ライフサイエンスコーパス: bacterial DNA

1 amples did not contain significant levels of bacterial DNA.

2 LR9) activation is attributed to delivery of bacterial DNA.

3 involves activation of TLR9-ERK signaling by bacterial DNA.

4 y unrecognized potential for the exchange of bacterial DNA.

5 CpG motifs are present at high frequency in bacterial DNA.

6 ge regions, accounting for 2.7% of the total bacterial DNA.

7 (PFGE) of NotI restriction enzyme digests of bacterial DNA.

8 to contamination of laboratory reagents with bacterial DNA.

9 r label-free and ultrasensitive detection of bacterial DNA.

10 through cGAS-STING-dependent recognition of bacterial DNA.

11 8 log10 gene copies (GC)/g, respectively, in bacterial DNA; 5.5 and 4.4 log10 GC/g, respectively, in

12 The monomeric bacterial DNA adenine methyltransferase (Dam) is respons

13 Short-term expression of the bacterial DNA adenine methyltransferase Dam, tethered to

14 etermine whether exposure of immune cells to bacterial DNA affects DNA binding and internalization.

15 ing is able to induce some compaction of the bacterial DNA, although to a lesser extent than demixing

16 is required for transient expression of the bacterial DNA, an early step in the transformation proce

17 nicircle' DNA, a vector type that is free of bacterial DNA and capable of high expression in cells, f

18 binding to two distant operator sites on the bacterial DNA and causing the intervening DNA to form a

19 Bacterial DNA and CpG DNA induce the secretion of ADAM10

20 easingly clear that eukaryotes have acquired bacterial DNA and function through horizontal gene trans

21 o demonstrate that the third detector senses bacterial DNA and identify it as Aim2, a receptor that h

22 Bacterial DNA and immunostimulatory CpG oligodeoxynucleo

23 duced upon DNA damage, co-localized with the bacterial DNA and is required for the DDR.

24 s DNA from reactive intermediates by binding bacterial DNA and physically protecting it.

25 ethylated DNA sequences that mimic viral and bacterial DNA and protect against infectious agents and

26 to spacer acquisition from both foreign and bacterial DNA and results in multiple spacers incapable

27 )17 cell-derived IL-26 formed complexes with bacterial DNA and self-DNA released by dying bacteria an

28 a significant correlation between levels of bacterial DNA and serum tumor necrosis factor-alpha (P =

29 cytosolic surveillance pathway, which senses bacterial DNA and signals through STING, TBK1, IRF3 and

30 Bacterial DNA and synthetic oligodeoxynucleotides (ODN)

31 these, TLR9, is activated intracellularly by bacterial DNA and synthetic oligodeoxynucleotides (ODN),

32 Bacterial DNA and synthetic oligomers containing CpG din

33 idate the mechanisms of immunostimulation by bacterial DNA and synthetic oligonucleotides, the effect

34 Minicircle DNA vectors are free of bacterial DNA and thus capable of high expression in mam

35 Although the pathways involved in sensing bacterial DNA and viral RNA are now well established, on

36 also resulted in the presence of contaminant bacterial DNA and yielded fewer reads from the known pat

37 ivated by un-methylated CpG motifs, found in bacterial DNA, and beta-glucans, found in the cell wall

38 olysaccharides, lipoproteins, flagellin, and bacterial DNA, and signaling through TLRs leads to the p

39 s, gram-negative (GN) and gram-positive (GP) bacterial DNA, and the antibiotic-resistance gene bla(TE

40 xcises phage lambda from the chromosome, the bacterial DNA architectural protein Fis recruits multipl

41 cast the action of depletants on supercoiled bacterial DNA as an effective solvent quality.

42 time, the extent of cytosine methylation of bacterial DNA at single-base resolution.

43 ) reciprocal recombination between phage and bacterial DNA at specific sites on both partners.

44 Bacterial DNA attenuation of Treg suppressive activity m

45 Previous work showed that the bacterial DNA backbone of the plasmid has potent adjuvan

46 Bacterial DNA (Bact-DNA) in MLNs was identified by polym

47 Pretreatment blood levels of bacterial DNA (bDNA) were measured in 731 patients.

48 Fis is an abundant bacterial DNA binding protein that functions in many dif

49 is unknown; CbpA lacks motifs found in other bacterial DNA binding proteins.

