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1 asion as the parasite moves into the nascent parasitophorous vacuole.
2 rusion to accomplish cell entry and form the parasitophorous vacuole.
3 space, as well as secreted into the primary parasitophorous vacuole.
4 asite-derived compartment referred to as the parasitophorous vacuole.
5 nvasion of host cells and establishment of a parasitophorous vacuole.
6 lication of C. burnetii and formation of the parasitophorous vacuole.
7 within the host cell cytosol and within the parasitophorous vacuole.
8 cretes a variety of proteins that modify the parasitophorous vacuole.
9 ctor proteins that direct the formation of a parasitophorous vacuole.
10 n serves as a source of membrane to form the parasitophorous vacuole.
11 rotein translocon within the membrane of the parasitophorous vacuole.
12 e intracellular replication compartment, the parasitophorous vacuole.
13 oving junction and subsequent formation of a parasitophorous vacuole.
14 that replicates within an intraerythrocytic parasitophorous vacuole.
15 om within a phagosomal compartment to form a parasitophorous vacuole.
16 utside the parasites and is found within the parasitophorous vacuole.
17 lar protozoan parasite that resides inside a parasitophorous vacuole.
18 mic parasite residing in a host cell-derived parasitophorous vacuole.
19 the RBC and the coordinated induction of the parasitophorous vacuole.
20 junction formation and the induction of the parasitophorous vacuole.
21 ompartment of the host cell that is termed a parasitophorous vacuole.
22 ds, glucose being a limiting nutrient in the parasitophorous vacuole.
23 n acidified (pH 4.5 to 5) phagolysosome-like parasitophorous vacuole.
24 when CD40 was ligated after the formation of parasitophorous vacuoles.
25 ss program are revealed: (1) swelling of the parasitophorous vacuole accompanied by shrinkage of the
28 n network that connects parasites within the parasitophorous vacuole and allows vesicles to be exchan
29 rrangement persisted for the duration of the parasitophorous vacuole and contributed to the formation
32 nd b, the 452 aa Pfs230 is secreted into the parasitophorous vacuole and released as a soluble protei
33 arum infects an erythrocyte, it resides in a parasitophorous vacuole and remarkably exports proteins
34 1 clone (C9) formed morphologically unusual parasitophorous vacuoles and another (A2) was avirulent
35 nfected with T. gondii resulted in fusion of parasitophorous vacuoles and late endosomes/lysosomes.
36 Ligation of CD40 caused colocalization of parasitophorous vacuoles and LC3, a marker of autophagy,
37 , inhibitory compounds must cross host cell, parasitophorous vacuole, and parasite membranes and cyst
38 mulation of LC3-containing vesicles near the parasitophorous vacuole, and to the relocalization towar
39 the rupture of infected erythrocytes but not parasitophorous vacuoles, and independently interfering
40 ndicating that formation of the junction and parasitophorous vacuole are molecularly distinct steps i
41 sion and survival of the parasite within the parasitophorous vacuole are required to induce and maint
42 are required for peptide degradation in the parasitophorous vacuole as the degradation of the marker
43 GRA6, a polymorphic protein secreted in the parasitophorous vacuole, as the source of the immunodomi
44 a unique intracellular but extracytoplasmic parasitophorous vacuole at the apical surface of infecte
45 the liver, invade hepatocytes, and develop a parasitophorous vacuole but do not significantly persist
46 s produced in the parasite mitochondrion and parasitophorous vacuole by decarboxylation of phosphatid
47 structure is produced by modification of the parasitophorous vacuole by the parasite and is important
50 elin hydrolysis, is detected in newly formed parasitophorous vacuoles containing trypomastigotes but
51 lar pathogen that replicates in an acidified parasitophorous vacuole derived from host lysosomes.
52 f host protective responses, escape from the parasitophorous vacuole, differentiation, and other acti
53 revealed that the protein is present in the parasitophorous vacuole during growth and is later recru
54 the rhoptries are released into the nascent parasitophorous vacuole during invasion into the host ce
56 pathways of host-parasite interaction at the parasitophorous vacuole employed by Toxoplasma and host,
59 II molecules and FcR were excluded from the parasitophorous vacuole formed by active parasite invasi
61 brane proteins are excluded from the forming parasitophorous vacuole hence conferring the resistance
65 ell, Toxoplasma forms a novel organelle, the parasitophorous vacuole, in which it resides during its
66 fore invading a hepatocyte by formation of a parasitophorous vacuole, in which they developed into th
67 atis elementary bodies and in the chlamydial parasitophorous vacuole (inclusion) membrane of infected
68 ranslation inhibits early trafficking of the parasitophorous vacuole (inclusion) to the microtubule-o
70 -specific Ab, did not block formation of the parasitophorous vacuole, indicating that formation of th
71 granules--serves to establish and maintain a parasitophorous vacuole inside the host cell in which th
72 that Toxoplasma proteins can escape from the parasitophorous vacuole into the host cytoplasm and be p
73 st cellular attack physically disrupting the parasitophorous vacuole, involves autophagy to collect c
75 se interaction of host mitochondria with the parasitophorous vacuole is connected to lipoate supply b
78 apical membranes overlying the parasite and parasitophorous vacuole may be the unsuspected major rou
79 es specific for proteins associated with the parasitophorous vacuole membrane (Pfs16 or Exp-1) or Mau
