Literature DB >> 33115844

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

Aurélie Hennebique1,2, Fabienne Gas3, Hélène Batina3, Cécilia De Araujo4, Karine Bizet4, Max Maurin5,2.   

Abstract

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 cross-amplification 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.
Copyright © 2020 American Society for Microbiology.

Entities:  

Keywords:  Francisella tularensiszzm321990; diagnosis; real-time PCR; tularemia

Year:  2020        PMID: 33115844      PMCID: PMC7771460          DOI: 10.1128/JCM.01434-20

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  3 in total

Review 1.  Applications of polymerase chain reaction-based methods for the diagnosis of plague (Review).

Authors:  Yanan Zhang; Zhanli Wang; Wenrui Wang; Hui Yu; Min Jin
Journal:  Exp Ther Med       Date:  2022-06-14       Impact factor: 2.751

Review 2.  Recent Progress on Tick-Borne Animal Diseases of Veterinary and Public Health Significance in China.

Authors:  Weijuan Jia; Si Chen; Shanshan Chi; Yunjiang He; Linzhu Ren; Xueli Wang
Journal:  Viruses       Date:  2022-02-09       Impact factor: 5.048

3.  Development and evaluation of a multiplex droplet digital polymerase chain reaction method for simultaneous detection of five biothreat pathogens.

Authors:  Yipu Du; Ziheng Yan; Kai Song; Junyan Jin; Liting Xiao; Zhulin Sun; Yafang Tan; Pingping Zhang; Zongmin Du; Ruifu Yang; Yong Zhao; Yajun Song
Journal:  Front Microbiol       Date:  2022-07-28       Impact factor: 6.064

  3 in total

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