It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
In 1998 an outbreak of fatal encephalitis among pig farm workers in Malaysia and Singapore led to the discovery of Nipah henipavirus (NiV), a novel paramyxovirus closely related to Hendra henipavirus with case fatality rates of nearly 40%. Following its initial emergence nearly annual outbreaks of NiV have occurred in Bangladesh with a different, NiV Bangladesh, genotype, where the role of pigs in its transmission remains unknown. The present study provides the first report on susceptibility of domestic pigs to NiV Bangladesh following experimental infection, characterizing acute and long-term phases of disease and pathogenesis. All pigs were successfully infected with NiV Bangladesh following oronasal inoculation, with viral shedding confirmed by a novel genotype-specific qRT-PCR in oral, nasal and rectal excretions and dissemination from the upper respiratory tract to the brain, lungs, and associated lymphatic tissues. Unlike previous NiV Malaysia findings in pigs, clinical signs were absent, viremia was undetectable throughout the study, and only low level neutralizing antibody titers were measured by 28/29 days post-NiV-B infection. Results obtained highlight the need for continued and enhanced NiV surveillance in pigs in endemic and at-risk regions, and raise questions regarding applicability of current serological assays to detect animals with previous NiV-B exposure.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
1 Canadian Food Inspection Agency, National Centre for Foreign Animal Disease, Winnipeg, Canada (GRID:grid.418040.9) (ISNI:0000 0001 2177 1232); Public Health Agency of Canada, National Microbiology Laboratory, Winnipeg, Canada (GRID:grid.415368.d) (ISNI:0000 0001 0805 4386)
2 Public Health Agency of Canada, National Microbiology Laboratory, Winnipeg, Canada (GRID:grid.415368.d) (ISNI:0000 0001 0805 4386)
3 Canadian Food Inspection Agency, National Centre for Foreign Animal Disease, Winnipeg, Canada (GRID:grid.418040.9) (ISNI:0000 0001 2177 1232); University of Manitoba, Department of Medical Microbiology, Winnipeg, Canada (GRID:grid.21613.37) (ISNI:0000 0004 1936 9609)
4 Canadian Food Inspection Agency, National Centre for Foreign Animal Disease, Winnipeg, Canada (GRID:grid.418040.9) (ISNI:0000 0001 2177 1232)
5 Public Health Agency of Canada, National Microbiology Laboratory, Winnipeg, Canada (GRID:grid.415368.d) (ISNI:0000 0001 0805 4386); University of Manitoba, Department of Medical Microbiology, Winnipeg, Canada (GRID:grid.21613.37) (ISNI:0000 0004 1936 9609)