Babesia equi was continuously cultured through 90 passages in an enric
hed chemically defined basal medium (HL-1) supplemented with 20% fetal
bovine serum and serum replacement factors, including lipid-rich bovi
ne serum albumin, bovine insulin, and human transferrin. Cryopreservat
ion and subsequent recovery of B. equi were easily achieved. Inoculati
on of a splenectomized and an intact horse with cultured infected eryt
hrocytes resulted in parasitemias and B. equi in vitro reisolation fro
m both animals. In vitro forms of the parasite resembled in vivo forms
. After establishment, parasitemias of 10-15% were commonly observed.