Optimization of culture conditions for in vitro fertilization and reproduction of Microphallus turgidus (Trematoda: Microphallidae).

Most attempts to culture adult digeneans in vitro are unsuccessful. Even progenetic digeneans typically fail to produce infective eggs in axenic culture. However, metacercariae of Microphallus turgidus grown in vitro mature into adults and release eggs infective to the hydrobiid snail Spurwinkia salsa. The objectives of the present study were to verify the reproducibility of the M. turgidus culture protocol, to define optimal culture conditions for M. turgidus further, and to investigate why the parasite can be grown successfully in the absence of the definitive host. In the original cultivation protocol, excysted M. turgidus metacercariae from grass shrimp (Palaemonetes pugio) were incubated overnight in a conical-bottom centrifuge tube containing Hank's balanced salt solution and then cultivated in flat-bottom culture plate wells containing RPMI-1640 plus 20% horse serum. The gas phase was air. Worms cultured under this protocol consistently deposited eggs infective to snails. Worms grown in anaerobic conditions deposited few eggs, and those cultured in a gas phase of 5% CO(2) survived longer and produced more eggs than those cultured in air. However, snails were less likely to become infected when fed eggs deposited by worms cultured in 5% CO(2). Additionally, worms incubated with conspecifics in conical-bottom tubes prior to cultivation were more likely to be inseminated than worms incubated in flat-bottom culture wells; the highest percentages of inseminated worms occurred when metacercariae were incubated 24 hr in conical-bottom tubes at a density of 50 worms/tube and at a temperature of 37 C. Worms incubated in the absence of conspecifics were not fertilized and failed to produce infective eggs.

In vitro cultivation of Microphallus turgidus (Trematoda: Microphallidae) from metacercaria to ovigerous adult with continuation of the life cycle in the laboratory.

In vitro cultivation of trematodes would aid studies on the basic biology of the parasites and the development of chemotherapies and vaccines. Our goal was to measure the in vitro survival and maturation of metacercariae of Microphallus turgidus under different culture conditions. Metacercariae of M. turgidus from grass shrimp (Palaemonetes pugio) were excysted and cultured in humidified air at 37 degrees C in RPMI-1640 medium supplemented with 20% calf, chicken, or horse serum. Deposition of eggs was greatest in media containing horse or calf serum. Worms survived longest at 37 C, but did not produce greater numbers of eggs than worms cultured in RPMI-1640-supplemented horse serum at 42 degrees C. Most eggs deposited in vitro (>80%) were normal in shape and, after incubation for 10 days at 30 degrees C in brackish water, approximately 30% of them contained miracidia. Eighteen percent of hydrobiid snails (Spurwinkia salsa) fed these eggs shed cercariae 5-6 wk later. The cercariae were infective to grass shrimp (Palaemonetes vulgaris) and developed into metacercariae. This study is significant because it is the second instance in which a digenean, and the first time that a microphallid, has been demonstrated to develop in vitro from metacercariae into adult worms capable of producing infective eggs.