Most reported isolates of
Sarcocystis
spp. derived from Brazilian opossums (
Didelphis
sp.) have genetic characteristics distinct from the known species of
Sarcocystis
, but behave similarly as
Sarcocystis falcatula
, as they are infective to budgerigars. In previous studies, these Brazilian isolates, classified as
Sarcocystis falcatula
-like, were originated from South and Southeast regions of Brazil. In the current work, we aimed to culture and to perform multilocus sequence analysis of
Sarcocystis
sp. derived from a Brazilian opossum (
D. aurita
/
D. marsupialis
) that inhabited the city of Salvador, Bahia, in the Northeast of Brazil. The parasite was isolated in Vero cells, referred here as Sarco-BA1, and propagated in avian cells (DF-1). Molecular analysis of Sarco-BA1 revealed that the nucleotide sequence of the internal transcribed spacer 1 (ITS1) of the rDNA was identical to all isolates (n = 19) of
Sarcocystis
spp. reported in two studies from South and Southeast regions of the country. Two budgerigars were inoculated with 10 and 1000 sporocysts of Sarco-BA1, respectively, and developed acute sarcocystosis, showing that the parasite behaves like
S. falcatula
. It was interesting to observe that Sarco-BA1 had almost identical ITS1 and SAG sequences to all 16 isolates of
S. falcatula
-like recently described in Magellanic penguins (
Spheniscus magellanicus
) rescued on the coast of Espírito Santo state, Brazil. Our results suggest that Sarco-BA1 and
S. falcatula
-like may represent a single species of
Sarcocystis
. Propagation of the parasite in a permanent avian cell line significantly improved the yield of merozoites in cell culture. To our knowledge, this is the first molecular study and
in vitro
isolation of
S. falcatula
-like derived from Northeastern Brazil. Studies are under way to determine the infectivity of Sarco-BA1 to other animal species, as well as to investigate serological cross-reactivity among Sarco-BA1,
S. neurona
and related species.