k 2016

Real-time PCR a digital PCR v diagnostice parazitů v potravinách

RESLOVÁ, Nikol, Martin KAŠNÝ, Michal SLANÝ, Silvia MONTEIRO, Ricardo SANTOS et. al.

Základní údaje

Originální název

Real-time PCR a digital PCR v diagnostice parazitů v potravinách

Název česky

Real-time PCR a digital PCR v diagnostice parazitů v potravinách

Název anglicky

Real-time PCR a digital PCR in disgnostics of parasitological agents in food

Autoři

RESLOVÁ, Nikol (203 Česká republika, garant, domácí), Martin KAŠNÝ (203 Česká republika, domácí), Michal SLANÝ (203 Česká republika), Silvia MONTEIRO (620 Portugalsko) a Ricardo SANTOS (620 Portugalsko)

Vydání

XV. Tomáškovy dny mladých mikrobiologů, 2016

Další údaje

Jazyk

čeština

Typ výsledku

Prezentace na konferencích

Obor

10600 1.6 Biological sciences

Stát vydavatele

Česká republika

Utajení

není předmětem státního či obchodního tajemství

Kód RIV

RIV/00216224:14310/16:00090148

Organizační jednotka

Přírodovědecká fakulta

ISBN

978-80-210-8255-7

Klíčová slova česky

real-time PCR; digitální PCR; diagnostika potravinových parazitů; giardia intestinalis; toxoplasma gondii

Klíčová slova anglicky

real-time PCR; digital PCR; diagnostics of foodborne parasites; giardia intestinalis; toxoplasma gondii
Změněno: 25. 3. 2017 08:10, RNDr. Martin Kašný, Ph.D.

Anotace

V originále

In recent years, the increase of reported outbreaks causing human-diseases associated with food-borne parasitic infections (uni/multi-cellular) arising from meat consumption has been recorded. This trend could be affected e.g. by the changes in farming management towards bio-production, globalization of food market, global climate change and also by the meat processing. This situation is consequently inducing the need for improvement of the diagnostic applications. Our work is focused on development of a reliable comprehensive molecular diagnostic method useful for rapid control of meat products. We adopted high sensitive multiplex oligonucleotide ligation-PCR assay - MOL-PCR, enabling direct and simultaneous detection of multiple nucleic acid signatures of parasites from complex samples and xMAP technology representing a novel detection platform based on magnetic microspheres. Visualization of the products is then realized via qualitative and quantitative MAGPIX instrumentation. Up to this date, the specific molecular probes allowing the detection and capturing of targeted DNA originating from two parasitic worms - Trichinella spiralis (nematode; partial sequence of 18S rRNA gene) and Taenia saginata (cestode; partial sequence of mitochondrial COX1 gene) were designed. Reaction conditions of MOL-PCR were optimized for simultaneous duplex assay. Currently, the calibration of MAGPIX system is in process.

Anglicky

In recent years, the increase of reported outbreaks causing human-diseases associated with food-borne parasitic infections (uni/multi-cellular) arising from meat consumption has been recorded. This trend could be affected e.g. by the changes in farming management towards bio-production, globalization of food market, global climate change and also by the meat processing. This situation is consequently inducing the need for improvement of the diagnostic applications. Our work is focused on development of a reliable comprehensive molecular diagnostic method useful for rapid control of meat products. We adopted high sensitive multiplex oligonucleotide ligation-PCR assay - MOL-PCR, enabling direct and simultaneous detection of multiple nucleic acid signatures of parasites from complex samples and xMAP technology representing a novel detection platform based on magnetic microspheres. Visualization of the products is then realized via qualitative and quantitative MAGPIX instrumentation. Up to this date, the specific molecular probes allowing the detection and capturing of targeted DNA originating from two parasitic worms - Trichinella spiralis (nematode; partial sequence of 18S rRNA gene) and Taenia saginata (cestode; partial sequence of mitochondrial COX1 gene) were designed. Reaction conditions of MOL-PCR were optimized for simultaneous duplex assay. Currently, the calibration of MAGPIX system is in process.

Návaznosti

MUNI/A/1325/2015, interní kód MU
Název: Analýzy diverzity biologických systémů různých úrovní a na různých škálách prostředí (Akronym: BIDA5)
Investor: Masarykova univerzita, Analýzy diverzity biologických systémů různých úrovní a na různých škálách prostředí, DO R. 2020_Kategorie A - Specifický výzkum - Studentské výzkumné projekty