ライフサイエンスコーパス: resistance gene

1 tes (MIC of >0.06 mg/liter and presence of a resistance gene).

2 (800-1200 bps, designed to cover the entire resistance genes).

3 regulators of TSSG and copy gains of a drug resistance gene.

4 rtant for the protective function of the Mx1 resistance gene.

5 ecrosis in the presence of the corresponding resistance gene.

6 es have access to routine tests for the mecA resistance gene.

7 er and carries the emerging NDM-1 antibiotic resistance gene.

8 g the corresponding expression of antibiotic resistance gene.

9 e adaptive changes in expression of the drug-resistance gene.

10 of expression stochasticity of an antifungal resistance gene.

11 aumannii complex and to detect antimicrobial resistance genes.

12 s and the need to search for new/alternative resistance genes.

13 portant carriers of virulence and antibiotic resistance genes.

14 epends on the matching between virulence and resistance genes.

15 esponsible for the spread of some antibiotic resistance genes.

16 rogenase; and (iii) downregulation of copper resistance genes.

17 as bacterial virulence genes and antibiotic resistance genes.

18 r to be directly associated with insecticide-resistance genes.

19 of these drugs to trigger the expression of resistance genes.

20 ustrate an in vivo approach for finding drug resistance genes.

21 revealed an overrepresentation of antibiotic resistance genes.

22 o truncatula host carrying the RAP1 and RAP2 resistance genes.

23 nd ERas (ES-cell expressed Ras) as candidate resistance genes.

24 ble evolutionary responses and adaptation to resistance genes.

25 250, Tn6251 and Tn6252, two of which contain resistance genes.

26 ession of respiration and nitrosative stress resistance genes.

27 ence of virulence and acquired antimicrobial resistance genes.

28 r50 locus holds promise for mining effective resistance genes.

29 iffer in resistance and to predict candidate resistance genes.

30 onsidered the gold standard for detection of resistance genes.

31 al breast cancer cells to identify candidate resistance genes.

32 es two beta-lactamase and two aminoglycoside resistance genes.

33 rategies in slowing the spread of antibiotic resistance genes.

34 iates transcriptional derepression of copper resistance genes.

35 power to prospectively detect emerging drug resistance genes.

36 ic resistance, including lateral transfer of resistance genes.

37 cocci to prevent the spread of plasmid-borne resistance genes.

38 g the prevalence and diversity of antibiotic resistance genes.

39 the gut microbiome, and spread of antibiotic resistance genes.

40 two genes in a six-gene cluster of tellurite resistance genes.

41 naviridae genomes, and a group of antibiotic resistance genes.

42 are based on either antibiotic or herbicide resistance genes.

43 r carbohydrate-active enzymes and antibiotic resistance genes.

44 haracterized dominant or recessive potyvirus resistance genes.

45 ping files, and a database of anti-microbial resistance genes.

46 dentification of virulence and antimicrobial resistance genes.

47 xchange genetic material, notably antibiotic resistance genes.

48 s of host susceptibility genes and sometimes resistance genes.

49 pulations with low frequencies of antibiotic resistance genes.

50 moters, or that allow effector activation of resistance genes.

51 and interferon-induced genes such as myxoma resistance gene 1 (Mx1) and retinoic acid-inducing gene-

52 transporter PfMDR1 (P. falciparum multidrug resistance gene-1) as a determinant of parasite resistan

53 ein, using the mouse model of PSC (multidrug resistance gene 2 knockout), the hepatic knockdown of Gn

54 tration on hepatic fibrosis in the multidrug resistance gene 2-knockout (Mdr2(-/-)) mouse model of PS

55 -inducible gene-1), IRF3, and MxA (myxovirus resistance gene A) but not IRF7.

56 le selectable marker gene, the spectinomycin resistance gene aadA.

57 of transplastomic lines as the spectinomycin resistance gene aadA.

58 l and eukaryotic genes, including antibiotic resistance genes, activated by binding of macrolide drug

59 s: an allele-specific avirulence effector, a resistance gene allele, and a pathogen-encoded suppresso

60 ids, which harbor a wide range of antibiotic resistance genes, also encode the protein factors necess

61 mediates the dangerous spread of antibiotic resistance genes among bacterial populations.

62 ng, for instance the detection of ampicillin resistance gene (ampR).

