ライフサイエンスコーパス: trophozoite

1 the nuclei of cysts, but not the vegetative trophozoite.

2 n from the dormant cyst form into the active trophozoite.

3 PHIST/CVC-81(95) is most highly expressed in trophozoites.

4 and attachment mechanisms of Giardia lamblia trophozoites.

5 tially in nonencysting and encysting Giardia trophozoites.

6 ar algae, and preferentially, Perkinsus spp. trophozoites.

7 ith serially diluted cultured E. histolytica trophozoites.

8 nes, and levels of these target proteases in trophozoites.

9 falcipain-2, the hydrolysis of hemoglobin in trophozoites.

10 e of the main host defenses against invading trophozoites.

11 rafts were then infected with E. histolytica trophozoites.

12 VSPs were detected on the surface of single trophozoites.

13 on of plasminogen activators by Acanthamoeba trophozoites.

14 nt did not affect encystment of Acanthamoeba trophozoites.

15 60-kDa enzyme in extracts of E. histolytica trophozoites.

16 n contrast to P. falciparum, does not affect trophozoites.

17 recognition of and response to Acanthamoeba trophozoites.

18 ced the number of acidic compartments in the trophozoites.

19 ntify the pathogenic behavior of the amoebic trophozoites.

20 12-kDa protein localized to the cytoplasm of trophozoites.

21 Trophozoites (10(6)) were injected into the AC of hamste

22 hamoeba cysts/10 microl and 2.3 Acanthamoeba trophozoites/10 microl by both real-time PCR assays.

23 mine specifically arrested the maturation of trophozoites, a stage at which the parasite synthesizes

24 Amoebic trophozoites activate the transcription factor NF-kappa

25 This may explain why Giardia trophozoites adhere to the small intestinal epithelium d

26 Against trophozoites, All-in-One, ReNu Multiplus, and Optifree E

27 lower sensitivity to short drug pulses than trophozoites, although we identify a subpopulation of ri

28 ble number approach were used to compare the trophozoite and cysticidal efficacy of four multipurpose

29 s further indicate that FCP is essential for trophozoite and FV maturation and that it traffics to th

30 pypAg-2 expression was localized to both the trophozoite and merozoite membranes.

31 For Pf-RBCs at trophozoite and schizont stages, the presence of cytoadh

32 son, the H3-K9 acetylation increased in late trophozoite and schizont stages, while H4-K16 acetylatio

33 y decreases by approximately 50% at the late trophozoite and schizont stages.

34 g activity is markedly increased at the late trophozoite and schizont stages.

35 ponents of the red cell skeleton at the late trophozoite and schizont stages.

36 ge and reaches its maximal level in the late trophozoite and schizont stages.

37 imals bound to the surface of E. histolytica trophozoites and accelerated amebic lysis via activation

38 efficacies against Acanthamoeba castellanii trophozoites and cysts by using a most probable number (

39 excystment, proliferation, and encystment of trophozoites and cysts of A. castellanii was examined in

40 nly All-in-One proved effective against both trophozoites and cysts over the same time period.

41 ibitor management strategy effective against trophozoites and cysts that may be useful for formulatin

42 ther show that exposure of M. bovis-infected trophozoites and cysts to Balb/c mice leads to pulmonary

43 termining the susceptibility of Acanthamoeba trophozoites and cysts to contact lens care systems has

44 dings indicate that exposure of Acanthamoeba trophozoites and cysts to dexamethasone increases the pa

45 The proliferation of trophozoites and cysts was examined by optical density a

46 (ii) by determining their ability to detect trophozoites and cysts, and (iii) by testing a battery o

47 bin-hydrolyzing activity is maximum in early trophozoites and declines rapidly at late stages, wherea

48 e the key adherence lectin on E. histolytica trophozoites and decrease their adherence to epithelial

49 Both active trophozoites and dormant cysts of a pathogenic strain of

50 revealed that both kinases were expressed in trophozoites and encysting cells as 44- and 41-kDa polyp

51 The inability to coculture trophozoites and epithelial cells under optimal conditio

52 ring the parasite growth from rings to early trophozoites and from late trophozoites to schizonts and

53 arasite life cycle (sporozoites, merozoites, trophozoites and gametocytes) by multidimensional protei

54 PN technique, which uses axenically produced trophozoites and mature, double-walled cysts, has the po

55 Here we overexpressed this enzyme in Giardia trophozoites and observed a significantly enhanced susce

56 Growth and maturation of trophozoites and schizonts was markedly inhibited in the

57 limited to ring stage, but also occurred in trophozoites and schizonts.

