ライフサイエンスコーパス: resistance gene

1 me 5 near a previously characterized disease resistance gene.

2 plasmid coexpressing BC200 and the neomycin resistance gene.

3 fic target genes, including an antimicrobial resistance gene.

4 Fhb1-1 (aka WFhb1-c1) as a candidate for FHB resistance gene.

5 of expression stochasticity of an antifungal resistance gene.

6 ggesting an opportunity to introduce a novel resistance gene.

7 es carrying at least 1 horizontally acquired resistance gene.

8 ate its deployment and pyramiding with other resistance genes.

9 rons into the coding sequences of antibiotic-resistance genes.

10 and, consequently, the harboured antibiotic resistance genes.

11 h the removal of the hosts harbouring mobile resistance genes.

12 ed methods for identifying new antimicrobial-resistance genes.

13 bacteriophage capsid to target antimicrobial resistance genes.

14 ociated strains, linked to key virulence and resistance genes.

15 ave epistatic effects on qualitative disease resistance genes.

16 quisite for the efficient deployment of host resistance genes.

17 ploid wheat and rapidly clone four stem rust resistance genes.

18 rotype, virulence factors, and antimicrobial resistance genes.

19 co-occur with antibacterial biocide or metal resistance genes.

20 exaploid wheats, harbors many powdery mildew resistance genes.

21 lower than expected contribution from known resistance genes.

22 em amplifications, typically including known resistance genes.

23 of several transcription factors and disease resistance genes.

24 e expression of the most abundant antibiotic resistance genes.

25 ry systems, and antimicrobial production and resistance genes.

26 re and we could accurately detect antibiotic resistance genes.

27 ulatory system VanSR to induce expression of resistance genes.

28 in the spread of virulence or antimicrobial resistance genes.

29 is confirmed the presence of seven stem rust resistance genes.

30 r carbohydrate-active enzymes and antibiotic resistance genes.

31 revealed an overrepresentation of antibiotic resistance genes.

32 overed the presence of several antimicrobial resistance genes.

33 nd clinical samples with known antimicrobial resistance genes.

34 otentially pathogenic taxa and antimicrobial resistance genes.

35 isease of wheat that can be controlled using resistance genes.

36 i population carrying multiple antimicrobial resistance genes.

37 ce via inducing the expression of antibiotic resistance genes.

38 s by recognizing corresponding antimicrobial resistance genes.

39 ear-isogenic lines that differ for leaf rust resistance genes.

40 e continuously evolved to become more potent resistance genes.

41 virulence factors and no relevant antibiotic resistance genes.

42 istance evolution via horizontal transfer of resistance genes.

43 LR genes within the intervals of mapped rust resistance genes.

44 were performed in BDL rats and the multidrug resistance gene 2 knockout (Mdr2(-/-) ) mouse model of P

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

46 identified as ClaPMR2, Citrullus lanatus PM Resistance gene 2 {Chr2 : 26750001 ..

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

48 resistance, being the most relevant hosts of resistance genes acquired through horizontal gene transf

49 pite being the primary vectors of antibiotic resistance genes across many key pathogens.

50 s long-term maintenance of diversity in host resistance genes across smallholder agroecosystems, prov

51 omote replacement of a candidate gene with a resistance gene; adapted MS-based glycomics workflows to

52 ite the high and relatively stable levels of resistance genes against the main antimicrobials used, t

53 iome beta-diversity and increased antibiotic resistance gene alpha-diversity and prevalence.

54 ge plasmids enables the spread of antibiotic resistance genes among human enteric pathogens(1-3).

55 production, but the prevalence of antibiotic resistance genes among the species of bacteria that colo

56 to disease is the selection in breeding for resistance gene analogs (RGAs).

57 is an effective high-temperature adult-plant resistance gene and confers resistance to a broad spectr

58 mental samples revealed extensive sharing of resistance genes and bacteria following exposure and aft

59 ted in enrichment and exchange of antibiotic resistance genes and bacteria.

60 gene frequently occurs in clusters of copper resistance genes and can be recognized by the presence o

61 T-cell activation while repressing multidrug resistance genes and cancer-related genes, thereby rende

62 ete is highly variable and rapidly overcomes resistance genes and fungicides.

