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Identification of lipopolysaccharide-binding proteins in porcine milk

机译:猪乳中脂多糖结合蛋白的鉴定

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摘要

Septicemia and endotoxemia initiated by bacterial lipopolysaccharide (LPS) are relatively common in suckling and weaned piglets. Maternal milk is a source of both nutrition and immune protection for piglets. Passive transfer of colostral antibodies is necessary for protection of neonatal piglets against diseases, but the concentration of immunoglobulins in milk rapidly declines during the 1st wk of lactation in all mammals. We hypothesized, therefore, that nonimmunoglobulin substances in milk contribute to the innate protection of neonates against septicemia during the suckling period. Using LPS-affinity chromatography for isolation of LPS-binding proteins and liquid chromatography–mass spectrometry for their identification, we identified in porcine milk the following proteins with LPS-binding capacity: lactoferrin, soluble CD14, serum amyloid A, α-S1 casein, β-casein, and κ-casein. For lactoferrin, α-S1 casein, and κ-casein, in vitro pepsin digestion did not inhibit LPS-binding activity, whereas combined digestion with pepsin and pancreatin abolished it. The biologic functions of these LPS-binding proteins and peptides were not determined.
机译:由细菌脂多糖(LPS)引发的败血病和内毒素血症在哺乳和断奶仔猪中相对普遍。母乳是仔猪营养和免疫保护的来源。初乳的被动转移对于保护新生仔猪免受疾病是必不可少的,但是在所有哺乳期的哺乳期第一周中,牛奶中免疫球蛋白的浓度迅速下降。因此,我们假设牛奶中的非免疫球蛋白物质有助于新生儿在哺乳期抵抗败血病。使用LPS亲和色谱法分离LPS结合蛋白,并通过液相色谱-质谱法对其进行鉴定,我们在猪乳中鉴定出以下具有LPS结合能力的蛋白:乳铁蛋白,可溶性CD14,血清淀粉样蛋白A,α-S1酪蛋白, β-酪蛋白和κ-酪蛋白。对于乳铁蛋白,α-S1酪蛋白和κ-酪蛋白,体外胃蛋白酶消化不抑制LPS结合活性,而与胃蛋白酶和胰酶联合消化则废除了它。这些LPS结合蛋白和肽的生物学功能尚未确定。

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