Impact of Nosema sp. Infection on Nutritional Physiology and Growth of the Tasar Silkworm Antheraea mylitta

  • Published : 2009.12.31

Abstract

Nosema sp. infection in the Indian tasar silkworm, Antheraea mylitta exerts a complex of influences on its host. The instar duration was extended significantly (P<0.001) except in $1^{st}$ instar. The infected larvae took about 48 days to reach the spinning stage against 40 days in the uninfected ones. The final weight attained by the larva at the end of each instar of development declined significantly following infection, as did weight gain and relative growth rate (RGR). The growth recorded/ day declined in infected larvae compared to uninfected ones from 8.2% during $1^{st}$ instar to 43.3% during $5^{th}$ instar. Food ingestion and digestion increased with advancement of the instar significantly irrespective of the status of the larvae but the relative consumption rate (RCR) declined. These parameters significantly declined in infected larvae (except food digested during $2^{nd}$ instar). The decline was more during $3^{rd}$ instar. In contrast, the approximate digestibility (AD %) was significantly higher in infected larvae than uninfected ones leaving the $1^{st}$ instar larvae unaffected. The efficiency of conversion of ingested food (ECI) and efficiency of conversion of digested food (ECD) did not change in a patterned way following the microsporidia (Nosema sp.) infection. The values of ECI significantly changed during $2^{nd}$, $3^{rd}$ and $5^{th}$ instars; while the change in ECD during $2^{nd}$, $4^{th}$ and $5^{th}$ were significant. During the entire larval life all the parameters tends to decline significantly following microsporidia infection but AD registered a significant increase. Nosema sp. spore concentration has increased 270.7 times during larval development in the course of experimentation.