58 We showed that both Acanthamoeba trophozoites and soluble amoebic products induce an earl

59 ciated with the disappearance of intraocular trophozoites and suggests that cells of the innate immun

60 We show that most parasite mRNAs derive from trophozoites and that the asynchronicity of P. vivax inf

61 differentiate various malaria stages (ring, trophozoite, and schizont stage) due to their varied def

62 patic inoculation with Entamoeba histolytica trophozoites, and 12 h after amebic inoculation, reduced

63 its life cycle inside erythrocytes as rings, trophozoites, and schizonts, before egress and reinvasio

64 a cocultures grew better than nonconditioned trophozoites, and the cell lines differed in their abili

65 /perinuclear targeting of bodipy-ceramide in trophozoites, and this could be reversed by 3-ketosphing

66 BCH070 preferentially kills early ring-form trophozoites, and, importantly, equally inhibits ring-st

67 (PyMIF) were used to localize expression in trophozoite- and schizont-stage parasites and demonstrat

68 Entamoeba histolytica trophozoites are covered by lipophosphoglycan-peptidogly

69 When Acanthamoeba castellanii trophozoites are grown in methyl-alpha-D-mannopyranoside

70 phoresis demonstrates that within 24 h after trophozoites are induced to encyst, the level of glucosa

71 tracellular cysteine proteinases from amebic trophozoites are key virulence factors and have a number

72 Raft-like structures in trophozoites are located in the plasma membranes and on

73 The data show that IRBCs with late trophozoites are more resistant to trypsin treatment tha

74 re capable of detecting as few as 100 viable trophozoites as determined by ethidium bromide staining,

75 le the Pf MDH protein level remained high in trophozoites as well as schizonts.

76 Trophozoites attach to enterocytes that mature and die.

77 Trophozoites attached to host cells, in contrast, respon

78 on by host secretions reduces proclivity for trophozoite attachment, while inducing virulence factors

79 wall proteins to the plasma membrane of the trophozoite before laying down the protective cyst wall.

80 nthamoeba keratitis begins when Acanthamoeba trophozoites bind specifically to mannosylated glycoprot

81 toxic, its presence increased A. castellanii trophozoites biomass and delayed encystation by 96 h.

82 the maturation of early trophozoites to late trophozoites but not during the development of rings to

83 were introduced into GLV-infected G. lamblia trophozoites by electroporation and stablized in the tra

84 ipt was introduced into GLV-infected Giardia trophozoites by electroporation.

85 ynthesis of FBPA was demonstrated in Giardia trophozoites by using an antibody-based fluorescence ass

86 The second hypothesis proposed that the trophozoites can enter the AC; however, the aqueous humo

87 The first hypothesis proposed that trophozoites cannot penetrate Descemet's membrane and th

88 fection have begun to illuminate how amoebic trophozoites cause intestinal disease and liver abscess,

89 Invasion by Entamoeba histolytica trophozoites causes secretion of proinflammatory cytokin

90 Infection in Muc2(-/-) mice elevated trophozoite colonization in the small intestine and impa

91 E. histolytica trophozoites colonize the colon, where they induce infla

92 ced 4- to 10-fold increases in the number of trophozoites compared with untreated control cultures.

93 Trophozoites conditioned on one cell line and then grown

94 gene expression level of 68% of genes under trophozoite conditions.

95 d was used to determine whether Acanthamoeba trophozoites could penetrate this membrane in vitro.

96 A principal trophozoite cysteine protease was purified by affinity c

97 es linked to virulence, are both aberrant in trophozoites deficient in the metallosurface protease Eh

98 at these kinases may play a critical role in trophozoite differentiation into cysts.

99 ring intra-erythrocytic development, malaria trophozoites digest hemoglobin, which leads to parasite

100 A high proportion of ring forms and trophozoites disintegrates within a subset of CC cells,

101 castellanii and reversion of cysts to amoeba trophozoites, dotA and dotB mutants exhibited intracellu

102 stics of helminth eggs, protozoan cysts, and trophozoites, ease of use, and cost.

