Genotyping and phylogenetic analysis of canine parvovirus circulating in Egypt
Aim: This study aimed to detect and characterize current genotypes of canine parvovirus (CPV) in Egypt during 2018. Materials and Methods: A total of 50 fecal swabs were collected from clinically infected domestic dogs of 2-5 months of age, suspected to suffer from CPV infection, from Cairo and G...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Veterinary World
2020-02-01
|
Series: | Veterinary World |
Subjects: | |
Online Access: | http://www.veterinaryworld.org/Vol.13/February-2020/14.pdf |
id |
doaj-a47c8d73070b410394b348d7d1295ddf |
---|---|
record_format |
Article |
spelling |
doaj-a47c8d73070b410394b348d7d1295ddf2021-08-02T14:37:16ZengVeterinary WorldVeterinary World0972-89882231-09162020-02-0113232633310.14202/vetworld.2020.326-333Genotyping and phylogenetic analysis of canine parvovirus circulating in EgyptKawther Sayed Zaher0Wahid Hussein El-Dabae1Mostafa Mohamed El-Sebelgy2Naglaa Ibrahim Aly3Zeinab Taha Salama4Department of Microbiology and Immunology, Veterinary Research Division, National Research Centre, Dokki 12622, Giza, Egypt.Department of Microbiology and Immunology, Veterinary Research Division, National Research Centre, Dokki 12622, Giza, Egypt.Department of Microbiology and Immunology, Veterinary Research Division, National Research Centre, Dokki 12622, Giza, Egypt.Department of Pet Animal Vaccine Research, Veterinary Serum and Vaccine Research Institute, Abbasia, Egypt.Department of Pet Animal Vaccine Research, Veterinary Serum and Vaccine Research Institute, Abbasia, Egypt.Aim: This study aimed to detect and characterize current genotypes of canine parvovirus (CPV) in Egypt during 2018. Materials and Methods: A total of 50 fecal swabs were collected from clinically infected domestic dogs of 2-5 months of age, suspected to suffer from CPV infection, from Cairo and Giza Governorates. The samples were subjected to qualitative antigen detection using the rapid test, followed by isolation on Madin-Darby Canine Kidney (MDCK) cells, molecular characterization with partial amplification of VP2 gene using polymerase chain reaction (PCR), followed by sequencing and phylogenetic analysis. Results: Out of 50 fecal samples, 20 samples were positive (40%) by Rapid CPV/canine coronavirus Ag Test Kit. These positive samples were cultured successfully on MDCK cells. Nine randomly chosen samples out of 30 apparently negative samples were amplified using PCR with primers Hfor and Hrev to yield a typical 630 bp fragment. Then, six randomly chosen samples out of nine were amplified using PCR with primers Pbs and Pbas to yield a typical 427 bp fragment. Sequencing, BLAST analysis and assembly of the two fragments (630 bp and 427 bp) to produce 912 bp fragments, in the six samples, revealed two serotypes CPV-2b and CPV-2c. The obtained strains were submitted to GenBank and given accession numbers MK642272, MK642273, MK642274, MK642275, MK642276, and MK642277. Phylogenetic analysis of the Egyptian strains serotype 2b illustrated that they were closely related to Thailand strains (accession numbers KP715709, KP715694, KP715701, and KP715700); while Egyptian strains serotype 2c was closely related to Thailand strains (accession numbers MH711894 and MH711902), Taiwanese strain (KU244254), Chinese strain (MF467242), and Vietnamese strain (accession number LC216910). Conclusion: The current research recommends further epidemiological studies to assess the extent of the occurrence of different serotypes of CPV in Egypt and the efficiency of imported and locally produced vaccines in protection against CPV infection.http://www.veterinaryworld.org/Vol.13/February-2020/14.pdfcanine parvovirusegyptgenotypingphylogenetic analysisserotyping |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kawther Sayed Zaher Wahid Hussein El-Dabae Mostafa Mohamed El-Sebelgy Naglaa Ibrahim Aly Zeinab Taha Salama |
