ライフサイエンスコーパス: endosymbiont

1 rmore, we discuss what it takes to become an endosymbiont.

2 the eukaryotic host cell or the prokaryotic endosymbiont.

3 from the nucleus or (less likely) a cryptic endosymbiont.

4 es to altered proteome and physiology of the endosymbiont.

5 ular alterations to accommodate their fungal endosymbiont.

6 nding the host lineage for the mitochondrial endosymbiont.

7 of our cells, are remnants of a eubacterial endosymbiont.

8 contain the obligate intracellular Wolbachia endosymbiont.

9 o the compartment derived from the bacterial endosymbiont.

10 ated by infection of plants with a bacterial endosymbiont.

11 and about 12-fold coverage of its Wolbachia endosymbiont.

12 ted protein degradation (ERAD) system of the endosymbiont.

13 e host cell to harvest ATP from the enslaved endosymbiont.

14 report of pure culture of a thioautotrophic endosymbiont.

15 with the hosting of the proto-mitochondrion endosymbiont.

16 alaria parasites once contained a chlamydial endosymbiont.

17 occur to enable accommodation of the fungal endosymbiont.

18 cost-effective sequencing of the pathogen or endosymbiont.

19 chromosomes of O. volvulus and its Wolbachia endosymbiont.

20 virulence-enhancing properties of bacterial endosymbionts.

21 interactions between host species and their endosymbionts.

22 parallels that observed in some other insect endosymbionts.

23 istant past and have subsequently shed their endosymbionts.

24 amoebae, which are known to harbor bacterial endosymbionts.

25 to impose major morphological changes on the endosymbionts.

26 ction in many bacterial and eukaryotic algal endosymbionts.

27 of which are infected by Wolbachia bacterial endosymbionts.

28 the loss of adults, perhaps associated with endosymbionts.

29 ch 71% of species horizontally acquire algal endosymbionts [9].

30 Altogether, our study shows that an insect endosymbiont acquires specific lipidic metabolites from

31 most likely originated from a Rickettsiales endosymbiont already residing in the host, but not from

32 We show that these endosymbionts also attenuate the systemic release of vol

33 ort the hypothesis that plant infection with endosymbionts alters plant volatile profiles, and infect

34 centor ticks suggests that they may be viral endosymbionts, although further studies are needed to de

35 rones primarily inherited from its bacterial endosymbiont ancestor.

36 through an epistatic interaction between an endosymbiont and a paternally acting locus on the X chro

37 asts arose from a free-living cyanobacterial endosymbiont and divide by binary fission.

38 arly plastid endosymbiosis by connecting the endosymbiont and host carbon storage networks.

39 s established using components from both the endosymbiont and host cell through a modification of the

40 ts that created a stable association between endosymbiont and host during the process of organellogen

41 bilizing the partnership between the plastid endosymbiont and host through retargeting of proteins to

42 h may in turn alter interactions between the endosymbiont and its host.

43 genetic neighbor Frankia, a mesophilic plant endosymbiont and soil dweller.

44 s in cross-kingdom communication between the endosymbiont and the host.

45 -2 Proteobacteria, including N2-fixing plant endosymbionts and Brucella, a worldwide pathogen that fi

46 atus under these conditions in both Aiptasia endosymbionts and cultured Symbiodinium.

47 ourage radical genome erosion in mutualistic endosymbionts and other intracellular bacteria is discus

48 Antibiotic treatment eliminated both endosymbionts and restored an even sex ratio to subseque

49 ondria are derived from primordial bacterial endosymbionts and retain partial genomes.

50 strains, we found no evidence that bacterial endosymbionts and rhizoxin contribute to the pathogenesi

51 , nor did antibiotic-mediated eradication of endosymbionts and rhizoxin production decrease the virul

52 rences in heat tolerance caused by bacterial endosymbionts and showed the potential for rapid evoluti

53 ggest that hosts exerted strong control over endosymbionts and that there were no conditions where th

54 reasing rate, particularly between Wolbachia endosymbionts and their diverse invertebrate hosts.

55 t of intimate relationships such as those of endosymbionts and their invertebrate hosts, particularly

56 We differentially cured E. inaron of each endosymbiont, and crossed hosts of different infection s

57 The human body louse, its primary endosymbiont, and the bacterial pathogens that it vector

58 NCRs are targeted to the endosymbionts, and concerted action of different sets of

59 the genomes of other actinobacteria, legume endosymbionts, and plant pathogens.

