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WAVLD Symposium Handbook_V4.indd - csiro

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World Association of Veterinary Laboratory Diagnosticians – 13 th International <strong>Symposium</strong>, Melbourne, Australia, 11-14 November 2007<br />

0815 - 1000 Plenary Sessions - Preparing for the Future<br />

LABS OF THE FUTURE<br />

Dr. Martyn Jeggo<br />

Director, Australian Animal Health Laboratory, Geelong, Victoria,<br />

Australia<br />

Today, veterinary laboratories are faced with a range of challenges that constantly threaten their resource<br />

base, yet globally the need for veterinary diagnostic services and the underpinning research activities has<br />

never been greater. The occurrence and risks from infectious diseases has steadily been increasing during<br />

the past 20 years. Whilst many endemic production diseases have been on the wane, infectious disease e.g.<br />

avian influenza, foot and mouth disease, West Nile, bluetongue continues to threaten livestock and in a<br />

growing number of cases, man.<br />

How best can veterinary laboratories utilize current and new technologies to provide an effective diagnostic<br />

service and do so in a growing regulatory environment that makes the delivery of these services evermore<br />

complex and resource hungry?<br />

During the past few years, the development of molecular technologies based around the polymerase chain<br />

reaction (PCR) offer a quantum leap in diagnostic levels of sensitivity and specificity, in a timely and<br />

increasingly, quality assured manner. But where will this take us in the next ten years and can we genuinely<br />

equate the presence of genetic material with that of an infectious agent? Can the laboratory of the future<br />

dispense with causative agent isolation and characterization and rely on these newer gene based<br />

approaches? On the one hand, the promises of multiplex assays for multiple agent detection in a single test<br />

provides an opportunity to check for an enormously wide range of potential pathogens, whilst at the other<br />

end of the spectrum, the development of pen-side assays offers the opportunity to dispense with the need to<br />

even submit samples to a laboratory. How will these contrasting approaches impinge on activities<br />

undertaken by a veterinary laboratory in ten year time?<br />

In considering the regulatory and operating environment that laboratories now find themselves, a wide range<br />

of health, safety and environmental priorities must be taken into account for every activity undertaken.<br />

Invariably processes involving gene based technologies are now carefully regulated and activities involving<br />

the use of animals overseen by welfare and ethic committees. But beyond this, a new biosecurity regulatory<br />

environment is being created for anyone working with a range of pathogens, and increasingly this deals not<br />

only with biosafety and bio-containment but the potential element of bioterrorism. This increasing regulation<br />

of the operational environment of a veterinary laboratory must lead to changes in the way they operate, but<br />

what is the likely outcome?<br />

The biggest challenge though, maybe in the area of bio-informatics, information exchange and the decision<br />

making processes that this will underpin. The technologies embraced today have an ability to generate large<br />

amounts of data, that need to be collated, processed and re-organized to assist the veterinary diagnostician<br />

and the disease management services he supports. What will be the impact of the continuing information<br />

technology explosion on the activities of the veterinary laboratory in the future?<br />

This paper attempts to answer the questions posed above, taking examples from a number of recent disease<br />

outbreaks both in Australia and elsewhere, illustrating trends taking place today, that are likely to shape the<br />

veterinary laboratory of the future.<br />

Wed 14 November<br />

Wed 14 November<br />

World Association of Veterinary Laboratory Diagnosticians – 13 th International <strong>Symposium</strong>, Melbourne, Australia, 11-14 November 2007<br />

Biosafety and Biosecurity Concerns Of High Security Animal Pathogen Laboratories<br />

Luis L. Rodriguez, D.V.M., Ph.D.<br />

Overview:<br />

In response to the global spread of emerging infectious diseases and the threat of bioterrorism, highcontainment<br />

biosafety laboratories (BSL)--specifically biosafety level (BSL)-3 and BSL-4--have been<br />

proliferating in the United States as well as throughout the world. Specific incidents such as the anthrax<br />

terrorist attacks in the USA in 2001; the emergence of SARS and the infection of humans with H5N1 Avian<br />

influenza in Asia generated great concern and interest in around the world and in particular in the USA. A<br />

new industry; biodefense has emerged with academia, government and industry adapting and responding to<br />

this new niche for biodefense-related research, diagnostics, laboratory equipment, high-containment<br />

construction and pharmaceuticals. This multi-billion dollar industry ($5.24 billion in 2007 in the US alone)<br />

places great demand for BL3 and BL4 labs in government, academia and private sector.<br />

High-consequence human and animal pathogens, which traditionally have been studied in Public Health or<br />

Agriculture government laboratories, have become potential targets for bioterrorists. For example, foreign<br />

animal diseases such as Foot-and-Mouth Disease were determined to be high threats for US agriculture and<br />

food security. This increased concern for protecting an infrastructure critical to national security resulted in<br />

the transfer of the Administration and Operations of the Plum Island Animal Disease Center facility from the<br />

US Department of Agriculture (USDA) to the newly created Department of Homeland Security (DHS) in<br />

2003, while maintaining the research and diagnostics mission in USDA. Laws were revised and or created<br />

in 2002 to ensure the proper handling, storage and tracking of high consequence agents for both human and<br />

animal health.<br />

Although investment in biodefense research has been significant over the last 5 years, particularly in the<br />

area of human health, some of the critical infrastructure in animal health has lagged behind and only recently<br />

have plans been made to replace or renovate high-containment laboratories such as the Pirbright laboratory<br />

in the UK and the Plum Island laboratory in the US. These aging facilities have come under close scrutiny<br />

after a recent FMD outbreak was linked to the Pirbright site. This incident as well as recent incidents in US<br />

labs handling select agents motivated ongoing investigations at the congressional level. Similar inquiries are<br />

likely to follow in the UK as well as other countries with high-security laboratories.<br />

This lecture will present an overview of the current biosafety and biosecurity concerns, including the real as<br />

well as perceived risks from the construction and operation of high-security animal disease laboratories.

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