Identification of circulating antibodies in fasciolosis and localization of 66 kDa antigenic target using monoclonal antibodies.

We identified three specific circulating antibodies in serum of cattle naturally infected with Fasciola gigantica. Two of the antibodies were found to react specifically to 97 and 66 kDa antigenic molecules of adult worm tegumental membrane extract. The third antibody was identified by the reaction with 26-28 kDa molecule of the excretory/secretory antigens. Monoclonal antibody against 66 kDa protein was developed and used for localization of its antigenic target in adult worm frozen sections. The experiment demonstrated that 66 kDa protein is a component on the outer surface membrane and on the membrane lining of the caecal epithelial of adult worm. The 66 kDa antigen was considered as a promising candidate for immunodiagnosis and vaccine.

Sex ratio and susceptibility of the golden apple snail, Pomacea canaliculata.

Golden apple snails, Pomacea canaliculata, were collected at two localities having different ecological environments. In both canal and pond, P. canaliculata males were found more than females during the dry season (summer and winter). In the canal, the male snails were highest in number (86.67%) in May. When rain started, they began decreasing and were lowest at 33.33% in August. Of 575 snails collected, 30.6% were infected by one or more of the three groups of amphistome, distome and echinostome metacercariae. There were two high peaks of infection in April and October, as 60.7% and 68.4%, respectively, during which there were more males than females. The average number of parasites per snail which was highest at 54 was found in the medium-sized males (25 out of 35 males) in October. The number of parasites per snail was significantly correlated with the collected males (p < 0.01), but such relationship was not occurred with the females. Of the females, only the large-sized individuals were infected. In the pond, the female snails were present in much greater numbers than the males during the reproductive time (June-September). The females were highest (94.23%) in August. Only 24 (4.0%) of 605 snails were infected; most of the infected snails were large.

Natural parasitic infection of the golden apple snail, Pomacea canaliculata.

Golden apple snails, Pomacea canaliculata, were collected once a month during a year to search for their natural parasites. The collections were made at two localities having different ecological environments. Of 576 collected snails from a canal, 176 individuals (30.6%) were infected by three groups of metacercariae. These parasites were amphistome, distome and echinostome metacercariae, which had prevalences of 23.5, 19.5 and 0.5%, respectively. The incidence of infection was highest (68.4% in October) when the snail population was composed of the old, juvenile and young Pomacea. Amphistome metacercariae were found most frequently and echinostome metacercariae the least frequently; both parasites were localized in the foot muscle of the snails and had a Shannon index of zero. The range of amphistomes was 1 to 115 with the mean +/- SD of 1 +/- 2 and 95% CL of 1, 2. Distome metacercariae were found primarily in the heart (range: 1-13), and also in the foot muscle (range: 1-5) and kidney (range: 1-14), with a Shannon index of 0.4. The means +/- SD (with 95% CL) were 3 +/- 4 (95% CL = 1, 5), 3 +/- 4 (95% CL = 2, 4) and 2 +/- 1 (95% CL = 1, 2) for the foot muscle, heart and kidney, respectively. The snails from a pond, another locality, had a low proportion of infected individuals. Of 605 snails, only 24 individuals (4.0%) were infected, with the prevalence of amphistomes, distomes and echinostomes being 0.8, 1.8 and 2.1%, respectively. The incidence of infection for each month was zero or less than 10%, except in May when it was 30.2%.

Genetic response of Aedes aegypti to different environmental temperatures.

Three groups of Aedes aegypti maintained 8 generations in the laboratory at 20 degrees C, 27 +/- 1 degree C (normal control), and at 35 degrees C, respectively were analyzed for allozyme variability. Of the 8 larval loci examined Est alpha-1 and Lap-2 in generation 8 were still variable, while the other allozymes became uniform. The 35 degrees C population had mean level of heterozygosity of about 6% of individual per locus, less than those observed in the 20 degrees C and the control populations which were 14% and 13%, respectively. It is suggested that in the experimental populations, the rate of loss of alleles can be increased by high temperature which must not be higher than the optimum temperature of enzymes.