ライフサイエンスコーパス: histolytica

1 parvum or C. hominis) or trichrome stain (E. histolytica).

2 erent kinetics of ubiquitin activation in E. histolytica.

3 codon 223 were intracecally infected with E. histolytica.

4 low for a unique polyubiquitin linkage in E. histolytica.

5 nserved mode of E2/RING-E3 interaction in E. histolytica.

6 the initiation of erythrophagocytosis in E. histolytica.

7 mechanism is not very well understood in E. histolytica.

8 ityca) and microarray expression data for E. histolytica.

9 isolated crypts from mice inoculated with E. histolytica.

10 ion during various endocytic processes in E. histolytica.

11 I3-kinase signaling in these processes in E. histolytica.

12 he early stages of phagosome formation in E. histolytica.

13 allei, Clostridium perfringens and Entamoeba histolytica.

14 -specific manner, while ERE2 is unique to E. histolytica.

15 main of C1q were all chemoattractants for E. histolytica.

16 bat disease caused by the parasite Entamoeba histolytica.

17 cteria, the usual source of nutrients for E. histolytica.

18 de transcriptional regulatory patterns in E. histolytica.

19 n V prior to adherence to or ingestion by E. histolytica.

20 rlying erythrocyte phagocytosis by Entamoeba histolytica.

21 iated TGS in the deep-branching eukaryote E. histolytica.

22 polymorphisms on intestinal infection by E. histolytica.

23 Entamoeba histolytica, a protozoan intestinal parasite, is the cau

24 ntified and characterized EVs from Entamoeba histolytica, a protozoan parasite and a human pathogen.

25 Entamoeba histolytica, a protozoan parasite, is an important human

26 + ADP), with the exception of the Entamoeba histolytica ACK (EhACK) which uses pyrophosphate (PPi)/i

27 dditionally, through trogocytosis, Entamoeba histolytica acquires and displays human cell membrane pr

28 Entamoeba histolytica adherence and cell migration, two phenotypes

29 the mechanism of phagocytosis, we used an E. histolytica Affymetrix microarray chip to measure the to

30 species while ERE2 was likely acquired by E. histolytica after its separation from E. dispar.

31 m of Ca(2+)-mediated regulation of Entamoeba histolytica alpha-actinin-2 (EhActn2) with features expe

32 We examined rhomboid function in Entamoeba histolytica, an extracellular, parasitic ameba that is s

33 Infection with Entamoeba histolytica and associated complications are relatively

34 be harnessed for the prevention of Entamoeba histolytica and Cryptosporidium species infection in chi

35 ntly been published for identification of E. histolytica and differentiation from the morphologically

36 re found at syntenic break points between E. histolytica and E. dispar and hence, could work as recom

37 human intestinal IgA antibody response to E. histolytica and E. dispar infection and revealed that AL

38 aks that are associated with clearance of E. histolytica and E. dispar infection.

39 und a putative transposase-coding gene in E. histolytica and E. dispar related to the mariner transpo

40 We demonstrate that E. histolytica and E. dispar share their entire repertoire

41 uplex real-time PCR (capable of detecting E. histolytica and E. dispar), our tetraplex real-time PCR

42 of a PS receptor on the surfaces of both E. histolytica and E. dispar.

43 Archamoebae, including pathogenic Entamoeba histolytica and free-living Mastigamoeba balamuthi, the

44 atistically significant associations with E. histolytica and G. intestinalis were not found.

45 dy-state levels in the plasma membrane of E. histolytica and that these levels, unlike those in mamma

46 ll as in the phagolysosomal biogenesis in E. histolytica and thus contributes to the pathogenicity of

47 In contrast, recombinant Entamoeba histolytica and Trypanosoma brucei Tgs are capable of ca

48 ptosporidium, Giardia lamblia, and Entamoeba histolytica), and helminths (Ascaris lumbricoides and Tr

49 lamblia, Cryptosporidium spp., and Entamoeba histolytica), and viruses (norovirus GI and GII, adenovi

50 nd infection with Cryptosporidium, Entamoeba histolytica, and Giardia intestinalis in children.

