ライフサイエンスコーパス: symbiotic

1 n nature vary from competitive to neutral to symbiotic.

2 m); (2) cosmopolitan distributions, (3) non-symbiotic, (4) solitary or small colonies and (5) bleach

3 Symbiotic algae also have an elevated carbon-to-nitrogen

4 coral animal in concert with its unicellular symbiotic algae and a wide diversity of closely associat

5 nic nutrients reduced the diversity of coral-symbiotic algal interactions and caused nutrient and car

6 lmata and Porites porites) to test how coral-symbiotic algal interactions changed under real-world co

7 AraC-like transcription factor CuxR in plant symbiotic alpha-proteobacteria.

8 genes showed similar expression patterns in symbiotic and aposymbiotic anemones, suggesting that thi

9 Compared with symbiotic and free-living chemoautotrophs, Ca R. santand

10 s a versatile fungus with saprophytic, plant symbiotic and insect pathogenic lifestyle options.

11 small molecule signals is important for both symbiotic and pathogenic relationships, but is often poo

12 We traced the macroevolutionary history of symbiotic and phenotypic diversification in an iconic sy

13 ition of dinoflagellates from free-living to symbiotic and propose strategies for future research to

14 ccurate differentiation between the healthy (symbiotic) and unhealthy (dysbiotic) microbial state has

15 bacteria ample opportunity for mutualistic, symbiotic, and pathogenic interactions.

16 embly and global-scale biogeography of plant symbiotic arbuscular mycorrhizal (AM) fungal communities

17 Here we modelled the global diversity of symbiotic arbuscular mycorrhizal (AM) fungi using curren

18 first virus found to infect Nanoarchaeota, a symbiotic archaean found in acidic hot springs of Yellow

19 ermites, and beetles independently evolved a symbiotic association with lignocellulolytic fungi culti

20 abolic integration impacts the benefits of a symbiotic association, and the potential evolution of no

21 n adaptive response by fine roots to promote symbiotic association, as evidenced by the higher coloni

22 proaches will improve understanding of these symbiotic associations and, in the long term, their usef

23 uscular mycorrhizas (AM) are the most common symbiotic associations between a plant's root compartmen

24 ncreasing our understanding of the role that symbiotic associations have in animals.

25 er, our results reveal that establishment of symbiotic associations in M. truncatula requires DREPP i

26 Symbiotic associations in the rhizosphere between plants

27 it aerial eCO(2) cues to roots, to alter the symbiotic associations remain unknown.

28 IV MLOs are involved in the establishment of symbiotic associations with beneficial fungi, a role tha

29 izobia are soil bacteria that form important symbiotic associations with legumes, and rhizobial surfa

30 errestrial environments where they thrive in symbiotic associations with plants and animals and are i

31 pressure for saprotrophic fungi to switch to symbiotic associations with plants.

32 ological niches across the broad spectrum of symbiotic associations, from free-living to putative obl

33 Given its role in such diverse symbiotic associations, we hypothesized that the CSP als

34 ction as effector proteins that may regulate symbiotic associations.

35 Environmental pH can be an important cue for symbiotic bacteria as they colonize their eukaryotic hos

36 Symbiotic bacteria assist in maintaining homeostasis of

37 Although engineered symbiotic bacteria have been shown to render mosquitoes

38 ious microenvironments of the gut, with some symbiotic bacteria having evolved traits to invade the e

39 en coral bleaching and disease, the roles of symbiotic bacteria in holobiont resistance and susceptib

40 which may contribute to the biogeography of symbiotic bacteria in the gut.

41 Here, we investigated whether symbiotic bacteria isolated from toxic newts could produ

42 The symbiotic bacteria of entomopathogenic nematodes, Xenorh

43 spectrum antibacterial activity against some symbiotic bacteria of leguminous plants.

44 were more abundant in predatory mites, while symbiotic bacteria prevailed in prey mites.

45 In addition to metabolic benefits, symbiotic bacteria provide the host with several functio

46 l have orthologs in other phytopathogenic or symbiotic bacteria, and are involved in the modulation a

47 ulate TTX from their food or acquire it from symbiotic bacteria, but its origin in amphibians is uncl

48 requires infection of the root hairs by soil symbiotic bacteria, collectively referred to as rhizobia

49 bacteriocytes, the specialized cells housing symbiotic bacteria, during their cell death.

