4 +/- 1.8 vs 1.0 +/- 0.6 pg/mL; P < .01).

141 ion limits 10(3)cfu/mL TB in sputum and 10(2)cfu/mL Ab in blood within 2h after sample loading.

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

143 es for Gram-negative bacteriuria at >/=10(4) CFU/ml and >/=10(5) CFU/ml were 96% and 99%, respectivel

144 The detection limit are 1 CFU/mL and 10 CFU/mL correspondingly.

145 in, with high selectivity and sensitivity (5 CFU/mL and 10 microg/g for bacteria and meat, respective

146 mL and 17 CFU/mL for E. coli and 7.4 x 10(3) CFU/mL and 11.7 x 10(3)CFU/mL for Salmonella sp., respec

147 hamburger extracts were determined to be 57 CFU/mL and 17 CFU/mL for E. coli and 7.4 x 10(3) CFU/mL

148 Detection limits of 21 CFU/mL and 18 CFU/mL were achieved in stool and blood, r

149 The LODs of the system were 2.5 x 10(4)CFU/ml and 2.5 x 10(5)CFU/ml for cells spiked into water

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

151 he sensitivity of biosensor was as few as 50 CFU/ml and it showed no responses to other entric bacter

152 the sensitivity range is from 10(1) to 10(7)CFU/ml and LOD is calculated as 9x10(2)CFU/ml.

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

154 The detection limit are 1 CFU/mL and 10 CFU/mL correspondingly.

155 ns of E. coli O157:H7 from 3x10(1) to 3x10(7)cfu/mL could be detected.

156 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

157 genome equivalents (GE) per reaction and 10 CFU/ml F. tularensis in both human and macaque blood.

158 The detection limit was 10 CFU/mL for both E. coli and N. gonorrhoeae, while commer

159 1 CFU/mL for C. tropicalis and C. krusei, 2 CFU/mL for C. albicans and C. glabrata, and 3 CFU/mL for

160 el sensor has a detection limit of around 32 CFU/mL for C. albicans.

161 FU/mL for C. albicans and C. glabrata, and 3 CFU/mL for C. parapsilosis.

162 The limit of detection was 1 CFU/mL for C. tropicalis and C. krusei, 2 CFU/mL for C.

163 system were 2.5 x 10(4)CFU/ml and 2.5 x 10(5)CFU/ml for cells spiked into water and sputum, respectiv

164 racts were determined to be 57 CFU/mL and 17 CFU/mL for E. coli and 7.4 x 10(3) CFU/mL and 11.7 x 10(

165 ial pathogens with a detection limit of 10(2)CFU/mL for four bacterial strains including Escherichia

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

167 coli and 7.4 x 10(3) CFU/mL and 11.7 x 10(3)CFU/mL for Salmonella sp., respectively.

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

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

170 a dynamic response range from 10(1) to 10(6)cfu/mL in water, juice and milk samples.

171 la detection, a limit of detection of 8x10(4)CFU/mL is achieved within a total assay time of 3h.

172 ase in sensitivity enabled us to detect 10(3)CFU/mL of Escherichia coli in broth after 7h, and by add

173 In contrast, after exposure to 10(6) CFU/ml of methicillin-sensitive S. aureus (MSSA) attenua

174 was able to detect luminescence from 10(6) CFU/mL of the bio-reporter, which corresponds to 10(7)

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

176 n of inoculated (2.3 x 10(2) and 3.1 x 10(1) CFU/mL or g of E. coli and E. faecium, respectively) spr

177 f the standard regimen based by both TTP and CFU/mL over 28 days of treatment.

178 H7 and L. monocytogenes by 1.48 and 0.47 log cfu/ml respectively after 6 h of contact time.

179 baumanii (Ab) with the detection limits 10(3)cfu/mL TB in sputum and 10(2)cfu/mL Ab in blood within 2

180 ow detection limit and sensitivity of 10(1)cfu/mL towards E. coli O78:K80:H11 with a dynamic respon

181 Bacteriuria with any CFU/mL was also reduced in men in the universal decoloni

182 nced beef and tap water with 10(3) and 10(4) CFU/mL were 94.7 and 90.4 (in beef) and 91.3 and 94.8% (

183 bacteriuria at >/=10(4) CFU/ml and >/=10(5) CFU/ml were 96% and 99%, respectively.

184 Detection limits of 21 CFU/mL and 18 CFU/mL were achieved in stool and blood, respectively, c

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

186 agalactiae and detection of bacteremia at <1 CFU/ml were unreliable.

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

188 that the limit of quantitation is 1.9x10(5) CFU/mL with this simple device, which is more than 10,00

189 Ex vivo studies showed that 108 CFU/mL yielded greater IL-10 than did 103 CFU/mL (4.4 +/

190 f 0-100ng/ml (R(2)=0.992) and log10 (1-10(4) CFU/ml) (R(2)=0.9918), respectively.

