This Author published in this journals
All Journal bionature
Claim Missing Document
Check
Articles

Found 2 Documents
Search

Pembentukan Kapsul/Nodul Larva Helicoverpa armigera Hubner (Lepidoptera : Noctuidae) Pasca Infeksi HaNPV (Helicoverpa armigera NUCLEAR POLYHEDROSIS VIRUS) Nani, Kurnia
bionature Vol 11, No 1 (2010): April
Publisher : Fakultas MIPA UNM

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (147.088 KB) | DOI: 10.35580/bionature.v11i1.1375

Abstract

NPV is one of the biological insecticides that kills the target by infecting their cells including hemocytes. Hemocytes play a key role on defence mechanism against pathogens like NPV. This defense mechanism may cause the insect to become more tolerant as well as to chemical insectisides. The tolerances of insect to NPV could be induced by cellular immune system (CIS). One of the CIS is capsules/nodules formation. Based on that assumption, this research was conducted to observe the alteration of capsules/nodules formation of Helicoverpa armigera larvae post sublethal infection of HaNPV (Helicoverpa armigera nuclear polyhedrosis viruses). The fifth instar Helicoverpa armigera ware infected by sublethal doses of HaNPV. 24 hour post infection, partly of survive larvae reared to get their first (NPV-F1) and second filial (NPV-F2). Another survivor induced by hit killed Bacillus cereus, and then its haemocoel were exposed under stereo microscope (total magnification, 60 X) to watch capsules/nodules that appear as black spots on haemolymph. This procedure also conducted to fifth instar larvae of NPV-F1, NPV-F2, control (K-P) and their filial (K-F1 and K-F2), blank and placebo. The result showed that the number of nodules/capsules on larvae were not significant between control and the NPV-treat larvae on every generation, which was about 4 nodules/capsules. It showed that there is no cellular immune respon changed on NPV-P larvae, so their immune ability are similar to larvae K-P. The recoveries of NPV-P larvae cause it have a good capability to produce offspring with good immune response. So, NPV-F1 and NPV-F2 larvae have same ability as K-F1 and K-F2 larvae. It can be concluded that the use of sublethal dosage of HaNPV has not changed formation of capsules/nodules of H. armigera larvae and their offspring.
Respon Imun Humoral Pada Larva Helicoverpa armigera hubner (Lepidoptera : Noctuidae) Pasca Infeksi HaNPV (Helicoverpa armigera Nuclear Polyhedrosis Virus) dan Keturunannya Nani, Kurnia
bionature Vol 12, No 1 (2011): April
Publisher : Fakultas MIPA UNM

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (143.748 KB) | DOI: 10.35580/bionature.v12i1.1396

Abstract

NPV is one of the biological insecticides that kill the target by infecting their cells including hemocytes. Hemocytes play a key role on defense mechanism against pathogens like NPV. This defense mechanism may cause the insect to become more tolerant as well as to chemical insecticides. The tolerances of insect to NPV could be induced by humoral immune system (HIS). The HIS can be recorded by watch prophenoloxidase (PPO) activity or the presence of antibacterial compound (AC). Based on that assumption, this research was conducted to observe the alteration of PPO and AC due to sublethal infection of HaNPV (Helicoverpa armigera nuclear polyhedrosis viruses) on Helicoverpa armigera larvae and their offspring. PPO was detected as PO and measured spectrometrically on microplate-reader. Protein concentration was measured based on the color which appears due to protein-CBG (PO and Bradford reagent) bond at 570 nm. Protein concentration was calibrated with BSA. The occurrence of antibacterial activity was tested using modified Hoffman method. Inhibition zones were used to measure the antibacterial activity from E. coli (Gram negative) and B. cereus (Gram positive). Immune responses were observed on the fifth instar Helicoverpa armigera after 24 hpi by HaNPV (NPV-P) and their offspring (NPV-F1 and NPV-F2). Also, immune response on control larvae (K-P) were monitored and their filial (K-F1 and K-F2). The titer of PO enzyme were not significantly different for each generation. There was no inhibition zone on antibacterial activity test in every generation on NPV-P and K-P larvae.