ライフサイエンスコーパス: isolate of

1 crodilution method, we found that the serial isolates of 11% of the patients infected with strains of

2 A total of 78 clinical isolates of 13 Gram-negative species collected between A

3 We tested 187 blood culture isolates of 5 Candida spp. (120 C. albicans, 38 C. glabr

4 nstructed a deletion of 530 bps in a primate isolate of A. actinomycetemcomitans, which produced leuk

5 her the laboratory Neff strain or a clinical isolate of A. castellaniiIn vitro real-time imaging demo

6 lis were fertile when paired with the MAT1-1 isolate of A. felis but not with any of the other specie

7 c heterogeneity is commonly observed between isolates of a given pathogen.

8 Ten isolates of a novel reovirus (genus Dinovernavirus) were

9 omes of three toxigenic and three atoxigenic isolates of A. flavus in aflatoxin conducive and non-con

10 o biologically incompatible, with the MAT1-2 isolates of A. parafelis and A. pseudofelis being the ex

11 Recently, isolates of A. pleuropneumoniae that were serologically

12 The MAT1-2 isolates of A. pseudofelis were fertile when paired with

13 coincubated with trophozoites of a clinical isolate of Acanthamoeba (genotype T4) or stimulated with

14 er, macrophages cocultured with the clinical isolate of Acanthamoeba produced significantly less IL-1

15 have the greatest overall inhibition for all isolates of Acanthamoeba castellanii and Acanthamoeba po

16 was assessed for 206 clinically significant isolates of aerobic Gram-positive bacilli representing 2

17 ere, we examined resistance of P. falciparum isolates of African origin (NF54, NF165 and NF166) to TE

18 The rectal and clinical isolates of all 9 men with paired isolates had indisting

19 possible to produce HCV particles resembling isolates of all HCV genotypes in human hepatoma cells (H

20 ly inhibits cellular entry of representative isolates of all known ebolavirus species in vitro and sh

21 LV-J strain PDRC-59831, a newly studied U.S. isolate of ALV-J.

22 symptomatic and lethal outcomes than in EPEC isolates of asymptomatic outcomes.

23 Here we report that a gastrointestinal isolate of B. subtilis sporulates with high efficiency d

24 Fluoroquinolone-resistant clinical isolates of bacteria have emerged readily and recent dat

25 effect against multi-drug resistant clinical isolates of bacterial pathogens and include three novel

26 ons, ferrets were challenged with a clinical isolate of BDBV.

27 Here we screened infant-gut isolates of Bifidobacterium longum subsp. infantis and B

28 ins and is prevalent in livestock-associated isolates of both species.

29 bjectives of this study were to characterize isolates of bovine milk origin from a collection that ha

30 gel electrophoresis for typing of S. aureus isolates of bovine origin.

31 Some isolates of Bradyrhizobium have been shown to be non-sym

32 Both a laboratory strain and a clinical isolate of C. albicans were used for SCFS experiments.

33 In a genetically divergent isolate of C. parvum, a majority of sequences was found

34 rmed a plasmid-free lymphogranuloma venereum isolate of C. trachomatis, serovar L2, with either the o

35 Among the 60 isolates of C. albicans (9 isolates), C. tropicalis (5 i

36 inst numerous fluconazole-resistant clinical isolates of C. albicans and non-albicans species, and it

37 Paired isolates of C. difficile were available from 93 of 199 p

38 Natural isolates of C. elegans differ in their sensitivity to ph

39 SKN-1 in both laboratory-derived and natural isolates of C. elegans.

40 tural selection, and to compare with 40 wild isolates of C. elegans.

41 Drug-resistant clinical isolates of C. glabrata most commonly contain point muta

42 da species (702 isolates, 13 species) and 44 isolates of C. neoformans against fluconazole.

