Nosema sp. isolated from Cabbage White Butterfly(Pieris rapae) Collected in Korea

  • Park, Ji-Young (Department of Sericulture and Entomology, National Institute of Agricultural Science and Technology) ;
  • Kim, Jong-Gill (Department of Sericulture and Entomology, National Institute of Agricultural Science and Technology) ;
  • Park, Young-Cheol (Department of Sericulture and Entomology, National Institute of Agricultural Science and Technology) ;
  • Goo, Tae-Won (Department of Sericulture and Entomology, National Institute of Agricultural Science and Technology) ;
  • Chang, Jin-Hee (School of Agricultural Biotechnology, Seoul National University) ;
  • Je, Yeon-Ho (Department of Biology, Imperial College of Science, Technology and Medicine) ;
  • Kim, Keun-Young (Department of Sericulture and Entomology, National Institute of Agricultural Science and Technology)
  • Published : 2002.09.01

Abstract

A microsporidium, from cabbage white bntteflies, Pieris rapae, collected in Korea, was purified and characterized according to its gene structure, spore morphology and pathogenicity. From the observation of the isolate by SEM and TEM, the endospores, exospores and nuclei, about 12 polar filament coils of the polar tube and posterior vacuoles were all identified. The nucleotide sequence was determined for a portion of genomic DNA which spans the V4 variable region of the small subunit rRNA gene. Comparison with the GenBank database for 15 other microsporidia species suggests that this isolate is most closely related to Nosema species. The pathogenicity against cabbage white butterflies was quantified by inoculating variable doses of spores to the second instar larvae. Peroral inoculation at a dosage of 10$\^$8/ spores/ml resulted in the death of all larvae prior to adult eclosion, but at lower spore dosages of 10$\^$4/-10$\^$5/ spores/ml, many adults successfully emerged. The median lethal dose (LD$\_$50/) was deter-mined to be 4.6$\times$10$\^$6/ spores/ml and the isolate also transmitted transovarially to the progeny eggs at a frequency of 92%.

Keywords

References

  1. The Microsporidia of Vertebrates Canning, E. U;J. Lom
  2. J. Invertebr. Pathol v.74 Nosema tyriae n.sp. and Nosema sp., Microsporidian Parasites of Cinnabar Moth Tyria Jacobaeae Canning, E. U;A. Curry;S. A. Cheney;N. J. Lafranchi-Tristem;Y. Kawakami;Y. Hatakeyama;H. Iwano;R. Ishihara
  3. Protoplasma v.186 Electron microscopic studies on Nosema mesnili Paillot(Microsporidia: Nosematidae)infecting the malpighian tubules of Pieris canidia larva Cheung, W. W. K;J. B. Wang
  4. Cell v.16 On spacers Fedoroff, N. V
  5. Evolution v.29 Confidence limits on phylogenics : an approach using the bootstrap Felsenstein, J
  6. PHYLIP(Phylogeny Inference Package)ver.3.5c. Department of Genetics Felsenstein, J
  7. Prog. Protozool. Proc. Int. Congr. Protozool v.3 On possible ways of speciation among Microsporidia Issi, I. V
  8. J. Stored Prod. Res v.7 Mode of transmission of Nosema plodiae Kellen and Lindegren, a pathogen of Plodia interpunctella(Hubner) Kellen, W. R;J. E. Lindegren
  9. J. Mole. Evol v.116 A simple method for estimating evolutionary rate of base substition through comparative studies of nucleotide sequence Kimura, M
  10. J. Invertebr. Pathol v.8 A microsporidian, Thelohania sp., in Pieris rapae Laigo, F. M;J. D. Paschke
  11. Annu. Rev. Biochem v.49 Repeated genes in eukaryotes Long, E. O;I. B. Dawid
  12. J. Invertebr. Pathol v.64 Ribosomal RNA genes of two microporidia, Nosema apis and Vavraia oncoperae, are very variable Malone, L. A;A. H. Broadwell;E. T. Lindridge;C. A. McIvor;J. A. Ninham
  13. J. Invertebr. Pathol v.68 Use of nucleotide sequence data to identify a microsporidian pathogen of Pieris rapae (Lepidoptera, Pieridae) Malone, L. A;C. A. Mclvor
  14. Clin Diagn Lab Immunol v.6 A powerful DNA extraction method and PCR for detection of microsporidia in clinical stool specimens Muller, A;K. Stellermann;P. Hartmann;M. Schrappe;G. Fatkenheuer;B. Salzberger;V. Diehl;C. Franzen
  15. Parasitol Res v.86 Ribosomal RNA of Nosema algerae and phylogenetic relationship to other microsporidia Muller, A;T. Trammer;G. Chioralia;H. M. Seitz;V. diehl;C. Franzen
  16. Bot. Z v.15 Uber die neue Krankheit der Seidenraupe und verwandte Organismen Nageli, K. W
  17. C. R. Soc. Biol v.81 Deux microsporidies nouvelles parasites des chenilles de Pieris brassicae Paillot, A
  18. L. C. R. Soc. Biol v.90 Sur Thelohania mesnili, microsporidie nouvelle parasite de Pieris brassicae Paillot, A
  19. Gene v.246 Microsporidia: accumulating molecular evidence that a group of amitochondriate and suspectedly primitive eukaryotes are just curious fungi Peer, Y.V.D;A. B. Ali;A. Meyer
  20. J. seric. Sci. Japan v.49 Purification of mature microsporidian spores by iso-density equilibrium centrifugation Sato, R;H. Watanabe
  21. Comparative pathobiology v.2 Systematics of the microsporidia Sprague, V;J. Vavra;L.A. Bulla(Eds.);T.C. cheug(Eds.)
  22. Synopsis and classification of living organism v.1 Microspora Sprague,V;S.P. Parker(Eds.)
  23. Crit. Rev. Microbiol v.18 Taxonomy of phylum Microspora Sprague, V;J. J. Becnel;E. I. Hazard
  24. The Microbiology and Microsporidiosis Appendix: Checklist of available generic names for microsporidia with type species and type hosts Sprague, V;J. J. Becnel;Wittner M(Eds.);L. M. Weiss(Eds.)
  25. PAUP: Phylogenetic analysis using parsi???? National History Survey ???
  26. ? Microsc v.39 ?? wainability of modified Satos staining ??? ???;T. Hanaichi;T. Iwamoto;L. Tin
  27. Proc. Hawaii. Entomol. Soc v.15 ??? parasite of the imported cabbage ??? ???
  28. Structure of the microsporidia, ??? ???L.M. Weiss(Eds.)
  29. Cesk. Parasitol v.3 Plistophora aporiae n. sp., ein parasit des Baumweisslinges Aporia crataegi Veber, J
  30. Nature v.326 Ribosomal RNA sequence suggests microsporidia are extremely ancient eukaryotes Vossbrinck, C. R;J. V. Maddox;S. Friedman;B. A. Debrunner-Vossbrink;C. R. Woese
  31. Clin. Microbiol. Rev v.7 Human microsporidial infections Weber, R;R. T. Bryan;D. A. Schwartz;R. L. Owen