50 re array compatibly accommodates N(2)-fixing symbiotic bacteria, which receive energy and reducing eq

51 , in part, mediated by EVs released by these symbiotic bacteria.

52 roducts has been traced to partnerships with symbiotic bacteria.

53 hosts of CPB by chemical elicitors and their symbiotic bacteria.

54 es which inject and feed on entomopathogenic symbiotic bacteria.

55 ecture important for pathogenic oomycete and symbiotic bacterial interactions in legumes.

56 l for the interactions of many pathogenic or symbiotic bacterial species with their respective eukary

57 d light organ impacts the physiology of this symbiotic bacterium in vivo through CysB-dependent gene

58 This symbiotic bacterium was present in almost all individual

59 We show that a single sponge symbiotic bacterium, Entotheonella sp., constitutes the

60 We engineered a symbiotic bee gut bacterium, Snodgrassella alvi, to indu

61 fields of treatment and diagnosis as in vivo symbiotic bioelectronics.

62 Finally, an hnoX mutant formed larger symbiotic biofilms.

63 assimilation transcripts become elevated in symbiotic Breviolum minutum algae as they reach high-den

64 hila Jonah66Ci is upregulated in response to symbiotic (carrying the mutualistic bacterium Xenorhabdu

65 ion threads, endocytotic uptake of bacteria, symbiotic cells carrying thousands of intracellular bact

66 of nodule organogenesis, the functioning of symbiotic cells, and the evolution of symbiosis in the N

67 Many of these genes are only active in symbiotic cells, reflecting the unique nature of nodules

68 s to thousands of genes, mostly expressed in symbiotic cells.

69 ccess is inexorably linked to their diet and symbiotic cellulolytic intestinal microorganisms.

70 N into host and symbiont cells of the model symbiotic cnidarian Aiptasia (Exaiptasia pallida) when c

71 terol transporter are vastly up-regulated in symbiotic cnidarians.

72 Efficient symbiotic colonization of the squid Euprymna scolopes by

73 bacteria undergo during the early stages of symbiotic colonization.

74 als have coevolved with a large community of symbiotic, commensal, and some potentially pathogenic mi

75 our data demonstrate that specific pulmonary symbiotic commensals can promote lung fibrosis by regula

76 animals studied to date are associated with symbiotic communities of microorganisms.

77 Individual genomes in these symbiotic complexes differ dramatically in relative abun

78 for the diurnal rhythms underlying a dynamic symbiotic conversation.

79 biome, which is achieved at least in part by symbiotic cooperation with innate host defense.

80 profiles of endophyte and host plant imply a symbiotic cross-species biosynthesis pathway for astin C

81 cs to investigate how the acquisition of the symbiotic cyanobacterium Candidatus Synechococcus feldma

82 h similarities between the genes used by the symbiotic Cycloclasticus to degrade short-chain alkanes

83 ructures in species with different levels of symbiotic dependence has impacted leaf/stem scaling.

84 h chronic skin GVHD and confirm parallel but symbiotic developmental pathways of Th22 and Th17 differ

85 e plants fix atmospheric nitrogen by hosting symbiotic diazotrophic rhizobia or Frankia bacteria in r

86 Many corals harbour symbiotic dinoflagellate algae.

87 ain promotes colonization of the host by the symbiotic dinoflagellate Symbiodinium minutum.

88 response to high temperature across various symbiotic dinoflagellates in four common Pacific coral s

89 Interactions between symbiotic ectomycorrhizal (EM) and free-living saprotrop

90 n host investment could promote variation in symbiotic effectiveness and prevent the extinction of in

91 th three Bradyrhizobium strains that vary in symbiotic effectiveness on sympatric hosts.

92 Using symbiotic farming methods [cover crops and chicken grazi

93 al biofilms by up-regulating expression of a symbiotic filamentous inoviral prophage, Pf4.

94 ould be considered as powerful regulators of symbiotic function.

95 aded between mutualists, thereby influencing symbiotic function.