63 two previously unreported P. falciparum drug resistance genes, an acetyl-CoA transporter (pfact) and

64 o look for an association between antibiotic resistance genes and antimicrobial chemicals in dust.

65 nt evolutionary selection both in known drug resistance genes and at new loci, and these varied marke

66 Patterns of other resistance genes and common virulence factors, represent

67 Efforts to discover resistance genes and DNA markers have been dominated by

68 talloregulatory proteins to upregulate metal resistance genes and enable the organism to preclude met

69 mes that express marker proteins (antibiotic resistance genes and Green Fluorescent Protein), and can

70 aphylococcal plasmids that harbor antibiotic resistance genes and immunizes avirulent staphylococci t

71 bjected to PCR-based detection of antibiotic resistance genes and repetitive sequence-based PCR (rep-

72 vironment selects for resistant bacteria and resistance genes and stimulates bacterial mutation, reco

73 explore the relationship between antibiotic resistance genes and the antimicrobial chemicals triclos

74 The resistance genes and the induction mechanism remain full

75 sm genes, and promote the expression of acid resistance genes and the non-LEE-encoded effector NleA.

76 We then explored the hosts of these resistance genes and the shared resistome of pig, chicke

77 rial, including pathogenicity and antibiotic resistance genes and their maintenance in the absence of

78 sistant cultivars, and, to date, 21 seedling resistance genes and two adult plant resistance (APR) ge

79 ontal gene transfer, in spread of antibiotic resistance genes, and as sites of phage attachment.

80 production, relative abundance of antibiotic resistance genes, and microbial community structure.

81 re and function of biotic and abiotic stress-resistance genes, and QTLs could shed light on the evolu

82 es like neurotoxicity as well as antibiotics resistance genes, and taxonomic gene markers for pathoge

83 ntibiotic resistant bacteria, and antibiotic resistance genes, and thus could serve as a contributing

84 was characterized by identifying antibiotic resistance genes annotated in the Comprehensive Antibiot

85 assemblies sufficient for full antimicrobial resistance gene annotation were obtained with as few as

86 to displace their resistant counterparts if resistance genes are costly.

87 gens and pests in plants, typically dominant resistance genes are deployed.

88 conjugative transposons carrying antibiotic resistance genes are found in a diverse range of bacteri

89 defense mechanism and prioritizing candidate resistance genes are important to the development of res

90 The incidence of classic malaria resistance genes are lower in the Fulani than in other s

91 racking environmental pathways of antibiotic resistance gene (ARG) dissemination, we sought to determ

92 pment of models for understanding antibiotic resistance gene (ARG) persistence and transport is a cri

93 the extent to which antibiotics, antibiotic resistance genes (ARG), and ruminant-associated microbes

94 eria (MRB) and even intracellular antibiotic resistance genes (ARG), but information on the latter is

95 The co-occurrence of antibiotic-resistance genes (ARGs) and mobile genetic elements (MGE

96 Substantial quantities of antibiotic resistance genes (ARGs) are discharged with treated resi

97 Antibiotic resistance genes (ARGs) are increasingly appreciated to

98 tablish a pipeline for annotating antibiotic resistance genes (ARGs) based on metagenomic assembly to

99 by a lower abundance of selected antibiotic resistance genes (ARGs) compared with ambient dust, asse

100 Environmental dissemination of antibiotic resistance genes (ARGs) has become an increasing concern

101 Ancient and diverse antibiotic resistance genes (ARGs) have previously been identified

102 The emergence and prevalence of antibiotic resistance genes (ARGs) in the environment is a serious

103 d wastewater on the quantities of antibiotic resistance genes (ARGs) in the Upper Mississippi River.

104 f selected clinically significant antibiotic resistance genes (ARGs) showed that their relative abund

105 d are recognized as reservoir for antibiotic-resistance genes (ARGs) that are associated with clinica

106 Antibiotic resistance genes (ARGs), human pathogenic bacteria (HPB)

107 ften conferred by the presence of antibiotic resistance genes (ARGs), which are readily found in the

108 iota is an important reservoir of antibiotic resistance genes (ARGs).

109 ds are a significant reservoir of antibiotic resistance genes (ARGs).

110 as their associated plasmid-borne antibiotic resistance genes (ARGs).