60 coordinate the assembly and activity of the endosymbiont- and host-derived plastid division componen

61 In galegoid plants, the endosymbionts are terminally differentiated, uncultivabl

62 um genomes sequenced so far suggest that the endosymbionts are variable in their genome size, gene co

63 hondria, more so than plastids and bacterial endosymbionts, are prone to the repeated evolution of mu

64 host glutamine may be utilized by the algal endosymbiont as a primary nitrogen source.

65 cellular and intracellular pathogens as also endosymbionts as effectors targeting nucleic acids of ho

66 highly compartmentalized and have integrated endosymbionts as organelles, namely mitochondria and pla

67 iotics targeting common classes of bacterial endosymbionts attenuated Acanthamoeba virulence, as indi

68 ion will be particularly useful for devising endosymbiont-based strategies to intervene in insect imm

69 Endosymbiont-bearing fauna were very important in suppor

70 Paramoeba species harbor endosymbionts belonging to the Kinetoplastea, a diverse

71 ckroaches harbor the obligate flavobacterial endosymbiont Blattabacterium sp., which resides within t

72 ll size of the proteome of the Gram-negative endosymbiont Blochmannia floridanus to search for novel

73 m 2.3 x 10(-5) per nucleotide in mRNA of the endosymbiont Buchnera aphidicola to 5.2 x 10(-5) per nuc

74 s are sap-feeding plant pests and harbor the endosymbiont Buchnera aphidicola, which is essential for

75 t and are supplied by the obligate bacterial endosymbiont (Buchnera), which lives inside specialized

76 obligate and maternally inherited bacterial endosymbiont, Buchnera, were identified as differentiall

77 g blight fungus Rhizopus microsporus and its endosymbiont Burkholderia rhizoxinica form an unusual, h

78 izopus have been shown to harbor a bacterial endosymbiont (Burkholderia) that produces rhixozin, a pl

79 ing after the acquisition of a mitochondrial endosymbiont by a prokaryotic host cell >1.8 billion yea

80 ndependent incorporation of a cyanobacterial endosymbiont by Paulinella Our analyses include both bro

81 an Type Culture Collection were screened for endosymbionts by amplifying and sequencing bacterial 16S

82 e Leishmania guyanensis (L.g) harbor a viral endosymbiont called Leishmania RNA virus 1 (LRV1).

83 ting approach for this is to use a bacterial endosymbiont called Wolbachia that can populate mosquito

84 ional traits such that the combined host and endosymbiont can exploit vacant ecological niches and oc

85 strain of Francisella, indicating that tick endosymbionts can evolve from mammalian pathogens.

86 Theory suggests that maternally inherited endosymbionts can promote their spread and persistence i

87 that sex ratio distorters, such as Wolbachia endosymbionts, can be powerful agents of evolutionary tr

88 cicada species of the genus Tettigades, the endosymbiont Candidatus Hodgkinia cicadicola has split i

89 The genome of the obligatory louse endosymbiont Candidatus Riesia pediculicola encodes less

90 of the body louse and its primary bacterial endosymbiont Candidatus Riesia pediculicola.

91 ed the first complete genome of the obligate endosymbiont, Candidatus 'Uzinura diaspidicola', of armo

92 feeding insects is the presence of bacterial endosymbionts capable of providing essential nutrients t

93 ron is naturally infected with two unrelated endosymbionts, Cardinium and Wolbachia, both of which ha

94 o 5.2 x 10(-5) per nucleotide in rRNA of the endosymbiont Carsonella ruddii The similarity of transcr

95 mitogenome) sequences from three green algal endosymbionts (Chlorella heliozoae, Chlorella variabilis

96 isms were derived originally from prokaryote endosymbionts, chloroplasts retain comparatively few gen

97 s well as Coxiella-like and Francisella-like endosymbionts (CLEs and FLEs, respectively) occur in tic

98 A novel endosymbiont closely related to Mycobacterium spp. was i

99 tigated the potential effect of Acanthamoeba-endosymbiont coinfection in a human corneal tissue model

100 Host-microbe symbioses involving bacterial endosymbionts comprise some of the most intimate and lon

101 ssion profile of the cell lineage from which endosymbiont-containing host cells, called bacteriocytes

102 These endosymbionts contribute to inflammatory disease pathoge

103 splayed seasonal fluctuations in biomass and endosymbiont density related to annual temperature varia

