Isolation of peste des petits ruminants virus using primary goat kidney cell culture from kidneys obtained at slaughter
Abstract Background Traditionally isolation of peste des petits ruminant virus (PPRV) is performed in Vero cells that takes several blind passages before observing typical cytopathic effects (CPEs). As an alternate, researchers have been using lamb kidney (LK) cells but day‐old lambs are difficult t...
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doaj-528ad469e9ea4643ac22f7b6aa83f9932021-05-20T18:47:35ZengWileyVeterinary Medicine and Science2053-10952021-05-017391592210.1002/vms3.413Isolation of peste des petits ruminants virus using primary goat kidney cell culture from kidneys obtained at slaughterShahana Begum0Mohammed Nooruzzaman1Azmary Hasnat2Mst. Murshida Parvin3Rokshana Parvin4Mohammad Rafiqul Islam5Emdadul Haque Chowdhury6Department of Pathology Faculty of Veterinary Science Bangladesh Agricultural University Mymensingh BangladeshDepartment of Pathology Faculty of Veterinary Science Bangladesh Agricultural University Mymensingh BangladeshDepartment of Pathology Faculty of Veterinary Science Bangladesh Agricultural University Mymensingh BangladeshDepartment of Pathology Faculty of Veterinary Science Bangladesh Agricultural University Mymensingh BangladeshDepartment of Pathology Faculty of Veterinary Science Bangladesh Agricultural University Mymensingh BangladeshDepartment of Pathology Faculty of Veterinary Science Bangladesh Agricultural University Mymensingh BangladeshDepartment of Pathology Faculty of Veterinary Science Bangladesh Agricultural University Mymensingh BangladeshAbstract Background Traditionally isolation of peste des petits ruminant virus (PPRV) is performed in Vero cells that takes several blind passages before observing typical cytopathic effects (CPEs). As an alternate, researchers have been using lamb kidney (LK) cells but day‐old lambs are difficult to obtain and requires animal sacrifice. Objective We established a primary goat kidney (GK) cell culture from the kidneys obtained at slaughter. Methods The kidney of Black Bengal goats were collected from slaughter house and processed to make single cell suspension. The cells were resuspended in appropriate culture medium and maintained under optimum culture condition. Results The 80% confluent monolayer of GK cells was obtained after 15–20 days post seeding. Upon infection with a field isolate of PPRV, the well‐developed CPEs characterized by cell rounding, vacuolation in the cytoplasm and fusion of cells were observed after 48 hr post infection. Virus quantification in the culture supernatant revealed more viral RNA in GK cells than LK cells. The multicycle growth analysis of PPRV showed a steady increase in the virus loads in the culture supernatant of infected GK cells, suggesting an adaptation of the PPRV in GK cells. Conclusions The findings suggest that primary GK cells can be successfully prepared from the mature kidney cortical tissues and can be used for the isolation of PPRV. This system could reduce the unnecessary sacrifice of lambs or kids. Since kidneys of slaughtered goats are available throughout the year, using this protocol primary cell culture from mature goat kidney can provide primary cells to the laboratory throughout the year.https://doi.org/10.1002/vms3.413Black Bengal goatsgoat kidney cell culturepeste des petits ruminantsvirus isolation |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shahana Begum Mohammed Nooruzzaman Azmary Hasnat Mst. Murshida Parvin Rokshana Parvin Mohammad Rafiqul Islam Emdadul Haque Chowdhury |
spellingShingle |
Shahana Begum Mohammed Nooruzzaman Azmary Hasnat Mst. Murshida Parvin Rokshana Parvin Mohammad Rafiqul Islam Emdadul Haque Chowdhury Isolation of peste des petits ruminants virus using primary goat kidney cell culture from kidneys obtained at slaughter Veterinary Medicine and Science Black Bengal goats goat kidney cell culture peste des petits ruminants virus isolation |
author_facet |
Shahana Begum Mohammed Nooruzzaman Azmary Hasnat Mst. Murshida Parvin Rokshana Parvin Mohammad Rafiqul Islam Emdadul Haque Chowdhury |
author_sort |
Shahana Begum |
title |
Isolation of peste des petits ruminants virus using primary goat kidney cell culture from kidneys obtained at slaughter |
title_short |
Isolation of peste des petits ruminants virus using primary goat kidney cell culture from kidneys obtained at slaughter |
title_full |
Isolation of peste des petits ruminants virus using primary goat kidney cell culture from kidneys obtained at slaughter |
title_fullStr |
Isolation of peste des petits ruminants virus using primary goat kidney cell culture from kidneys obtained at slaughter |
title_full_unstemmed |
Isolation of peste des petits ruminants virus using primary goat kidney cell culture from kidneys obtained at slaughter |
title_sort |
isolation of peste des petits ruminants virus using primary goat kidney cell culture from kidneys obtained at slaughter |
publisher |
Wiley |
series |
Veterinary Medicine and Science |
issn |
2053-1095 |
publishDate |
2021-05-01 |
description |
Abstract Background Traditionally isolation of peste des petits ruminant virus (PPRV) is performed in Vero cells that takes several blind passages before observing typical cytopathic effects (CPEs). As an alternate, researchers have been using lamb kidney (LK) cells but day‐old lambs are difficult to obtain and requires animal sacrifice. Objective We established a primary goat kidney (GK) cell culture from the kidneys obtained at slaughter. Methods The kidney of Black Bengal goats were collected from slaughter house and processed to make single cell suspension. The cells were resuspended in appropriate culture medium and maintained under optimum culture condition. Results The 80% confluent monolayer of GK cells was obtained after 15–20 days post seeding. Upon infection with a field isolate of PPRV, the well‐developed CPEs characterized by cell rounding, vacuolation in the cytoplasm and fusion of cells were observed after 48 hr post infection. Virus quantification in the culture supernatant revealed more viral RNA in GK cells than LK cells. The multicycle growth analysis of PPRV showed a steady increase in the virus loads in the culture supernatant of infected GK cells, suggesting an adaptation of the PPRV in GK cells. Conclusions The findings suggest that primary GK cells can be successfully prepared from the mature kidney cortical tissues and can be used for the isolation of PPRV. This system could reduce the unnecessary sacrifice of lambs or kids. Since kidneys of slaughtered goats are available throughout the year, using this protocol primary cell culture from mature goat kidney can provide primary cells to the laboratory throughout the year. |
topic |
Black Bengal goats goat kidney cell culture peste des petits ruminants virus isolation |
url |
https://doi.org/10.1002/vms3.413 |
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