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

192 bition, selectivity, sensitivity (10(1)-10(2)CFU/mL) and reproducibility (below 12.5%).

193 ng both colony-forming units per milliliter (CFU/mL) and time to positivity (TTP).

194 ly low concentration of E. coli O157:H7 (~10 CFU/mL) could be detected within 1h and 3h from both pur

195 nd nonpathogenic E. coli isolates and (10(0) CFU/mL) E. faecalis and E. faecium strains were detected

196 ow the clinical diagnostic criterion (>10(5) CFU/mL) for UTI.

197 Low concentrations (10(1) CFU/mL) of pathogenic and nonpathogenic E. coli isolates

198 ceeded total aerobic plate count of 2 log10 (cfu/ml) on 15th day of storage.

199 rom samples with low bacterial counts (10(4) cfu/mL) using a custom-designed microfluidic chip and mo

200 hetic urine at low concentrations (1 x 10(2) CFU/ml) was detected in FCDI cell lysates using real-tim

201 e 10(0) colony forming units per milliliter (CFU/mL) with a detection limit of 9.4 x 10(-12) mol L(-1

202 ropathogen, high-level candiduria (>/=50 000 CFU/mL), and any bacteriuria with uropathogens.

203 strains of heterologous genera (all at 10(4) CFU/ml), or tissue samples from mice infected with MRSA,

204 was 1.2 x 10(2) colony-forming-units per mL (CFU/mL), which is well below the clinical diagnostic cri

205 und to be 2.17x10(2) colony forming unit/ml (CFU/ml).

206 d at just 10(1) colony forming units per mL (CFU/mL).

207 t medium, an inoculum size of 1 to 3 x 10(3) CFU/ml, and an incubation time and temperature of 96 h a

208 low bacterium concentration, i.e., below 100 CFU/mL, blood samples show a random nature.

209 st strip also had a detection limit of 10(6) CFU/mL, but this method is not antibody-based and thus n

210 With the detection limit of 10(3) CFU/mL, crn-1 and crn-2 based platforms detected target

211 At 1 to 10 CFU/ml, Escherichia coli, Staphylococcus epidermidis, St

212 L. monocytogenes count by 2.51 and 1.64 log cfu/ml, respectively.

213 1, there was a >12-fold decrease (23 and 331 CFU/mL, respectively; P < .0001).

214 ised in a wide range between 10(4) and 10(8) CFU/mL, where linear relation was found between conducti

215 d out within the range of 1.0x10(2)-1.0x10(7)CFU/mL.

216 chieve a low limit of detection (LOD) of 100 CFU/mL.

217 0.978 and R(2)=0.992, in range of 10(2)-10(5)CFU/mL.

218 eria, even at concentrations as high as 10(7)CFU/mL.

219 portional to the bacterial concentrations in CFU/ml.

220 evaluated from 9.14 x 10(7) to 1.17 x 10(10) cfu/mL.

221 imit of the detection of the assay, 0.01-1.0 CFU/ml.

222 10(7)CFU/ml and LOD is calculated as 9x10(2)CFU/ml.

223 li O157:H7 and approximately 500 E. coli K12 cfu/mL.

224 O was defined as equal to or more than 10(3) cfu/ml.

225 ore than 95% was bound in vitro to 5 x 10(9) cfu/mL.

226 e sensitive measure of bacterial burden than CFU/mL.

227 98 with high detection limit as much as 10(7)cfu/mL.

228 or Staphylococcus saprophyticus at >/=10(3) CFU/ml.

229 nd the linear range of the assay up to 10(7) CFU/mL.

230 ith plate counting at a range of 10(3)-10(7) CFU/mL.

231 The lower limit of detection was 10(3) CFU/mL.

232 rence was most prominent at lower numbers of CFU/ml.

233 stically significant impedance change was 10 CFU/mL.

234 rapid kit showed a detection limit of 10(6) CFU/mL.

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

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

237 linear response over the range of 10(3)-10(7)cfu/mL.

238 lony growth at 24 h from as few as 1 x 10(2) CFU/ml.

239 acteria concentration between 10(1) to 10(8) CFU/mL.

240 respectively, yielding a LOD of 1.0 x 10(5) CFU/ml.

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

242 at 2:1 than at 3:1 for almost all numbers of CFU/ml; this difference was most prominent at lower numb

243 bacteriuria (>/=50 000 colony forming units [CFU]/mL) with any uropathogen, high-level candiduria (>/

244 2 survive a dose of C. albicans (2.5 x 10(5) CFU/mouse) that is uniformly lethal to wild-type mice wi

245 er limit of detection was determined to be 1 CFU/mul.