104 We describe endosymbiont-derived, bacterial-like division systems co

105 nvolves the assembly and constriction of the endosymbiont-derived, tubulin-like FtsZ ring on the stro

106 The morphology and physiology of endosymbionts, despite their common function, are highly

107 However, fungal strains with or without endosymbionts did not differ in their ability to cause e

108 e known role of NCR peptides as effectors of endosymbionts' differentiation to nitrogen-fixing bacter

109 catalogue of the nuclear, mitochondrial and endosymbiont DNA variants generated in this study will s

110 ochondrial genes demonstrated that the three endosymbionts do not form a monophyletic group, indicati

111 uminosarum bv. viciae 3841, a pea-nodulating endosymbiont, encodes a sensor histidine kinase containi

112 ecognized as an important mechanism by which endosymbionts enhance host fitness.

113 d due to their intracellular lifestyle, many endosymbionts, especially those that switch hosts, are r

114 ed fundamental theories of bacteriophage and endosymbiont evolution, namely the phage Modular Theory

115 for import into the organelle into which the endosymbiont evolved.

116 Bacterial endosymbionts exert a variety of beneficial effects on i

117 tudy, we identified a novel Francisella-like endosymbiont (FLEs-Hd) from the tick Haemaphysalis doeni

118 Francisella-like endosymbionts (FLEs) with significant homology to Franci

119 oove, indicating a large dependence on their endosymbionts for nutrition.

120 nscription errors in Escherichia coli and in endosymbionts for which mutation and/or substitution rat

121 bacteria are obligate, maternally-inherited, endosymbionts found frequently in insects and other inve

122 rancisella philomiragia and Francisella-like endosymbionts found in ticks.

123 e of a previously uncharacterized Rickettsia endosymbiont from Culicoides newsteadi (RiCNE).

124 tionally defined when loss or removal of the endosymbiont from the host results in the death of both.

125 mpletion of essential pathways requires host/endosymbiont genome complementarity.

126 Overall, our data suggest that endosymbiont genome evolution alters tRNA characteristic

127 ads from endosymbiont-host LGTs can confound endosymbiont genome projects, erroneously altering the c

128 dicted wood-degrading enzymes encoded in the endosymbiont genomes, accumulate in the gut to the near

129 if there is no evidence for evolution in the endosymbiont genotype.

130 ween scleractinian corals and photosynthetic endosymbionts (genus Symbiodinium) are the foundation of

131 A Chlamydia-like endosymbiont has previously enhanced Acanthamoeba virule

132 DNA from the endosymbionts has bombarded nuclei since the ancestral p

133 deacylation of lipid A among nitrogen-fixing endosymbionts has not been characterized.

134 Although many functions of the original endosymbiont have been usurped by nuclear genes or inter

135 s and plastomes of the three newly sequenced endosymbionts have a standard set of genes compared with

136 our understanding of this globally pandemic endosymbiont, highlighting genetic patterns associated w

137 In contrast, the genome of the endosymbiont Hodgkinia cicadicola has fractured into mul

138 Sulcia's partner endosymbiont, Hodgkinia cicadicola, similarly remains co

139 nt ingests amoeba cytoplasm, a novel form of endosymbiont-host communication.

140 data, illustrating that sequence reads from endosymbiont-host LGTs can confound endosymbiont genome

141 ulating renewed interest in the long-dormant endosymbiont hypothesis of organelle origins.

142 Under the endosymbiont hypothesis, over a billion years ago a hete

143 ges in vector fecundity, physiology, primary endosymbionts (i.e. yeast-like symbionts, YLS) and feedi

144 e autophagy of bacteria and bacteria-derived endosymbionts-i.e., mitochondria.

145 coli genome, sequencing of minimal bacterial endosymbionts, identification of essential genes, and in

146 We detected a Francisella endosymbiont in 174 ticks (70%), and Rickettsia spp. in

147 xplain why some hosts are uninfected by this endosymbiont in nature.

148 EPNs harbor a bacterial endosymbiont in their gut that assists in insect killing

149 Endosymbionts in more recent and/or facultative relation

150 to define the role of rhizoxin production by endosymbionts in the pathogenesis of mucormycosis.

151 ent information on the involvement of insect endosymbionts in the response to parasitic nematode infe

152 related Gammaproteobacteria as intracellular endosymbionts in their gills.

