ライフサイエンスコーパス: DNA virus

1 etect both siRNAs and a novel miRNA from the DNA virus.

2 highly structurally complex double stranded DNA virus.

3 f Bean dwarf mosaic virus, a single-stranded DNA virus.

4 ted with vaccinia virus (VACV), a vertebrate DNA virus.

5 derstanding the life cycle of this oncogenic DNA virus.

6 vaccinia virus (VV), a large (200 kB genome) DNA virus.

7 gainst a large range of viruses, including a DNA virus.

8 subsequent immune evasion by this prominent DNA virus.

9 sequences from a widespread single-stranded DNA virus.

10 oductive infection of this large cytoplasmic DNA virus.

11 of both is needed to control infection by a DNA virus.

12 igation of the oncogenic mechanisms for this DNA virus.

13 o largely take over study of double-stranded DNA viruses.

14 STING to initiate the antiviral response to DNA viruses.

15 s antiviral activity against several RNA and DNA viruses.

16 ba species are infected by the largest known DNA viruses.

17 replication intermediates produced by other DNA viruses.

18 stant to geminiviruses, a damaging family of DNA viruses.

19 f the suitability of bone for exploration of DNA viruses.

20 cellular immune response to infections with DNA viruses.

21 ical functions in defending the cell against DNA viruses.

22 gs to the Hepadnaviridae family of enveloped DNA viruses.

23 hologies associated with nuclear replicating DNA viruses.

24 aging motors in many complex double-stranded DNA viruses.

25 ositive-sense RNA viruses, retroviruses, and DNA viruses.

26 tly belonging to the nucleocytoplasmic large DNA viruses.

27 cytosolic DNA, cyclic di-GMP (c-di-GMP), and DNA viruses.

28 has not been described previously for human DNA viruses.

29 ed from polymerase II transcripts encoded by DNA viruses.

30 h antiviral activity against several RNA and DNA viruses.

31 ew is to explore recombination strategies in DNA viruses.

32 DNA structures generated upon replication of DNA viruses.

33 ulator of infection by VSV and other RNA and DNA viruses.

34 erferon responses to intracellular dsDNA and DNA viruses.

35 exhaustively studied of the double-stranded DNA viruses.

36 tivity against CMV and other double-stranded DNA viruses.

37 equences within the genomes of certain large DNA viruses.

38 of non-enveloped, circular, single-stranded DNA viruses.

39 sid expansion in the complex double-stranded DNA viruses.

40 ent results from other small single-stranded DNA viruses.

41 ycodnaviruses, and nuclear-cytoplasmic large DNA viruses.

42 f antiviral activity against a wide range of DNA viruses.

43 ories induced by the nucleocytoplasmic large DNA viruses.

44 proach as a treatment for diseases caused by DNA viruses.

45 or RNA viruses whereas PVG PCR detected more DNA viruses.

46 innate immune response to exogenous DNA and DNA viruses.

47 uction by a panel of pathogenic bacteria and DNA viruses.

48 obustly induced upon infection with multiple DNA viruses.

49 in that can be found in many double-stranded DNA viruses.

50 sponses against RNA viruses, but not against DNA viruses.

51 ral drugs for the treatment of infections by DNA viruses.

52 s of the protein kinase R pathway with large DNA viruses.

53 o cytosolic DNA, c-di-GMP, cGAMP, HIV-1, and DNA viruses.

54 the host innate immune response to HIV-1 and DNA viruses.

55 otinia sclerotiorum hypovirulence-associated DNA virus 1 and aNCV as within the insect-infecting Crip

56 leave us with a lesser understanding of how DNA viruses adapt to hosts and how the host responds to

57 dynamics and identify genes that are key to DNA virus adaptation, improving our understanding of how

58 Similar to the case for most DNA viruses, after receptor binding and entry, AAV trave

59 s have deficient inflammasome responses to a DNA virus and fungal infection.

60 The virus is a large DNA virus and is the only member of the Asfarviridae fam

61 ssential for innate immune responses against DNA viruses and bacteria such as Francisella and Listeri

62 osely classed into two groups: slow-evolving DNA viruses and fast-evolving RNA viruses.

63 ontaining proteins are encoded by many large DNA viruses and found in all domains of life, studies of

64 ity of RNA-Seq in detecting tumor-associated DNA viruses and identifying viral integration sites that

65 e, with implications for the interactions of DNA viruses and retroviruses with their hosts.

