Detection of biological threats. A challenge for directed molecular evolution

被引:73
作者
Petrenko, VA [1 ]
Sorokulova, IB [1 ]
机构
[1] Auburn Univ, Coll Vet Med, Dept Pathobiol, Auburn, AL 36849 USA
关键词
phage display; detection; monitoring; threat agents; landscape library; phage antibodies; Salmonella typhimurium; fluorescence-activated cell sorting; electron microscopy; food safety; food security;
D O I
10.1016/j.mimet.2004.04.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The probe technique originated from early attempts of Anton van Leeuwenhoek to contrast microorganisms under the microscope using plant juices, successful staining of tubercle bacilli with synthetic dyes by Paul Ehrlich and discovery of a stain for differentiation of gram-positive and gram-negative bacteria by Hans Christian Gram. The technique relies on the principle that pathogens have unique structural features, which can be recognized by specifically labeled organic molecules. A hundred years of extensive screening efforts led to discovery of a limited assortment of organic probes that are used for identification and differentiation of bacteria. A new challenge-continuous monitoring of biological threats-requires long lasting molecular probes capable of tight specific binding of pathogens in unfavorable conditions. To respond to the challenge, probe technology is being revolutionized by utilizing methods of combinatorial chemistry, phage display and directed molecular evolution. This review describes how molecular evolution methods are applied for development of peptide, antibody and phage probes, and summarizes the author's own data on development of landscape phage probes against Salmonella typhimurium. The performance of the probes in detection of Salmonella is illustrated by a precipitation test, enzyme-linked immunosorbent assay (ELISA), fluorescence-activated cell sorting (FACS) and fluorescent, optical and electron microscopy. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:147 / 168
页数:22
相关论文
共 166 条
[51]   Comparison of commercially available kits with standard methods for detection of Salmonella strains in foods [J].
Hanai, K ;
Satake, M ;
Nakanishi, H ;
Venkateswaran, K .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (02) :775-778
[53]   High-throughput antibody isolation [J].
Hayhurst, A ;
Georgiou, G .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2001, 5 (06) :683-689
[54]   Isolation and expression of recombinant antibody fragments to the biological warfare pathogen Brucella melitensis [J].
Hayhurst, A ;
Happe, S ;
Mabry, R ;
Koch, Z ;
Iverson, BL ;
Georgiou, G .
JOURNAL OF IMMUNOLOGICAL METHODS, 2003, 276 (1-2) :185-196
[55]   Smallpox as a biological weapon - Medical and public health management [J].
Henderson, DA ;
Inglesby, TV ;
Bartlett, JG ;
Ascher, MS ;
Eitzen, E ;
Jahrling, PB ;
Hauer, J ;
Layton, M ;
McDade, J ;
Osterholm, MT ;
O'Toole, T ;
Parker, G ;
Perl, T ;
Russell, PK ;
Tonat, K .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 281 (22) :2127-2137
[56]   Sensitive and rapid identification of biological threat agents [J].
Higgins, JA ;
Ibrahim, MS ;
Knauert, FK ;
Ludwig, GV ;
Kijek, TM ;
Ezzell, JW ;
Courtney, BC ;
Henchal, EA .
FOOD AND AGRICULTURAL SECURITY: GUARDING AGAINST NATURAL THREATS AND TERRORIST ATTACKS AFFECTING HEALTH, NATIONAL FOOD SUPPLIES, AND AGRICULTURAL ECONOMICS, 1999, 894 :130-148
[57]  
Himmelweit F., 1960, COLLECTED PAPERS P E
[58]   Protein design and phage display [J].
Hoess, RH .
CHEMICAL REVIEWS, 2001, 101 (10) :3205-3218
[59]  
HOFSCHNEIDER PH, 1963, Z NATURFORSCH PT B, VB 18, P203
[60]  
HOLLING CS, 1999, CONSERV ECOL, V3, P1