63 contained target alleles for five stem rust resistance genes and had a high level of stem rust resis

64 amplifies environmental pools of antibiotic resistance genes and increases the likelihood for the se

65 rum-sensing circuitry, to acquire antibiotic resistance genes and initiate its attack on the human ho

66 bears bla(CTX-M-15), seven other functional resistance genes and multiple resistance pseudogenes.

67 e respiratory disease (BRD) on antimicrobial resistance genes and mutation in quinolone resistance-de

68 tment contributed to reduce the abundance of resistance genes and of plasmid replicons, coinciding wi

69 adaptation to different repertoires of host resistance genes and other challenges.

70 Sequence type, antimicrobial resistance genes and plasmid replicons were identified f

71 s few differences between the acquisition of resistance genes and the phenotypic resistance profile,

72 e potential relationships between antibiotic resistance genes and their phenotypic traits.

73 ic resistance genes detected, five macrolide resistance genes and two tetracycline resistance genes w

74 efficiently removes the hosts of antibiotic resistance genes and, consequently, the harboured antibi

75 0 Gram-positive bacteria, four antimicrobial resistance genes, and both Pan Candida and Pan Gram-Nega

76 ds were utilized to identify FIB, antibiotic resistance genes, and human enteric viruses in the final

77 als, fecal indicator bacteria, antimicrobial resistance genes, and human enteric viruses with struvit

78 n failed to acquire some of these beneficial resistance genes, and we found some chromosomal resistan

79 Carbapenemases and other types of antibiotic resistance genes are carried almost exclusively on large

80 One explanation for this is that resistance genes are commonly associated with 'fitness c

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

82 als, the highest abundances of antimicrobial resistance genes are found in the oral cavity, but the o

83 rtially because they are fully synthetic and resistance genes are unlikely to exist in nature; noneth

84 lin on gram-negative bacteria and antibiotic resistance genes are warranted.

85 human migration on gut microbiome antibiotic resistance gene (ARG) carriage.

86 metabolized antimicrobials and antimicrobial resistance genes (ARG) into the environment.

87 vestigated community profiles and antibiotic resistance genes (ARGs) as a function of anthropogenic c

88 Antibiotic resistance genes (ARGs) can spread among pathogens via h

89 nmental spread of antibiotics and antibiotic resistance genes (ARGs) from the land application of liv

90 reaction (PCR) identified several antibiotic resistance genes (ARGs) in our isolates.

91 a on bacterial communities and antimicrobial resistance genes (ARGs) in the environment; we show that

92 ssociated sequences and 2-fold of antibiotic resistance genes (ARGs) in the Ganges relative to other

93 inical relevance, and mobility of antibiotic resistance genes (ARGs) in watersheds.

94 rne and the human populations, antimicrobial resistance genes (ARGs) may be shared by horizontal gene

95 In total, 1206 antibiotic resistance genes (ARGs) of 52 different categories were

96 cation of principal reservoirs of antibiotic resistance genes (ARGs) plus an understanding of drivers

97 s serves as a reservoir of 329 antimicrobial resistance genes (ARGs) presumably conferring resistance

98 ute the gut microbiota can harbor antibiotic resistance genes (ARGs), including those encoding beta-l

99 ants of emerging concern, such as antibiotic resistance genes (ARGs), remains largely unknown.

100 ducive for horizontal exchange of antibiotic resistance genes (ARGs), thereby facilitating the emerge

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

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

103 romycin, Puromycin, Neomycin and Blasticidin resistance genes as well as mScarlet fluorescent protein

104 concentration of ampicillin and tetracycline resistance genes, as measured with quantitative polymera

105 The occurrence of resistance genes associates with the timing of antibioti

106 The pepper (Capsicum annuum) resistance gene bacterial spot3 (Bs3) is transcriptional

107 ressing Lr34res, another wheat multipathogen resistance gene, barley flavonoids are unlikely to have

108 itive (GP) bacterial DNA, and the antibiotic-resistance gene bla(TEM) with femtomolar sensitivity.

