ライフサイエンスコーパス: isolate of

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

2 In total, the spectra of 141 isolates of 17 bacteria have been used.

3 We apply MGEfinder to 12,374 sequenced isolates of 9 prevalent bacterial pathogens, including M

4 verage nucleotide identity among the Mexican isolates of 98.3%, ranging from 91.1 to 100%.

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

6 itional cloning showed that resistance to an isolate of A. candida race 2 (Ac2V) can be explained in

7 was identified that confers resistance to an isolate of A. candida race 9 (AcBoT) that infects B. ole

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

9 and epidemiological analyses have identified isolates of a single serotype, M28, as being nonrandomly

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

11 Recently, isolates of A. pleuropneumoniae that were serologically

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

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

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

15 veral hundred genes in a multidrug-resistant isolate of Acinetobacter baumannii that are required for

16 es mice from lethal infections with clinical isolates of Acinetobacter baumannii, Klebsiella pneumoni

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

18 5 available GAS macrolide-resistant clinical isolates of all infection types collected at the nationa

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

20 The ability to sense prey among wild isolates of Arthrobotrys oligospora varied greatly, as d

21 The laboratory also received 46 isolates of Aspergillus fumigatus from COVID-19 patients

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

23 MDMs were infected with CF clinical isolates of B. cenocepacia and P. aeruginosa.

24 We reviewed human and veterinary isolates of B. helicus identified among Blastomyces and

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

28 Comparison of eight isolates of bovine and ovine origin at three key time-po

29 pathogenic and non-pathogenic M. haemolytica isolates of bovine and ovine origin.

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

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

32 ular basis for successful spread of virulent isolates of bovine tuberculosis among animals and to est

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

34 n a BSL-3 model with an aerosolized clinical isolate of Burkholderia pseudomallei from Thailand.

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

36 entiated cells were infected with a clinical isolate of C. trachomatis, and inclusions containing chl

37 perimentally infected with scrapie or bovine isolates of C-BSE and L-BSE, respectively.

38 5) and thus was further evaluated against 18 isolates of C. albicans (n = 9), C. glabrata (n = 4), an

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

40 Among 35 isolates of C. auris, Vitek 2 yielded correct identifica

41 control infection caused by azole-resistant isolates of C. auris.

42 n) were further screened against 20 clinical isolates of C. difficile.

43 s ranging from 3 to 800 muM against clinical isolates of C. difficile.

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

45 Finally, we demonstrate that wild isolates of C. elegans display variation in seam cell se

46 ain-specific insertions among different wild isolates of C. elegans.

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

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

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

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

51 Public Health England received 25 isolates of Campylobacter jejuni from an individual with

52 A panel of 44 isolates of Candida species (C. auris, n = 35; Candida h

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

54 eron-deficient mice infected with a clinical isolate of CCHFV develop a severe inflammatory disease b

55 fference between genital and ocular clinical isolates of Chlamydia trachomatis is that only the forme

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

57 test data from excised-leaf assays for three isolates of Colletotrichum sublineola, the results showe

58 e that during pneumonia caused by a clinical isolate of CRKP-ST258 (KP35) there is an early recruitme

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

60 es investigated, with the exception of three isolates of DENV in the pre-treatment only regimen.

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

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

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

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

65 extended-spectrum cephalosporins in clinical isolates of E. coli.

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

67 pulmonary endothelium infected with clinical isolates of either Pseudomonas aeruginosa, Klebsiella pn

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 ar-identical clinical Streptococcus pyogenes isolates of emm subtype emm43.4 with a pbp2x missense mu

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

72 resistant) and challenge (12 MEV resistant) isolates of Enterobacterales (excluding P. mirabilis) an

73 MacConkey, and Mueller-Hinton agars with 110 isolates of Enterobacterales and P. aeruginosa These res

74 inor errors (mE) with clinical and challenge isolates of Enterobacterales Individual species demonstr

75 ods were evaluated using a collection of 270 isolates of Enterobacterales, 122 Pseudomonas aeruginosa

76 d classification of CPOs for the majority of isolates of Enterobacterales, Acinetobacter baumannii, a

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

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

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

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

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

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

83 rains and reliably detected 48 environmental isolates of enterococci.

84 S. equi subsp. zooepidemicus isolates of equine and human origins were compared with

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

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

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

88 -bit HiPR-FISH can distinguish between 1,023 isolates of Escherichia coli, each fluorescently labelle

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

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

91 Optimisation was completed on 15 isolates of Escherichia coli, showing 5 W in pulsatile m

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

93 dextran sulfate sodium-treated mice with an isolate of F. rodentium (F.

94 nhibition of mycotoxin production in the two isolates of F. graminearum.

