ライフサイエンスコーパス: bacteriophage

1 usiformis expressed on the surface of the fd bacteriophage.

2 late cycle, and reduce infection activity of bacteriophage.

3 self-assembly of genetically engineered M13 bacteriophage.

4 a 936-type Lactococcus lactis subsp. lactis bacteriophage.

5 oducts conferred resistance to a WTA-binding bacteriophage.

6 y of DNA modifications found in bacteria and bacteriophages.

7 ing motor assembly, as predicted for several bacteriophages.

8 each other and from previously described RNA bacteriophages.

9 iruses, including the herpesviruses and many bacteriophages.

10 ems benefit bacteria by protecting them from bacteriophages.

11 promote DNA transfers between eukaryotes and bacteriophages.

12 ontext of the arms race between bacteria and bacteriophages.

13 vention, including vaccines, probiotics, and bacteriophages.

14 ses frequently encoded in the genome of many bacteriophages.

15 nting protein similar to those found in many bacteriophages.

16 proteins or cross-linking, as occur in other bacteriophages.

17 ymptoms of CDI showed a complex signature of bacteriophages.

18 Two bacteriophages (536_P1 and 536_P7) were isolated from se

19 otably in the form of viral pathogens termed bacteriophages (8-12) , which are the most abundant repl

20 bov1, is derepressed by the dUTPase (Dut) of bacteriophage 80alpha (Dut80alpha) and its phage varphi1

21 guanosine, was found in the Escherichia coli bacteriophage 9 g, as predicted from the presence of hom

22 nal import (TAxI), that enriched recombinant bacteriophage accumulation and delivered protein cargo i

23 aging motors, including those of dsDNA/dsRNA bacteriophages, adenoviruses, poxviruses, herpesviruses,

24 ivibrio, Oscillospira and Ruminococcus after bacteriophage administration.

25 galactosylated WTA was directly required for bacteriophage adsorption and that mutant WTA lacked appr

26 s spectrometry to monitor the replication of bacteriophage after it is used to infect samples thought

27 idermidis, Saccharomyces cerevisiae, and MS2 Bacteriophage after light treatment of a medical grade s

28 Using a previous dataset of 820 bacteriophage and 2699 bacterial genomes, [Formula: see

29 properties were then used to isolate His6-T7 bacteriophage and His6-GroEL directly from cell lysates.

30 ired through horizontal gene transfer from a bacteriophage and is classified as an atypical A-family

31 alyzed a deep DNA sequence dataset of active bacteriophages and available metagenomic datasets of the

32 cs studies and discusses the contribution of bacteriophages and eukaryotic viruses to human health.

33 ource tracking (MST) tools using enterococci bacteriophages and evaluated their performance with univ

34 Tailed bacteriophages and herpes viruses use powerful molecular

35 Tailed bacteriophages and herpesviruses assemble infectious par

36 eformed protein capsid exemplified by tailed bacteriophages and herpesviruses.IMPORTANCE Adenovirus i

37 e proteins related to D10 in archaebacteria, bacteriophages and in viruses known to infect a range of

38 Bacteriophages and large dsDNA viruses encode sophistica

39 RISPR-Cas systems defend prokaryotes against bacteriophages and mobile genetic elements and serve as

40 Starting with bacteriophages and moving to the retroviruses, my use of

41 ike proteins encoded by bacteria, as well as bacteriophages and other extrachromosomal elements.

42 arget and degrade nucleic acids derived from bacteriophages and other foreign genetic elements.

43 systems capture DNA fragments from invading bacteriophages and plasmids and integrate them as spacer

44 In addition to DNA, capsids of tailed bacteriophages and their distant relatives, herpesviruse

45 sponse to the evolutionary arms race between bacteriophages and their hosts.

