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1 ent a pH-sensor (as in similar toxins, e.g., Listeriolysin).
2                               The hemolysin, listeriolysin 0 (LLO), produced by Listeria monocytogene
3 micked by Listeria monocytogenes and soluble listeriolysin, a pore-forming hemolysin derived from it,
4 he host response is markedly attenuated in a listeriolysin-deficient (Deltahly) mutant despite its ab
5 trations that inhibited hemolysis by ALO and listeriolysin did not prevent these toxins from binding
6 ene hly (encoding the pore-forming cytolysin listeriolysin) is under negative regulation by readily m
7  I molecules present three nonamer peptides, listeriolysin (LLO) 91-99, p60 217-225, and p60 449-457,
8 ; however, WTLM and L. monocytogenes lacking listeriolysin O (DeltahlyLM) induce similar levels of cy
9 anomer peptides amino acids (aa) 91 to 99 of listeriolysin O (LLO 91-99) and aa 217 to 225 of the p60
10 by the cholesterol-dependent cytolysin (CDC) listeriolysin O (LLO) acts within the infected cell, (ii
11 ast two critical secreted virulence factors: listeriolysin O (LLO) and a broad-specificity phospholip
12                                              Listeriolysin O (LLO) and a phosphatidylinositol-specifi
13                                              Listeriolysin O (LLO) and ActA are essential virulence d
14              Listeria monocytogenes requires listeriolysin O (LLO) and ActA, the products of hly and
15 tron microscopy that LM expressing truncated listeriolysin O (LLO) and amino acid fragments 311 to 66
16  on the expression of two secreted proteins: listeriolysin O (LLO) and phosphatidylcholine-preferring
17 to 200 nm, containing the pore-forming toxin listeriolysin O (LLO) and phosphatidylinositol-specific
18 virulence factors of Listeria monocytogenes, listeriolysin O (LLO) and phosphatidylinositol-specific
19 91 to 99 (aa91-99) immunodominant peptide of listeriolysin O (LLO) and to the aa217-225 immunodominan
20 n host cells by using the pore-forming toxin listeriolysin O (LLO) and two phospholipase C enzymes.
21 ) that are deficient in the virulence factor listeriolysin O (LLO) are highly attenuated and are thou
22  the Listeria monocytogenes virulence factor listeriolysin O (LLO) enhances the immunogenicity and an
23                                              Listeriolysin O (LLO) is a cholesterol-dependent cytolys
24                       The pore-forming toxin listeriolysin O (LLO) is a major virulence factor implic
25                       The pore-forming toxin listeriolysin O (LLO) is a major virulence factor secret
26                                              Listeriolysin O (LLO) is a pore-forming cytolysin that m
27           The Listeria monocytogenes protein listeriolysin O (LLO) is a pore-forming protein essentia
28                                              Listeriolysin O (LLO) is a pore-forming toxin of the cho
29                                              Listeriolysin O (LLO) is a pore-forming toxin that media
30                                              Listeriolysin O (LLO) is a secreted pore-forming protein
31                                              Listeriolysin O (LLO) is a secreted pore-forming toxin o
32 ved cells tested, the pore-forming cytolysin listeriolysin O (LLO) is absolutely required for lysis o
33                                              Listeriolysin O (LLO) is an essential determinant of pat
34                                              Listeriolysin O (LLO) is an essential virulence factor f
35              The secreted pore-forming toxin listeriolysin O (LLO) of the intracellular pathogen List
36 ould be attributed partially to insufficient listeriolysin O (LLO) production, indicating a requireme
37 mediated, and a nonamer CTL epitope from the listeriolysin O (LLO) protein has been identified in BAL
38 ,258) fused to the first 441 residues of the listeriolysin O (LLO) protein.
