A new diagnostic technique for identifying Angiostrongylus spp. larvae in intermediate snail species by examining the buccal cavity.

BACKGROUND: Angiostrongyliasis is a zoonotic parasitic disease caused by the rat lungworm Angiostrongylus cantonensis. The intermediate hosts of A. cantonensis are gastropods, and snail species such as Pomacea canaliculata play a key role in the transmission of human angiostrongyliasis. Detecting A. cantonensis infection in snails is an important component of epidemiological surveillance and the control of angiostrongyliasis. METHODS: In this study, a new method for diagnosing A. cantonensis infection in gastropods was developed by recovering larvae from the buccal cavity of three snail species. The entire buccal cavity of a snail was extracted, and the tissue was pressed between two microscope slides to observe whether A. cantonensis larvae were present. Our new method was compared with traditional pathogenic detection methods of lung microscopy, tissue homogenization, and artificial digestion. We artificially infected 160 P. canaliculata, 160 Cipangopaludina chinensis, and 160 Bellamya aeruginosa snails with A. cantonensis. Then, the four different detection methods were used to diagnose infection in each snail species at 7, 14, 21, and 28 days post exposure. RESULTS: We found no significant difference in the percentages of infected P. canaliculata snails using the four methods to detect A. cantonensis larvae. The radula pressing method had a mean detection rate of 80%, while the lung microscopy (81.3%), tissue homogenization (83.8%), and artificial digestion (85%) methods had slightly greater detection rates. Similarly, the percentages of infected C. chinensis snails that were detected using the radula pressing (80%), tissue homogenization (82.1%), and artificial digestion (83.8%) methods were not significantly different. Finally, the percentages of infected B. aeruginosa snails that were detected using the radula pressing (81.3%), tissue homogenization (81.9%), and artificial digestion (81.4%) methods were not significantly different. These results showed that the radula pressing method had a similar detection rate to traditional lung microscopy, tissue homogenization, or artificial digestion methods. CONCLUSIONS: This study demonstrates a new method for the qualitative screening of gastropods that act as intermediate hosts of A. cantonensis (and other Angiostrongylus species), provides technical support for the control of human angiostrongyliasis, and furthers research on A. cantonensis.

[Molluscicidal effect of buried niclosamide sustained-release method in plateau mountainous areas].

OBJECTIVE: To evaluate the molluscicidal effect of the buried niclosamide sustained-release method in Oncomelania snail-infested terraced environments of mountainous areas in Yunnan Province. METHODS: A piece of relatively isolated snail-infested terraced environment was selected as experimental plot and randomly divided into four groups. The buried niclosamide sustained-release methods were performed in Group A, B, C with the doses of 6 g/m2, 12 g/m2, 24 g/m2 respectively, and Group D was sprayed with 50% niclosamide ethanolamine salt wettable powder (2 g/m2) as the control. RESULTS: In Group C (with the buried niclosamide sustained-release method of 24 g/m2), the half-year reduction of living snail density was 89.90%, and one-year reduction of living snail density was 96.80%, which were significantly higher than those of Group D (40.35% and 59.11%) (Both P < 0.01) CONCLUSION: The buried niclosamide sustained-release method is effective and suitable for snail control in mountainous terrace areas.

[Molluscicidal effect of WPN and MNSC on Lymnaea].

OBJECTIVE: To evaluate the molluscicidal effect of wettable powder of 50% niclosamide ethanolamide salt (WPN) and suspension concentrate of 26% metaldehyde and niclosamide (MNSC) on Lymnaea. METHODS: WPN and MNSC were prepared as a series of solutions containing the active ingredient concentrations of 0.06, 0.13, 0.25, 0.50, 1.00, 2.00 mg/L and 4.00 mg/L, and the adult Lymnaea snails were soaked in the above mentioned series of solutions in the laboratory, and the LC50 values were calculated. The doses of active ingredient concentrations of 0.03, 0.06, 0.13, 0.25, 0.50, 1.00 g/m2 and 2.00 g/m2 of WPN and MNSC were adopted to spray on Lymnaea snails in the laboratory, and the LC50 values were calculated. A series of solutions containing the active ingredient concentrations of 1.00 mg/L, 0.50 mg/L, 0.25 mg/L, and 0.13 mg/L of WPN and MNSC were prepared, and the adult Lymnaea snails were put into the bowls with each concentration solution above mentioned and the climbing situation of the snails was observed at different time. RESULTS: By the immersion method, LC50 values of WPN at 48 h and 72 h were 0.93 mg/L and 0.64 mg/L respectively; LC50 values of MNSC at 48 h and 72 h were 0.74 mg/L and 0.51 mg/L respectively; by the spray method, when active ingredient concentrations of WPN and MNSC were 1.00 g/m2 or more, the death rates were both 100% after 3 days. In the climbing test, the Lymnaea snails did not climb in the solutions containing the active ingredient concentration of 1.00 mg/L of WPN and MNSC, however, a few snails climbed in the low concentrations. CONCLUSIONS: WPN and MNSC both have the effect of killing Lymnaea snails and inhibiting their climbing. By using the immersion method in the field, the active ingredient concentration of 2.00 mg/L of WPN and MNSC for 48 h is appropriate; by using the spray method, the active ingredient content of 1.00 g/m2 of WPN and MNSC for 3 days is appropriate.