Biological Threat Detection Via Host Gene Expression Profiling. Biological Threat Detection Via Host Gene Expression Profiling.

Biological Threat Detection Via Host Gene Expression Profiling‪.‬

Clinical Chemistry 2003, July, 49, 7

    • $5.99
    • $5.99

Publisher Description

The task of detecting biological threats is far more complicated than monitoring for other weapons of mass destruction. Measuring and quantifying radiation and chromatographic profiles indicative of nuclear and chemical threats, respectively, are relatively straightforward compared with the detection of biological weapon threats amid the tremendous biological background that comprises our environment. Most of the current biological warfare and environmental agent detection systems in field use or under prototype development rely on structural recognition approaches to identify anticipated agents or rely on "gold standard" culture conditions. Such assays, based primarily on antibodies, are highly specific for anticipated targets but provide only partial information concerning the pathogenicity of the threat. Current systems the military has implemented for threat identification have performed with limited success. In fact, the Pentagon Inspector General has criticized the "Joint Biological Point Detection System" for erratic limited performance (1). In addition, it is unclear how such an approach is applicable to the civilian population, where mass deployment of point detectors is not a feasible solution. Even with ideal detectors, proximity to a biological threat does not guarantee infection or illness. For threats such as Bacillus anthracis, the ability to preemptively treat individuals who were near dissemination sources with antibiotics is an option, if the dissemination source can be identified. Of further concern, a report has been published of a B. anthracis vaccine strain that had been engineered by Russian scientists to resist tetracycline antibiotics (2), raising the possibility that a quinolone-resistant B. anthracis could emerge as a biological weapon threat. Thus, not all biological threats can be treated as readily as during recent events, and there is a critical need to be able to quickly discern those individuals who are ill as a result of a bioagent etiology and to yield insight to the severity of illness.

GENRE
Science & Nature
RELEASED
2003
July 1
LANGUAGE
EN
English
LENGTH
15
Pages
PUBLISHER
American Association for Clinical Chemistry, Inc.
SELLER
The Gale Group, Inc., a Delaware corporation and an affiliate of Cengage Learning, Inc.
SIZE
171.6
KB
Gene Discovery for Disease Models Gene Discovery for Disease Models
2011
Microbial Forensics Microbial Forensics
2005
Chemical Diagnostics Chemical Diagnostics
2013
Applications of Advanced Omics Technologies: From Genes to Metabolites Applications of Advanced Omics Technologies: From Genes to Metabolites
2014
Molecular Analysis and Genome Discovery Molecular Analysis and Genome Discovery
2011
Animal Biotechnology Animal Biotechnology
2013
Doping in Sport: Misuse, Analytical Tests, And Legal Aspects (Editorial) Doping in Sport: Misuse, Analytical Tests, And Legal Aspects (Editorial)
1997
Vitamin E and Coronary Heart Disease in Tunisians (Nutrition) (Clinical Report) Vitamin E and Coronary Heart Disease in Tunisians (Nutrition) (Clinical Report)
2000
Endothelial Nitric Oxide Synthase Haplotypes Are Associated with Features of Metabolic Syndrome (Endocrinology and Metabolism) (Survey) Endothelial Nitric Oxide Synthase Haplotypes Are Associated with Features of Metabolic Syndrome (Endocrinology and Metabolism) (Survey)
2007
Alanine Aminotransferase As an Independent Predictor of Incident Nonalcoholic Fatty Liver Disease (Letters) (Letter to the Editor) Alanine Aminotransferase As an Independent Predictor of Incident Nonalcoholic Fatty Liver Disease (Letters) (Letter to the Editor)
2007
T-Cell Regulatory Gene CTLA-4 Polymorphism/Haplotype Association with Autoimmune Pancreatitis (Clinical Immunology) T-Cell Regulatory Gene CTLA-4 Polymorphism/Haplotype Association with Autoimmune Pancreatitis (Clinical Immunology)
2007
Percent Free Prostate-Specific Antigen in Assessing the Probability of Prostate Cancer Under Optimal Analytical Conditions (Enzymes and Protein Markers) Percent Free Prostate-Specific Antigen in Assessing the Probability of Prostate Cancer Under Optimal Analytical Conditions (Enzymes and Protein Markers)
1998