109 De novo identification of the antibiotic resistance genes bla(NDM-5), bla(NDM-7), bla(CTX-M-15) a

110 eaeA, sta, and lt) as well as the antibiotic-resistance genes (bla(TEM), bla(KPC), and bla(CTX)).

111 rL, exoS, phzM, and toxA) and the antibiotic-resistance genes (bla(TEM), tetA, and bla(CTX-M)).

112 lones, are phenotypically MDR, and have high resistance gene burdens.

113 ssociation studies (GWAS) can identify novel resistance genes but must control for genetic confounder

114 allele frequency change or selection for Bd resistance genes, but we uncovered a set of candidate ge

115 of the microorganisms or their antimicrobial resistance genes can lead to false-negative results.

116 rious genetic variants, including antibiotic resistance genes, can establish in populations without s

117 vels of antibiotic resistance and antibiotic resistance gene carriage.

118 eneity in virulence factor and antimicrobial resistance genes carried by LA-S. aureus and CA-MRSA str

119 tion without allele replacement at SARC acid resistance genes caused changes in both phenotype and ex

120 to assess the bacterial shift and antibiotic resistance gene changes employing 16S rRNA gene sequenci

121 ecological niches of microbes and antibiotic resistance genes characterized by biofilm-forming and hu

122 fferences in the prevalence of antimicrobial resistance genes, classes and mechanisms in oral and sto

123 Disease resistance gene clusters, which often exist as SVs, exhi

124 he oral cavity contains a lower diversity of resistance genes compared to the gut.

125 ad assembly also identifies 94 antimicrobial resistance genes, compared to only seven alleles in the

126 despite annual fluctuations in antimicrobial resistance gene content in the sampled genomes.

127 ergence of plasmid-mediated, mobile colistin resistance genes creates potential for rapid spread of p

128 revisiae strain that expresses a cantharidin resistance gene (CRG1), encoding a SAM-dependent methylt

129 high levels of eccDNA containing the copper-resistance gene CUP1.

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

131 ase, suggests that members carrying multiple resistance genes date back to at least the 1970s.

132 points, we create 3- and 6-split Hygromycin resistance genes, demonstrating that higher-degree split

133 l characterization of Pm41, a powdery mildew resistance gene derived from WEW, which encodes a coiled

134 Pm1a, the first powdery mildew resistance gene described in wheat, is part of a complex

135 The only resistance genes detected were aac(6')Ib-cr (n = 13), bl

136 Of the 89 antibiotic resistance genes detected, five macrolide resistance gen

137 vis-a-vis bacterial detection and antibiotic resistance gene detection for predicting staphylococcal

138 mpiric treatment decisions that are based on resistance gene detection in P. aeruginosa, acknowledgin

139 orresponded to the previously identified TLS resistance gene ds1.

140 e loci was significantly less than for other resistance genes during cultivated sunflower evolution.

141 , benzoxazinone synthesis (bx7, 9) and known resistance genes (e.g. maize insect resistance 1, mir1).

142 Many resistance genes (e.g., bla(NDM), bla(OXA) carbapenamase

143 d a beta-lactamase-encoding (bla) antibiotic resistance gene, enabling isolation of pure cssDNA with

144 Disease resistance genes encoding nucleotide-binding and leucine

145 expression of the blaZ and pbp2a antibiotic-resistance genes, encoding PC1 and PBP2a, respectively.

146 bulked segregant analysis was combined with resistance gene enrichment sequencing (MapRenSeq).

147 Previously, resistance gene enrichment sequencing (RenSeq) was devel

148 eate comparative NLR resources, we conducted resistance gene enrichment sequencing (RenSeq) with sing

149 ta-lactam, fluoroquinolone, and tetracycline resistance genes exists and is independent of disease st

150 o decouple noise from the mean for Puromycin resistance gene expression in Chinese Hamster Ovary cell

151 ome analysis showed an increase in macrolide resistance gene expression in gut microbiota in communit

152 nding, leucine-rich-repeat) form the largest resistance gene family in plants, with lineage-specific

153 Here, we cloned the FHB resistance gene Fhb7 by assembling the genome of Thinopy

154 CF10 promote horizontal spread of antibiotic resistance genes following induction of plasmid-containi

155 of in vivo testing and direct sequencing of resistance genes folP1, rpoB, and gyrA.

