ライフサイエンスコーパス: amoeba

1 g a certain plasticity of the pathway in the amoeba.

2 en's long term intracellular survival in the amoeba.

3 nt in an attempt to reflect the situation in amoeba.

4 had not been tested before in more than one amoeba.

5 at is coassembled with Mimivirus in the host amoeba.

6 t in the differentiation program of a social amoeba.

7 travacuolar proliferation in macrophages and amoeba.

8 vives in mammals, arthropods, and freshwater amoeba.

9 is thought to promote transmission to a new amoeba.

10 es such as nonseed plants, algae, fungi, and amoeba.

11 amoeba sori, and disseminates along with the amoeba.

12 nd late phases of erythrophagocytosis by the amoeba.

13 ases in viroids to 670 billion bases in some amoebas.

14 fungi (16 species), plants (6), diatoms (1), amoebas (2), protists (1) and animals (17).

15 AMOEBA, a second-generation force field, was chosen as i

16 tions of three dimorphic fungi with the soil amoeba Acanthameobae castellanii.

17 cessing of L. pneumophila by the free-living amoeba Acanthamoeba castellanii shows many similarities

18 as unable to multiply within the free-living amoeba Acanthamoeba castellanii yet was able to kill HL-

19 ffect on intracellular multiplication in the amoeba Acanthamoeba castellanii, indicating that certain

20 In the small, free-living amoeba Acanthamoeba castellanii, rRNA transcription requ

21 umophila genes necessary for survival in the amoeba Acanthamoeba castellanii.

22 a potential protozoan host, the water-borne amoeba Acanthamoeba castellanii.

23 ncystment phenotype (REP) in the free-living amoeba, Acanthamoeba castellanii.

24 uscle actin filaments (Kd = 0.5 microM) than amoeba actin filaments (Kd = 5 microM) even though the a

25 = 0.03 microM-1 s-1) to and dissociates from amoeba actin filaments in a simple bimolecular reaction,

26 ibits TH-2/3 binding to muscle actin but not amoeba actin filaments.

27 1 microM, for Acanthamoeba profilins binding amoeba actin monomers with bound Mg-ATP.

28 o-cultivated bacteria resemble arthropod- or amoeba-adapted Francisella is unknown.

29 that mannose-based saccharides which inhibit amoeba adhesion to corneal epithelial cells were also po

30 in vacuoles isolated from P2X(A)R knock-out amoeba and ablated in cells devoid of P2XRs.

31 ion that resulted in loss of infectivity for amoeba and HeLa cells and loss of Dot/Icm T4SS-mediated

32 the ankB null mutant in proliferation within amoeba and human cells is rescued by supplementation of

33 la pneumophila proliferates in environmental amoeba and human cells within the Legionella-containing

34 Both amoeba and human macrophages were challenged with L. pne

35 s, endogenous triuret has been identified in amoeba and human urine, the latter being diagnostic for

36 Following Ers treatment entry into amoeba and macrophage hosts does not require dotA, which

37 required for proper intracellular growth in amoeba and macrophage hosts.

38 hat function in the entry of Legionella into amoeba and macrophage hosts.

39 us that translocates bacterial proteins into amoeba and macrophage hosts.

40 Identification of these amoeba and mycobacteria strains indicated that the main

41 a is an intracellular pathogen of freshwater amoeba and of alveolar macrophages in human hosts.

42 ber of ADF/cofilin family, with filaments of amoeba and rabbit skeletal muscle actin.

43 Here we describe such a screen in a social amoeba and show that cheating is multifaceted by reveali

44 shed a model predator-prey system using this amoeba and Synechococcus elongatus PCC 7942.

45 uding chemical reactions, metal rust, yeast, amoeba and the heart and brain.

46 lution between bacterial husbandry in social amoebas and fungus farming in social insects makes sense

47 ve evolved mechanisms that are used to enter amoebas and human macrophages.

48 Upon entry of Legionella pneumophila into amoebas and macrophages, host-mediated farnesylation of

49 hing animals such as amphioxus, sea anemone, amoebas and Trichoplax, and in plants and algae.

50 nst four different taxa: insects, nematodes, amoeba, and mammalian macrophages.

51 chetes, cyanobacteria, ciliates, heliozoans, amoeba, and many others.

