Giardia undergo antigenic variation. Cloned populations contain small numbers of Giardia with unique surface antigens and these can be selected for by exposing Giardia to cytotoxic MAbs which react with original major antigen. Antigens present in the original isolate are not present in subsequent progeny and later antigens are not present in the original isolate. The major antigen of the original WB isolate (170 Kd) and one of the newly detected surface antigen are cysteine containing compounds. The DNA of clones of the original isolate (parents) were compared to the DNA of populations which grew following exposure to cytotoxic MAb (progeny). Multiple bands were seen in Southern blots using part of the cloned 170 kd antigen as a probe. Most progeny differed from each other but parent-progeny pairs were the same. Although frequent rearrangements were seen in the area encoding for this varying antigen, the differences in the banding patterns did not correlate with the loss of the major antigen. The major antigen of the parent isolate is a 170 kd antigen. Part of this gene was sequenced and showed two tandem repeats (65 amino acids) and part of a third. The entire segment has 12% cysteine. A Giardia gene was identified which hybridized under non- stringent conditions to hsp-70 of Drosphila. Sequence analysis of a 2 kb fragment revealed an open reading frame but no similarity to hsp-70. The promotor region had the typical heat shock promotor. The chromosomes of Giardia were identified using pulse field electrophoresis. Five chromosomes were identified and a number of minor less brightly staining Giardia DNA containing bands. Isolates differ in the position of the major bands and the number and position of the minor bands. Clones of the same isolate differ in the position of the minor bands.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000350-06
Application #
3822042
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
6
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Niaid Extramural Activities
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Worgall, Tilla S; Davis-Hayman, Sara R; Magana, Marissa M et al. (2004) Sterol and fatty acid regulatory pathways in a Giardia lamblia-derived promoter: evidence for SREBP as an ancient transcription factor. J Lipid Res 45:981-8
Davis-Hayman, Sara R; Hayman, J Russell; Nash, Theodore E (2003) Encystation-specific regulation of the cyst wall protein 2 gene in Giardia lamblia by multiple cis-acting elements. Int J Parasitol 33:1005-12
Davis-Hayman, Sara R; Nash, Theodore E (2002) Genetic manipulation of Giardia lamblia. Mol Biochem Parasitol 122:1-7
Nash, Theodore E (2002) Surface antigenic variation in Giardia lamblia. Mol Microbiol 45:585-90
Hayman, J R; Hayes, S F; Amon, J et al. (2001) Developmental expression of two spore wall proteins during maturation of the microsporidian Encephalitozoon intestinalis. Infect Immun 69:7057-66
Nash, T E; Lujan, H T; Mowatt, M R et al. (2001) Variant-specific surface protein switching in Giardia lamblia. Infect Immun 69:1922-3
Elmendorf, H G; Singer, S M; Nash, T E (2001) The abundance of sterile transcripts in Giardia lamblia. Nucleic Acids Res 29:4674-83
Singer, S M; Elmendorf, H G; Conrad, J T et al. (2001) Biological selection of variant-specific surface proteins in Giardia lamblia. J Infect Dis 183:119-24
Elmendorf, H G; Singer, S M; Pierce, J et al. (2001) Initiator and upstream elements in the alpha2-tubulin promoter of Giardia lamblia. Mol Biochem Parasitol 113:157-69