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Title: Exploiting the explosion of information associated with whole genome sequencing to tackle Shiga toxin-producing Escherichia coli (STEC) in global food production systems

Author
item FRANZ, EELCO - National Institute For Public Health And The Environment (RIVM)
item DELAQUIS, PASCAL - Agriculture And Agri-Food Canada
item STEFANO, MORABITO - Istituto Superiore Di Sanità
item BEUTIN, LOTHAR - Federal Institute Of Technology
item GOBIUS, KARI - Commonwealth Scientific And Industrial Research Organisation (CSIRO)
item RASKO, DAVID - University Of Maryland
item Bono, James - Jim
item FRENCH, NIGEL - Massey University
item OSEK, JACEK - Dept Of Hygiene Of Food And Animal Origin
item LINDSTEDT, BJORN_ARNE - The Norwegian Institute Of Public Health
item MUNIESA, MAITE - University Of Barcelona
item MANNING, SHANNON - Michigan State University
item LEJEUNE, JEFF - Ohio Agricultural Research & Development Center
item Callaway, Todd
item BEATSON, SCOTT - University Of Queensland
item EPPINGER, MARK - University Of Texas At San Antonio
item DALLMAN, TIM - Health Protection Agency
item FORBES, KEN - University Of Aberdeen
item AARTS, HENK - National Institute For Public Health And The Environment (RIVM)
item PEARL, DAVID - University Of Aberdeen
item STRACHAN, NORVAL - University Of Aberdeen

Submitted to: International Journal of Food Microbiology
Publication Type: Other
Publication Acceptance Date: 7/4/2014
Publication Date: 7/11/2014
Citation: Franz, E., Delaquis, P., Stefano, M., Beutin, L., Gobius, K., Rasko, D., Bono, J.L., French, N., Osek, J., Lindstedt, B., Muniesa, M., Manning, S., LeJeune, J., Callaway, T.R., Beatson, S., Eppinger, M., Dallman, T., Forbes, K., Aarts, H., Pearl, D., Strachan, N.J. 2014. Exploiting the explosion of information associated with whole genome sequencing to tackle Shiga toxin-producing Escherichia coli (STEC) in global food production systems. International Journal of Food Microbiology. 187:57-72.

Interpretive Summary: Shiga toxin-encoding Escherichia coli (STEC) are important contributors to foodborne human illness in both the developed and developing worlds. One of the primary challenges in studying STEC is to see that new technologies are effectively utilised to help address the issues associated with these pathogenic organisms. The purpose of this position paper is to investigate the potential benefits and pitfalls of whole genome sequencing of STECs. A number of key recommendations are made to ensure the methods used are valid, data is freely available, software is developed for non-bioinformaticians, and prioritization of funding. Currently the benefits of WGS are being slowly teased out by both government and academic researchers around the world. The next phase will require a coordinated international approach to ensure that its potential to contribute to the challenge of STEC disease can be realized in a cost effective and timely manner.

Technical Abstract: The rates of foodborne disease caused by gastrointestinal pathogens continue to be a concern in both the developed and developing worlds. The growing world population, the increasing complexity of agri-food networks and the wide range of foods now associated with STEC are potential drivers for increased risk of human disease. It is vital that new developments in technology, such as whole genome sequencing (WGS), are effectively utilised to help address the issues associated with these pathogenic organisms. This position paper, arising from an OECD funded workshop, provides a brief overview of next generation sequencing technologies and software. It then uses the agent-host-environment paradigm as a basis to investigate the potential benefits and pitfalls of WGS in (1) the evolution and virulence of STEC, (2) epidemiology from bedside diagnostics to investigations of outbreaks and sporadic cases and (3) food protection from routine analysis of foodstuffs to global food networks. A number of key recommendations are made that include: validation and standardization of acquisition, processing and storage of sequence data including the development of an open access “WGSNET”; building up of sequence databases from both prospective and retrospective isolates; development of a suite of open-access software specific for STEC accessible to non-bioinformaticians; prioritisation of research funding to both produce and integrate genotypic and phenotypic information suitable for risk assessment; training to develop a supply of individuals working in bioinformatics/software development; training for clinicians, epidemiologists, the food industry etc. to ensure take-up of the technology and finally review of progress of implementation of WGS. Currently the benefits of WGS are being slowly teased out by both government and academic researchers around the world. The next phase will require a coordinated international approach to ensure that its potential to contribute to the challenge of STEC disease can be realized in a cost effective and timely manner.