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Some pathological effects and transmission potential of a microsporidian isolate (Nosema sp.) from the teak defoliator Hyblaea puera (Lepidoptera: Hyblaeidae)

Published online by Cambridge University Press:  01 September 2010

O.K. Remadevi*
Affiliation:
Wood Bio-degradation Division, Institute of Wood Science and Technology, 18th Cross, Malleswaram PO, Bangalore560 003, India
T.O. Sasidharan
Affiliation:
Ashoka Trust for Research in Ecology and the Environment, Royal Enclave, Srirampura, Jakkur PO, Bangalore560 064, India
Jayeeta Bhattacharya
Affiliation:
Wood Bio-degradation Division, Institute of Wood Science and Technology, 18th Cross, Malleswaram PO, Bangalore560 003, India
Charles R. Vossbrinck
Affiliation:
The Connecticut Agricultural Experiment Station, 123 Huntington Street, PO Box 1106, New Haven, CT06504, USA
Priyadarsanan Dharma Rajan
Affiliation:
Ashoka Trust for Research in Ecology and the Environment, Royal Enclave, Srirampura, Jakkur PO, Bangalore560 064, India
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Abstract

We report here the pathological effects of a microsporidian isolate (Nosema sp.) from the lepidopteran teak defoliator Hyblaea puera Cramer. The spores were ovo-cylindrical and had a mean size of 5.1 × 2.8 μm. The midgut and fat body were the primary organs infected by the microsporidium. Subsequently, infection was observed in Malphigian tubules, tracheal epithelium and gonads. The sequence of infection observed was: midgut – fat body – tracheal membrane – Malpighian tubule – gonad. Infection of this microsporidium produced a marked negative effect on the growth and development of larvae. The weight of healthy larvae increased about 22 times from the 3rd instar to pupation while the increase was about 12 times in the infected larvae. Rearing experiments conducted in the laboratory revealed a high potential for horizontal transmission (>90%) of the microsporidium among the defoliator larvae developing together. A nearly equal degree of vertical transmission (88.7%) was also observed from the infected females to the progeny larvae. The observations reported here indicate the prospect of the microsporidium as a bio-control agent against the defoliator pest if exploited properly. Small subunit rRNA gene sequence analysis revealed that this microsporidium differed from Nosema bombycis of silk moth by only two nucleotides. The teak moth and the silk moth are not as closely related as these two parasites appear to be, implying the likelihood of host switching.