103 In E. histolytica trophozoites, EhROM1 changed localization to vesicles du

104 monstrated that putrescine induces protozoan trophozoite encystment and adversely affects cyst viabil

105 Exposure of hemocytes to Perkinsus spp. trophozoites enhanced this process further, and their ph

106 ebic DNA corresponding to as little as a 0.1 trophozoite equivalent of any of these species.

107 synthetic peptide from Plasmodium falciparum trophozoite exported protein 1 (TEX1), the target of hum

108 ending pseudopodia and in phagosomal cups in trophozoites exposed to erythrocytes but did not localiz

109 Trophozoites exposed to Ru(II) compounds die through an

110 Acanthamoeba trophozoites express a mannose binding receptor that fac

111 Transcripts for three trophozoite-expressed genes were lost in AN3661-treated

112 SCID mice were infected with E. histolytica trophozoites expressing an antisense message to ehcp5.

113 by H2O2 in vitro, and infection with Rahman trophozoites expressing higher levels of peroxiredoxin w

114 sient shrinkage of infected cells with young trophozoites followed by continuous volume increase to a

115 reviously showed that falcipain-2 is a major trophozoite food vacuole cysteine protease.

116 Research using the trophozoite form of Entamoeba histolytica has clearly sh

117 sion were identified between the blood stage trophozoite form of the malarial parasite and the sexual

118 With trophozoites, four of four MPDSs and the one-step peroxi

119 l lines differed in their ability to support trophozoite growth in the order of RIT > Cos7 > Caco2.

120 and 92 cases with hyperparasitemia (asexual trophozoites, >500,000/mm3).

121 Falcipain-2-knockout trophozoites had markedly diminished cysteine protease a

122 increased deformability of both Pf-free and trophozoite-harboring RBCs.

123 alciparum cysteine protease falcipain-2 is a trophozoite hemoglobinase and potential antimalarial dru

124 de on presence of target images, clusters or trophozoite images (at least 1 of the 3 features), the p

125 Specificity of both target and trophozoite images was 100%.

126 sites, whereas EVs from metabolically active trophozoites impeded encystation.

127 Furthermore, culturing of trophozoites in dialyzed medium containing fetal bovine

128 ion of helminth eggs and protozoan cysts and trophozoites in fecal specimens.

129 e we tested the virulence of amoebapore A(-) trophozoites in models of the two major forms of amebic

130 useful in confirming the presence of viable trophozoites in respiratory specimens collected by nonin

131 gest there is frequently a failure to detect trophozoites in routine examination, resulting in an und

132 on of ADP could be obtained in permeabilized trophozoites in the presence of succinate, citrate, alph

133 for the specific detection of E. histolytica trophozoites in unfixed frozen clinical stool samples.

134 inhibits G. lamblia CK and kills G. lamblia trophozoites in vitro at submicromolar IC50 values.

135 rypsin treatment than those containing early trophozoites, indicating that parasite proteins expresse

136 onstrate that antibodies against PfGARP kill trophozoite-infected erythrocytes in culture by inducing

137 By killing trophozoite-infected erythrocytes, PfGARP could synergiz

138 In contrast, trophozoite-infected RBCs exhibited voltage-dependent, n

139 ence phenotype, and E. histolytica HM-1:IMSS trophozoites infecting human intestinal xenografts show

140 Finally, expression of a PH domain in trophozoites inhibited erythrophagocytosis and enhanced

141 inside the infected host cell, we find that trophozoites (intermediate-stage iRBCs) tend to flip due

142 es outside of the host by differentiation of trophozoites into infectious cysts.

143 These data suggest that once trophozoites invade the cornea, MIP-133 production is ne

144 and engulfing red blood cells, E histolytica trophozoites invade the intestinal mucosa, causing amoeb

145 When E. histolytica trophozoites invade the lamina propria of a host colon,

146 testinal epithelial colonization of invasive trophozoites involves a complex interplay in which the u

147 ing, while no signal was obtained from 10(6) trophozoites killed by heat, desiccation, or UV radiatio

148 Moreover, even though Giardia trophozoites lack a morphologically discernible Golgi ap

149 Although Giardia trophozoites lack a morphologically discernible Golgi ap

150 racecal inoculation of Entamoeba histolytica trophozoites led to established infection in 60% of C3H

151 Target images and trophozoite-like images are pathognomonic of AK.

152 rreflective objects (diameter, <30 mum); and trophozoite-like objects (diameter, >30 mum).