46 have never before been reported in packaged bacteriophages and their phylogeny, distribution and seq

47 primarily to be part of an arms race between bacteriophages (and other genomic parasites) and their h

48 ases to defend against infection by viruses, bacteriophages, and mobile elements, while these foreign

49 We expressed in E. coli VLPs from the bacteriophage AP205 genetically fused to SpyCatcher.

50 Bacteriophages are believed to increase the diversity by

51 Bacteriophages are present in virtually all ecosystems,

52 Bacteriophages are widely recognized for their importanc

53 Bacterial viruses (bacteriophages) are a particularly rich but still undere

54 We used bacteriophage as a nanofiber model system to exploit its

55 e specificity and rapid-acting properties of bacteriophages as a potential prophylaxis therapy for ch

56 performed human subject studies using three bacteriophages as pathogenic virus surrogates: nonenvelo

57 ings provide novel insights into the role of bacteriophages as potentially pathogenic for mammals and

58 Using bacteriophages as surrogates for human pathogenic viruse

59 itous in nature, because they are present in bacteriophage, bacteria, archaea, and simple and complex

60 Recently, we have established a bacteriophage-based biomimetic process, called 'self-tem

61 roof-of-concept study was conducted using T2 bacteriophage-based biosensors for electrochemical detec

62 hat low concentrations (0.09 mg/mL of the R5 bacteriophage, below the concentration range used in oth

63 nomic diversification of naturally occurring bacteriophages by analyzing the full genomic sequences o

64 ase that provides efficient immunity against bacteriophages by inducing abortive infection.

65 An enzyme produced by a bacteriophage can enter human cells and kill intracellul

66 ture which is composed of functionalized M13 bacteriophage can simultaneously improve the sensitivity

67 Predation by bacteriophages can significantly influence the populatio

68 protocol to the 3.3-A map of the mature P22 bacteriophage capsid, a large and complex macromolecular

69 Bacteriophage capsids constitute icosahedral shells of e

70 nflammation-related cytokines, following the bacteriophage challenge.

71 versity index values increased following the bacteriophage challenge.

72 ing a WIG1 tethering system based on the MS2 bacteriophage coat protein and a reporter construct cont

73 el, we examined the effects of exposure to a bacteriophage cocktail on intestinal permeability and re

74 iruses typically co-opt eukaryotic genes and bacteriophages commonly harbour bacterial genes.

75 We propose that the core and common bacteriophage communities are globally distributed and c

76 nd available metagenomic datasets of the gut bacteriophage community from healthy individuals.

77 The bacteriophage community in the human gut is a mixture of

78 ysis, we identified disease-associated viral bacteriophage contigs after subtraction of age-associate

79 Recently, a novel bacteriophage, crAssphage, was discovered by metagenomic

80 nase from the Geobacillus stearothermophilus bacteriophage D6E shows a unique relative orientation of

81 Conditional gene targeting using the bacteriophage-derived Cre recombinase is widely applied

82 eaving the polysialic acid moiety, using the bacteriophage-derived enzyme endoneuraminidase N, comple

83 We used two M13-bacteriophage display biopanning strategies to search fo

84 We show for the T4 bacteriophage DNA replication system that primer-primase

85 e-stranded DNA breaks and the degradation of bacteriophage DNA.

86 Small bacteriophage-encoded anti-CRISPR proteins (Acrs) can in

87 PlyC, a bacteriophage-encoded endolysin, lyses Streptococcus pyo

88 Bacteriophage-encoded small proteins that either modulat

89 orm of the host RNAP can also be targeted by bacteriophage-encoded transcription regulatory proteins.

90 temperature during infection, the truncated bacteriophage endolysin CHAPK and the staphylococcal bac

91 As an alternative mode of treatment both bacteriophage endolysins and bacteriocins have been show

92 itution of WTA determines the recognition by bacteriophage endolysins.

93 to detect different bacteria using specific bacteriophages engineered with gene encoding for appropr

94 n of Escherichia coli (E. coli) using the T7 bacteriophages engineered with lacZ operon encoding for

95 Serine integrases are bacteriophage enzymes that carry out site-specific integ

96 quimolar mixtures of genomic DNA from lambda bacteriophage, Escherichia coli (strain K12, MG1655) and

97 Studies of bacteriophage evolution thus provide unparalleled insigh

98 Here, we show that bacteriophages evolve within two general evolutionary mo

99 ate immunity centered on Argonaute proteins, bacteriophage exclusion, and new types of CRISPR-Cas sys

100 resent a new approach to phage therapy where bacteriophages exert selection for MDR bacteria to becom

101 Although an abundance of bacteriophages exists, little is known about interaction

102 ases, DNA site-specific recombinases used by bacteriophages for integration and excision of their DNA

103 l observations of single-cell lysis times in bacteriophage [Formula: see text] Here, lysis of an infe

104 than one-half of all people, a common set of bacteriophages found in 20-50% of individuals, and a set

105 have found a high level of heterogeneity in bacteriophages from healthy individuals.