66 by a range of viruses including RNA viruses, DNA viruses and retroviruses.

67 A damage response, presenting challenges for DNA viruses and retroviruses.

68 origin of several groups of large eukaryotic DNA viruses and self-replicating plasmids.

69 as the replication and pathogenesis of many DNA viruses and some RNA viruses.

70 a gene conserved in nucleo-cytoplasmic large DNA viruses) and Organic Lake virophage OLV2 (conserved

71 ine tune host response to intracellular DNA, DNA virus, and c-di-GMP.

72 sing mechanism of hepatitis B virus (HBV), a DNA virus, and the subsequent downstream signaling event

73 requirement in the antiviral response to two DNA viruses, and an unappreciated contribution to the in

74 e limited encoding capacity compared to many DNA viruses, and as a likely consequence, most open read

75 RV) and human Herpes simplex virus (HSV) are DNA viruses, and their pathogenesis and immunobiology ar

76 , large systems including protein binding to DNA, viruses, and membranes.

77 umber of sequences (P = 0.047) of persistent DNA viruses (anelloviruses, herpesviruses, papillomaviru

78 igin of the glycosylation machinery in giant DNA virus are also discussed.

79 recognized by RIG-I during infection with a DNA virus are largely unknown.

80 Single-stranded (ss)DNA viruses are extremely widespread, infect diverse hos

81 Various types of DNA viruses are known to elicit the formation of a large

82 Although several DNA viruses are sensed by cGAS, viral strategies targeti

83 hich have the largest genome of nonenveloped DNA viruses, are being extensively explored for use in g

84 ge dsDNA viruses.IMPORTANCE Unlike all other DNA viruses, ascoviruses code for an executioner caspase

85 n 20 previously undetected RNA viruses and a DNA virus associated with wild D. melanogaster.

86 Polyomaviruses are small circular DNA viruses associated with chronic infections and tumor

87 viruses 1 and 2 (HSV-1 and HSV-2) are large DNA viruses associated with recurring oral or genital er

88 Elucidation of tumor-DNA virus associations in many cancer types has enhanced

89 e novo assembly of a novel, highly divergent DNA virus at the interface between the Parvoviridae and

90 s in GT frequencies have been achieved using DNA virus-based replicons.

91 nfection by a rapidly evolving single-strand DNA virus, beak and feather diseases virus (BFDV), which

92 less dependent on host functions than other DNA viruses because of their cytoplasmic site of replica

93 nase Hopscotch to infections by seven RNA or DNA viruses belonging to different families.

94 s (STING) is known be involved in control of DNA viruses but has an unexplored role in control of RNA

95 ttenuated cytokine responses to both DNA and DNA viruses but not to RNA or RNA virus infection.

96 lyzing motor, formed in many double-stranded DNA viruses by a complex of a small terminase (S-termina

97 These results suggest that a nuclear DNA virus can selectively interfere with RNA export to r

98 litis in susceptible mice.IMPORTANCE RNA and DNA viruses can cause encephalitis; in some cases, this

99 Whether DNA viruses can prevent activation of the cGAS-STING pat

100 Human papillomaviruses (HPVs) are small DNA viruses causally associated with benign warts and mu

101 Hepatitis B virus (HBV), a small enveloped DNA virus, chronically infects more than 350 million peo

102 nt a global map of abundant, double-stranded DNA viruses complete with genomic and ecological context

103 For many double-stranded DNA viruses, confinement of the large DNA molecule withi

104 ophages and certain nucleo-cytoplasmic large DNA viruses contain an unexpectedly diverse range of DNA

105 ral activity against a wide range of RNA and DNA viruses despite specifically targeting different pro

106 Our results provide a glimpse into how DNA viruses differ from RNA viruses in their evolutionar

107 ing of bacteriophages and eukaryotic RNA and DNA viruses, during the first years of life.

108 Surprisingly, unlike other DNA viruses (e.g., adenovirus [Ad] and herpes simplex vi

109 The discovery that animals, plants and DNA viruses encode microRNAs (miRNAs) has transformed ou

110 merous viral microRNAs (miRNAs) expressed by DNA viruses, especially herpesvirus family members, have

111 Accordingly, Nlrx1(-/-) mice infected with DNA viruses exhibit enhanced innate immunity and reduced

112 human cytomegalovirus (HCMV), a large human DNA virus, exploits IFITMs to facilitate the formation o

113 In this study, we used a recombinant DNA virus expressing different forms of a model Ag to st

114 rom veterinary herpesviruses and other large DNA virus families.

