ライフサイエンスコーパス: agar

1 pplemented with 0.01% (w/v) cholesterol (LBC agar).

2 ecimens plated onto chromID CPS Elite (CPSE) agar.

3 ential, assessed by colony formation in soft agar.

4 forcement of fluid that permeated out of the agar.

5 rentially toward algae embedded in a disk of agar.

6 t conditions analogous to growth in the soft agar.

7 tiple Wnt-addicted cancer cell lines in soft agar.

8 d to a reduction of colony formation in soft agar.

9 solubilizing the cholesterol micelles in LBC agar.

10 oma proliferation in both monolayer and soft agar.

11 h subculture on Mycoplasma-specific Hayflick agar.

12 genotypes was lower from McC + CTX than ESBL agar.

13 s colony-forming units (cfus) when plated on agar.

14 um-stimulated epithelial cell growth in soft agar.

15 pontaneous mutants able to move through soft agar.

16 d prostate cancer cell colony growth in soft agar.

17 H9 broth and 7H10 agar or 7H9 broth and 7H11 agar.

18 richment followed by plating to Baird-Parker agar.

19 form xenografts in mice and colonies in soft agar.

20 h and migration and colony formation in soft agar.

21 ody gait and locomotion of animals reared on agar.

22 late agar, MacConkey agar, and mannitol salt agar.

23 using two non-tumorigenic cell lines in soft agar.

24 several were able to inhibit growth in soft agar.

25 ethod were 100% for both blood and MacConkey agars.

26 res plated onto standard blood and MacConkey agars.

27 00% for blood, MacConkey, and Mueller-Hinton agars.

28 and Eggerthella lenta (broth, 1 to 4 mug/ml; agar, 1 to 8 mug/ml) were approved by the Clinical and L

29 emporal dynamics of Escherichia coli in soft agar(12,17,18).

30 30 degrees C, 64.7%; P = 0.005), and in BHI agar (63.0%; P = 0.001).

31 versus 59.4%; P = 0.01) or Middlebrook 7H11 agar (76.7% versus 47.4%; P = 0.0001) alone, but it was

32 hich includes both MGIT and Middlebrook 7H11 agar (76.7% versus 63.9%; P = 0.0647).

33 nd 94.0% for software reading of chromogenic agar, 83.3% and 97.7% for technologist reading for beta-

34 7.7% for technologist reading of chromogenic agar, 90.6% and 94.0% for software reading of chromogeni

35 nologist reading for beta-hemolysis on blood agar accompanied by any zone of inhibition around a baci

36 The effects of agar, alginate, lecithin and glycerol on the rheological

37 Immobilizing AQDS in agar also limited its diffusion, which resembled electro

38 d for bedaquiline MICs determined using 7H10 agar and 7H11 agar but not for bedaquiline MICs determin

39 This study also showed that agar and alginate in addition to potato puree could be v

40 These data demonstrate that the use of CPSE agar and automated plate reading has the potential to im

41 nd displayed increased clonogenicity in soft agar and broad drug-resistance in vitro and in vivo.

42 , Italy) software to analyze VRE chromogenic agar and compared the results to technologist plate read

43 ng all suspected colonies on the chromogenic agar and identifying 3 additional true-positive specimen

44 re inoculated into MGIT and Middlebrook 7H11 agar and incubated at 35 degrees C for 42 days.

45 Silver electrodes were overlaid with agar and lawn biofilms grown for 24 h.

46 breast cancer cells to form colonies in soft agar and metastasize to the lungs or liver.

47 ls contained HPV-16, formed colonies in soft agar and rapidly produced tumors in immunodeficient mice

48 The use of both CPSE agar and the WASPLab software improved the time to resul

49 TGM2 suppressed colony formation in soft agar and tumor formation in a xenograft mouse model.

50 rent volumes of urine onto 7 combinations of agars and environments.

51 al culture techniques (aerobic and anaerobic agars and thioglycolate broth) compared to inoculation i

52 tryptic soy agar with 5% sheep blood (blood agar) and MacConkey agar were tested, and the results we

53 nologist reading for beta-hemolysis on blood agar, and 39.5% and 83.1% for technologist reading for b

54 feration, abolishes colony formation in soft agar, and decreases NO generation.

55 liferation, reduced colony formation in soft agar, and induction of apoptosis.