51 sequence similarity to adhesin in Entamoeba histolytica, and we observed that Alix is secreted, we d

52 sensitive detection for individual Entamoeba histolytica antigen EHI_115350 (limit of detection = 1 p

53 h for the capture and detection of Entamoeba histolytica antigens from disinfected stool, within a sp

54 Cyclospora, Isospora, Giardia, and Entamoeba histolytica are discussed.

55 Complex N-glycans of E. histolytica are made by the addition of alpha1,2-linked

56 Here, we used Entamoeba histolytica as the model MIF-secreting protozoan, and a

57 nce for Golgi apparatus-like functions in E. histolytica as well as for components of glycoprotein fo

58 The lack of a defined Golgi apparatus in E. histolytica as well as in other protists led to the hypo

59 s colitis and liver abscess due to Entamoeba histolytica as well as to bacterial peritonitis.

60 named E. histolytica ILWEQ (EhILWEQ) and E. histolytica BAR (EhBAR), were chosen for localization vi

61 esses following intrahepatic injection of E. histolytica by a combined rate of 68% in two independent

62 mately 80% of children were infected with E. histolytica by the age of 2 years.

63 is aggregated into caps on the surface of E. histolytica by the N-glycan-specific, anti-retroviral le

64 measure the activity of Dbr1 from Entamoeba histolytica by using a synthetic, dark-quenched bRNA sub

65 determine if calreticulin functions as an E. histolytica C1q receptor during phagocytosis of host cel

66 Finally, E. histolytica calreticulin bound specifically to apoptotic

67 The protozoan parasite Entamoeba histolytica can invade both intestinal and extra intesti

68 ay in erythrophagocytosis was observed in E. histolytica cells overexpressing S428A and KDDeltaC prot

69 PI(4,5)P2 were enhanced upon treatment of E. histolytica cells with cholesterol.

70 proteolytic rhomboid (EhROM1) from Entamoeba histolytica cleaves cell surface galactose-binding or N-

71 asB) and Clostridium histolyticum (Hathewaya histolytica) collagenase (ColH) play a significant role

72 spectively studied the natural history of E. histolytica colonization and diarrhea among infants in a

73 The parasite Entamoeba histolytica contains an abundant repertoire of 27 nt ant

74 The virulence of E. histolytica correlates with the degree of host cell engu

75 are caused by Giardia duodenalis, Entamoeba histolytica, Cryptosporidium parvum, and Cryptosporidium

76 cholerae, Yersinia enterocolitica, Entamoeba histolytica, Cryptosporidium spp., and E. coli O157:H7;

77 alnourished at birth had increased Entamoeba histolytica, Cryptosporidium, and ETEC infections and mo

78 ith an increase in phagocytic ability, as E. histolytica cultures exposed to an initial stimulus of p

79 to each specifically detect their cognant E. histolytica cyst antigens was demonstrated in a biologic

80 -free electrochemical detection of Entamoeba histolytica cyst antigens.

81 ves of bovine xanthine oxidase and Entamoeba histolytica cysteine protease 1 allowed active stocks to

82 Entamoeba histolytica cysteine proteinases (EhCPs) play a key role

83 inal cathelicidins is a novel function of E. histolytica cysteine proteinases in the evasion of the i

84 screte mechanisms of innate resistance to E. histolytica depending on the host background and, in con

85 hment of intestinal infection with Entamoeba histolytica depends on the mouse strain; C57BL/6 mice ar

86 pressive histone mark to be identified in E. histolytica, dimethylation of H3K27 (H3K27Me2), and demo

87 nfection with P. falciparum, hookworm and E. histolytica/dispar, as well as co-infection with each pa

