Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1996 Aug;62(8):2789–2797. doi: 10.1128/aem.62.8.2789-2797.1996

Prevalence of Giardia cysts and Cryptosporidium oocysts and characterization of Giardia spp. isolated from drinking water in Canada.

P M Wallis 1, S L Erlandsen 1, J L Isaac-Renton 1, M E Olson 1, W J Robertson 1, H van Keulen 1
PMCID: PMC168064  PMID: 8702271

Abstract

This study was carried out to estimate the prevalence and potential for human infectivity of Giardia cysts in Canadian drinking water supplies. The presence of Cryptosporidium oocysts was also noted, but isolates were not collected for further study. A total of 1,760 raw water samples, treated water samples, and raw sewage samples were collected from 72 municipalities across Canada for analysis, 58 of which treat their water by chlorination alone. Giardia cysts were found in 73% of raw sewage samples, 21% of raw water samples, and 18.2% of treated water samples. There was a trend to higher concentration and more frequent incidence of Giardia cysts in the spring and fall, but positive samples were found in all seasons. Cryptosporidium oocysts were found in 6.1% of raw sewage samples, 4.5% of raw water samples, and 3.5% of treated water samples. Giardia cyst viability was assessed by infecting Mongolian gerbils (Meriones unguiculatus) and by use of a modified propidium iodide dye exclusion test, and the results were not always in agreement. No Cryptosporidium isolates were recovered from gerbils, but 8 of 276 (3%) water samples and 19 of 113 (17%) sewage samples resulted in positive Giardia infections. Most of the water samples contained a low number of cysts, and 12 Giardia isolates were successfully recovered from gerbils and cultured. Biotyping of these isolates by isoenzyme analysis and karyotyping by pulsed-field gel electrophoresis separated the isolates into the same three discrete groups. Karyotyping revealed four or five chromosomal bands ranging in size from 0.9 to 2 Mb, and four of the isolates had the same banding pattern as that of the WB strain. Analysis of the nucleotide sequences of the 16S DNA coding for rRNA divided the isolates into two distinct groups corresponding to the Polish and Belgian designations found by other investigators. The occurrence of these biotypes and karyotypes appeared to be random and was not related to geographic or other factors (e.g., different types were found in both drinking water and sewage from the same community). Biotyping and karyotyping showed that isolates from this study were genetically and biochemically similar to those found elsewhere, including well-described human source strains such as WB. We conclude that potentially human-infective Giardia cysts are commonly found in raw surface waters and sewage in Canada, although cyst viability is frequently low. Cryptosporidium oocysts are less common in Canada. An action level of three to five Giardia cysts per 100 liters in treated drinking water is proposed on the basis of the monitoring data from outbreak situations. This action level is lower than that proposed by Haas and Rose (C. N. Haas and J. B. Rose, J. Am. Water Works Assoc. 87(9):81-84, 1995) for Cryptosporidium spp. (10 to 30 oocysts per 100 liters).