43 In diploid isolates of C. neoformans var. grubii (serotype AA) and

44 While most isolates of C. neoformans var. grubii belong to one of t

45 examining over 800,000 DNA variants in wild isolates of Caenorhabditis elegans, we made a discovery

46 Among the 62 isolates of Candida albicans (4 isolates), C. tropicalis

47 6 Cryptococcus neoformans strains), and 746 isolates of Candida species (702 isolates, 13 species) a

48 was also inhibitory to fluconazole-resistant isolates of Candida species.

49 isolates of Enterobacteriaceae, including 25 isolates of carbapenem-resistant Enterobacteriaceae.

50 sing a CHIKV replicon cell line and clinical isolate of CHIKV of Central/East African genotype.

51 ized by both a vaccine strain and a clinical isolate of CHIKV to mediate virus binding.

52 chloropsis oceanica CCAP 849/10 and a marine isolate of Chlorella vulgaris CCAP 211/21A as the best l

53 e, convallatoxin was able to inhibit primary isolates of CMV, including those resistant to the anti-C

54 antimicrobial agents against clinical equine isolates of Corynebacterium pseudotuberculosis.

55 ed against the commercially used Mexican (M) isolate of CpGV, infection experiments of larvae of the

56 of the anthelmintics against 16 C. difficile isolates of defined PCR-ribotype.

57 d intravenously with a low-passage, clinical isolate of DENV-2, and this resulted in sustained viremi

58 nally influences Caenorhabditis elegans wild isolates of distinct mtDNA lineages and geographic origi

59 comparisons of numerous species, strains, or isolates of diverse origins.

60 Live isolates of dromedary 229E viruses were obtained and stu

61 We also sequenced the complete genome of an isolate of DWV that covertly infects the AmE-711 cell li

62 y in which a heterogeneous collection of 196 isolates of E. coli and K. pneumoniae (PRIMERS II) were

63 te quantification of both stock and clinical isolates of E. coli in spiked blood within a broad range

64 ion, and virulence of oropharyngeal and lung isolates of E. coli, suggesting that cranberry proanthoc

65 Two VMEs were observed for daptomycin in isolates of E. faecalis and 2 ME, 1 for high-level genta

66 he molecular origin of the outbreak using 22 isolates of E. rostratum retrieved from 19 case patients

67 Representative isolates of each species were used to create reference M

68 he same mutation is also found in most human isolates of emergent avian H7N9 and H10N8 viruses whose

69 n, PA-K356R, in avian H9N2 viruses and human isolates of emergent H7N9 and H10N8 viruses.

70 atories' perspective on why having access to isolates of enteric pathogens is essential for public he

71 We screened IncX4 plasmids among 2,470 isolates of Enterobacteriaceae and determined the mcr-1

72 lobal surveillance program collected 103,960 isolates of Enterobacteriaceae from 2008 to 2014.

73 Both tests were challenged with 294 isolates of Enterobacteriaceae spp., Pseudomonas aerugin

74 The practice of screening clinical isolates of Enterobacteriaceae that test as susceptible

75 nd accounted for 1.4% (1,493/103,960) of all isolates of Enterobacteriaceae The most frequently ident

76 We identified 21 621 non-duplicate isolates of Enterobacteriaceae, Acinetobacter spp, and P

77 ed by CLSI broth microdilution (BMD) for 255 isolates of Enterobacteriaceae, including 25 isolates of

78 accumulation of mobile elements in hospital isolates of enterococci can include those that are inher

79 rains and reliably detected 48 environmental isolates of enterococci.

80 picture of natural enterococci diversity, 11 isolates of Enterococcus faecalis recovered from freshwa

81 against beta-lactams in 72 highly resistant isolates of Escherichia coli and Klebsiella pneumoniae (

82 t OmpC proteins from four different clinical isolates of Escherichia coli obtained sequentially from

83 ctivity against multidrug-resistant clinical isolates of Escherichia coli, Acinetobacter baumannii, K

84 activity in vitro, including recent clinical isolates of Escherichia coli, Enterococcus faecalis, Kle

85 ates (MIC, >/=1 mug/ml; n = 3,428) and 9,371 isolates of Escherichia coli, Klebsiella pneumoniae, Kle

