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Handbook Part 2 - International Mycological Association

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S40IS2 - 0796<br />

Biosecurity: latest developments in systems and tools for fungal identification and disease diagnostics<br />

M.E. Palm<br />

USDA/APHIS, Beltsville, MD, United States<br />

Early detection, accurate identification and rapid response are key components of an effective plant disease<br />

management system for agricultural biosecurity. The detection and accurate identification of a fungal pathogen<br />

rely on a strong base of systematic knowledge and the resulting identification tools. Tools include access to published<br />

and interactive web-based keys, distance diagnostics capabilities, and an array of molecular and biochemical tests.<br />

An effective system also relies on a network of people that include early detectors, trained diagnosticians, and<br />

specialized mycologists. The U.S. utilizes a network of personnel for detection and identification of exotic pathogens<br />

at its borders. More recently a biosecurity network has been established to identify pathogens within the US. This<br />

network utilizes state departments of agriculture and diagnosticians from land-grant universities, which form the<br />

National Plant Diagnostic Network (NPDN), in conjunction with scientists in federal laboratories. In both networks<br />

distance diagnostics can be useful to make a preliminary and sometimes a final identification, if the fungus is<br />

particularly distinctive. In most cases morphological tools are used for a final identification. Increasingly molecular<br />

and biochemical tests are being developed and utilized for targeted pathogens and many of these are being<br />

adapted for rapid determinations in the field. For some groups of fungal pathogens, such as some ascomycetes and<br />

ascomycetous anamorphs, the knowledge base on which to make an accurate identification is lacking. For some<br />

groups of fungi an adequate knowledge base exists but rapid access to that information is lacking. Many fungal<br />

species have yet to be discovered and thus it is not surprising that a number of recently emerging pathogens must be<br />

studied and described as new species. Because these species were not known previously it is impossible to predict<br />

their origin and potential damaging effects. Support for systematics is essential to provide the basis for developing<br />

tools and tests for accurate identification of fungi.<br />

S40IS3 - 0961<br />

A major exotic disease outbreak, emergency response and eradication: banana black Sigatoka, Tully,<br />

Australia, 2001.<br />

PJL Whittle<br />

Department of Primary Industries and Fisheries, Brisbane, Queensland, Australia<br />

Australia’s geographical isolation has assisted its plant industries to remain free of many serious pests and diseases.<br />

Strong quarantine measures have been used to support this status. In the past decade, this approach has evolved<br />

substantially towards a cohesive national biosecurity system that supports international phytosanitary standards,<br />

structured around the shared responsibilities of governments and industries. A good example of the functioning of this<br />

system is provided by the response to an incursion of black Sigatoka (Mycosphaerella fijiensis Morelet) in Tully in April<br />

2001. The ‘hothouse’ of this response provided many lessons for the continued development of Australia’s plant<br />

biosecurity system.<br />

Freedom from black Sigatoka is a benefit the Australian banana industry values greatly. Fungicide and labour inputs<br />

are far lower than would be required if this disease was present. The industry, producing 300 000T per year worth over<br />

$300 million, is based primarily in tropical far north Queensland. Black Sigatoka is endemic nearby in the Torres Strait<br />

and Papua New Guinea. Since 1981, as part of a specific black Sigatoka biosecurity program, nine outbreaks were<br />

detected and eradicated on Cape York Peninsula in remote areas and in one case in an isolated commercial<br />

plantation. Detection of black Sigatoka in Tully, the heart of the 9 000 ha industry, came as a great shock. Industry’s<br />

concern about the expected yield losses and control costs was exacerbated by strict market access restrictions that<br />

were placed immediately on fruit from a 50 km radius around infected areas. An emergency response was mounted,<br />

based on an incursion management plan and the national system for managing exotic pest incursions. Initially,<br />

infected fields were destroyed, with voluntary compensation paid by the industry. As this became unaffordable, the<br />

approach changed to a zero-disease standard to be achieved by removal of diseased leaf tissue, a compulsory areawide<br />

fungicide program and intensive surveillance. Over 13 000 feral and unmanaged residential plants were killed.<br />

Industry and community participation was exceptional, although regulatory enforcement was available when<br />

required. A PCR-based molecular diagnostic assay was developed and was of great assistance. Disease was found<br />

in 25 sites in over 8 900 diagnostic samples. Efforts were assisted by the occurrence of two dry years. Eradication was<br />

completed in May 2002. Area freedom surveillance was conducted, with over 6 300 samples examined leading to a<br />

declaration of pest freedom in March 2005. Full market access was restored and early warning surveillance resumed.<br />

This paper will use the response to black Sigatoka in Tully and other examples to illustrate the functioning of the<br />

emergency plant pest response system in Australia.<br />

267

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