J 2021

Development and Inter-Laboratory Validation of Diagnostics Panel for Detection of Biothreat Bacteria Based on MOL-PCR Assay

JELINKOVA, Pavlina, Jakub HRDÝ, Jirina MARKOVA, Jiri DRESLER, Petr PAJER et. al.

Základní údaje

Originální název

Development and Inter-Laboratory Validation of Diagnostics Panel for Detection of Biothreat Bacteria Based on MOL-PCR Assay

Autoři

JELINKOVA, Pavlina (203 Česká republika), Jakub HRDÝ (203 Česká republika, domácí), Jirina MARKOVA (203 Česká republika), Jiri DRESLER (203 Česká republika), Petr PAJER (203 Česká republika), Oto PAVLIS (203 Česká republika), Pavel BRANICH (203 Česká republika), Gabriela BORILOVA (203 Česká republika), Marketa REICHELOVA (203 Česká republika), Vladimir BABAK (203 Česká republika), Nikol RESLOVÁ (203 Česká republika, garant, domácí) a Petr KRALIK (203 Česká republika)

Vydání

Microorganisms, Basel, MDPI, 2021, 2076-2607

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10606 Microbiology

Stát vydavatele

Švýcarsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 4.926

Kód RIV

RIV/00216224:14310/21:00120920

Organizační jednotka

Přírodovědecká fakulta

UT WoS

000610579000001

Klíčová slova anglicky

MOL-PCR; biothreat bacteria; magnetic bead; bioterrorism; detection panel

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 16. 2. 2021 11:15, Mgr. Marie Šípková, DiS.

Anotace

V originále

Early detection of biohazardous bacteria that can be misused as biological weapons is one of the most important measures to prevent the spread and outbreak of biological warfare. For this reason, many instrument platforms need to be introduced into operation in the field of biological warfare detection. Therefore the purpose of this study is to establish a new detection panel for biothreat bacteria (Bacillus anthracis, Yersinia pestis, Francisella tularensis, and Brucella spp.) and confirm it by collaborative validation by using a multiplex oligonucleotide ligation followed by polymerase chain reaction and hybridization to microspheres by MagPix detection platform (MOL-PCR). Appropriate specific sequences in bacterial DNA were selected and tested to assemble the detection panel, and MOLigo probes (short specific oligonucleotides) were designed to show no cross-reactivity when tested between bacteria and to decrease the background signal measurement on the MagPix platform. During testing, sensitivity was assessed for all target bacteria using serially diluted DNA and was determined to be at least 0.5 ng/mu L. For use as a diagnostic kit and easier handling, the storage stability of ligation premixes (MOLigo probe mixes) was tested. This highly multiplex method can be used for rapid screening to prevent outbreaks arising from the use of bacterial strains for bioterrorism, because time of analysis take under 4 h.