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Issue 1105 coverFrancisella Tularensis: Biology, Pathogenicity, Epidemiology, and Biodefense Volume 1105 published June 2007
Ann. N.Y. Acad. Sci. 1105: 405–417 (2007). doi: 10.1196/annals.1409.002
Copyright © 2007 by the New York Academy of Sciences
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Biosafety and Selectable Markers

RICHARD W. TITBALLa,b, ANDERS SJOSTEDTc, MARTIN S. PAVELKA, JRd AND FRANCIS E. NANOe

a Defence Science and Technology Laboratory, Porton Down, Salisbury, United Kingdom b Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom c Department of Clinical Bacteriology, Umeå University, Umeå, Sweden d University of Rochester Medical Center, Rochester, New York, USA. e Department of Biochemistry and Microbiology, University of Victoria, Victoria, British Columbia, Canada

Key Words: Francisella tularensis • containment • laboratory • biosafety • genetic manipulation • vaccine

Address for correspondence: Richard W. Titball, Defence Science and Technology Laboratory, Porton Down, Salisbury, SP4 0JQ, United Kingdom. Voice: 44-1980-613301; fax: 44-1980-614307.  rwtitball{at}dstl.gov.uk

Francisella tularensis (F. tularensis) is one of the most infectious pathogens known. Although the disease caused by this bacterium is rarely fatal with appropriate antibiotic therapy, it is often severely debilitating. Laboratory work with F. tularensis poses a significant hazard, and it is essential that appropriate laboratory facilities, trained personnel, and suitable working practices are in place in any organization working with this pathogen. Work with human virulent strains should be carried out at containment level 3. Vaccines play an important potential role in the protection of individuals working with F. tularensis, but the live vaccine strain (LVS) vaccine is not currently licensed for use in humans. Because antibiotic therapy is central to the treatment of human tularemia, antibiotic resistance markers for use in genetic manipulation studies should be carefully selected.




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