Full Text

The Full Text of this article is available as a PDF (295.9 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Belosevic M., Faubert G. M., MacLean J. D., Law C., Croll N. A. Giardia lamblia infections in Mongolian gerbils: an animal model. J Infect Dis. 1983 Feb;147(2):222–226. doi: 10.1093/infdis/147.2.222. [DOI] [PubMed] [Google Scholar]
  2. Hoff J. C., Rice E. W., Schaefer F. W., 3rd Comparison of animal infectivity and excystation as measures of Giardia muris cyst inactivation by chlorine. Appl Environ Microbiol. 1985 Oct;50(4):1115–1117. doi: 10.1128/aem.50.4.1115-1117.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Homan W. L., van Enckevort F. H., Limper L., van Eys G. J., Schoone G. J., Kasprzak W., Majewska A. C., van Knapen F. Comparison of Giardia isolates from different laboratories by isoenzyme analysis and recombinant DNA probes. Parasitol Res. 1992;78(4):316–323. doi: 10.1007/BF00937090. [DOI] [PubMed] [Google Scholar]
  4. Isaac-Renton J. L., Cordeiro C., Sarafis K., Shahriari H. Characterization of Giardia duodenalis isolates from a waterborne outbreak. J Infect Dis. 1993 Feb;167(2):431–440. doi: 10.1093/infdis/167.2.431. [DOI] [PubMed] [Google Scholar]
  5. LeChevallier M. W., Norton W. D., Lee R. G. Giardia and Cryptosporidium spp. in filtered drinking water supplies. Appl Environ Microbiol. 1991 Sep;57(9):2617–2621. doi: 10.1128/aem.57.9.2617-2621.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. LeChevallier M. W., Norton W. D., Lee R. G. Occurrence of Giardia and Cryptosporidium spp. in surface water supplies. Appl Environ Microbiol. 1991 Sep;57(9):2610–2616. doi: 10.1128/aem.57.9.2610-2616.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. LeChevallier M. W., Norton W. D., Siegel J. E., Abbaszadegan M. Evaluation of the immunofluorescence procedure for detection of Giardia cysts and Cryptosporidium oocysts in water. Appl Environ Microbiol. 1995 Feb;61(2):690–697. doi: 10.1128/aem.61.2.690-697.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Meloni B. P., Lymbery A. J., Thompson R. C. Genetic characterization of isolates of Giardia duodenalis by enzyme electrophoresis: implications for reproductive biology, population structure, taxonomy, and epidemiology. J Parasitol. 1995 Jun;81(3):368–383. [PubMed] [Google Scholar]
  9. Roach P. D., Olson M. E., Whitley G., Wallis P. M. Waterborne Giardia cysts and Cryptosporidium oocysts in the Yukon, Canada. Appl Environ Microbiol. 1993 Jan;59(1):67–73. doi: 10.1128/aem.59.1.67-73.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Rose J. B., Landeen L. K., Riley K. R., Gerba C. P. Evaluation of immunofluorescence techniques for detection of Cryptosporidium oocysts and Giardia cysts from environmental samples. Appl Environ Microbiol. 1989 Dec;55(12):3189–3196. doi: 10.1128/aem.55.12.3189-3196.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Schupp D. G., Erlandsen S. L. A new method to determine Giardia cyst viability: correlation of fluorescein diacetate and propidium iodide staining with animal infectivity. Appl Environ Microbiol. 1987 Apr;53(4):704–707. doi: 10.1128/aem.53.4.704-707.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Symons J. M., Xia R. Technical note: interference of Br-, BrO3-, and ClO3- with DOX determination. J Am Water Works Assoc. 1995 Aug;87(8):81–84. [PubMed] [Google Scholar]
  13. Tibayrenc M. Entamoeba, giardia and toxoplasma: clones or cryptic species? Parasitol Today. 1993 Mar;9(3):102–105. doi: 10.1016/0169-4758(93)90217-4. [DOI] [PubMed] [Google Scholar]
  14. Wallis P. M., Wallis H. M. Excystation and culturing of human and animal Giardia spp. by using gerbils and TYI-S-33 medium. Appl Environ Microbiol. 1986 Mar;51(3):647–651. doi: 10.1128/aem.51.3.647-651.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Weiss J. B., van Keulen H., Nash T. E. Classification of subgroups of Giardia lamblia based upon ribosomal RNA gene sequence using the polymerase chain reaction. Mol Biochem Parasitol. 1992 Aug;54(1):73–86. doi: 10.1016/0166-6851(92)90096-3. [DOI] [PubMed] [Google Scholar]
  16. van Keulen H., Homan W. L., Erlandsen S. L., Jarroll E. L. A three nucleotide signature sequence in small subunit rRNA divides human Giardia in two different genotypes. J Eukaryot Microbiol. 1995 Jul-Aug;42(4):392–394. doi: 10.1111/j.1550-7408.1995.tb01600.x. [DOI] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES