2020
DOI: 10.1186/s13028-020-0505-x
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Paradigm shift in the diagnosis of peste des petits ruminants: scoping review

Abstract: Peste des petits ruminants virus causes a highly contagious disease, which poses enormous economic losses in domestic animals and threatens the conservation of wild herbivores. Diagnosis remains a cornerstone to the Peste des petits ruminants Global Control and Eradication Strategy, an initiative of the World Organisation for Animal Health and the Food and Agriculture Organisation. The present review presents the peste des petits ruminants diagnostic landscape, including the practicality of commercially availa… Show more

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Cited by 19 publications
(28 citation statements)
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“…Multiple wildlife and atypical host species can be infected with PPRV, which poses diagnostic challenges in multi-host system testing [ 3 , 15 , 16 ]. Commercially available serological and molecular diagnostic tools to detect PPRV infection were mainly developed for domestic sheep and goats [ 17 , 18 , 19 ]. Thus, accurate diagnosis and standard protocols for interpretation of PPR diagnostic tests in atypical host species need to be established.…”
Section: Introductionmentioning
confidence: 99%
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“…Multiple wildlife and atypical host species can be infected with PPRV, which poses diagnostic challenges in multi-host system testing [ 3 , 15 , 16 ]. Commercially available serological and molecular diagnostic tools to detect PPRV infection were mainly developed for domestic sheep and goats [ 17 , 18 , 19 ]. Thus, accurate diagnosis and standard protocols for interpretation of PPR diagnostic tests in atypical host species need to be established.…”
Section: Introductionmentioning
confidence: 99%
“…The differences between PPRV H cELISA and neutralisation tests in buffalo sera have also been reported, indicating that differential antiviral immune responses among host species may affect the serology and interpretation of results [ 24 ]. The serological tool spectrum for PPR diagnosis (Virus Neutralization Test, immunochromatographic lateral flow devices, blocking ELISA, pseudotype-based neutralization assays, and PPR-Luciferase Immunoprecipitation System) have inherent strengths and weaknesses that require parallel optimization and validation [ 17 , 25 ]. Diagnostic tools to detect active infection, such as antigen ELISA and reverse transcriptase polymerase chain reaction (RT-PCR), are critical to the prompt implementation of control measures [ 26 ].…”
Section: Introductionmentioning
confidence: 99%
“…In order to achieve this goal, effective diagnostic tools play a vital role for the timely diagnosis of the disease. Antigen detection methods such as the agar gel immunodiffusion test (AGID)/AGPT, counterimmunoelectrophoresis (CIE), dot enzyme immunoassays, and differential immunohistochemical staining on tissue sections were initial diagnostic methods, but these techniques are less sensitive and unreliable for use in the routine diagnosis of PPR (13). With the advancement of molecular biology, advanced techniques like virus isolation, RT-PCR and its variants, PCR ELISA, and loop-mediated isothermal amplification (LAMP) have been developed (14)(15)(16)(17).…”
Section: Introductionmentioning
confidence: 99%
“…A number of tests can be deployed in the diagnosis of PPR, which includes virus isolation, serological and molecular techniques [18]. Currently, virus isolation in primary cell cultures is up to 1000 times less effective than in lymphoid cells containing a glycoprotein known as Signaling Lymphocyte Activation Molecule (SLAM).…”
Section: Introductionmentioning
confidence: 99%
“…Currently, virus isolation in primary cell cultures is up to 1000 times less effective than in lymphoid cells containing a glycoprotein known as Signaling Lymphocyte Activation Molecule (SLAM). The later paves the way to the use of new cell line (BST-34) technique which performs even better than the known Vero Cells [19,18]. The serological diagnosis of PPR targets the antibodies to the pathogen or pathogen [20,15] and these include the virus neutralization or immunodiffusion.…”
Section: Introductionmentioning
confidence: 99%