1. Effective, appropriate and simple culture, egg hatching and cryopreserving of the nematode Cheilospirura hamulosa.
- Author
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Rouhani, S., Ebrahimi, M., Rostami, A., and Fallahi, SH.
- Subjects
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NEMATODES , *CRYOPRESERVATION of organs, tissues, etc. , *EGG incubation , *PARASITES , *HOSTS (Biology) - Abstract
1. Successful invasion by nematode parasites is associated with several factors including egg hatching at the right time in their hosts. To determine a simple and appropriate medium for culture and egg hatching of the highly pathogenic species of theAcuariidaefamily,Cheilospirura hamulosawere cultured in three different media. In addition the viability ofC. hamulosaeggs was determined after storage in frozen infected gizzards. 2. Eggs removed from the uteri of the female worms in infected gizzards were pooled and washed in distilled water and screened under a stereo dissecting microscope. Eggs were counted and cultured in three different media, nutrient agar, normal saline 0.9% and Bearman, at room temperature. Additionally, 10 infected gizzards were kept at −20°C for 2 and 8 months. 3. After 4–5 d there had been no growth in the nutrient agar medium, whereas 11% of the cultured eggs in the Bearman medium contained larvae 2–3 d after culturing. In 0.9% normal saline medium the two polar knobs appeared on the two poles of the eggs at 2 d post cultivation, and 74% of the eggs contained a larva on the third day. Mature larvae gradually exited from the eggs. 4. Eggs collected from female worms in gizzards frozen at −20°C were cultured in the same three culture media at room temperature. Larvae were visible in the eggs after 2–3 d in the Bearman and 0.9% normal saline media and hatched thereafter. 5. The 0.9% normal saline medium is recommended for egg hatching and cultivation ofC. hamulosadue for simplicity, efficacy and cost effectiveness. Moreover, freezing of the infected gizzards at −20°C is proposed for long-term storage of the eggs. [ABSTRACT FROM AUTHOR]
- Published
- 2014
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