39 ytogenes and its secreted pore-forming toxin listeriolysin O (LLO) to identify key signaling events a
40 uction of the hly-encoded secreted hemolysin listeriolysin O (LLO) was also found to significantly en
41                                              Listeriolysin O (LLO), a cholesterol-binding cytolysin o
42                               Among these is listeriolysin O (LLO), a pore-forming hemolysin that is
43                  We prove in this study that listeriolysin O (LLO), a pore-forming molecule and a maj
44 e with an Escherichia coli strain expressing listeriolysin O (LLO), a pore-forming toxin from L. mono
45 which is dependent on the pore-forming toxin listeriolysin O (LLO), followed by rupture.
46 the Listeria monocytogenes virulence factor, listeriolysin O (LLO), induces an immune response that c
47  of L. monocytogenes, the pore-forming toxin listeriolysin O (LLO), is sufficient to induce L. monocy
48 ore-forming cholesterol-dependent cytolysin, listeriolysin O (LLO), mediates bacterial escape from ve
49 gen which secretes a pore-forming cytolysin, listeriolysin O (LLO), necessary for intracellular growt
50               Here, the pore-forming protein listeriolysin O (LLO), secreted by Listeria monocytogene
51                  We report here that the CDC listeriolysin O (LLO), secreted by the facultative intra
52 e of macrophages from liposomes that contain listeriolysin O (LLO), the hemolytic protein of Listeria
53 ment of mice with a neutralizing mAb against listeriolysin O (LLO), the pore-forming toxin of Listeri
54 r PrfA, including the pore-forming cytolysin listeriolysin O (LLO), two phospholipases C (PlcA and Pl
55                    Using a prototypical CDC, listeriolysin O (LLO), we provide a microscopic connecti
56 o reduced cytokine production in response to Listeriolysin O (LLO), which activates MC by a TLR2-inde
57 hat secretes a pore-forming cytolysin called listeriolysin O (LLO), which disrupts the phagosomal mem
58 rane is initiated by the secreted haemolysin listeriolysin O (LLO), which is essential for vacuolar e
59 pecific for the L. mono cytogenes-encoded Ag listeriolysin O (LLO).
60  amino acid 91 to 99 (aa91-99) sequence from listeriolysin O (LLO).
61 tion through the secreted pore-forming toxin listeriolysin O (LLO).
62 intracellular life cycle that is mediated by listeriolysin O (LLO).
63 osol by secreting the pore-forming cytolysin listeriolysin O (LLO).
64 om the phagosome using a secreted cytolysin, listeriolysin O (LLO).
65 otein with a truncated, nonhemolytic form of listeriolysin O (LLO).
66 actions of the pore-forming virulence factor listeriolysin O (LLO).
67 diated by the bacterial pore-forming protein listeriolysin O (LLO).
68 lls via the action of the pore-forming toxin listeriolysin O (LLO).
69 as a fusion protein joined to a nonhemolytic listeriolysin O (LLO).
70 (PI-PLC), a broad-range phospholipase C, and listeriolysin O (LLO).
71 T cells is the secreted bacterial hemolysin, listeriolysin O (LLO).
72              T cell populations specific for listeriolysin O (LLO)91-99, the immunodominant epitope r
73 CD8+ T cells specific for the immunodominant listeriolysin O (LLO91-99) epitope provide immunity to L
74                          Mice immunized with listeriolysin O 91-99-coated BMDCs are protected against
75  that pH-sensitive liposomes containing both listeriolysin O and gelonin were more effective than con
76 pression of the phagosome-lysing pore former listeriolysin O and on type I IFN receptor signaling.