86 trations (MICs) of imipenem against clinical isolates of Eschericia coli and Klebsiella pneumoniae ha

87 Oral gavage of BALB/c mice with a clinical isolate of extraintestinal pathogenic E. coli (ExPEC) le

88 novo assembly of 312 blood- or urine-derived isolates of extraintestinal pathogenic (ExPEC) Escherich

89 Shedding results differed among isolates of five different pneumococcal types.

90 h-throughput sequencing of the RNAs from 275 isolates of five fungal plant pathogens, 66 previously u

91 crotiter trays on caspofungin MICs using 209 isolates of four Candida species, including 16 C. albica

92 ribotype 027 clinical isolates and clinical isolates of four other ribotypes (001, 002, 014, and 053

93 reak was caused by genotype II, although two isolates of genotype I were also detected for the first

94 omplete genomic sequences of recent virulent isolates of genotypes II and IX from China, Egypt, and I

95 Of the 100 isolates of giant viruses, we demonstrated the human pat

96 in swelling power and solubility of starches isolated of grains stored at 40 degrees C.

97 ssment of prevalence of MCRPE infection from isolates of Gram-negative bacteria collected at the hosp

98 model) to predict the potential virulence of isolates of H. parasuis based on a subset of 10 genes fr

99 new diagnostic mPCR was tested on 143 field isolates of H. parasuis that had previously been whole-g

100 y protective vaccine against nonencapsulated isolates of Haemophilus influenzae (NTHi) lies in the ge

101 e-orchestrated inflammation using a clinical isolate of HCMV (TR) and macrophages derived from primar

102 target remains unchanged across 30 clinical isolates of HCoV-NL63 strains.

103 With a single exception, all isolates of hepatitis C virus (HCV) require adaptive mut

104 e used to compare clinical and environmental isolates of Herbaspirillum spp.

105 It demonstrates activity against isolates of heterogeneous vancomycin-intermediate S. aur

106 Overall, these data indicate that a recent isolate of HFMG is greatly attenuated in the chicken hos

107 ver, in contrast to other avian IAVs, recent isolates of highly pathogenic H5N1 influenza viruses had

108 ein PB1-F2 is frequently truncated in recent isolates of highly pathogenic H5N1 viruses.

109 susceptibility patterns of multiple clinical isolates of Histoplasma representing different phylogene

110 osylation is one of the reasons that primary isolates of HIV and SIV are so heavily resistant to anti

111 t it was recently observed that most primary isolates of HIV-1 can mediate HLA-C downmodulation.

112 However, only some isolates of HIV-1 subtype C can use the CD4 receptor enc

113 o acid of RNase H never varied in over 1,850 isolates of HIV-1 that we compared.

114 ed the susceptibilities of different primary isolates of HIV-1 to the inhibition of viral infectivity

115 s functional entry receptors for early-stage isolates of HIV-1.

116 ur data indicate that we have detected a new isolate of HPV38 that appears to be integrated into the

117 that one patient was infected with this new isolate of HPV38, which was integrated into his/her geno

118 ular challenge with a neurovirulent clinical isolate of HSV-1.

119 e replication of HSV-2 and a recent clinical isolate of HSV-1.

120 binant trimers based on the env genes of two isolates of human immunodeficiency virus type 1 (HIV-1),

121 Most isolates of human rhinovirus, the common cold virus, rep

122 al expansion to include a number of clinical isolates of important Gram-negative species-Enterobacter

123 idemic, and Virginia 2013 (VA2013), a recent isolate of increased house finch virulence.

124 Forty-six of 51 isolates of Indian origin displayed decreased susceptibi

125 All isolates of Indonesian origin were susceptible to ciprof

126 olar efficacy against several human clinical isolates of influenza A viruses, including both oseltami

127 s rapidly accumulated in respective clinical isolates of interest including MDROs such as methicillin

128 3 strains emerge frequently within clinical isolates of invasive diseases.