50 The bacterial DNA-binding protein HU and the yeast HMGB prot

51 se studies thus identified a novel family of bacterial DNA-binding proteins, developed a model of Spo

52 hii Ptr2, a member of the Lrp/AsnC family of bacterial DNA-binding proteins, is an activator of its e

53 idylate kinase (TMK), an essential enzyme in bacterial DNA biosynthesis, is an attractive therapeutic

54 f 10(4) CFU/ml was correlated with increased bacterial DNA burden (P < 0.01), decreased community div

55 ture-independent indices of infection (total bacterial DNA burden and low bacterial community diversi

56 was ineffective with genomic double stranded bacterial DNA, but it allowed down to 16 amole detection

57 lex amplification and detection of viral and bacterial DNA by a flow-based chemiluminescence microarr

58 ype phages can randomly package and transfer bacterial DNA by a process called generalized transducti

59 ained model description of the compaction of bacterial DNA by H-NS.

60 Recognition of extracelluar bacterial DNA by the STING-dependent cytosolic pathway i

61 Bacterial DNA can be damaged by reactive nitrogen and ox

62 Methylation of bacterial DNA can regulate microbial growth and virulenc

63 In this study the ability of bacterial DNA, characterized by unmethylated CpG islands

64 functional specificity, as we illustrate for bacterial DNA clamp loader ATPases.

65 signature that is unaffected by the initial bacterial DNA concentration.

66 Bacterial DNA concentrations were raised in 16 of 16 blo

67 Bacterial DNA concentrations were raised in 4 of 29 epis

68 Bacterial DNA containing unmethylated CpG dinucleotide m

69 Bacterial DNA containing unmethylated CpG motifs is a pa

70 Bacterial DNA contains a high frequency of unmethylated

71 Bacterial DNA contains immunostimulatory CpG motifs that

72 Many studies have reported the presence of bacterial DNA contamination in commercial Taq DNA polyme

73 mmon to all four methods, and revealed trace bacterial DNA contamination in TFF-concentrated metageno

74 atory good practice was required to minimize bacterial DNA contamination.

75 Here we report that bacterial DNA (CpG DNA) and mitochondrial DNA impair pha

76 imulatory unmethylated CpG motifs present in bacterial DNA (CpG DNA) induce expression of cyclooxygen

77 Unmethylated CpG motifs present in bacterial DNA (CpG DNA) induce innate inflammatory respo

78 Bacterial DNA (CpG DNA) persists in tissues and blood un

79 xpression of TLR4 and TLR9, the receptor for bacterial DNA (CpG-DNA).

80 The bacterial DNA cytosine methyltransferase M.HhaI sequence

81 o investigate the catalytic mechanism of the bacterial DNA cytosine methyltransferase M.HhaI.

82 iously identified base flipping motif in the bacterial DNA cytosine methyltransferase, M.HhaI.

83 s pathway is a disease-enhancing response to bacterial DNA damage inflicted by the host immune system

84 tress in its specific niche, and this causes bacterial DNA damage.

85 itations have hampered broad applications of bacterial DNA delivery.

86 try analysis, this protein was identified as bacterial DNA-dependent RNA polymerase (RNAP).

87 f the beta, beta', and sigma(70) subunits of bacterial DNA-dependent RNA polymerases (DdRp), combined

88 ssive oligodeoxynucleotides; 3) simulated by bacterial DNA derived from HKBA; and 4) abrogated by DNa

89 ociated with an increase of the diversity of bacterial DNA detected in the blood.

90 g of bacterial 16S rRNA genes to investigate bacterial DNA diversity in milk samples of mastitic and

91 s end joining (NHEJ) is a recently described bacterial DNA double-strand break (DSB) repair pathway t

92 pathway and PriA, suggesting a mechanism of bacterial DNA DSB repair involving the establishment of

93 otein curli, irreversibly formed fibers with bacterial DNA during biofilm formation.

94 Can homology between vector and bacterial DNA enable the uptake of these foreign DNA ins

95 A ligase D (PaeLigD) exemplifies a family of bacterial DNA end-joining proteins that consist of a lig

96 e-inducible GAL1 promoter joined to PvuII, a bacterial DNA endonuclease gene, are toxic to yeast cell

97 Certain CpG motifs found in bacterial DNA enhance immune responses through Toll-like

98 We hypothesised that bacterial DNA extraction methodology from breast milk sa

99 secretion samples were used for analysis of bacterial DNA for Porphyromonas gingivalis (Pg), Prevote

100 broad-range detection and identification of bacterial DNA from clinical specimens are a foundational

101 was approximately equal to genotyping using bacterial DNA from cultures.

