Delayed access to feed affects broiler small intestinal morphology and goblet cell ontogeny

Broilers are often deprived of feed and water for up to 48 h after hatch. This delayed access to feed (DAF) can inhibit small intestine development. The objective of this study was to determine the effects of DAF on small intestinal morphology, mRNA abundance of the goblet cell marker Muc2 and absor...

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Main Authors: K. Liu, M. Jia, E.A. Wong
Format: Article
Language:English
Published: Elsevier 2020-11-01
Series:Poultry Science
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0032579120305216
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author K. Liu
M. Jia
E.A. Wong
author_facet K. Liu
M. Jia
E.A. Wong
author_sort K. Liu
collection DOAJ
description Broilers are often deprived of feed and water for up to 48 h after hatch. This delayed access to feed (DAF) can inhibit small intestine development. The objective of this study was to determine the effects of DAF on small intestinal morphology, mRNA abundance of the goblet cell marker Muc2 and absorptive cell marker PepT1, and the distribution of goblet cells in young broilers. Cobb 500 chicks, hatching within a 12-h window, were randomly allocated into 3 groups: control with no feed delay (ND), 24-h feed delay (DAF24), and 36-h feed delay (DAF36). Morphology, gene expression, and in situ hybridization analyses were conducted on the duodenum, jejunum, and ileum at 0, 24, 36, 72, 120, and 168 h after hatch. Statistical analysis was performed using a t test for ND and DAF24 at 24 h. A 2-way ANOVA and Tukey's HSD test (P < 0.05) were used for ND, DAF24, and DAF36 from 36 h. At 24 to 36 h, DAF decreased the ratio of villus height/crypt depth (VH/CD) in the duodenum but increased VH/CD in the ileum due to changes in CD, whereas at 72 h, DAF decreased VH/CD due to a decrease in VH. The mRNA abundance of PepT1 was upregulated, while Muc2 mRNA was downregulated in DAF chicks. Cells expressing Muc2 mRNA were present along the villi and in the crypts. The ratio of the number of goblet cells found in the upper half to the lower half of the villus was greater in DAF chicks than in ND chicks, suggesting that DAF affected the appearance of new goblet cells. The number of Muc2 mRNA-expressing cells in the crypt, however, was generally not affected by DAF. In conclusion, DAF transiently affected small intestinal morphology, upregulated PepT1 mRNA, downregulated Muc2 mRNA, and changed the distribution of goblet cells in the villi. By 168 h, however, these parameters were not different between ND, DAF24, and DAF36 chicks.
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spelling doaj.art-1b59c3c493234e5e8a1232bc040b60b22022-12-22T00:57:29ZengElsevierPoultry Science0032-57912020-11-01991152755285Delayed access to feed affects broiler small intestinal morphology and goblet cell ontogenyK. Liu0M. Jia1E.A. Wong2Department of Animal and Poultry Sciences, Virginia Tech, Blacksburg, VA 24061, USADepartment of Animal and Poultry Sciences, Virginia Tech, Blacksburg, VA 24061, USACorresponding author:; Department of Animal and Poultry Sciences, Virginia Tech, Blacksburg, VA 24061, USABroilers are often deprived of feed and water for up to 48 h after hatch. This delayed access to feed (DAF) can inhibit small intestine development. The objective of this study was to determine the effects of DAF on small intestinal morphology, mRNA abundance of the goblet cell marker Muc2 and absorptive cell marker PepT1, and the distribution of goblet cells in young broilers. Cobb 500 chicks, hatching within a 12-h window, were randomly allocated into 3 groups: control with no feed delay (ND), 24-h feed delay (DAF24), and 36-h feed delay (DAF36). Morphology, gene expression, and in situ hybridization analyses were conducted on the duodenum, jejunum, and ileum at 0, 24, 36, 72, 120, and 168 h after hatch. Statistical analysis was performed using a t test for ND and DAF24 at 24 h. A 2-way ANOVA and Tukey's HSD test (P < 0.05) were used for ND, DAF24, and DAF36 from 36 h. At 24 to 36 h, DAF decreased the ratio of villus height/crypt depth (VH/CD) in the duodenum but increased VH/CD in the ileum due to changes in CD, whereas at 72 h, DAF decreased VH/CD due to a decrease in VH. The mRNA abundance of PepT1 was upregulated, while Muc2 mRNA was downregulated in DAF chicks. Cells expressing Muc2 mRNA were present along the villi and in the crypts. The ratio of the number of goblet cells found in the upper half to the lower half of the villus was greater in DAF chicks than in ND chicks, suggesting that DAF affected the appearance of new goblet cells. The number of Muc2 mRNA-expressing cells in the crypt, however, was generally not affected by DAF. In conclusion, DAF transiently affected small intestinal morphology, upregulated PepT1 mRNA, downregulated Muc2 mRNA, and changed the distribution of goblet cells in the villi. By 168 h, however, these parameters were not different between ND, DAF24, and DAF36 chicks.http://www.sciencedirect.com/science/article/pii/S0032579120305216delayed access to feedpeptide transporter 1mucin 2stem cellgoblet cell
spellingShingle K. Liu
M. Jia
E.A. Wong
Delayed access to feed affects broiler small intestinal morphology and goblet cell ontogeny
Poultry Science
delayed access to feed
peptide transporter 1
mucin 2
stem cell
goblet cell
title Delayed access to feed affects broiler small intestinal morphology and goblet cell ontogeny
title_full Delayed access to feed affects broiler small intestinal morphology and goblet cell ontogeny
title_fullStr Delayed access to feed affects broiler small intestinal morphology and goblet cell ontogeny
title_full_unstemmed Delayed access to feed affects broiler small intestinal morphology and goblet cell ontogeny
title_short Delayed access to feed affects broiler small intestinal morphology and goblet cell ontogeny
title_sort delayed access to feed affects broiler small intestinal morphology and goblet cell ontogeny
topic delayed access to feed
peptide transporter 1
mucin 2
stem cell
goblet cell
url http://www.sciencedirect.com/science/article/pii/S0032579120305216
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AT mjia delayedaccesstofeedaffectsbroilersmallintestinalmorphologyandgobletcellontogeny
AT eawong delayedaccesstofeedaffectsbroilersmallintestinalmorphologyandgobletcellontogeny