111 ds to the widespread induction of antibiotic-resistance genes (ARGs).

112 orthologs control expression of two MAs(III) resistance genes, arsP that encodes the ArsP MAs(III) ef

113 rella forsythia and also identify antibiotic resistance genes, bacterial virulence factors and host i

114 luble NSF attachment protein (Gm-alpha-SNAP) resistance gene because homologs of these genes physical

115 This problem is exacerbated by exchange of resistance genes between pathogens and benign microbes f

116 ater; synthetic DNA containing an ampicillin resistance gene (bla) from cloning vectors was not detec

117 d plasmid pWH1266, which contains ampicillin resistance gene blaTEM-1 and tetracycline resistance gen

118 rred by Xo1 and that conferred by the tomato resistance gene Bs4 suggests that monocots and dicots sh

119 irulence has been detected for most seedling resistance genes but is unknown for the APR genes Rph20

120 derstanding the differences in antimicrobial resistance gene carriage between different species of St

121 We report the cloning of a P. pachyrhizi resistance gene CcRpp1 (Cajanus cajan Resistance against

122 d abundance of FRGs, including the linezolid resistance genes cfr and optrA, in adjacent soils, and a

123 amplification and overexpression of the drug resistance gene CKS1B, which we recapitulated in hypoxic

124 n-specific gene family expansions, including resistance gene clusters, predate the split of the Mesoa

125 overy identifies a new type of durable plant resistance gene conferring quantitative disease resistan

126 eIF2Bbeta represents a new class of virus resistance gene conferring resistance to any pathogen.

127 The Sr35 resistance gene confers immunity against this pathogen's

128 turnaround time, full annotation of plasmid resistance gene content could be obtained in under 6 h f

129 expansion of both ceftiofur and tetracycline resistance gene copies/gram of feces.

130 directly demonstrate that CNV of the copper-resistance gene CUP1 is stimulated by environmental copp

131 g99 race group is virulent to most stem rust resistance genes currently deployed in wheat and poses a

132 netic polymorphism analysis of the three key resistance genes, CYP6P9a, CYP6P9b, and CYP6M7, support

133 Analysis of the prevalence of antibiotic resistance genes demonstrated the effect of eliminating

134 rogramming the nuclease to target antibiotic resistance genes destroys staphylococcal plasmids that h

135 enchtop genomic sequencing and antimicrobial resistance gene detection in clinical isolates.

136 and rapid 1D) with the goal of antimicrobial resistance gene detection.

137 CR (rmPCR) detection of bacteria, fungi, and resistance genes directly from positive BCBs.

138 Two types of antibiotic resistance gene discoveries will be discussed: the use o

139 titative risk assessment and surveillance of resistance gene dissemination across interconnected habi

140 Mapping resistance gene dissemination between humans and their e

141 enes Rwt3 and Rwt4 Studies on avirulence and resistance gene distributions, together with historical

142 a more extensive description of the two main resistance genes employed against tospoviruses: the Sw5

143 Additionally, putative multidrug resistance genes (emrE) were found in YSLPV1 and YSLPV2

144 In plants, most disease resistance genes encode nucleotide binding Leu-rich repe

145 The repetitive nature of plant disease resistance genes encoding for nucleotide-binding leucine

146 t are predominantly generated from canonical resistance genes encoding nucleotide binding-leucine ric

147 a ten times higher mutation rate in pathogen resistance genes, expected to be under positive or balan

148 Prolamin and resistance gene families are important in wheat food use

149 ch-repeat proteins (NLRs), the major disease-resistance gene families, has been unexplored in plants.

150 Here, we have tested a bifunctional resistance gene for its suitability as a selectable mark

151 resistant to EAB and may eventually provide resistance genes for introgression into North American s

152 ave been suggested to serve as reservoirs of resistance genes for more pathogenic streptococci and ma

153 al food-production scenario, we profiled hop-resistance gene frequencies and bacterial and fungal com

154 e emergence and dissemination of florfenicol resistance genes (FRGs, including fexA, fexB, cfr, optrA

155 in plants by means of an endogenous disease resistance gene from Arabidopsis thaliana named RPS5, wh

156 edator cells functionally acquiring adaptive resistance genes from adjacent prey.