102 teins play a major role in the protection of bacterial DNA from damage by reactive oxygen species.

103 lunteers with liver cirrhosis, 50% contained bacterial DNA from Enterobactericaea, Clostridium leptum

104 n with specific primers and probes to detect bacterial DNA from several oral species and Chlamydia pn

105 The presence of bacterial DNA from Streptococcus mutans, Porphyromonas g

106 Bacterial DNA from the cecum was extracted for deep meta

107 Lastly, we analyzed ancient samples of bacterial DNA from the Copper Age 'Iceman' mummy and fro

108 lammatory response by enhancing clearance of bacterial DNA from the extracellular environment.

109 ion of WDM for rapid, automated detection of bacterial DNA from whole blood may have an enormous impa

110 for point-of-care or molecular detection of bacterial DNA from whole blood.

111 ome is facilitated by the directed motion of bacterial DNA generated during chromosome replication, i

112 tomyces sahachiroi AlkZ (previously Orf1), a bacterial DNA glycosylase that protects its host by exci

113 AlkD is a recently discovered bacterial DNA glycosylase that removes positively charge

114 MutM is a bacterial DNA glycosylase that removes the mutagenic les

115 MutM is a bacterial DNA glycosylase that serves as the first line

116 g (DXL) technology to obtain structures of a bacterial DNA glycosylase, MutM, interrogating undamaged

117 MutM, a bacterial DNA glycosylase, protects genome integrity by

118 MutM, a bacterial DNA-glycosylase, plays a critical role in main

119 -2(1H)-ones, exemplified by 34, that inhibit bacterial DNA gyrase and topoisomerase IV and display po

120 g the GyrB/ParE ATP-binding sites located on bacterial DNA gyrase and topoisomerase IV and not utiliz

121 Bacterial DNA gyrase and topoisomerase IV are essential

122 Bacterial DNA gyrase and topoisomerase IV are well-chara

123 Bacterial DNA gyrase and topoisomerase IV control the to

124 e and represent a new antibacterial class of bacterial DNA gyrase and topoisomerase IV inhibitors.

125 rt their activity through dual inhibition of bacterial DNA gyrase and topoisomerase IV.

126 ntibacterial agents that specifically target bacterial DNA gyrase and topoisomerase IV.

127 es are bifunctional antibiotics that inhibit bacterial DNA gyrase by preventing DNA binding to the en

128 Bacterial DNA gyrase introduces negative supercoils into

129 Bacterial DNA gyrase is a well-established and validated

130 Bacterial DNA gyrase is a well-known and validated targe

131 arin natural product antibiotics that target bacterial DNA gyrase is assembled from tyrosine by nonri

132 A recent study has analysed the action of bacterial DNA gyrase on a single substrate DNA molecule,

133 Albicidin is a nanomolar inhibitor of the bacterial DNA gyrase with a strong activity against vari

134 A1 is a natural aminocoumarin that inhibits bacterial DNA gyrase, a member of the GHKL proteins supe

135 antibacterial agents that act by inhibiting bacterial DNA gyrase, a target of clinical significance.

136 t act through validated drug targets such as bacterial DNA gyrase.

137 iety that is the pharmacophore for targeting bacterial DNA gyrase.

138 intracellular bacteria, cytosolic sensing of bacterial DNA has also been implicated in eliciting immu

139 in the human genome, but the integration of bacterial DNA has not been described.

140 motifs (CpG ODN), which mimic the effects of bacterial DNA, have been shown to enhance type-1 cytokin

141 erised Geobacillus stearothermophilus Bad, a bacterial DNA helicase-nuclease with similarity to human

142 Bacterial DNA helicases are nucleic acid-dependent NTPas

143 qPCR detected 16s bacterial DNA in 37 patients (66%), compared to 19 (34%)

144 estimates the relative amounts of fungal and bacterial DNA in a sample in comparison to the endogenou

145 The total bacterial DNA in autopsy liver was associated with the p

146 osomal DNA was used to measure the levels of bacterial DNA in blood samples drawn through the CVC in

147 Levels of bacterial DNA in blood were low regardless of HIV status

148 been demonstrated by the presence of similar bacterial DNA in both prostatic secretion and subgingiva

149 We analyzed plant and bacterial DNA in fecal samples from an assemblage of 33

150 This is the first report of bacterial DNA in human breast ductal fluid and the diffe

151 6S rDNA PCR analysis reveals the presence of bacterial DNA in incubated blood samples but also in neg

152 Differences exist among oral bacterial DNA in inducing immune responses.

153 recent reports suggest that the presence of bacterial DNA in peritoneal fluid in patients with cirrh

154 on analysis of the reassociation kinetics of bacterial DNA in soil, Gans et al. claimed that millions

155 e provide evidence, for the first time, that bacterial DNA in the context of heat-killed Brucella abo

156 nal age were associated with the presence of bacterial DNA in the human placenta.

