Summary
Expert Review of Molecular Diagnostics
http://www.future-drugs.com/loi/erm;jsessionid=jA2HJq9doX1h
July 2004, Vol. 4, No. 4, Pages 559-569
(doi:10.1586/14737159.4.4.559)
Molecular diagnosis of human granulocytic anaplasmosis
J Stephen Dumler, Philippe Brouqui
Future Drugs - Expert Review of Molecular Diagnostics - 4(4):559 - Summary
http://www.future-drugs.com/doi/abs/10.1586/14737159.4.4.559?cookieSet=1
Human granulocytic anaplasmosis, formerly known as human granulocytic
ehrlichiosis, is caused by the microorganism Anaplasma phagocytophilum that is
transmitted by Ixodes tick bites. The disease state ranges from subclinical to
fatal but may be difficult to differentiate from other febrile conditions
without specific tests. Rapid and early diagnosis is important since the
infection may be fatal and specific antibiotic therapy is required. The
bacterium is an obligate intracellular pathogen of neutrophils. Thus, early
diagnosis is best achieved by amplification of nucleic acids from the blood. An
increasing number of potential gene targets for diagnostic assays have been
described and the incipient release of an Anaplasma phagocytophilum genome
sequence will not only help to better understand the disease but may facilitate
improvements in diagnostic strategies.