153 Endosymbionts infect most arthropods and cause a wide va

154 vores initially settled on plants exposed to endosymbiont-infected psyllids but later defected and ov

155 Wolbachia pipientis is an intracellular endosymbiont infecting many arthropods and filarial nema

156 f M. fradeorum, we detected these same three endosymbionts infecting 55% of the spiders in almost all

157 controlled for the effects of herbivory and endosymbiont infection by exposing potato plants (Solanu

158 respect to both herbivory and herbivory plus endosymbiont infection when compared to undamaged contro

159 isms, and electron microscopy shows that the endosymbiont ingests amoeba cytoplasm, a novel form of e

160 However, what happens when multiple endosymbionts inhabit the same host?

161 evelopmental and cellular mechanisms of host/endosymbiont integration, work that heralds a new era in

162 s, yet how the nematodes and their bacterial endosymbionts interact with the insect immune system is

163 volutionary, genetic, developmental and host-endosymbiont interaction studies.

164 particularly useful taxon for investigating endosymbiont interactions, because they are host to a pl

165 Conversion of the bacterial endosymbionts into cell organelles involved the massive

166 instance of a non-photosynthetic, eukaryotic endosymbiont involves members of the genus Paramoeba, am

167 The endosymbiont is involved in complete or partial synthesi

168 tion, we show that the proliferation of this endosymbiont is limited by the availability of hemolymph

169 e 2 secretion system (T2SS) of the bacterial endosymbiont is required for the formation of the endosy

170 luence of genome reduction on translation in endosymbionts is largely unknown.

171 Wolbachia, one of the most widespread endosymbionts, is a target for biological control of mos

172 arasitism is male-killing which involves the endosymbiont killing all of the sons of infected females

173 te in the gut to the near exclusion of other endosymbiont-made proteins.

174 sets of peptides governs different stages of endosymbiont maturation, whereas the symbiotic function

175 Also, our findings suggest that the endosymbiont may not place negative selection pressure o

176 Among these partners, microbial endosymbionts may affect Se speciation in hyperaccumulat

177 ur results suggest that a dynamic network of endosymbionts may interact both within multiply infected

178 e results predicts that infection with these endosymbionts may reduce malaria prevalence in human pop

179 E. gennaroi (EG), not infected by bacterial endosymbionts, may have diverged because of the compleme

180 and an alphaproteobacterial (mitochondrial) endosymbiont merged together, resulting in the first euk

181 the use of a living contrast agent, magneto-endosymbionts (MEs) derived from magnetotactic bacteria

182 may explain differences in patterns of host/endosymbiont metabolic collaboration between the sap-fee

183 suggests that protein import into bacterial endosymbionts might be a phenomenon much more widespread

184 In the endosymbionts, mitochondria and chloroplasts, the vast m

185 bled the complete circular chromosome of its endosymbiont, Mycoavidus cysteinexigens, which we place

186 ansmission electron microscopy localized the endosymbiont near hydrogenosomes in the posterior part a

187 y altered the evolution of life by providing endosymbionts necessary for the emergence of eukaryotes

188 eficial apicomplexan: the mutualistic marine endosymbiont Nephromyces.

189 The endosymbiont nuclear genome is 9.5 Mbp in size, the sma

190 e the exchange of nutrients between host and endosymbiont occurs.

191 ary plastids descend from the cyanobacterial endosymbiont of an ancient eukaryotic host, but the init

192 Hamiltonella defensa, an endosymbiont of aphids and other sap-feeding insects, pr

193 era aphidicola, the reduced-genome bacterial endosymbiont of aphids, possess altered translational fe

194 h of the proteome of Wolbachia, the obligate endosymbiont of Bm that also expressed proteins in a sta

195 lts from Candidatus Hodgkinia cicadicola, an endosymbiont of cicadas, revealed that some lineages of

196 xemplified by Sulcia muelleri, a nutritional endosymbiont of cicadas.

197 Wolbachia is a ubiquitous intracellular endosymbiont of invertebrates.

198 present the draft genome for the Rickettsia endosymbiont of Ixodes scapularis (REIS), a symbiont of

199 green alga (Chlorella heliozoae) that is an endosymbiont of the heliozoon Acanthocystis turfacea, ca

200 Wolbachia species are endosymbionts of a wide range of invertebrates, includin

201 sp. strains, the nitrogen-fixing facultative endosymbionts of actinorhizal plants, have long been pro

202 nsmitted genetic elements, such as bacterial endosymbionts of arthropods.

