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Quantitative PCR to detect, discriminate and quantify intracellular parasites in their host: an example from three microsporidians in Daphnia

Published online by Cambridge University Press:  27 March 2006

D. REFARDT  and
D. EBERT
D. REFARDT
Affiliation:
Unité Ecologie et Evolution, Département de Biologie, Université de Fribourg, chemin du Musée 10, CH-1700 Fribourg, Switzerland Current address of both authors: Zoologisches Institut der Universität Basel, Evolutionsbiologie, Vesalgasse 1, CH-4051 Basel, Switzerland.
D. EBERT
Affiliation:
Unité Ecologie et Evolution, Département de Biologie, Université de Fribourg, chemin du Musée 10, CH-1700 Fribourg, Switzerland Current address of both authors: Zoologisches Institut der Universität Basel, Evolutionsbiologie, Vesalgasse 1, CH-4051 Basel, Switzerland.
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Abstract

Reliable detection, discrimination and quantification of parasites are important for host-parasite studies and diagnostics. Microsporidial infections are problematic in this respect. Their discrimination and quantification using light microscopy is difficult because spores are the only light microscopically visible form of the parasite and they offer few distinct characters. We developed a quantitative PCR (qPCR) assay based on SYBR Green chemistry to quantify the microsporidia Glugoides intestinalis, Octosporea bayeri and Ordospora colligata in their host, the freshwater crustacean Daphnia magna. The assay allows the quantification of infection intensities in whole animals and is more than an order of magnitude more sensitive than light microscopy. Sampling and DNA extraction account for more than 90% of the residual variance in infection intensity data and this variance considerably impairs the resolution of qPCR. Where higher resolution is required, we propose using the ratio of parasite to host DNA as the measure of infection intensity. We show that this measure is robust and greatly improves resolution of qPCR. Additionally, this method can be applied to compare samples of unequal volume.

Keywords

GlugoidesOctosporeaOrdosporaMicrosporidiaDaphniareal-time quantitative PCRinfection intensityquantificationdiagnostics
Type
Research Article
Information
Parasitology , Volume 133 , Issue 1 , July 2006 , pp. 11 - 18
Copyright
2006 Cambridge University Press

