Research articles
ScienceAsia (): 581-588 |doi:
10.2306/scienceasia1513-1874...581
Effects on detoxification enzymes of Helicoverpa
armigera (Lepidoptera: Noctuidae) infected by
Beauveria bassiana spores and detection of its infection
by PCR
Wanida Petlamula,*, Sawai Boukaewa, Caroline Hauxwellb, Poonsuk Prasertsanc
ABSTRACT: This research aimed to investigate virulence of Beauveria bassiana36 and its pathogenicity on the infected
larvae of Helicoverpa armigera. The virulence was measured by LD50 values and pathogenicity was monitored from detoxification enzymatic changes and pathogenic detection using polymerase chain reaction (PCR). LD50 of B. bassiana
against H. armigera larvae was highly effective at a very low dose of 7.2 × 108 spores/ml. Phenoloxidase (PO), glutathione S-transferase (GST), esterase (EST), and glucose oxidase (GOX) activities were found from the hemolymph of the infected H. armigera larvae. PO and GST activities from the infected larval sample increased from 53.72 ± 1.10
to 79.03 ± 1.22 U/mg protein and from 3.81 ± 0.17 to 5.77 ± 0.09 U/mg protein, respectively, from 0–48 h and then decreased from 61.75 ± 1.12 to 37.46 ± 1.06 U/mg protein and from 4.45 ± 0.09 to 2.61 ± 0.12 U/mg protein from 72–120 h, respectively. EST and GOX activities from the infected larval sample increased from 10.24 ± 0.44 to
21.84 ± 0.64 U/mg protein and from 3.38 ± 0.30 to 10.76 ± 0.34 U/mg protein, respectively, from 0–72 h, but decreased slightly from 21.72 ± 0.76 to 16.00 ± 0.89 U/mg protein and from 4.33 ± 0.55 to 4.02 ± 0.41 U/mg protein from 96–120 h, respectively. The presence of B. bassiana in the infected larvae was detected at post-inoculation using PCR with the specific primers (P1–P3). B. bassiana was successfully and rapidly detected and identified within 72–120 h with molecular techniques.
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a |
College of Innovation and Management, Songkhla Rajabhat University, Songkhla, Thailand |
b |
Earth Environmental and Biological Sciences, Bioscience, Faculty of Science and Engineering,
Queensland University of Technology, Brisbane, Queensland, Australia |
c |
Research and Development Office, Prince of Songkla University, Hat Yai, Songkhla, Thailand |
* Corresponding author, E-mail: wanida.pe@skru.ac.th
Received 6 Nov 2018, Accepted 29 Nov 2019
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