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

157 ool, as a valuable resource for discovery of resistance genes for improvement of modern wheat cultiva

158 gies for metagenomic detection of antibiotic resistance genes for predicting staphylococcal antibacte

159 he origins of clinically relevant antibiotic resistance genes found in human pathogens have been trac

160 Multiple independent acquisitions of resistance genes from 5 classes of antibiotics character

161 sient expression of selected putative insect resistance genes from C. platycarpus viz., chitinase (CH

162 al culture followed by PCR identification of resistance genes from colonies, the Carba-R assay reduce

163 ng with a decline in the number of intrinsic resistance genes from Enterobacteriaceae, as well as wit

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

165 ) for the rapid identification of antibiotic resistance genes from various formats of whole genome se

166 tion, we assessed the presence of fosfomycin resistance genes from whole-genome sequencing (WGS) data

167 We find mutations in known resistance genes (FUR1 and FCY2) and in a gene UXS1, pre

168 Our results suggest that specific antibiotic resistance genes have spread among Campylobacter isolate

169 f intracellular and extracellular antibiotic resistance genes (iARGs and eARGs) from an AnMBR.

170 Resistance gene identification-based approaches provided

171 k factor-, pathogen sequence type [ST]-, and resistance gene identification-based approaches) for cla

172 A few resistance genes identified to date provide partial, dur

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

174 tome analysis and prediction, such as CARD's Resistance Gene Identifier (RGI) software.

175 mid DNA carrying ampicillin and tetracycline resistance genes in aged urine, including its ability to

176 recent reports on the prevalence of colistin resistance genes in animals, especially wildlife and aqu

177 studies on the prevalence of mobile colistin resistance genes in aquaculture and their transmission b

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

179 Plasmids may maintain antibiotic resistance genes in bacterial populations through conjug

180 rt of a long-term goal to define key disease resistance genes in cacao, here we use a transcriptomic

181 defense response initiated by powdery mildew resistance genes in chromosomes 3S(l)#2 and 6S(l)#3.

182 eveal the diverse trajectories of antibiotic resistance genes in clinical settings, summarized as usi

183 The roles of heavy metal resistance genes in environmental adaptation and virulen

184 the abundance and diversity of antimicrobial resistance genes in feces.

185 cation of small plasmids carrying antibiotic resistance genes in Gram-positive bacteria.

186 y aims to test the presence of antimicrobial resistance genes in milk metagenome, investigate their g

187 trating the detection of multiple antibiotic resistance genes in parallel.

188 am-positive pathogens and four antimicrobial resistance genes in positive blood culture bottles.

189 we applied it to detection of antimicrobial resistance genes in respiratory fluid and dried blood sp

190 tribute to maintaining a stable frequency of resistance genes in the absence of selection pressure fr

191 gut resistome, a reservoir of antimicrobial resistance genes in the body, of twice-yearly administra

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

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

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

195 We detected 28 antibiotic resistance genes in the hospital-adapted clade, of which

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

197 chitinase gene clusters and NBS-LRR disease resistance genes in this region suggest the possible inv

198 tability of the genetic elements linked with resistance genes in V. cholerae Here we present details

199 iticina are highly variable for virulence to resistance genes in wheat and adapt quickly to resistanc

200 sistance genes in wheat and adapt quickly to resistance genes in wheat cultivars.

201 ill support the identification of functional resistance genes in wheat to accelerate the breeding and

202 In addition, other frequently identified resistance genes included blaZ, qacA/B and dfrC.

203 DR, with the presence of multiple antibiotic resistance genes, including 3 (40.11%) and 4 (9.13%) gen

204 nt microbial community, even though we found resistance genes, including a highly effective resistanc

205 The ST16 clone carried up to 14 resistance genes, including blaKPC-2 in an IncFIBpQIL pl

206 ST16 clone carried up to 14 resistance genes, including blaKPC-2 in an IncFIBpQIL pl

207 ted loci were especially common from disease resistance genes, including from a large number of monoc

208 identified all well characterised Triclosan resistance genes, including the primary target, fabI.