106 Bacteriophages from the family Myoviridae use double-lay

107 rge terminase nuclease from the thermophilic bacteriophage G20c show that it is most similar to the R

108 ial RNAP to allow the temporal regulation of bacteriophage gene expression often target the activity

109 ine nucleotide biosynthetic pathway using T4 bacteriophage genes to achieve approximately 63% replace

110 ditional domains to forge one of the largest bacteriophage genes to date (14,256 bp).

111 a web application which creates databases of bacteriophage genes, grouped by gene similarity.

112 a-proteobacteria and are encoded on multiple bacteriophage genomes, also accumulate in the predivisio

113 C-terminal domain, that are uninterrupted in bacteriophage genomes, enriched with eukaryotic protease

114 standing the structure and origin of natural bacteriophage genomic diversity is important in elucidat

115 orm of interdigital capacitor coated with T4 bacteriophage gp37 adhesin.

116 roperties using a MST toolbox containing two bacteriophage groups (phage infecting GB-124 and ARABA-8

117 A network analysis identified 44 bacteriophage groups of which 9 (20%) were shared in mor

118 Bacteriophage has been recognized as a novel approach to

119 ted proteins present in various bacteria and bacteriophages have diverged from msRNAPs before the Las

120 Studies on dsDNA bacteriophages have revealed that a DNA packaging comple

121 binding peptide (His Pro Gln: HPQ) gives M13 bacteriophage high selectivity for the streptavidin.

122 In the T=7 capsids of Escherichia coli bacteriophage HK97 and other phages, 60 capsomers are he

123 manifest as a complex of insertions around a bacteriophage HK97 gp5-like domain, which gives rise to

124 amine against murine norovirus (MNV) and MS2 bacteriophage in secondary effluent MWW and phosphate bu

125 The role of bacteriophages in influencing the structure and function

126 We found 23 shared bacteriophages in more than one-half of 64 healthy indiv

127 However, the presence of bacteriophages in obligate intracellular bacteria of euk

128 RT-PCR)-based screening for two specific RNA bacteriophages in stool samples from a longitudinal coho

129 a has spurred renewed interest in the use of bacteriophages in therapy.

130 role of bacteriophages with RNA genomes (RNA bacteriophages) in these processes is poorly understood,

131 or commensals, including bacteria, fungi and bacteriophages, in modulating skin functions in health a

132 equences, protecting bacterial cells against bacteriophage infection by attacking foreign DNA.

133 f a unique protein product resulting from T7 bacteriophage infection of E. coli, illustrating that na

134 ch as twitching motility, biofilm formation, bacteriophage infection, surface attachment, virulence,

135 cific RNA-guided nucleases to defend against bacteriophage infection.

136 ttle about how the stressed cells respond to bacteriophage infection.

137 la flexneri (S. flexneri) as a first step of bacteriophage infection.

138 need it most: in high-density cultures, when bacteriophage infections can be most detrimental.

139 s with higher restriction efficiency against bacteriophage infections exhibit a higher rate of self-r

140 For bacteriophage infections, the cell walls of bacteria, co

141 de prokaryotes with adaptive defense against bacteriophage infections.

142 ic diversity is important in elucidating how bacteriophages influence the mortality rates and composi

143 During replication of the varphi29 bacteriophage inside a bacterial host cell, a DNA packag

144 g protein [gene product 32 (gp32)] of the T4 bacteriophage is a central integrating component of the

145 Bacteriophages isolated from known E. coli reservoirs ly

146 evolutionary trajectory of a group of dsDNA bacteriophages known as the phiKMVviruses.

147 ctural tail protein of Klebsiella pneumoniae bacteriophage KP32, and is responsible for adhering the

148 as an example the directed evolution of the bacteriophage lambda cI TF against two synthetic bidirec

149 witches for orthogonal logic gates, based on bacteriophage lambda cI variants and multi-input promote

150 tions affects the lysis-lysogeny decision of bacteriophage lambda despite variable infection times be

151 To counteract the latter activity, bacteriophage lambda encodes a small protein inhibitor c

152 The bacteriophage lambda is a convenient source of high qual

153 es to survey the roles of P-loop residues in bacteriophage lambda motor function.

