A newly identified intraerythrocytic Babesia-like organism, WA1, and i
ts relatives were recently shown to be infectious for humans in the we
stern United States. The purpose of the present study was to determine
the susceptibilities of selected mouse genotypes to WA1 infection in
an attempt to develop a murine model of the human disease, Several mou
se strains were inoculated intraperitoneally with various passages of
WA1-parasitized erythrocytes. Parasitemia was evaluated by blood smear
s and by PCR with blood samples collected at various intervals after i
noculation, Hematologic parameters were monitored in blood samples at
all intervals. C57BL/6 and C57BL/10 mice exhibited mortality rates of
< 10%. BALB/cJ, CBAJ, and 129/J mice had higher peak parasitemias than
did C57BL mice, with mortality rates of 40, 50, and 50%, respectively
, A/J, AKR/N, C3H, and DBA/1J mice also had higher peak parasitemia an
d mortality rates (>95%), An F-1 cross of C57BL/6 (resistant) and C3H.
RKK (susceptible) mice had a mortality rate similar to that of the res
istant parental strain. Histopathology of BALB/cJ and C3H mice at 9 an
d 14 days after inoculation revealed erythrophagocytosis and depositio
n of an iron-negative pigment in multiple organs, Morbidly ill C3H mic
e at 14 days had severe pulmonary edema, hemoglobinuria, and glomerulo
nephritis.