52 Understanding why organisms as different as amoebas, ants, and birds cooperate remains an important

53 As amoebas are natural environmental predators of both bact

54 Free-living amoebas are thought to serve as a reservoir for Legionel

55 By using survival in amoeba as a selection, we have isolated mutant strains w

56 potential role of an L. pneumophila-infected amoeba as an infectious particle in replicative L. pneum

57 We found six phyla of amoeba-associated bacteria: Proteobacteria, Bacteroidete

58 questions about the natural ecology of these amoeba-bacteria symbioses along the pathogen-mutualist s

59 Recently, another type of free-living amoeba, Balamuthia mandrillaris, has been shown to cause

60 In some cases amoebas breach the mucosal barrier and travel through th

61 n myosin heavy chain kinases (MHCKs) in this amoeba but that has a completely novel domain organizati

62 g the underlying in situ metabolism for this amoeba but the potential exists to exploit differentiall

63 ows that B. bronchiseptica not only inhabits amoebas but can persist and multiply through the social

64 ence of surface antibodies specific for this amoeba by immunofluorescence.

65 evels of resistance to, and survival within, amoeba by these bacteria and their known virulence mutan

66 This suggests that the amoeba catecholamine receptor functions downstream of th

67 ow that adaptation of L. pneumophila to each amoeba causes the accumulation of distinct virulence gen

68 uthia mandrillaris, a pathogenic free-living amoeba, causes cutaneous skin lesions as well as granulo

69 s considerably delayed in both mammalian and amoeba cells.

70 A draft genome of Cochliopodium minus, an amoeba characterized by extensive cellular and nuclear f

71 ancelets, insects, nematodes, fungi, plants, amoebas, ciliates, and excavates spontaneously and rapid

72 linical microbiology laboratories (including amoeba co-culture and shell-vial culture) and through th

73 was isolated from an environmental sample by amoeba coculture.

74 On food depletion, Dictyostelium discoideum amoebas collect into aggregates, which first transform i

75 Dictyostelium discoideum amoebas coordinate aggregation and morphogenesis by secr

76 AMOEBA correctly predicted over 80% of the observed NOEs

77 saE, PsaK1, and PsaK2 are synthesized in the amoeba cytoplasm and traffic into CRs, where they assemb

78 croscopy shows that the endosymbiont ingests amoeba cytoplasm, a novel form of endosymbiont-host comm

79 nt virus particles, Sputnik 2 particles, and amoeba cytoplasm.

80 and phagocytosis of yeast cells resulted in amoeba death and fungal growth.

81 Cytokinesis in animals, fungi, and amoebas depends on the constriction of a contractile rin

82 canthamoeba (genotype T4) or stimulated with amoeba-derived cell-free conditioned medium.

83 From the timing of amoeba development to the maintenance of stem cell pluri

84 The social amoebas (Dictyostelia) display conditional multicellular

85 ent organisms, such as humans and the social amoeba Dictyostelium (Dd).

86 al. (2016) identified in cells of the social amoeba Dictyostelium a G protein-coupled receptor (GPCR)

87 on after fertilization of an egg, the social amoeba Dictyostelium achieves multicellularity by the ag

88 review addresses these issues for the social amoeba Dictyostelium and highlights some of the organism

89 In the social amoeba Dictyostelium and probably many other unicellular

90 that mediates O(2) regulation of the social amoeba Dictyostelium and the parasite Toxoplasma gondii

91 hich L. pneumophila is grown within the soil amoeba Dictyostelium discoideum and how D. discoideum ge

92 predator-prey association between the social amoeba Dictyostelium discoideum and the free soil living

93 Farmer clones of the social amoeba Dictyostelium discoideum carry bacteria to seed o

94 Here, we show that the amoeba Dictyostelium discoideum coordinates Ras and Rac

95 The social amoeba Dictyostelium discoideum diverged from the line l

96 The amoeba Dictyostelium discoideum expresses a simple compl

97 The amoeba Dictyostelium discoideum feeds on, and is coloniz

98 Here we show that the social amoeba Dictyostelium discoideum has a primitive farming

99 The life cycle of the social amoeba Dictyostelium discoideum includes a multicellular

100 The social amoeba Dictyostelium discoideum integrates into a multic

101 starvation-induced aggregation of the social amoeba Dictyostelium discoideum into a multicellular slu