154 Bacteriophage lambda of Escherichia coli has two alterna

155 relief of TI by CI or Cro repressors in the bacteriophage lambda PR-PRE system show strong relief of

156 component of the Red recombination system of bacteriophage lambda that promotes a single strand annea

157 ightly regulated pathway for the excision of bacteriophage lambda viral DNA out of the E. coli host c

158 We propagated bacteriophage lambda, a virus with rapid generations and

159 he bacterium Escherichia coli and its virus, bacteriophage lambda, is paradigmatic for gene regulatio

160 cles in the lysogeny maintenance promoter of bacteriophage lambda, P(RM).

161 Bacteriophage lambda-terminase, which serves as a protot

162 r a complete narrative for the life cycle of bacteriophage lambda.

163 on of the N and Q antiterminator proteins of bacteriophage lambda.

164 ation signal, to an RNA binding peptide from bacteriophage lambda.

165 argeting various positions in the genomes of bacteriophages lambda, T5, T7, T4 and R1-37 and investig

166 PIs), such as SaPI1, exploit specific helper bacteriophages, like 80alpha, for their high frequency m

167 oduce gene transfer agents (GTAs), which are bacteriophage-like particles that exclusively package pi

168 the first time that the known tropism of RNA bacteriophages may include gram-positive bacteria.

169 s that bacterial components, metabolites, or bacteriophages mediate many of the effects of FMT, and t

170 vo, and are applicable to both bacterial and bacteriophage-mediated laboratory evolution platforms.

171 Bacteriophage modulation of microbial populations impact

172 man blood, using a novel LAMP primer set for bacteriophage MS2 (a model RNA virus particle).

173 the viral genome, as exemplified by the RNA bacteriophage MS2 and as proposed for other RNA viruses

174 sed RNA oligomer segments from the genome of bacteriophage MS2 to UV254, simulated sunlight, and sing

175 surrogate viruses murine norovirus (MNV) and bacteriophage MS2 under identical experimental condition

176 xtrinsic controls (phocine herpesvirus 1 and bacteriophage MS2) were included to ensure extraction an

177 f of concept for the label-free detection of bacteriophage MS2, a model indicator of microbiological

178 igated the inactivation of Escherichia coli, bacteriophage MS2, and Bacillus subtilis spores as surro

179 single-stranded RNA (ssRNA) viruses, such as bacteriophage MS2, co-assemble their capsid with the gen

180 o model microorganisms: Escherichia coli and bacteriophage MS2.

181 n the capsid proteins and the genomic RNA of bacteriophage MS2.

182 ynamics of negatively charged viruses (i.e., bacteriophages MS2, fr, GA, and Qbeta) and polystyrene n

183 ruses (MHV and varphi6) and two nonenveloped bacteriophages (MS2 and T3) in raw wastewater samples.

184 ystematically studied the adsorption of four bacteriophages (MS2, fr, GA, and Qbeta) to five model su

185 The transposition of bacteriophage Mu serves as a model system for understand

186 e exception of the tailed viruses related to bacteriophages of the order Caudovirales and the familie

187 h a management strategy, we isolated a lytic bacteriophage, OMKO1, (family Myoviridae) of Pseudomonas

188 The enormous prevalence of tailed DNA bacteriophages on this planet is enabled by highly effic

189 can be transferred into chromosomes by: (i) bacteriophage P1 transduction; and (ii) transformation o

190 ural evidence that the portal protein of the bacteriophage P22 exists in two distinct dodecameric con

191 genase, sequestered within the capsid of the bacteriophage P22 through directed self-assembly.

192 acteriophage T7 tail protein gp11 and gp4 of bacteriophage P22, but TTPA contains an additional antip

193 tral pH structure of three tail needles from bacteriophage P22, HK620, and Sf6.

194 ese methods to new cryoEM maps of the mature bacteriophage P22, reconstructed without imposing icosah

195 harge-directed, orientated immobilization of bacteriophage particles on carbon nanotubes was achieved

196 y increases the production of filamentous Pf bacteriophage (Pf phage).

197 Bacteriophage (phage) amplification is an attractive met

198 mune systems that provide protection against bacteriophage (phage) and other parasites.

199 Here, we report a new bacteriophage, phage DSS3Phi8, which infects marine rose

200 Both lytic and temperate bacteriophages (phages) can be applied in nanomedicine,

201 Bacteriophages (phages) defend mucosal surfaces against

202 Bacteriophages (phages) infect many bacterial species, b

203 stems to defend themselves from infection by bacteriophages (phages).

