PSIII-19 Copper and zinc hydroxychloride co-supplementation reduce the diarrhea frequency of finishing pigs

Abstract The study aimed to investigate the effects of the co-supplementation of copper (Cu) and zinc (Zn) hydroxychloride (CHC and ZHC) minerals on diarrhea frequency of growing and finishing pigs. A total of 256 pigs were distributed into 4 treatments with 8 replicate/treatment. The diets from 70 to 112 days of age (d) were T1: 100 mg/kg CuSO4 + 80 mg/kg ZnO; T2: 150 mg/kg CuSO4 + 80 mg/kg ZnO; T3: 100 mg/kg CHC + 80 mg/kg ZHC; T4: 150 mg/kg CHC + 80 mg/kg ZHC and from 112 to 154 d T1: 90 mg/kg CuSO4 + 70 mg/kg ZnO; T2: 150 mg/kg CuSO4 + 70 mg/kg ZnO; T3: 90 mg/kg CHC + 70 mg/kg ZHC; T4: 150 mg/kg CHC + 70 mg/kg ZHC. Visual analysis of the feces was carried out daily, with scores ranging from 1 to 3 for each pen: 1=solid feces (normal); 2=feces softer than normal (pasty); and 3 = liquid feces (severe diarrhea). The values of frequency were transformed into arc-sine. Data were analyzed using the MIXED procedure of SAS software, according to the block design. The treatment was considered a fixed effect. The effect was considered significant when P < 0.05. From 112 to 154 d, pigs that received the hydroxychloride sources showed a lower diarrhea frequency compared to the pigs fed with CuSO4 and ZnO (P < 0.05). Possibly the reduction of diarrhea in animals with CHC and ZHC was due to the higher bioavailability of these minerals, improving their functions (e.g. Cu on microbial load reduction and Zn on the protection and renewal of intestinal epithelial cells). It can be concluded that the co-supplementation of copper and zinc hydroxychloride sources reduce the diarrhea frequency of finishing pigs.

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Rotavirus VP3 targets MAVS for degradation to inhibit type III interferon expression in intestinal epithelial cells

eLife ◽

10.7554/elife.39494 ◽

2018 ◽

Vol 7 ◽

Cited By ~ 15

Author(s):

Siyuan Ding ◽

Shu Zhu ◽

Lili Ren ◽

Ningguo Feng ◽

Yanhua Song ◽

...

Keyword(s):

Epithelial Cells ◽

Intestinal Epithelial Cells ◽

Mammalian Species ◽

Intestinal Epithelial ◽

Structural Protein ◽

Severe Diarrhea ◽

Multiple Strategies ◽

Type Iii Interferon ◽

Proline Rich Region

Rotaviruses (RVs), a leading cause of severe diarrhea in young children and many mammalian species, have evolved multiple strategies to counteract the host innate immunity, specifically interferon (IFN) signaling through RV non-structural protein 1 (NSP1). However, whether RV structural components also subvert antiviral response remains under-studied. Here, we found that MAVS, critical for the host RNA sensing pathway upstream of IFN induction, is degraded by the RV RNA methyl- and guanylyl-transferase (VP3) in a host-range-restricted manner. Mechanistically, VP3 localizes to the mitochondria and mediates the phosphorylation of a previously unidentified SPLTSS motif within the MAVS proline-rich region, leading to its proteasomal degradation and blockade of IFN-λ production in RV-infected intestinal epithelial cells. Importantly, VP3 inhibition of MAVS activity contributes to enhanced RV replication and to viral pathogenesis in vivo. Collectively, our findings establish RV VP3 as a viral antagonist of MAVS function in mammals and uncover a novel pathogen-mediated inhibitory mechanism of MAVS signaling.

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Three-dimensional organization and functional relationships of endocytotic compartments in pig intestinal epithelial cells

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100123283 ◽

1992 ◽

Vol 50 (1) ◽

pp. 576-577

Author(s):

Julian P. Heath ◽

Buford L. Nichols ◽

László G. Kömüves

Keyword(s):

Electron Microscopy ◽

Epithelial Cells ◽

Intestinal Epithelial Cells ◽

Three Dimensional ◽

Intestinal Epithelial ◽

Cell Surfaces ◽

Basal Surface ◽

Functional Relationships

The newborn pig intestine is adapted for the rapid and efficient absorption of nutrients from colostrum. In enterocytes, colostral proteins are taken up into an apical endocytotic complex of channels that transports them to target organelles or to the basal surface for release into the circulation. The apical endocytotic complex of tubules and vesicles clearly is a major intersection in the routes taken by vesicles trafficking to and from the Golgi, lysosomes, and the apical and basolateral cell surfaces.Jejunal tissues were taken from piglets suckled for up to 6 hours and prepared for electron microscopy and immunocytochemistry as previously described.

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