56 cquired anchorage-independent growth in soft agar, and led to enlarged, disorganized, three-dimension

57 ted on blood agar, chocolate agar, MacConkey agar, and mannitol salt agar.

58 uced proliferation, colony formation in soft agar, and NO generation of KSHV-transformed cells, which

59 including conventional culture, chromogenic agar, and polymerase chain reaction.

60 i in tissue culture plates, colonies in soft agar, and tumors in nude mice.

61 Agars are sulfated galactans from red macroalgae and are

62 e model of bacterial diffusion and growth in agar, are compared with our experimental measurements of

63 the illumigene assay using culture on blood agar as the "gold standard" and following discrepancy an

64 slime; and (4) the comets etch trails in the agar as they move forwards.

65 caeca on MacConkey + cefotaxime (McC + CTX) agar, as recommended by the European Commission, or ESBL

66 ndent cell growth ability was tested by soft agar assay following FA exposure.

67 Because the soft agar assay is unsuitable for high throughput screens (HT

68 In a soft agar assay, treatment of HC11-Int3 cells with P50-siRNA

69 se activity in bacteria, producing a lighter agar background coloration facilitating visualization of

70 We have developed an in vitro agar based model using a bioluminescent strain of Pseudo

71 stem, and had been screened previously in an agar based system.

72 developed microsystem is integrated with an agar-based growth medium and monitors the metabolism of

73 his shortcoming, we developed a customizable agar-based medium modified from an established plant cel

74 Nevertheless, using an agar-based MIC assay, we found that propionylation of Ly

75 RGM medium to Burkholderia cepacia selective agar (BCSA) and a standard acid-fast bacillus (AFB) cult

76 incubation on Burkholderia cepacia selective agar (BCSA) has been recommended as an expedient culture

77 We have developed an adapted agar bead murine model using a clinical mucoid strain th

78 zation and counting of bacterial colonies on agar before they became visible to the naked eye.

79 ed to glycerol>lecithin>alginate, whereas 1% agar behaved differently, increasing all rheological val

80 , bacterial polysaccharidases that hydrolyze agars (beta-agarases and beta-porphyranases) have been c

81 le-colony selection on antibiotic-containing agar, blinded to sequencing results.

82 crete, agarose gel, vaginal tissue, polymer, agar, bone, spider silk, and hydrogel demonstrate that t

83 ine MICs determined using 7H10 agar and 7H11 agar but not for bedaquiline MICs determined using 7H9 b

84 ient for suppressing migration and growth in agar, but their Rho-GAP activity was similar to that of

85 Chromogenic agar can expedite culture results, but technologist revi

86 oMATRIX CDM software and the Colorex Strep A agar can improve detection of GAS from throat specimens,

87 ating negative and "nonnegative" chromogenic agar can reduce the labor cost of these screens and pote

88 Specimens were inoculated on blood agar, chocolate agar, MacConkey agar, and mannitol salt

89 Colorex Strep A agar (CHROMagar, Paris, France) was evaluated with Pheno

90 onventional media and into chromID CPS Elite agar (chromID).

91 or cells showed significantly increased soft-agar clonogenic ability and tumor sphere formation.

92 ot CRAF WT, transformed NIH3T3 cells in soft-agar colony formation assays, increased kinase activity

93 19 could promote cell proliferation and soft agar colony formation in HNSCC cells with low FGF19 expr

94 rofibrotic targets, cell migration, and soft agar colony formation stimulated by TGF-beta required GL

95 tion) signaling, transwell invasion and soft agar colony formation, and in vivo promoted lung metasta

96 led to decreased transwell invasion and soft agar colony formation, without affecting proliferation.

97 nregulation increased cell invasion and soft agar colony formation; this was dependent on NF-kappaB a

98 The number of cells detected by conventional agar colony forming unit (CFU) and most probable number

99 Soft agar colony growth assays were applied to examine iAs-in

100 Generally, Luria-Bertani (LB) agar colony is a conventional method to evaluate the pho

101 could not be achieved by the traditional LB agar colony method.

102 cement of cell proliferation, increased soft agar colony size, and elevated ERK1/2 phosphorylation we

103 so increased cell growth as assessed by soft-agar colony survival and cell growth assays, and pretrea

104 MALDI-TOF MS might be able to replace the LB agar colony to evaluate the photodynamic effect.

105 logical patterns were altered by varying the agar concentration.

