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[Factors affecting the in vitro excystation of Cryptosporidium sp]
B C Pezzani1, E Bautista, A Córdoba
1Cátedra de Microbiología y Parasitología, Facultad de Ciencias Médicas, Universidad Nacional de La Plata, Provincia de Buenos Aires, Argentina.
Abstract:
To assess the viability of the oocysts from Cryptosporidium sp, an in vitro excystation technique was developed and optimized. To this end, oocysts from Cryptosporidium sp were isolated from a sample of fecal material from a child with symptomatic cryptosporidiosis. The specimen was processed by a discontinuous-sucrose-gradient technique yielding a final suspension of purified and concentrated oocysts. The resulting oocysts were quantified by counting an aliquot in a Neubauer hemocytometer chamber and the remainder were preserved in phosphate-buffered saline at pH 7.2 and 4 degrees C. The two protocols tested through the use of 100-microliter aliquots containing 178,000 oocytes/mm3 were: I. Treatment at 37 degrees C for 24 h with 1% (v/v) bile plus 0.44% (w/v) sodium bicarbonate. Group A: pretreated with acidified trypsin (pH 2.75) at 37 degrees C for 1 h; Group B: not pretreated. II. Treatment at 37 degrees C for 24 h with 1% (v/v) bile at pH 6 and at pH 8 either with or without 0.44% (w/v) sodium bicarbonate in air or an atmosphere containing 10% (v/v) CO2. Group 1: bile, pH 6; Group 2: bile, pH 6 plus CO2; Group 3: bile, pH 6 plus bicarbonate; Group 4: bile, pH 8 plus bicarbonate; Group 5: bile, pH 6 plus bicarbonate plus CO2; Group 6: bile, pH 8 plus bicarbonate plus CO2; Group 7: bile, pH 8; and Group 8: bile, pH 8 plus CO2. We then assessed the degree of excystation in all the groups by counting the number of intact oocysts in the hemocytometer. For the first protocol, the oocyst count after excystation revealed an average of 28,000 oocysts/mm3 in Group A and 22,000 in Group B. These values indicate excystation frequencies of 84.3% and 87.6% for these two groups, respectively. The corresponding excystation percentages for groups 1-8 of protocol II were 49.5, 56.7, 83.2, 88.3, 88.3, 92.7, and 94.1, respectively. Preincubation with trypsin failed to augment oocyst excystation in Cryptosporidium in any of these experimental circumstances. The optimal conditions for oocyst excystation in these 24 h incubations were thus seen to be in the presence of 1% (v/v) bile at pH 8, and 37 degrees C under an atmosphere of 10% (v/v) CO2.
Insights
This study optimized an in vitro excystation technique for Cryptosporidium oocysts. Optimal conditions involve 1% bile at pH 8 and 37°C with 10% CO2, achieving high excystation rates.
Area of Science:
- * Parasitology
- * Molecular Biology
- * Infectious Diseases
Context:
- * Cryptosporidium sp. is a significant cause of diarrheal disease in humans and animals.
- * Oocyst viability is crucial for understanding transmission and developing control strategies.
- * Current methods for assessing oocyst viability have limitations.
Purpose:
- * To develop and optimize an in vitro excystation technique for Cryptosporidium oocysts.
- * To determine the optimal conditions for oocyst excystation, including bile concentration, pH, temperature, and atmospheric composition.
- * To evaluate the effect of pre-treatment with acidified trypsin on excystation rates.
Summary:
- * Cryptosporidium oocysts were isolated from infected fecal material and purified using a sucrose-gradient technique.
- * Two protocols were tested: Protocol I involved bile and sodium bicarbonate with or without trypsin pretreatment; Protocol II varied bile pH, bicarbonate presence, and CO2 atmosphere.
- * Optimal excystation was achieved with 1% bile at pH 8, 37°C, and 10% CO2, yielding high excystation frequencies (up to 94.1%).
- * Trypsin pre-treatment did not enhance excystation.
Impact:
- * Provides a reliable and optimized in vitro method for assessing Cryptosporidium oocyst viability.
- * Facilitates research into Cryptosporidium biology, pathogenesis, and drug development.
- * Contributes to improved diagnostics and control measures for cryptosporidiosis.