96 ent in saprotrophic ancestors to fulfill new symbiotic functions, (3) diversification of novel, linea

97 e bacterial diversity or to govern important symbiotic functions.

98 species, yet interactions between plants and symbiotic fungi (mutualists and potential pathogens) aff

99 Symbiotic fungi associated with plant roots can shuttle

100 Applying the species pool concept to symbiotic fungi facilitated a better understanding of ho

101 phytes are one of the most diverse guilds of symbiotic fungi found in the photosynthetic tissues of e

102 seudohyphal growth, and transcription in non-symbiotic fungi from the Ascomycete and Basidiomycete ph

103 he DNA of opportunistic, phytopathogenic and symbiotic fungi were detected, which might have been int

104 use and greatest photosynthate allocation to symbiotic fungi.

105 sue colonization by saprobic, pathogenic and symbiotic fungi.

106 lem to complete their life cycle, feeding on symbiotic fungi.

107 Here, we show how a symbiotic fungus mediates trade with a host root in resp

108 ocado where they have been found to vector a symbiotic fungus, Raffaelea lauricola, the causal agent

109 al guilds for which there were previously no symbiotic genomes available, including ectomycorrhizal R

110 Symbiotic Glbs derive from class 1 or class 2 Glbs and t

111 This symbiotic glioma-macrophage interplay provides therapeut

112 dy by Sugiura and coworkers reported the non-symbiotic growth and spore production of an arbuscular m

113 We previously showed that symbiotic gut bacteria from CPB larvae suppressed jasmon

114 The symbiotic gut microbiota play pivotal roles in host phys

115 hin legume nodules, but the functions of non-symbiotic hemoglobins or phytoglobins (Glbs) are much le

116 Symbiotic hemoglobins provide O(2) to N(2) -fixing bacte

117 t and stable 'mixed' GRN rather than being a symbiotic heterogeneous mix of cells.

118 commensal microbes has led to development of symbiotic host-microbiota relationships(1).

119 A (PSA) of Bacteroides fragilis is the model symbiotic immunomodulatory molecule.

120 archaeon association is both mutualistic and symbiotic; in this case, each microbe relies on its part

121 We studied the symbiotic infection phenotypes of S. meliloti mutants de

122 cast new light on a critical early stage of symbiotic initiation in the V. fischeri-squid model symb

123 In holometabolous symbiotic insects, metamorphosis entails a complete and

124 The symbiotic interaction between legumes and nitrogen-fixin

125 al CelC2 cellulase in different steps of the symbiotic interaction Rhizobium leguminosarum-Trifolium

126 nd drought tolerance; and (3) CO2 effects on symbiotic interactions and eco-evolutionary feedbacks.

127 roles of bacteria, host, and environment on symbiotic interactions and microbiome formation in basal

128 We posit that mutual symbiotic interactions are well described by three eleme

129 Symbiotic interactions between eukaryotes and prokaryote

130 understand the evolutionary significance of symbiotic interactions in nature, microbiome studies can

131 ous stages of macronutrient deficiencies and symbiotic interactions with rhizobia and mycorrhiza were

132 In legume plants, low-nitrogen soils promote symbiotic interactions with rhizobial bacteria, leading

133 se the likelihood of establishing beneficial symbiotic interactions.

134 ism and cellular physiology, morphology, and symbiotic interactions.

135 g of tissues as well as for host-parasite or symbiotic interactions.

136 ial to manipulate the relative proportion of symbiotic interfaces via modulation of RAM1 However, the

137 rected approaches to increase the density of symbiotic interfaces will require a more focused, potent

138 Thus, symbiotic intestinal bacteria modulate antiviral immunit

139 ghly specific and intimate associations with symbiotic, intracellular bacteria and highlights that sy

140 ies are enriched in functions related to the symbiotic lifestyle (e.g., CRISPR system, Eukaryotic-lik

141 and functional diversity contributes to the symbiotic lifestyle and aids in nutrient cycling.

142 cavity-provide a rare glimpse into the novel symbiotic lifestyle of these enigmatic human-associated

143 derstand the molecular underpinning of their symbiotic lifestyle.

144 umerous adaptations are gained in light of a symbiotic lifestyle.

145 Our work expands the range of archaeal symbiotic lifestyles and provides a genetically tractabl

146 c fungi observed in culture can translate to symbiotic lifestyles.