209 tionary pressure to accelerate the spread of resistance genes, including those encoding beta-lactamas

210 uencing techniques to monitor the profile of resistance genes, known as the resistome, in microbial p

211 The study of pathogen resistance genes, largely aided by mouse models, has sig

212 >420 kb) carrying large arrays of antibiotic resistance genes located in discrete, complex and dynami

213 entify the presence or absence of antibiotic resistance genes/loci are increasingly being developed.

214 The antibiotic resistance gene may encode spectinomycin or kanamycin re

215 hat long-term balancing selection on disease resistance genes may have maintained ancestral haplotype

216 qPCR for the detection of the antimicrobial resistance gene MCR-2.

217 ed our BIGSI search function to rapidly find resistance genes MCR-1, MCR-2, and MCR-3, determine the

218 However, the role of macrophage multidrug resistance gene MDR1 on intracellular M. tuberculosis su

219 (mean -0.050; 95% CI [-0.084, -0.017]), and resistance gene (mean -0.13; 95% CI [-0.17, -0.099]) bet

220 (mean, -0.050 [95% CI, -.084 to -.017]), and resistance gene (mean, -0.13 [95% CI, -.17 to -.099]) be

221 thogen abundance, and carriage of antibiotic resistance genes.Methods: 16S rRNA sequencing and quanti

222 , rplV and 23S rRNA) mutations, 10 macrolide resistance genes (MRGs) and efflux pump overexpression w

223 the drug had higher prevalence of macrolide-resistance genes msr(A) and ermC at 28 days but not at 1

224 vancomycin resistance genes while mupirocin resistance gene mupR (n = 2) and cfr gene (n = 1) were r

225 , PCR-detection of virulence, and antibiotic-resistance genes of E. coli isolated from secondary infe

226 rous genetically encoded markers, antibiotic resistance genes or enzymes, such as Cre recombinase.

227 trols pathogen entry through the penetration-resistance genes PEN2 and PEN3, encoding an atypical myr

228 port the map-based cloning of powdery mildew resistance gene Pm24 from Chinese wheat landrace Hulutou

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

230 d clouds enabled the placement of antibiotic resistance genes present in multiple copies both within

231 In contrast, resistance gene prevalence (P = .00719) and alpha-divers

232 In contrast, resistance gene prevalence (p=0.00719) and alpha-diversi

233 ese differences increased over time for both resistance gene prevalence measured by log normalized ab

234 ese differences increased over time for both resistance gene prevalence measured by log-normalized ab

235 generated taxonomic, functional pathway, and resistance gene profiles for each sample and compared mi

236 generated taxonomic, functional pathway, and resistance gene profiles for each sample and compared mi

237 oacae) and their corresponding antimicrobial resistance gene profiles within as little as 1 h of sequ

238 l(17) was identified, encoding a typical TNL resistance gene protein.

239 ial H3K9 histone demethylase and the disease resistance gene RECOGNITION OF PERONOSPORA PARASITICA7 B

240 expanded its aerobic respiration and salt/UV resistance gene repertoire.

241 ht harbor new stripe rust and powdery mildew resistance genes, respectively, therefore, they could be

242 ogression process involving networks of host resistance genes, RNA silencing/antiviral defense genes,

243 We cloned the first leaf rust resistance gene Rph1 (Rph1 a) from cultivated barley (Ho

244 thogen Phytophthora sojae evades the soybean Resistance gene Rps1b through transcriptional polymorphi

245 liams 82, a soybean variety that encodes the resistance gene Rps1k, rendered it compatible with race

246 To fine map the resistance gene Sbwm1, 205 wheat accessions was genotype

247 resistance, software to predict the optimal resistance gene set for a specific geographic region, an

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

249 The resulting model-associated adaptive resistance gene signature negatively correlated with GBM

250 aper reports the identification of stem rust resistance gene Sr60, a race-specific gene from diploid

251 d rapid spread of large spectrum beta-lactam resistance genes such as carbapenemases is detrimental t

252 st known for its regulation of Candida azole resistance genes such as MDR1, regulates other genes tha

253 nalysis showed a significant loss of disease-resistance genes such as those encoding NB-ARC domain-co

254 ive abundance of bacteria and beta-lactamase resistance genes (TEM-1) was observed over 6 months for

255 ere, we report two unique mobile tigecycline-resistance genes, tet(X3) and tet(X4), in numerous Enter

256 ibiotic, and vaccine serotypes harbored more resistance genes than nonvaccine serotypes (P < .05).