203 from numerous studies on the dinoflagellate endosymbionts of corals, and yet the multi-copy nature a

204 a are the most abundant maternally inherited endosymbionts of insects and cause various reproductive

205 Many bacterial endosymbionts of insects are capable of manipulating the

206 Wolbachia bacteria are common endosymbionts of insects, and some strains are known to

207 Although some information on certain endosymbionts of N. cucumeris and T. putrescentiae exist

208 es characterized thus far have been found in endosymbionts of protozoa or pathogens of higher-order a

209 of the genus Symbiodinium are photosynthetic endosymbionts of stony corals that provide the foundatio

210 pheroid bodies' of Epithemia turgida and the endosymbionts of the amoeba Paulinella chromatophora.

211 tochondrion sHSPs did not originate from the endosymbionts of the chloroplast and mitochondria.

212 ood and other organic deposits, and that the endosymbionts of these progenitors made use of hydrogen

213 research is to establish the impact of this endosymbiont on vector competence.

214 de infections, and the influence of nematode endosymbionts on specific aspects of the insect immune s

215 s, these cells assemble into groups, such as endosymbionts or multicellular organisms; in turn, multi

216 tain their photosynthetic ability by hosting endosymbionts or stealing plastids from their prey - are

217 This feature could limit endosymbiont over-proliferation under conditions of host

218 ble genomic resources for understanding host-endosymbiont/parasitoid evolutionary relationships, reso

219 zone and by the extraordinary ability of its endosymbiont Pedinomonas noctilucae to fix carbon more e

220 criptomes of Paramoeba pemaquidensis and its endosymbiont Perkinsela sp.

221 , yet few studies have documented concurrent endosymbiont phenotypes or explored their potential inte

222 3-O-deacylated lipid A among nitrogen-fixing endosymbionts, plant endophytes, and plant pathogens has

223 Bioinformatic studies predict that tsetse endosymbionts possess part (up to homoserine in Wigglesw

224 The environmental protozoan endosymbiont Protochlamydia amoebophila UWE25 encodes fi

225 s had a minority of the reads supporting the endosymbiont reference base call using the capture data,

226 In this study, two strains of the endosymbiont Regiella insecticola (R. insecticola 5.15 a

227 oms and other chromalveolates from a cryptic endosymbiont related to prasinophyte-like green algae.

228 sporters, in contrast to their environmental endosymbiont relatives, without compromising their abili

229 rent obligate symbionts, and full or partial endosymbiont replacement.

230 The endosymbiont represents a new bacterial lineage in the g

231 esized to collectively play key roles in the endosymbiont's virulence against parasitoids, resulting

232 origins, although the unbiased genome of the endosymbiont Sodalis acted as an attractor for them.

233 The vertically transmitted endosymbionts (Sodalis glossinidius and Wigglesworthia g

234 opulations, were Wigglesworthia (the primary endosymbiont), Sodalis and Wolbachia as previously chara

235 ids (Acyrthosiphon pisum), several inherited endosymbiont species protect their hosts against parasit

236 estacea, which is protected by the bacterial endosymbiont Spiroplasma when parasitized by the nematod

237 mbiosis in composite P. vulgaris plants with endosymbionts such as Rhizobium tropici and Rhizophagus

238 or curing arthropods infected with bacterial endosymbionts such as Wolbachia.

239 g likewise host peptides for manipulation of endosymbionts, suggest convergent evolution.

240 f free-living algae alongside the hosts with endosymbionts, suggesting that symbionts could escape sy

241 lbachia, a widespread arthropod and nematode endosymbiont, suggests that this bacterium could be an e

242 ), with its closest known relative being the endosymbiont Sulcia muelleri, which is found in many sap

243 Interactions between the dinoflagellate endosymbiont Symbiodinium and its cnidarian hosts (e.g.

244 ear genomes that originated from the plastid endosymbiont: symbiogenetic genes (S genes).

245 sm is capable of generating blooms for other endosymbiont-targeting viruses.

246 Cyanobacteria, descendants of the endosymbiont that gave rise to modern-day chloroplasts,

247 s, derived from the ancestral cyanobacterial endosymbiont that gave rise to plastids.