88 denale and/or Necator americanus), Entamoeba histolytica/dispar, Mycobacterium tuberculosis, and HIV,

89 tions between hookworm, P. falciparum and E. histolytica/dispar, were assessed using multivariable lo

90 E. histolytica displays a relatively low level of nucleotid

91 ch as Cryptosporidium, Giardia, or Entamoeba histolytica) disrupt cell functions and cause short- or

92 lso determined that this assay can detect E. histolytica DNA in the presence of 10-fold more DNA from

93 We used an E. histolytica DNA microarray consisting of 2,110 genes to

94 th the virulent protozoan parasite Entamoeba histolytica do not develop invasive disease.

95 As E. histolytica does not readily form cysts in vitro, we ass

96 erstanding the mechanisms by which Entamoeba histolytica drives gut inflammation is critical for the

97 reticulin was localized to the surface of E. histolytica during interaction with both Jurkat lymphocy

98 Of these, four species (Entamoeba histolytica, E. dispar, E. moshkovskii, and E. banglades

99 Entamoeba histolytica (Eh) colonizes the mucus layer by binding of

100 moebic colitis is the detection of Entamoeba histolytica (Eh) trophozoites with ingested erythrocytes

101 for the detection of antibodies to Entamoeba histolytica (Eh) was positive.

102 and Lys(53) in the oxygen reducing Entamoeba histolytica EhFdp1.

103 e FNT from the amoebiasis parasite Entamoeba histolytica, EhFNT, and also show that BtFdhC from Bacil

104 E. histolytica encodes a homolog of the human cytokine macr

105 Despite its large genome, E. histolytica encodes only one rhomboid (EhROM1) with resi

106 highly repetitive amoeba genomes, Entamoeba histolytica, Entamoeba dispar, and Entamoeba invadens, w

107 school age, for infection by the parasite E. histolytica every other day over 9 years and evaluated t

108 The parasite was named "histolytica" for its ability to destroy host tissues, wh

109 ty of each assay to correctly distinguish E. histolytica from E. dispar was evaluated with DNA extrac

110 Entamoeba histolytica was named 'histolytica' (from histo-, 'tissue'; lytic-, 'dissolving

111 own that vaccination with purified Entamoeba histolytica Gal/GalNAc lectin or recombinant subunits ca

112 n A (IgA) antibody response to the Entamoeba histolytica galactose-inhibitable adherence lectin is mo

113 The E. histolytica genome contains two homologues to the metall

114 The E. histolytica genome encodes several Rho family GTPases kn

115 The release of the Entamoeba histolytica genome has facilitated the development of te

116 omposition bias and repetitiveness of the E. histolytica genome provide a challenge for short-read ma

117 lication of the protozoan parasite Entamoeba histolytica genome provides new insights into eukaryotic

118 e process has been the publication of the E. histolytica genome, from which has come an explosion in

119 entified a MIF gene homolog in the Entamoeba histolytica genome, raising the question of whether E. h

120 gene transfer of bacterial genes into the E. histolytica genome, the effects of which centre on expan

121 Rotavirus, adenovirus, Entamoeba histolytica, Giardia enterica, and Cryptosporidium speci

122 n a variety of parasites including Entamoeba histolytica, Giardia intestinalis, Leishmania spp., Plas

123 ium spp., Cyclospora cayetanensis, Entamoeba histolytica, Giardia lamblia, adenovirus F 40/41, astrov

124 tract include the deadly parasite Entamoeba histolytica;Giardia lamblia, the most common cause of wa

125 The intestinal parasite Entamoeba histolytica harbors an extensive ubiquitin-proteasome sy

126 Our previous data show that Entamoeba histolytica has a robust RNAi pathway that links to TGS

127 E. histolytica has been listed by the National Institutes o

128 arch using the trophozoite form of Entamoeba histolytica has clearly shown us the importance of the i

129 Together, these studies demonstrate that E. histolytica has different vesicles that play a role in p

130 an archetypal family member, from Entamoeba histolytica, has been determined to 1.2 A resolution in

131 phagocytosis-related signaling events in E. histolytica have been characterized, the functions of li

132 E. histolytica HM-1:IMSS is a virulent strain, E. histolyti

133 d with a reduced virulence phenotype, and E. histolytica HM-1:IMSS trophozoites infecting human intes

134 n the nonvirulent species/strains than in E. histolytica HM-1:IMSS.