115 he ubiquitous human circular single-stranded DNA virus family Anelloviridae, there is still no convin

116 Parvovirus 4 (PARV4) is a DNA virus frequently associated with human immunodeficie

117 Vaccinia virus (VV) is an enveloped DNA virus from the poxvirus family and has played a cruc

118 In many DNA viruses, genome packaging is initiated by the small

119 on silencing, especially for newly infecting DNA virus genomes entering the nucleus.

120 de editing through assembly methods in large DNA virus genomes raises dual-use concerns, we believe t

121 Herpesviruses are DNA viruses harboring the capacity to establish lifelong

122 chanisms that a small RNA virus and a larger DNA virus have evolved to drive the fusion of viral and

123 Throughout evolution, large DNA viruses have been usurping genes from their hosts to

124 For example, many vertebrate DNA viruses have hijacked cellular genes encoding cytoki

125 In contrast to RNA viruses, double-stranded DNA viruses have low mutation rates yet must still adapt

126 The large DNA viruses, herpes simplex and pseudorabies viruses, us

127 lication and demonstrate a novel strategy of DNA virus-host interaction.

128 The DNA virus human cytomegalovirus (HCMV) encodes a viral C

129 Mimivirus is one the largest DNA virus identified so far, infecting several Acanthamo

130 ctional transcription factors of other large DNA viruses, IE1 is an essential, site-specific DNA-bind

131 ovides the first evidence of an encephalitic DNA virus in its natural host causing increased MMP acti

132 but the cellular mechanisms that inhibit the DNA virus in macrophages are unknown.

133 nflammatory responses after infection with a DNA virus in vivo.

134 lation of the type I IFN response to RNA and DNA viruses in antiviral immunity.

135 ase, is activated by single stranded RNA and DNA viruses in endocytic compartments resulting in endos

136 s a large-scale overview of the landscape of DNA viruses in human malignant cancers.

137 functions broadly to inhibit replication of DNA viruses in nondividing macrophages.

138 It is suitable for sequencing either RNA or DNA viruses in the field during outbreaks or as an inexp

139 ls were highly susceptible to infection with DNA viruses including HSV1, a variant of which is being

140 During assembly, double-stranded DNA viruses, including bacteriophages and herpesviruses,

141 well-studied inhibitor of a range of RNA and DNA viruses, including influenza A virus (FLUAV) and hep

142 ic effector that restricts enveloped RNA and DNA viruses, including influenza A, Zika, Ebola, Sindbis

143 ice enhances infectivity by multiple RNA and DNA viruses, including orthomyxoviruses (influenza A), p

144 gly conserved in the complex double-stranded DNA viruses, including the herpesviruses and many bacter

145 zed as a broadly acting inhibitor of RNA and DNA viruses, including the orthomyxovirus influenza A vi

146 ism illustrates another novel means by which DNA viruses incorporate host death regulators that are m

147 dsDNA or infection of dendritic cells with a DNA virus induced the formation of dsDNA-Rad50-CARD9 sig

148 Here we found that infection with DNA viruses induced interaction of the metabolic checkpo

149 for recruitment to ALRs, as an inhibitor of DNA virus-induced activation of ALR inflammasomes in viv

150 The largest known DNA viruses infect Acanthamoeba and belong to two marked

151 Circular single-stranded DNA viruses infect archaea, bacteria, and eukaryotic org

152 The curiosity-driven discovery of giant DNA viruses infecting amoebas has triggered an intense d

153 alpha-helical TM proteins in double-stranded DNA viruses infecting bacteria and archaea reveals large

154 uses are a group of single-stranded circular DNA viruses infecting humans and other animal species.

155 ablished long before that of double-stranded DNA viruses infecting more complex organisms.

156 r that is essential for host defense against DNA virus infection and appears important in defense aga

157 radigm of the role of Rb inactivation during DNA virus infection and uncovers the existence of an alt

158 he biology of these SINE ncRNAs, explore how DNA virus infection may lead to their induction, and des

159 DNA transfection or DNA virus infection of mammalian cells also triggered cG

160 Here, we analyzed the role of RNAi in DNA virus infection using Drosophila melanogaster infect

161 n (IFN) response to transfected DNA ligands, DNA virus infection, and lentivirus infection.

