Effects of bile and bile salts on growth and membrane lipid uptake by Giardia lamblia. Possible implications for pathogenesis of intestinal disease
- PMID: 4056050
- PMCID: PMC424194
- DOI: 10.1172/JCI112162
Effects of bile and bile salts on growth and membrane lipid uptake by Giardia lamblia. Possible implications for pathogenesis of intestinal disease
Abstract
We have shown previously that ox and pig bile accelerate in vitro growth of Giardia lamblia. We have now investigated the possible mechanisms by which mammalian biles promote parasite growth. Growth effects of (a) ox, pig, guinea pig, and human biles, (b) pure bile salts, and (c) egg and soybean lecithins were studied in the presence of a lecithin-containing growth medium. Individually, dilute native bile and pure sodium taurocholate (TC), glycocholate (GC), and taurodeoxycholate (TDC) promoted parasite growth; growth was most marked with biles of high phospholipid content, with biles enriched in more hydrophobic bile salts (ox approximately equal to human greater than pig greater than guinea pig) and with micellar concentrations of GC and submicellar concentrations of TC and TDC. By measuring uptake of radiolabeled biliary lipids from bile and bile salt-supplemented growth medium, we showed that the parasite consumed bile lipids, with the rank order lecithin greater than bile salts. Apparent net uptake of cholesterol was considered to be due to exchange, since net loss of cholesterol from the growth medium was not detected. Although bile and bile salt-stimulated parasite growth was associated with enhanced lecithin uptake, reduction in generation time was observed at low bile and bile salt concentrations when lecithin uptake was similar to bile free controls. Thus, bile salts may stimulate Giardia growth initially by a mechanism independent of enhanced membrane phospholipid uptake. However, since Giardia has no capacity to synthesize membrane lipid, biliary lecithin may be a major source of phospholipid for growth of this parasite.
Similar articles
-
Biliary lipids support serum-free growth of Giardia lamblia.Infect Immun. 1986 Sep;53(3):641-5. doi: 10.1128/iai.53.3.641-645.1986. Infect Immun. 1986. PMID: 3744557 Free PMC article.
-
Cholesterol enhances membrane-damaging properties of model bile by increasing the intervesicular-intermixed micellar concentration of hydrophobic bile salts.J Surg Res. 1999 Jun 1;84(1):112-9. doi: 10.1006/jsre.1999.5625. J Surg Res. 1999. PMID: 10334899
-
Giardia-bile salt interactions in vitro and in vivo.Trans R Soc Trop Med Hyg. 1988;82(3):428-32. doi: 10.1016/0035-9203(88)90153-8. Trans R Soc Trop Med Hyg. 1988. PMID: 3232181
-
Separation and quantitation of cholesterol "carriers" in bile.Hepatology. 1990 Sep;12(3 Pt 2):94S-104S; discussion 104S-105S. Hepatology. 1990. PMID: 2210665 Review.
-
Cholesterol carriers in human bile: are "lamellae" involved?Hepatology. 1993 Dec;18(6):1522-31. Hepatology. 1993. PMID: 8244279 Review.
Cited by
-
Mechanisms of Giardia lamblia differentiation into cysts.Microbiol Mol Biol Rev. 1997 Sep;61(3):294-304. doi: 10.1128/mmbr.61.3.294-304.1997. Microbiol Mol Biol Rev. 1997. PMID: 9293183 Free PMC article. Review.
-
Biliary lipids support serum-free growth of Giardia lamblia.Infect Immun. 1986 Sep;53(3):641-5. doi: 10.1128/iai.53.3.641-645.1986. Infect Immun. 1986. PMID: 3744557 Free PMC article.
-
Attachment of Giardia lamblia to rat intestinal epithelial cells.Gut. 1988 Jun;29(6):795-801. doi: 10.1136/gut.29.6.795. Gut. 1988. PMID: 3384364 Free PMC article.
-
Molecular Cloning and Characterization of a Fasciola gigantica Nuclear Receptor Subfamily 1 (FgNR1).Pathogens. 2022 Dec 1;11(12):1458. doi: 10.3390/pathogens11121458. Pathogens. 2022. PMID: 36558792 Free PMC article.
-
The biology of Giardia spp.Microbiol Rev. 1991 Dec;55(4):706-32. doi: 10.1128/mr.55.4.706-732.1991. Microbiol Rev. 1991. PMID: 1779932 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous