Molecular Characterization of Lineage-IV Peste Des Petits Ruminants Virus and the Development of In-House Indirect Enzyme-Linked Immunosorbent Assay (IELISA) for its Rapid Detection”

Abstract Peste des petits ruminants (PPRV), a highly contagious viral disease, causes significant economic losses concerning sheep and goats. Recently, PPR viruses (PPRVs), have adopted new hosts and lineage IV of PPRVs represents genetic diversity within the same lineage. 350 samples, including blo...

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التفاصيل البيبلوغرافية
الحاوية / القاعدة:Biological Procedures Online
المؤلفون الرئيسيون: Tahira Kamal, Saeed-ul-Hassan Khan, Fariha Hassan, Amir-bin- Zahoor, Amman Ullah, S. Murtaza Hassan Andrabi, Ghulam Muhammad Ali, Tayyaba Afsar, Fohad Mabood Husain, Huma Shafique, Suhail Razak
التنسيق: مقال
اللغة:الإنجليزية
منشور في: BMC 2024-07-01
الموضوعات:
الوصول للمادة أونلاين:https://doi.org/10.1186/s12575-024-00249-y
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author Tahira Kamal
Saeed-ul-Hassan Khan
Fariha Hassan
Amir-bin- Zahoor
Amman Ullah
S. Murtaza Hassan Andrabi
Ghulam Muhammad Ali
Tayyaba Afsar
Fohad Mabood Husain
Huma Shafique
Suhail Razak
author_facet Tahira Kamal
Saeed-ul-Hassan Khan
Fariha Hassan
Amir-bin- Zahoor
Amman Ullah
S. Murtaza Hassan Andrabi
Ghulam Muhammad Ali
Tayyaba Afsar
Fohad Mabood Husain
Huma Shafique
Suhail Razak
author_sort Tahira Kamal
collection DOAJ
container_title Biological Procedures Online
description Abstract Peste des petits ruminants (PPRV), a highly contagious viral disease, causes significant economic losses concerning sheep and goats. Recently, PPR viruses (PPRVs), have adopted new hosts and lineage IV of PPRVs represents genetic diversity within the same lineage. 350 samples, including blood, swabs, and tissues from sheep/goats, were collected during the 2020–2021 disease outbreaks in Pakistan. These samples were analysed through RT-PCR and three isolates of PPRV with accession numbers, MW600920, MW600921, and MW600922, were submitted to GenBank, based on the partial N-gene sequencing. This analysis provides a better understanding of genetic characterizations and a targeted RT-PCR approach for rapid PPRV diagnosis. An IELISA test was developed using the semi-purified antigen MW600922 isolate grown in Vero cells. The PPRV isolates currently present high divergence with the Turkish strain; conversely, similarities equivalent to 99.73% were observed for isolates collected from Pakistan. The developed indirect ELISA (IELISA) test demonstrated antibody detection rates at dilutions of 1:200 for antibodies (serum) and 1:32 for antigens. In comparison to cELISA, high specificity (85.23%) and sensitivity (90.60%) rates were observed. In contrast to the virus neutralization test (VNT), IELISA was observed to be 100% specific and 82.14% sensitive in its results. Based on these results, serological surveys conducted for PPR antibodies using IELISA can be a more effective strategy on a larger scale. Furthermore, our results demonstrate a significant breakthrough in the research in terms of cost-effectiveness and storage efficiency, and the developed IELISA test is highly recommended for use in developing countries.
