1996
DOI: 10.1056/nejm199601253340401
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Direct Cultivation of the Causative Agent of Human Granulocytic Ehrlichiosis

Abstract: We describe the cultivation of the agent of human granulocytic ehrlichiosis in cell culture. The ability to isolate this organism should lead to a better understanding of the biology, treatment, and epidemiology of this emerging infection.

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Cited by 430 publications
(398 citation statements)
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“…[13][14][15][16] Thus, a history of a tick bite or well established exposure to ticks is an important historical clue. Ticks in the Ixodes persulcatus-complex serve as competent vectors for multiple pathogens that can infect humans including A. phagocytophilum, 11 Borrelia burgdorferi (the agent of Lyme borreliosis), 17 Babesia microti (the agent of babesiosis), 18 Ehrlichia muris-like agent, 19 Borrelia miyamotoi, 3 and Powassan virus 20 Vector ticks in North American endemic habitats include Ixodes scapularis in the northeastern and upper Midwest regions of the USA, and I. pacificus along the northern Pacific coast.…”
Section: Patient Historymentioning
confidence: 99%
See 1 more Smart Citation
“…[13][14][15][16] Thus, a history of a tick bite or well established exposure to ticks is an important historical clue. Ticks in the Ixodes persulcatus-complex serve as competent vectors for multiple pathogens that can infect humans including A. phagocytophilum, 11 Borrelia burgdorferi (the agent of Lyme borreliosis), 17 Babesia microti (the agent of babesiosis), 18 Ehrlichia muris-like agent, 19 Borrelia miyamotoi, 3 and Powassan virus 20 Vector ticks in North American endemic habitats include Ixodes scapularis in the northeastern and upper Midwest regions of the USA, and I. pacificus along the northern Pacific coast.…”
Section: Patient Historymentioning
confidence: 99%
“…41,49,50 At least 20%, and in some studies up to 100% of patients present with morulae in the cytoplasm of peripheral blood neutrophils in the first week of illness. 15,50,51 PCR amplification of A. phagocytophilum-specific DNA from acute phase blood 14,15,52 or isolation of A. phagocytophilum in HL-60 promyelocytic leukemia cell cultures inoculated with acute phase blood 13,41,53 can also confirm the diagnosis during the early stage of infection, but these test modalities are available in only a limited number of public health and commercial reference laboratories. Acute and convalescent serologic testing using an indirect fluorescent antibody method for A. phagocytophilum IgG with demonstration of four-fold change or seroconversion is the most sensitive confirmatory laboratory test, and has been used most commonly to confirm HGA.…”
Section: Diagnostic Testing and Imagingmentioning
confidence: 99%
“…These actual and potential functions are facilitated by the range of tick species from which cell lines are now available, and the well-documented ability of some of these lines to support growth of microorganisms that are not transmitted by the parent tick, or even, in the case of some arboviruses, not transmitted by ticks at all [6,10,25]. The first isolations of A. phagocytophilum from human blood were made using tick (IDE8) and human (HL60) cells [32]; although growth was initially much faster in the HL60 cells, the principle of isolating unknown pathogens using tick cells was established. Subsequently, a previously uncultivable Anaplasma sp.…”
Section: Isolation Of Pathogensmentioning
confidence: 99%
“…Ehrlichia canis (NCSU, DJ strain) was grown as described previously by in vitro propagation in the DH82-cell line [40]. Anaplasma phagocytophilum (strain 96HE158) was grown as described previously by in vitro propagation in the HL60 [14] cell line. Antigen for the IFA was prepared as previously described [14,40].…”
Section: Questionnairesmentioning
confidence: 99%
“…Anaplasma phagocytophilum (strain 96HE158) was grown as described previously by in vitro propagation in the HL60 [14] cell line. Antigen for the IFA was prepared as previously described [14,40].…”
Section: Questionnairesmentioning
confidence: 99%