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1 as infected with both E. intestinalis and E. cuniculi.
2 nents of these organelles in Encephalitozoon cuniculi.
3 tive immune response against Encephalitozoon cuniculi.
4 ficant sequence similarity to proteins in E. cuniculi.
5 chizosaccaromyces pombe) and Encephalitozoan cuniculi.
6 r had positive serologic test results for E. cuniculi.
7 the microsporidian parasite Encephalitozoon cuniculi.
8 s (CTL) in survival of mice infected with E. cuniculi.
9 pecies-specific primers for E. hellem and E. cuniculi.
10 n intestinalis (2.3 Mbp) and Encephalitozoon cuniculi (2.9 Mbp) revealed massive gene losses and redu
11 0 tpr homologs in Treponema paraluiscuniculi Cuniculi A strain and determined their sequence architec
13 (Bosnia strain), Treponema paraluiscuniculi (Cuniculi A, H, and K strains), and a little-characterize
19 his study, we show that both Encephalitozoon cuniculi and Encephalitozoon intestinalis are preferenti
20 rikingly similar to those of Encephalitozoon cuniculi and Encephalitozoon intestinalis in both form a
21 scence histograms showed that rabbit anti-E. cuniculi and rabbit anti-E. intestinalis sera were react
24 oridian spores of Encephalitozoon hellem, E. cuniculi, and E. intestinalis were propagated in axenic
25 from the eukaryotic pathogen Encephalitozoon cuniculi bound to tryptophan, a HisRS from Burkholderia
26 ochondrion and host has been subverted in E. cuniculi, by reductive evolution and analogous gene repl
27 of the N-terminal domain of Encephalitozoon cuniculi Cdc27 (Cdc27(Nterm)), revealing a homo-dimeric
28 n solution, and abolishes the capacity of E. cuniculi Cdc27 to complement Saccharomyces cerevisiae Cd
30 the microsporidian parasite Encephalitozoon cuniculi consists of 15 heptad repeats, which approximat
33 lysis provides a basis for distinguishing E. cuniculi, E. hellem, and E. intestinalis in clinical spe
35 cleotide probes specific for Encephalitozoon cuniculi, E. hellem, and Encephalitozoon (Septata) intes
37 l and structural analyses of Encephalitozoon cuniculi Ecm1, a prototypal cellular cap methyltransfera
38 challenged with the parasite Encephalitozoon cuniculi, effector CD8+ T cell survival and polyfunction
39 es: Enterocytozoon bieneusi, Encephalitozoon cuniculi, Encephalitozoon hellem, and Encephalitozoon in
40 t the intracellular parasite Encephalitozoon cuniculi encodes a complete mRNA capping apparatus consi
43 genome of the microsporidian Encephalitozoon cuniculi has lost all of its genes for MCF proteins.
45 uman E. cuniculi isolate was identical to E. cuniculi III, which had been isolated only from domestic
48 neration of CD8(+) T-cell immunity during E. cuniculi infection and the cytokines involved in this pr
50 In the current study, we demonstrate that E. cuniculi infection causes strong Toll-like receptor 4 (T
51 imals, CD4(-/-) mice were able to resolve E. cuniculi infection even at a very high challenge dose (5
52 he present study, immune response against E. cuniculi infection in CD4(+) T-cell-deficient mice was e
53 ta obtained in these studies suggest that E. cuniculi infection induces a strong and early CD8+ T res
54 an IFN-gamma-mediated protection against E. cuniculi infection that is independent of NO production.
57 The role of gamma(delta) T cells against E. cuniculi infection was further evaluated by using gene-k
59 ntigen-specific CD8(+) T-cell response to E. cuniculi infection was observed in CD4(-/-) mice (precur
62 it greater susceptibility to Encephalitozoon cuniculi infection, and their ability to evoke an Ag-spe
72 it is able to grow in vitro, Encephalitozoon cuniculi is currently the best-studied microsporidian.
73 of a recently cultured human Encephalitozoon cuniculi isolate was analyzed by gene amplification and
77 uence analysis of the PTP gene divided 11 E. cuniculi isolates into three genotypes in congruence wit
80 chain reaction testing were positive for E. cuniculi of genotype III in each recipient; the organism
81 crophages were infected with Encephalitozoon cuniculi or Encephalitozoon intestinalis, and the recrui
82 rown Encephalitozoon hellem, Encephalitozoon cuniculi, or Vittaforma corneae or with Enterocytozoon b
86 mples reacted with anti-E. hellem or anti-E. cuniculi sera, nor were they amplified with species-spec
87 ) cultures from knockout mice pulsed with E. cuniculi spores were unable to develop a robust CD8(+) T
89 s, and E. hellem, as well as Encephalitozoon cuniculi, spores in fecal samples and is a useful tool f
93 he existence of functional APC/C genes in E. cuniculi, the evolutionarily conserved dimeric propertie
95 consistent with this hypothesis, all four E. cuniculi transporters can transport ATP, and three of th
96 ot Encephalitozoon hellem or Encephalitozoon cuniculi was confirmed in 6 of 8 mammalian stool samples
98 In this study, the genetic diversity of E. cuniculi was examined at the polar tube protein (PTP) an
100 donors protected SCID mice infected with E. cuniculi, whereas administration of CD8(+) T cells from
102 ted in vivo activity against Encephalitozoon cuniculi, with prolonged survival and the prevention of
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