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Page 17

Journal of Nutrition and Human Health | Volume 3

May 23-24, 2019 | Vienna, Austria

Joint Event

2

nd

International Conference on

Gastroenterology and Digestive Disor

ders

17

th

International Conference on

Nutrition and Fitness

&

F

ish meat consumption increases worldwide, even in

landlocked countries, due to its health benefits. In this

context, it is becoming critical to control the fish market of

developed countries, also regarding the proper labelling

according to the zoological origin of the traded fish. This

is important economically, as mislabelling can result from

the fraudulent substitution of species of high value with

some less expensive fish. Proper labelling is also important

in terms of the impact on health as fish parvalbumin

can trigger allergic reactions in sensitive consumers. The

severity of the reaction varies, according to some reports,

for each individual patient based on the species of fish.

Methods based on polymerase chain reaction (PCR) can be

employed in fish species determination from small piece of

meat devoid of morphological traits. Approaches based on

mitochondrial markers play dominant role so far. However,

intron regions of nuclear genes can serve as a platform for

such approaches as well. Second intron in protein coding

region of fish parvalbumin gene was used as such marker

in a model species Black seabream. In interlaboratory study

all participating laboratories detected Black seabream with

no false positivities in panel of other fish species. Also, Real

Time PCR modification can be designed. This approach

brings ability to quantify the amount of target fish species

as an extra readout of the assessment. Such information can

be very useful in inspection of fish market as adulteration

usually takes place in complex foods and extent of admixed

species is important criterion. Cloning of fragment of nuclear

gene intron into plasmid vector can lead to recombinant

calibrators for such detection methods based on Real Time

PCR and bring these assays on more defined, precise and

generally more sophisticated in methods.

Speaker Biography

Petr Hanak graduated in biology in 1990 at Charles University, Prague,

Czech Republic. He obtained his PhD in biochemistry at Safarik´s

University in Kosice, Slovakia in 2006. Currently, he is the head of

laboratory of molecular biology in Food Research Institute in Prague.

His research interest includes employment of PCR in fraud detection

of food, in particular fish species determination by various PCR

modifications.

e:

petr.hanak@vupp.cz

Petr Hanak

Food Research Institute, Czech Republic

Polymerase Chain Reaction in the assessment of fish meat

taxonomic identity

Notes: