The p44 gene of the agent of human granulocytic ehrlichiosis (aoHGE) encode
s a 44-kDa major outer surface protein. A technique was developed for the t
yping of the aoHGE based on the PCR amplification of the p44 gene followed
by a multiple restriction digest with HindIII, EcoRV, and AspI to generate
restriction fragment length polymorphism patterns. Twenty-four samples of t
he aoHGE were collected from geographically dispersed sites in the United S
tates and included isolates from humans, equines, canines, small mammals, a
nd ticks. Six granulocytic ehrlichiosis (GE) types were identified. The GE
typing method is relatively simple to perform, is reproducible, and is able
to differentiate among the various isolates of granulocytic ehrlichiae in
the United States. These characteristics suggest that this GE typing method
may be an important epizootiological and epidemiological tool.