<abstract xmlns="http://www.w3.org/1999/xhtml"><p>The family Taeniidae is of great importance in the medical and veterinary fields, particularly in the tropics and subtropics. Identification of eggs of different <italic>Taenia</italic> spp. in the final host by morphological examination is difficult owing to their similarity. Therefore, a multiplex polymerase chain reaction (PCR) targeting a mitochondrial gene was applied to identify morphologically indistinguishable eggs. Fecal samples from 100 domestic dogs, from the Mazandaran province in Iran, were examined using the flotation/sieving method followed by multiplex PCR. Taeniid eggs were observed in 24 % samples, of which 12 %, 10 %, and 2 % were infected with <italic>Echinococcus granulosus, Taenia</italic> spp., and both <italic>E. granulosus</italic> and <italic>Taenia</italic> spp., respectively. <italic>E. multilocularis</italic> was absent in these samples. The prevalence of <italic>E. granulosus</italic> in the examined domestic dogs as definitive hosts in north of Iran was high (14 %). Therefore, people living in this region of Iran are in danger of acquiring hydatid cyst, which is a serious public health problem.</p></abstract>

The family Taeniidae is of great importance in the medical and veterinary fields, particularly in the tropics and subtropics. Identification of eggs of different Taenia spp. in the final host by morphological examination is difficult owing to their similarity. Therefore, a multiplex polymerase chain reaction (PCR) targeting a mitochondrial gene was applied to identify morphologically indistinguishable eggs. Fecal samples from 100 domestic dogs, from the Mazandaran province in Iran, were examined using the flotation/sieving method followed by multiplex PCR. Taeniid eggs were observed in 24 % samples, of which 12 %, 10 %, and 2 % were infected with Echinococcus granulosus, Taenia spp., and both E. granulosus and Taenia spp., respectively. E. multilocularis was absent in these samples. The prevalence of E. granulosus in the examined domestic dogs as definitive hosts in north of Iran was high (14 %). Therefore, people living in this region of Iran are in danger of acquiring hydatid cyst, which is a serious public health problem.

Application of multiplex PCR for the simultaneous detection of <italic>Taenia</italic> spp. from domestic dogs in the north of Iran

Toxoplasmosis Research Center, Mazandaran University of Medical Science, Sari, Iran

Student Research Committee, Mazandaran University of Medical Sciences

Infectious and Tropical Diseases Research Centre, Tabriz University of Medical Sciences, Tabriz, Iran

Helminthologia

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Application of multiplex PCR for the simultaneous detection of  spp. from domestic dogs in the north of Iran

The family Taeniidae is of great importance in the medical and veterinary fields, particularly in the tropics and subtropics. Identification of eggs of...

Application of multiplex PCR for the simultaneous detection of Taenia spp. from domestic dogs in the north of Iran

Article Category: Research Note

Publié en ligne: 22 juil. 2016

Pages: 285 - 289

Reçu: 06 sept. 2015

Accepté: 23 mars 2016

DOI: https://doi.org/10.1515/helmin-2016-0017

Mots clés
Cestoda, spp, Multiplex Polymerase Chain Reaction (PCR)

© 2016 Institute of Parasitology, SAS, Košice

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Application of multiplex PCR for the simultaneous detection of Taenia spp. from domestic dogs in the north of Iran

Article Category: Research Note

Publié en ligne: 22 juil. 2016

Pages: 285 - 289

Reçu: 06 sept. 2015

Accepté: 23 mars 2016

DOI: https://doi.org/10.1515/helmin-2016-0017

Mots clésCestoda, spp, Multiplex Polymerase Chain Reaction (PCR)

© 2016 Institute of Parasitology, SAS, Košice

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Mots clés
Cestoda, spp, Multiplex Polymerase Chain Reaction (PCR)