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Changes in Intestinal Morphology, Number of Mucus-producing Cells and Expression of Coronavirus Receptors APN, DPP4, ACE2 and TMPRSS2 in Pigs with Aging

Overview
Journal Vet Res
Publisher Biomed Central
Date 2023 Apr 13
PMID 37055856
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Abstract

Porcine enteric viral infections cause high morbidity and mortality in young piglets (<3 weeks). Later, these rates decrease with age. This age-dependent infectivity remains largely unexplored. This study investigated the changes in intestinal morphology, number of mucus-producing cells and expression level of coronavirus receptors in three age groups of pigs. Villus height and crypt depth increased with age from 3 days to 3 months in duodenum and ileum but not in mid-jejunum, where the villus height decreased from 580 µm at 3 days to 430 µm at 3 months. Enterocyte length-to-width ratio increased from 3 days to 3 months in all intestinal regions. The number of mucus-producing cells increased with age in the intestinal villi and crypts. The Brunner's glands of the duodenum contained the highest concentration of mucus-producing cells. The expression of coronavirus receptor APN was highest in the small intestinal villi at all ages. DPP4 expression slightly decreased over time in jejunum and ileum; it was highest in the ileal villi of 3-day-old piglets (70.2% of cells). ACE2 and TMPRSS2 positive cells increased with age in jejunal and ileal crypts and were particularly dominant in the ileal crypts (> 45% of cells). Except for the expression of DPP4 in the jejunum and ileum of young pigs, the expression pattern of the selected coronavirus receptors was very different and not correlated with the age-dependent susceptibility to viral infections. In contrast, the number of mucus-producing cells increased over time and may play an essential role in protecting enteric mucosae against intestinal viruses.

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References
1.
Li W, Luo R, He Q, van Kuppeveld F, Rottier P, Bosch B . Aminopeptidase N is not required for porcine epidemic diarrhea virus cell entry. Virus Res. 2017; 235:6-13. PMC: 7114539. DOI: 10.1016/j.virusres.2017.03.018. View

2.
Glowacka I, Bertram S, Muller M, Allen P, Soilleux E, Pfefferle S . Evidence that TMPRSS2 activates the severe acute respiratory syndrome coronavirus spike protein for membrane fusion and reduces viral control by the humoral immune response. J Virol. 2011; 85(9):4122-34. PMC: 3126222. DOI: 10.1128/JVI.02232-10. View

3.
Schneeberger K, Roth S, Nieuwenhuis E, Middendorp S . Intestinal epithelial cell polarity defects in disease: lessons from microvillus inclusion disease. Dis Model Mech. 2018; 11(2). PMC: 5894939. DOI: 10.1242/dmm.031088. View

4.
Liu J, Wang H, Lin L, Miao C, Zhang Y, Zhou B . Intestinal barrier damage involved in intestinal microflora changes in fluoride-induced mice. Chemosphere. 2019; 234:409-418. DOI: 10.1016/j.chemosphere.2019.06.080. View

5.
Yamamoto K, Takeshita H, Rakugi H . ACE2, angiotensin 1-7 and skeletal muscle: review in the era of COVID-19. Clin Sci (Lond). 2020; 134(22):3047-3062. PMC: 7687025. DOI: 10.1042/CS20200486. View