135 pression in E. histolytica Rahman than in E. histolytica HM-1:IMSS.

136 te-limiting role in the process of Entamoeba histolytica host cell engulfment.

137 scribe the crystal structure of an Entamoeba histolytica hybrid IP6K/IP3K, an enzymatic parallel to a

138 Nine of 12 (75%) people with anti-E. histolytica IgG also had EhMSP-1-specific IgG antibodies

139 nsitivity and specificity compared to the E. histolytica II ELISA of 98.0% (95% confidence interval [

140 ytica microplate assay from Remel and the E. histolytica II enzyme-linked immunosorbent assay (ELISA)

141 creen Entamoeba test (R-Biopharm) and the E. histolytica II test (Techlab), and we found that the E.

142 II test (Techlab), and we found that the E. histolytica II test detects E. histolytica infections mo

143 the five encoded proteins, which we named E. histolytica ILWEQ (EhILWEQ) and E. histolytica BAR (EhBA

144 tially increases susceptibility to Entamoeba histolytica in children.

145 r rheumatoid arthritis, as active against E. histolytica in culture.

146 tual interactions between host and Entamoeba histolytica in human and experimental amebiasis.

147 d lines of the eukaryotic pathogen Entamoeba histolytica in order to develop a picture of genetic div

148 The early establishment of E. histolytica in the colon occurs in the presence of antim

149 onas spp, Cryptosporidium spp, and Entamoeba histolytica increased risk of death.

150 ss K(+) protected diverse cell types from E. histolytica-induced death.

151 Prior to phagocytosis of host cells, E. histolytica induces apoptotic host cell death, using a m

152 Entamoeba histolytica induces host cell apoptosis and uses ligands

153 of this subunit were more susceptible to E. histolytica infection as measured by culture results, ce

154 eaks were of higher amplitude following a E. histolytica infection compared to E. dispar (P = 0.01) a

155 E. histolytica infection generally does not cause symptoms,

156 Invasive amebiasis due to Entamoeba histolytica infection is an important cause of morbidity

157 The paradigm of Entamoeba histolytica infection is changing with recent reports of

158 sera of children living in an area where E. histolytica infection is endemic.

159 A prior E. histolytica infection was associated with the occurrence

160 In conclusion, E. histolytica infection was confirmed in 9 (15.8%) of the

161 Thus, E. histolytica infection was confirmed in 9 cases (15.8%) i

162 E. histolytica infection was prevalent in this population,

163 n function may increase susceptibility to E. histolytica infection.

164 t contributes to resistance of the gut to E. histolytica infection.

165 tosis of host cells characterize invasive E. histolytica infection.

166 ic liver abscesses due to invasive Entamoeba histolytica infections are an important cause of morbidi

167 d that the E. histolytica II test detects E. histolytica infections more accurately.

168 ella, Shigella, Campylobacter, and Entamoeba histolytica infections, and their impact on long-term ef

169 on and shape the colonic microenvironment E. histolytica infects.

170 During the process of invasion E. histolytica ingests red blood and host cells using phago

171 ine vaccine efficacy against asymptomatic E. histolytica intestinal infection.

