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Early induction and late abrogation of respiratory burst in A. phagocytophilum-infected neutrophils.

Abstract
Human granulocytic ehrlichiosis is an emerging tick-borne disease caused by the obligate intracellular pathogen, Anaplasma phagocytophilum. This organism is unique because it survives and propagates in neutrophil vacuoles. During phagocytosis professional phagocytes increase oxygen consumption (respiratory burst) through the activity of NADPH-oxidase, which generates superoxide anion (O2(-)) and hydrogen peroxide (H(2)O(2)). We assayed the ability of A. phagocytophilum-infected neutrophils to generate O2(-) in response to early infection (0, 3, and 5 hours) by using 2',7'-dichlorodihydrofluorescein diacetate (DCFH-DA), a fluorogenic probe commonly used to detect cellular production of reactive oxygen species (ROS). Our flow cytometric analyses showed that cell-free A. phagocytophilum induced respiratory burst 6.9-fold greater than that of LPS, an effect still evident to a lesser degree after 3 h, but absent by 5h. A. phagocytophilum initially induces and then represses respiratory burst in neutrophils. The long-term reduction in respiratory burst activity may be important for survival of A. phagocytophilum and other infectious agents in neutrophils. The effect of this may be to generate a limited functional equivalent of chronic granulomatous disease that predisposes to infections by opportunistic pathogens.
AuthorsKyoung-Seong Choi, J Stephen Dumler
JournalAnnals of the New York Academy of Sciences (Ann N Y Acad Sci) Vol. 990 Pg. 488-93 (Jun 2003) ISSN: 0077-8923 [Print] United States
PMID12860678 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Lipopolysaccharides
Topics
  • Anaplasma phagocytophilum (growth & development, physiology)
  • Cell-Free System
  • Humans
  • In Vitro Techniques
  • Lipopolysaccharides (pharmacology)
  • Neutrophils (drug effects, microbiology, physiology)
  • Respiratory Burst (physiology)

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