77 atural L. monocytogenes-derived soluble Ags (listeriolysin O and p60) revealed that tethering of thes
78              HD-5 was very effective against listeriolysin O but less effective against the other tox
79     In in vitro experiments, co-encapsulated listeriolysin O enabled liposomal gelonin-mediated B16 c
80 lipid biosynthesis, enhanced the toxicity of listeriolysin O expressed in the host cell cytosol, lead
81 smid containing the invasin gene Inv and the listeriolysin O gene HlyA, which encode two bacterial fa
82 irement for the essential pore-forming toxin listeriolysin O in mediating escape from phagocytic vacu
83 cytoplasmic entry of Listeria facilitated by listeriolysin O is an essential feature not only of the
84                     The pore-forming protein listeriolysin O mediates escape from host vacuoles and u
85 -2Kb-restricted CD8 T cells specific for the listeriolysin O molecule mediate significant immunity in
86 cua and a mutant strain of L. monocytogenes (listeriolysin O negative), which do not enter the cytoso
87  provided only pore-forming activity because listeriolysin O of Listeria monocytogenes could substitu
88              Nonetheless it is possible that listeriolysin O potentiates the effect(s) of an other mo
89                      These data suggest that listeriolysin O production by infecting L. monocytogenes
90  single LFn fusion protein containing NP and listeriolysin O protein epitopes in tandem mount a CTL r
91  r30 linked in frame to the L. monocytogenes listeriolysin O signal sequence and driven by the hly pr
92 train was constructed in which expression of listeriolysin O was placed under the inducible control o
93  accounted for by a decrease in LM-specific (listeriolysin O(91-99) tetramer(+)) effector CD8(+) T ce
94 aracterize changes in SUMOylation induced by listeriolysin O, a bacterial toxin that impairs the host
95                            Immunization with listeriolysin O, a potent inducer of cell death, also pr
96       Cellular immune responses specific for listeriolysin O, a secreted bacterial protein required f
97 ree of these exotoxins: anthrolysin O (ALO), listeriolysin O, and pneumolysin.
98 xpression of other critical virulence genes (Listeriolysin O, and two phospholipases plcA and plcB) i
99 when the matrix protein was coexpressed with listeriolysin O, but not when expressed alone.
100 ndent cytolysin (CDC) family, which includes listeriolysin O, perfringolysin O, and streptolysin O.
101 specific cells were similar to those against listeriolysin O, the immunodominant Ag of L. monocytogen
102 n with WT, heat-killed, or mutant Lm lacking listeriolysin O, the pore-forming hemolysin that promote
103 apsulated inside pH-sensitive liposomes with listeriolysin O, the pore-forming protein that mediates
104 production of the critical virulence factor, listeriolysin O, was compromised by FA modulation, sugge
105                               Infection with listeriolysin O-expressing, cytosolic Bacillus subtilis
106 ncentrations fractions significantly reduced listeriolysin O-induced haemolysis (p < 0.05), and ameli
107  on uninfected cells and may be triggered by listeriolysin O-mediated activation of host response mec
108 nocytogenes and induced a subset of effector listeriolysin O-specific CD11a(+) CD8(+) T cells in sple
109       However, significant levels of Gag and listeriolysin O-specific CD8(+) T cells were observed in
110 se animals is characterized by activation of listeriolysin O-specific CD8(+) T cells, which are capab
111 with L. monocytogenes dal dat/pRRR generated listeriolysin O-specific effector and memory CD8(+) T ce
112  requires the presence of pore-forming toxin listeriolysin O.
113 ecame ill had elevated levels of antibody to listeriolysin O.
114 erum samples were tested for IgG antibody to listeriolysin O.
115  requires the presence of pore-forming toxin listeriolysin O.
116 rotein Ags: hen egg white lysozyme, OVA, and listeriolysin O.
117 s not limited to CD8+ T cells that recognize listeriolysin O.
118  partially dependent on the virulence factor listeriolysin O; however, WTLM and L. monocytogenes lack
119 l liver kinase-1) to the microbial adjuvant, listeriolysin-O, and used Lm to deliver the Ags and elic
120                                           Lm-listeriolysin-O-fetal liver kinase-1 was able to eradica
121                                              Listeriolysin S (LLS) is a thiazole/oxazole-modified mic
122                    Here, we demonstrate that Listeriolysin S (LLS), a virulence factor only present i

 
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