162 cated in antiviral cell death signaling upon DNA virus infection.

163 ents of rare diseases and valuable models of DNA virus infection.

164 rferon-beta induction by DNA transfection or DNA virus infection.

165 cytokines in response to DNA transfection or DNA virus infection.

166 ng that vsiRNAs contribute to the control of DNA virus infection.

167 n the intrinsic antiviral immune response to DNA virus infection.

168 ered a potential anti-inflammatory agent for DNA-virus infection.

169 However, the roles of IFITMs in DNA virus infections have not been studied in detail.

170 ar staining was also present in some RNA and DNA virus infections.

171 no known latency mechanism for chronic small DNA virus infections.

172 nate immunity, leading to the persistence of DNA virus infections.Proteins of the TRIM family have re

173 oma-associated herpesvirus (KSHV), a nuclear DNA virus, inhibits mRNA export in a transcript-selectiv

174 mutant flies to many viruses, including the DNA virus invertebrate iridescent virus 6.

175 Host innate immune responses to DNA viruses involve members of the nucleotide-binding do

176 viral particle stability for double-stranded DNA viruses is the energetically unfavorable state of th

177 roviruses (family Phycodnaviridae) are large DNA viruses known to infect certain eukaryotic green alg

178 -36 to regulate infection of closely related DNA viruses: KSHV, Epstein-Barr virus (EBV), and herpes

179 nderstanding of the evolution of other large DNA viruses, like poxviruses, that are reported to share

180 Polyomaviruses (PyVs) are small DNA viruses, long known to be important as etiological a

181 f baculoviruses, a group of insect-infecting DNA viruses, many of which have been used in biocontrol.

182 These putative large DNA viruses may be infected by B. natans virophages.

183 observation that the genomes of other large DNA viruses might bear SLAM family homologs further unde

184 omes make evolution in these double-stranded DNA viruses more efficient than that in smaller RNA viru

185 tibility to infection by the double-stranded DNA viruses mouse cytomegalovirus (MCMV) and human adeno

186 rus, vesicular stomatitis virus (VSV), and a DNA virus, murine gammaherpes virus (MHV-68).

187 other viruses of the nucleocytoplasmic large DNA virus (NCLDV) clade.

188 of related viruses, nucleo-cytoplasmic large DNA viruses (NCLDV).

189 ey on giant viruses (nucleocytoplasmic large DNA viruses; NCLDVs), which are themselves parasites of

190 , is nearly identical by sequence to another DNA virus, NIH-CQV, previously detected in Chinese patie

191 s an evolutionarily conserved strategy among DNA viruses of insects and mammals.

192 Poxviruses are large DNA viruses of vertebrates and insects causing disease i

193 important in immunity to cytosolic bacteria, DNA viruses, or HIV.

194 Some DNA viruses overcome plant defenses by producing a suppr

195 h histones are found in the capsids of small DNA viruses (papovaviruses), none are found in the capsi

196 to have a role in the antiviral response to DNA viruses, physiological RNA species recognized by RIG

197 cribed to occur in 3 other families of large DNA viruses, poxviruses, baculoviruses, and mimiviruses,

198 egin to study natural variation, we analyzed DNA viruses present in the lower gastrointestinal tract

199 The recombinant baculoviruses produced viral DNA, virus progeny, and some viral proteins earlier duri

200 ion of a wide variety of analytes, including DNA, viruses, proteins, chemical vapors, and pesticides.

201 Poxviruses, a family of large cytoplasmic DNA viruses, rely on the intracellular membranes to deve

202 Most DNA viruses replicate in the nucleus and exit it either

203 ruses, unlike many well-characterized animal DNA viruses, replicate entirely within the cytoplasm of

204 DNA viruses replicating in the nucleus challenge the res

205 t report of a proviral function of IFITMs in DNA virus replication.

