






Vol.3 , No. 4, Publication Date: Aug. 29, 2017, Page: 37-44
[1] | Md. Tarek Hossain, Department of Pathology, Bangladesh Agricultural University, Mymensingh, Bangladesh. |
[2] | Rahman M. M., Department of Pathology, Bangladesh Agricultural University, Mymensingh, Bangladesh. |
[3] | Begum J. A., Department of Pathology, Bangladesh Agricultural University, Mymensingh, Bangladesh. |
[4] | Haque M. E., Department of Pathology, Bangladesh Agricultural University, Mymensingh, Bangladesh. |
[5] | Habib M. A., Department of Pathology, Bangladesh Agricultural University, Mymensingh, Bangladesh. |
[6] | Islam M. R., Department of Pathology, Bangladesh Agricultural University, Mymensingh, Bangladesh. |
[7] | Emdadul Haque Chowdhury, Department of Pathology, Bangladesh Agricultural University, Mymensingh, Bangladesh. |
Peste des petits ruminants (PPR) is an acute viral disease of goats and sheep. The disease causes a huge loss of small ruminant production per year in Bangladesh. Diagnosis of PPR from suspected field samples is not properly carried out due to unreliable transportation and poor infrastructure. This study was planned to develop and validate a hazard free, time saving and specific sampling technique for the diagnosis of PPRV (Peste des petits ruminants vaccine). Two categories of samples including bronchial lymph node and viral suspensions from nasal swab (from dead and live animals) were collected from 25 goats and from each case corresponding nasal swab smeared filter paper was also taken as sample. All the samples were subjected to RT-PCR with (lymph node and viral suspension from nasal swab) or without (smeared filter paper) RNA extraction using N gene specific primer. Twenty three goats found PPR positive for both categories of samples. One found positive where extracted RNA is used as template but negative to smeared filter paper RNA. On the other hand, one found negative to extracted RNA but positive to filter paper RNA. One goat found negative for both the cases. The result of the study has suggested that sampling through filter paper could be easiest, less time consuming and hazardless for transportation of samples from the field through which diagnosis of PPRV can be done by RT-PCR.
Keywords
Peste Des Petits Ruminants (PPR), Filter Paper, RT-PCR, N Gene, Sequencing
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