106 erol compared with those of potato puree and agar, consequently affecting the rheological properties

107 were used in three different assays: insert, agar contact and glass-bottom well assays.

108 contact with the membranes in the insert and agar contact assays, thus better mimicking bacterial adh

109 The agar culture plate has played a crucial role in bacterio

110 tely sort positive from negative chromogenic agar cultures regardless of the pigmentation produced.

111 on inhibits PC3 growth in monolayer and soft agar cultures.

112 Different agars designed for the isolation of B. cepacia complex v

113 Antimicrobial activity was evaluated by agar diffusion and microdilution methods and antioxidant

114 Although gradient agar diffusion is commonly performed for other antimicro

115 tial agreement for calcium-enhanced gradient agar diffusion were 73.7% and 65.5%, respectively, compa

116 Performing gradient agar diffusion with calcium enhancement of susceptibilit

117 microdilution (BMD), macrodilution (MD), and agar dilution (AD) methods were compared.

118 -adjusted Mueller-Hinton broth (ID-BMD), and agar dilution (AD) using standard Mueller-Hinton agar we

119 Agar dilution and broth microdilution methods were evalu

120 Agreement rates were analyzed using both agar dilution and broth microdilution with a resulting h

121 esistance using standard MIC testing by both agar dilution and broth microdilution, as well as genosp

122 termined to be 256 mug/ml and 512 mug/ml for agar dilution and broth microdilution, respectively.

123 In conclusion, agar dilution and Etest yielded comparable results to BM

124 s to regional laboratories for culture-based agar dilution AST with seven antibiotics and for whole-g

125 CLSI document M23-defined tier 2 study, the agar dilution MIC QC range for zoliflodacin against the

126 For the agar dilution MIC, a 4-dilution QC range (0.015 to 0.12

127 : 0.015 to 0.12 mug/ml for the 7H10 and 7H11 agar dilution MICs and 0.015 to 0.06 mug/ml for the 7H9

128 sults of the assay were 100% concordant with agar dilution susceptibility test results for 100 clinic

129 rsity of Washington and CDC for confirmatory agar dilution testing; sequence data were sent to CDC fo

130 Categorical agreement was 98.0% for agar dilution, 73.1% for disk diffusion, 96.3% for Etest

131 Essential agreement was 95.6% for agar dilution, 90.6% for Etest, and 85.2% for MTS.

132 ere tested for colistin susceptibility using agar dilution, and characterised by whole genome sequenc

133 animal isolates were determined in vitro by agar dilution, biofilm formation, adhesion, invasion and

134 testing agreement rates across four methods: agar dilution, broth microdilution, disk diffusion, and

135 MIC values for agar dilution, Etest, and MTS were not significantly dif

136 This study aimed to determine whether agar dilution, research-use-only disk diffusion (Mast Gr

137 cified method for MIC determination, namely, agar dilution, which is not widely available and is both

138 ailable in a clinical laboratory compared to agar dilution.

139 l minimal inhibitory concentrations (MIC) by agar dilution.

140 Etest, 70% (67/96) by DD, and 88% (84/96) by agar dilution.

141 e results were compared to those obtained by agar dilution.

142 5 had ceftriaxone MICs = 0.125 microg/mL by agar dilution.

143 broth microdilution and that to carbadox by agar dilution.

144 minimum inhibitory concentrations (MICs) by agar dilution.

145 ) major errors in categorical agreement with agar dilution.

146 ound the geometric mean included 95.8% (7H10 agar dilution; 204/213 observations with one data set ex

147 s with one data set excluded) or 95.9% (7H11 agar dilution; 232/242) of bedaquiline MICs.

148 ies were tested against 4 bacteria b y using agar disc diffusion and tube dilution tests.

149 Agar disc diffusion assay was used to analyse the antimi

150 robial effects by DPPH, ABTS, FRAP, ORAC and agar disc diffusion methods, respectively.

151 Antimicrobial activity was evaluated by the agar disk diffusion method, and in vitro cytotoxic activ

152 Agr mutants can be monitored on blood agar due to their nonhemolytic phenotype.

153 eye model, which is made of a hemispherical agar embedded with pencil lead fragments simulating as F

154 In contrast to agar environments that pose specific drawbacks for chara

155 ted keratitis, were cultured on non-nutrient agar examined by microscope for the presence of free-liv

156 A2S-G, released by the activity of ZgAgaC on agar extracted from Osmundea pinnatifida By resolving th

157 upport iron acquisition on unsupplemented LB agar, Feo, Fbp, Vct, and Vib, remains functional.