129 irst ten carbapenem non-susceptible clinical isolates of K pneumoniae or E coli and ten susceptible s

130 targeting Gram-negative bacteria on clinical isolates of Klebsiella pneumoniae, containing highly-res

131 ikely to be XDR, or (iii) is identical to an isolate of known resistance (i.e., a likely transmission

132 aluated using DNA extracted from 91 clinical isolates of known geographic subspecies, while the assay

133 sceptible Staphylococcus aureus (MSSA) CC398 isolates of known human origin.

134 (i) raw reads from genomes of 308 Salmonella isolates of known serotype; (ii) raw reads from genomes

135 lineages and was validated using 515 E. coli isolates of known STs.

136 Many isolates of L. braziliensis (>25%) contain a double-stra

137 o the mechanisms by which resistant clinical isolates of L. donovani induce intracellular events rele

138 genetic analyses indicate that environmental isolates of L. pneumophila have a potential positive sel

139 rophages infected with 3 ATCC and 5 clinical isolates of L.V. guyanensis, and L.V. panamensis for 24

140 for screening the aromatic potential of new isolates of LAB.

141 Human isolates of Lactobacillus spp. have differing site assoc

142 l SidE orthologs encoded by the Philadelphia isolate of Legionella pneumophila were toxic to yeast, a

143 d case caused by reinfection with a separate isolate of M. avium.

144 The tedizolid MIC90 values for 81 isolates of M. abscessus subsp. abscessus and 12 isolate

145 seful for treating approximately 20% of U.S. isolates of M. abscessus subsp. abscessus.

146 ates of M. abscessus subsp. abscessus and 12 isolates of M. abscessus subsp. massiliense were 8 mug/m

147 nd that PRELP binds the majority of clinical isolates of M. catarrhalis (n = 49) through interaction

148 We show that the majority of clinical isolates of M. catarrhalis (n = 49), but not other teste

149 Twenty-two isolates of M. chelonae had tedizolid and linezolid MIC9

150 ast, the absence of a detectable erm gene in isolates of M. chelonae, M. senegalense, and M. peregrin

151 The MIC90 values for 20 isolates of M. fortuitum were 2 mug/ml for tedizolid and

152 enome comparison of pretreatment and relapse isolates of M. intracellulare uncovered mutations in a p

153 e did not affect the virulence of compatible isolates of M. oryzae.

154 There were no isolates of M. terrae or M. nonchromogenicum, including

155 emergence of drug resistance among clinical isolates of M. tuberculosis, we show that the ancestral

156 drug-susceptible and drug-resistant clinical isolates of M. tuberculosis.

157 Here, we compared genome sequence of 6 isolates of Magnaporthe species obtained from three diff

158 Two isolates of maize chromosome 3 proved to contain neocent

159 A clinical isolate of methicillin-resistant S. aureus was killed by

160 s in all bloodstream infections and clinical isolates of methicillin-resistant Staphylococcus aureus

161 as a drug of last resort; however, clinical isolates of methicillin-resistant Staphylococcus aureus

162 We consistently observe that isolates of Methicillin-resistant Staphylococcus aureus

163 a, Staphylococcus aureus (including clinical isolates of MRSA and MSSA) and Staphylococcus epidermidi

164 laboratory using serially passaged clinical isolates of MRSA and MSSA.

165 were able to clearly distinguish a clinical isolate of MTB from a nonTB species of the genus Mycobac

166 f 224 temporal and spatial diverse S. aureus isolates of multilocus sequence type (ST) 8 to reconstru

167 he corresponding glycoproteins of a clinical isolate of MuV (hMuV).