248 ins descended from the alpha-proteobacterial endosymbiont that gave rise to the mitochondrion and was

249 n-related organelle exist, implying that the endosymbiont that gave rise to the mitochondrion was pre

250 HLB appears to have originated as an insect endosymbiont that has moved into plants.

251 lsonii is a maternally transmitted bacterial endosymbiont that is naturally associated with Drosophil

252 oduction was probably acquired with an algal endosymbiont that was retained as a non-photosynthetic p

253 nium are commonly recognized as invertebrate endosymbionts that are of central importance for the fun

254 tor of the nucleated cell engulfed bacterial endosymbionts that gradually evolved into the mitochondr

255 , pattern of tRNA loss in Buchnera and other endosymbionts that have undergone genome shrinkage.

256 clustered within a lineage of several insect endosymbionts that included Buchnera aphidicola.

257 Both organisms contain endosymbionts that possess the ability to interfere with

258 closely related to pathogens but function as endosymbionts that provide nutrients that are missing fr

259 Bacterial endosymbionts that provide nutrients to hosts often have

260 hloroplasts are relicts of ancient bacterial endosymbionts that ultimately extended the range of acce

261 Mitochondria are evolutionary endosymbionts that were derived from bacteria and so mig

262 tid-targeted proteins may originate from the endosymbiont, the host, or other sources entirely.

263 In stark contrast to its algal endosymbiont, the salamander cells did not exhibit major

264 nd originated from plastid and mitochondrial endosymbionts: the alpha and beta subunits of ATP syntha

265 gh the movement of cyanobacterial genes from endosymbiont to host is well studied, less is known abou

266 Like many insects, mosquitoes, rely on endosymbionts to grow and develop.

267 be a particularly common way for facultative endosymbionts to increase in frequency within host popul

268 The importance of microbial facultative endosymbionts to insects is increasingly being recognize

269 transcription error rates in these bacterial endosymbionts to that in E. coli (4.63 x 10(-5) per nucl

270 genes were functionally transferred from the endosymbionts to the nucleus.

271 this relies on unexamined assumptions about endosymbiont-to-host gene transfer [3-5].

272 cytoplasmic conflicts generated by Wolbachia endosymbionts triggered recurrent turnovers of sex deter

273 evidence indicating that Wolbachia bacterial endosymbionts triggered the evolution of new sex chromos

274 y reserves and changes in the dominant algal endosymbiont type (Symbiodinium spp.) facilitated rapid

275 Phenotypic plasticity in the dominant endosymbiont type of Orbicella faveolata did not prevent

276 The endosymbiont usurps or integrates into core host process

277 symbiosis at high light intensity, carrying endosymbionts was costly to hosts in the dark and confer

278 bolic reconstruction of the nematode and its endosymbiont, we identified enzymes that are likely to b

279 (MGDG) and phosphatidylglycerol (PG), of the endosymbiont were selected to function as the AKR2A rece

280 blood and included genes from the Wolbachia endosymbiont, which shows a simultaneous and coordinated

281 olution of the relationships of other insect endosymbionts, which appear to have had multiple origins

282 , despite a high prevalence of the Wolbachia endosymbiont--which is known to be protective against vi

283 estors of chloroplasts and mitochondria were endosymbionts whose genes became copied to the genomes o

284 rypanosomes, have coevolved with mutualistic endosymbiont Wigglesworthia glossinidiae.

285 tic lifestyle and likely replaced an ancient endosymbiont with degraded functionality.

286 bon fixation from its chlorophyll-containing endosymbiont with ingestion of prey.

287 mealybug Planococcus citri has two bacterial endosymbionts with an unusual nested arrangement: the ga

288 targeting the Onchocerca volvulus Wolbachia endosymbionts with doxycycline for these individuals wit

289 otrophs and that plants provide their fungal endosymbionts with fatty acids.

290 nstrates stage-specific expression by the Bm endosymbiont Wolbachia as well.

291 The endosymbiont Wolbachia is common among insects and known

292 The common bacterial endosymbiont Wolbachia manipulates its host's reproducti

293 melanogaster after removal of the bacterial endosymbiont Wolbachia pipientis by antibiotic treatment

294 Mosquito infection with the bacterial endosymbiont Wolbachia pipientis wMel is a novel strateg

295 azole (ABZ) and drugs depleting the filarial endosymbiont Wolbachia, a proven macrofilaricide target,

296 Interestingly, the endosymbionts Wolbachia and Rickettsia were detected onl

297 One endosymbiont, Wolbachia pipientis, infects a vast number

298 e, we show that in mosquitoes the introduced endosymbiont, Wolbachia, significantly suppresses expres

299 The target of doxycycline is the essential endosymbiont, Wolbachia.

300 e WO might be likened to phage lambda of the endosymbiont world.