157 rinciples are defined to discard contaminant bacterial DNA in the subsequent data analysis.

158 The median value for the total amount of bacterial DNA in thrombi was 16 times higher than that f

159 We aimed to measure bacterial DNA in thrombus aspirates of patients with ST-

160 technique were investigated by using various bacterial DNAs in drinking and tap water.

161 glycan and double-stranded RNA, but not with bacterial DNA, indicating that Rip2 is downstream of TLR

162 ne-deoxyguanosine dinucleotides, which mimic bacterial DNA, induced hemophagocytosis only in IFN-gamm

163 pG oligodeoxynucleotides (ODNs), which mimic bacterial DNA, inhibit allergic airways disease and prom

164 Here we present evidence that bacterial DNA integrates into the human somatic genome t

165 The Cancer Genome Atlas (TCGA), we examined bacterial DNA integration into the human somatic genome.

166 foundation for future experiments to test if bacterial DNA integrations alter the transcription of th

167 will lead to the more frequent detection of bacterial DNA integrations in tumors that are in close p

168 ctional and biological consequences of these bacterial DNA integrations remain unknown.

169 at role these factors play in compacting the bacterial DNA into a distinct organelle-like entity, the

170 We first purify the bacterial DNA into a PCR solution using our DM-based sam

171 subsequent passive leakage of extracellular bacterial DNA into the host cell cytosol is sensed by th

172 ible for the generation and transport of the bacterial DNA into the host cell has resulted in the est

173 Bacterial DNA invertases of the serine site-specific rec

174 patient by a newly developed method in which bacterial DNA is amplified directly from sputum Gram-sta

175 Bacterial DNA is protected from restriction endonuclease

176 rep Spin miniprep kit [Qiagen] and the urine bacterial DNA isolation kit [Norgen]) for the direct DNA

177 is to identify the structural components of bacterial DNA ligase that interact with NAD(+) and then

178 irement, and widespread existence in nature, bacterial DNA ligases appear to be valuable targets for

179 To explore bacterial DNA ligases as antibacterial targets and furth

180 Bacterial DNA ligases catalyze a NAD(+)-dependent DNA li

181 Bacterial DNA ligases, NAD(+)-dependent enzymes, are dis

182 Sequential bacterial DNA loads in the blood were measured by a quan

183 Higher baseline bacterial DNA loads of bacteria other than those of S ep

184 on 5 of a pyrimidine nucleotide, such as the bacterial DNA m(5)C methyltransferases, utilize their si

185 evention of coagulation in pathologies where bacterial DNA may abundantly be present.

186 Mitochondrial DNA that shows similarities to bacterial DNA may be released after tissue damage and ac

187 -function mutations or transient exposure to bacterial DNA may drive persistent inflammatory mononucl

188 ch in guanine nucleotides and the integrated bacterial DNA may have complex transcript secondary stru

189 Beyond its role in host defense, bacterial DNA methylation also plays important roles in

190 ing antibiotic stress and suggests targeting bacterial DNA methylation as a viable approach to enhanc

191 Bacterial DNA methylation has been well characterized in

192 reasing number of studies have reported that bacterial DNA methylation has important functions beyond

193 e present a binning method that incorporates bacterial DNA methylation signatures, which are detected

194 man DNA methyltransferase 1 (hDNMT1) and the bacterial DNA methyltransferase (M.EcoRII) and that it i

195 n to characterize the specificity of several bacterial DNA methyltransferases (MTases).

196 Th1 phenotype, raising the possibility that bacterial DNA might play a role in the generation of pat

197 Copy-out/paste-in transposition is a major bacterial DNA mobility pathway.

198 Clinically relevant concentrations of bacterial DNA molecules are separated by digitization ac

199 solution melt (HRM) to quantify and identify bacterial DNA molecules.

