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1 E. chaffeensis binding to and subsequent infection of mo
2 E. chaffeensis BolA bound to the promoters of genes enco
3 E. chaffeensis bolA complemented a stress-sensitive E. c
4 E. chaffeensis cannot synthesize phosphatidylcholine or
5 E. chaffeensis CtrA bound to the promoters of late-stage
6 E. chaffeensis experiences temperature changes during tr
7 E. chaffeensis expresses a sensor kinase, PleC, and a co
8 E. chaffeensis has a multigene family of major outer mem
9 E. chaffeensis inclusions were labeled with the transfer
10 E. chaffeensis induced rapid tyrosine phosphorylation of
11 E. chaffeensis infection activated the phosphatidylinosi
12 E. chaffeensis infection did not result in dramatic chan
13 E. chaffeensis infection in a human monocyte cell line (
14 E. chaffeensis strains induce strikingly variable inflam
15 E. chaffeensis TRP75 and E. canis TRP95 were immunopreci
16 E. chaffeensis was sensitive to closantel, an HK inhibit
17 E. chaffeensis, therefore, can recruit interacting signa
18 E. chaffeensis-EHRL-4-TRIM21 complexes caused significan
19 E. chaffeensis-specific cytotoxic T cells were not detec
20 responses to E. chaffeensis lipoproteins, 13 E. chaffeensis lipoprotein genes were cloned into a mamm
22 to analyze the antibody responses of the 37 E. chaffeensis indirect fluorescent-antibody assay (IFA)
24 129S6-Cd4(tm1Knw) mice also developed active E. chaffeensis-specific immunoglobulin G responses that
29 The addition of oxytetracycline 6 h after E. chaffeensis infection caused a decrease in TfR mRNA w
32 the hypothesis that immune responses against E. chaffeensis would be different if the mice are challe
36 ss spectrometry identified the protein as an E. chaffeensis 12.3-kDa hypothetical protein, which was
37 ted strongly with antibodies in sera from an E. chaffeensis-infected dog and human monocytotropic ehr
38 rophoretic mobility shift assays revealed an E. chaffeensis-encoded protein that specifically bound t
39 ast two-hybrid analysis demonstrated that an E. chaffeensis type 1 secretion system substrate, TRP32,
48 peptide repeat units from E. canis gp36 and E. chaffeensis gp47 were substantially less immunoreacti
50 peptides are conserved between E. muris and E. chaffeensis OMP-19, and they elicited IFN-gamma produ
51 B4, and virB6) of both A. phagocytophila and E. chaffeensis were arranged downstream from a sodB gene
52 ese five genes in both A. phagocytophila and E. chaffeensis were polycistronically transcribed and co
53 d endocytosis directs A. phagocytophilum and E. chaffeensis to an intracellular compartment secluded
54 cal sensitivities for A. phagocytophilum and E. chaffeensis were 93% and 84%, respectively, and speci
57 his macrophage-tropic bacterium, we assessed E. chaffeensis infections in three mouse strains with di
58 Recently, molecular interactions between E. chaffeensis 47-kDa tandem repeat (TR) protein (TRP47)
59 sferrin receptors (TfRs) accumulated on both E. chaffeensis and E. sennetsu, but not HGE agent, inclu
60 retic mobility shift assays showed that both E. chaffeensis and E. sennetsu infection increased the b
61 which peaked at 24 h postinfection with both E. chaffeensis and E. sennetsu infection in THP-1 or HL-
64 y indistinguishable from infection caused by E. chaffeensis or the agent of human granulocytic ehrlic
65 protein-processing enzymes were expressed by E. chaffeensis cultured in the human promyelocytic leuke
67 r VirB6 proteins and VirB9 were expressed by E. chaffeensis in THP-1 cells, and amounts of these five
71 t canonical and noncanonical Wnt pathways by E. chaffeensis TRP effectors stimulates phagocytosis and
73 n of host cytokine and chemokine profiles by E. chaffeensis strains underlies the distinct host liver
74 nslocation of bacterially encoded protein by E. chaffeensis and to identify a specific binding motif
77 Anaplasma phagocytophilum, Ehrlichia canis, E. chaffeensis, E. ewingii, Rickettsia rickettsii, R. co
79 m mutagenesis is a valuable tool in defining E. chaffeensis genes critical for its persistent growth
83 CL11, which were strongly upregulated during E. chaffeensis infection and were also upregulated by di
87 ntibodies reactive to E. chaffeensis and for E. chaffeensis-specific 16S rRNA gene fragments by an in
90 rs of tandem repeats, were characterized for E. chaffeensis from white-tailed deer (Odocoileus virgin
92 nucleotide salvage pathway is essential for E. chaffeensis replication and that it may be important
97 ge PCR assay, but not by assays specific for E. chaffeensis or the agent of human granulocytic ehrlic
100 not amplify the 200-bp target amplicon from E. chaffeensis, the human granulocytic ehrlichiosis agen
101 esota or Wisconsin were found not to be from E. chaffeensis or E. ewingii and instead to be caused by
