Attempted experimental reproduction of porcine periweaning-failure-to-thrive syndrome using tissue homogenates.

Porcine periweaning failure-to-thrive syndrome (PFTS) is characterized by anorexia and progressive debilitation of newly weaned pigs, of which some also demonstrate repetitive oral behaviour. Although no relevant porcine pathogens have been shown to be causally associated, inoculation of susceptible...

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Main Authors: Yanyun Huang, John C S Harding
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3940845?pdf=render
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spelling doaj-668e8fe042a44ca98daa6c4309a1261e2020-11-24T21:44:21ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0193e9006510.1371/journal.pone.0090065Attempted experimental reproduction of porcine periweaning-failure-to-thrive syndrome using tissue homogenates.Yanyun HuangJohn C S HardingPorcine periweaning failure-to-thrive syndrome (PFTS) is characterized by anorexia and progressive debilitation of newly weaned pigs, of which some also demonstrate repetitive oral behaviour. Although no relevant porcine pathogens have been shown to be causally associated, inoculation of susceptible pigs using tissue homogenates is needed to rule out infectious etiologies. Eight snatched-farrowed porcine-colostrum-deprived (SF-pCD) pigs were inoculated with tissue homogenates made from PFTS-affected pigs orally, or combined orally, intraperitoneally (i.p.) and intramuscularly (i.m.) at day (D) 14 of age (INOC). On D21, i.p. and i.m. inoculation were repeated. Four sham-inoculated pigs served as control (CTRL). Three INOC pigs developed mixed bacterial septicemia between the first and second inoculation. All other pigs survived until termination on D49. Average daily gain (ADG) and the frequencies of diarrhea did not differ between INOC and CTRL pigs D14 and D29. Additionally, the progressive debilitation characteristic of PFTS was not observed in any pig, and repetitive oral behaviour was observed in both groups. In conclusion, PFTS was not experimentally reproduced by the current experimental approach providing evidence that PFTS may not have an infectious etiology.http://europepmc.org/articles/PMC3940845?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yanyun Huang
John C S Harding
spellingShingle Yanyun Huang
John C S Harding
Attempted experimental reproduction of porcine periweaning-failure-to-thrive syndrome using tissue homogenates.
PLoS ONE
author_facet Yanyun Huang
John C S Harding
author_sort Yanyun Huang
title Attempted experimental reproduction of porcine periweaning-failure-to-thrive syndrome using tissue homogenates.
title_short Attempted experimental reproduction of porcine periweaning-failure-to-thrive syndrome using tissue homogenates.
title_full Attempted experimental reproduction of porcine periweaning-failure-to-thrive syndrome using tissue homogenates.
title_fullStr Attempted experimental reproduction of porcine periweaning-failure-to-thrive syndrome using tissue homogenates.
title_full_unstemmed Attempted experimental reproduction of porcine periweaning-failure-to-thrive syndrome using tissue homogenates.
title_sort attempted experimental reproduction of porcine periweaning-failure-to-thrive syndrome using tissue homogenates.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Porcine periweaning failure-to-thrive syndrome (PFTS) is characterized by anorexia and progressive debilitation of newly weaned pigs, of which some also demonstrate repetitive oral behaviour. Although no relevant porcine pathogens have been shown to be causally associated, inoculation of susceptible pigs using tissue homogenates is needed to rule out infectious etiologies. Eight snatched-farrowed porcine-colostrum-deprived (SF-pCD) pigs were inoculated with tissue homogenates made from PFTS-affected pigs orally, or combined orally, intraperitoneally (i.p.) and intramuscularly (i.m.) at day (D) 14 of age (INOC). On D21, i.p. and i.m. inoculation were repeated. Four sham-inoculated pigs served as control (CTRL). Three INOC pigs developed mixed bacterial septicemia between the first and second inoculation. All other pigs survived until termination on D49. Average daily gain (ADG) and the frequencies of diarrhea did not differ between INOC and CTRL pigs D14 and D29. Additionally, the progressive debilitation characteristic of PFTS was not observed in any pig, and repetitive oral behaviour was observed in both groups. In conclusion, PFTS was not experimentally reproduced by the current experimental approach providing evidence that PFTS may not have an infectious etiology.
url http://europepmc.org/articles/PMC3940845?pdf=render
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