172 Entamoeba histolytica is a protozoan intestinal parasite that caus

173 Entamoeba histolytica is a protozoan parasite of humans that cause

174 Entamoeba histolytica is a protozoan parasite that causes colitis

175 Entamoeba histolytica is a protozoan parasite that causes dysenter

176 Entamoeba histolytica is a significant cause of disease worldwide.

177 Entamoeba histolytica is an intestinal ameba that causes dysentery

178 Entamoeba histolytica is an intestinal parasite and the causative

179 Entamoeba histolytica is an intestinal parasite that infects 50-10

180 Entamoeba histolytica is an intestinal protozoan parasite and is t

181 Entamoeba histolytica is an intestinal protozoan parasite that cau

182 The parasitic protozoan Entamoeba histolytica is aptly named for its capacity to destroy h

183 monstrate that G3-based gene silencing in E. histolytica is mediated by an siRNA pathway, which utili

184 Entamoeba histolytica is not a common causative agent of acute app

185 Entamoeba histolytica is the agent of amebic colitis.

186 Entamoeba histolytica is the causative agent of amebiasis, a disea

187 The protozoan parasite Entamoeba histolytica is the causative agent of amebiasis, an infe

188 Entamoeba histolytica is the causative agent of amoebiasis, a pote

189 The enteric protozoan parasite Entamoeba histolytica is the cause of potentially fatal amebic col

190 The transmissive form of E. histolytica is the cyst, with a single infected individu

191 Entamoeba histolytica is the protozoan parasite that causes amebic

192 Entamoeba histolytica is the protozoan parasite that causes invasi

193 Entamoeba histolytica is the third-leading cause of parasitic mort

194 ancient eukaryotic human pathogen, Entamoeba histolytica, is a nucleo-base auxotroph (i.e. lacks the

195 the calcium-binding proteins from Entamoeba histolytica, is a two-domain EF-hand protein.

196 Entamoeba histolytica kills human cells by ingesting fragments of

197 The parasite Entamoeba histolytica kills human cells resulting in ulceration, i

198 Entamoeba histolytica, Leishmania spp., Trypanosoma cruzi and Tric

199 E. histolytica makes an unusual truncated N-glycan precurso

200 potential for novel metabolic pathways in E. histolytica may allow for the development of new chemoth

201 The discovery of amoebic trogocytosis in E. histolytica may also shed light on an evolutionarily con

202 of the sequenced genomes, suggesting that E. histolytica may reproduce sexually.

203 otic cells, monoclonal antibodies against E. histolytica membrane antigens were screened for inhibiti

204 afts, and the actin-rich fractions of the E. histolytica membrane.

205 In this study, we sought to characterize E. histolytica metallosurface protease 1 (EhMSP-1).

206 he commercially available ProSpecT Entamoeba histolytica microplate assay from Remel and the E. histo

207 Here, we investigated the role of E. histolytica MIF (EhMIF) during infection.

208 a genome, raising the question of whether E. histolytica MIF (EhMIF) has proinflammatory activity sim

209 ith metronidazole when combined with anti-E. histolytica MIF antibodies, compared to metronidazole al

210 ier family (MCF) complement of the Entamoeba histolytica mitochondrial homolog, also known as a crypt

211 The Entamoeba histolytica mitosome has lost all but a single type of M

212 talloprotease leishmanolysin gene, Entamoeba histolytica MSP-1 (EhMSP-1) and EhMSP-2, while the comme

213 lence multiple amebic genes, including an E. histolytica Myb gene, which is upregulated during oxidat

214 n(5)GlcNAc(2), which is the most abundant E. histolytica N-glycan, is aggregated into caps on the sur

215 In summary, E. histolytica N-glycans include unprocessed Man(5)GlcNAc(2

216 apio anubis) are natural hosts for Entamoeba histolytica; naturally infected baboons raised in captiv

217 In Entamoeba histolytica, neither PTA nor XFP was found as a partner

218 lower odds of B hominis (0.52, 0.34-0.78), E histolytica or E dispar (0.61, 0.38-0.99), G intestinali

219 antly lower odds of infection with Entamoeba histolytica or Entamoeba dispar (OR 0.56, 95% CI 0.42-0.