80 mma enhanced the recruitment of LC3 onto the parasitophorous vacuole membrane (PVM) and increased the
81 lasma-secreted protein that localizes to the parasitophorous vacuole membrane (PVM) and mediates pass
82 screte subcellular reservoirs and attack the parasitophorous vacuole membrane (PVM) as orchestrated,
86 f phosphorylated IkappaB that is seen at the parasitophorous vacuole membrane (PVM) of T. gondii was
88 ausative agent of malaria, wraps itself in a parasitophorous vacuole membrane (PVM), which constitute
91 to an inability to rapidly permeabilize the parasitophorous vacuole membrane and host plasma membran
92 he export of hundreds of proteins across the parasitophorous vacuole membrane and into the human host
93 B1-deficient parasites failed to rupture the parasitophorous vacuole membrane and to egress from hepa
94 where it resides with little turnover in the parasitophorous vacuole membrane for most of the remaind
95 s reduced in uis4(-) parasites, which lack a parasitophorous vacuole membrane protein and arrest duri
96 s located on the gametocyte plasma membrane, parasitophorous vacuole membrane, and the membranes of c
97 for the disruption of the gamete-containing parasitophorous vacuole membrane, and thus for parasite
98 across its plasma membrane and a surrounding parasitophorous vacuole membrane, into its host erythroc
99 its parasite plasma membrane and surrounding parasitophorous vacuole membrane, most of which are like
101 Based on these findings we propose that parasitophorous vacuoles not only offer protection but a
102 incorporation into the vacuole generates the parasitophorous vacuole occupied by TOXOPLASMA: The char
103 findings reveal the presence in the malarial parasitophorous vacuole of a regulated, PfSUB1-mediated
108 ding protein family that is recruited to the parasitophorous vacuole of the intracellular parasite To
109 ichia coli beta-lactamase, secreted into the parasitophorous vacuole of transgenic tachyzoites was co
110 's membranous nanotubular network within the parasitophorous vacuole play a major role in determining
112 0-12-h parasites is found released into the parasitophorous vacuole (PV) and in apposition with the
113 rasite Plasmodium falciparum reside within a parasitophorous vacuole (PV) and set up unique "extrapar
114 tii generates a replication niche termed the parasitophorous vacuole (PV) by directing fusion with au
118 parasite proficiently adapted to thrive in a parasitophorous vacuole (PV) formed in the cytoplasm of
120 parasite Toxoplasma gondii develops within a parasitophorous vacuole (PV) in mammalian cells, where i
121 stem (T4SS) to generate a phagolysosome-like parasitophorous vacuole (PV) in which to replicate.
122 gosomes and lysosomes, establishing a unique parasitophorous vacuole (PV) in which to replicate.
125 r macrophages in a unique phagolysosome-like parasitophorous vacuole (PV) required for survival.
126 en Coxiella burnetii directs biogenesis of a parasitophorous vacuole (PV) that acquires host endolyso
127 Toxoplasma multiplies in a membrane-bound parasitophorous vacuole (PV) that interacts with mammali
128 omplexa that resides within an intracellular parasitophorous vacuole (PV) that is selectively permeab
129 ted biogenesis of a large, growth-permissive parasitophorous vacuole (PV) with phagolysosomal charact
130 i directs biogenesis of a phagolysosome-like parasitophorous vacuole (PV), in which it replicates.
131 king processes, particularly export from the parasitophorous vacuole (PV), is poorly understood and a
132 xoplasma gondii resides within a specialized parasitophorous vacuole (PV), isolated from host vesicul
133 asmodium, replicates inside a membrane-bound parasitophorous vacuole (PV), which shields this intrace
148 nitroblue tetrazolium, we found that 25% of parasitophorous vacuoles (PVs) that harbor promastigotes
150 olesale transport of LDs into the lumen of a parasitophorous vacuole represents a unique mechanism of
151 ich are secreted via dense granules into the parasitophorous vacuole shortly after invasion, become p
156 d) inhibited formation of the mature (large) parasitophorous vacuole that is characteristic of C. bur
157 ides in a specialized compartment termed the parasitophorous vacuole that is derived from the host ce
158 ted/secreted antigen fraction as well as the parasitophorous vacuole that T. gondii occupies during i
159 esides within a specialized compartment, the parasitophorous vacuole, that sequesters the parasite an
160 s invade erythrocytes and replicate within a parasitophorous vacuole to form daughter cells that even
161 of host cell lysosomes, and escape from the parasitophorous vacuole to liberate amastigotes to multi
162 ufficient methionine is available within the parasitophorous vacuole to meet the needs of the parasit
163 results may suggest that TgPL1 moves to the parasitophorous vacuole to protect parasites from nitric
166 complex membrane network, which connects the parasitophorous vacuole to the host plasma membrane and
167 parasite divides within an intraerythrocytic parasitophorous vacuole until rupture of the vacuole and
169 ishes a replicative niche in a lysosome-like parasitophorous vacuole where it carries out a lengthy i
170 parasite that invades host cells, creating a parasitophorous vacuole where it communicates with the h
171 protease called SUB1 is discharged into the parasitophorous vacuole, where it proteolytically proces
172 intracellular pathogen, replicates within an parasitophorous vacuole with lysosomal characteristics.
174 tachyzoites, host cells, tachyzoites inside parasitophorous vacuoles within host cells, extracellula
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