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1 hilum, supporting its placement in the genus Anaplasma.
6 obligatory intracellular bacterial pathogens Anaplasma and Ehrlichia infect leukocytes by hijacking h
8 porates melt curve analysis to differentiate Anaplasma and Ehrlichia species with blood smear and ser
10 th intracellular survival and replication of Anaplasma and Ehrlichia spp. in granulocytes or monocyte
11 ription of the three virB genes in these two Anaplasma and Ehrlichia spp. is regulated by factors tha
12 lection for divergence in Ank function among Anaplasma and Ehrlichia spp. is supported by both locus
13 Although the basic developmental cycle of Anaplasma and Ehrlichia spp. within the tick has been de
14 widely applicable to bacteria in the genera Anaplasma and Ehrlichia, removing a major technical impe
15 n fragmentation are common in the genomes of Anaplasma and other obligate intracellular bacteria.
19 positive amplicons revealed the presence of Anaplasma bovis, an agent not known to be present in Nor
21 lasma marginale subsp. centrale (synonym for Anaplasma centrale) induces protection against severe di
23 The broad-range assay detected Ehrlichia or Anaplasma DNA in 20 (26%) of the symptomatic dogs and 2
26 roEL and gltA genes revealed the presence of Anaplasma, Ehrlichia, Candidatus Neoehrlichia, and Ricke
29 hermal in situ technique to detect localized Anaplasma gene sequences by using rolling-circle amplifi
34 Ectopically expressed Ats-1 targeted the Anaplasma inclusions and enhanced infection, whereas hos
36 nd preliminary immunofluorescent staining of Anaplasma-infected tissues suggest that endothelial cell
40 incubated at 34 degrees C, and 8 days later, Anaplasma-like inclusions were demonstrated in Giemsa-st
43 , major surface protein 2 (MSP2) and MSP3 of Anaplasma marginale and Anaplasma ovis, Anaplasma phagoc
44 an immunodominant outer membrane protein of Anaplasma marginale and Anaplasma phagocytophilum pathog
46 to the model obligate intracellular pathogen Anaplasma marginale and the human pathogen Anaplasma pha
47 red unique to the intraerythrocytic agent of Anaplasma marginale and the intragranulocytic agent of A
48 of the persistent bovine ehrlichial pathogen Anaplasma marginale are immunodominant proteins that und
53 SP1a and MSP1b) of the erythrocytic stage of Anaplasma marginale conferred protection against homolog
58 the hypothesis that challenge of cattle with Anaplasma marginale expressing MSP2 variants to which th
62 ive immunity against the ehrlichial pathogen Anaplasma marginale has been hypothesized to require ind
64 he highly transmissible St. Maries strain of Anaplasma marginale in Dermacentor andersoni as a positi
65 protein 1 (MSP1) of the ehrlichial pathogen Anaplasma marginale induces protective immunity in calve
66 r membranes induces protection against acute Anaplasma marginale infection and disease, and a proteom
70 ve major surface protein 1 (MSP1) complex of Anaplasma marginale is a heteromer of MSP1a and MSP1b, e
78 ly variant major surface protein 2 (MSP2) of Anaplasma marginale is expressed from a 3.5-kb operon th
80 nalyzing the CD4(+) T lymphocyte response to Anaplasma marginale major surface protein 1a (MSP1a).
83 erogeneity in this species, the homologue of Anaplasma marginale major surface protein 4 gene (msp4)
86 ly unique strains of the tick-borne pathogen Anaplasma marginale occur and are transmitted within reg
93 sed an unbiased proteomic screen to identify Anaplasma marginale proteins specifically upregulated in
97 s were fed on animals superinfected with the Anaplasma marginale subsp. centrale vaccine strain (low
102 distinct strains of the tick-borne pathogen Anaplasma marginale that encode distinctly different sur
104 This question was addressed by tracking the Anaplasma marginale variant population and corresponding
105 We examined allelic usage in generating Anaplasma marginale variants during in vivo infection in
106 the conservation of MSP3 between strains of Anaplasma marginale was evaluated by using immunoblots o
107 ofluorescence, Anaplasma phagocytophilum and Anaplasma marginale were successfully localized in situ
108 e protein 2 (MSP2) variants are expressed by Anaplasma marginale within the tick salivary gland and,
109 t study, we examined the strain structure of Anaplasma marginale, a genogroup II ehrlichial pathogen,
110 , broad population immunity develops against Anaplasma marginale, a highly antigenically variant rick
111 immunodominant surface proteins, we examined Anaplasma marginale, a rickettsia with two highly immuno
113 We investigated this by using infection with Anaplasma marginale, a ruminant pathogen that replicates
117 nulocytic ehrlichiosis, msp-2 and msp-4 from Anaplasma marginale, and map-1 from Cowdria ruminantium.