157 dwide and, to protect against these viruses, resistance genes from different wild tomato species are

158 y emerge mainly by acquisition of antibiotic-resistance genes from other S. aureus strains or even fr

159 ecific contamination of the known retrovirus resistance gene Fv1.

160 ine resistance genes (manures) and multidrug resistance genes (greenhouse soils).

161 gered immunity that is directed by the wheat resistance genes H6 and H9.

162 However, few recessive disease resistance genes have been characterized.

163 soybean resistance loci have been mapped, no resistance genes have been cloned.

164 se to wheat genotypes carrying different RWA resistance genes have been initiated in our group; howev

165 ity (S) genes, here referred to as recessive resistance genes, have promise for providing broad durab

166 protein-coding genes, including 292 disease resistance gene homologs, and nine genes determining ess

167 s problem for Plum Pox Virus (PPV) candidate resistance gene identification in Prunus species, we imp

168 All late blight resistance genes identified to date belong to the coiled

169 of novel genome analysis tools, such as the Resistance Gene Identifier (RGI) for resistome predictio

170 strate the functionality of the GmSHMT08 SCN resistance gene in a transgenic soybean plant.

171 brane eliciting activation of the antibiotic resistance gene in E. coli.

172 Selection based on the puromycin resistance gene in KSHV.219 yielded cultures with all ce

173 GTPase 1) gene has been described as a major resistance gene in mice and humans.

174 very from Friend virus 3 (Rfv3), a classical resistance gene in mice that promotes the neutralizing a

175 The expression of antibiotic resistance gene in the E. coli bioreporter responded lin

176 voke very different expression of antibiotic resistance gene in the exposed bacteria due to different

177 94.2%, respectively, for detection of known resistance genes in 108 multidrug-resistant Gram-negativ

178 hisms (SNPs) in 4 Plasmodium falciparum drug resistance genes in 668 archived parasite-positive blood

179 ity demonstrates the existence of antibiotic resistance genes in a population with little antibiotic

180 tential to provide typing results and detect resistance genes in a single assay, thus guiding timely

181 e to assess the usefulness and durability of resistance genes in agricultural settings.

182 ification of stress tolerance and antibiotic resistance genes in bacteria.

183 mber heterogeneity and the emergence of drug resistance genes in cancer.

184 Characterizations of durable resistance genes in crop plants are coming to the fore.

185 on quantities of ceftiofur and tetracycline resistance genes in feedlot cattle.

186 munity structure, function and antimicrobial resistance genes in lab-scale anaerobic digesters.

187 ce of NLR genes including functional disease-resistance genes in pepper plants.

188 performing a 4-plex PCR targeting antibiotic resistance genes in S. aureus using only 2 color channel

189 y associated with horizontal transmission of resistance genes in the absence of antimicrobial selecti

190 d successful identification of antimicrobial resistance genes in the draft assembly corresponding to

191 ces could help reduce the load of antibiotic-resistance genes in the environment.

192 lation between the presence of antimicrobial resistance genes in the gut microbiota and the administr

193 ept of an oral resistome, which includes all resistance genes in the microbiome.

194 icated the up-regulation of oxidative stress resistance genes in the observed resistance to external

195 . bethesdensis altered the expression of ROS resistance genes in the presence of normal but not CGD P

196 lated to the use of antibiotic and herbicide resistance genes in the production of transgenic crops.

197 s were the most prevalent (25.9%) antibiotic resistance genes in these samples.

198 t strategies in reducing faecal bacteria and resistance genes in these settings representative of low

199 nctional metagenomics identified beta-lactam-resistance genes in treated and untreated soil, and indi

200 ns (which often carry multiple antimicrobial resistance genes), in the fecal microbiota of 147 mother

201 Core resistance genes include a transcriptional regulator of

202 erial riboregulators that control antibiotic resistance genes including metabolite-binding riboswitch

203 and the relative abundance of an antibiotic resistance gene, including one between the ubiquitous an

204 ved in plasmids encoding multiple antibiotic resistance genes, including extended spectrum beta-lacta

205 and previously unidentified drug targets and resistance genes, including novel roles for phosphatases

206 ds on the chromosomal neighborhood of a drug-resistance gene inserted at different positions of the E

207 issemination of them and their antimicrobial resistance genes into animal and human populations.

