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PMID: 12933880 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Ehrlichia chaffeensis and Anaplasma phagocytophilum lack genes for lipid A biosynthesis and incorporate cholesterol for their survival.

Infection and immunity ·Vol. 71 ·No. 9 ·2003-09-00 ·Pages 5324-31

Lin M, Rikihisa Y

Abstract

Ehrlichia chaffeensis and Anaplasma phagocytophilum are agents of human monocytic and granulocytic ehrlichioses, respectively. They are extremely sensitive to mechanical stress and are pleomorphic gram-negative bacteria. Membrane incorporation of cholesterol from the eukaryotic host is known to be essential for other fragile and pleomorphic bacteria and mycoplasmas that lack a cell wall. Thus, we tested whether cholesterol is required for E. chaffeensis and A. phagocytophilum. Using a freeze fracture technique and biochemical analysis, these bacteria were found to contain significant levels of membrane cholesterol. These bacteria lack genes for cholesterol biosynthesis or modification. However, host cell-free bacteria had the ability to take up directly exogenous cholesterol or NBD-cholesterol, a fluorescent cholesterol derivative. Treatment of the bacteria with cholesterol extraction reagent methyl-beta-cyclodextrin caused their ultrastructural changes. Furthermore, pretreatment of the bacteria with methyl-beta-cyclodextrin or NBD-cholesterol deprived these bacteria of the ability to infect leukocytes, thus killing these obligate intracellular bacteria. Analysis of E. chaffeensis and A. phagocytophilum genome sequences revealed that these bacteria lack all genes for the biosynthesis of lipid A and most genes for the biosynthesis of peptidoglycan, which confer structural strength to gram-negative bacteria. Taken together, these results suggest that human ehrlichiosis agents became cholesterol dependent due to the loss of these genes. As the first report of gram-negative bacteria incorporating cholesterol for survival, these findings offer insight into the unique nature of their parasitism and imply that cholesterol is important in the control of human ehrlichioses.

MeSH Terms
4-Chloro-7-nitrobenzofurazan/analogs & derivatives,pharmacokinetics Anaplasma phagocytophilum/genetics,metabolism,pathogenicity Cholesterol/analogs & derivatives,metabolism,pharmacokinetics Ehrlichia chaffeensis/genetics,metabolism,pathogenicity Ehrlichiosis/etiology,metabolism,microbiology Fluorescent Dyes/pharmacokinetics Freeze Fracturing Genes, Bacterial Humans In Vitro Techniques Leukocytes/metabolism,microbiology Lipid A/biosynthesis,genetics Membrane Lipids/metabolism Microscopy, Electron Peptidoglycan/biosynthesis,genetics
Chemicals
7-nitrobenz-2-oxa-1,3-diazol-4-ylcholesterol Fluorescent Dyes Lipid A Membrane Lipids Peptidoglycan Cholesterol 4-Chloro-7-nitrobenzofurazan
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lin Mingqun
Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio 43210, USA.
Rikihisa Yasuko
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
2003-09-00
Pages
5324-31
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC187327
Subset
IM
Grants
NIAID NIH HHS · R01 AI030010 · United States
NIAID NIH HHS · R01 AI047885 · United States
NIAID NIH HHS · R01 AI30010 · United States
NIAID NIH HHS · R01 AI47885 · United States
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