153 roteins expressed on the IRBC surface during trophozoite maturation partially mask accessibility of a

154 ect corneal epithelial or stromal cells from trophozoite-mediated cytolysis in vitro.

155 Acanthamoeba trophozoite migration is also voltage-dependent, with in

156 We find that the trophozoite migration response is voltage-dependent, wit

157 In 2-microm channels, trophozoites mimicked "pitting," a normal process in the

158 transition from free swimming to attachment, trophozoites modified their swimming behavior from a rap

159 oxiredoxin in Rahman rendered the transgenic trophozoites more resistant to killing by H2O2 in vitro,

160 ese data suggest an important role of PKA in trophozoite motility during vegetative growth and the ce

161 Acanthamoeba trophozoites move at random in the absence of an EF, but

162 Acanthamoeba trophozoites move directionally in response to an EF in

163 Trophozoite mucosal invasion is triggered only when both

164 Despite strong CvGal1 binding to P. marinus trophozoites, no binding of ABH blood group antibodies w

165 intimate contact with cells, suggesting that trophozoites obtain an essential nutrient or growth fact

166 A concentration of 10(4) trophozoites of 3 well-characterized clinical strains of

167 ved macrophages were either coincubated with trophozoites of a clinical isolate of Acanthamoeba (geno

168 Trophozoites of A. castellanii bound avidly to corneal e

169 um from the 2004-2006 keratitis outbreak and trophozoites of Acanthamoeba castellanii were inoculated

170 In vitro real-time imaging demonstrated that trophozoites of both strains often established evanescen

171 row-derived macrophages were cocultured with trophozoites of either the laboratory Neff strain or a c

172 Analysis of trophozoites of five different species of Acanthamoeba e

173 ucing ability, and MBP expression pattern of trophozoites of four different isolates of Acanthamoeba

174 demonstrated lower detection limits of five trophozoites of G. lamblia.

175 ia swim, we used video microscopy to observe trophozoites of Giardia intestinalis, which were labeled

176 consisting of eggs, larvae, cysts, and a few trophozoites of Giardia intestinalis.

177 and the mitochondrial membrane potential of trophozoites of the malaria parasite Plasmodium berghei

178 Trophozoites of the malaria parasite Plasmodium falcipar

179 Trophozoites of the WB isolate but not the GS isolate we

180 site numbers (n = 7) or specimens containing trophozoites only (n = 3); one specimen with a false-neg

181 Dexamethasone-treated trophozoites or cysts induced a significant cytopathic e

182 ein on the surfaces of axenic E. histolytica trophozoites or from solubilized amebae.

183 on the development of either rings to early trophozoites or late trophozoites to schizonts and meroz

184 not during the development of rings to early trophozoites or late trophozoites to schizonts and meroz

185 colitis, we demonstrate that E. histolytica trophozoites or their released proteinases, including cy

186 of IL-10; furthermore, challenge with either trophozoites or their soluble metabolites stimulate both

187 surface proteins and by flow cytometry using trophozoites overexpressing epitope-tagged calreticulin.

188 indirect immunofluorescence assay with whole trophozoites (P < 0.01) and Western blot analysis confir

189 otocol was capable of detecting as few as 20 trophozoites per PCR on fecal DNA isolated using a comme

190 A isolated using a commercial method or 1.25 trophozoites per PCR on fecal DNA isolated using a G. la

191 Development proceeds rapidly from the trophozoite phase of nutrient acquisition and growth thr

192 Here we show that in isolated trophozoite phase parasites: (i) both CPA and Thg releas

193 at kill asexual blood-stage parasites at the trophozoite phase, and the most promising compound 24 al

194 evealed the existence of distinct, nonclonal trophozoite populations with high and low EhMSP-1 surfac

195 Entamoeba histolytica trophozoites produce amoebapores, a family of small amph

196 Besides, all compounds inhibit the trophozoite proliferation in amoebic liver abscess induc

197 Acceleration of trophozoite proliferation was observed when trophozoites

198 In trophozoites, pyruvate-ferredoxin oxidoreductase (PFOR)

199 Finally, trophozoite quorum sensing via the lectin initiates the

200 eding, the healthy oysters ingest P. marinus trophozoites released to the water column by the infecte

201 Most of the SOD activity in P. marinus trophozoites resides in a major component of subunit mol

202 Inside oyster hemocytes, trophozoites resist oxidative killing, proliferate, and

203 Motile trophozoites respond to soluble secreted signals, which

204 Overexpression of EhEBP1 in E. histolytica trophozoites resulted in a 7-fold drop in promoter activ

205 development and that this persists until the trophozoite-schizont boundary.