257 nes have been identified, there are no known resistance genes that confer immunity to MCMV.

258 at the integration site, and the addition of resistance genes that do not disrupt the target gene cod

259 Pl(17) and Pl(19) are two broad-spectrum DM resistance genes that have been previously mapped to a g

260 TEM), and tetA genes are the main antibiotic-resistance genes that induce resistance patterns to cefo

261 iously described virulence and antimicrobial resistance genes that promote the dissemination of CA-MR

262 cter species clusters carrying multiple drug resistance genes that segregated with these isolates.

263 obacter spp. clusters carrying multiple drug resistance genes that segregated with these isolates.

264 s containing promoters regulating antibiotic resistance genes that shift to the ON orientation after

265 oncerning the distribution of the antibiotic resistance genes, the examined strains harbored bla(TEM)

266 a low potential for the spread of antibiotic resistance genes to bacteria once it is released to the

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

268 ile element that facilitates the transfer of resistance genes to other bacteria, e.g. to the ones liv

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

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

271 erichia coli TEM-1 beta-lactamase antibiotic resistance gene using growth competition experiments in

272 DNA sequences or knock out their antibiotic resistance genes using CRISPR technology.

273 or cephalosporin, quinolone and tetracycline resistance genes using PCR.

274 ted by the horizontal transfer of antibiotic resistance genes via conjugative plasmids.

275 owed the most potential in scenarios where a resistance gene was detected or in scenarios where a res

276 on SNPs identification and CAPS markers, the resistance gene was identified as ClaPMR2, Citrullus lan

277 ce gene was detected or in scenarios where a resistance gene was not detected and the prevalence of r

278 ty of our tool for the positional cloning of resistance genes, we estimated the number of NLR genes w

279 ates expression of blaZ and pbp2a antibiotic resistance genes, we suggest further consideration and r

280 lates revealed that six groups of antibiotic resistance genes were carried by all seven phage suscept

281 Notably, antibiotic resistance genes were found in similar genetic contexts

282 rolide resistance genes and two tetracycline resistance genes were increased significantly.Conclusion

283 Several antibiotic-resistance genes were observed.

284 Antibiotic resistance genes were widespread, and debridement, rathe

285 ed genes, pattern recognition receptors, and resistance genes, which could be critical for the abilit

286 ng microbial contaminants such as antibiotic resistance genes, which leads to better protection of pu

287 ) (n = 179) genes, none harboured vancomycin resistance genes while mupirocin resistance gene mupR (n

288 stool sample harbors 46 known antimicrobial resistance genes, while all other species from the pre-t

289 or ceritinib, identifying PIM1 as a putative resistance gene, whose high expression is associated wit

290 detection and surveillance of antimicrobial resistance genes will decrease the turnaround time for D

291 Therefore, WFhb1-1 is an important FHB resistance gene with a potential antifungal function and

292 GECI was driven by coupling to a blasticidin resistance gene with a self-cleaving cis-acting hydrolas

293 teria in the environment, as well as uncover resistance genes with an environmental origin.

294 nent of transgenic cassettes including other resistance genes with complementary resistance profiles.

295 hibitory concentration (MIC) and beta-lactam resistance genes with mortality in the MERINO trial.

296 ethods may not perform well when identifying resistance genes with sequences having low sequence iden

297 ern and wastewater is thought to disseminate resistance genes within bacteria.

298 ques that detect pathogens and antimicrobial resistance genes within clinical samples present a treme

299 n skin sites and dissemination of antibiotic resistance genes within-individual.

300 (including many plasmids carrying antibiotic-resistance genes) without significant similarities to cu