206 Immunity against plasmids and DNA viruses requires DNA, but not RNA, cleavage activity

207 Human adenoviruses are double-stranded DNA viruses responsible for numerous infections, some of

208 w that TRIM29 is induced upon infection with DNA viruses, resulting in degradation of STING, decrease

209 ahedral, membrane-containing double-stranded DNA virus--Salisaeta icosahedral phage 1 (SSIP-1) and it

210 ages are recently discovered double-stranded DNA virus satellites that prey on giant viruses (nucleoc

211 clic GMP-AMP synthase (cGAS) is an essential DNA virus sensor that triggers type I interferon (IFN) s

212 A novel circular DNA virus sequence is reported from grapevine.

213 viral reads, followed by 9 to 17% for CRESS DNA virus sequences.

214 During infection with DNA viruses STING is activated downstream of cGAMP synth

215 which IFNs, particularly IFN-gamma, inhibit DNA viruses such as cytomegalovirus (CMV) is still not f

216 DNA viruses such as herpesviruses have relatively large

217 than in the context of large double-stranded DNA viruses such as herpesviruses.

218 The genomes of DNA viruses such as human cytomegalovirus (HCMV) are dev

219 The assembly of "complex" DNA viruses such as the herpesviruses and many tailed ba

220 h suppresses infection by a range of RNA and DNA viruses (such as influenza A virus [FluAV]), is inef

221 latively recent emergence of single-stranded DNA viruses, such as chicken anemia virus (CAV) and porc

222 Many double-stranded DNA viruses, such as Epstein-Barr virus, can establish p

223 cator of the possible presence of pathogenic DNA viruses, suggests that the thawing of permafrost eit

224 Most vertebrate and plant RNA and small DNA viruses suppress genomic CpG and UpA dinucleotide fr

225 mplex modifications of HSV-1 and other large DNA viruses than previous technologies, facilitating man

226 ia virus (CAV) is a single-stranded circular DNA virus that carries 3 genes, the most studied of whic

227 simplex virus-1 (HSV-1) is a double-stranded DNA virus that causes life-long infections.

228 virus (HCMV) is an enveloped double-stranded DNA virus that causes severe disease in newborns and imm

229 galovirus (HCMV) is a large, double-stranded DNA virus that causes significant human disease, particu

230 bursaria chlorella virus 1 (PBCV-1), a large DNA virus that infects green algae, encodes a histone H3

231 Hepatitis B is a DNA virus that infects liver cells and can cause both ac

232 African swine fever virus, a double-stranded DNA virus that infects pigs, is the only known member of

233 g multiple viral proteins encoded by a human DNA virus that inhibit the cGAS-STING DNA sensing pathwa

234 s sarcoma-associated herpesvirus (KSHV) is a DNA virus that is linked to several human malignancies.

235 JCV is a ubiquitous small DNA virus that leads to persistent infection of humans w

236 BKPyV is a nonenveloped DNA virus that must traffic through the endoplasmic reti

237 is B and prototypic hepadnavirus, is a small DNA virus that replicates by protein-primed reverse tran

238 simplex virus 1 (HSV-1) is a double-stranded DNA virus that replicates in the nucleus of the host cel

239 newly discovered icosahedral double-stranded DNA virus that was isolated from an environmental sample

240 omaviruses are nonenveloped, double-stranded DNA viruses that are associated with both benign and mal

241 Polydnaviruses are large, double-stranded DNA viruses that are beneficial symbionts of parasitoid

242 e a unique group of circular double-stranded DNA viruses that are considered parasites of giant DNA v

243 Baculoviruses are insect-specific DNA viruses that are highly pathogenic to their insect h

244 on of a family of proteins encoded by insect DNA viruses that are homologous to a 12-kDa circulating

245 irus are small, nonenveloped single-stranded DNA viruses that are nonpathogenic in humans but have po

246 lomaviruses (PVs) are small, double-stranded DNA viruses that are responsible for cervical, oropharyn

247 sses, but also as a natural barrier for most DNA viruses that assemble their nucleocapsids in the nuc

248 ted viruses (AAVs) are small single-stranded DNA viruses that can package and deliver nongenomic DNA

249 ruses (HAdVs) are ubiquitous double-stranded DNA viruses that cause a wide array of diseases in human

250 nother potential target for gene editing are DNA viruses that cause chronic pathogenic diseases that

251 (HSV-1) and HSV-2 are large, double-stranded DNA viruses that cause lifelong persistent infections ch

252 Geminiviruses are single-stranded DNA viruses that cause serious diseases in many crops.

253 constitute a large family of single-stranded DNA viruses that cause serious losses in important crops

