Biosafety and selectable markers

被引:14
作者
Titball, Richard W. [1 ]
Sjostedt, Anders
Pavelka, Martin S., Jr.
Nano, Francis E.
机构
[1] Def Sci & Technol Lab, Salisbury SP4 0JQ, Wilts, England
[2] London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1, England
[3] Umea Univ, Dept Clin Bacteriol, Umea, Sweden
[4] Univ Rochester, Med Ctr, Rochester, NY 14642 USA
[5] Univ Victoria, Dept Biochem & Microbiol, Victoria, BC, Canada
来源
FRANCISELLA TULARENSIS: BIOLOGY, PATHOGENICITY, EPIDEMIOLOGY, AND BIODEFENSE | 2007年 / 1105卷
关键词
Francisella tularensis; containment; laboratory; biosafety; genetic manipulation; vaccine;
D O I
10.1196/annals.1409.002
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:405 / 417
页数:13
相关论文
共 33 条
[1]   TRANSFORMATION AND ALLELIC REPLACEMENT IN FRANCISELLA SPP [J].
ANTHONY, LSD ;
GU, M ;
COWLEY, SC ;
LEUNG, WWS ;
NANO, FE .
JOURNAL OF GENERAL MICROBIOLOGY, 1991, 137 :2697-2703
[2]   The Bla2 β-lactamase from the live-vaccine strain of Francisella tularensis encodes a functional protein that is only active against penicillin-class β-lactam antibiotics [J].
Bina, Xiaowen R. ;
Wang, Chunmei ;
Miller, Mark A. ;
Bina, James E. .
ARCHIVES OF MICROBIOLOGY, 2006, 186 (03) :219-228
[3]   IMMUNIZATION AGAINST TULAREMIA - ANALYSIS OF EFFECTIVENESS OF LIVE FRANCISELLA-TULARENSIS VACCINE IN PREVENTION OF LABORATORY-ACQUIRED TULAREMIA [J].
BURKE, DS .
JOURNAL OF INFECTIOUS DISEASES, 1977, 135 (01) :55-60
[4]   Tularemia as a biological weapon - Medical and public health management [J].
Dennis, DT ;
Inglesby, TV ;
Henderson, DA ;
Bartlett, JG ;
Ascher, MS ;
Eitzen, E ;
Fine, AD ;
Friedlander, AM ;
Hauer, J ;
Layton, M ;
Lillibridge, SR ;
McDade, JE ;
Osterholm, MT ;
O'Toole, T ;
Parker, G ;
Perl, TM ;
Russell, PK ;
Tonat, K .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (21) :2763-2773
[5]  
DIENST F T Jr, 1963, J La State Med Soc, V115, P114
[6]  
Eigelsbach H T, 1967, Med Ann Dist Columbia, V36, P282
[7]   Tularemia [J].
Ellis, J ;
Oyston, PCF ;
Green, M ;
Titball, RW .
CLINICAL MICROBIOLOGY REVIEWS, 2002, 15 (04) :631-+
[8]   An outbreak of primary pneumonic tularemia on martha's vineyard [J].
Feldman, KA ;
Enscore, RE ;
Lathrop, SL ;
Matyas, BT ;
McGuill, M ;
Schriefer, ME ;
Stiles-Enos, D ;
Dennis, DT ;
Petersen, LR ;
Hayes, EB .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (22) :1601-1606
[9]   The identification of five genetic loci of Francisella novicida associated with intracellular growth [J].
Gray, CG ;
Cowley, SC ;
Cheung, KKM ;
Nano, FE .
FEMS MICROBIOLOGY LETTERS, 2002, 215 (01) :53-56
[10]   TNMAX - A VERSATILE MINI-TRANSPOSON FOR THE ANALYSIS OF CLONED GENES AND SHUTTLE MUTAGENESIS [J].
HAAS, R ;
KAHRS, AF ;
FACIUS, D ;
ALLMEIER, H ;
SCHMITT, R ;
MEYER, TF .
GENE, 1993, 130 (01) :23-31