A gene encoding the manganese superoxide dismutase (Mn-SOD) of Spirometra erinacei was identified, and the biochemical properties of the recombinant enzyme were partially characterized. The S. erinacei Mn-SOD gene consisted of 669 bp, which encoded 222 amino acids. A sequence analysis of the gene showed that it had typical molecular structures, including characteristic metal-binding residues and motifs that were conserved in Mn-SODs. An analysis of the N-terminal presequence of S. erinacei Mn-SOD revealed that it had physiochemical characteristics commonly found in mitochondria-targeting sequences and predicted that the enzyme is located in the mitochondria. A biochemical analysis also revealed that the enzyme is a typical Mn-SOD. The enzyme was consistently expressed in both S. erinacei plerocercoid larvae and adult worms. Our results collectively suggested that S. erinacei Mn-SOD is a typical mitochondrial Mn-SOD and may play an important role in parasite physiology, detoxifying excess superoxide radicals generated in the mitochondria.Spirometra erinacei is a pseudophyllidean tapeworm that inhabits the intestines of cats and dogs. The infections are usually asymptomatic, but in more severe cases, the infected animals may exhibit weight loss, irritability, and changes in appetite. The most important clinical manifestation, sparganosis, is developed when the plerocercoid larvae of the parasite (spargana) infect other intermediate vertebrate hosts, including humans. Human infections are mainly acquired by ingesting water containing Cyclops spp. in which tapeworm eggs mature into procercoid larvae, by ingesting uncooked mammalian, reptilian, or amphibian flesh, or by placing frog poultices on open lesions (Sarma and Weilbaecher, 1986). Spargana can invade muscle, subcutaneous tissues, visceral and urogenital organs, orbital tissue, and occasionally the central nervous system, causing inflammation and fibrosis (Chang et al., 1992). Symptoms differ depending on the particular tissues or organs involved.Highly reactive oxygen species (ROS), including superoxide anions, hydrogen peroxide, hydroxyl radicals, and singlet oxygen, are generated through numerous pathways in aerobic organisms (Fridovich, 1995). ROS induce peroxidation of membrane lipids, DNA damage, and inactivation of proteins (Imlay and Linn, 1988). Oxidative stress resulting from ROS is much greater in parasitic organisms because they must detoxify ROS produced endogenously as well as those produced by host immune effector cells. Activated host immune effector cells undergo an oxidative burst and produce ROS as a part of their defense against parasitic infections (Butterworth, 1984;Callahan et al., 1988;Brophy and Pritchard, 1992;Maizels et al., 1993). Therefore, effective detoxification of host-generated ROS is important for parasitic organisms in evading host immune responses and for surviving inside the host (Callahan et al., 1988;Mkoji et al., 1988;Nare et al., 1990;Batra et al., 1993;Maizels et al., 1993;Vaca-Paniagua et al., 2008;Mourã o ...