scholarly journals Histopathological and RT-PCR Detection of Mycobacterium paratuberculosis in Tissues of Clinically Suspected Small Ruminants

Author(s):  
Mohamed AI. Hamid ◽  
Galal Eldin E. Mohammed ◽  
Amel O. Bakhiet ◽  
Elhassan M. A. Saeed
2021 ◽  
pp. 114286
Author(s):  
Xiaoqin Li ◽  
Yu Li ◽  
Wenli Hu ◽  
Yingjuan Li ◽  
Yan Li ◽  
...  
Keyword(s):  

2011 ◽  
Vol 175 (2) ◽  
pp. 236-245 ◽  
Author(s):  
Oliver Lung ◽  
Mathew Fisher ◽  
Anne Beeston ◽  
Kimberley Burton Hughes ◽  
Alfonso Clavijo ◽  
...  

2011 ◽  
Vol 27 (3) ◽  
pp. 291-296 ◽  
Author(s):  
Jong-Seung Lee ◽  
Won-Kyong Cho ◽  
Hong-Soo Choi ◽  
Kook-Hyung Kim
Keyword(s):  

Author(s):  
Ying Zhang ◽  
Xue Cai ◽  
Weigang Ge ◽  
Donglian Wang ◽  
Guangjun Zhu ◽  
...  

2021 ◽  
Vol 77 (05) ◽  
pp. 226-231
Author(s):  
WIESŁAW NIEDBALSKI ◽  
ANDRZEJ FITZNER ◽  
KRZYSZTOF BULENGER ◽  
ANDRZEJ KĘSY

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 However, these conventional methods have been superseded by more rapid, sensitive and accurate molecular diagnostic techniques based on the amplification of parts of either nucleocapsid (N) or fusion (F) protein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


BioTechniques ◽  
1997 ◽  
Vol 23 (4) ◽  
pp. 616-618 ◽  
Author(s):  
Michael A. Drebot ◽  
Spencer H.S. Lee

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