102 produce PCR products with DNA extracted from E. chaffeensis-, E. canis-, or E. phagocytophila-infecte
107 cores, identity of the primers to homologous E. chaffeensis sequences, and the availability of simila
108 med if the ELISA is positive), we identified E. chaffeensis or a serologically and antigenically simi
111 the N-terminal TR region (18 amino acids) in E. chaffeensis and the complete TR (24 amino acids) in E
112 own to be surface exposed), were detected in E. chaffeensis cultured in human monocytic leukemia THP-
114 e sequence polymorphisms in several genes in E. chaffeensis strains have been reported, global genomi
116 y that documents that insertion mutations in E. chaffeensis that cause attenuated growth confer prote
119 ssion of penicillin-binding protein (PBP) in E. chaffeensis was analyzed by reverse-transcription pol
120 cted, which was strikingly more prevalent in E. chaffeensis-containing vacuoles than in vacuole-free
125 inhibitor, globomycin, was found to inhibit E. chaffeensis infection and lipoprotein processing in H
126 strate that huMAbs are capable of inhibiting E. chaffeensis infection by distinct effector mechanisms
127 -butyldimethysilyl)-c-di-GMP (CDGA) inhibits E. chaffeensis internalization into host cells by facili
129 these five proteins were similar in isolated E. chaffeensis-containing vacuoles and vacuole-free E. c
132 eral cytokines and chemokines by leukocytes, E. chaffeensis lacks lipopolysaccharide and peptidoglyca
141 detected, and EHRL-4-mediated degradation of E. chaffeensis was abrogated by the autophagy inhibitor
143 e to that of the nested PCR for detection of E. chaffeensis in infected DH82 cells, experimentally in
144 more sensitive than the PCR for detection of E. chaffeensis regardless of the nature of the specimens
145 Thus, this RT-PCR is useful for detection of E. chaffeensis when a high sensitivity is required.
146 During the intracellular development of E. chaffeensis, both P28 and OMP-1F were expressed mostl
149 f the members of the p28 multigene family of E. chaffeensis, sera from two beagle dogs experimentally
154 These data suggest that the rMAP2 homolog of E. chaffeensis may have potential as a test antigen for
158 c diversity of the P28 among the isolates of E. chaffeensis suggest that P28s may be involved in immu
160 res infected with nine different isolates of E. chaffeensis, blood samples from seven patients with m
164 d in this study suggest that the membrane of E. chaffeensis is very complex, having many expressed pr
165 munofluorescent microscopy in the nucleus of E. chaffeensis-infected host cells and was detected in n
166 f E. canis and the corresponding ortholog of E. chaffeensis (47 kDa) were identified and the proteins
167 p30 of Ehrlichia canis (< or =71.3%), p28 of E. chaffeensis (< or =68.3%), and map1 of Cowdria rumina
168 protein with < or =69.1% identity to P28 of E. chaffeensis, < or =67.3% identity to P30 of E. canis,
169 n or closely related interacting partners of E. chaffeensis TRP32, TRP47, and TRP120 demonstrate a mo
171 d chromatography purified, and native PBP of E. chaffeensis were investigated for their ability to in
173 ts revealed distinct virulence phenotypes of E. chaffeensis strains with defined genome sequences.
176 sponses to another outer membrane protein of E. chaffeensis (GP120) showed similar temporal and quant
177 recognizing four outer membrane proteins of E. chaffeensis (Arkansas strain) including the 25-, 26-,
178 34 sera reacted with any native proteins of E. chaffeensis ranging from 44 to 110 kDa, and 30 sera r
180 otal, membrane, and immunogenic proteomes of E. chaffeensis originating from macrophage and tick cell
182 ci was downregulated prior to the release of E. chaffeensis from host THP-1 cells and was upregulated
183 ral responses and the in vivo replication of E. chaffeensis suggests that D. melanogaster is a suitab
185 This is the first demonstration of RNA of E. chaffeensis in infected blood and acquisition-fed mal
186 aling regulates aggregation and sessility of E. chaffeensis within the inclusion through stabilizatio
187 t immunization with the p28 of one strain of E. chaffeensis would confer cross-protection against oth
188 tigenic variants of p28 among the strains of E. chaffeensis and the presence of multiple copies of he
189 o compare the genome sequences of strains of E. chaffeensis and to examine the virulence potentials o
190 ikingly different among the three strains of E. chaffeensis: gamma interferon, CCL5, CXCL1, CXCL2, CX
192 protease HtrA was detected on the surface of E. chaffeensis, and TRP120 was degraded by treatment of
193 d macrophage activation and the synthesis of E. chaffeensis-specific Th1-type immunoglobulin G respon
198 sis, and TRP120 was degraded by treatment of E. chaffeensis with recombinant E. chaffeensis HtrA.