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spelling doaj-art-c4a04ce4b0c14dff92e2ff0ffeca9bf42025-08-20T00:36:30ZengBMCBiological Procedures Online1480-92222024-07-0126111410.1186/s12575-024-00249-yMolecular Characterization of Lineage-IV Peste Des Petits Ruminants Virus and the Development of In-House Indirect Enzyme-Linked Immunosorbent Assay (IELISA) for its Rapid Detection”Tahira Kamal0Saeed-ul-Hassan Khan1Fariha Hassan2Amir-bin- Zahoor3Amman Ullah4S. Murtaza Hassan Andrabi5Ghulam Muhammad Ali6Tayyaba Afsar7Fohad Mabood Husain8Huma Shafique9Suhail Razak10National Institute for Genomics and Advanced Biotechnology, National Agricultural Research CenterDepartment of Zoology, Faculty of Biological Sciences, Quaid-i-Azam UniversityDepartment of Microbiology, Faculty of Biological Sciences, Quaid-i-Azam UniversityAnimal Sciences Institute, Animal Health, National Agricultural Research CenterAnimal Sciences Institute, Animal Health, National Agricultural Research CenterAnimal Sciences Institute, Animal Health, National Agricultural Research CenterNational Institute for Genomics and Advanced Biotechnology, National Agricultural Research CenterDepartment of Community Health Sciences, College of Applied Medical Sciences, King Saud UniversityDepartment of Food Science and Nutrition, College of Food and Agriculture Sciences, King Saud UniversityInstitute of Cellular Medicine, Newcastle University Medical School, Newcastle UniversityDepartment of Community Health Sciences, College of Applied Medical Sciences, King Saud UniversityAbstract Peste des petits ruminants (PPRV), a highly contagious viral disease, causes significant economic losses concerning sheep and goats. Recently, PPR viruses (PPRVs), have adopted new hosts and lineage IV of PPRVs represents genetic diversity within the same lineage. 350 samples, including blood, swabs, and tissues from sheep/goats, were collected during the 2020–2021 disease outbreaks in Pakistan. These samples were analysed through RT-PCR and three isolates of PPRV with accession numbers, MW600920, MW600921, and MW600922, were submitted to GenBank, based on the partial N-gene sequencing. This analysis provides a better understanding of genetic characterizations and a targeted RT-PCR approach for rapid PPRV diagnosis. An IELISA test was developed using the semi-purified antigen MW600922 isolate grown in Vero cells. The PPRV isolates currently present high divergence with the Turkish strain; conversely, similarities equivalent to 99.73% were observed for isolates collected from Pakistan. The developed indirect ELISA (IELISA) test demonstrated antibody detection rates at dilutions of 1:200 for antibodies (serum) and 1:32 for antigens. In comparison to cELISA, high specificity (85.23%) and sensitivity (90.60%) rates were observed. In contrast to the virus neutralization test (VNT), IELISA was observed to be 100% specific and 82.14% sensitive in its results. Based on these results, serological surveys conducted for PPR antibodies using IELISA can be a more effective strategy on a larger scale. Furthermore, our results demonstrate a significant breakthrough in the research in terms of cost-effectiveness and storage efficiency, and the developed IELISA test is highly recommended for use in developing countries.https://doi.org/10.1186/s12575-024-00249-yIELISAPPRVRT-PCRCost-effectiveDiagnostic assays
spellingShingle Tahira Kamal
Saeed-ul-Hassan Khan
Fariha Hassan
Amir-bin- Zahoor
Amman Ullah
S. Murtaza Hassan Andrabi
Ghulam Muhammad Ali
Tayyaba Afsar
Fohad Mabood Husain
Huma Shafique
Suhail Razak
Molecular Characterization of Lineage-IV Peste Des Petits Ruminants Virus and the Development of In-House Indirect Enzyme-Linked Immunosorbent Assay (IELISA) for its Rapid Detection”
IELISA
PPRV
RT-PCR
Cost-effective
Diagnostic assays
title Molecular Characterization of Lineage-IV Peste Des Petits Ruminants Virus and the Development of In-House Indirect Enzyme-Linked Immunosorbent Assay (IELISA) for its Rapid Detection”
title_full Molecular Characterization of Lineage-IV Peste Des Petits Ruminants Virus and the Development of In-House Indirect Enzyme-Linked Immunosorbent Assay (IELISA) for its Rapid Detection”
title_fullStr Molecular Characterization of Lineage-IV Peste Des Petits Ruminants Virus and the Development of In-House Indirect Enzyme-Linked Immunosorbent Assay (IELISA) for its Rapid Detection”
title_full_unstemmed Molecular Characterization of Lineage-IV Peste Des Petits Ruminants Virus and the Development of In-House Indirect Enzyme-Linked Immunosorbent Assay (IELISA) for its Rapid Detection”
title_short Molecular Characterization of Lineage-IV Peste Des Petits Ruminants Virus and the Development of In-House Indirect Enzyme-Linked Immunosorbent Assay (IELISA) for its Rapid Detection”
title_sort molecular characterization of lineage iv peste des petits ruminants virus and the development of in house indirect enzyme linked immunosorbent assay ielisa for its rapid detection
topic IELISA
PPRV
RT-PCR
Cost-effective
Diagnostic assays
url https://doi.org/10.1186/s12575-024-00249-y
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