206 s unable to induce excystation and increased trophozoite sensitivity to APC16.

207 subcellular localization of ERK1 and ERK2 in trophozoites showed ERK1 staining mostly in the median b

208 ggest the presence of an H(+) conductance in trophozoites similar to that produced by a mitochondrial

209 les, and was responsible for at least 93% of trophozoite soluble cysteine protease activity.

210 Babesia can also be confused with the early trophozoite stage (ring forms) of Plasmodium parasites.

211 rotease that cleaves hemoglobin at the early trophozoite stage and erythrocyte membrane ankyrin and p

212 tide increases dramatically during the early trophozoite stage and reaches its maximal level in the l

213 ashion, with high levels detected during the trophozoite stage at the peak of parasite membrane bioge

214 The parasite asexual trophozoite stage is susceptible to iron-induced oxidati

215 e as the organelle forms upon entry into the trophozoite stage of development and that this persists

216 rmation and swelling of the IRBCs during the trophozoite stage of P. falciparum that is followed by s

217 es are transcribed simultaneously during the trophozoite stage of the IDC and that only a small subse

218 alarial drug dihydroartemisinin (DHA) at the trophozoite stage resulted in a ~ fourfold increase in s

219 parum-infected red blood cells (RBCs) in the trophozoite stage were simultaneously loaded with the Ca

220 ript pattern was unique, peaking at mid-late trophozoite stage, but absent in late-stage schizonts.

221 e growth of the parasite specifically at the trophozoite stage, preventing further development to sch

222 ycle, at the highly transcriptionally active trophozoite stage, the genome adopts a more open chromat

223 obin in the acidic food vacuole at the early trophozoite stage, whereas it cleaves specific component

224 replicative stage of the asexual cycle, the trophozoite stage.

225 organelle forms and persists throughout the trophozoite stage.

226 ages, while H4-K16 acetylation peaked in mid-trophozoite stage.

227 le of the parasite but induced mainly at the trophozoite stage.

228 inhibits parasite differentiation beyond the trophozoite stage.

229 in parasitised cells up to the mature, late trophozoite stage.

230 h Plasmodium falciparum, at the mature, late trophozoite stage.

231 t is significantly elevated during the early trophozoite stage.

232 he Pfmc-2tm genes are transcribed during the trophozoite stage; this narrow time frame of transcripti

233 parasites were more barrier disruptive than trophozoite-stage P. falciparum-IE and prolonged thrombi

234 Whereas trophozoite-stage P. falciparum-IE have limited effect o

235 ce of erythrocytes infected by early-to-late-trophozoite-stage parasites.

236 ound distributed on the surface of ring- and trophozoite-stage parasites.

237 Trophozoite stages failed to freely traverse 2- to 4-mic

238 nst HEK293 cells and inhibited both ring and trophozoite stages of the malaria parasite life cycle.

239 core histone gene expression during the late trophozoite stages, consistent with their role in replic

240 f the parasite life cycle at the ring or the trophozoite stages.

241 CLAG9 at two stages--the early ring and late trophozoite stages.

242 f variant histones decreased in mid- or late trophozoite stages.

243 nant var gene occurs in the later (pigmented trophozoite) stages, whereas Northern blot data indicate

244 bition of FBPA gene transcription in Giardia trophozoites suggested that the enzyme is necessary for

245 abscesses consisting of a few E histolytica trophozoites surrounding dead and dying hepatocytes and

246 row mammalian cells does not support healthy trophozoite survival for more than a few hours.

247 Trophozoite survival required intimate contact with cell

248 Recently, E. histolytica trophozoites that are totally deficient in the productio

249 of amebic liver abscess, but E. histolytica trophozoites that do not express amoebapore-A can still

250 The mucus gel layer prevents those trophozoites that escape the hydrolases from reaching th

251 nal morphologic features of the 2 strains of trophozoites that received treatment were similar to tho

252 ally expressed in nonencysting and encysting trophozoites, the giardial ceramide glucosyltransferase

253 th dependent efficacy against A. castellanii trophozoites, the latter producing death via permeabiliz

254 ytic enzymes that facilitate the invasion of trophozoites through the basement membrane.