102 The microbial soil amoeba Dictyostelium discoideum is a model system for th

103 The social amoeba Dictyostelium discoideum is a professional phagoc

104 The social amoeba Dictyostelium discoideum is a widely used model o

105 The genome of the social amoeba Dictyostelium discoideum is known to have a very

106 f the multicellular slug stage of the social amoeba Dictyostelium discoideum produce ETs upon stimula

107 New research indicates that the social amoeba Dictyostelium discoideum recognizes distinctions

108 ow here that dedifferentiation in the social amoeba Dictyostelium discoideum relies on a sequence of

109 Experiments on the social amoeba Dictyostelium discoideum show that the origins of

110 ria's host is a "farmer" clone of the social amoeba Dictyostelium discoideum that carries and dispers

111 with chemical mutagenesis in the social soil amoeba Dictyostelium discoideum Through genome sequencin

112 The social amoeba Dictyostelium discoideum was selected for functio

113 Using the amoeba Dictyostelium discoideum, a model system for the

114 kly related gene in the genome of the social amoeba Dictyostelium discoideum, and show, with the use

115 In many systems, including the social amoeba Dictyostelium discoideum, development is often ma

116 tingly some eukaryotes, including the social amoeba Dictyostelium discoideum, encode both a class I a

117 In the social amoeba Dictyostelium discoideum, four signaling pathways

118 ular act of cooperation occurs in the social amoeba Dictyostelium discoideum, in which some cells die

119 In the social amoeba Dictyostelium discoideum, starvation-triggered mu

120 involved in cheating behaviors in the social amoeba Dictyostelium discoideum, testing whether these g

121 o regulate spore encapsulation in the social amoeba Dictyostelium discoideum, the metabolic profile a

122 Using the social amoeba Dictyostelium discoideum, we provide a possible e

123 composition can be manipulated in the social amoeba Dictyostelium discoideum, which allows us to test

124 One such system is represented by the social amoeba Dictyostelium discoideum.

125 ffraction experiments on single cells of the amoeba Dictyostelium discoideum.

126 s the model organism database for the social amoeba Dictyostelium discoideum.

127 thailandensis to predation by the phagocytic amoeba Dictyostelium discoideum.

128 for extracting DNA from cells of the social amoeba Dictyostelium discoideum.

129 model organism database (MOD) for the social amoeba Dictyostelium discoideum.

130 gus Ustilago maydis and spores of the social amoeba Dictyostelium discoideum.

131 isseminate via the complex life cycle of the amoeba Dictyostelium discoideum.

132 iation in loner behavior in the model social amoeba Dictyostelium discoideum.

133 metal efflux or uptake systems in the social amoeba Dictyostelium discoideum.

134 he illusion of social cheating in the social amoeba Dictyostelium discoideum.

135 icellularity is mainly studied in the social amoeba Dictyostelium discoideum.

136 e, we confirm this prediction for the social amoeba Dictyostelium discoideum; relatedness in natural

137 conventional myosin 7 (DdMyo7) in the social amoeba Dictyostelium However, the exact roles of these M

138 Here we show that the social amoeba Dictyostelium purpureum prefers to form groups wi

139 In live cells of the soil amoeba Dictyostelium that were expressing GFP-ABD, the t

140 IFalpha-type PHDs is expressed in the social amoeba Dictyostelium where it also exhibits characterist

141 In the social amoeba Dictyostelium, a terminal step in development is

142 ates multicellular development of the social amoeba Dictyostelium, suggesting it may serve as an impo

143 similar modification is found in the social amoeba Dictyostelium, where it regulates SCF assembly an

144 A primary example is the social amoeba Dictyostelium, which migrates to the source of tr

145 mes, and the contractile vacuole (CV) of the amoeba Dictyostelium.

146 trigger the rapid sporulation of the social amoeba Dictyostelium.

147 The social amoeba, Dictyostelium discoideum, is known to use peptid

148 The social amoeba, Dictyostelium discoideum, is widely used as a si

149 ices formed during development of the social amoeba, Dictyostelium discoideum.

150 n forces measured in chemotaxing unicellular amoeba, Dictyostelium discoideum.

151 hows that both non-enucleated and enucleated amoebas display the same kind of dynamic migration struc

152 ose-rich cyst wall, leading to subversion of amoeba encystation.