200 ondensed and became toroidal, similar to the bacterial DNA morphology seen during tetracycline treatm

201 nd examined for epithelial morphology, SIgA, bacterial DNA, nuclear factor-kappaB activation, neutrop

202 Cirrhotics had in median 27 times more bacterial DNA of Enterobactericaea in faeces compared to

203 evelop resistance following stimulation with bacterial DNA or CpG oligodeoxynucleotide.

204 Unmethylated CpG motifs in bacterial DNA or synthetic oligodeoxynucleotides (ODN) a

205 by unmethylated CpG-containing sequences in bacterial DNA or synthetic oligonucleotides (ODNs) in th

206 23, PMAP-36, and protegrin-1 to complex with bacterial DNA or synthetic RNA molecules and facilitate

207 romote NET formation, as did preparations of bacterial DNA, outer membrane proteins, and lipooligosac

208 expectation, animals receiving alum-GTF plus bacterial DNA (P. gingivalis in particular) demonstrated

209 mass spectrometry and normalized for mass of bacterial DNA per sample to exclude confounding by varyi

210 ncluding three essential proteins related to bacterial DNA pol I (POLIB, POLIC and POLID).

211 wist to this paradigm, a naturally occurring bacterial DNA polymerase I member isolated from Geobacil

212 l III) is the catalytic alpha subunit of the bacterial DNA Polymerase III holoenzyme.

213 capacity to inhibit the replication-specific bacterial DNA polymerase IIIC (pol IIIC) and the growth

214 are potent and selective inhibitors of Gram+ bacterial DNA polymerase IIIC (pol IIIC).

215 ts of these reactions with several phage and bacterial DNA polymerases capable of strand-displacement

216 tes, consistent with replication by accurate bacterial DNA polymerases in the integrated prophage sta

217 archaeal FEN1 or the 5'-nuclease domains of bacterial DNA polymerases is a double-flap structure con

218 act using 16S rRNA gene sequence analysis of bacterial DNA prepared from intestinal content.

219 Bacterial DNA primase DnaG synthesizes RNA primers requi

220 o interact with and facilitate import of the bacterial DNA-protein transport (T) complexes into the p

221 Humans express nine paralogs of the bacterial DNA repair enzyme AlkB, an iron/2-oxoglutarate

222 The phosphoesterase (PE) domain of the bacterial DNA repair enzyme LigD possesses distinctive m

223 Bacterial DNA replicases contain multiple subunits that

224 plasmid-borne RepA binding sites to inhibit bacterial DNA replication and delay host cell division w

225 on is also evident during the termination of bacterial DNA replication and during the induction of th

226 Initiation of bacterial DNA replication at oriC is mediated by primoso

227 ilis, in contrast to the prevailing model of bacterial DNA replication based on Escherichia coli DnaA

228 The process of bacterial DNA replication generates chromosomal topologi

229 Recent studies of bacterial DNA replication have led to a picture of the r

230 The level of DnaA, a key bacterial DNA replication initiation factor, increases d

231 rio extends our fundamental understanding of bacterial DNA replication initiation, and because of the

232 lethal infection in mice, demonstrating that bacterial DNA replication is inhibited during host-patho

233 The bacterial DNA replication machinery presents new targets

234 Summary It has been postulated that bacterial DNA replication occurs via a factory mechanism

235 ading onto repaired DNA replication forks in bacterial DNA replication restart pathways.

236 complexes and R-loops using a reconstituted bacterial DNA replication system.

237 We propose that DnaA serves to coordinate bacterial DNA replication with the onset of chromosome s

238 to those in eukaryal DNA replication than in bacterial DNA replication, but have some archaeal-specif

239 In the initiation of bacterial DNA replication, DnaA protein recruits DnaB he

240 endosomes, TLR9 is activated by unmethylated bacterial DNA, resulting in proinflammatory cytokine sec

241 s, bacterial antibodies, bacteriophages, and bacterial DNA/RNA hybrid nucleotide oligomers.

242 Starting with extracted bacterial DNA, samples are fragmented by restriction enz

243 this study is to determine the expression of bacterial DNA sensors, including Toll-like receptor 9 (T

244 t self-transmissible is dissimilarity in the bacterial DNA sequences concerned.

245 Here, we use bacterial DNA sequencing from serially collected vaginal

246 additional information on the quantities of bacterial DNA shed.

