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Serial subcultivation of Giardia lamblia in Keister's modified TYI-S-33 medium containing ultroser G
1Environmental Monitoring Systems Laboratory, United States Environmental Protection Agency, Cincinnati, Ohio 45268.
Abstract:
The ability of Giardia strains of the duodenalis type to grow in Keister's modified TYI-S-33 medium varies with serum lot. Recently, strains of Giardia including MR4, WB, and Human-1-Portland, have been cultivated in Keister's modified TYI-S-33 medium containing the serum substitute Ultroser G and have been cultured serially as least 40 times. An optimal concentration of 8% Ultroser G promotes maximal growth in Keister's modified TYI-S-33 medium for all three strains. This concentration of Ultroser G will produce a two-log increase in the number of trophozoites in approximately three days post-inoculation. Generation times for the trophozoites ranging from 6 to 11 h have been achieved in Keister's modified TYI-S-33 containing 10% adult bovine serum and from 8 to 13 h in Keister's modified TYI-S-33 with 8% Ultroser G. Despite the excellent growth of Giardia strains in medium containing Ultroser G, the maximum trophozoite density is only about half of that achieved in Keister's modified TYI-S-33 medium supplemented with 10% adult bovine serum. Comparisons of trophozoites grown with serum or the serum substitute reveal no discernable differences in morphology and motility. Additionally, these strains have been successfully cryopreserved and revived in Keister's modified TYI-S-33 medium supplemented with Ultroser G. Because Ultroser G is a characterized mixture of six main groups of ingredients (growth factors, adhesion factors, mineral trace elements, hormones, binding proteins, and vitamins), the variability in cell proliferation that may occur when changing serum lots should be minimized when using this product.
Insights
Ultroser G, a serum substitute, supports serial cultivation of Giardia duodenalis strains in Keister
Area of Science:
- Parasitology
- Cell Culture
- Microbiology
Background:
- Giardia duodenalis cultivation in Keister's modified TYI-S-33 medium is limited by serum lot variability.
- Consistent Giardia growth is crucial for research and diagnostics.
Purpose of the Study:
- To evaluate Ultroser G as a serum substitute for Giardia duodenalis cultivation.
- To determine optimal Ultroser G concentration for Giardia growth and serial propagation.
Main Methods:
- Cultivation of Giardia strains (MR4, WB, Human-1-Portland) in Keister's modified TYI-S-33 medium with varying Ultroser G concentrations.
- Serial subculturing for at least 40 passages.
- Assessment of growth kinetics, trophozoite density, morphology, motility, and cryopreservation.
Main Results:
- Optimal growth achieved with 8% Ultroser G, supporting serial cultivation over 40 passages.
- Generation times ranged from 8–13 hours with Ultroser G, comparable to adult bovine serum.
- Trophozoite density was approximately half that achieved with adult bovine serum; no differences in morphology or motility observed.
- Successful cryopreservation and revival of Giardia strains using Ultroser G.
Conclusions:
- Ultroser G provides a consistent and effective alternative to serum for Giardia duodenalis cultivation.
- Minimizes variability associated with serum lot changes, enhancing reproducibility in Giardia research.
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