153 cm mutants following incubation in water and amoeba encystment and was required for delay of phagosom

154 mined the effects of incubation in water and amoeba encystment on L. pneumophila strain JR32 and null

155 Amoeba encystment was inhibited by addition of beta(1)-a

156 First, amoebas exhibit a reduction in growth rate when they swi

157 The cysteine proteinase-deficient amoeba failed to induce intestinal epithelial cell produ

158 Unlike bacteria that serve as an amoeba food source, B. bronchiseptica evades amoeba pred

159 evades amoeba predation, survives within the amoeba for extended periods of time, incorporates itself

160 septica continues to be transferred with the amoeba for months, through multiple life cycles of amoeb

161 l-studied development of dictyostelid social amoebas, for example, Dictyostelium discoideum However,

162 All considered, our characterization of amoeba foraging identifies amoeba mobility, and not amoe

163 multipole refinement method assisted by the AMOEBA force field for macromolecular crystallography.

164 pole electrostatics model implemented in the AMOEBA force field is applicable and informative for cry

165 ), dead-end elimination with the polarizable AMOEBA force field lowered Rfree by 2.8-26.7% and improv

166 ASA.S1 was obtained from single amoeba, from cultures of all known 18S rDNA genotypes, a

167 quencing of 16S rRNA amplicons directly from amoeba fruiting bodies.

168 Division of amoebas, fungi, and animal cells into two daughter cells

169 cytokinesis in cells with contractile rings (amoebas, fungi, and animals) depends on shared molecular

170 exons and 5 introns that span 3.6 kb of the amoeba genome and that MBP cDNA codes for a precursor pr

171 ly and annotation of three highly repetitive amoeba genomes, Entamoeba histolytica, Entamoeba dispar,

172 ing status previously has been attributed to amoeba genotype, but the role of bacterial partners in i

173 30 % of actophorin is phosphorylated in live amoebas grown in suspension culture.

174 To explore whether amoeba-grown L. pneumophila differs from BCYE-grown L. p

175 Although amoeba-grown L. pneumophila displays enhanced entry into

176 In addition, amoeba-grown L. pneumophila displays increased replicati

177 Entry of amoeba-grown L. pneumophila into monocytes occurred more

178 Furthermore, amoeba-grown M. avium was also more virulent in the beig

179 Posaconazole was found to inhibit amoeba growth within the first 12 hours of exposure, whi

180 foraging identifies amoeba mobility, and not amoeba growth, as the core determinant of predation effi

181 es of the coprophilic, fruiting body-forming amoeba Guttulinopsis vulgaris and its non-fruiting relat

182 This amoeba had previously been found only in environmental s

183 ing during the first 24h of infection of the amoeba Hartmanella vermiformis.

184 infection was investigated in vivo with the amoeba Hartmannella vermiformis, a natural reservoir of

185 mophila which have reduced virulence for the amoeba Hartmannella vermiformis.

186 The finding that this amoeba has caused infection in some healthy children has

187 ven discovery of giant DNA viruses infecting amoebas has triggered an intense debate about the origin

188 s problem, we have isolated a heterolobosean amoeba, HGG1, that grazes upon unicellular and filamento

189 However, in the amoeba host a mutant lacking both sidJ and sdjA does not

190 rium finds itself in a hot mammalian or cool amoeba host environment.

191 e identified in Acanthamoeba castellanii, an amoeba host for many giant viruses.

192 it because it can confer an advantage to the amoeba host when grown in food-limiting conditions.

193 relationship between Perkinsela sp. and its amoeba host, and provide a foundation for understanding

194 and multiply through the social stage of an amoeba host, Dictyostelium discoideum.

195 enera (Legionella and mycobacteria), and two amoeba hosts (Acanthamoeba spp. and Hartmanella vermifor

196 ificant growth defect in both macrophage and amoeba hosts, but an sdjA mutant is detectably defective

197 fferentially abundant taxa between different amoeba hosts.

198 Acanthamoeba amoeba in 16 solutions (80 %) collected from 12 patients

199 s not significantly affect the locomotion of amoeba in 2D environments.

200 l cell apoptosis occurred in the vicinity of amoeba in histological specimens.

201 erates within a diverse range of free-living amoeba in the environment, but upon transmission to huma

202 poptosis occurred rapidly on co-culture with amoeba in vitro as measured by annexin positivity, DNA d

203 during Legionnaires' disease and invasion of amoebas in the environment.