204 Many dsDNA bacterial viruses (bacteriophages/phages) have long tail structures that se

205 he three-way junction (3WJ) of the pRNA from bacteriophage phi29 DNA packaging motor were examined pr

206 th the clip region of the portal proteins of bacteriophages phi29, SPP1 and T4.

207 In this study, the enveloped bacteriophage Phi6 was evaluated as a surrogate for enve

208 In the prototypic dsRNA bacteriophage phi6, the assembly reaction is promoted by

209 ction of Pseudomonas aeruginosa by the giant bacteriophage phiKZ is resistant to host RNA polymerase

210 The E. coli O157:H7 bacteriophage PhiV10 was modified to express NanoLuc luc

211 he Encyclopedia of DNA Elements project, and bacteriophage PhiX DNA samples.

212 eir genomes into a host bacterium, the ssDNA bacteriophage PhiX174 is tailless.

213 identify partial genome sequences of 122 RNA bacteriophage phylotypes that are highly divergent from

214 bI expression caused restriction of incoming bacteriophage/plasmid DNA and endogenous chromosomal DNA

215 How temperate bacteriophages play a role in microbial infection and di

216 The sophisticated tail structures of DNA bacteriophages play essential roles in life cycles.

217 Bacteriophages play key roles in microbial evolution(1,2

218 nd another member of the structural lineage, bacteriophage PM2, extends to the capsid organization (p

219 e characterized the inactivation kinetics of bacteriophage PR772, a member of the Tectiviridae family

220 Bacteriophages produce endolysins, which lyse the bacter

221 ses have been observed in the genomic DNA of bacteriophages, prokaryotes, and eukaryotes that play a

222 ce diversity imply lateral transfers between bacteriophage/prophage and animal genomes.

223 detailed interactions between SP and CP in a bacteriophage, providing unique insights into macromolec

224 sassembly of (19)F-labeled VLPs derived from bacteriophage Qbeta by (19)F NMR.

225 Hfq (host factor for RNA bacteriophage Qbeta replication), a bacterial Lsm family

226 tion, packaging and delivery system based on bacteriophage Qbeta.

227 could be effectively replaced by those from bacteriophage RB69, and could carry out chromosomal DNA

228 s to identify an expansive, diverse group of bacteriophages related to crAssphage and predict the fun

229 eviously unidentified mechanism that confers bacteriophage resistance.

230 netic modification of functional peptides of bacteriophage results in structures that can be used as

231 e genes, and thus represents a novel type of bacteriophage RNAPs.

232 These novel RNA bacteriophage sequences were present in samples collecte

233 Bacteriophage serine integrases are extensively used in

234 te atomic model of the headful DNA-packaging bacteriophage Sf6 at 2.9 A resolution determined by elec

235 e studied the tailspike protein (TSP) of the bacteriophage Sf6.

236 is a mixture of three classes: a set of core bacteriophages shared among more than one-half of all pe

237 t because of the limited number of known RNA bacteriophage species.

238 he structural particle of bacterial viruses (bacteriophages) specifically infecting Gram-positive bac

239 t six different 2-deoxyadenosines in the M13 bacteriophage ssDNA genome.

240 In single-stranded RNA bacteriophages (ssRNA phages) a single copy of the matur

241 n of molecular networks consisting of entire bacteriophage structure, displaying specific peptides, d

242 eralizing peptide component displayed on the bacteriophage surface, we found that low concentrations

243 In a process called sigma appropriation, bacteriophage T4 activates a class of phage promoters us

244 ingle-stranded DNA-binding protein gp32 from bacteriophage T4 and a strand-displacing DNA polymerase.

245 al for efficient homologous recombination in bacteriophage T4 and is the functional analog of the euk

246 cture of the 860-A-diameter isometric mutant bacteriophage T4 capsid has been determined.

247 ty DNA polymerases such as pol delta and the bacteriophage T4 DNA polymerase replicating 8-oxo-G in a

248 Tailed bacteriophage T4 employs one of the fastest and most pow

249 Bacteriophage T4 infects the bacterial host (Escherichia

250 Mutation of the zinc-hook in bacteriophage T4 is lethal, indicating the ability to bi

251 lf of the ribosomes translating a particular bacteriophage T4 mRNA bypass a region of 50 nt, resuming

252 cted mutations to perturb this domain in the bacteriophage T4 Rad50 homolog.

