Evaluation of the Biotoxis qPCR Detection Kit for Francisella tularensis Detection in Clinical and Environmental Samples

被引:7
作者
Hennebique, Aurelie [1 ,2 ]
Gas, Fabienne [3 ]
Batina, Helene [3 ]
De Araujo, Cecilia [4 ]
Bizet, Karine [4 ]
Maurin, Max [1 ,2 ]
机构
[1] Ctr Hosp Univ Grenoble Alpes, Ctr Natl Reference Francisella, Inst Biol & Pathol, Grenoble, France
[2] Univ Grenoble Alpes, Ctr Natl Rech Sci, TIMC IMAG, UMR5525, Grenoble, France
[3] Univ Paris Saclay, SPI, Dept Medicaments & Technol Sante, CEA,INRAE, Bagnols Sur Ceze, France
[4] Berlin Technol, Montigny Le Bretonneux, France
关键词
Francisella tularensis; diagnosis; real-time PCR; tularemia; TULAREMIA; PCR; FRANCE;
D O I
10.1128/JCM.01434-20
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Rapid and reliable detection and identification of Francisella tularensis (a tier 1 select agent) are of primary interest for both medical and biological threat surveillance purposes. The Biotoxis qPCR detection kit is a real-time quantitative PCR (qPCR) assay designed for the detection of Bacillus anthracis, Yersinia pestis, and F. tularensis in environmental or biological samples. Here, we evaluated its performance for detecting F. tularensis in comparison to previously validated qPCR assays. The Biotoxis qPCR was positive for 87/87 F. tularensis subsp. holarctica (type B) strains but also for F. tularensis subsp. novicida. It was negative for Francisella philomiragia and 24/24 strains belonging to other bacterial species. For 31 tularemia clinical specimens, the Biotoxis qPCR displayed a sensitivity between 90.32% and 96.55%, compared to qPCR tests targeting ISFtu2 or a type B-specific DNA sequence, respectively. All 30 nontularemia clinical specimens were Biotoxis qPCR negative. For water samples, the Biotoxis qPCR limit of detection was 1,000 CFU/liter of F. tularensis. For 57 environmental water samples collected in France, the Biotoxis qPCR was positive for 6/15 samples positive for ISFtu2 qPCR and 4/4 positive for type B qPCR. In conclusion, the Biotoxis qPCR detection kit demonstrated good performances for F. tularensis detection in various biological and environmental samples, although crossamplification of F. tularensis subsp. novicida must be considered. This plate format assay could be useful to test a large number of clinical or environmental specimens, especially in the context of natural or intentional tularemia outbreaks.
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页数:8
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