118 s on three unrelated vector-borne pathogens, Anaplasma marginale, Borrelia hermsii and Trypanosoma br
120 Native major surface protein 1 (MSP1) of Anaplasma marginale, composed of covalently associated M
121 chia phagocytophila, and the bovine pathogen Anaplasma marginale, express a markedly immunodominant o
122 protein 2 (Msp2) of the tick-borne pathogen, Anaplasma marginale, is thought to be involved in antige
125 f template DNA from closely related species (Anaplasma marginale, the white-tailed deer agent, and ad
135 ces of selected amplicons from the assay for anaplasma matched sequences of the white-tailed deer age
136 s technique to detect, localize, and analyze Anaplasma nucleotide sequences in the tissues of infecte
140 2 (MSP2) and MSP3 of Anaplasma marginale and Anaplasma ovis, Anaplasma phagocytophilum MSP2 (p44), Eh
143 sms in the genera Rickettsia, Ehrlichia, and Anaplasma, persists in ticks and mammalian hosts; howeve
144 burgdorferi (33.6%), Babesia microti (8.4%), Anaplasma phagocytophila (1.9%), and Bartonella spp. (34
146 nant 44 kDa major outer membrane proteins of Anaplasma phagocytophila (human granulocytic ehrlichiosi
147 ck-vectored pathogen transmission, including Anaplasma phagocytophila an etiologic agent of granulocy
148 ng tick-borne zoonosis caused by a strain of Anaplasma phagocytophila called the HGE agent, an obliga
152 The human granulocytic ehrlichiosis agent, Anaplasma phagocytophila, resides and multiplies exclusi
153 determined the frequencies of antibodies to Anaplasma phagocytophila, the agent of human granulocyti
158 ing of the region directly downstream of the Anaplasma phagocytophilum (strain MRK) 16S rRNA gene ide
160 nd von Willebrand factor immunofluorescence, Anaplasma phagocytophilum and Anaplasma marginale were s
162 Pennsylvania and tested for the presence of Anaplasma phagocytophilum and Borrelia burgdorferi by PC
164 amine TH 1 and TH 17 immunity infection with Anaplasma phagocytophilum and Citrobacter rodentium resp
166 nt outer membrane proteins (P44 proteins) of Anaplasma phagocytophilum are encoded by the p44 polymor
168 ngton State suspected of being infected with Anaplasma phagocytophilum because of the finding of moru
171 Colonization of neutrophils by the bacterium Anaplasma phagocytophilum causes the disease human granu
174 A polymorphic multigene family (p44) of Anaplasma phagocytophilum encodes the immunodominant 44-
175 from 16S rRNA gene-based genetic variants of Anaplasma phagocytophilum from dogs in the western Unite
176 to determine the presence and prevalence of Anaplasma phagocytophilum human agent (AP-ha) and a gene
201 during infection with the rickettsial agent Anaplasma phagocytophilum Macrophages deficient in annex
202 3 of Anaplasma marginale and Anaplasma ovis, Anaplasma phagocytophilum MSP2 (p44), Ehrlichia chaffeen
203 membrane protein of Anaplasma marginale and Anaplasma phagocytophilum pathogens that cause bovine an
206 Borellia burgdorferi, Babesia microti and Anaplasma phagocytophilum rely almost exclusively on a s
207 et al. demonstrate that ticks infected with Anaplasma phagocytophilum show enhanced fitness against
208 first tissue culture isolates of the unique Anaplasma phagocytophilum strain, Ap-Variant 1, were obt
209 owledge regarding the strategies employed by Anaplasma phagocytophilum to evade or subvert neutrophil
210 ce-exposed major membrane proteins, P44s, of Anaplasma phagocytophilum were hypothesized to be garner
211 he agent of human granulocytic ehrlichiosis (Anaplasma phagocytophilum) is intensely enzootic in rabb
220 gen, seventy-four (40%) were seroreactive to Anaplasma phagocytophilum, and five (2.7%) were seroposi
221 ate substrates, an ankyrin repeat protein of Anaplasma phagocytophilum, AnkA, is delivered into the h
222 intracellular bacteria such as Ehrlichia and Anaplasma phagocytophilum, as well as obligate intracell
223 egative for all tick-borne pathogens tested (Anaplasma phagocytophilum, Ehrlichia canis, and Ricketts
224 hogens in the order Rickettsiales, including Anaplasma phagocytophilum, Ehrlichia canis, E. chaffeens
225 ighly conserved with orthologous proteins in Anaplasma phagocytophilum, Ehrlichia chaffeensis, and Eh
226 ptional regulator, tr1, and a homolog of the Anaplasma phagocytophilum, identified here as A. platys
227 n Anaplasma marginale and the human pathogen Anaplasma phagocytophilum, in order to examine the abili
229 ated first to Anaplasma platys and second to Anaplasma phagocytophilum, supporting its placement in t
230 recent studies of the granulocyte pathogen, Anaplasma phagocytophilum, the agent of granulocytic ehr
231 burgdorferi, the agent of Lyme disease, and Anaplasma phagocytophilum, the agent of human anaplasmos
233 s harbor numerous human pathogens, including Anaplasma phagocytophilum, the agent of human granulocyt
235 y proteomics and transcriptome sequencing to Anaplasma phagocytophilum, the agent of human granulocyt
240 increases tick colonization by the bacterium Anaplasma phagocytophilum, the causative agent of human
242 ertain Ixodes ticks, which can also transmit Anaplasma phagocytophilum, the cause of human granulocyt
243 des scapularis tick, which can also transmit Anaplasma phagocytophilum, the cause of human granulocyt
249 ic ehrlichiosis was recently reclassified as Anaplasma phagocytophilum, unifying previously described
250 his report, we show that the AnkA protein of Anaplasma phagocytophilum, which is translocated into th
261 he isolate was most closely related first to Anaplasma platys and second to Anaplasma phagocytophilum
264 cells and other potentially cryptic sites of Anaplasma sp. infection in mammalian tissues, a sensitiv
265 Transmission electron microscopy of this Anaplasma sp. organism in tick cell cultures revealed la
269 antibody (MAb) ANAF16C1, is conserved among Anaplasma species and is expressed in the salivary gland
272 l for cross-reactivity among closely related Anaplasma species has made the accurate determination of
278 r membrane suggests that the porin feeds the Anaplasma TCA cycle and that the relatively large pore s
280 ts known pathogenic species of Ehrlichia and ANAPLASMA: The species was determined by using species-s
282 that the relatively large pore size provides Anaplasma with the necessary metabolic intermediates fro
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