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Proteomic assessment of resistance to the fumigant phosphine in the lesser grain borer, Rhyzopertha dominica (F.)

Publication Type  Journal Article
Year of Publication  2008
Authors  Campbell, P.
Journal Title  Journal of Stored Products Research
Volume  44
Pages  389-393

Biosecurity defends key rural industry

CRC researchers are studying genetic codes to learn how insects like the lesser grain borer are developing resistance to the world’s most widely used grain fumigant – phosphine.

Media Release: 30 November 2009

 

This project aims to develop mathematical models to investigate the emergence of resistance to fumigants, particularly phosphine based fumigants. A particularly important aspect is the possibility that resistance is directly influenced due to the migration of resistant stored grain insects from silos to and from surrounding farmland, where they breed with non-resistant insects. Computer software will be developed to assess different fumigation strategies with the aim to reduce (or eliminate) resistance, taking into account ecological data on movement of insects to surrounding farmland.

What is the biosecurity problem?

Phosphine is the most common fumigant used today to treat stored grain infestations. Resistance to phosphine is a major threat to the grain industry and inadequate fumigation strategies may result in infestations of resistant insects that are difficult to control. Grain borers tend to reach unnaturally high population numbers due to mass storage of grain food. There is a need to understand the impact of refuges on the emergence of resistance.

The main outputs of this project are to:

  • understand the impact of refuges on the emergence of resistance
  • develop a management tool for farmers to allow more effective management strategies to be applied
  • develop much needed skills in mathematical model development in the grains industries, and
  • limit the risk of resistant strains of stored grain insects becoming endemic to the Australian grain industry.

Who will be the end-users of your research?

Grain handling companies and farmers will have a fumigation management tool (as computer software) that will help them decide the most effective fumigation management strategies.
 

STUDENT


Mr Jason Thorne
Student CRC60129: Mathematical modelling of fumigant resistance - PhD

j1.thorne@student.qut.edu.au

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PROJECT DETAILS

Status
Complete
Supervisor
Dr Glenn Fulford (QUT), Dr Ian Turner (QUT), Dr Andrew Ridley (QPI&F) and Dr David Schipallus (QPI&F)
Supervising Institution
Queensland University of Technology
Term
June 2009 - June 2012

LOCATION

This project aimed to provide rapid identification of the phosphine resistance status of any individual R. dominica or T. castaneum collected from grain in storage across Australia. The resistance genes that are directly responsible for phosphine resistance in these insects were identified and used as indicators of resistance status.

Research outcomes

Key outcomes of the research are:

  1. Phosphine resistance is mediated by two major genes in both T. castaneum and R. dominica. These two genes have been named rph1 and rph2 (i.e. resistance to phosphine 1 and 2).
  2. The two genes are incompletely recessive and individually confer weak resistance when homozygous for the resistance mutation.
  3. The two genes are synergistic in effect and confer strong resistance in R. dominica and T. castaneum when both are present and homozygous for the resistance alleles.
  4. The two genes are expressed in all insect life stages suggesting a constitutively expressed resistance factor that does not appear to be 'switched off' at any stage of development.
  5. The location of the rph1 gene has been narrowed down to a very small number of candidate genes (about six) for T. castaneum. However the location for R. dominica is less clear with a region of about 100 genes identified as the source area.
  6. While gene expression profiling was achieved for R. dominica and T. castaneum the results indicate that the technique is not suitable as the basis for development of a diagnostic test for resistance as the known resistance genes are not differentially expressed in resistant and sensitive strains and do not change expression in response to phosphine.

Research implications

Implication 1

The research has shown that there are two major genes that confer resistance in the two insect species studied and that both these genes are expressed in all insect life stages. This means that:

  1. Selection for resistance can occur in all life stages of the two studied insects, and
  2. There are no vulnerable life-stages that could have been targeted in attempts to manage resistance development

Implication 2

The finding that the two genes are synergistic in effect and confer strong resistance only when both genes are homozygous (for resistance) explains why strong resistance has taken a relatively long time to increase in frequency and appear in enough numbers to be detected. This is because you must have, in one individual, both resistance genes present and both homozygous and the chances of this occurring in random mating events in nature are not high.

Implication 3

It was found that the gene rph2 is highly conserved between R. dominica and T. castaneum. The significance of this finding is that a similar mechanism for resistance could be common across all major grain storage pest species where phosphine is used for control.

Implication 4

The research has shown that mutations in rph2 vary between populations of R. dominica and T. castaneum. This indicates that industry is unlikely to gain a universal molecular diagnostic test for phosphine resistance that could be applied across Australian grain growing areas. 

Acknowledgements

The authors would like to acknowledge the support of the Australian Government’s Cooperative Research Centres Program. We would also like to acknowledge the contributions of the University of Queensland which contributed to two PhD scholarships that worked on this project.

PROJECT LEADER


Dr David Schlipalius
Project Leader CRC20080:Phosphine Resistance - Molecular

David.Schlipalius@deedi.qld.gov.au
Phone: 07 3365 2516
Fax: 07 3354 1655

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PROJECT DETAILS

Status
Complete
Term
July 2007 – July 2010
Budget
$1,341,599 (cash and in-kind resources)

PROGRAM DETAILS

LOCATION