158 riolus versicolor, pre-grown on kenaf/lignin agar followed by either vacuum evaporation or acid preci

159 Software reading of the chromogenic agar for suspected colonies detected 110 orange colonies

160 ator tube (MGIT) system and Middlebrook 7H11 agar for the isolation of all nontuberculous mycobacteri

161 cobacteria [RGM] medium and Middlebrook 7H11 agar), for their abilities to isolate NTM.

162 superior option, compared to other selective agars, for the isolation of rapidly growing mycobacteria

163 Using MH agar from BD and Oxoid, susceptibility rates determined

164 With the disk diffusion method using MH agar from BD and Oxoid, susceptibility rates were 82.2%

165 quantifying potential ESBL E. coli MacConkey agar from eight manufacturers, representing seven countr

166 ation of bacteria isolated on Columbia blood agar from milk samples of dairy cows.

167 hydrolyzes not only agarose but also complex agars from Ceramiales species.

168 mass transfer kinetics of solid coatings: in agar gel at static conditions, in PBS solution with agit

169 Short-term release into an agar gel was evaluated using a fluorescent tracer (fluor

170 r-sized particles sprinkled over a semisolid agar gel.

171 s was followed by standard samples for blood agar, Gram stain, Sabouraud agar, thioglycolate broth, a

172 Using agar-grown Bartonella henselae San Antonio type 2 (SA2)

173 ZNF322A promoted cell proliferation and soft agar growth by prolonging cell cycle in S phase in multi

174 naling pathways regulate proliferation, soft agar growth, and invasion of human lung adenocarcinoma c

175 snitzii strain 16-6-I 40 fastidious anaerobe agar had the greatest effect.

176 ms of localized corrosion in soil, semisolid agar has been developed as an analogue for soil.

177 g the colony expansion of cells deposited on agar have shown that the expansion rate increases with i

178 agar with gentamicin (SDA), inhibitory mold agar (IMA), and brain heart infusion (BHI) agar with chl

179 sensor bacteria either in liquid culture or agar-immobilized, respectively, at a distance of 50 m in

180 We deposited fractions onto nutrient agar in a Petri dish for microbial culturing, and we sub

181 aping was inoculated onto Sabouraud Dextrose Agar in C-shaped streaks and incubated at 25 degrees C a

182 se VAT failed to stimulate growth in soft of agar in cells deficient in FGFR-1 (FGF2 receptor).

183 ls enhanced proliferation and growth in soft agar in vitro but was insufficient to drive tumorigenesi

184 colistin-nalidixic acid (CNA), and MacConkey agars in 5% CO2 for 48 h.

185 ity testing was done in selected isolates by agar incorporation, and we used sequence data to determi

186 ard urine culture inoculated at 1 mul onto 2 agars incubated aerobically; expanded-spectrum EQUC inoc

187 MRSASelect II agar is a simple, rapid, and robust method to routinely

188 robiology laboratory; the use of chromogenic agar is one method by which the laboratory might expedit

189 For disk diffusion, standard Mueller-Hinton agar is recommended, presumably because iron is bound in

190 rmed by high MIC/MBC, and a no inhibition on agar lawns.

191 Incorporation of a secondary agar layer as a biocompatible passivation layer protects

192 ens were inoculated on blood agar, chocolate agar, MacConkey agar, and mannitol salt agar.

193 ecovery of E. coli 13457 from four MacConkey agar manufacturers was reduced by up to 4 log CFU/ml, an

194 across a wide P concentration gradient in an agar matrix, we demonstrated a shift in the effect of ba

195 s unable to tumble become trapped within the agar matrix.

196 at in low-prevalence settings, CPE screening agars may lack specificity, and confirmation of putative

197 s of Chlamydomonas strains by propagation on agar media and by cryogenic storage, (2) identify mutage

198 nd Gram-positive clinical isolates) grown on agar media by liquid extraction surface analysis mass sp

199 and P. aeruginosa colonies on commonly used agar media.

200 designed to lyse cells grown in colonies on agar media.

201 ( Triticum aestivum) cultivated on free iron agar medium plates.

202 readily visualized blue pigmentation on ABM agar medium supplemented with X-gal (ABMX-gal).