220 ozoa such as Dientamoeba fragilis, Entamoeba histolytica, or Cyclospora cayetanensis.

221 Contact with E. histolytica parasites triggered K(+) channel activation

222 Motility is a key factor in E. histolytica pathogenesis, and this process relies on a d

223 e is known about the role of PI(4,5)P2 in E. histolytica pathogenicity.

224 ost cell engulfment, or phagocytosis, and E. histolytica phagocytosis alters amebic gene expression i

225 y implicate the SREHP as a participant in E. histolytica phagocytosis and suggest that it may play an

226 calreticulin as a receptor for C1q during E. histolytica phagocytosis of host cells.

227 psonins on apoptotic cells that stimulate E. histolytica phagocytosis, an effect mediated at least in

228 the collectins are ligands that stimulate E. histolytica phagocytosis, we used a flow cytometry-based

229 set demonstrating feed-forward control of E. histolytica phagocytosis.

230 Together, our data suggest that in E. histolytica, PI(4,5)P2 may signal from lipid rafts and c

231 We showed previously that Entamoeba histolytica PIG-L exhibits a novel metal-independent alb

232 a significantly higher leukocyte count in E. histolytica-positive patients than in negative patients

233 The single-celled human parasite Entamoeba histolytica possesses a dynamic actin cytoskeleton vital

234 In contrast, E. histolytica possesses only single genes encoding NifS an

235 sion of the GalNAc lectin and serine-rich E. histolytica protein (SREHP) receptors.

236 aphy-mass spectrometry as the serine-rich E. histolytica protein (SREHP).

237 red to the ProSpecT microplate assay, the E. histolytica Quik Chek (Quik Chek) assay exhibited 97.0%

238 lyzed the ability of the third-generation E. histolytica Quik Chek assay developed by Techlab to dete

239 After discrepant resolution, The E. histolytica Quik Chek assay exhibited sensitivity and sp

240 stolytica HM-1:IMSS is a virulent strain, E. histolytica Rahman is a nonvirulent strain, and Entamoeb

241 par and 32 genes with lower expression in E. histolytica Rahman than in E. histolytica HM-1:IMSS.

242 :IMSS, the prototype virulent strain, and E. histolytica Rahman, a strain that was reportedly less vi

243 Vietnam, a novel and simple-to-use Entamoeba histolytica rapid antigen test had 97% sensitivity and 1

244 In this study, we compared three E. histolytica real-time PCR techniques published by Decemb

245 he pattern of polymorphism indicates that E. histolytica reproduces sexually, or has done so in the p

246 rvum or C. hominis, and 100% and 100% for E. histolytica, respectively.

247 Insight into how E. histolytica responds to oxidative stress increases our u

248 overexpression of calreticulin increased E. histolytica's ability to phagocytose apoptotic lymphocyt

249 s of which centre on expanding aspects of E. histolytica's metabolic repertoire.

250 estinalis, Cryptosporidium parvum, Entamoeba histolytica, Salmonella enterica, enterotoxigenic Escher

251 We previously demonstrated that Entamoeba histolytica secretes a protease capable of dissolving th

252 In Entamoeba histolytica seminal aspects of pathogenesis are transcri

253 a, we first defined the phenotypes of two E. histolytica strains, HM-1:IMSS, the prototype virulent s

254 evaluate genetic variability among Entamoeba histolytica strains, we sequenced 9,077 bp from each of

255 ranofin was ten times more potent against E. histolytica than metronidazole.

256 es less likely to be infected with Entamoeba histolytica than those carrying the mutant R223 allele.