147 iving, Symbiodiniaceae diversified mainly as symbiotic lineages.

148 aper presents two 1:10 scale prototypes of a Symbiotic Machine for Ocean uRanium Extraction (SMORE) w

149 ryo and ensuing lethality in crosses between symbiotic males and either aposymbiotic females or femal

150 will aid in the elucidation of the different symbiotic mechanisms(s).

151 onditions that alter the relationships among symbiotic members.

152 acterial and archaeal cells that underwent a symbiotic merger.

153 Herein, we review recent progress on symbiotic microbe-arbovirus interactions and summarize t

154 tance to pathogens or the ability to recruit symbiotic microbes from the environment.

155 Symbiotic microbes impact the function and development o

156 further studies should routinely incorporate symbiotic microbes in their experimental designs.

157 in host defense, but less is known about how symbiotic microbes mediate pathogen-induced damage to ho

158 There is growing evidence that symbiotic microbes play key roles in host defense, but l

159 the dissemination in mosquitoes of inherited symbiotic microbes to block Plasmodium transmission.

160 system to accommodate invasive structures of symbiotic microbes.

161 Symbiotic microbial communities are important for host h

162 ic metals, sponges lack organs but harbour a symbiotic microbiome performing various functions.

163 It is increasingly recognized that symbiotic microbiota (especially those present in the gu

164 as evolved to promote the separation between symbiotic microorganisms and the intestinal epithelium a

165 More than 100 trillion symbiotic microorganisms constitutively colonize through

166 idence has established an important role for symbiotic microorganisms in vector-virus interactions wh

167 The trillion symbiotic microorganisms inhabiting the mammalian gastro

168 Social insect symbiotic microorganisms play a key role in intraspecifi

169 In arthropod vectors, symbiotic microorganisms residing in the gut lumen and/o

170 m pathogens is crucial for plants that allow symbiotic microorganisms to infect and colonize their in

171 Accumulating evidence suggests that symbiotic microorganisms, specifically the microbiota th

172 sophila rather than completely domesticated, symbiotic mobile elements.

173 These data support a symbiotic model of collective invasion where phenotypica

174 The early Frankia-Alnus symbiotic molecular exchanges were analyzed in detail by

175 Human disturbance inhibited non-symbiotic N fixation but not symbiotic N fixation.

176 dance can help improve the representation of symbiotic N fixation in Earth System Models.

177 not N-fixing trees, but the total amount of symbiotic N fixation was sufficient to account for most

178 of stem inventory data, in-situ measures of symbiotic N fixation, and simulations of N demand to eva

179 e inhibited non-symbiotic N fixation but not symbiotic N fixation.

180 creasing drought frequency, which may affect symbiotic N2 fixation (SNF), a process that facilitates

181 Symbiotic nitrogen (N) fixation has been shown to suppor

182 Symbiotic nitrogen (N)-fixing trees supply significant N

183 have uncovered nearly 200 genes required for symbiotic nitrogen fixation (SNF) in legumes.

184 ertainty in the land carbon cycle is whether symbiotic nitrogen fixation acts to enhance the tropical

185 f nodule cells and a substantial decrease in symbiotic nitrogen fixation and plant growth.

186 Symbiotic nitrogen fixation by rhizobia in legume root n

187 Symbiotic nitrogen fixation in legumes is mediated by an

188 Iron is an essential cofactor for symbiotic nitrogen fixation, required by many of the enz

189 on, seed oil content, disease resistance and symbiotic nitrogen fixation.

190 enes expressed during nodule development and symbiotic nitrogen fixation.

191 um cofactor of nitrogenase, is essential for symbiotic nitrogen fixation.

192 Symbiotic nitrogen fixers-which are insensitive to clima

193 Establishment of symbiotic nitrogen-fixation in legumes is regulated by t

194 tional traits, such as mycorrhizal types and symbiotic nitrogen-fixation.

195 e we use a theoretical model to suggest that symbiotic nitrogen-fixing trees could either mitigate (C

196 atula model to regulate root nitrogen-fixing symbiotic nodulation.

197 for receptor-mediated cytokinin signaling in symbiotic nodule organogenesis.