203 performed using a liquid medium and a solid agar medium with an incubation period of up to 60 days.

204 sor consists of Agrobacterium mannitol (ABM) agar medium, X-gal, and a biosensor.

205 ed, homogenized, and cultured in tryptic soy agar medium.

206 bles had a minimal effect on gepotidacin pH, agar method, atmospheric condition, temperature, and add

207 routine AST media, including Mueller-Hinton agar (MHA) and cation-adjusted Mueller-Hinton broth.

208 growing cells of Escherichia coli in curved agar microchambers, and find that chemoreceptor cluster

209 gene responsible for halo production on LBC agar, named choA, was identified as an N-acyltransferase

210 phorylated ERK, and slows the growth in soft agar of HCT116 cells.

211 l proliferation and colony formation in soft agar of KSHV-transformed cells by attenuating mTORC1 act

212 obese human donors stimulated growth in soft agar of non-tumorigenic epithelial cells.

213 ine MICs determined using 7H9 broth and 7H10 agar or 7H9 broth and 7H11 agar.

214 methods developed in the mid-1800s-growth on agar or in broth-identification and susceptibility profi

215 ansform normal cells enabling growth in soft agar or in immunodeficient mice.

216 ability of C6 cells to form colonies in soft agar or spheres when grown in suspension.

217 al cultures from multiwell plates onto large agar pads using inexpensive replicator pins and automati

218 g: 100 mul of urine plated onto blood (blood agar plate [BAP]), colistin-nalidixic acid (CNA), and Ma

219 tions of povidone iodine (PI) solution in an agar plate experiment of respiratory flora.

220 icantly different than a previously reported agar plate experiment, again owing to subtle but very si

221 duce efficient fibrin clot lysis in a fibrin-agar plate model and the encapsulated tPA retained 97.4

222 owever, the time investment for conventional agar plate or microtiter plate-based screening assays re

223 a standardised script for 5 min over a blood agar plate positioned at 20 cm in a simulated position o

224 n ophthalmic examination chair with an blood agar plate secured to the forehead and wearing various f

225 of meropenem and subcultured to a MacConkey agar plate with a 10-mug meropenem disk) and for sequenc

226 Treponema bacteria and the development of an agar plate-based detection system will enable similar st

227 Using agar plate-based infection assays with different Arabido

228 ith height variations up to 0.8 mm above the agar plate.

229 were performed from growth on BMHA and blood agar plates (BAP), with and without cefoxitin disk induc

230 aluated by plating Salmonella typhimurium on agar plates and showed that the catholyte possesses a lo

231 on Module (CDM) for categorizing chromogenic agar plates as negative or "nonnegative" for vancomycin-

232 ditionally, throat swabs are inoculated onto agar plates for isolation of the large-zone beta-hemolyt

233 oratory procedures were subcultured on blood agar plates for MALDI-TOF analysis.

234 of images obtained from bacterial cell-grown agar plates using colony forming units as well as conflu

235 The blood agar plates were subject to a randomised pre-application

236 ies of a 6PGDH mutant library growing on the agar plates were treated by heat to minimize the backgro

237 f metabolites in tissues, cell cultures, and agar plates with cellular resolution, but it is hampered

238 y collecting surface profiles of colonies on agar plates with high vertical resolution (3-5 nanometer

239 ptomic profiles of E. coli OP50 in vitro (on agar plates) versus in vivo (fed to C. elegans host).

240 ing Bacillus subtilis ATCC 49760 colonies on agar plates.

241 ed in stronger seedling growth inhibition on agar plates.

242 (AST) systems and five selective chromogenic agar plates.

243 ed on two different types of VRE chromogenic agar plates.

244 Overexpression of bsrE causes cell lysis on agar plates.

245 at cultures on selective streptococcal blood agar plates.

246 on of clones with promoter-containing GCs on agar plates.

247 Polymyxins diffuse poorly into agar, potentially giving inaccurate disk diffusion and E

248 linical MRSA isolates were grown on nutrient agar, prepared in suspension, and adjusted to concentrat

249 om archival type specimens of ten species in agar-producing red algal genera Gelidium and Pterocladie

250 Three methods were used: Middlebrook 7H11 agar proportion (AP) assay, broth microdilution (BMD) as

251 How bacteria can degrade complex agars remains therefore an open question.

252 A novel selective agar (RGM medium) has been advocated for the isolation o

253 s and outdoors at 8 locations with automatic agar samplers.