204 revealed independent origins of filopodiated amoebas in two lineages, one related to fungi and the ot

205 Diverse soil amoebas including Dictyostelium and Acanthamoeba can hos

206 eukocytes (PMNs) or Dictyostelium discoideum amoeba induced formation of filamentous actin.

207 hesion of the parasites to host cells or the amoeba-induced CPE.

208 amoeba to host cells is also an inhibitor of amoeba-induced CPE.

209 thelial cells were also potent inhibitors of amoeba-induced CPE.

210 oeba to host cells is a prerequisite for the amoeba-induced cytolysis of target cells and have implic

211 bohydrate binding properties and the role in amoeba-induced cytopathic effect (CPE).

212 Amoebas infected with mimivirus were disrupted at sequen

213 of a new giant virus that is related to the amoeba-infecting pathogen Marseillevirus was recovered f

214 The revival of such an ancestral amoeba-infecting virus used as a safe indicator of the p

215 isinfected biofilms was 1-2 times higher and amoeba infectivity was 2-29 times lower than that from u

216 gnificant advantages for the study of fungus-amoeba interactions.

217 The transition from spore to amoeba is accompanied by developmentally regulated chang

218 The earliest record of a terrestrial testate amoeba is reported.

219 ough the internal environment of free-living amoebas is similar in many ways to that of mammalian mac

220 lular pathogenic strategy in macrophages and amoebas is similar, leading to the proposal that it orig

221 yostelium discoideum, a soil-dwelling social amoeba, is a model for the study of numerous biological

222 TS region was performed in order to identify amoeba isolates, and the presence of Legionella pneumoph

223 such as Dictyostelium discoideum This social amoeba kills bacteria via phagocytosis for nutrient acqu

224 ogical systems such as dictyostelids, social amoeba known to form multicellular aggregates observed a

225 a "remembering" prior nutritional status and amoeba "learning" to anticipate future environmental con

226 Sugar inhibition assays revealed that the amoeba lectin has the highest affinity for alpha-Man and

227 s a major virulence protein suggest that the amoeba lectin has the potential to serve as a marker of

228 We characterized the amoeba lectin with respect to its carbohydrate binding p

229 produce flagellated cells, but many produce amoeba-like cells.

230 At low densities, NPCs moved randomly in an amoeba-like fashion.

231 ctor alpha, LCs showed amplified dSEARCH and amoeba-like lateral migration between keratinocytes.

232 constantly crawled around hair follicles via amoeba-like movements with a mean velocity of 1.0+/-0.4

233 ad and decaying tail and moving and dividing amoeba-like structures with sharp edges.

234 tion defects in Hartmannella vermiformis, an amoeba linked to hospital outbreaks of Legionella pneumo

235 In highly polarized Dictyostelium discoideum amoebas, membrane-associated betagamma subunits of heter

236 roM) even though the affinity for muscle and amoeba Mg-ADP-actin monomers (Kd = 0.1 microM) is the sa

237 of their soil habitat, and soil pH affected amoeba microbiome diversity.

238 aracterization of amoeba foraging identifies amoeba mobility, and not amoeba growth, as the core dete

239 s isolated with enhanced virulence in a soil amoeba model that nevertheless exhibits dramatically red

240 e (MIHCK) phosphorylates the heavy chains of amoeba myosins I, increasing their actin-activated ATPas

241 ith a Delta24 sterol reductase from the soil amoeba Naegleria gruberi.

242 at T2S is also critical for infection of the amoeba Naegleria lovaniensis.

243 with the other known pathogenic free-living amoebas (Naegleria fowleri and Acanthamoeba species), dr

244 nella, mycobacteria, P. aeruginosa, and both amoebas naturally colonized the six SDSs, but L. pneumop

245 rajectories of enucleated and non-enucleated amoebas on flat two-dimensional (2D) surfaces using adva

246 ogy and immunohistochemistry for free-living amoebas on the brain biopsy tissue were positive.

247 The amoeba originally identified as Sappinia diploidea was i

248 The amoeba Paulinella chromatophora contains nascent photosy

249 The photosynthetic amoeba Paulinella chromatophora represents a unique mode

250 perspective on this issue is provided by the amoeba Paulinella chromatophora, which contains photosyn

251 ithemia turgida and the endosymbionts of the amoeba Paulinella chromatophora.