247 s from myeloperoxidase, serum amyloid A, and bacterial DNA, shifting the balance of pro- and anti-sur

248 Sequencing of bacterial DNA showed the slow development of a bacterial

249 bosomal RNA gene sequencing detected diverse bacterial DNA signatures in the filtrates.

250 Unmethylated CpG motifs present in bacterial DNA stimulate a rapid and robust innate immune

251 Unmethylated CpG motifs present in bacterial DNA stimulate a strong innate immune response.

252 This response is similar to that seen with bacterial DNA stimulation of B cells.

253 ylate kinase (TMK) is an essential enzyme in bacterial DNA synthesis.

254 Our findings demonstrate that bacterial DNA through Toll-like receptor 9 shifted the b

255 nsive to CpG ODN but are fully responsive to bacterial DNA, thus implying that microbial recognition

256 bined this approach with quantitative PCR of bacterial DNA to normalize the amount of gene expression

257 We then transfer the purified bacterial DNA to our microfluidic nanoarray to amplify 1

258 Intracolonic administration of bacterial DNA to wild-type mice induced expression of ca

259 Bacterial DNA topoisomerase I is responsible for prevent

260 DNA gyrase is a bacterial DNA topoisomerase that catalyzes ATP-dependent

261 Bacterial DNA topoisomerases are essential for bacterial

262 DNA gyrase and topoisomerase IV control bacterial DNA topology by breaking DNA, passing duplex D

263 lism; it is also suggested to participate in bacterial DNA transactions.

264 robiology, the most commonly used methods of bacterial DNA transfer are conjugation and electroporati

265 ng the viral DNA-packaging motor, beside the bacterial DNA translocases, that uses a revolving mechan

266 Because so far no clear homologs of bacterial DNA transporters have been identified among th

267 Bacterial DNA transposition is an important model system

268 Bacterial DNA typical for endodontic infection, mainly o

269 Here, we interpret bacterial DNA uptake and release in the context of sexua

270 ng approach for the broad range detection of bacterial DNA using broad-range 16S rRNA gene hybrid cap

271 lli identified by Gram staining, we isolated bacterial DNA using spin columns (BC-C) and rapid water

272 etic readout of rolling circle products from bacterial DNA utilizing the dynamic properties of MNBs i

273 ve qPCR detection of the extracted S. aureus bacterial DNA was achieved with a detection limit of 5+/

274 were collected from children, and extracted bacterial DNA was amplified for the V4 region of the 16S

275 Among the 46 samples associated with PTB, bacterial DNA was amplified from all (16/16) of the cult

276 Bacterial DNA was amplified from the only patient with c

277 No bacterial DNA was amplified in AF collected from the asy

278 Blood bacterial DNA was analyzed both quantitatively by 16S ri

279 ization and microbial diversity on the skin, bacterial DNA was analyzed from swabs collected from les

280 Bacterial DNA was analyzed using terminal restriction fr

281 .1% and 11.4% of vascular and blood samples, bacterial DNA was detected.

282 Bacterial DNA was extracted from and subjected to Illumi

283 Bacterial DNA was extracted from mouse fecal samples to

284 Bacterial DNA was extracted, and qPCR was used to determ

285 Bacterial DNA was extracted, and the 16S rRNA genes were

286 ted at the deepest site of each sextant, and bacterial DNA was extracted.

287 cimens with no culture growth, the amount of bacterial DNA was greater than that in reagent and rinse

288 Bacterial DNA was isolated and 16S ribsomal RNA gene lib

289 Bacterial DNA was isolated and was processed and analyze

290 Bacterial DNA was isolated from 123 "donuts" of patients

291 Bacterial DNA was isolated from the same milk samples an

292 Bacterial DNA was isolated, and the 16S ribosomal RNA ge

293 Bacterial DNA was isolated, and the 16S rRNA gene was am

294 ide LL-37 and the abundance and diversity of bacterial DNA was measured.

295 Using qPCR, we show that bacterial DNA was present in the atherosclerotic plaque

296 n events leading to the stable expression of bacterial DNA was unexplored.

297 ment may be systematically contaminated with bacterial DNA, which appears to be sampled by metagenome

298 s were positive for spiroplasma or any other bacterial DNA, while control Spiroplasma mirum genomic D

299 larensis revealed striking colocalization of bacterial DNA with endogenous AIM2 and inflammasome adap

300 how that neighboring transgenic elements and bacterial DNA within the transgene cause profound silenc