254 Paired Sabouraud dextrose agar (SDA) plates were always positive for fungi within

255 We present results from agar-solidified experimental incubations, containing eit

256 n a dose-dependent manner when applied on an agar substrate.

257 developing Vibrio cholerae biofilms grown on agar substrates in which the spatiotemporal morphologica

258 e perform experiments with isolated cells on agar substrates of varying stiffness and find the measur

259 damide is capable of producing a halo on LBC agar suggesting that this molecule is solubilizing the c

260 sed in Escherichia coli, produce halos on LB agar supplemented with 0.01% (w/v) cholesterol (LBC agar

261 We evaluated MacConkey agar supplemented with ceftriaxone or cefotaxime as a sc

262 that populations confined to grow on a flat agar surface are more susceptible than their well-mixed

263 (PHE) to a model soil-atmosphere interface (agar surface) in the presence and absence of glass fiber

264 e and non-motile bacterial species on a soft agar surface.

265 own that S. aureus can passively move across agar surfaces in a process called spreading.

266 a swab with an anaerobic transport semisolid agar system for their capacities to maintain the viabili

267 tin broth disk elution (CBDE) and a colistin agar test (CAT), the latter of which was evaluated using

268 obilized AQDS/AH(2)QDS was 10 times lower in agar than in water, the iron(III) mineral reduction rate

269 ificantly fewer and smaller colonies in soft agar than their 2D-irradiated counterparts (gamma P = 0.

270 io alginolyticus isolate B522 on carrageenan agar that may lay the foundation for swarming studies of

271 ransformation, as measured by growth in soft agar, the gold-standard in vitro transformation assay.

272 amples for blood agar, Gram stain, Sabouraud agar, thioglycolate broth, and brain heart infusion brot

273 taining molecules in NOM) was immobilized in agar to achieve a spatial separation between the iron-re

274 nt conditions as an alternative to growth in agar to discover compounds that inhibit transformation.

275 results between disk manufacturers and some agar types and also with potassium and thymidine for S.

276 Chromogenic agar used at these sites included MRSASelect (Bio-Rad La

277 ommended by the European Commission, or ESBL agar, used additionally by United Kingdom.

278 The quality and reproducibility of MacConkey agar varied by manufacturer, which suggests that a singl

279 sm identification was decreased with chromID agar versus conventional media for E. coli (mean of 24.4

280 arming from colonies grown on MacConkey soft agar was delayed in the mutant in comparison to the wild

281 liquid and embedded in glucose-limited soft agar, we evaluate the fit of this model to experimental

282 In the agar well diffusion tests, zones of inhibition for the d

283 inst test microorganisms was assessed by the agar well-diffusion method.

284 ned for proteolytic activity using skim milk agar-well diffusion test.

285 lls for anchorage independent growth in soft agar were dependent on GIT1.

286 ically in hemolysis or growth on human blood agar were identified by comparing the mutants to the par

287 dilution (AD) using standard Mueller-Hinton agar were performed according to Clinical and Laboratory

288 th 5% sheep blood (blood agar) and MacConkey agar were tested, and the results were compared to those

289 nts HeLa cells from forming colonies in soft agar, when paxillin is knocked down together with Cat-1,

290 motes their ability to form colonies in soft agar, whereas ectopically expressing paxillin in these c

291 axis response, migration in classic motility agar, which constitutes a fluid-filled porous medium, is

292 e in the order of glycerol>alginate>lecithin>agar, while at 1% concentration, the order changed to gl

293 isolates were only confirmed from MacConkey agar with 4 mug/ml cefotaxime, where 45% and 16.6% of E.

294 Colonies from tryptic soy agar with 5% sheep blood (blood agar) and MacConkey agar

295 for bacterial culture were plated onto CPSE agar with a 1-mul loop using the WASP.

296 After recovery was assessed, US-1 MacConkey agar with cefotaxime was used to further evaluate the re

297 d agar (IMA), and brain heart infusion (BHI) agar with chloramphenicol and gentamicin.

298 culture media, including Sabouraud dextrose agar with gentamicin (SDA), inhibitory mold agar (IMA),

299 5 from blood, MacConkey, and Mueller-Hinton agars with 110 isolates of Enterobacterales and P. aerug

300 sults were similar using the three different agars with a sensitivity of 100% and specificity ranging