252 The thecate amoeba Paulinella is a valuable model for understanding

253 se 1 (ITPK1)-found in Asgard archaea, social amoeba, plants, and animals-phosphorylates I(3)P(1) orig

254 sing molecular dynamics simulations with the AMOEBA polarizable force field and perturbation techniqu

255 (LDE), using atomistic simulations with the AMOEBA polarizable force field.

256 amoeba food source, B. bronchiseptica evades amoeba predation, survives within the amoeba for extende

257 food-rich conditions, Burkholderia-colonized amoebas produce fewer spores than uncolonized counterpar

258 is about 10 microM proline decamer units for amoeba profilin and 20-30 microM for human profilin.

259 led X-bacteria), present in the xD strain of Amoeba proteus as required cell components, synthesize a

260 the role of the nucleus in the migration of Amoeba proteus we have analyzed the movement trajectorie

261 ere we show that a locus ('Tgr') of a social amoeba represents a polychromatic greenbeard.

262 Among these amoeba resistant bacteria are numerous members of the ge

263 ncing moderate field strengths; in contrast, AMOEBA robustly recapitulates the TDM electric fields.

264 the role that mannose stimulation has in the amoeba's growth, secreted products, and ability to desqu

265 and 0.003%) with hydrogen peroxide (3%) and amoeba saline controls.

266 cipients remained susceptible as measured by amoeba score and culture, whereas CBA BM --> B6 recipien

267 L-10(-/-)Rag2(-/-) mice exhibited diminished amoeba scores and culture rates vs IL-10(-/-) mice, indi

268 --> IL-10(-/-) recipients, exhibited higher amoeba scores than their wild-type controls.

269 eriods of time, incorporates itself into the amoeba sori, and disseminates along with the amoeba.

270 These bacteria were present in multiple amoeba species across multiple locations.

271 netically and morphologically diverse social amoeba species using next-generation sequencing of 16S r

272 commonly required in all host cell types and amoeba-specific auxiliary genes that determine host rang

273 However, studies in amoeba suggest that P2X receptors are also present intra

274 the ability of Burkholderia to colonize new amoebas, suggests a mixed mode of symbiont transmission.

275 The amoeba surface lectin that binds mucin is presumed to co

276 Amoeba survival was calculated using the most probable n

277 sentative selection of 19 Arcellinid testate amoeba taxa.

278 Both fusaria and amoeba tended to be observed in discrete regions of the

279 telium discoideum farming symbiosis, certain amoebas (termed "farmers") stably associate with bacteri

280 Acanthamoeba castellanii is an amoeba that inhabits soil and water in every part of the

281 Dictyostelium is a social amoeba that undergoes a basic developmental program, and

282 Dictyostelium discoideum are social amoebas that propagate as unicellular organisms but aggr

283 Within macrophages and amoeba, the Legionella-containing vacuole (LCV) membrane

284 n relationships, but the general response of amoeba to bacteria is not well understood.

285 (GlcNAc) which does not inhibit adhesion of amoeba to host cells is also an inhibitor of amoeba-indu

286 ryotic hosts that extends from single-celled amoeba to mammals.

287 ic flagellated bacterivores and filopodiated amoebas to cell-walled osmotrophic parasites and saprotr

288 In Dictyostelium (a social amoeba), Toxoplasma gondii (the agent for human toxoplas

289 atecholamine binding sites on the surface of amoeba trophozoites was confirmed using radiolabeled cat

290 amoeba castellanii and reversion of cysts to amoeba trophozoites, dotA and dotB mutants exhibited int

291 ion years ago and includes the "brain-eating amoeba." Unlike nearly all other known eukaryotic cells,

292 sity where the buoyant force should push the amoeba upward.

293 mal RNA (ssrRNA) gene from the naked, marine amoeba, Vannella anglica (subclass Gymnamoebia), was det

294 The affinity-purified protein of the amoeba was shown to bind specifically to mannose-BSA.

295 a previously unknown cell type in the social amoeba, which appears to provide detoxification and immu

296 sin (DdMVII) in the Dictyostelium discoideum amoeba, which is a model for phagocytosis, is reported h

297 fore bacteria infected humans, they infected amoebas, which remain a potentially important reservoir

298 rstood why multicellularity emerged in these amoebas while the majority of other members of Amoebozoa

299 oeba castellanii is a ubiquitous free-living amoeba with a worldwide distribution that can occasional

300 itis was reported that was caused by another amoeba with morphological features suggestive of Sappini