Rapid Detection of Bacillus anthracis Bloodstream Infections by Use of a Novel Assay in the GeneXpert System

被引:9
作者
Banada, Padmapriya P. [1 ]
Deshpande, Srinidhi [1 ]
Russo, Riccardo [1 ]
Singleton, Eric [1 ]
Shah, Darshini [2 ]
Patel, Bhavana [2 ]
Burday, Michele [2 ]
Koshy, Ranie [3 ]
Wang, Qing [2 ]
Jones, Martin [4 ]
Gall, Alexander [5 ]
Lokhov, Sergey [5 ]
Kwiatkowski, Robert [4 ]
Persing, David [4 ]
Connell, Nancy [1 ]
Alland, David [1 ]
机构
[1] Rutgers Biomed & Hlth Sci Univ, New Jersey Med Sch, Div Infect Dis, Ctr Emerging Pathogens, Newark, NJ 07103 USA
[2] Univ Hosp, Dept Pathol & Lab Med, Newark, NJ USA
[3] Univ Hosp, Blood Bank, Transfus Serv, Newark, NJ USA
[4] Cepheid, Sunnyvale, CA USA
[5] Cepheid, Bothell, WA USA
基金
美国国家卫生研究院;
关键词
Bacillus anthracis; diagnostic; whole blood; GeneXpert; diagnostics; MYCOBACTERIUM-TUBERCULOSIS; FRANCISELLA-TULARENSIS; YERSINIA-PESTIS; XPERT MTB/RIF; CEREUS; CAPABILITIES; VIRULENCE; SAMPLES; GENES;
D O I
10.1128/JCM.00466-17
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bacillus anthracis is a tier 1 select agent with the potential to quickly cause severe disease. Rapid identification of this pathogen may accelerate treatment and reduce mortality in the event of a bioterrorism attack. We developed a rapid and sensitive assay to detect B. anthracis bacteremia using a system that is suitable for point-of-care testing. A filter-based cartridge that included both sample processing and PCR amplification functions was loaded with all reagents needed for sample processing and multiplex nested PCR. The assay limit of detection (LOD) and dynamic range were determined by spiking B. anthracis DNA into individual PCR mixtures and B. anthracis CFU into human blood. One-milliliter blood samples were added to the filter-based detection cartridge and tested for B. anthracis on a GeneXpert instrument. Assay specificity was determined by testing blood spiked with non-anthrax bacterial isolates or by testing blood samples drawn from patients with concurrent non-B. anthracis bacteremia or nonbacteremic controls. The assay LODs were 5 genome equivalents per reaction and 10 CFU/ml blood for both the B. anthracis Sterne and V1B strains. There was a 6-log(10) dynamic range. Assay specificity was 100% for tests of non-B. anthracis bacterial isolates and patient blood samples. Assay time was less than 90 min. This automated system suitable for point-of-care detection rapidly identifies B. anthracis directly from blood with high sensitivity. This assay might lead to early detection and more rapid therapy in the event of a bioterrorism attack.
引用
收藏
页码:2964 / 2971
页数:8
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