168 RGM medium supported the growth of all isolates of mycobacteria and was more selective than any

169 One hundred isolates of Mycobacterium avium complex and eight M. sim

170 drug susceptibility testing on 337 clinical isolates of Mycobacterium tuberculosis collected in KwaZ

171 Multidrug-resistant (MDR) isolates of Mycobacterium tuberculosis complex (MTBC) ar

172 ipids synthesized by clinical drug-resistant isolates of Mycobacterium tuberculosis reactivate HIV-1

173 strains with mutations in gatA from clinical isolates of Mycobacterium tuberculosis show increased mi

174 selected mutations found in Australian field isolates of MYXV that fall in known or potential virulen

175 We sequenced the genomes of 236 isolates of N gonorrhoeae collected by the Centers for D

176 All isolates of N. cyriacigeorgica, N. asteroides, N. absces

177 One hundred fifteen clinical and laboratory isolates of N. gonorrhoeae were tested following the Cli

178 en evaluating solithromycin against clinical isolates of N. gonorrhoeae.

179 rude whole-genome assemblies, we analyzed 25 isolates of Neisseria gonorrhoeae by using a high-resolu

180 All isolates of NG-STAR ST-42, ST-43, ST-63, ST-81, and ST-1

181 d ofloxacin were determined for 100 clinical isolates of nontyphi Salmonella with or without resistan

182 ralia and New Zealand, the unique population isolate of Norfolk Island has been shown to exhibit incr

183 here that, in the guinea pig model, a human isolate of novel H7N9 influenza virus, A/Anhui/1/2013 (A

184 enerated high-quality draft genomes from 265 isolates of NVT pneumococci not susceptible to penicilli

185 One isolate of Ochroconis cordanae was found, being reported

186 ement and orientation of an invasive corneal isolate of P. aeruginosa in the corneal stroma during in

187 l isolates and approximately 50% of clinical isolates of P. aeruginosa from chronic airway infection

188 Both laboratory standard strains and CF isolates of P. aeruginosa induce DNA, MPO, and HNE relea

189 Determination of exoU expression in clinical isolates of P. aeruginosa may be helpful in directing cl

190 s showed increased activity against clinical isolates of P. aeruginosa, further confirming the target

191 throcytes were refractory to invasion by all isolates of P. falciparum because parasites failed to at

192 Isolates of P. triticina found worldwide on cultivated d

193 eport the sequence variation of 16 different isolates of parainfluenza virus 5 (PIV5) that were isola

194 We included N. gonorrhoeae isolates of patients visiting the Amsterdam STI Clinic b

195 We included N. gonorrhoeae isolates of patients who visited the Amsterdam STI Clini

196 In clinical isolates of PBMCs from lymphangioleiomyomatosis patients

197 releases a diverse array of metabolites, and isolates of physically associated taxa use unique subset

198 al isolates of PIV5-RSV-G (HN-L), but plaque isolates of PIV5-RSV-F (HN-L) had no mutations.

199 in RSV G and PIV5 L were found in individual isolates of PIV5-RSV-G (HN-L), but plaque isolates of PI

200 e drug responses of K13 wild-type and mutant isolates of Plasmodium falciparum sourced from a region

201 peptides may explain why nearly all clinical isolates of pneumococci conserve this enzyme despite the

202 rogenic acids (CHAs) from green coffee, with isolates of proteins from egg white (EWP), whey (WPC) an

203 evealed that genetic divergence among Hainan isolates of PRSV has allowed the virus to overcome the C

204 er antimicrobial performance against two MDR isolates of Pseudomonas aeruginosa and Acinetobacter bau

205 Inspired by new data from 28 clinical isolates of Pseudomonas aeruginosa and strains evolved i

206 We identified here melanogenic clinical isolates of Pseudomonas aeruginosa with large chromosoma

207 ) reference broth microdilution (BMD) for 99 isolates of Pseudomonas aeruginosa, 26 Acinetobacter bau

208 resistance against a broad spectrum of field isolates of Puccinia graminis f.sp. tritici, including t

209 rus infection and that the M protein of wild isolates of rabies virus is a viral immune-modulatory fa

210 The matrix (M) protein of wild isolates of rabies virus such as Tha (M-Tha) was previou

211 All seven media were challenged with 147 isolates of rapidly growing mycobacteria and 185 isolate

212 microdilution, susceptibility testing of 170 isolates of rapidly growing mycobacteria showed equivale

213 The peptides from the protein isolate of raw bean with molecular mass lower than 3kDa

214 Sequencing of independent clonal isolates of replication-competent virus revealed that 57

215 Isolates of rhinovirus C (RV-C), a recently identified E

216 pin, gentamicin, and doxycycline against 101 isolates of Rhodococcus equi were determined by broth ma

217 d in vitro and transfected into a virus-free isolate of S. sclerotiorum, DK3.

