A rapid bioassay screen for quantifying nucleopolyhedroviruses (Baculoviridae) in the environment

Citation
Ar. Richards et Pd. Christian, A rapid bioassay screen for quantifying nucleopolyhedroviruses (Baculoviridae) in the environment, J VIROL MET, 82(1), 1999, pp. 63-75
Citations number
30
Categorie Soggetti
Microbiology
Journal title
JOURNAL OF VIROLOGICAL METHODS
ISSN journal
01660934 → ACNP
Volume
82
Issue
1
Year of publication
1999
Pages
63 - 75
Database
ISI
SICI code
0166-0934(199909)82:1<63:ARBSFQ>2.0.ZU;2-T
Abstract
A quantitative bioassay method for the detection of Helicoverpa armigera (L epidoptera: Noctuidae) singly encapsulated nucleopolyhedroviruses (HaSNPVs) in soil is described. Calibration curves used for estimating soil virus ti tres in environmental samples were generated by incorporating a sterilised soil into a semi-synthetic insect diet then inoculating known concentration s of an HaSNPV into the soil-diet mixture. Calibration curves were construc ted for soil diets containing varying proportions of soil: 0, 1, 5, 10 and 25% soil (w/v). Their accuracy was assessed in a series of blind tests in w hich the actual soil virus concentration fell within the estimated mean 95% confidence region for each of three samples. The five soil-diet incorporat ion rates were compared in terms of larval survivorship and growth rate. Th ere was no significant difference in larval survivorship after 10 days (i.e . for the duration of the bioassay period). The stage structure of bioassay larvae at 10 days and pupal weight at 20 days was significantly different for individuals reared on 25% soil-diet in terms of both a slower growth ra te and a lower mean pupal weight compared to individuals reared on 10, 5 an d 1% soil diets. This did not, however, appear to lead to greater variabili ty in bioassay response at the high soil rate at 10 days. The level of sens itivity of virus detection achieved using this method was extremely good wi th the LC,, value for mid-first instar H. armigera larvae reared on the 25% soil-diet estimated at 26 polyhedral inclusion bodies (PIBs) per gram of s oil. The suitability of using this approach for quantifying Helicoverpa NPV s in Australian soils was assessed by comparing percent bioassay infection across a range of five isolates known to be present in Australia. The effec t of soil pH and soil management (cultivated versus non-cultivated) on perc ent bioassay infection was also examined. In both cases, no significant dif ferences were observed. Finally, percent idopathic mortality, percent NPV i nfection and estimates of Helicoverpa SNPV concentration in a selection of samples from the Australian environment are presented. (C) 1999 Elsevier Sc ience B.V. All rights reserved.