246 her group B streptococcus (GBS) at 1 x 10(6) CFU (n = 5) or saline (n = 5) in the choriodecidual spac

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

248 Between 4 h and 10 days, CFU numbers increased to numbers comparable to the inocu

249 infected via the footpad with 10(3) to 10(6) CFU of Brucella spp. display neutrophil and monocyte inf

250 ecreased the biofilm biomass and reduced the CFU of E. coli isolates, K. pneumoniae isolates were obs

251 nucleic acid fragments of Ebola virus, and 8 CFU of Escherichia coli carrying Ebola virus-derived pla

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

253 infection, and the second, with 1.2 x 10(8) cfu of heat shock-treated S. aureus to generate sterile

254 voltammetry (DPV) response from as low as 1 CFU of Mtb bacilli DNA input material, having shown its

255 The LOD was 300 CFU of Mycobacterium tuberculosis in 1 ml sputum.

256 rupting preformed biofilms or decreasing the CFU of P. aeruginosa and K. pneumoniae within a biofilm.

257 in which we used 25 mug of CRP and 5 x 10(7) CFU of pneumococci, mutant CRP was not protective while

258 The CFU of recoverable P. aeruginosa and K. pneumoniae isola

259 inoculated intramuscularly with 1.2 x 10(8) cfu of S. aureus to provoke infection, and the second, w

260 ation ( approximately 10(0), 10(1), or 10(2) CFU of spores) from test surfaces (a bed rail, a stainle

261 type were bronchoscopically infected with 41 CFU of the M. tuberculosis Erdman strain.

262 excellent linearity in a range of 10(2)-10(9)cfu of UPEC mL(-1) with a current sensitivity of 7.162mu

263 Volunteers ingested approximately 1 x 10(5) CFU of wild-type V. cholerae O1 El Tor Inaba strain N169

264 Notably, MET-1 did not decrease CFUs of Salmonella in the intestine.

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

266 ples were analyzed for colony forming units (CFUs) of E. coli, and households were evaluated for thei

267 ned as the decrease in colony forming units (CFUs) of Mycobacterium tuberculosis in the sputum of pat

268 10 C. difficile count (colony-forming units [CFU]) of 6.7 +/- 2.0 at study entry; vancomycin treatmen

269 in the E. coli numbers determined as either CFU or gene copies during the summer for the field-expos

270 pproximately 5 x 10(8) colony-forming units [CFU]) or placebo in double-blind fashion.

271 e number of colony-forming unit osteoblasts (CFU-Os), a surrogate marker of undifferentiated mesenchy

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

273 MazFsa in the cshA mutant resulted in lower CFU per milliliter accompanied by a precipitous drop in

274 he lateral tail vein), and muscle (1 x 10(8) CFU per mouse intramuscularly) at three timepoints after

275 yeast transformation efficiency up to 10(7) CFU per mug plasmid DNA and per 10(8) cells with a 13.8

276 to draining lymph nodes (controls median 183 CFU per node [IQR 8-5800] vs trauma group 20 000 [1875-6

277 U) per reaction for L. pneumophila and three CFU per reaction for S. typhimurium and S. aureus.

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

279 PCR assay achieved two colony-forming units (CFU) per reaction for L. pneumophila and three CFU per r

280 sence of inhibitors, colony formation units (CFUs) per milliliter in blood from all 12 immunized subj

281 challenge of 1 x 10(7) colony forming units [CFU] per mouse), intravenous (1 x 10(7). per mouse via t

282 uria (ie, at least 105 colony-forming units [CFUs] per milliliter of 1 or 2 microorganisms in urine c

283 distinguish VISA from hVISA, a cutoff of 16 CFU provided 83.3% sensitivity and 94.7% specificity; th

284 umococcal infection increased the numbers of CFU recovered from an intranasal mouse model of infectio

285 idal activity, demonstrated by the decreased CFU recovery of internalized yeasts, with comparable pha

286 aused the reduction in colony forming units (CFUs) substantially for almost 3 orders of magnitude.

287 limit of 0.1 ng of the extracted DNAs and 10 CFU/test, can be achieved.

288 nterally in a daily dose of 8.2 to 9.2 log10 CFU; the placebo was dilute infant formula alone.

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

290 bronchoalveolar lavage fluid (BALF) and lung CFU values were determined.

291 ion and increased BALF and lung pneumococcal CFU values.

292 In MS-WF-exposed mice CV-3988 reduced BALF CFU values.

293 Bacterial growth of more than 0 CFU was noted in 16.1% duodenoscopes in the sHLD group,

294 Bacterial growth or 10 or more CFU was noted in 2.3% of duodenoscopes in the sHLD group

295 Paratyphi A at a dose of 1-5 x 103 CFU was well tolerated and associated with an acceptable

296 Lethal challenge (>4.0 x 10(6) CFU) was characterized by fulminate hemorrhagic pneumoni

297 [tdT+] BM cells), circulating and splenic EC-CFUs were BM-derived (tdT+), whereas cells positive for

298 The circulating WBCs and LSKs, and CFUs were reduced in both models with a shorter duration

299 ssing markers of EC colony-forming units (EC-CFUs) were detected.

300 at they do not grow as colony-forming units (cfus) when plated on agar.

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