198 hylation was found in only a small subset of symbiotic nodule-specific genes, including more than hal

199 abeae legumes such as pea and faba bean form symbiotic nodules with a large diversity of soil Rhizobi

200 s of postembryonic organs, lateral roots and symbiotic nodules.

201 egume nodules have two types of hemoglobins: symbiotic or leghemoglobins (Lbs) and nonsymbiotic or ph

202 cibacteria have small genomes and a presumed symbiotic or parasitic lifestyle, but the difficulty in

203 trition to relationships that are commensal, symbiotic, or parasitic.

204 bust aggregate on the surface of the nascent symbiotic organ.

205 Such translocation strategies can help symbiotic organisms cope with exposure to resource inequ

206 when using metagenomic DNA from inseparable symbiotic organisms, RADseq loci may belong to any numbe

207 lants of the nitrogen-fixing clade (NFC) are symbiotic organs that function in the maintenance and me

208 sient nature of establishment makes study of symbiotic origins difficult, but experimental comparison

209 COs, when present in a mix with COs, drive a symbiotic outcome and this mix of signals is essential f

210 identities avoid immune activation and drive symbiotic outcome is still not fully understood.

211 should develop breeding methods to optimize symbiotic outcomes in crop species.

212 Here, we demonstrate a fully implanted symbiotic pacemaker based on an implantable triboelectri

213 The symbiotic pacemaker successfully corrects sinus arrhythm

214 xpression in the presence and absence of the symbiotic partner.

215 meliloti symbiosis, incompatibility between symbiotic partners frequently occurs, leading to the for

216 papers report nonrandom associations between symbiotic partners.

217 ed process involving many components of both symbiotic partners.

218 A symbiotic partnership with Blochmannia bacteria is thoug

219 t also impede the establishment of essential symbiotic partnerships.

220 ual framework to analyse trade strategies in symbiotic partnerships.

221 and how its biosynthesis is regulated by the symbiotic pathway.

222 Dwarf14-Like (D14L) receptor conditions pre-symbiotic perception of AM fungi, and also detects the s

223 f lichens, and reshapes our understanding of symbiotic persistence in a classic model of symbiosis.

224 nction to include the negative regulation of symbiotic persistence in host-strain interactions.

225 Furthermore, while symbiont identity and symbiotic phenotype influence the ecology and physiology

226 Root nodules are agricultural-important symbiotic plant-microbe composites in which microorganis

227 centrations and F(v) /F(m) ) are enhanced in symbiotic plants at low (-1 to 15 degrees C), but not at

228 ion arm, 1354 patients received prebiotic or symbiotic preparations, whereas 1369 patients in the con

229 dynamics of fixers and non-fixers along the symbiotic process in the Cupriavidus taiwanensis-Mimosa

230 l infections, but further progression of the symbiotic process was blocked.

231 t known when succinoglycan intervenes in the symbiotic process, and it is not known whether the plant

232 ays an important, but different role in this symbiotic process.

233 rane physiology as V. fischeri initiates its symbiotic program.

234 ignalling activation, de-represses essential symbiotic programmes and increases strigolactone hormone

235 lleled those of sTeLIC, a pLGIC from another symbiotic prokaryote.

236 This is further strengthened by the symbiotic quest of cardiac imaging and therapy for an in

237 to map the phosphorylation site(s) of plant symbiotic receptor-like kinases.

238 The critical symbiotic relation between host and mutualistic bacteria

239 The symbiotic relationship between legumes and rhizobium bac

240 Taken together, this study illustrates a symbiotic relationship between P2 and its marine host, t

241 The symbiotic relationship between the gut microbiome and th

242 Most of the microorganisms living in a symbiotic relationship in different animal body sites (m

243 e mechanisms for planted soybean that have a symbiotic relationship with bacteroids in their root nod

244 member of the oral microbiota and can have a symbiotic relationship with its hosts.

245 , possibly, the breakdown of this ostensibly symbiotic relationship.

246 isms that have co-evolved with the host in a symbiotic relationship.

247 ntrol within the host is needed to sustain a symbiotic relationship.

