Immunoblot Patterns of Taenia asiatica Taeniasis

Differential diagnosis of Taenia asiatica infection from other human taeniases by serology has been tested. An enzyme-linked immunoelectrotransfer blot (EITB) was applied to subjected human sera and tapeworm materials. Thirty-eight proteins reactive to serum IgG were observed between 121 and 10 kDa in adult worms, and more than 22 serum-reactive components between 97 kDa and 21.5 kDa were observed in eggs of T. asiatica. Antigens of adult T. asiatica revealed immunoblot bands between 120 and 21.5 kDa against T. asiatica infected sera. Antigens of adult Taenia saginata revealed 110-100, 66, 58-56, and 46 kDa immunoblot bands against T. asiatica infected sera. Antigens of adult Taenia solium also revealed 99-97, 68-66, and 46 kDa bands against T. asiatica infected sera. The immunoblot band of 21.5 kDa exhibited specificity to T. asiatica.

Fundamental study of expression-library immunization against Taenia taeniaeformis in rats.

Expression-library immunization has been proposed as an effective means to screen a large number of genes of the pathogen as candidate protective molecules. In this study, we examined the efficacy of expression-library immunization using a T. taeniaeformis rat model system. Total RNAs were isolated from the last 15 segments of adult T. taeniaeformis and poly A RNA was purified. cDNA library was produced using SuperScript Plasmid System, which contains a mammalian expression vector, pCMV*SPORT6. From about 3,500 clones examined, more than 800 clones were found to contain DNA fragments. About 200 clones were sequenced and the homology search was carried out. The blast search revealed that 29% of the expression genes were mitochondrial genes (rRNA; 17%, protein; 12%). Nuclear rRNA genes (10%), nuclear protein (9%) and genes from Escherichia coli were also detected. Forty-two percent of sequences did not show a significant similarity to any genes deposited in the public database. Rats were immunized with expression-library and injected orally with 1,000 T. taeniaeformis eggs. However the protective effect of expression-library vaccine was not confirmed.

Teniosis y detección de anticuerpos anticisticerco en personas de una comunidad rural del estado de Guerrero / Taeniosis and detection of antibodies against cysticerci among inhabitants of a rural community in Guerrero State, Mexico

OBJETIVO: Determinar la frecuencia de portadores de Taenia sp. y su relación con el diagnóstico de cisticercos en humanos en una comunidad rural del estado de Guerrero, México. MATERIAL Y MÉTODOS: Para detectar portadores de Taenia sp. se analizaron 403 muestras de heces de personas, por medio de ELISA para coproantígenos de Taenia sp., así como 92 muestras de suero para detectar anticuerpos anticisticerco mediante inmunoelectrotransferencia. El diseño del estudio fue transversal y se llevó a cabo durante 1998. Se hizo estadística descriptiva y se estimó razón de momios. RESULTADOS: De 403 muestras de heces evaluadas, cinco resultaron positivas (1.2 por ciento). Sólo en dos de las cinco personas positivas se obtuvo el cestodo adulto. En 3 (3.26 por ciento) de los 92 sueros se encontraron anticuerpos anticisticerco. Del total de sueros, 17 fueron de las personas con diagnóstico positivo a teniosis por coproantígenos o que cohabitaban con ellos (primer grupo), los restantes 75 provenían de personas en quienes no se detectaron casos en las viviendas (segundo grupo). En el primer grupo se detectaron 2 (11.8 por ciento) sueros positivos, mientras que en el segundo sólo 1 (1.3 por ciento) (RM= 9.87, I.C 0.64-295.56, p= 0.086). CONCLUSIONES: La dificultad para obtener el parásito adulto en las personas positivas a coproantígenos puede deberse a características propias de éste que dificultan su expulsión, a que la permanencia del cestodo en su huésped es menor a la esperada o a que el tratamiento fue insuficiente para obtener el parásito, o bien, a problemas de especificidad de la prueba. Es necesario realizar estudios tendientes a evaluar estas posibilidades, lo cual permitiría conocer mejor la dinámica de transmisión de esta parasitosis, con el fin de establecer medidas de prevención y control, además de poder comparar con mayor veracidad la eficacia de las pruebas diagnósticas en condiciones de campo

Ensayo de la proliferación celular en cultivo de linfocitos de cerdo / Assay kinetics cell proliferations lymphocytes from pigs

Se reporta el cultivo de linfocitos de sangre periférica completa de cerdos sanos e infectados, para evaluar la cinética de proliferación celular; 0.5 ml de sangre fue cultivada en 6.0 ml de RPMI-11640 suplementado, en presencia de fitohemaglutinina y 5-BrdU, a 37§C. Al cabo de 48 horas de incubación se cosecharon y fueron teñidos de acuerdo a la técnica de fluorescencia más Giemsa, obteniéndose así células en diferentes etapas de diferenciación, identificándolas en primera, segunda y tercera división. La actividad proliferativa se midió bajo dos parámetros: índice mitótico e índice de replicación. Los resultados son reproducibles y se pueden diferenciar los efectos citotóxicos de los citostáticos sobre los linfocitos del huésped

ELISA antibodies to cysticerci of Taenia solium in human populations in New Guinea, Oceania, and Southeast Asia.

The presence of ELISA antibodies to cysticerci of Taenia solium was surveyed in populations of New Guinea, Micronesia, and several areas of Southeast Asia. It is confirmed that cysticercosis in New Guinea remains limited to the primary Wissel Lakes focus in Irian Jaya, where the disease was introduced by the importation of infected pigs, and that it has not spread to populations east or south of the Wissel Lakes, or to Papua New Guinea. On the island of Bali, Indonesia, 21% of sera were positive from one village where pigs are especially numerous, whereas in Sumatra, Indonesia, only 3%-4% of sera were positive. In Singapore, there was a higher proportion of positive sera among the Chinese (13%) than among the Indian (5%) or Malay (3%) Moslems. From 3 to 13% of sera from populations in Micronesia, Burma, Vietnam, and the Philippines were also found to react with cysticercus antigen. However, the problem of incomplete ELISA specificity raises the possibility that in areas not known to be endemic for T. solium, seropositive results could represent either subclinical infection with cysticerci or crossreactivity to other parasitic infections.

The role of cell-mediated immunity in Taenia taeniaeformis infections.

A functional cell mediated immunity (CMI) response was recorded in rats experimentally infected with Taenia taeniaeformis larvae. The presence of CMI was manifested in the delayed type hypersensitivity (DTH) reaction recorded between 12 hours and 24 hours on elicitation with antigen. The time course of the immediate type hypersensitivity (ITH) over 10 weeks showed 2 peaks around the 2nd and the 6th weeks of infection, whereas the DTH response was generally weaker and more uniform over the same time course. Transfer of peritoneal cells from infected rats conferred partial protection to normal recipient rats against a challenge infection. However, optimal protection was only about 50% with transfer of 0.625 X 10(7) cells/rat, and no increase in protection was possible even with transfer of higher cell concentrations.