Rapid Detection of Equine Piroplasms Using Multiplex PCR and First Genetic Characterization of <i>Theileria haneyi</i> in Egypt
Equine Piroplasmosis (EP) is an infectious disease caused by the hemoprotozoan parasites <i>Theileria equi</i>, <i>Babesia caballi</i>, and the recently identified species <i>T. haneyi</i>. Hereby, we used a multiplex PCR (mPCR) targeting the 18S rRNA gene of <...
Guardado en:
Autores principales: | , , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
MDPI AG
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/7f2096120bc4460ea58148e2efe9ecb0 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:7f2096120bc4460ea58148e2efe9ecb0 |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:7f2096120bc4460ea58148e2efe9ecb02021-11-25T18:38:05ZRapid Detection of Equine Piroplasms Using Multiplex PCR and First Genetic Characterization of <i>Theileria haneyi</i> in Egypt10.3390/pathogens101114142076-0817https://doaj.org/article/7f2096120bc4460ea58148e2efe9ecb02021-10-01T00:00:00Zhttps://www.mdpi.com/2076-0817/10/11/1414https://doaj.org/toc/2076-0817Equine Piroplasmosis (EP) is an infectious disease caused by the hemoprotozoan parasites <i>Theileria equi</i>, <i>Babesia caballi</i>, and the recently identified species <i>T. haneyi</i>. Hereby, we used a multiplex PCR (mPCR) targeting the 18S rRNA gene of <i>T. equi</i> and <i>B. caballi</i> for the simultaneous detection of EP in Egyptian equids and examined the presence of <i>T. haneyi</i> infections in Egypt. Blood samples from 155 equids (79 horses and 76 donkeys) collected from different governorates of Egypt were examined by mPCR and PCR targeting <i>T. hayeni</i>. The mPCR method revealed a prevalence of <i>T. equi</i> of 20.3% in horses and of 13.1% in donkeys and a prevalence of <i>B</i>. <i>caballi</i> of 1.2% in horses. <i>B</i>. <i>caballi</i> was not detected in donkeys in the current study. The mPCR method also detected coinfections with both species (2.5% and 1.3% in horses and donkeys, respectively). Additionally, we report the presence of <i>T. haneyi</i> in Egypt for the first time in 53.1% of the horse and 38.1% of the donkey tested samples. Coinfection with <i>T. haneyi</i> and <i>T. equi</i> was found in 13.5% of the samples, while infection with the three EP species was found in 1.9% of the samples.Bassma S. M. ElsawyAhmed M. NassarHeba F. AlzanRaksha V. BhooraSezayi OzubekMona S. MahmoudOmnia M. KandilOlfat A. MahdyMDPI AGarticleequids<i>Babesia caballi</i><i>Theileria equi</i><i>Theileria haneyi</i>multiplex PCRcPCRMedicineRENPathogens, Vol 10, Iss 1414, p 1414 (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
equids <i>Babesia caballi</i> <i>Theileria equi</i> <i>Theileria haneyi</i> multiplex PCR cPCR Medicine R |
spellingShingle |
equids <i>Babesia caballi</i> <i>Theileria equi</i> <i>Theileria haneyi</i> multiplex PCR cPCR Medicine R Bassma S. M. Elsawy Ahmed M. Nassar Heba F. Alzan Raksha V. Bhoora Sezayi Ozubek Mona S. Mahmoud Omnia M. Kandil Olfat A. Mahdy Rapid Detection of Equine Piroplasms Using Multiplex PCR and First Genetic Characterization of <i>Theileria haneyi</i> in Egypt |
description |