255 ive infection, (b) developmental change from trophozoite to cyst, or (c) invasion and potential death

256 abeling is detected predominantly during the trophozoite to schizont and schizont to ring transitions

257 From the trophozoite to the schizont stage that ensues within 24-

258 treatment on the capacity of A. castellanii trophozoites to adhere to and kill corneal epithelial ce

259 lactose-specific adherence of E. histolytica trophozoites to Chinese hamster ovary cells in vitro (P,

260 Interestingly, adherence of E. histolytica trophozoites to CHO cells was inhibited by MAbs against

261 was upregulated in phagocytic E. histolytica trophozoites to determine whether these genes actually f

262 igated the in vitro response of Acanthamoeba trophozoites to electric fields (EFs).

263 s exclusively during the maturation of early trophozoites to late trophozoites but not during the dev

264 inding receptor that facilitates adhesion of trophozoites to mannosylated proteins on corneal epithel

265 The results suggest that binding of trophozoites to mannosylated proteins on the corneal sur

266 of thioredoxin and enhancing sensitivity of trophozoites to reactive oxygen-mediated killing.

267 om rings to early trophozoites and from late trophozoites to schizonts and merozoites.

268 f either rings to early trophozoites or late trophozoites to schizonts and merozoites.

269 pment of rings to early trophozoites or late trophozoites to schizonts and merozoites.

270 n on corneal epithelial cells and stimulates trophozoites to secrete a mannose-induced 133 kDa protea

271 In addition, the capacity of trophozoites to survive in AH was determined in vitro.

272 The capacity of trophozoites to sustain oxidative phosphorylation was ad

273 x bead treatment did not affect adherence of trophozoites to the corneal epithelium or protect cornea

274 Adherence of EhMSP-1-deficient trophozoites to tissue culture cell monolayers was more

275 Giardia lamblia trophozoites transfected with the transcript of this con

276 vered that, during rapid swimming of Giardia trophozoites, undulations of the caudal region contribut

277 By comparison, host-cell attached trophozoites up-regulated intracellular pathways for ubi

278 revealed that the trailing edge of polarized trophozoites, uroids, are highly enriched in lipid rafts

279 While using this planar swimming motion, the trophozoites used the flagella for propulsion and direct

280 ed transcripts of luciferase gene in Giardia trophozoites via transfection and observed that when the

281 The migration of A. castellanii trophozoites was analyzed and quantified with ImageJ sof

282 amine binding sites on the surface of amoeba trophozoites was confirmed using radiolabeled catecholam

283 d stage parasites, as maturation of rings to trophozoites was markedly stalled.

284 Falcipain-2 was predominantly expressed in trophozoites, was concentrated in food vacuoles, and was

285 of mitochondria of Plasmodium yoelii yoelii trophozoites were assayed in situ after permeabilization

286 ree-dimensional culture system, Acanthamoeba trophozoites were cultured in agar, exposed to an EF, di

287 In all cases, cysts and trophozoites were detected 24 hours after treatment at a

288 Despite induction, E. histolytica trophozoites were found to be resistant to killing by th

289 Acanthamoeba castellanii trophozoites were grown in peptone-yeast extract glucose

290 Giardia trophozoites were persuaded to encyst in vitro by mimick

291 trophozoite proliferation was observed when trophozoites were treated with dexamethasone.

292 The organism has two life cycle stages, trophozoites, which are responsible for tissue invasion,

293 model, M. bovis would be taken up by amoebal trophozoites, which are the actively feeding, replicatin

294 -expressed genes were lost in AN3661-treated trophozoites, which was not observed in parasites select

295 evels of Pf MDH transcripts were detected in trophozoites while the Pf MDH protein level remained hig

296 domains, as evidenced by reduced staining of trophozoites with CTXB and GM1 antibodies.

297 t of a synchronized culture of P. falciparum trophozoites with gossypol caused induction in expressio

298 the detection of Entamoeba histolytica (Eh) trophozoites with ingested erythrocytes.

299 ur finding that co-culture of E. histolytica trophozoites with mucin-producing T84 cells increased eh

300 inhibitors blocked hemoglobin hydrolysis in trophozoites, with a subsequent block in rupture of eryt