254 Geminiviruses are DNA viruses that cause severe crop losses in different p

255 Papillomaviruses are small, double-stranded DNA viruses that encode the E2 protein, which controls t

256 s 1 and 2 (HSV-1 and HSV-2) are large-genome DNA viruses that establish a persistent infection in sen

257 Adenoviruses are linear double-stranded DNA viruses that infect human and rodent cell lines, occ

258 Poxviruses are unique among DNA viruses that infect mammalian cells, in that their r

259 Ascoviruses are insect-specific large DNA viruses that mainly infect noctuid larvae, and are t

260 pe 2 (GHV-2) genomes, generating recombinant DNA viruses that now circulate in wild birds and poultry

261 t and heterogeneous group of double-stranded DNA viruses that preferentially infect the cutaneous and

262 eport 18 genome sequences of double-stranded DNA viruses that putatively infect widespread sulfur-oxi

263 Poxviruses are large DNA viruses that replicate within the cytoplasm and enco

264 viridae is a large family of double-stranded DNA viruses that selectively infect insects.

265 Parvoviruses are single-stranded DNA viruses that use the palindromic structures at the e

266 h the previously described icosahedral large DNA viruses, the Pandoraviruses appear unrelated to them

267 In most icosahedral double-stranded (ds) DNA viruses, the viral genome enters and exits the capsi

268 uppressed replication of a broad spectrum of DNA viruses through inhibition of mRNA transcription.

269 y mechanism we report allows double-stranded DNA viruses to achieve rapid, high-density packing of th

270 r evidence of the ability of double-stranded DNA viruses to acquire drug resistance through gene dupl

271 gene duplications can enable double-stranded DNA viruses to adapt rapidly to environmental pressures

272 HRVs were less likely than DNA viruses to be codetected with another virus, suggest

273 ribe the structure of faustovirus, the first DNA virus (to our knowledge) that has been found to use

274 No DNA virus transcripts were detected in acute myeloid leu

275 merges during infection with a retrovirus or DNA virus triggers antiviral type I interferon responses

276 Infection of cells with DNA viruses triggers innate immune responses mediated by

277 The small DNA virus TTV was unexpectedly found in all culture-nega

278 Many DNA viruses use powerful molecular motors to cleave conc

279 arr virus and possible other double-stranded DNA viruses use TRIM29 to suppress local innate immunity

280 estimated the relative abundances of RNA and DNA viruses using a mass ratio approach and conducted sh

281 hat the genetic diversity of double-stranded DNA viruses was generated over long periods of time, sim

282 of influenza B viruses but not other RNA or DNA viruses was seen.

283 viruses and host genomes or between RNA and DNA viruses, was previously thought to be practically no

284 h human cytomegalovirus (HCMV), an enveloped DNA virus, we performed a semiquantitative, temporal ana

285 Herpes simplex virus (HSV) is a large DNA virus which is characterized by its ability to form

286 rgence of previously unknown double-stranded DNA viruses which delineate and extend the diversity of

287 Many double-stranded DNA viruses which parasitize such hosts, including the f

288 rdance in exit strategies among some RNA and DNA viruses, which exploit autophagy pathway for their r

289 ruses that are considered parasites of giant DNA viruses, which in turn are known to infect eukaryoti

290 Unlike double-stranded DNA viruses, which pump their genome into a preformed ca

291 cytoplasmic innate recognition molecule for DNA viruses whose function is lost in a variety of cance

292 Human cytomegalovirus (HCMV) is a complex DNA virus with a 230-kb genome encoding 170 and up to 75

293 SFV) is a highly pathogenic, double-stranded DNA virus with a marked tropism for cells of the monocyt

294 tive cycle of vaccinia virus (VACV), a large DNA virus with about 200 genes.

295 epatitis B virus is a partly double-stranded DNA virus with several serological markers: HBsAg and an

296 available database of 3908 isolate reference DNA viruses with 264 413 computationally identified vira

297 n may provide a way for poxviruses and other DNA viruses with high-fidelity DNA polymerases to adjust

298 H(2)O(2) rapidly inactivates both RNA and DNA viruses with minimal damage to antigenic structure o

299 pic, nonenveloped, circular, double-stranded DNA viruses within the family Papillomaviridae that are

300 We hypothesized that DNA viruses would target inflammasomes to overcome host