218 We obtained 331 clinical isolates of S flexneri serotype 3a, including 275 from l

219 natants from laboratory strains and clinical isolates of S. aureus caused galectin-3 degradation.

220 of nonsynonymous SNPs in fnbA among clinical isolates of S. aureus that cause endovascular infections

221 a collection of genetically diverse clinical isolates of S. aureus, community-associated methicillin-

222 ts when requested to perform AST on atypical isolates of S. aureus.

223 By whole-genome sequence analysis of 675 isolates of S. Enteritidis from 45 countries, we show th

224 These data indicate that nearly all isolates of S. lugdunensis are susceptible to narrow-spe

225 Here, we used whole-genome sequencing of 140 isolates of S. pneumoniae recovered from bloodstream inf

226 onmental survival of clinical and laboratory isolates of S. pyogenes and S. pneumoniae as both organi

227 ary to this view, we found that many natural isolates of Saccharomyces cerevisiae display short or no

228 Antibiotic-resistant isolates of Salmonella enterica were selected on plates

229 genomes of pre- and posttherapy MDR clinical isolates of Salmonella Typhimurium from a patient that f

230 termine the species diversity of 23 clinical isolates of Schizophyllum from the United States using m

231 ain samples, in which ovine BSE and distinct isolates of scrapie are mixed at various ratios ranging

232 enome sequencing (WGS) was carried out on 87 isolates of sequence type 111 (ST-111) of Pseudomonas ae

233 o variants shared the same serotype, the SC2 isolates of sequence type 14 (ST14) harbored intact SPI-

234 There are no cultivated isolates of several bacteria identified using molecular

235 ollected and whole-genome sequenced clinical isolates of Shigella flexneri serotype 3a from high-risk

236 In contrast, three different isolates of sporadic CJD prions failed to transmit disea

237 We have discovered an isolate of Staphylococcus epidermidis harboring the gene

238 f infections caused by methicillin-resistant isolates of Staphylococcus aureus (MRSA).

239 sequencing was used to compare longitudinal isolates of Staphylococcus aureus that developed resista

240 United States were invited to submit ocular isolates of Staphylococcus aureus, coagulase-negative st

241 ctivity against multidrug-resistant clinical isolates of staphylococcus aureus, including methicillin

242 ctam resistance in human and animal clinical isolates of Staphylococcus intermedius group, Staphyloco

243 Beta-lactam resistant clinical isolates of Streptococcus pneumoniae contain altered pen

244 nce typing was successfully completed on 494 isolates of Streptococcus uberis from clinical mastitis

245 at were significantly more prevalent in EPEC isolates of symptomatic and lethal outcomes than in EPEC

246 yzing the full genomic sequences of over 100 isolates of Synechococcus-infecting cyanophages collecte

247 We corrected an initial isolate of synV to perfectly match the designed sequence

248 des survival and persistence benefits to TcI isolates of T. cruzi.

249 ant mutations (17.1%) was obtained among the isolates of TB patients suspected of having MDR-TB.

250 of ZIKV that was generated using a clinical isolate of the Asian lineage.

251 quencing data from 10 global isolates and an isolate of the closely-related Schistosoma rodhaini, whi

252 se finches-Virginia 1994 (VA1994), the index isolate of the epidemic, and Virginia 2013 (VA2013), a r

253 hat Pelagibacterales sp. strain HTCC7211, an isolate of the SAR11 clade of marine alpha-proteobacteri

254 rameshift mutation in pgp1 of our laboratory isolate of the straight genome sequenced variant of 1116

255 ex subjects, 182 (55%) were infected with an isolate of the USA300 methicillin-resistant S. aureus (M

256 BMD) assays were performed on 90 bloodstream isolates of the 4 most common gram-negative bacteria cau

257 the viral envelope (E) protein, whereas many isolates of the African lineage virus lack this site.

