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Exposure to maternal feces in lactation influences piglet enteric microbiota, growth, and survival preweaning

It is known that gilt progeny performance is reduced compared with sow progeny. Previous research suggests that the presence of maternal feces in early life improves the health and survival of offspring. Therefore, we aimed to determine whether contact with feces from multiparous (MP) sows would imp...

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Autores principales: Nowland, Tanya L, Kirkwood, Roy N, Plush, Kate J, Barton, Mary D, Torok, Valeria A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259832/
https://www.ncbi.nlm.nih.gov/pubmed/34036347
http://dx.doi.org/10.1093/jas/skab170
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author Nowland, Tanya L
Kirkwood, Roy N
Plush, Kate J
Barton, Mary D
Torok, Valeria A
author_facet Nowland, Tanya L
Kirkwood, Roy N
Plush, Kate J
Barton, Mary D
Torok, Valeria A
author_sort Nowland, Tanya L
collection PubMed
description It is known that gilt progeny performance is reduced compared with sow progeny. Previous research suggests that the presence of maternal feces in early life improves the health and survival of offspring. Therefore, we aimed to determine whether contact with feces from multiparous (MP) sows would improve the growth and survival of piglets born and reared on primiparous (P1) sows and if so, whether these differences are associated with the gut microbiota. Four treatments were applied for 10 days: Donor (n = 29) piglets had limited access to maternal feces as, each morning, sow feces were removed and placed in the crate of a P1 sow (P1-FT; n = 30 piglets) and P1-Con (n = 29) and MP-Con (n = 33) piglets had access to their own mothers’ feces. All piglets were weighed on days 1, 3, 10, and 18. Fecal samples were collected from a subset of sows (n = 10/treatment) 3 days post farrow and from two female piglets/litter on days 10 and 18 (n = 20/treatment) and subject to 16S rRNA amplicon analysis. Escherichia, Clostridium, Campylobacter, and Treponema were more abundant in MP sows, while P1 sows had a higher abundance of Lactobacillus and Prevotella. At 10 days, P1 progeny fecal microbiota differed, and growth and survival were reduced when compared with MP progeny. No treatment effect was observed for P1-FT piglets (P > 0.05). Donor piglets had a different fecal microbiota and improved weight and survival then all other treatments (P < 0.05). Overall, the removal of sow feces from the farrowing crate improved piglet microbiota development, growth, and survival.
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spelling pubmed-82598322021-07-07 Exposure to maternal feces in lactation influences piglet enteric microbiota, growth, and survival preweaning Nowland, Tanya L Kirkwood, Roy N Plush, Kate J Barton, Mary D Torok, Valeria A J Anim Sci Microbiology and Microbiome It is known that gilt progeny performance is reduced compared with sow progeny. Previous research suggests that the presence of maternal feces in early life improves the health and survival of offspring. Therefore, we aimed to determine whether contact with feces from multiparous (MP) sows would improve the growth and survival of piglets born and reared on primiparous (P1) sows and if so, whether these differences are associated with the gut microbiota. Four treatments were applied for 10 days: Donor (n = 29) piglets had limited access to maternal feces as, each morning, sow feces were removed and placed in the crate of a P1 sow (P1-FT; n = 30 piglets) and P1-Con (n = 29) and MP-Con (n = 33) piglets had access to their own mothers’ feces. All piglets were weighed on days 1, 3, 10, and 18. Fecal samples were collected from a subset of sows (n = 10/treatment) 3 days post farrow and from two female piglets/litter on days 10 and 18 (n = 20/treatment) and subject to 16S rRNA amplicon analysis. Escherichia, Clostridium, Campylobacter, and Treponema were more abundant in MP sows, while P1 sows had a higher abundance of Lactobacillus and Prevotella. At 10 days, P1 progeny fecal microbiota differed, and growth and survival were reduced when compared with MP progeny. No treatment effect was observed for P1-FT piglets (P > 0.05). Donor piglets had a different fecal microbiota and improved weight and survival then all other treatments (P < 0.05). Overall, the removal of sow feces from the farrowing crate improved piglet microbiota development, growth, and survival. Oxford University Press 2021-05-24 /pmc/articles/PMC8259832/ /pubmed/34036347 http://dx.doi.org/10.1093/jas/skab170 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the American Society of Animal Science. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Microbiology and Microbiome
Nowland, Tanya L
Kirkwood, Roy N
Plush, Kate J
Barton, Mary D
Torok, Valeria A
Exposure to maternal feces in lactation influences piglet enteric microbiota, growth, and survival preweaning
title Exposure to maternal feces in lactation influences piglet enteric microbiota, growth, and survival preweaning
title_full Exposure to maternal feces in lactation influences piglet enteric microbiota, growth, and survival preweaning
title_fullStr Exposure to maternal feces in lactation influences piglet enteric microbiota, growth, and survival preweaning
title_full_unstemmed Exposure to maternal feces in lactation influences piglet enteric microbiota, growth, and survival preweaning
title_short Exposure to maternal feces in lactation influences piglet enteric microbiota, growth, and survival preweaning
title_sort exposure to maternal feces in lactation influences piglet enteric microbiota, growth, and survival preweaning
topic Microbiology and Microbiome
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259832/
https://www.ncbi.nlm.nih.gov/pubmed/34036347
http://dx.doi.org/10.1093/jas/skab170
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