2014
DOI: 10.3389/fmicb.2014.00092
|View full text |Cite
|
Sign up to set email alerts
|

Quantitative and sensitive RNA based detection of Bacillus spores

Abstract: The fast and reliable detection of bacterial spores is of great importance and still remains a challenge. Here we describe a direct RNA-based diagnostic method for the specific detection of viable bacterial spores which does not depends on an enzymatic amplification step and therefore is directly appropriate for quantification. The procedure includes the following steps: (i) heat activation of spores, (ii) germination and enrichment cultivation, (iii) cell lysis, and (iv) analysis of 16S rRNA in crude cell lys… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
4
0

Year Published

2016
2016
2023
2023

Publication Types

Select...
4
1

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(4 citation statements)
references
References 64 publications
0
4
0
Order By: Relevance
“…Overall, compared to reported conventional ELISAs for anthrax spore detection [4,22], PHAD has improved sensitivity, robustness and/or substantially reduced run times. Nucleic acid sequence (DNA or RNA), dipicolinic acid (DPA), and surface resonance (Raman spectroscopy)-based methods of anthrax spore detection all require sample processing procedures (often including sample enrichment) and equipment limiting the portability and practicality in the field [6,23,24,25]. …”
Section: Discussionmentioning
confidence: 99%
“…Overall, compared to reported conventional ELISAs for anthrax spore detection [4,22], PHAD has improved sensitivity, robustness and/or substantially reduced run times. Nucleic acid sequence (DNA or RNA), dipicolinic acid (DPA), and surface resonance (Raman spectroscopy)-based methods of anthrax spore detection all require sample processing procedures (often including sample enrichment) and equipment limiting the portability and practicality in the field [6,23,24,25]. …”
Section: Discussionmentioning
confidence: 99%
“…The supernatant was loaded into the microfluidic chips with a 500 µl syringe through a single channel, with a flow rate of 300 µm s −1 . After the CNF fibrils entangled behind the pillars to form a solid transparent membrane, the CNF solution was switched to H 2 O. Phasecontrast and fluorescent images were acquired using an Axio Observer Z1 microscope (Carl Zeiss, Jena, Germany) 45 . Images were acquired every 2 min at ×20 magnification during the experiment.…”
Section: Particle Specificitymentioning
confidence: 99%
“…After the CNF fibrils entangled behind the pillars to form a solid transparent membrane, the CNF solution was switched to H2O. Phase-contrast and fluorescent images were acquired using an Axio Observer Z1 microscope (Carl Zeiss, Jena, Germany) 40 . Images were acquired every two minutes at 20x magnification during the experiment.…”
Section: Microfluidistic Set-up and Fluorescence Microscopymentioning
confidence: 99%