Type
Research Paper
Copyright
Copyright © ICIPE 2010

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References

Ananthalakshmi, K. V. V., Samson, M. V., Baig, M. and Datta, R. K. (1994) The developmental stages and site of infection of Nosema bombycis in the silkworm, Bombyx mori L. Indian Journal of Sericulture 33, 180181.Google Scholar
Becnel, J. J. and Undeen, A. H. (1992) Influence of temperature on developmental parameters of the parasite/host system Edhazardia aedis (Microsporidia: Amblyosporidae) and Aedes aegypti (Diptera: Culicidae). Journal of Invertebrate Pathology 60, 299303.Google Scholar
Hylis, M., Pilarska, D. K., Obornik, M., Vavra, J., Solter, L. F., Weiser, J., Linde, A. and McManus, M. L. (2006) Nosema chrysorrhoeae n. sp. (Microsporidia), isolated from browntail moth (Euproctis chrysorrhoea L.) (Lepidoptera: Lymantridae) in Bulgaria: characterization and phylogenetic relationships. Journal of Invertebrate Pathology 91, 105114.CrossRefGoogle Scholar
Johny, S., Kanginakudru, S., Muralirangan, M. C. and Nagaraju, J. (2006) Morphological and molecular characterisation of a new microsporidian (Protozoa: Microsporidia) isolated from Spodoptera litura (Fabricius) (Lepidoptera: Noctuidae). Parasitology 132, 803814.Google Scholar
Kyei-Poku, G., Gauthier, D. and Frankenhuyzen, K. (2008) Molecular data and phylogeny of Nosema infecting lepidopteran forest defoliators in the genera Choristoneura and Malacosoma. Journal of Eukaryotic Microbiology 55, 5158.CrossRefGoogle ScholarPubMed
McManus, M. L., Maddox, J. V., Jeffords, M. R. and Webb, R. E. (1989) Evaluation and selection of candidate European microsporidia for introduction into U.S. gypsy moth populations, pp. 455468. Proceedings, Lymantriidae: A Comparison of Features of New and Old World Tussock Moths. USDA Forest Service, General Technical Report NE-123 Technical Coordinators: W.E. Wallner and K.A. McManus. USDA Forest Service, Northeastern Forest Experiment Station, Broomall, PA.Google Scholar
Maddox, J. V., Baker, M. D., Jeffords, M. R., Kuras, M., Linde, A., Solter, L. E., McManus, M. L., Vavra, J. and Vossbrinck, C. R. (1999) Nosema portugal, n. sp. isolated from gypsy moths (Lymantria dispar L.) collected in Portugal. Journal of Invertebrate Pathology 73, 192200.CrossRefGoogle Scholar
Maddox, J. V., Brooks, W. M. and Fuxa, J. R. (1981) Vairimorpha necatrix, a pathogen of agricultural pests: Potential for pest control, pp. 587594. In Microbial Control of Pests and Plant Diseases (edited by Burges, H. D.). Academic Press, London.Google Scholar
Maddox, J. V., McManus, M. L. and Solter, L. F. (1998) Microsporidia affecting forest Lepidoptera, pp. 187197. In Proceedings, Population Dynamics, Impacts and Integrated Management of Forest Defoliating Insects (edited by McManus, M. L. and Liebhold, A. M.). USDA Forest Service, General Technical Report NE-247. USDA Forest Service, Radnor, PA.Google Scholar
Nair, K. S. S., Sudheendrakumar, V. V., Varma, R. V. and Chacko, K. C. (1985) Studies on the seasonal incidence of defoliators and the effect of defoliation on volume increment of teak, KFRI Research Report No. 30. Kerala Forest Research Institute, Peechi. 78 pp.Google Scholar
Nair, K. S. S., Sudheendrakumar, V. V., Varma, R. V., Chacko, K. C. and Jayaraman, K. (1996) Effect of defoliation by Hyblaea puera and Eutectona machaeralis (Lepidoptera) on volume increment of teak, pp. 257273. In Impact of Diseases and Insect Pests in Tropical Forests. Proceedings of the IUFRO Symposium held at KFRI, Peechi, Kerala, India.Google Scholar
Nordin, G. L. and Maddox, J. V. (1974) Microsporidia of the fall webworm, Hyphantria cunea. Identification, distribution and comparison of Nosema sp. with similar Nosema spp. from other Lepidoptera. Journal of Invertebrate Pathology 24, 113.Google Scholar
Sajeev, T. V. and Sudheendrakumar, V. V. (2005) HpNPV Technology for Biocontrol of Teak Defoliator, Hyblaea puera, KFRI Handbook 23. Kerala Forest Research Institute, Peechi. 28 pp.Google Scholar
Sasidharan, T. O., Remadevi, O. K., Anitha Rani, A., Priyadarsanan, D. and Bhattacharya, J. (2008) New record of a microsporidian parasite from the teak defoliator, Hyblaea puera Cramer (Lepidoptera: Hyblaeidae). Hexapoda 15, 97101.Google Scholar
Sasidharan, T. O., Singh, R. N., Samson, M. V., Manjula, A., Santha, P. C. and Shekhariah, C. (1994) Spore replication rate of Nosema bombycis (Microsporidia: Nosematidae) in the silkworm Bombyx mori L. in relation to pupal development and age of moths. Insect Science and Its Application 15, 427431.Google Scholar
Sato, R. and Watanabe, H. (1980) Purification of mature microsporidian spores by iso-density equilibrium centrifugation. Journal of Sericulture Sciences of Japan 49, 512516.Google Scholar
Thomson, H. M. (1959) A microsporidian parasite of the forest tent caterpillar Malacosomadisstria Hbn. Canadian Journal of Zoology 37, 217221.CrossRefGoogle Scholar
Vossbrinck, C. R., Andreadis, T. G. and Debrunner-Vossbrinck, B. A. (1998) Verification of intermediate hosts in the life cycles of microsporidia by small subunit rDNA sequencing. Journal of Eukaryotic Microbiology 45, 290292.CrossRefGoogle ScholarPubMed
Wang, C. Y., Solter, L. F., T'sui, W. H. and Wang, C. H. (2005) An Endoreticulatus species from Ocinara lida (Lepidoptera: Bombycidae) in Taiwan. Journal of Invertebrate Pathology 89, 123135.Google Scholar
Wilson, G. G. (1977) Effects of the microsporidia Nosema disstriae and Pleistophora schubergi on the survival of the forest tent caterpillar, Malacosoma disstria (Lepidoptera: Lasicampidae). Canadian Journal of Entomology 109, 10211022.Google Scholar
Wilson, G. G. (1980) Effects of Nosema fumiferanae (Microsporidia) on rearing stock of spruce budworm, Choristoneura fumiferana (Lepidoptera: Tortricidae). Proceedings of the Entomological Society of Ontario 3, 115116.Google Scholar
Wilson, G. G. and Burke, J. M. (1971) Nosema thomsoni n. sp., a microsporidian from Choristoneura conflictana (Lepidoptera: Tortricidae). Canadian Journal of Zoology 49, 786788.CrossRefGoogle Scholar