spellingShingle |
Kawther Sayed Zaher Wahid Hussein El-Dabae Mostafa Mohamed El-Sebelgy Naglaa Ibrahim Aly Zeinab Taha Salama Genotyping and phylogenetic analysis of canine parvovirus circulating in Egypt Veterinary World canine parvovirus egypt genotyping phylogenetic analysis serotyping |
author_facet |
Kawther Sayed Zaher Wahid Hussein El-Dabae Mostafa Mohamed El-Sebelgy Naglaa Ibrahim Aly Zeinab Taha Salama |
author_sort |
Kawther Sayed Zaher |
title |
Genotyping and phylogenetic analysis of canine parvovirus circulating in Egypt |
title_short |
Genotyping and phylogenetic analysis of canine parvovirus circulating in Egypt |
title_full |
Genotyping and phylogenetic analysis of canine parvovirus circulating in Egypt |
title_fullStr |
Genotyping and phylogenetic analysis of canine parvovirus circulating in Egypt |
title_full_unstemmed |
Genotyping and phylogenetic analysis of canine parvovirus circulating in Egypt |
title_sort |
genotyping and phylogenetic analysis of canine parvovirus circulating in egypt |
publisher |
Veterinary World |
series |
Veterinary World |
issn |
0972-8988 2231-0916 |
publishDate |
2020-02-01 |
description |
Aim: This study aimed to detect and characterize current genotypes of canine parvovirus (CPV) in Egypt during 2018.
Materials and Methods: A total of 50 fecal swabs were collected from clinically infected domestic dogs of 2-5 months of age, suspected to suffer from CPV infection, from Cairo and Giza Governorates. The samples were subjected to qualitative antigen detection using the rapid test, followed by isolation on Madin-Darby Canine Kidney (MDCK) cells, molecular characterization with partial amplification of VP2 gene using polymerase chain reaction (PCR), followed by sequencing and phylogenetic analysis.
Results: Out of 50 fecal samples, 20 samples were positive (40%) by Rapid CPV/canine coronavirus Ag Test Kit. These positive samples were cultured successfully on MDCK cells. Nine randomly chosen samples out of 30 apparently negative samples were amplified using PCR with primers Hfor and Hrev to yield a typical 630 bp fragment. Then, six randomly chosen samples out of nine were amplified using PCR with primers Pbs and Pbas to yield a typical 427 bp fragment. Sequencing, BLAST analysis and assembly of the two fragments (630 bp and 427 bp) to produce 912 bp fragments, in the six samples, revealed two serotypes CPV-2b and CPV-2c. The obtained strains were submitted to GenBank and given accession numbers MK642272, MK642273, MK642274, MK642275, MK642276, and MK642277. Phylogenetic analysis of the Egyptian strains serotype 2b illustrated that they were closely related to Thailand strains (accession numbers KP715709, KP715694, KP715701, and KP715700); while Egyptian strains serotype 2c was closely related to Thailand strains (accession numbers MH711894 and MH711902), Taiwanese strain (KU244254), Chinese strain (MF467242), and Vietnamese strain (accession number LC216910).
Conclusion: The current research recommends further epidemiological studies to assess the extent of the occurrence of different serotypes of CPV in Egypt and the efficiency of imported and locally produced vaccines in protection against CPV infection. |
topic |
canine parvovirus egypt genotyping phylogenetic analysis serotyping |
url |
http://www.veterinaryworld.org/Vol.13/February-2020/14.pdf |
work_keys_str_mv |
AT kawthersayedzaher genotypingandphylogeneticanalysisofcanineparvoviruscirculatinginegypt AT wahidhusseineldabae genotypingandphylogeneticanalysisofcanineparvoviruscirculatinginegypt AT mostafamohamedelsebelgy genotypingandphylogeneticanalysisofcanineparvoviruscirculatinginegypt AT naglaaibrahimaly genotypingandphylogeneticanalysisofcanineparvoviruscirculatinginegypt AT zeinabtahasalama genotypingandphylogeneticanalysisofcanineparvoviruscirculatinginegypt |
_version_ |
1721231157356396544 |