253 ulting in different triangulation numbers in bacteriophage T4.

254 gle-stranded (ss) DNA binding protein of the bacteriophage T4.

255 putative helicase encoded by the D10 gene of bacteriophage T5.

256 in Ocr (overcome classical restriction) from bacteriophage T7 acts as a mimic of DNA and inhibits all

257 pproximately 650-kDa functional replisome of bacteriophage T7 assembled on DNA resembling a replicati

258 Bacteriophage T7 belongs to the Podoviridae family and h

259 DNA-duplex stability affects replication by bacteriophage T7 DNA polymerase.

260 ensuring a high-fidelity replication of the bacteriophage T7 genome.

261 talytic activity is known to increase during bacteriophage T7 infection, reflecting the expression of

262 The single-subunit RNA polymerase (RNAP) of bacteriophage T7 is able to perform all steps of transcr

263 other in vitro display technologies such as bacteriophage T7 or mRNA display.

264 expression levels in 6,348 experiments using bacteriophage T7 polymerase to synthesize messenger RNA

265 olling Okazaki fragment initiation using the bacteriophage T7 replication system.

266 proach to visualize this coordination in the bacteriophage T7 replisome by simultaneously monitoring

267 developed to control the expression of both bacteriophage T7 RNA polymerase and recombinant gene(s)

268 tal structure of TTPA resembles those of the bacteriophage T7 tail protein gp11 and gp4 of bacterioph

269 Here, we show that bacteriophage T7 undergoes apparent stress-induced mutag

270 )CACONH, and (H)CBCANH spectra of the 20 kDa bacteriophage tail-tube protein gp17.1 in a total time o

271 chanism related to the action of contractile bacteriophage tails.

272 that YonO is a bona fide RNAP of the SPbeta bacteriophage that specifically transcribes its late gen

273 found in 20-50% of individuals, and a set of bacteriophages that are either rarely shared or unique t

274 f tailless, icosahedral, membrane-containing bacteriophages that can be divided into two groups by th

275 sly, we discovered small proteins encoded by bacteriophages that inhibit the CRISPR-Cas systems of th

276 We propose that predation by bacteriophages that use T4P as receptors selects for str

277 In the Phi29 bacteriophage, the DNA packaging nanomotor packs its dou

278 is cell rescue program, and the induction of bacteriophages, the movement of pathogenicity islands, a

279 Here we investigated the efficacy of bacteriophage-therapy (phage) alone or combined with ant

280 ge KP32, and is responsible for adhering the bacteriophage to host cells.

281 bination (HR) protein that is conserved from bacteriophage to humans.

282 bacterial virulence factors, utilization of bacteriophages to kill bacteria, and manipulation of the

283 complex molecular architectures ranging from bacteriophages to nuclear pores, cilia, and synaptonemal

284 t in the well-studied nuclear, bacterial, or bacteriophage transcription systems but that similaritie

285 ments and occurs primarily by conjugation or bacteriophage transduction, with the latter traditionall

286 rther, this material rapidly inactivates MS2 bacteriophage under sunlight illumination, oxidizes vari

287 stem after infection with the staphylococcal bacteriophage varphi12.

288 he ATPase ring in the DNA packaging motor of bacteriophage varphi29 is regulated by an arginine finge

289 The T2 bacteriophage (virus) served as the biorecognition eleme

290 Furthermore, one RNA bacteriophage was detected in the transcriptome of a pur

291 of the C-dots and the DNA fragment of lambda bacteriophage was performed, and the DNA binding resulte

292 elbrueckii subsp. bulgaricus (Ldb)-infecting bacteriophages, was shown to hydrolyze, besides the simp

293 For bacteriophages, we found higher Shannon diversity and ri

294 These shared bacteriophages were found in a significantly smaller per

295 AIM06 and SR14 bacteriophages were present in human sewage at 2-4 order

296 However, our knowledge on bacteriophage which infects the Roseobacter clade is sti

297 Unlike tailed bacteriophages, which use a preformed tail for transport

298 However, the role of bacteriophages with RNA genomes (RNA bacteriophages) in

299 we report a metagenomic analysis of purified bacteriophage WO particles of Wolbachia and uncover a eu

300 Genomic analyses of these novel bacteriophages yielded multiple novel genome organizatio