RESLOVÁ, Nikol, Martin KAŠNÝ, Michal SLANÝ, Silvia MONTEIRO a Ricardo SANTOS. Real-time PCR a digital PCR v diagnostice parazitů v potravinách. In XV. Tomáškovy dny mladých mikrobiologů. 2016. ISBN 978-80-210-8255-7.
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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
Originální 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
Změnil Změnil: RNDr. Martin Kašný, Ph.D., učo 11259. Změněno: 25. 3. 2017 08:10.
Anotace
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.
Anotace 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 MUNázev: 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
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