Equine Piroplasmosis (EP) is an infectious disease caused by the hemoprotozoan parasites <i>Theileria equi</i>, <i>Babesia caballi</i>, and the recently identified species <i>T. haneyi</i>. Hereby, we used a multiplex PCR (mPCR) targeting the 18S rRNA gene of <i>T. equi</i> and <i>B. caballi</i> for the simultaneous detection of EP in Egyptian equids and examined the presence of <i>T. haneyi</i> infections in Egypt. Blood samples from 155 equids (79 horses and 76 donkeys) collected from different governorates of Egypt were examined by mPCR and PCR targeting <i>T. hayeni</i>. The mPCR method revealed a prevalence of <i>T. equi</i> of 20.3% in horses and of 13.1% in donkeys and a prevalence of <i>B</i>. <i>caballi</i> of 1.2% in horses. <i>B</i>. <i>caballi</i> was not detected in donkeys in the current study. The mPCR method also detected coinfections with both species (2.5% and 1.3% in horses and donkeys, respectively). Additionally, we report the presence of <i>T. haneyi</i> in Egypt for the first time in 53.1% of the horse and 38.1% of the donkey tested samples. Coinfection with <i>T. haneyi</i> and <i>T. equi</i> was found in 13.5% of the samples, while infection with the three EP species was found in 1.9% of the samples. |
format |
article |
author |
Bassma S. M. Elsawy Ahmed M. Nassar Heba F. Alzan Raksha V. Bhoora Sezayi Ozubek Mona S. Mahmoud Omnia M. Kandil Olfat A. Mahdy |
author_facet |
Bassma S. M. Elsawy Ahmed M. Nassar Heba F. Alzan Raksha V. Bhoora Sezayi Ozubek Mona S. Mahmoud Omnia M. Kandil Olfat A. Mahdy |
author_sort |
Bassma S. M. Elsawy |
title |
Rapid Detection of Equine Piroplasms Using Multiplex PCR and First Genetic Characterization of <i>Theileria haneyi</i> in Egypt |
title_short |
Rapid Detection of Equine Piroplasms Using Multiplex PCR and First Genetic Characterization of <i>Theileria haneyi</i> in Egypt |
title_full |
Rapid Detection of Equine Piroplasms Using Multiplex PCR and First Genetic Characterization of <i>Theileria haneyi</i> in Egypt |
title_fullStr |
Rapid Detection of Equine Piroplasms Using Multiplex PCR and First Genetic Characterization of <i>Theileria haneyi</i> in Egypt |
title_full_unstemmed |
Rapid Detection of Equine Piroplasms Using Multiplex PCR and First Genetic Characterization of <i>Theileria haneyi</i> in Egypt |
title_sort |
rapid detection of equine piroplasms using multiplex pcr and first genetic characterization of <i>theileria haneyi</i> in egypt |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/7f2096120bc4460ea58148e2efe9ecb0 |
work_keys_str_mv |
AT bassmasmelsawy rapiddetectionofequinepiroplasmsusingmultiplexpcrandfirstgeneticcharacterizationofitheileriahaneyiiinegypt AT ahmedmnassar rapiddetectionofequinepiroplasmsusingmultiplexpcrandfirstgeneticcharacterizationofitheileriahaneyiiinegypt AT hebafalzan rapiddetectionofequinepiroplasmsusingmultiplexpcrandfirstgeneticcharacterizationofitheileriahaneyiiinegypt AT rakshavbhoora rapiddetectionofequinepiroplasmsusingmultiplexpcrandfirstgeneticcharacterizationofitheileriahaneyiiinegypt AT sezayiozubek rapiddetectionofequinepiroplasmsusingmultiplexpcrandfirstgeneticcharacterizationofitheileriahaneyiiinegypt AT monasmahmoud rapiddetectionofequinepiroplasmsusingmultiplexpcrandfirstgeneticcharacterizationofitheileriahaneyiiinegypt AT omniamkandil rapiddetectionofequinepiroplasmsusingmultiplexpcrandfirstgeneticcharacterizationofitheileriahaneyiiinegypt AT olfatamahdy rapiddetectionofequinepiroplasmsusingmultiplexpcrandfirstgeneticcharacterizationofitheileriahaneyiiinegypt |
_version_ |
1718410900288831488 |