Cargando…

Multiplex PCR and Sequence Analysis to Investigate Genetic Diversity of Fasciola Isolates from Cattle and Sheep in Turkey

Fasciolosis is a highly prevalent helminthic infection caused by Fasciola hepatica and F. gigantica. With the aim of identifying hybrid Fasciola flukes, multiplex PCR was performed to amplify the pepck gene. Furthermore, to determine Fasciola haplotypes, mitochondrial nad1 gene was amplified and seq...

Descripción completa

Detalles Bibliográficos
Autores principales: Uzun, Veysel, Celik, Figen, Simsek, Sami, Kesik, Harun Kaya, Kilinc, Seyma Gunyakti, Zhang, Xiaocheng, Ahmed, Haroon, Cao, Jianping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692402/
https://www.ncbi.nlm.nih.gov/pubmed/36364987
http://dx.doi.org/10.3390/pathogens11111235
_version_ 1784837256726446080
author Uzun, Veysel
Celik, Figen
Simsek, Sami
Kesik, Harun Kaya
Kilinc, Seyma Gunyakti
Zhang, Xiaocheng
Ahmed, Haroon
Cao, Jianping
author_facet Uzun, Veysel
Celik, Figen
Simsek, Sami
Kesik, Harun Kaya
Kilinc, Seyma Gunyakti
Zhang, Xiaocheng
Ahmed, Haroon
Cao, Jianping
author_sort Uzun, Veysel
collection PubMed
description Fasciolosis is a highly prevalent helminthic infection caused by Fasciola hepatica and F. gigantica. With the aim of identifying hybrid Fasciola flukes, multiplex PCR was performed to amplify the pepck gene. Furthermore, to determine Fasciola haplotypes, mitochondrial nad1 gene was amplified and sequenced, and phylogenetic analyses were performed. Adult Fasciola isolates were collected from 51 cattle and 51 sheep, genomic DNA was isolated, and one-step multiplex PCR was subsequently performed to amplify pepck. Isolates that generated a 510 bp band were identified as F. gigantica, those that generated a 241 bp band were identified as F. hepatica, and those that generated both bands were identified as hybrid (aspermic) flukes. Multiplex PCR data identified four isolates as F. gigantica and 84 as F. hepatica. Fourteen hybrid isolates (five cattle and nine sheep) were identified. On unidirectional DNA sequence analysis of nad1 PCR products, three sequences were identified as F. gigantica and 99 as F. hepatica. In addition, only 4 of 87 haplotypes detected for F. hepatica nad1 sequences were found to be previously reported, while the remaining 83 are unique to this study. To summarize, this study is the first to report the existence of hybrid Fasciola flukes and 83 unique haplotypes of F. hepatica in Turkey.
format Online
Article
Text
id pubmed-9692402
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-96924022022-11-26 Multiplex PCR and Sequence Analysis to Investigate Genetic Diversity of Fasciola Isolates from Cattle and Sheep in Turkey Uzun, Veysel Celik, Figen Simsek, Sami Kesik, Harun Kaya Kilinc, Seyma Gunyakti Zhang, Xiaocheng Ahmed, Haroon Cao, Jianping Pathogens Article Fasciolosis is a highly prevalent helminthic infection caused by Fasciola hepatica and F. gigantica. With the aim of identifying hybrid Fasciola flukes, multiplex PCR was performed to amplify the pepck gene. Furthermore, to determine Fasciola haplotypes, mitochondrial nad1 gene was amplified and sequenced, and phylogenetic analyses were performed. Adult Fasciola isolates were collected from 51 cattle and 51 sheep, genomic DNA was isolated, and one-step multiplex PCR was subsequently performed to amplify pepck. Isolates that generated a 510 bp band were identified as F. gigantica, those that generated a 241 bp band were identified as F. hepatica, and those that generated both bands were identified as hybrid (aspermic) flukes. Multiplex PCR data identified four isolates as F. gigantica and 84 as F. hepatica. Fourteen hybrid isolates (five cattle and nine sheep) were identified. On unidirectional DNA sequence analysis of nad1 PCR products, three sequences were identified as F. gigantica and 99 as F. hepatica. In addition, only 4 of 87 haplotypes detected for F. hepatica nad1 sequences were found to be previously reported, while the remaining 83 are unique to this study. To summarize, this study is the first to report the existence of hybrid Fasciola flukes and 83 unique haplotypes of F. hepatica in Turkey. MDPI 2022-10-26 /pmc/articles/PMC9692402/ /pubmed/36364987 http://dx.doi.org/10.3390/pathogens11111235 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Uzun, Veysel
Celik, Figen
Simsek, Sami
Kesik, Harun Kaya
Kilinc, Seyma Gunyakti
Zhang, Xiaocheng
Ahmed, Haroon
Cao, Jianping
Multiplex PCR and Sequence Analysis to Investigate Genetic Diversity of Fasciola Isolates from Cattle and Sheep in Turkey
title Multiplex PCR and Sequence Analysis to Investigate Genetic Diversity of Fasciola Isolates from Cattle and Sheep in Turkey
title_full Multiplex PCR and Sequence Analysis to Investigate Genetic Diversity of Fasciola Isolates from Cattle and Sheep in Turkey
title_fullStr Multiplex PCR and Sequence Analysis to Investigate Genetic Diversity of Fasciola Isolates from Cattle and Sheep in Turkey
title_full_unstemmed Multiplex PCR and Sequence Analysis to Investigate Genetic Diversity of Fasciola Isolates from Cattle and Sheep in Turkey
title_short Multiplex PCR and Sequence Analysis to Investigate Genetic Diversity of Fasciola Isolates from Cattle and Sheep in Turkey
title_sort multiplex pcr and sequence analysis to investigate genetic diversity of fasciola isolates from cattle and sheep in turkey
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692402/
https://www.ncbi.nlm.nih.gov/pubmed/36364987
http://dx.doi.org/10.3390/pathogens11111235
work_keys_str_mv AT uzunveysel multiplexpcrandsequenceanalysistoinvestigategeneticdiversityoffasciolaisolatesfromcattleandsheepinturkey
AT celikfigen multiplexpcrandsequenceanalysistoinvestigategeneticdiversityoffasciolaisolatesfromcattleandsheepinturkey
AT simseksami multiplexpcrandsequenceanalysistoinvestigategeneticdiversityoffasciolaisolatesfromcattleandsheepinturkey
AT kesikharunkaya multiplexpcrandsequenceanalysistoinvestigategeneticdiversityoffasciolaisolatesfromcattleandsheepinturkey
AT kilincseymagunyakti multiplexpcrandsequenceanalysistoinvestigategeneticdiversityoffasciolaisolatesfromcattleandsheepinturkey
AT zhangxiaocheng multiplexpcrandsequenceanalysistoinvestigategeneticdiversityoffasciolaisolatesfromcattleandsheepinturkey
AT ahmedharoon multiplexpcrandsequenceanalysistoinvestigategeneticdiversityoffasciolaisolatesfromcattleandsheepinturkey
AT caojianping multiplexpcrandsequenceanalysistoinvestigategeneticdiversityoffasciolaisolatesfromcattleandsheepinturkey