95 y variability and was applicable to multiple isolates of F. tularensis Further improvements in the ac

96 nriched for mild ID (>50%) from a population isolate of Finland.

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

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

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

100 nanoemulsion forms were determined using two isolates of Fusarium graminearum.

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

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

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

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

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

106 ic but with HGT from an antibiotic-resistant isolate of H. pylori We find that HGT increases the rate

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

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

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

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

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

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

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

114 We find that most primary isolates of HIV-1 from the blood, including early isolat

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

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

117 It is widely held that clinical isolates of human cytomegalovirus (HCMV) are highly cell

118 nce of the filamentous phenotype in clinical isolates of IAV.

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

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

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

122 All isolates of Indonesian origin were susceptible to ciprof

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

124 With this method, we have detected clinical isolates of influenza in just one minute, significantly

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

126 3 strains emerge frequently within clinical isolates of invasive diseases.

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

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

129 sses growth of antibiotic-resistant clinical isolates of Klebsiella pneumoniae, Escherichia coli, and

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

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

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

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

134 One isolate of Lb. plantarum produced the highest concentrat

135 timonials and miltefosine-resistant clinical isolates of Leishmania infantum, indicating its potentia

136 persistent (but not a slow-spreading acute) isolate of lymphocytic choriomeningitis virus induced la

137 of susceptible mice infected with a clinical isolate of M. tuberculosis resembles that of active huma

138 o the reference strain, independent clinical isolates of M. abscessus also readily establish infectio

139 Isolates of M. abscessus from sputum do not always refle

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

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

142 erformed whole-genome sequencing (WGS) on 32 isolates of M. abscessus that were taken from multiple b

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

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

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

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

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

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

149 Clinical isolates of M. tuberculosis differed in their ability to

150 Clinical isolates of M. tuberculosis from both Egypt and Saudi Ar

151 tant and extensively drug-resistant clinical isolates of M. tuberculosis, suggesting that PIPD1's mod

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

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

154 using colony-bred ERBs inoculated with a bat isolate of MARV, we use species-specific antibodies and

155 wn to be rapidly fungicidal against clinical isolates of MDR C. albicans in vitro.

156 A clinical isolate of measles virus (MeV) bearing a single amino ac

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

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

159 ing A549 epithelial cells, we assessed nasal isolates of Moraxella, Staphylococcus, and Corynebacteri

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

161 ng ofloxacin resistance in cultured clinical isolates of Mtb and benchmark its performance with stand

162 their ability to inhibit growth of clinical isolates of multidrug-resistant ESKAPE pathogens.

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

164 tiple methods with 96 KPC-producing clinical isolates of multiple strains and species collected at a

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

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

167 ted in rpoB in rifampicin-resistant clinical isolates of Mycobacterium tuberculosis (Mtb).

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

169 resistant (DR) and multidrug-resistant (MDR) isolates of Mycobacterium tuberculosis.

170 We inoculated 55 isolates of Mycoplasma gallisepticum, collected over 20

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

172 te and aurothioglucose inhibited 48 clinical isolates of N. gonorrhoeae including multidrug-resistant

173 trations of 5 different antibiotics in 1,102 isolates of Neisseria gonorrhoeae that were confirmed in

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

175 es derived from a common ancestor or between isolates of nonmodel organisms.

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

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

178 The authors injected a unique human isolate of P. vivax that reached high gametocyte density

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

180 Natural isolates of P. aeruginosa that exhibit diverse genomes d

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

182 l US isolates and a subset of Czech Republic isolates of P. destructans were infected with PdPV-1.

183 e (CRISPRi) system for use in diverse strain isolates of P. fluorescens, SBW25, WH6 and Pf0-1.

184 A total of 558 isolates of P. triticina from wheat producing regions in

185 t reticulocyte invasion by multiple clinical isolates of P. vivax.

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

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

188 In clinical isolates of PBMCs from lymphangioleiomyomatosis patients

189 An Australian estuarine isolate of Penicillium sp. MST-MF667 yielded 3 tetrapept

190 we demonstrate that sporophytes of some wild isolates of Physcomitrella patens are associated with AH

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

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

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

194 scherichia coli, and a complex environmental isolate of primary sewage effluent.

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

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

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

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

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

200 Multiple clinical isolates of Pseudomonas aeruginosa, an important human p

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

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

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

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

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

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

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

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

209 Although bacterial isolates of S. aureus differ in their virulence potentia

210 Cultured wound isolates of S. aureus elicited differential phenotypes i

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

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

213 cularly in the context of divergent clinical isolates of S. aureus.

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

215 mediated beta-lactam resistance in 100 human isolates of S. epidermidis (48 mecA-positive isolates an

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

217 are broadly applicable to emerging clinical isolates of S. marcescens causing bacteremia.