208 These results indicate that the pepper Bs2 resistance gene is also functional in a family other tha

209 loci is also found when a NAT to hygromycin resistance gene is driven off the endogenous vivid (vvd)

210 ancient human-associated putative antibiotic resistance genes, (iv) a genome reconstruction of the pe

211 encing approaches, we identified a novel BPH resistance gene, LOC_Os06g03240 (MSU LOCUS ID), from the

212 highest relative abundance was tetracycline resistance genes (manures) and multidrug resistance gene

213 al implications, as stochastic expression of resistance genes may be widespread, allowing populations

214 and 5 yeast species) and three antimicrobial resistance genes (mecA, vanA/B, and blaKPC) from positiv

215 The resistance gene, mecA, is carried on a large (20 kb to >

216 of effectors and their functions as well as resistance gene-mediated recognition and signaling.

217 through estrogen receptor alpha, whereas the resistance genes modulate the PI3K signaling pathway.

218 ude mobile genetic elements (MGEs) and metal resistance genes (MRGs).

219 The dominant tobacco mosaic virus (TMV) resistance gene N induces a hypersensitive response upon

220 Nucleotide-binding site leucine-rich repeat resistance genes (NLRs) allow plants to detect microbial

221 to explain the rapid exchange of antibiotic resistance genes observed in S. aureus.

222 In cereals, several mildew resistance genes occur as large allelic series; for exam

223 lic potential and the presence of antibiotic resistance genes of these different bacterial communitie

224 void suicide, an antibiotic producer harbors resistance genes often found within the same biosyntheti

225 etic screen, we show that AphB represses ROS resistance gene ohrA, which is also repressed by another

226 ecificity by reprogramming the expression of resistance genes or their corresponding avirulence genes

227 ates (MIC of </=0.06 mg/liter and absence of resistance genes) or non-wild-type isolates (MIC of >0.0

228 However, many resistance genes persist for long periods in the absence

229 rast, variant alleles of the novel candidate resistance genes pfap2mu (S160N/T; P = .006) and pfubp-1

230 e factors Avr-Pia (corresponding to the rice resistance gene Pia) and Avrpiz-t (the cognate Avr gene

231 ) and Avrpiz-t (the cognate Avr gene for the resistance gene Piz-t) proteins.

232 lasmid that has evolved to harbor antibiotic resistance genes plays a role in the differentiation of

233 The convergence of virulence and resistance genes potentially could lead to the emergence

234 Ps, potentially in combination with specific resistance genes, precedes full resistance, we retrogres

235 virulence protein triggering each of the two resistance gene products; epidemiology of RB isolates is

236 Race-specific resistance genes protect the global wheat crop from stem

237 , and quinolones (plasmid-mediated quinolone resistance gene qnrB7).

238 Plant resistance genes (R genes) harbor tremendous allelic div

239 omes, we identified a heretofore unknown RIF resistance gene, RIF phosphotransferase (rph).

240 ers a dual specificity of recognition by two resistance genes (Rlm4 and Rlm7) and is strongly involve

241 effector-triggered immunity mediated by the resistance genes RPS2, RPS4, RPS6 and RPM1.

242 wheat cultivars containing the corresponding resistance genes Rwt3 and Rwt4 Studies on avirulence and

243 es near the gip-1 locus suggest that a novel resistance gene(s) confers immunity.

244 quences were further tested using the zeocin resistance gene sh-ble as a reporter in monocistronic an

245 ed a complement of chromosomal antimicrobial resistance genes similar to that of more recent isolates

246 We applied MutRenSeq to clone stem rust resistance genes Sr22 and Sr45 from hexaploid bread whea

247 We identify the wheat stem rust resistance gene Sr50 (using physical mapping, mutation a

248 n levels was observed for the main metabolic resistance genes, suggesting that metabolic resistance h

249 hia coli and its plasmid-encoded sulfonamide resistance gene sul1 in different water matrixes.

250 lla pertussis, and B. anthracis (sulfonamide resistance gene, sul1), respectively.