201 lecule inhibitor had a significant impact on E. chaffeensis replication and recruitment of the TRP120
202 tigated the effects of c-di-GMP signaling on E. chaffeensis infection of the human monocytic cell lin
203 nt is unique because it is thus far the only E. chaffeensis recombinant antigen that has been shown t
204 5.8%) goats were positive by diagnostic PCR; E. chaffeensis was isolated in cell culture from one goa
205 To survive and replicate within phagocytes, E. chaffeensis exploits the host cell by modulating a nu
206 his study, we assessed two clonally purified E. chaffeensis mutants with insertions within the genes
207 Genomic DNA was extracted from purified E. chaffeensis strains Wakulla and Liberty, and comparat
210 odies in patients' sera with the recombinant E. chaffeensis 120- and 28-kDa proteins as well as the 1
211 by protein immunoblotting using recombinant E. chaffeensis proteins expressed in Escherichia coli.
216 n particular, despite its small genome size, E. chaffeensis has four tandem virB6 paralogs (virB6-1,
218 isiae) two-hybrid analysis demonstrated that E. chaffeensis-secreted tandem repeat protein 120 (TRP12
221 Therefore, we tested the hypothesis that E. chaffeensis can infect adult Drosophila melanogaster.
235 trafficked to autophagosomes induced by the E. chaffeensis type IV secretion system effector Etf-1,
236 e (1,620 bp), and a 2-repeat region from the E. chaffeensis P120 gene (520 bp) were expressed in Esch
237 the same chromosomal location; however, the E. chaffeensis VLPT gene (594 bp) has tandem repeats tha
238 ovel tandem repeat DNA-binding domain in the E. chaffeensis 120-kDa tandem repeat protein (TRP120) th
240 ed proteins provides novel insights into the E. chaffeensis surface and lays the foundation for ratio
242 ve genes and that antigenic variation of the E. chaffeensis 28-kDa proteins may result from different
245 rly one-fourth of all predicted genes of the E. chaffeensis genome, validating that they are function
247 el treatment induced lysosomal fusion of the E. chaffeensis inclusion in a human monocytic leukemia c
254 ween TRP32 and host targets localized to the E. chaffeensis morulae or in the host cell cytoplasm adj
256 tly different between mice infected with the E. chaffeensis originating from tick cells or macrophage
259 owed a very high prevalence of antibodies to E. chaffeensis (97 of 112; 87%) and a low prevalence of
262 probable human monocytic ehrlichiosis due to E. chaffeensis also had antibodies to the HGE agent in a
263 that residents of Connecticut are exposed to E. chaffeensis, A. americanum ticks were collected in Co
264 uman leukemia cell line THP-1 was exposed to E. chaffeensis, significant upregulation of IL-8, IL-1be
265 38 (73.7%) goats had antibodies reactive to E. chaffeensis (>/=1:128), and 6 of 38 (15.8%) goats wer
266 icity were tested for antibodies reactive to E. chaffeensis and for E. chaffeensis-specific 16S rRNA
268 5, an ehrlichial organism closely related to E. chaffeensis isolated from Ixodes ovatus ticks in Japa
269 rlichia muris, a pathogen closely related to E. chaffeensis, resulted in anemia, thrombocytopenia, an
272 These data suggest that the host response to E. chaffeensis depends on the source of the bacteria and
274 tein expression and host immune responses to E. chaffeensis lipoproteins, 13 E. chaffeensis lipoprote
275 veral E. chaffeensis native proteins and two E. chaffeensis recombinant I-site proteins, and this bin
276 Ech_0379 mutant and challenge with wild-type E. chaffeensis 1 month following inoculation with the mu
277 ere tested by immunofluorescence (IFA) using E. chaffeensis antigen and by protein immunoblotting usi
278 ay for immunoglobulin M (IgM) and IgG, using E. chaffeensis antigen, identified 44 and 33% of the iso
281 t could mediate bacterial clearance in vivo, E. chaffeensis-specific mAbs were generated and administ
283 genes suggest a possible mechanism by which E. chaffeensis might evade the host immune defenses.
284 h lysosomes or Golgi-derived vesicles, while E. chaffeensis resides in an early endosomal compartment
285 oxyl-terminal amino acid homology (59%) with E. chaffeensis VLPT and the same chromosomal location; h
286 strongly with TRP120 in HeLa cells and with E. chaffeensis dense-cored morulae and areas adjacent to
288 ; 1 patient had evidence of coinfection with E. chaffeensis and a spotted fever group rickettsia.
290 a pattern different from that of humans with E. chaffeensis infection but similar to that of a dog ex
291 two beagle dogs experimentally infected with E. chaffeensis were evaluated for the presence of specif
292 naive dogs, or when dogs were infected with E. chaffeensis, the animals developed delayed-type hyper
293 cteria and that of macrophages infected with E. chaffeensis, we have identified few genes that are co
295 three sera that were IFA positive only with E. chaffeensis, and three sera that were IFA positive on
296 st recombinant P43 (rP43) did not react with E. chaffeensis as detected by indirect fluorescent antib
297 cence contained antibodies that reacted with E. chaffeensis and E. canis antigens in a pattern differ
298 gainst the recombinant proteins reacted with E. chaffeensis P120 and E. canis P140, respectively.
299 nstrated to contain antibodies reactive with E. chaffeensis by indirect immunofluorescence assays (IF