[PubMed] [Google Scholar] 5. extruded from geminated spores exist and suggest that such antibodies may play a part in protective immunity. is usually a microsporidian parasitic pathogen listed in a 1996 WHO report as an emerging infectious agent (17). The pathogen is also considered a zoonotic parasite (4). Various animals can be naturally infected by contamination in rabbits and in squirrel monkeys in zoos is usually of current concern (1, 5). The rate of contamination is considered to increase each year, and the contamination has now spread throughout Japan. However, to the best of our knowledge, the only case of human microsporidiosis reported in Japan was in a 9-year-old boy in 1958 (10). Although immunological conditions Chlorobutanol of the Japanese case were not recorded, almost all other patients infected with this pathogen in other nations have been immunocompromised groups Mouse monoclonal to PR of human immunodeficiency virus (HIV)-infected patients (16). A few cases have Chlorobutanol also been found among renal transplant recipients (6, 11). can thus be regarded as an opportunistic pathogen (2). Cases of HIV-associated infections with are increasingly reported, although they remain less common than those due to and (2). Many reports around the seroprevalence of human infection have been published (3, 8). However, the reported rates of microsporidial seropositivity vary greatly, depending on the serological technique used, probably due to the use of antigens unsuitable for measurement of specific antibodies and the use of secondary antibodies without differential specificities. Recently, specific immunoglobulin G (IgG) antibodies against the polar tube (PT) of were demonstrated in a healthy laboratory worker accidentally infected with (14). The PT is usually a typical microsporidian spore structure with an extrusion that is essential for invasion of a host cell, as sporoplasm flows through the discharged PT and into the host cell (13). We have recently developed an enzyme immunostaining assay (EIA) for measuring anti-PT antibodies using 96-well microplates coated with germinated spores. This method allows us to screen human sera for anti-PT antibodies on a large scale for seroepidemiological analysis. This study reports around the screening of sera from 380 healthy persons and 78 HIV-infected persons seroepidemiologically analyzed by this particular EIA, which is usually capable of measuring anti-PT antibodies of each Ig class, that is, IgM, IgG, and IgA. MATERIALS AND METHODS Serum samples. For this study we used serum samples from 380 healthy people living in Hokkaido Prefecture, Japan; serum samples from 180 residents who underwent a serological test for parasitosis in 2000 but who showed negative results; and serum samples from 200 blood donors collected in 2005. Serum samples from 78 HIV-infected persons, collected in 1999 from the Kanto region of Japan, were also provided for this study. These included sera from 51 persons with CD4 cell levels below 250/l and sera from 27 persons with CD4 cell levels between 251 and 900/l. The 51 persons in the former group were of various ages, while the 27 persons in the latter group were younger than 30 years of age. Assessments for HIV contamination and determination of CD4 lymphocyte counts were performed by standard laboratory protocols. spores. For this study we used the HF strain, isolated from a rabbit with encephalitozoonosis. Strain HF was then cultivated in RK-13 cells (ATCC CCL-37) (5). Culture supernatants of HF-infected RK-13 cells were collected, centrifuged, and used for Chlorobutanol serological tests. Strain HF was genetically analyzed beforehand by PCR, followed by direct DNA sequencing (1). The internal transcribed spacer gene sequence revealed that strain HF was classified into genotype I, since it contained three GTTT repeats. Sequence analysis of the spore wall protein I gene revealed that the strain belonged to genotype Ia because of the amplification of a 399-bp PCR product. Microplate enzyme immunostaining assay. Sediments containing germinated spores, nongerminated spores, and heavily infected cells detached from cell sheets, were suspended in Gibco minimal essential medium including Earle’s salts and glutamine (Invitrogen Corporation, Grand Island, NY) and supplemented with 1,000 U/ml penicillin G, 1,000 g/ml streptomycin, and 10% fetal bovine serum; this medium was also.