257 stress-responsive transcription factor in E. histolytica that controls a transcriptional regulatory n

258 Entamoeba histolytica, the cause of invasive amebiasis, phagocytos

259 Finally, Entamoeba histolytica, the etiologic agent of invasive amebiasis,

260 identified the protozoan parasite Entamoeba histolytica, the etiological agent of amebiasis, as one

261 N-Glycans of Entamoeba histolytica, the protist that causes amebic dysentery an

262 e host immune response during invasion of E. histolytica, the protozoan cause of human amebiasis.

263 patients who may be infected with Entamoeba histolytica, the species that causes clinical amebiasis.

264 rdia spp, Cryptosporidium spp, and Entamoeba histolytica, the Tri-Combo parasite screen, was compared

265 says suggested that auranofin targets the E. histolytica thioredoxin reductase, preventing the reduct

266 The ability of E. histolytica to phagocytose host cells correlates with vi

267 The ability of the human parasite Entamoeba histolytica to survive reactive oxygen and nitrogen spec

268 e effects(3), and potential resistance of E. histolytica to the drug is an increasing concern(4,5).

269 deep-branching eukaryotic parasite Entamoeba histolytica, transcriptional gene silencing (TGS) of the

270 rase (OST) from Trypanosoma cruzi, Entamoeba histolytica, Trichomonas vaginalis, Cryptococcus neoform

271 o control animals bound to the surface of E. histolytica trophozoites and accelerated amebic lysis vi

272 eases degrade the key adherence lectin on E. histolytica trophozoites and decrease their adherence to

273 E. histolytica trophozoites colonize the colon, where they

274 obust assay for the specific detection of E. histolytica trophozoites in unfixed frozen clinical stoo

275 When E. histolytica trophozoites invade the lamina propria of a

276 lectin protein on the surfaces of axenic E. histolytica trophozoites or from solubilized amebae.

277 is of amebic colitis, we demonstrate that E. histolytica trophozoites or their released proteinases,

278 on of the galactose-specific adherence of E. histolytica trophozoites to Chinese hamster ovary cells

279 expression was upregulated in phagocytic E. histolytica trophozoites to determine whether these gene

280 Despite induction, E. histolytica trophozoites were found to be resistant to k

281 lated with our finding that co-culture of E. histolytica trophozoites with mucin-producing T84 cells

282 In E. histolytica trophozoites, EhROM1 changed localization to

283 les spiked with serially diluted cultured E. histolytica trophozoites.

284 we have cloned and characterized multiple E. histolytica ubiquitination components, spanning ubiquiti

285 However, no functional studies of the E. histolytica ubiquitination enzymes have yet emerged.

286 ches we have (a) cloned and expressed the E. histolytica UDP-galactose transporter in Saccharomyces c

287 ed that the Q223 allele protected against E. histolytica via STAT3-mediated transcription of genes re

288 EhILWEQ and EhBAR appear to contribute to E. histolytica virulence through their function in phagocyt

289 nvironmental factors in the regulation of E. histolytica virulence.

290 The seroprevalence of E. histolytica was 33% (14/43) from the available stored se

291 Entamoeba histolytica was named 'histolytica' (from histo-, 'tissu

292 To identify virulence factors of E. histolytica, we first defined the phenotypes of two E. h

293 om South Africans naturally infected with E. histolytica were examined by enzyme-linked immunosorbent

294 pathogenic E. coli, rotavirus, and Entamoeba histolytica were the most frequent probable contributors

295 postchallenge, all Q223 mice had cleared E. histolytica, whereas 39% of 223R mice were infected.

296 e invasion by the intestinal ameba Entamoeba histolytica, which causes amebic dysentery and liver abs

297 Here we present the genome of E. histolytica, which reveals a variety of metabolic adapta

298 esting confirmed an infection with Entamoeba histolytica, which was treated with metronidazole, follo

299 ed a new tool for genetic manipulation in E. histolytica with many advantages over currently availabl

300 n biosynthesis and the final N-glycans of E. histolytica with the following conclusions.

301 C57BL/6 (B6) mice clear Entamoeba histolytica within hours of challenge, whereas C3H and C