218 vel peptide-peptoid hybrid B1 against canine isolates of S. pseudintermedius and P. aeruginosa.

219 ased signaling system conserved in sequenced isolates of S. pyogenes Deletion of the QS system's tran

220 We previously showed that wild isolates of Saccharomyces cerevisiae tolerate chromosome

221 eduction neutralization test with a clinical isolate of SARS-CoV-2 at biosafety level 3.

222 Upon challenge with a human isolate of SARS-CoV-2, mice that expressed human ACE2 an

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

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

225 se distinct from an invasive-disease-causing isolate of serotype 4 (TIGR4).

226 strictly pathogen or serotype specific, with isolates of serotype A1, A2, A6 and A12 being capable of

227 d ST with pathotype identified a majority of isolates of serotypes 1, 1/2, 2, 7, 14, and 23 and ST1,

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

229 to bacteria, we show that they kill clinical isolates of several multidrug-resistant bacteria-includi

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

231 tween methicillin-resistant and -susceptible isolates of Staphylococcus aureus (MRSA and MSSA) with 8

232 he whole-genome sequences of 4 blood culture isolates of Staphylococcus aureus and 2 control organism

233 pothesis by challenging a diverse set of 222 isolates of Staphylococcus aureus with the antibiotic ci

234 Isolates of Staphylococcus capitis, Staphylococcus haemo

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

236 In this study, we characterized 31 isolates of Streptococcus agalactiae (group B Streptococ

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

238 hylation motif CACNNNNNTAC was only found in isolates of sublineage 2.

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

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

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

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

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

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

245 from a multiplex family, from the population isolate of the Central Valley of Costa Rica.

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

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

248 Interestingly, a human isolate of the highly pathogenic avian influenza (HPAI)

249 support growth requirements of an open-ocean isolate of the SAR11 clade, the most abundant group of m

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

251 We test isolates of the 3 causative pathogens of CRE infections

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

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

254 typhoidal (iNTS) infections are dominated by isolates of the antibiotic resistance-associated sequenc

255 eneity is driven by the diversity ofclinical isolates of the causative agent, Mycobacterium tuberculo

256 ur discrete clades, based on where the first isolates of the clade were reported, South Asian (clade

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

258 tent of intra-species variation between four isolates of the ECM fungus Pisolithus microcarpus, in te

259 to study different types of ICEs in clinical isolates of the emergent pathogen Shewanella spp., to co

260 es from 3 U.S. academic medical centers (126 isolates of the Enterobacterales, 50 Pseudomonas aerugin

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

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

263 copy number variation (CNV), in many diverse isolates of the human fungal pathogen Candida albicans (

264 Isolates of the human polyomavirus JC virus from patient

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

266 Hawaiian isolates of the nematode species Caenorhabditis elegans

267 -wide association study (GWAS) on a panel of isolates of the opportunistic pathogen Legionella pneumo

268 Clinical isolates of the opportunistic pathogen Pseudomonas aerug

269 inducible antagonistic behavior in multiple isolates of the order Bacillales, where large inhibition

270 Eighty-five isolates of the order Enterobacteriales (12 mcr positive

271 echanisms of heteroresistance in 41 clinical isolates of the pathogens Escherichia coli, Salmonella e

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

273 tative Disease Resistance (QDR) to different isolates of the plant root rot pathogen Aphanomyces eute

274 We characterize three respiratory isolates of the recently described species Mycobacterium

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

276 single strains, but 16 groups of two or more isolates of the same emm type had an identical amino aci

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

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

279 Connections between closely related isolates of the same strain are robustly identified, des

280 etic context of a global collection of 1,087 isolates of the seventh pandemic V. cholerae serogroups

281 Isolates of the South African and Japanese/Korean lineag

282 large cellular aggregates was seen only with isolates of the South African and Japanese/Korean lineag

283 exhibited significantly higher MICs against isolates of the South African lineage than against isola

284 , aggregation could be reversibly induced in isolates of the Southern Asian lineage by exposure to tr

285 es of the South African lineage than against isolates of the Southern Asian lineage.

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

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

288 elements in 99.3% of the macrolide-resistant isolates of these emm types.

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

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

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

292 ted filtrates and mycelium from 15 blueberry isolates of this endophyte revealed differences in their

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

294 greatly in its ability to transmit different isolates of TSWV.

295 Recently, natural isolates of V. cholerae with chromosomal fusion have bee

296 genetic regulation networks among different isolates of V. cholerae.

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

298 A total of 107 actinobacteria were isolated, of which 77 exhibited significant antagonistic

299 The American isolates of Zika virus appear to have acquired mutations

300 than adults infected with the same Brazilian isolate of ZIKV (n = 11 pregnant females, 4 males, and 4