258 lso protects against infection with multiple isolates of the closely related organism and causative a

259 detected within these regions, including in isolates of the current outbreak.

260 A set of 73 isolates of the emerging fungus Trichoderma isolated fro

261 HAdV-D8 isolates of the epidemic period had a very high sequence

262 H7 vaccines based on divergent isolates of the Eurasian and North American lineages hav

263 nce results were also obtained with clinical isolates of the four DENV serotypes verified by RT-PCR a

264 In contrast to isolates of the four Shigella species, which are widespr

265 discovery in 1989, efforts to grow clinical isolates of the hepatitis C virus (HCV) in cell culture

266 Here, we first use natural isolates of the highly social bacterium Myxococcus xanth

267 Isolates of the human polyomavirus JC virus from patient

268 We evaluated 26 isolates of the M. terrae complex associated with tenosy

269 nd micafungin were assessed for 290 clinical isolates of the most representative pathogenic molds (15

270 -coverage whole-genome sequencing of 37 wild isolates of the nematode C. briggsae and applied a pairw

271 is consistent across clinical and laboratory isolates of the North American type 1 and type 2 phyloge

272 co-cultured a diverse collection of natural isolates of the opportunistic pathogen Pseudomonas aerug

273 n as well as decreased resistance to several isolates of the plant pathogen Hyaloperonospora arabidop

274 Here we report that some isolates of the rice pathogen Xanthomonas oryzae use tru

275 lated, and their genotypes were common among isolates of the same serotype in South Africa.

276 interact with the genomes of diverse natural isolates of the same species.

277 observed for whole water samples than for OM isolates of the same water, suggesting differential reco

278 thicillin resistance in 115 human and animal isolates of the Staphylococcus intermedius group (SIG),

279 seq and full genome sequences for 85 diverse isolates of the yeast Saccharomyces cerevisiae-including

280 at are not observed for M3 or M18 GAS due to isolates of these serotypes naturally harboring mutant r

281 we detect nucleoid components in biochemical isolates of these structures.

282 Obtaining isolates of these targets, preferably in pure cultures,

283 ed a collection of archived human and animal isolates of these three species by deep-sequencing polym

284 the antibiotic susceptibility of subgingival isolates of these two bacterial species, this study dete

285 A total of 356 isolates of these two pathogenic RGM taxa from two refer

286 nome sequencing (WGS) was performed for each isolate of this collection, and discriminating molecular

287 The whole genome sequence of six isolates of this collection was analyzed.

288 n Rhodococcus equi, pVAPN, carried by bovine isolates of this facultative intracellular pathogenic ac

289 oDetection phylogenetic tree showed that all isolates of this outbreak cluster were strongly related,

290 he severity of invasive infections caused by isolates of this serotype.

291 coinfection of naive African buffaloes with isolates of three SAT serotypes from field buffaloes, pa

292 We provide evidence that a wild-type isolate of TMV is able to enter C71 cells grown in liqui

293 MS identified all 42 isolates of V. cholerae O1 and O139 and 7 of 9 non-O1/O1

294 f synthetic peptide BF2 against the clinical isolates of vancomycin-resistant and control strains of

295 of which 6 neutralized heterologous primary isolates of various HIV-1 subtypes in a standardized in

296 lates and comparing them with a set of CC398 isolates of various known origin might provide clues to

297 all, these data suggest that C. elegans wild isolates of varying geographic origins may adapt to envi

298 ecombination patterns were evaluated for 229 isolates of Wheat dwarf virus (WDV), which are important

299 MDR was found in 6.8% of 844 isolates, of which 593 (70.3%) were identified as belong

300 4 strains revealed OsSWEET13 induction by 42 isolates of X. oryzae pv. oryzae.