Keywords

References

  1. Bansal AK, Saxena NN, Shukla RM, Roy DK, Sinha BRRP, Sinha SS (1997) A new technique proposed for estimation of pebrine in grainages. Sericologia 37, 11-14
  2. Bauer LS, Nordin GL (1988) Nutritional physiology of the eastern spruce budworm, Choristoneura fumiferana, infected with Nosema fumiferanae, and interaction with dietary nitrogene. Oecologia (Heidelberg) 77, 44-50 https://doi.org/10.1007/BF00380923
  3. Cantwell GE (1974) Honey bee diseases, parasites, and pests;in Insects diseases, Cantwell GE (ed.), Vol. II, pp. 539-542. Marcell Dekker, INC NewYork
  4. Giordana B, Forcella M, Leonardi MG, Casartelli M, Fiandra L, Hanozet GM, Parenti P (2002) A novel regulatory mechanism for amino acid absorption in lepidopteran larval midgut. J Insect Physiol 48, 585-592 https://doi.org/10.1016/S0022-1910(02)00080-X
  5. Henn MW, Solter LF (2000) Food utilization values of gypsy moth Lymantria dispar (Lepidoptera: Lymantriidae) larvae infected with the microsporidium Vairimorpha sp. (Microsporidia:Burenellidae). J Invertebr Pathol 76 , 263-269 https://doi.org/10.1006/jipa.2000.4977
  6. Hoch G, Schopf A (2001) Effects of Glyptapanteles liparidis (Hym.: Braconidae) parasitism, polydnavirus, and venom on development of microsporidia-infected and uninfected Lymantria dispar (Lep.: Lymantriidae) larvae. J Invertebr Pathol 77, 37-43 https://doi.org/10.1006/jipa.2000.4987
  7. Jolly MS, Sen SK (1972) Infection of Antheaea mylitta Drury (Lepidoptera: Saturniidae) by a microsporidian (Nosema sp.). Indian J Seric 11, 52-57
  8. Leonardi MG, Casartelli M, Fiandra L, Parenti P, Giordana B (2001) Role of specific activatiors of intestinal amino acid transport in Bombyx mori larval growth and nutrition. Arch Insect Biochem Physiol 48, 190-198 https://doi.org/10.1002/arch.1071
  9. Lee KP, Behmer ST, Simpson SJ, Raubenheimer D (2002) A geometric analysis of nutrient regulations in the generalist caterpillar, Spodoptera littoralis (Boisduval). J Insect Physiol 48, 655-665 https://doi.org/10.1016/S0022-1910(02)00088-4
  10. Lue Hui-ping, Jun Cai, Gong-yin Ye, Hong-xing Xu, Cui Hu (2000) Effect of parasitism by Petromalus puparum on hemolymph protein and carbohydrate metabolism in over wintering pupa of Pieris rapae. J Zhejiang Univ (Agril and Life Sciences) 26, 611-615
  11. Mitchel MJ, Cali A (1994) Vairimorpha necatrix (Microsporidia:Burenellidae) affect growth and development of Heliothis zea (Lepidoptera: Noctuidae) raced at various temperatures. J Econ Entomol 87, 933-940 https://doi.org/10.1093/jee/87.4.933
  12. Nakamatsu Y, Gyotoku Y, Tanaka T (2001) The endoparasitoid Cotesia kariyai (Ck) regulates the growth and metabolic efficiency of Pseudaletia separate larvae by venom and Ck polydnavirus. J Insect Physiol 47, 573-584 https://doi.org/10.1016/S0022-1910(00)00147-5
  13. Rao SN, Muthulakshmi M, Kanginakudru S, Nagaraju J (2004) Phylogenetic relationship of three new microsporidian isolates from the silkworm, Bombyx mori. J Invertebr Pathol 86, 87-95 https://doi.org/10.1016/j.jip.2004.05.004
  14. Rath SS, Sinha BRRP (2005) Parasitization of fifth instar tasar silkworm, Antheraea mylitta, by the uzi fly, Blepharipa zebina; a host-parasitoid interaction and its effect on host’s nutritional parameters and parasitoid development. J Invertebr Pathol 88, 70-78 https://doi.org/10.1016/j.jip.2004.09.006
  15. Rath SS, Prasad BC, Sinha BRRP (2003) Food utilization efficiency in fifth instar larvae of Antheraea mylitta (Lepidoptera:Saturniidae) infected with Nosema sp. and its effect on reproductive potential and silk production. J Invertebr Pathol 83, 1-9 https://doi.org/10.1016/S0022-2011(03)00038-7
  16. Rath SS, Singh BMK, Sinha BRRP (2000) Effect of uzi parasitism on nutritional parameters and silk production in Antheraea mylitta D. Int J Wild Silkmoth & Silk 5, 179-188
  17. Raubenheimer D, Simpson SJ (1999) Integrating nutrition: a geometrical approach. Entomol Exp Appl 91, 67-82 https://doi.org/10.1023/A:1003682921131
  18. Reynolds SE, Nottingham SF, Stephens AE (1985) Food and water economy and its relation to growth in fifth instar larvae of tobacco hornworm, Manduca sexta. J Insect Physiol 31, 119-127 https://doi.org/10.1016/0022-1910(85)90016-2
  19. Schopf A, Steinberger P (1996) The influence of the endoparasitic wasp Glyptapanteles lipardis (Hymenoptera: Braconidae) on the growth, food consumption, and food utilization of its host larva, Lymantria dispar (Lepidoptera:Lymantriidae). Eur J Entomol 93, 555-568
  20. Thompson SN, Redak RA (2000) Integration of dietary protein and carbohydrate determine blood sugar level and regulate nutrient selection in the insect Manduca sexta L. Biochim Biophys Acta 1523, 91-102 https://doi.org/10.1016/S0304-4165(00)00102-1
  21. Thompson SN, Borchardt DB, Wang L-W (2003) Dietary nutrient levels regulate protein and carbohydrate intake, gluconeogenic/glycolytic flux and blood trehalose level in the insect Manduca sexta L. J Comp Physiol B 173, 149-163 https://doi.org/10.1007/s00360-002-0322-8
  22. Thompson SN, Redak RA, Borchardt DB (2002) The glucogenic response of a parasitized insect Manduca sexta L. is partially mediated by differential nutrient intake. Biochim Biophys Acta 1571, 138-150 https://doi.org/10.1016/S0304-4165(02)00208-8
  23. Thompson SN, Redak RA, Wang L-W (2001) Altered dietary nutrient intake maintains metabolic homeostasis in parasitized larvae of the insect Manduca sexta. J Exp Biol 204, 4065-4080
  24. Thompson SN, R. Redak A, Wang L-W (2005) Nutrition interacts with parasitism to influence growth and physiology of the insect Manduca sexta L. J Exp Biol 208, 611-623 https://doi.org/10.1242/jeb.01404
  25. Waldbauer GP (1968) The consumption and utilization of food by insects. Adv Insect Physiol 5, 229-288 https://doi.org/10.1016/S0065-2806(08)60230-1