TY - JOUR
T1 - Microbial adhesion of Cryptosporidium parvum
T2 - Identification of a colostrum-derived inhibitory lipid
AU - Schmidt, Joann
AU - Kuhlenschmidt, Mark S.
N1 - Funding Information:
This work was supported by grants from the U.S. National Institutes of Health (AI44967) and USDA (NC-1041-CSREES RRF ILLU-888-382) to MSK and a training fellowship grant (Agricultural Genome Science and Public Policy Training Program) from the USDA (2001-52100-11527) to JS. The mass spectrometer used in these studies was purchased in part with grants from the Division of Research Resources, National Institutes of Health (RR01575), the National Science Foundation (PCM 8121494), and the National Institute of General Medical Sciences (GM 27029). The AUCP-1 isolate of C. parvum used in these studies was originally a gift from Dr. Byron Blagburn, Auburn University. We thank Dr. Theresa Banet Kuhlenschmidt and Mr. William Hanafin for their excellent technical assistance; Spectral Data Services, Champaign, IL, and Professor Eric Oldfield, Department of Chemistry, University of Illinois for their assistance in NMR analyses; the Lipid Analysis Unit, Mylnefield Research Services Ltd., Mylnefield, Invergowrie, Dundee DD2 5DA, Scotland, for GC–MS analysis; and the Mass Spectrometry Laboratory, School of Chemical Sciences, University of Illinois for low-resolution fast-atom bombardment mass spectrometry (FAB-MS).
PY - 2008/11
Y1 - 2008/11
N2 - We previously described an unidentified lipid purified from calf small intestine that inhibits the in vitro adhesion of Cryptosporidium parvum sporozoites to host cells [Johnson JK, Schmidt J, Gelberg HB, Kuhlenschmidt MS. Microbial adhesion of Cryptosporidium parvum sporozoites: purification of an inhibitory lipid from bovine mucosa. J Parasitol 2004;90:980-90]. Intestinal mucosa from some calves, however, failed to yield this bioactive lipid. Accordingly, we examined other potential sources, especially dietary sources, of the inhibitory lipid and discovered it was principally derived from bovine colostrum. Interestingly, fresh colostrum yielded little or no inhibitory lipid, however, the lipid was found in relatively large quantities following incubation of colostrum with the aqueous fraction of calf intestinal contents. Using FAB-MS and NMR analysis, the sporozoite inhibitory lipid (SIL) was identified as oleic acid, a monounsaturated fatty acid likely released from colostrum triglycerides and phospholipids by digestion in the lumen of the calf small intestine. Oleic acid dose-dependently inhibited in vitro sporozoite-host cell adhesion with an inhibitory constant (IC50) of approximately 5 μM. Comparison of oleic acid with other C-18 fatty acids revealed linolenic, but not stearic acid, also displayed potent inhibitory activity. Neither linolenic nor oleic acid, however, affect either sporozoite or host cell viability at concentrations that inhibit sporozoite adhesion. These results suggest certain colostrum-derived long-chain fatty acids may serve as natural inhibitors of the early steps in C. parvum sporozoite-host cell interactions.
AB - We previously described an unidentified lipid purified from calf small intestine that inhibits the in vitro adhesion of Cryptosporidium parvum sporozoites to host cells [Johnson JK, Schmidt J, Gelberg HB, Kuhlenschmidt MS. Microbial adhesion of Cryptosporidium parvum sporozoites: purification of an inhibitory lipid from bovine mucosa. J Parasitol 2004;90:980-90]. Intestinal mucosa from some calves, however, failed to yield this bioactive lipid. Accordingly, we examined other potential sources, especially dietary sources, of the inhibitory lipid and discovered it was principally derived from bovine colostrum. Interestingly, fresh colostrum yielded little or no inhibitory lipid, however, the lipid was found in relatively large quantities following incubation of colostrum with the aqueous fraction of calf intestinal contents. Using FAB-MS and NMR analysis, the sporozoite inhibitory lipid (SIL) was identified as oleic acid, a monounsaturated fatty acid likely released from colostrum triglycerides and phospholipids by digestion in the lumen of the calf small intestine. Oleic acid dose-dependently inhibited in vitro sporozoite-host cell adhesion with an inhibitory constant (IC50) of approximately 5 μM. Comparison of oleic acid with other C-18 fatty acids revealed linolenic, but not stearic acid, also displayed potent inhibitory activity. Neither linolenic nor oleic acid, however, affect either sporozoite or host cell viability at concentrations that inhibit sporozoite adhesion. These results suggest certain colostrum-derived long-chain fatty acids may serve as natural inhibitors of the early steps in C. parvum sporozoite-host cell interactions.
KW - Adhesion
KW - Colostrum
KW - Cryptosporidium parvum
KW - Fatty acid
KW - Invasion
KW - Oleic acid
KW - Sporozoites
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U2 - 10.1016/j.molbiopara.2008.06.016
DO - 10.1016/j.molbiopara.2008.06.016
M3 - Article
C2 - 18675305
AN - SCOPUS:52049121506
SN - 0166-6851
VL - 162
SP - 32
EP - 39
JO - Molecular and Biochemical Parasitology
JF - Molecular and Biochemical Parasitology
IS - 1
ER -