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References

REFERENCES

Bedhomme, S., Agnew, P., Sidobre, C. and Michalakis, Y. ( 2004). Virulence reaction norms across a food gradient. Proceedings of the Royal Society of London, B 271, 739–744. DOI: 10.1098/rspb.2003.2657.CrossRefGoogle Scholar
Bustin, S. A. ( 2000). Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays. Journal of Molecular Endocrinology 25, 169–193. DOI: 10.1677/jme.0.0250169.CrossRefGoogle Scholar
Candotti, D., Temple, J., Owusu-Ofori, S. and Allain, J.-P. ( 2004). Multiplex real-time quantitative RT-PCR assay for hepatitis B virus, hepatitis C virus, and human immunodeficiency virus type 1. Journal of Virological Methods 118, 39–47. DOI: 10.1016/j.jviromet.2004.01.017.CrossRefGoogle Scholar
Canning, E. U., Refardt, D., Vossbrinck, C. R., Okamura, B. and Curry, A. ( 2002). New diplokaryotic microsporidia (Phylum Microsporidia) from freshwater bryozoans (Bryozoa, Phylactolaemata). European Journal of Protistology 38, 247–265. DOI: 10.1078/0932-4739-00867.CrossRefGoogle Scholar
Capaul, M. and Ebert, D. ( 2003). Parasite-mediated selection in experimental Daphnia magna populations. Evolution 57, 249–260.CrossRefGoogle Scholar
Cheesman, S. J., de Roode, J. C., Read, A. F. and Carter, R. ( 2003). Real-time quantitative PCR for analysis of genetically mixed infections of malaria parasites: technique validation and applications. Molecular and Biochemical Parasitology 131, 83–91. DOI: 10.1016/S0166-6851(03)00195-6.CrossRefGoogle Scholar
Decaestecker, E., Declerck, S., De Meester, L. and Ebert, D. ( 2005). Ecological implications of parasites in natural Daphnia populations. Oecologia 144, 382–390. DOI: 10.1007/s00442-005-0083-7.CrossRefGoogle Scholar
Ebert, D. ( 1994). Virulence and local adaptation of a horizontally transmitted parasite. Science 265, 1084–1086.CrossRefGoogle Scholar
Ebert, D. ( 2005). Ecology, Epidemiology, and Evolution of Parasitism in Daphnia [Internet]. National Library of Medicine, National Center for Biotechnology Information, Bethesda (MD). http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=Books
Ebert, D., Hottinger, J. W. and Pajunen, V. I. ( 2001). Temporal and spatial dynamics of parasite richness in a Daphnia metapopulation. Ecology 82, 3417–3434.CrossRefGoogle Scholar
Ebert, D., Lipsitch, M. and Mangin, K. L. ( 2000). The effect of parasites on host population density and extinction: Experimental epidemiology with Daphnia and six microparasites. American Naturalist 156, 459–477.CrossRefGoogle Scholar
Fischer, O. and Schmid-Hempel, P. ( 2005). Selection by parasites may increase host recombination frequency. Biology Letters 1, 193–195. DOI: 10.1098/rsbl.2005.0296.CrossRefGoogle Scholar
Green, J. ( 1974). Parasites and epibionts of Cladocera. Transactions of the Zoological Society of London 32, 417–515.CrossRefGoogle Scholar
Hester, J. D., Varma, M., Bobst, A. M., Ware, M. W., Lindquist, H. D. A. and Schaefer III., F. W. ( 2002). Species-specific detection of three human-pathogenic microsporidial species from the genus Encephalitozoon via fluorogenic 5′ nuclease PCR assays. Molecular and Cellular Probes 16, 435–444. DOI: 10.1006/mcpr.2002.0442.CrossRefGoogle Scholar
Higuchi, R., Fockler, C., Dollinger, G. and Watson, R. ( 1993). Kinetic PCR analysis: Real-time monitoring of DNA amplification reactions. Bio/Technology 11, 1026–1030.CrossRefGoogle Scholar
Jírovec, O. ( 1936). Über einige in Daphnia magna parasitierende Mikrosporidien. Zoologischer Anzeiger 116, 136–142.Google Scholar
Larsson, J. I. R., Ebert, D., Mangin, K. L. and Vávra, J. ( 1998). Ultrastructural study and description of Flabelliforma magnivora sp. n. (Microspora: Duboscqiidae), a microsporidian parasite of Daphnia magna (Crustacea: Cladocera: Daphniidae). Acta Protozoologica 37, 41–52.Google Scholar
Larsson, J. I. R., Ebert, D. and Vávra, J. ( 1997). Ultrastructural study and description of Ordospora colligata gen. et sp. nov. (Microspora, Ordosporidae fam. nov.), a new microsporidian parasite of Daphnia magna (Crustacea, Cladocera). European Journal of Protistology 33, 432–443.Google Scholar
Larsson, J. I. R., Ebert, D., Vávra, J. and Voronin, V. N. ( 1996). Redescription of Pleistophora intestinalis Chatton, 1907, a microsporidian parasite of Daphnia magna and Daphnia pulex, with establisment of the new genus Glugoides (Microspora, Glugeidae). European Journal of Protistology 32, 251–261.CrossRefGoogle Scholar
Lass, S. and Ebert, D. ( 2005). Apparent seasonality of parasite dynamics: analysis of cyclic prevalence patterns. Proceedings of the Royal Society of London, B. 273, 199–206. DOI: 10.1098/rspb.2005.3310.CrossRefGoogle Scholar
Lively, C. M. and Dybdahl, M. F. ( 2000). Parasite adaptation to locally common host genotypes. Nature 405, 679–1474. DOI: 10.1038/35015069.CrossRefGoogle Scholar
Mangin, K. L., Lipsitch, M. and Ebert, D. ( 1995). Virulence and transmission modes of two microsporidia in Daphnia magna. Parasitology 111, 133–142.CrossRefGoogle Scholar
Menotti, J., Cassinat, B., Porcher, R., Sarfati, C., Derouin, F. and Molina, J. M. ( 2003 a). Development of a real-time polymerase-chain-reaction assay for quantitative detection of Enterocytozoon bieneusi DNA in stool specimens from immunocompromised patients with intestinal microsporidiosis. Journal of Infectious Diseases 187, 1469–1474.Google Scholar
Menotti, J., Cassinat, B., Sarfati, C., Liguory, O., Derouin, F. and Molina, J. M. ( 2003 b). Development of a real-time PCR assay for quantitative detection of Encephalitozoon intestinalis DNA. Journal of Clinical Microbiology 41, 1410–1413. DOI: 10.1128/JCM.41.4.1410–1413.2003.CrossRefGoogle Scholar
Mouton, L., Dedeine, F., Henri, H., Boulétreau, M., Profizi, N. and Vavre, F. ( 2004). Virulence, multiple infections and regulation of symbiotic population in the Wolbachia-Asobara tabida symbiosis. Genetics 168, 181–189. DOI: 10.1534/genetics.104.026716.CrossRefGoogle Scholar
Mucklow, P. T., Vizoso, D. B., Jensen, K. H., Refardt, D. and Ebert, D. ( 2004). Variation in phenoloxidase activity and its relation to parasite resistance within and between populations of Daphnia magna. Proceedings of the Royal Society of London, B 271, 1175–1183. DOI: 10.1098/rspb.2004.2707.CrossRefGoogle Scholar
Pfaffl, M. W. ( 2004). Quantification strategies in real-time PCR. In A–Z of Quantitative PCR ( ed. Bustin, S. A.), pp. 78–120. International University Line (IUL), La Jolla, CA.
Pulkkinen, K. and Ebert, D. ( 2004). Host starvation decreases parasite load and mean host size in experimental populations. Ecology 85, 823–833.CrossRefGoogle Scholar
Rozen, S. and Skaletsky, H. J. ( 2000). Primer3 on the WWW for general users and for biologist programmers. In Bioinformatics Methods and Protocols: Methods in Molecular Biology ( ed. Krawetz, S. and Misener, S.), pp. 365–386. Humana Press, Totowa, NJ. http://frodo.wi.mit.edu/
Stirnadel, H. A. and Ebert, D. ( 1997). Prevalence, host specificity and impact on host fecundity of microparasites and epibionts in three sympatric Daphnia species. Journal of Animal Ecology 66, 212–222.CrossRefGoogle Scholar
Vizoso, D. B. and Ebert, D. ( 2004). Within-host dynamics of a microsporidium with horizontal and vertical transmission: Octosporea bayeri in Daphnia magna. Parasitology 128, 31–38. DOI: 10.1017/S0031182003004293.CrossRefGoogle Scholar
Vizoso, D. B., Lass, S. and Ebert, D. ( 2005). Different mechanisms of transmission of the microsporidium Octosporea bayeri: a cocktail of solutions for the problem of parasite permanence. Parasitology 130, 501–509. DOI: 10.1017/S0031182004006699.CrossRefGoogle Scholar
Wasson, K. and Barry, P. A. ( 2003). Molecular characterization of Encephalitozoon intestinalis (Microspora) replication kinetics in a murine intestinal cell line. Journal of Eukaryotic Microbiology 50, 169–174. DOI: 10.1111/j.1550-7408.2003.tb00112.x.CrossRefGoogle Scholar