251 in the laboratory, we evolved the antibiotic resistance gene TEM-1 in Escherichia coli hosts with eit

252 in resistance gene blaTEM-1 and tetracycline resistance gene tetA, with UV254 doses up to 430 mJ/cm(2

253 As such, this is an example of a pathogen resistance gene that has evolved to underlie two types o

254 tification of Sr13 expands the number of Pgt-resistance genes that can be incorporated into multigene

255 ong ecological gradients, but identified key resistance genes that cross habitat boundaries and deter

256 dentifying, mapping, and selecting for major resistance genes that tend to be highly effective but vu

257 evealed the integration of a chloramphenicol resistance gene, the deletion of the endogenous riboflav

258 examining the origins and rise of antibiotic resistance genes, their subsequent dissemination, and th

259 nase-expressing cassette and remove the drug-resistance gene, thus speeding up the generation of iKO

260 The Tomato mosaic virus (ToMV) resistance gene Tm-1 encodes a direct inhibitor of ToMV

261 tected in sewage, as well as MST markers and resistance genes to aminoglycosides, beta-lactams, and t

262 time explained the ability of antimicrobial resistance genes to disseminate among bacterial populati

263 ide range of ecological processes and stress resistance genes to estimate the functional potential of

264 orizontal transfer of these highly efficient resistance genes to pathogens.

265 te phages do not need to carry antimicrobial resistance genes to play a significant role in tolerance

266 al antibiotic pollution promotes transfer of resistance genes to the human microbiota.

267 We also screened samples directly for resistance genes to understand the true breadth and dept

268 s and use them to identify candidate disease resistance genes, to guide tetraploid transcript assembl

269 Additionally, resistance gene transfer can occur between Gram-negative

270 ere, we review the main routes of antibiotic resistance gene transfer in S. aureus in the context of

271 t the potential risk of antibiotic/herbicide-resistance gene transfer into neighboring plant species,

272 Similar to bacterial transfer of antibiotic resistance genes, transfer of a potent antibacterial gen

273 and transposable elements encoding multidrug resistance genes triggered the expansion of scarlet feve

274 bed, including the acquisition of antibiotic resistance genes via the transfer of mobile genetic elem

275 h to analyze the distributions of antibiotic-resistance genes, virulence factors, and phage sequences

276 rogression event involving the rodent poison resistance gene Vkorc1, in addition to other newly detec

277 A putative lysyl-tRNA synthetase resistance gene was identified in the cladosporin gene c

278 Recently, the Ty-1 resistance gene was identified, shown to code for an RNA

279 wide RNAi screen, a collection of host virus resistance genes was identified that, upon silencing, in

280 Transferability of resistance genes was studied using conjugation and trans

281 ource tracking (MST) markers, and antibiotic resistance genes was tested against DNA obtained from wh

282 fusion of xds to two consecutive antibiotic resistance genes was used to select transposon mutants t

283 Four different variants of the CTX-M ESBL-resistance gene were identified in our ST131 strains, wi

284 In our dataset, antimicrobial resistance genes were common among human carriage isolat

285 Quinolone resistance genes were detected in 42% of well water, 7%

286 multidrug, erythromycin, and aminoglycoside resistance genes were discovered in these fecal samples.

287 vely over-represented, suggesting that plant resistance genes were not the only drivers of viral adap

288 Putative virulence and antibiotic resistance genes were over-represented in L1, L2 and L3

289 species, 5 Candida spp., and 4 antimicrobial resistance genes were studied over sequential time perio

290 The three most highly abundant antibiotic resistance genes were tet(W), blaSRT-1, and erm(B).

291 Beta-lactamase and tetracycline resistance genes were the most prevalent (25.9%) antibio

292 , vancomycin, beta-lactam and aminoglycoside resistance genes were the top seven most abundant ARG ty

293 ended-spectrum ss-lactam- and aminoglycoside-resistance genes, were identified in the surface sedimen

294 Disease resistance is commonly based on resistance genes, which generally mediate the recognitio

295 n planthopper (Nilaparvata lugens Stal, BPH) resistance genes, which will allow the development of ri

296 o known as rhodanese) as a candidate obesity-resistance gene with selectively increased expression in

297 diagnostic tool to evaluate the presence of resistance genes with the added bonus of discriminating

298 in coordinating transcription regulation of resistance genes with the cell cycle.

299 c allele of OsSWEET13 known as the recessive resistance gene xa25 from the rice cultivar Minghui 63.

300 Here, we show that the broadly effective resistance gene xa5,for resistance to bacterial blight o