248 Symbiotic relationships between eukaryotic hosts and bac

249 form various regulatory functions to mediate symbiotic relationships between microbes and their hosts

250 s and nest-dwelling invertebrates may foster symbiotic relationships between them, but evidence is la

251 Symbiotic relationships encompass different lifestyles,

252 ve immunity, supporting that host-microbiota symbiotic relationships have evolved as a means to maint

253 genome-scale data from organisms involved in symbiotic relationships remains challenging.

254 Cyanobacteria are common in symbiotic relationships with diverse multicellular organ

255 Success depends exquisitely on their symbiotic relationships with microbial symbionts housed

256 helium form sophisticated barrier systems in symbiotic relationships with microbiota.

257 iation of orchids enables myriad fascinating symbiotic relationships with organisms across kingdoms.

258 gumes, and by some fungi that also establish symbiotic relationships with plants, notably the arbuscu

259 Moreover, soybean can form symbiotic relationships with Rhizobium bacteria to fix a

260 Legumes establish symbiotic relationships with soil bacteria (rhizobia), h

261 stic interactions between coexisting MGE and symbiotic relationships with the ir archaeal hosts.

262 are ubiquitous in cultivated soils, forming symbiotic relationships with the roots of major crop spe

263 dy size, each have the potential to decouple symbiotic relationships.

264 tanding of the factors controlling microbial symbiotic relationships.

265 may be important factors in shaping specific symbiotic relationships.

266 llus species, which benefit the host through symbiotic relationships.

267 Nature is full of examples of symbiotic relationships.

268 roduce, followed by the activation of either symbiotic responses that promote microbial colonization

269 n of intracellular host cell colonization by symbiotic rhizobia in Medicago truncatula requires repol

270 Symbiotic rhizobia-legume interactions are energy-demand

271 us, is the main route for delivering iron to symbiotic rhizobia.

272 hthora palmivora and colonization defects by symbiotic rhizobia.

273 ant responses to CelC2 during early steps of symbiotic rhizobial infection.

274 f the poplar rhizosphere showed evidence for symbiotic sharing of nutrients between the plant and the

275 + genotypes included orthologs to some known symbiotic signaling pathway genes, such as NFR5, NSP2, N

276 Beyond early, precontact symbiotic signaling, signal exchanges ensue throughout i

277 o-chitooligosaccharides (LCOs) are microbial symbiotic signals that also influence root growth.

278 oposed as arbuscular mycorrhizal (AM) fungal symbiotic signals.

279 Investigation of understudied and symbiotic sources has seen some success, yet no studies

280 t that NCR peptides are host determinants of symbiotic specificity in M. truncatula and possibly in c

281 clin gene expression between free-living and symbiotic states showed that several alveolate-specific

282 erate a spatially explicit global map of the symbiotic status of forests, using a database of over 1.

283 e regulatory protein NF-kappaB and cnidarian symbiotic status.

284 c oxide levels in response to infection with symbiotic Steinernema nematodes.

285 basidiomycete Hebeloma cylindrosporum before symbiotic structure differentiation with Pinus pinaster.

286 fungal determinants involved in ecto to endo symbiotic switch that occurs in desert truffle under dry

287 ology can determine the sRNAs present in any symbiotic system, but there are very few bioinformatic t

288 ta and shearinines in the fungus-growing ant symbiotic system.

289 noecy and dioecy, and codiversification in a symbiotic system.

290 expect it to be applicable to other similar symbiotic systems, especially other nodule-forming legum

291 and FISH approach for studies of complicated symbiotic systems.

292 olecules, which can be transposable to other symbiotic systems.

293 ences, affiliating with previously described symbiotic taxa were detected but their detection was rar

294 es whose much higher levels of expression in symbiotic than aposymbiotic anemones in the absence of s

295 tches resulting from divergence of secondary symbiotic traits could mediate host-symbiont specificity

296 The symbiotic unicellular cyanobacterium Candidatus Atelocya

297 sted three hypotheses for the maintenance of symbiotic variation in rhizobia that associate with a na

298 In essence, she presented a comprehensive symbiotic view of eukaryotic cell evolution (eukaryogene

299 N(2)-fixing cyanobacteria are symbiotic with diatoms and haptophytes.

300 These control templates are symbiotic with well-established mechanical templates, pr