Recent advances in the laboratory diagnosis of peste des petits ruminants

被引:0
作者
Niedbalski, Wieslaw [1 ]
Fitzner, Andrzej [1 ]
Bulenger, Krzysztof [1 ]
Kesy, Andrzej [1 ]
机构
[1] Natl Vet Res Inst, Dept Foot & Mouth Dis, Wodna 7, PL-98220 Zdunska Wola, Poland
来源
MEDYCYNA WETERYNARYJNA-VETERINARY MEDICINE-SCIENCE AND PRACTICE | 2021年 / 77卷 / 05期
关键词
peste des petits ruminants; laboratory diagnostics; molecular techniques; immunochromatographic tests; RT-PCR ASSAY; RAPID DETECTION; COMPETITIVE-ELISA; CLINICAL-SAMPLES; VIRUS-ANTIGEN; RINDERPEST; ANTIBODIES; DIFFERENTIATION; SYSTEM; GOATS;
D O I
10.21521/mw.6536
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Peste des petits ruminants (PPR) is a highly contagious and economically important, viral disease of small ruminants caused by the peste des petits ruminants virus (PPRV), which belongs to the genus Morbilivirus in the family Paramyxoviridae. PPR control is achieved mostly through vaccination and/or slaughter of susceptible animals coupled with clinical or laboratory-based diagnosis. Since clinical signs of PPR are not disease-specific and clinical diagnostics is not reliable, it should be confirmed by laboratory testing. Laboratory confirmation of clinical suspicions is made by detection of PPRV in blood, swabs or post-mortem tissues through classical virus isolation (VI), agar gel immunodiffusion (AGID)/agar gel precipitation test (AGPT), counter- immunoelectrophoresis ( CIE), immunoperoxidase test (IPT) or enzyme-linked immunosorbent (ELISA) assays. However, these conventional methods have been superseded by more rapid, sensitive and accurate molecular diagnostic techniques based on the amplification of parts of either nucleocapsid (N) or fusion (F) protein gene, such as RT-PCR, real-time RT-PCR, reverse transcription loop-mediated isothermal amplification (RT-LAMP), reverse transcription recombinase polymerase amplification (RT-RPA) and Oxford nanopore MinION technology. Although these molecular diagnostic assays are accurate, rapid and sensitive, they have to be performed in laboratory settings, and samples must be transported under appropriate conditions from the field to the laboratory, which can delay the confirmation of PPRV infection. The recently developed immunochromatographic lateral flow device (IC-LFD) assay can be used in the field ("pen-side") without the need for expensive equipment, so a well-established laboratory is not required. The control and eventual eradication of PPR is now one of the top priorities for the Food and Agriculture Organization (FAO) and the World Organization for Animal Health (OIE). In 2015, the international community agreed on a global strategy for PPR eradication, setting 2030 as a target date for elimination of the disease
引用
收藏
页码:226 / 231
页数:6
相关论文
共 44 条
  • [1] Utilization of protein-A in immuno-histochemical techniques for detection of Peste des Petits Ruminants (PPR) virus antigens in tissues of experimentally infected goats
    Abu Elzein, E. M. E.
    Al-Naeem, A.
    [J]. TROPICAL ANIMAL HEALTH AND PRODUCTION, 2009, 41 (01) : 1 - 4
  • [2] Peste des petits ruminants, the next eradicated animal disease?
    Albina, Emmanuel
    Kwiatek, Olivier
    Minet, Cecile
    Lancelot, Renaud
    de Almeida, Renata Servan
    Libeau, Genevieve
    [J]. VETERINARY MICROBIOLOGY, 2013, 165 (1-2) : 38 - 44
  • [3] Molecular characterization of Peste des petits ruminants viruses in the Marmara Region of Turkey
    Altan, Eda
    Parida, Satya
    Mahapatra, Mana
    Turan, Nuri
    Yilmaz, Huseyin
    [J]. TRANSBOUNDARY AND EMERGING DISEASES, 2019, 66 (02) : 865 - 872
  • [4] Development of one-step real-time RT-PCR assay for detection and quantitation of peste des petits ruminants virus
    Ba, Jingyue
    Li, Lin
    Wang, Zhiliang
    Barrett, Tom
    Suo, Longciren
    Zhao, Wenji
    Liu, Yutian
    Liu, Chunju
    Li, Jinming
    [J]. JOURNAL OF VIROLOGICAL METHODS, 2008, 148 (1-2) : 232 - 236
  • [5] Development of an indirect ELISA for the detection of antibodies against peste-des-petits-ruminants virus in small ruminants
    Balamurugan, V.
    Singh, R. P.
    Saravanan, P.
    Sen, A.
    Sarkar, J.
    Sahay, B.
    Rasool, T. J.
    Singh, R. K.
    [J]. VETERINARY RESEARCH COMMUNICATIONS, 2007, 31 (03) : 355 - 364
  • [6] One-step multiplex RT-PCR assay for the detection of Peste des petits ruminants virus in clinical samples
    Balamurugan, V.
    Sen, A.
    Saravanan, P.
    Singh, R. P.
    Singh, R. K.
    Rasool, T. J.
    Bandyopadhyay, S. K.
    [J]. VETERINARY RESEARCH COMMUNICATIONS, 2006, 30 (06) : 655 - 666
  • [7] Application of Semi-quantitative M Gene-Based Hydrolysis Probe (TaqMan) Real-Time RT-PCR Assay for the Detection of Peste des petitis ruminants Virus in the Clinical Samples for Investigation into Clinical Prevalence of Disease
    Balamurugan, V.
    Sen, A.
    Venkatesan, G.
    Yadav, V.
    Bhanot, V.
    Bhanuprakash, V.
    Singh, R. K.
    [J]. TRANSBOUNDARY AND EMERGING DISEASES, 2010, 57 (06) : 383 - 395
  • [8] Balamurugan Vinayagamurthy, 2012, Virologica Sinica, V27, P1, DOI 10.1007/s12250-012-3219-z
  • [9] Global distribution of peste des petits ruminants virus and prospects for improved diagnosis and control
    Banyard, Ashley C.
    Parida, Satya
    Batten, Carrie
    Oura, Chris
    Kwiatek, Olivier
    Libeau, Genevieve
    [J]. JOURNAL OF GENERAL VIROLOGY, 2010, 91 : 2885 - 2897
  • [10] Development and Testing of a Field Diagnostic Assay for Peste des Petits Ruminants Virus
    Baron, J.
    Fishbourne, E.
    Couacy-Hyman, E.
    Abubakar, M.
    Jones, B. A.
    Frost, L.
    Herbert, R.
    Chibssa, T. R.
    van't Klooster, G.
    Afzal, M.
    Ayebazibwe, C.
    Toye, P.
    Bashiruddin, J.
    Baron, M. D.
    [J]. TRANSBOUNDARY AND EMERGING DISEASES, 2014, 61 (05) : 390 - 396